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https://www.institutimagine.org/fr/impaired-eif5a-function-causes-mendelian-disorder-partially-rescued-model-systems-spermidine-13002022-01-13T16:33Znever https://www.institutimagine.org/fr/dysregulation-nrg1erbb-pathway-causes-developmental-disorder-gastrointestinal-dysmotility-humans2022-01-13T16:37Znever https://www.institutimagine.org/fr/phenotypic-spectrum-and-transcriptomic-profile-associated-germline-variants-traf7-13022022-01-13T16:41Znever https://www.institutimagine.org/fr/mn1-c-terminal-truncation-syndrome-novel-neurodevelopmental-and-craniofacial-disorder-partial-13032022-02-23T11:01Znever https://www.institutimagine.org/fr/novel-genome-editing-based-approaches-treat-motor-neuron-diseases-promises-and-challenges-13052022-01-20T17:00Znever https://www.institutimagine.org/fr/phosphatase-inhibition-lb-100-enhances-bmn-111-stimulation-bone-growth-13072022-01-28T08:16Znever 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https://www.institutimagine.org/fr/fgfr3-overactivation-brain-responsible-memory-impairments-crouzon-syndrome-mouse-model-14542022-11-28T09:11Znever https://www.institutimagine.org/fr/signaling-pathways-bone-development-and-their-related-skeletal-dysplasia-14552022-11-28T09:09Znever https://www.institutimagine.org/fr/biallelic-variants-slc35b2-cause-novel-chondrodysplasia-hypomyelinating-leukodystrophy-14562022-11-25T21:29Znever https://www.institutimagine.org/fr/ellis-van-creveld-syndrome-clinical-and-molecular-analysis-50-individuals-14572022-11-28T09:13Znever https://www.institutimagine.org/fr/repurposing-multiciliation-gene-regulatory-network-fate-specification-cajal-retzius-neurons-14612023-07-06T10:55Znever https://www.institutimagine.org/fr/multimorphic-mutation-irf4-causes-human-autosomal-dominant-combined-immunodeficiency-14882023-01-30T13:50Znever https://www.institutimagine.org/fr/cajal-retzius-cells-recent-advances-identity-and-function-14982025-04-14T09:54Zyearly 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https://www.institutimagine.org/fr/radiogenomics-diffuse-intrinsic-pontine-gliomas-dipgs-correlation-histological-and-biological-15172023-04-07T09:51Znever https://www.institutimagine.org/fr/ct-and-multimodal-mr-imaging-features-embryonal-tumors-multilayered-rosettes-children-15182023-04-07T09:52Znever https://www.institutimagine.org/fr/cerebral-blood-flow-changes-after-radiation-therapy-identifies-pseudoprogression-diffuse-02023-04-07T09:53Znever https://www.institutimagine.org/fr/multimodal-magnetic-resonance-imaging-treatment-induced-changes-diffuse-infiltrating-pontine2023-04-07T09:54Znever https://www.institutimagine.org/fr/neuroimaging-evidence-brain-abnormalities-mastocytosis-15212023-04-07T09:54Znever https://www.institutimagine.org/fr/arterial-spin-labeling-children-brain-tumor-meta-analysis-15222023-04-07T09:56Znever https://www.institutimagine.org/fr/cerebral-blood-flow-and-acute-episodes-leigh-syndrome-neurometabolic-disorders-15232023-04-07T09:57Znever https://www.institutimagine.org/fr/neuroimaging-manifestations-children-sars-cov-2-infection-multinational-multicentre-collaborative2023-04-07T09:58Znever https://www.institutimagine.org/fr/focal-areas-high-signal-intensity-children-neurofibromatosis-type-1-expected-evolution-mri-15252023-04-07T09:59Znever https://www.institutimagine.org/fr/arterial-spin-labeling-and-central-precocious-puberty-15262023-04-07T12:27Znever https://www.institutimagine.org/fr/high-predictive-value-brain-mri-imaging-primary-mitochondrial-respiratory-chain-deficiency-15272023-04-07T12:29Znever https://www.institutimagine.org/fr/aberrant-survival-hippocampal-cajal-retzius-cells-leads-memory-deficits-gamma-rhythmopathies-and2023-07-06T10:56Znever https://www.institutimagine.org/fr/activation-pi3kaktmtor-pathway-cajal-retzius-cells-leads-their-survival-and-increases2023-09-05T16:01Znever https://www.institutimagine.org/fr/diversity-within-olfactory-sensory-derivatives-revealed-contribution-dbx1-lineages-15492023-09-05T16:06Znever https://www.institutimagine.org/fr/transient-perinatal-metabolic-shifts-determine-neuronal-survival-and-functional-circuit-formation2025-04-14T09:55Zyearly https://www.institutimagine.org/fr/repurposing-multiciliation-gene-regulatory-network-fate-specification-cajal-retzius-neurons-15682023-11-01T08:30Znever https://www.institutimagine.org/fr/repurposing-multiciliation-gene-regulatory-network-fate-specification-cajal-retzius-neurons-15702023-11-02T09:34Znever https://www.institutimagine.org/fr/gpatch11-variants-cause-mis-splicing-and-early-onset-retinal-dystrophy-neurological-impairment-15712023-11-02T09:41Znever https://www.institutimagine.org/fr/identification-greb1l-genetic-determinant-crisscross-heart-mice-showing-torsion-heart-tube-shortage2025-07-30T10:45Zyearly https://www.institutimagine.org/fr/medrxiv-15762023-11-07T09:39Znever https://www.institutimagine.org/fr/tubb4b-variants-specifically-impact-ciliary-function-causing-ciliopathic-spectrum-15782024-09-25T09:10Zyearly https://www.institutimagine.org/fr/tubb4b-variants-specifically-impact-ciliary-function-causing-ciliopathic-spectrum-15872023-11-23T08:12Znever https://www.institutimagine.org/fr/association-missense-variants-vsx2-peculiar-form-congenital-stationary-night-blindness-affecting2023-11-23T08:18Znever https://www.institutimagine.org/fr/impaired-complex-i-repair-causes-recessive-lebers-hereditary-optic-neuropathy-15902023-11-23T08:22Znever https://www.institutimagine.org/fr/yif1b-mutations-cause-post-natal-neurodevelopmental-syndrome-associated-golgi-and-primary-cilium2023-11-23T08:23Znever https://www.institutimagine.org/fr/loss-function-rims2-causes-syndromic-congenital-cone-rod-synaptic-disease-neurodevelopmental-and-02023-11-23T08:23Znever https://www.institutimagine.org/fr/basal-exon-skipping-and-nonsense-associated-altered-splicing-allows-bypassing-complete-cep290-02023-11-23T08:24Znever https://www.institutimagine.org/fr/reply-expanding-neurological-phenotype-dnm1l-related-disorders-15942023-11-23T08:24Znever https://www.institutimagine.org/fr/neurologic-phenotypes-associated-mutations-rtn4ip1-opa10-children-and-young-adults-15952023-11-23T08:25Znever https://www.institutimagine.org/fr/mutations-tubb4b-cause-distinctive-sensorineural-disease-15962023-11-23T08:25Znever https://www.institutimagine.org/fr/mutations-dnm1l-opa1-result-dominant-optic-atrophy-despite-opposite-effects-mitochondrial-fusion2023-11-23T08:25Znever https://www.institutimagine.org/fr/compound-heterozygosity-severe-and-hypomorphic-mutations-cause-non-syndromic-lhon-optic-neuropathy2023-11-23T08:26Znever https://www.institutimagine.org/fr/ncboost-classifies-pathogenic-non-coding-variants-mendelian-diseases-through-supervised-learning2019-12-16T17:51Znever https://www.institutimagine.org/fr/autosomal-recessive-pathogenic-msto1-variants-hereditary-optic-atrophy-16002023-11-27T13:10Znever https://www.institutimagine.org/fr/autosomal-recessive-leber-hereditary-optic-neuropathy-new-neuro-ophthalmo-genetic-paradigm-16012023-11-27T13:10Znever https://www.institutimagine.org/fr/pcdh12-loss-results-premature-neuronal-differentiation-and-impeded-migration-cortical-organoid2023-11-27T13:11Znever https://www.institutimagine.org/fr/neurologic-phenotypes-associated-mutations-rtn4ip1-opa10-children-and-young-adults-16032023-11-27T13:12Znever https://www.institutimagine.org/fr/mutations-tubb4b-cause-distinctive-sensorineural-disease-16042023-11-27T13:13Znever https://www.institutimagine.org/fr/mutations-dnm1l-opa1-result-dominant-optic-atrophy-despite-opposite-effects-mitochondrial-fusion-02023-11-27T13:13Znever https://www.institutimagine.org/fr/compound-heterozygosity-severe-and-hypomorphic-ndufs2-mutations-cause-non-syndromic-lhon-optic-16062023-11-27T13:13Znever https://www.institutimagine.org/fr/recessive-and-dominant-de-novo-itpr1-mutations-cause-gillespie-syndrome-16072023-11-27T13:14Znever https://www.institutimagine.org/fr/identification-greb1l-genetic-determinant-crisscross-heart-mice-showing-torsion-heart-tube-02025-07-30T10:45Zyearly https://www.institutimagine.org/fr/submicroscopic-deletions-13q321-cause-congenital-microcoria-16102023-12-01T11:09Znever https://www.institutimagine.org/fr/mutations-dock7-individuals-epileptic-encephalopathy-and-cortical-blindness-16112023-12-01T11:09Znever 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https://www.institutimagine.org/fr/genome-editing-system-therapeutical-targeting-stem-cells-16682024-03-28T14:03Znever https://www.institutimagine.org/fr/de-novo-monoallelic-reelin-missense-variants-cause-dominant-neuronal-migration-disorders-dominant-02024-07-11T10:52Znever https://www.institutimagine.org/fr/ciliopathy-patient-variants-reveal-organelle-specific-functions-tubb4b-axonemal-microtubules-16892025-07-30T10:45Zyearly https://www.institutimagine.org/fr/four-unique-genetic-variants-three-genes-account-627-early-onset-severe-retinal-dystrophy-chile2025-07-30T10:45Zyearly https://www.institutimagine.org/fr/association-missense-variants-vsx2-peculiar-form-congenital-stationary-night-blindness-affecting-02025-07-30T10:45Zyearly https://www.institutimagine.org/fr/whole-locus-sequencing-identifies-prevalent-founder-deep-intronic-rpgrip1-pathologic-variant-french2025-07-30T10:45Zyearly 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https://www.institutimagine.org/fr/evolutionary-gain-dbx1-expression-drives-subplate-identity-cerebral-cortex-2562020-05-05T19:31Znever https://www.institutimagine.org/fr/somatic-genetic-rescue-mendelian-haematopoietic-diseases-2582020-07-23T09:46Znever https://www.institutimagine.org/fr/pediatric-evans-syndrome-associated-high-frequency-potentially-damaging-variants-immune-genes-2592020-07-23T09:42Znever https://www.institutimagine.org/fr/extracellular-pax6-regulates-tangential-cajal-retzius-cell-migration-developing-mouse-neocortex-2632019-12-04T23:39Znever https://www.institutimagine.org/fr/kremen1-induced-cell-death-regulated-homo-and-heterodimerization-2642020-05-05T19:30Znever https://www.institutimagine.org/fr/cortical-developmental-death-selected-survive-or-fated-die-2652023-02-13T12:53Znever https://www.institutimagine.org/fr/targeted-inactivation-bax-reveals-subtype-specific-mechanism-cajal-retzius-neuron-death-postnatal2019-12-04T22:59Znever https://www.institutimagine.org/fr/enhanced-abventricular-proliferation-compensates-cell-death-embryonic-cerebral-cortex-2672019-12-04T23:15Znever https://www.institutimagine.org/fr/neuronal-fate-specification-dbx1-transcription-factor-linked-evolutionary-acquisition-novel-2682020-05-05T19:27Znever https://www.institutimagine.org/fr/patterning-higher-order-cortical-areas-developmentally-regulated-distribution-cajal-retzius-cells2019-12-04T23:18Znever https://www.institutimagine.org/fr/tangential-migration-glutamatergic-neurons-and-cortical-patterning-during-development-lessons-cajal2019-12-04T23:18Znever https://www.institutimagine.org/fr/migration-speed-cajal-retzius-cells-modulated-vesicular-trafficking-controls-size-higher-order-2712020-05-05T19:27Znever https://www.institutimagine.org/fr/development-and-evolution-cortical-fields-2722019-12-04T23:21Znever https://www.institutimagine.org/fr/tangentially-migrating-transient-glutamatergic-neurons-control-neurogenesis-and-maintenance2019-12-04T23:40Znever https://www.institutimagine.org/fr/dbx1-expressing-cells-are-necessary-survival-mammalian-anterior-neural-and-craniofacial-structures2020-01-09T09:38Znever https://www.institutimagine.org/fr/novel-transient-glutamatergic-population-migrating-pallial-subpallial-boundary-contributes-2752019-12-04T23:22Znever https://www.institutimagine.org/fr/novel-role-dbx1-derived-cajal-retzius-cells-early-regionalization-cerebral-cortical-neuroepithelium2020-05-05T19:28Znever https://www.institutimagine.org/fr/patterning-cerebral-cortex-traveling-morphogens-2772019-12-04T23:23Znever https://www.institutimagine.org/fr/cerebral-cortex-development-progenitors-patterning-neocortical-size-during-evolution-2782019-12-04T23:24Znever https://www.institutimagine.org/fr/multiple-origins-cajal-retzius-cells-borders-developing-pallium-2792019-12-04T23:24Znever https://www.institutimagine.org/fr/kremen1-and-dickkopf1-control-cell-survival-wnt-independent-manner-2802020-05-05T19:28Znever https://www.institutimagine.org/fr/impaired-telomere-integrity-and-rrna-biogenesis-parn-deficient-patients-and-knock-out-models-2822019-12-06T10:21Znever https://www.institutimagine.org/fr/regulator-telomere-length-1-rtel1-mutations-are-associated-heterogeneous-pulmonary-and-extra-2842019-12-06T10:28Znever https://www.institutimagine.org/fr/efl1-mutations-impair-eif6-release-cause-shwachman-diamond-syndrome-2852020-07-23T09:25Znever https://www.institutimagine.org/fr/shared-genetic-predisposition-rheumatoid-arthritis-interstitial-lung-disease-and-familial-pulmonary2019-12-06T10:34Znever https://www.institutimagine.org/fr/cardiac-valve-involvement-adar-related-type-i-interferonopathy-2872021-09-10T09:13Znever https://www.institutimagine.org/fr/anti-mda5-juvenile-idiopathic-inflammatory-myopathy-specific-subgroup-defined-differentially-2882019-12-06T13:43Znever https://www.institutimagine.org/fr/defects-t6a-trna-modification-due-gon7-and-yrdc-mutations-lead-galloway-mowat-syndrome-2892020-10-27T15:21Znever https://www.institutimagine.org/fr/cilia-hereditary-cerebral-anomalies-2912019-12-06T15:06Znever https://www.institutimagine.org/fr/human-ift52-mutations-uncover-novel-role-protein-microtubule-dynamics-and-centrosome-cohesion-2922020-07-23T11:42Znever https://www.institutimagine.org/fr/ciliary-kinesins-beyond-ift-cilium-length-disassembly-cargo-transport-and-signalling-2932019-12-06T15:08Znever https://www.institutimagine.org/fr/copy-number-variation-landscape-congenital-anomalies-kidney-and-urinary-tract-2942019-12-06T15:09Znever https://www.institutimagine.org/fr/loss-function-mutations-kif14-cause-severe-microcephaly-and-kidney-development-defects-humans-and2019-12-06T15:10Znever https://www.institutimagine.org/fr/cell-type-specific-regulation-ciliary-transition-zone-assembly-vertebrates-2962019-12-06T15:10Znever https://www.institutimagine.org/fr/casein-kinase-1e-and-1a-novel-players-polycystic-kidney-disease-and-mechanistic-targets-r-2972019-12-06T15:11Znever https://www.institutimagine.org/fr/functional-characterization-tektin-1-motile-cilia-and-evidence-tekt1-new-candidate-gene-motile-2982019-12-06T15:12Znever https://www.institutimagine.org/fr/human-patient-derived-cellular-model-joubert-syndrome-reveals-ciliary-defects-which-can-be-rescued2019-12-06T15:14Znever https://www.institutimagine.org/fr/targeted-exome-sequencing-identifies-pbx1-involved-monogenic-congenital-anomalies-kidney-and2019-12-06T15:14Znever https://www.institutimagine.org/fr/genetic-drivers-kidney-defects-digeorge-syndrome-3022019-12-06T15:15Znever https://www.institutimagine.org/fr/kif13b-establishes-cav1-enriched-microdomain-ciliary-transition-zone-promote-sonic-hedgehog-3032019-12-06T15:16Znever https://www.institutimagine.org/fr/mutations-mapkbp1-cause-juvenile-or-late-onset-cilia-independent-nephronophthisis-3042019-12-06T15:17Znever https://www.institutimagine.org/fr/dcdc2-mutations-cause-neonatal-sclerosing-cholangitis-3052019-12-06T15:18Znever https://www.institutimagine.org/fr/novel-nek8-mutations-cause-severe-syndromic-renal-cystic-dysplasia-through-yap-dysregulation-3062019-12-06T15:18Znever https://www.institutimagine.org/fr/tmem107-recruits-ciliopathy-proteins-subdomains-ciliary-transition-zone-and-causes-joubert-syndrome2019-12-06T15:19Znever https://www.institutimagine.org/fr/mutations-traf3ip1ift54-reveal-new-role-ift-proteins-microtubule-stabilization-3082019-12-06T15:20Znever https://www.institutimagine.org/fr/phenotypic-similarity-rare-disease-ciliopathy-diagnoses-and-subtyping-3092020-07-23T09:43Znever https://www.institutimagine.org/fr/human-c-terminal-cubn-variants-associate-chronic-proteinuria-and-normal-renal-function-3102020-10-27T15:23Znever https://www.institutimagine.org/fr/mutations-sphingosine-1-phosphate-lyase-cause-nephrosis-ichthyosis-and-adrenal-insufficiency-3112020-10-27T15:18Znever https://www.institutimagine.org/fr/mutations-keops-complex-genes-cause-nephrotic-syndrome-primary-microcephaly-3122020-10-27T15:17Znever https://www.institutimagine.org/fr/endoplasmic-reticulum-retained-podocin-mutants-are-massively-degraded-proteasome-3132020-10-27T15:20Znever https://www.institutimagine.org/fr/lysosomal-targeting-cystinosin-requires-ap-3-3142019-12-06T15:35Znever https://www.institutimagine.org/fr/mutations-tubb4b-cause-distinctive-sensorineural-disease-3162020-07-23T09:41Znever https://www.institutimagine.org/fr/fdxr-mutations-cause-sensorial-neuropathies-and-expand-spectrum-mitochondrial-fe-s-synthesis-3172019-12-06T16:17Znever https://www.institutimagine.org/fr/differentiation-mouse-enteric-nervous-system-progenitor-cells-controlled-endothelin-3-and-requires2019-12-12T14:06Znever https://www.institutimagine.org/fr/mouse-models-hirschsprung-disease-and-other-developmental-disorders-enteric-nervous-system-old-and2019-12-16T17:44Znever https://www.institutimagine.org/fr/ebgene-trial-patient-preselection-outcomes-european-genegraft-ex-vivo-phase-iii-gene-therapy-trial2019-12-10T13:41Znever https://www.institutimagine.org/fr/digitoxin-metabolism-rat-liver-microsomes-3252024-02-14T07:59Znever https://www.institutimagine.org/fr/ebgene-trial-patient-preselection-outcomes-european-genegraft-ex-vivo-phase-iii-gene-therapy-02019-12-10T14:32Znever https://www.institutimagine.org/fr/ebgene-trial-patient-preselection-outcomes-european-genegraft-ex-vivo-phase-iii-gene-therapy-12020-07-23T09:22Znever https://www.institutimagine.org/fr/mutations-perp-cause-dominant-and-recessive-keratoderma-3292020-07-23T09:38Znever https://www.institutimagine.org/fr/ex-vivo-col7a1-correction-recessive-dystrophic-epidermolysis-bullosa-using-crisprcas9-and-homology2019-12-10T14:46Znever https://www.institutimagine.org/fr/apobec-mutation-drives-early-onset-squamous-cell-carcinomas-recessive-dystrophic-epidermolysis-3312019-12-10T14:49Znever https://www.institutimagine.org/fr/intradermal-injection-bone-marrow-mesenchymal-stromal-cells-corrects-recessive-dystrophic-3322019-12-10T14:50Znever https://www.institutimagine.org/fr/diacerein-orphan-drug-development-epidermolysis-bullosa-simplex-phase-23-randomized-placebo-3332019-12-10T14:51Znever https://www.institutimagine.org/fr/intradermal-injection-bone-marrow-mesenchymal-stromal-cells-corrects-recessive-dystrophic-3342019-12-10T15:06Znever https://www.institutimagine.org/fr/selective-substrates-and-inhibitors-kallikrein-related-peptidase-7-klk7-shed-light-klk-proteolytic2019-12-10T14:53Znever https://www.institutimagine.org/fr/targeted-exon-skipping-restores-type-vii-collagen-expression-and-anchoring-fibril-formation-vivo2019-12-10T14:54Znever https://www.institutimagine.org/fr/segmented-filamentous-bacterium-uses-secondary-and-tertiary-lymphoid-tissues-induce-gut-iga-and-3372019-12-10T14:55Znever https://www.institutimagine.org/fr/gene-corrected-fibroblast-therapy-recessive-dystrophic-epidermolysis-bullosa-using-self2019-12-10T14:57Znever https://www.institutimagine.org/fr/klk5-inactivation-reverses-cutaneous-hallmarks-netherton-syndrome-3392019-12-10T14:58Znever https://www.institutimagine.org/fr/transgenic-kallikrein-5-mice-reproduce-major-cutaneous-and-systemic-hallmarks-netherton-syndrome2019-12-10T14:59Znever https://www.institutimagine.org/fr/growth-and-host-interaction-mouse-segmented-filamentous-bacteria-vitro-3412020-07-23T09:29Znever https://www.institutimagine.org/fr/subnuclear-re-localization-sox10-and-p54nrb-correlates-unique-neurological-phenotype-associated-3612019-12-12T14:06Znever https://www.institutimagine.org/fr/striatal-progenitors-derived-human-es-cells-mature-darpp32-neurons-vitro-and-quinolinic-acid-3692019-12-12T09:47Znever https://www.institutimagine.org/fr/intracellular-offspring-released-sfb-filaments-are-flagellated-3712020-07-23T13:02Znever https://www.institutimagine.org/fr/modulation-gut-microbiota-improve-innate-resistance-3722019-12-12T13:23Znever https://www.institutimagine.org/fr/scratching-beneath-surface-linking-skin-pathology-food-allergy-3732019-12-12T13:25Znever https://www.institutimagine.org/fr/recent-advances-celiac-disease-and-refractory-celiac-disease-3742019-12-16T17:42Znever https://www.institutimagine.org/fr/de-novo-mutations-smchd1-cause-bosma-arhinia-microphthalmia-syndrome-and-abrogate-nasal-development2020-07-23T09:20Znever https://www.institutimagine.org/fr/biallelic-ppa2-mutations-cause-sudden-unexpected-cardiac-arrest-infancy-3762019-12-12T14:01Znever https://www.institutimagine.org/fr/mmp21-mutated-human-heterotaxy-and-required-normal-left-right-asymmetry-vertebrates-3772019-12-12T13:59Znever https://www.institutimagine.org/fr/mutations-endothelin-receptor-type-cause-mandibulofacial-dysostosis-alopecia-3782019-12-12T13:55Znever https://www.institutimagine.org/fr/mutations-endothelin-1-cause-recessive-auriculocondylar-syndrome-and-dominant-isolated-question2019-12-12T14:17Znever https://www.institutimagine.org/fr/eftud2-haploinsufficiency-leads-syndromic-oesophageal-atresia-3802019-12-12T14:20Znever https://www.institutimagine.org/fr/germline-deletion-mir-1792-cluster-causes-skeletal-and-growth-defects-humans-3812019-12-12T14:21Znever https://www.institutimagine.org/fr/epistasis-between-ret-and-bbs-mutations-modulates-enteric-innervation-and-causes-syndromic-3822019-12-12T14:22Znever https://www.institutimagine.org/fr/highly-conserved-non-coding-elements-either-side-sox9-associated-pierre-robin-sequence-3832019-12-12T14:26Znever https://www.institutimagine.org/fr/somatic-and-germline-activating-mutations-alk-kinase-receptor-neuroblastoma-3842019-12-12T14:27Znever https://www.institutimagine.org/fr/chronic-inflammation-etiology-disease-across-life-span-3962019-12-13T11:09Znever https://www.institutimagine.org/fr/recurrent-rhinovirus-infections-child-inherited-mda5-deficiency-3982019-12-13T12:46Znever https://www.institutimagine.org/fr/human-snora31-variations-impair-cortical-neuron-intrinsic-immunity-hsv-1-and-underlie-herpes2019-12-13T12:49Znever https://www.institutimagine.org/fr/chronic-mucocutaneous-candidiasis-and-connective-tissue-disorder-humans-impaired-jnk1-dependent-4002019-12-13T12:49Znever https://www.institutimagine.org/fr/candidate-predisposition-variants-kaposi-sarcoma-detected-whole-genome-sequencing-4022019-12-13T13:02Znever https://www.institutimagine.org/fr/human-embryonic-stem-cells-reveal-recurrent-genomic-instability-20q1121-4042019-12-13T13:15Znever https://www.institutimagine.org/fr/human-embryonic-stem-cells-and-genomic-instability-4052019-12-13T13:16Znever https://www.institutimagine.org/fr/recurrent-genomic-instability-chromosome-1q-neural-derivatives-human-embryonic-stem-cells-4062019-12-13T13:17Znever https://www.institutimagine.org/fr/early-transcriptional-changes-linked-naturally-occurring-huntingtons-disease-mutations-neural-4072019-12-13T13:18Znever https://www.institutimagine.org/fr/urine-derived-cells-provide-readily-accessible-cell-type-feeder-free-mrna-reprogramming-4082019-12-13T13:19Znever https://www.institutimagine.org/fr/high-n-glycan-multiplicity-critical-neuronal-adhesion-and-sensitizes-developing-cerebellum-n-4092020-07-23T09:30Znever https://www.institutimagine.org/fr/human-snora31-variations-impair-cortical-neuron-intrinsic-immunity-hsv-1-and-underlie-herpes-02019-12-17T09:51Znever https://www.institutimagine.org/fr/identification-endoglin-variant-associated-hcv-related-liver-fibrosis-progression-next-generation2020-07-23T09:34Znever https://www.institutimagine.org/fr/homozygous-nlrp1-gain-function-mutation-siblings-syndromic-form-recurrent-respiratory-12020-07-23T09:32Znever https://www.institutimagine.org/fr/prevalence-and-risk-factors-latent-tuberculosis-infection-among-healthcare-workers-morocco-4182019-12-16T09:24Znever https://www.institutimagine.org/fr/deep-intronic-splice-mutation-underlies-hyper-ige-syndrome-negative-dominance-4192019-12-17T09:55Znever https://www.institutimagine.org/fr/pleiotropic-effects-parkin-and-lrrk2-leprosy-type-1-reactions-and-parkinsons-disease-4202020-07-23T09:44Znever https://www.institutimagine.org/fr/inherited-ifnar1-deficiency-otherwise-healthy-patients-adverse-reaction-measles-and-yellow-fever2020-07-22T17:15Znever https://www.institutimagine.org/fr/severe-influenza-pneumonitis-children-inherited-tlr3-deficiency-4242019-12-13T14:58Znever https://www.institutimagine.org/fr/effectiveness-and-safety-tri-iodothyronine-analogue-triac-children-and-adults-mct8-deficiency-4262019-12-14T15:41Znever https://www.institutimagine.org/fr/glibenclamide-oral-suspension-suitable-and-effective-patients-neonatal-diabetes-4272019-12-14T15:44Znever https://www.institutimagine.org/fr/effectiveness-and-safety-long-term-treatment-sulfonylureas-patients-neonatal-diabetes-due-kcnj112020-07-23T16:46Znever https://www.institutimagine.org/fr/thyroid-hypoplasia-congenital-hypothyroidism-associated-thyroid-peroxidase-mutations-4302019-12-14T15:43Znever https://www.institutimagine.org/fr/mutations-borealin-cause-thyroid-dysgenesis-4312019-12-14T15:43Znever https://www.institutimagine.org/fr/update-thyroid-developmental-genes-4322019-12-14T15:43Znever https://www.institutimagine.org/fr/sulfonylurea-therapy-benefits-neurological-and-psychomotor-functions-patients-neonatal-diabetes-4332019-12-14T15:44Znever https://www.institutimagine.org/fr/dyrk1a-bac-transgenic-mouse-new-model-thyroid-dysgenesis-down-syndrome-4342019-12-14T15:44Znever https://www.institutimagine.org/fr/rfx6-regulates-insulin-secretion-modulating-ca2-homeostasis-human-b-cells-4352019-12-14T15:45Znever https://www.institutimagine.org/fr/tubb1-mutations-cause-thyroid-dysgenesis-associated-abnormal-platelet-physiology-4362019-12-14T15:41Znever https://www.institutimagine.org/fr/inherited-il-18bp-deficiency-human-fulminant-viral-hepatitis-4382019-12-17T09:57Znever https://www.institutimagine.org/fr/human-inborn-errors-immunity-infection-affecting-cells-other-leukocytes-immune-system-whole2019-12-17T09:58Znever https://www.institutimagine.org/fr/homozygosity-p1104a-underlies-tuberculosis-about-1-patients-cohort-european-ancestry-4402019-12-16T09:22Znever https://www.institutimagine.org/fr/seqtailor-user-friendly-webserver-extraction-dna-or-protein-sequences-next-generation-sequencing2019-12-16T09:00Znever https://www.institutimagine.org/fr/blacklisting-variants-common-private-cohorts-not-public-databases-optimizes-human-exome-analysis2019-12-16T09:27Znever https://www.institutimagine.org/fr/tuberculosis-and-impaired-il-23-dependent-ifn-g-immunity-humans-homozygous-common-missense-variant2019-12-16T09:28Znever https://www.institutimagine.org/fr/human-ifn-g-immunity-mycobacteria-governed-both-il-12-and-il-23-4442019-12-17T09:59Znever https://www.institutimagine.org/fr/popviz-webserver-visualizing-minor-allele-frequencies-and-damage-prediction-scores-human-genetic2019-12-16T09:02Znever https://www.institutimagine.org/fr/rescue-recurrent-deep-intronic-mutation-underlying-cell-type-dependent-quantitative-nemo-deficiency2019-12-19T09:45Znever https://www.institutimagine.org/fr/hcv-associated-liver-fibrosis-and-hsd17b13-4472020-04-15T16:12Znever https://www.institutimagine.org/fr/purely-quantitative-form-partial-recessive-ifn-gr2-deficiency-caused-mutations-initiation-or-second2020-07-22T17:16Znever https://www.institutimagine.org/fr/life-threatening-influenza-pneumonitis-child-inherited-irf9-deficiency-4492019-12-17T10:01Znever https://www.institutimagine.org/fr/disruption-antimycobacterial-circuit-between-dendritic-and-helper-t-cells-human-sppl2a-deficiency2019-12-17T10:02Znever https://www.institutimagine.org/fr/incomplete-penetrance-isolated-congenital-asplenia-humans-mutations-translated-and-untranslated-4512020-04-15T16:09Znever https://www.institutimagine.org/fr/human-cib1-ever1-ever2-complex-governs-keratinocyte-intrinsic-immunity-b-papillomaviruses-4522019-12-17T10:01Znever https://www.institutimagine.org/fr/cdg-online-server-detecting-biologically-closest-disease-causing-genes-and-its-application-primary2019-12-16T09:09Znever https://www.institutimagine.org/fr/variety-alu-mediated-copy-number-variations-can-underlie-il-12rb1-deficiency-4552019-12-19T09:41Znever https://www.institutimagine.org/fr/inherited-p40phox-deficiency-differs-classic-chronic-granulomatous-disease-4562019-12-17T10:04Znever https://www.institutimagine.org/fr/recessive-form-hyper-ige-syndrome-disruption-znf341-dependent-stat3-transcription-and-activity-4572019-12-17T10:04Znever https://www.institutimagine.org/fr/autosomal-dominant-ifn-gr1-deficiency-presenting-both-atypical-mycobacteriosis-and-tuberculosis-bcg2019-12-16T13:45Znever https://www.institutimagine.org/fr/microdeletion-chromosome-8p231-familial-form-severe-buruli-ulcer-4592019-12-16T09:12Znever https://www.institutimagine.org/fr/biallelic-mutations-dna-ligase-1-underlie-spectrum-immune-deficiencies-4622019-12-16T09:28Znever https://www.institutimagine.org/fr/inborn-errors-rna-lariat-metabolism-humans-brainstem-viral-infection-4632019-12-16T09:29Znever https://www.institutimagine.org/fr/eqtl-variant-zxdc-associated-ifn-g-production-following-mycobacterium-tuberculosis-antigen-specific2019-12-16T09:29Znever https://www.institutimagine.org/fr/deciphering-genetic-control-gene-expression-following-mycobacterium-leprae-antigen-stimulation-4652019-12-16T09:30Znever https://www.institutimagine.org/fr/kaposi-sarcoma-oral-malformations-mitral-dysplasia-and-scoliosis-associated-7q34-q363-heterozygous2019-12-16T09:30Znever https://www.institutimagine.org/fr/autosomal-recessive-cardiomyopathy-presenting-acute-myocarditis-4672019-12-16T09:31Znever https://www.institutimagine.org/fr/genome-wide-association-study-identifies-lncrna-risk-factor-pathological-inflammatory-responses-4682019-12-16T09:31Znever https://www.institutimagine.org/fr/population-pharmacokinetic-modeling-tenofovir-genital-tract-male-hiv-infected-patients-4692019-12-16T09:31Znever https://www.institutimagine.org/fr/new-3p25-locus-associated-liver-fibrosis-progression-human-immunodeficiency-virushepatitis-c-virus2019-12-16T09:32Znever https://www.institutimagine.org/fr/exome-and-genome-sequencing-inborn-errors-immunity-4712019-12-16T09:32Znever https://www.institutimagine.org/fr/coding-variants-are-associated-high-risk-hepatocellular-carcinoma-occurrence-patients-hcv-or-hbv2019-12-16T09:33Znever https://www.institutimagine.org/fr/whole-exome-sequencing-analyze-population-structure-parental-inbreeding-and-familial-linkage-4732019-12-16T09:33Znever https://www.institutimagine.org/fr/pauci-and-multibacillary-leprosy-two-distinct-genetically-neglected-diseases-4742019-12-16T09:34Znever https://www.institutimagine.org/fr/loss-b-cells-patients-heterozygous-mutations-ikaros-4752019-12-16T09:35Znever https://www.institutimagine.org/fr/missense-lrrk2-variant-risk-factor-excessive-inflammatory-responses-leprosy-4762019-12-16T09:35Znever https://www.institutimagine.org/fr/major-loci-chromosomes-8q-and-3q-control-interferon-g-production-triggered-bacillus-calmette-guerin2019-12-16T09:35Znever https://www.institutimagine.org/fr/impact-il28b-apoh-and-itpa-polymorphisms-efficacy-and-safety-tvr-or-boc-based-triple-therapy-4782019-12-16T09:36Znever https://www.institutimagine.org/fr/eqtl-variant-zxdc-associated-ifn-g-production-following-mycobacterium-tuberculosis-antigen-02019-12-17T10:06Znever https://www.institutimagine.org/fr/genetics-human-susceptibility-active-and-latent-tuberculosis-present-knowledge-and-future-4832019-12-17T10:07Znever https://www.institutimagine.org/fr/human-genetics-infectious-diseases-unique-insights-immunological-redundancy-4842019-12-17T10:07Znever https://www.institutimagine.org/fr/irf4-haploinsufficiency-family-whipples-disease-4852019-12-17T10:08Znever https://www.institutimagine.org/fr/novel-genetic-architecture-infectious-diseases-4862019-12-17T10:09Znever https://www.institutimagine.org/fr/mn1-c-terminal-truncation-syndrome-novel-neurodevelopmental-and-craniofacial-disorder-partial-4872019-12-19T09:47Znever https://www.institutimagine.org/fr/mariner-defective-myosin-viia-zebrafish-model-human-hereditary-deafness-4892019-12-19T09:39Znever https://www.institutimagine.org/fr/genomic-region-encompassing-newly-identified-exon-provides-enhancing-activity-sufficient-normal-4902019-12-17T13:58Znever https://www.institutimagine.org/fr/chronic-intestinal-pseudo-obstruction-and-lymphoproliferative-syndrome-novel-phenotype-associated2019-12-23T15:18Znever https://www.institutimagine.org/fr/human-ripk1-deficiency-causes-combined-immunodeficiency-and-inflammatory-bowel-diseases-5002019-12-23T15:17Znever https://www.institutimagine.org/fr/dynamic-formation-microvillus-inclusions-during-enterocyte-differentiation-deficient-intestinal-5022019-12-23T15:17Znever https://www.institutimagine.org/fr/gene-transfer-hematopoietic-stem-cells-reduces-hlh-manifestations-murine-model-munc13-4-deficiency2020-07-22T17:08Znever https://www.institutimagine.org/fr/hemophagocytic-syndrome-primary-forms-and-predisposing-conditions-5042019-12-23T15:15Znever https://www.institutimagine.org/fr/rab27a-duplication-several-cases-griscelli-syndrome-type-2-explanation-cases-lacking-genetic-5052019-12-23T15:15Znever https://www.institutimagine.org/fr/therapeutic-effect-jak12-blockade-manifestations-hemophagocytic-lymphohistiocytosis-mice-5062019-12-23T15:14Znever https://www.institutimagine.org/fr/kinesin-1-new-actor-involved-platelet-secretion-and-thrombus-stability-5072019-12-23T15:13Znever https://www.institutimagine.org/fr/kinesin-1-controls-mast-cell-degranulation-and-anaphylaxis-through-pi3k-dependent-recruitment-5082019-12-23T15:33Znever https://www.institutimagine.org/fr/terminal-transport-lytic-granules-immune-synapse-mediated-kinesin-1slp3rab27a-complex-5092019-12-23T15:32Znever https://www.institutimagine.org/fr/distinct-severity-hlh-both-human-and-murine-mutants-complete-loss-cytotoxic-effector-prf1-rab27a2019-12-23T15:32Znever https://www.institutimagine.org/fr/graded-defects-cytotoxicity-determine-severity-hemophagocytic-lymphohistiocytosis-humans-and-mice2019-12-23T15:22Znever https://www.institutimagine.org/fr/lyst-controls-biogenesis-endosomal-compartment-required-secretory-lysosome-function-5122019-12-23T15:31Znever https://www.institutimagine.org/fr/cytotoxic-granule-secretion-lymphocytes-and-its-link-immune-homeostasis-5132019-12-23T15:30Znever https://www.institutimagine.org/fr/polygenic-mutations-cytotoxicity-pathway-increase-susceptibility-develop-hlh-immunopathology-mice2019-12-23T15:30Znever https://www.institutimagine.org/fr/novel-immunoregulatory-role-nk-cell-cytotoxicity-protection-hlh-immunopathology-mice-5152019-12-23T15:29Znever https://www.institutimagine.org/fr/germline-havcr2-mutations-altering-tim-3-characterize-subcutaneous-panniculitis-t-cell-lymphomas2019-12-23T15:29Znever https://www.institutimagine.org/fr/gata-factor-transcriptional-activity-insights-genome-wide-binding-profiles-5182020-07-23T09:27Znever https://www.institutimagine.org/fr/extensive-multilineage-analysis-patients-mixed-chimerism-after-allogeneic-transplantation-sickle2019-12-23T15:28Znever https://www.institutimagine.org/fr/lentiviral-and-genome-editing-strategies-treatment-b-hemoglobinopathies-5202019-12-23T15:41Znever https://www.institutimagine.org/fr/gene-therapy-hemoglobinopathies-progress-and-future-challenges-5212019-12-23T15:30Znever https://www.institutimagine.org/fr/gene-therapy-targeting-haematopoietic-stem-cells-inherited-diseases-progress-and-challenges-5222020-07-23T09:28Znever https://www.institutimagine.org/fr/optimization-crisprcas9-delivery-human-hematopoietic-stem-and-progenitor-cells-therapeutic-genomic2019-12-23T15:30Znever https://www.institutimagine.org/fr/optimized-lentiviral-vector-efficiently-corrects-human-sickle-cell-disease-phenotype-5242019-12-23T15:32Znever https://www.institutimagine.org/fr/induction-fetal-hemoglobin-synthesis-crisprcas9-mediated-editing-human-b-globin-locus-5252019-12-23T15:44Znever https://www.institutimagine.org/fr/concise-review-epigenetic-regulation-hematopoiesis-biological-insights-and-therapeutic-applications2019-12-23T15:36Znever https://www.institutimagine.org/fr/transcriptional-epigenetic-and-retroviral-signatures-identify-regulatory-regions-involved-5282019-12-23T15:36Znever https://www.institutimagine.org/fr/dynamic-transcriptional-and-epigenetic-regulation-human-epidermal-keratinocyte-differentiation-5292019-12-23T15:37Znever https://www.institutimagine.org/fr/genome-wide-definition-promoter-and-enhancer-usage-during-neural-induction-human-embryonic-stem-5302019-12-23T15:51Znever https://www.institutimagine.org/fr/nup153-and-nup98-bind-hiv-1-core-and-contribute-early-steps-hiv-1-replication-5312019-12-23T15:52Znever https://www.institutimagine.org/fr/deletion-ltr-enhancerpromoter-has-no-impact-integration-profile-mlv-vectors-human-hematopoietic-5322019-12-23T15:52Znever https://www.institutimagine.org/fr/lentiviral-vector-integration-human-genome-induces-alternative-splicing-and-generates-aberrant-5332019-12-23T15:53Znever https://www.institutimagine.org/fr/gata1-hs2-enhancer-allows-persistent-and-position-independent-expression-b-globin-transgene-5342019-12-23T15:57Znever https://www.institutimagine.org/fr/role-gata-1fog-1nurd-pathway-expression-human-beta-globin-genes-5352019-12-23T15:53Znever https://www.institutimagine.org/fr/fog1-requires-nurd-promote-hematopoiesis-and-maintain-lineage-fidelity-within-megakaryocytic-5362019-12-23T15:54Znever https://www.institutimagine.org/fr/nurd-mediates-activating-and-repressive-functions-gata-1-and-fog-1-during-blood-development-5372019-12-23T15:54Znever https://www.institutimagine.org/fr/transcription-factor-binding-sites-are-genetic-determinants-retroviral-integration-human-genome-5382019-12-23T15:54Znever https://www.institutimagine.org/fr/vivo-selection-genetically-modified-erythroblastic-progenitors-leads-long-term-correction-beta-5392019-12-23T15:55Znever https://www.institutimagine.org/fr/homeodomain-transcription-factor-prep1-pknox1-required-hematopoietic-stem-and-progenitor-cell-5402019-12-23T15:55Znever https://www.institutimagine.org/fr/hot-spots-retroviral-integration-human-cd34-hematopoietic-cells-5412019-12-23T15:55Znever https://www.institutimagine.org/fr/hypomorphic-mutation-tale-gene-prep1-pknox1-causes-major-reduction-pbx-and-meis-proteins-and-5422019-12-23T15:55Znever https://www.institutimagine.org/fr/phosphorylation-synapsin-i-camp-dependent-protein-kinase-controls-synaptic-vesicle-dynamics-5432019-12-23T15:56Znever https://www.institutimagine.org/fr/activity-dependent-death-transient-cajal-retzius-neurons-required-functional-cortical-wiring-5712020-05-05T19:31Znever https://www.institutimagine.org/fr/paics-deficiency-new-defect-de-novo-purine-synthesis-resulting-multiple-congenital-anomalies-and2020-01-08T10:24Znever https://www.institutimagine.org/fr/nontoxic-transduction-enhancer-enables-highly-efficient-lentiviral-transduction-primary-murine-t2020-07-22T17:00Znever https://www.institutimagine.org/fr/plerixafor-enables-safe-rapid-efficient-mobilization-hematopoietic-stem-cells-sickle-cell-disease-02020-07-23T09:45Znever https://www.institutimagine.org/fr/generation-adult-human-t-cell-progenitors-immunotherapeutic-applications-5812021-04-28T15:18Znever https://www.institutimagine.org/fr/gene-therapy-x-linked-severe-combined-immunodeficiency-where-do-we-stand-5822020-07-22T17:02Znever https://www.institutimagine.org/fr/gene-therapy-hematopoietic-stem-cells-diseased-bone-marrows-point-view-5832020-07-22T17:03Znever https://www.institutimagine.org/fr/gene-corrected-human-munc13-4-deficient-cd8-t-cells-can-efficiently-restrict-ebv-driven-5842020-07-22T17:03Znever https://www.institutimagine.org/fr/loss-arhgef1-causes-human-primary-antibody-deficiency-5852020-07-22T17:04Znever https://www.institutimagine.org/fr/mutations-adaptor-binding-domain-and-associated-linker-region-p110d-cause-activated-pi3k-d-syndrome2020-07-22T17:05Znever https://www.institutimagine.org/fr/clinical-and-immunologic-phenotype-associated-activated-phosphoinositide-3-kinase-d-syndrome-2-5872021-04-30T17:07Znever https://www.institutimagine.org/fr/human-immunodeficiency-caused-mutations-pik3r1-gene-5882020-07-22T17:06Znever https://www.institutimagine.org/fr/x-linked-primary-immunodeficiency-associated-hemizygous-mutations-moesin-msn-gene-5892020-07-22T17:07Znever https://www.institutimagine.org/fr/gene-transfer-hematopoietic-stem-cells-reduces-hlh-manifestations-murine-model-munc13-4-02020-01-10T12:14Znever https://www.institutimagine.org/fr/ak2-deficiency-compromises-mitochondrial-energy-metabolism-required-differentiation-human2020-07-22T17:08Znever https://www.institutimagine.org/fr/human-t-lymphoid-progenitors-generated-feeder-cell-free-delta-4-culture-system-promote-t-cell-5922020-07-22T17:07Znever https://www.institutimagine.org/fr/loss-sphingolipid-desaturase-degs1-causes-hypomyelinating-leukodystrophy-6002020-01-14T10:48Znever https://www.institutimagine.org/fr/biallelic-mutations-neurofascin-cause-neurodevelopmental-impairment-and-peripheral-demyelination2020-01-14T10:50Znever https://www.institutimagine.org/fr/de-novo-mutation-screening-childhood-onset-cerebellar-atrophy-identifies-gain-function-mutations2020-01-14T10:50Znever https://www.institutimagine.org/fr/utility-whole-exome-sequencing-early-diagnosis-pediatric-onset-cerebellar-atrophy-associated-6052020-01-14T10:51Znever https://www.institutimagine.org/fr/innate-immune-cells-major-protagonists-sickle-cell-disease-pathophysiology-6072020-07-23T13:09Znever https://www.institutimagine.org/fr/novel-highly-potent-and-selective-phosphodiesterase-9-inhibitor-treatment-sickle-cell-disease-6082020-07-23T13:08Znever https://www.institutimagine.org/fr/enhanced-renewal-erythroid-progenitors-myelodysplastic-anemia-peripheral-serotonin-6092020-07-23T13:08Znever https://www.institutimagine.org/fr/new-publication-612019-10-30T17:02Znever https://www.institutimagine.org/fr/fas-and-ras-related-apoptosis-defects-autoimmunity-leukemia-6102020-01-21T13:46Znever https://www.institutimagine.org/fr/onset-autoimmune-lymphoproliferative-syndrome-alps-humans-consequence-genetic-defect-accumulation2020-01-21T13:44Znever https://www.institutimagine.org/fr/autoimmune-lymphoproliferative-syndrome-somatic-fas-mutations-6122020-01-21T13:48Znever https://www.institutimagine.org/fr/mutations-fas-associated-human-lymphoproliferative-syndrome-and-autoimmunity-6132020-01-21T12:39Znever https://www.institutimagine.org/fr/inactivation-fas-gene-alu-insertion-retrotransposition-intron-causing-splicing-variation-and-6142020-01-21T12:41Znever https://www.institutimagine.org/fr/inherited-and-somatic-cd3zeta-mutations-patient-t-cell-deficiency-6152020-01-21T12:42Znever https://www.institutimagine.org/fr/fas-l-il-10-and-double-negative-cd4-cd8-tcr-alphabeta-t-cells-are-reliable-markers-autoimmune-6162020-01-21T12:44Znever https://www.institutimagine.org/fr/reduced-expression-foxp3-and-regulatory-t-cell-function-severe-forms-early-onset-autoimmune-6172020-01-21T12:45Znever https://www.institutimagine.org/fr/survey-90-patients-autoimmune-lymphoproliferative-syndrome-related-tnfrsf6-mutation-6182020-01-21T12:47Znever https://www.institutimagine.org/fr/autoimmune-lymphoproliferative-syndrome-caused-homozygous-null-fas-ligand-faslg-mutation-6192020-01-21T13:37Znever https://www.institutimagine.org/fr/diagnosis-autoimmune-lymphoproliferative-syndrome-caused-fas-deficiency-adults-6202020-01-21T12:49Znever https://www.institutimagine.org/fr/ras-associated-lymphoproliferative-disease-evolves-severe-juvenile-myelo-monocytic-leukemia-6212020-01-21T13:38Znever https://www.institutimagine.org/fr/defective-anti-polysaccharide-response-and-splenic-marginal-zone-disorganization-alps-patients-6222020-01-21T12:51Znever https://www.institutimagine.org/fr/inherited-sting-activating-mutation-underlies-familial-inflammatory-syndrome-lupus-manifestations2020-01-21T13:43Znever https://www.institutimagine.org/fr/lrba-deficiency-autoimmunity-and-early-onset-chronic-erosive-polyarthritis-6242020-01-21T12:53Znever https://www.institutimagine.org/fr/efficacy-janus-kinase-12-inhibitor-ruxolitinib-treatment-vasculopathy-associated-tmem173-activating2020-01-21T12:54Znever https://www.institutimagine.org/fr/evolution-disease-activity-and-biomarkers-and-rapamycin-28-patients-autoimmune-lymphoproliferative2020-01-21T13:55Znever https://www.institutimagine.org/fr/intrinsic-antiproliferative-activity-innate-sensor-sting-t-lymphocytes-6272020-01-21T13:14Znever https://www.institutimagine.org/fr/whats-alps-6282020-01-21T13:15Znever https://www.institutimagine.org/fr/pediatric-onset-evans-syndrome-heterogeneous-presentation-and-high-frequency-monogenic-disorders2020-01-21T13:16Znever https://www.institutimagine.org/fr/autoimmune-lymphoproliferative-syndrome-fas-patients-have-abnormal-regulatory-t-cell-treg-phenotype2020-01-21T13:17Znever https://www.institutimagine.org/fr/autoimmune-lymphoproliferative-syndrome-defective-fas-or-fas-ligand-functions-6312020-01-21T13:18Znever https://www.institutimagine.org/fr/severe-combined-immunodeficiency-stimulator-interferon-genes-sting-v154mwild-type-mice-6322020-01-21T13:19Znever https://www.institutimagine.org/fr/comment-monogenic-mimics-behcets-disease-young-6342020-01-21T13:21Znever https://www.institutimagine.org/fr/fatal-hypogammaglobulinemia-3-years-after-rituximab-patient-immune-thrombocytopenia-underlying-6352020-01-21T13:22Znever https://www.institutimagine.org/fr/comprehensive-map-monocyte-derived-dendritic-cell-transcriptional-network-engaged-upon-innate-6372020-01-23T18:52Znever https://www.institutimagine.org/fr/neuromyelitis-optica-patients-increased-interferon-alpha-concentrations-6402021-09-10T09:45Znever https://www.institutimagine.org/fr/reverse-transcriptase-inhibitors-aicardi-goutieres-syndrome-6412021-09-10T09:13Znever https://www.institutimagine.org/fr/type-i-interferon-mediated-autoinflammation-due-dnase-ii-deficiency-6422021-09-10T09:00Znever https://www.institutimagine.org/fr/detection-interferon-alpha-protein-reveals-differential-levels-and-cellular-sources-disease-6432021-09-10T09:13Znever https://www.institutimagine.org/fr/contribution-rare-and-predicted-pathogenic-gene-variants-childhood-onset-lupus-large-genetic-panel2021-09-10T09:45Znever https://www.institutimagine.org/fr/opposite-modulation-rac1-mutations-trio-associated-distinct-domain-specific-neurodevelopmental-6682020-07-23T09:41Znever https://www.institutimagine.org/fr/whole-exome-sequence-analysis-highlights-role-unmasked-recessive-mutations-copy-number-variants-6692020-03-03T16:17Znever https://www.institutimagine.org/fr/ampa-receptor-specific-biogenesis-complexes-control-synaptic-transmission-and-intellectual-ability2020-03-03T16:18Znever https://www.institutimagine.org/fr/regulation-human-cerebral-cortical-development-exoc7-and-exoc8-components-exocyst-complex-and-roles2020-03-03T16:32Znever https://www.institutimagine.org/fr/expanding-genetic-and-phenotypic-relevance-kcnb1-variants-developmental-and-epileptic-6742020-03-04T10:34Znever https://www.institutimagine.org/fr/anatomical-and-functional-abnormalities-mri-kabuki-syndrome-6752021-02-08T09:45Znever https://www.institutimagine.org/fr/posterior-fossa-arachnoid-cyst-pediatric-population-associated-social-perception-and-rest-cerebral2025-03-24T11:12Zyearly https://www.institutimagine.org/fr/central-nervous-system-complications-adult-cystinosis-patients-6772021-02-08T09:51Znever https://www.institutimagine.org/fr/tuning-eye-gaze-perception-transitory-sts-inhibition-6782021-02-08T09:42Znever https://www.institutimagine.org/fr/kcnt1-epilepsy-migrating-focal-seizures-shows-temporal-sequence-poor-outcome-high-mortality-and-6822020-03-09T13:04Znever https://www.institutimagine.org/fr/gamma-aminobutyric-acidergic-transmission-underlies-interictal-epileptogenicity-pediatric-focal-6832020-03-09T13:04Znever https://www.institutimagine.org/fr/fenfluramine-treatment-resistant-seizures-patients-dravet-syndrome-receiving-stiripentol-inclusive2020-03-09T13:03Znever https://www.institutimagine.org/fr/intestinal-cell-kinase-and-juvenile-myoclonic-epilepsy-6852020-03-09T13:03Znever https://www.institutimagine.org/fr/trpv4-mediates-hypotonic-inhibition-central-osmosensory-neurons-taurine-gliotransmission-6862020-03-09T13:00Znever https://www.institutimagine.org/fr/trpv4-mediates-hypotonic-inhibition-central-osmosensory-neurons-taurine-gliotransmission-6872020-03-09T13:02Znever https://www.institutimagine.org/fr/depdc5-knockdown-causes-mtor-dependent-motor-hyperactivity-zebrafish-6882020-03-09T13:05Znever https://www.institutimagine.org/fr/most-prevalent-genetic-cause-als-ftd-c9orf72-synergizes-toxicity-atxn2-intermediate-polyglutamine2020-03-09T13:06Znever https://www.institutimagine.org/fr/cerebral-blood-flow-changes-after-radiation-therapy-identifies-pseudoprogression-diffuse-intrinsic2021-02-08T09:43Znever https://www.institutimagine.org/fr/extracting-3d-cell-parameters-dense-tissue-environments-application-development-mouse-heart-7042020-03-26T21:15Znever https://www.institutimagine.org/fr/regionalization-mouse-visceral-endoderm-blastocyst-transforms-egg-cylinder-7152020-03-26T21:19Znever https://www.institutimagine.org/fr/right-ventricular-myocardium-derives-anterior-heart-field-7202020-03-26T21:20Znever https://www.institutimagine.org/fr/mutations-complex-i-assembly-factor-tmem126b-result-muscle-weakness-and-isolated-complex-i-7242020-04-01T14:22Znever https://www.institutimagine.org/fr/recessive-mutations-trmt10c-cause-defects-mitochondrial-rna-processing-and-multiple-respiratory-7252020-04-01T14:21Znever https://www.institutimagine.org/fr/biallelic-ppa2-mutations-cause-sudden-unexpected-cardiac-arrest-infancy-7262020-04-01T14:20Znever https://www.institutimagine.org/fr/high-incidence-and-variable-clinical-outcome-cardiac-hypertrophy-due-acad9-mutations-childhood-7272020-04-01T14:19Znever https://www.institutimagine.org/fr/no-correlation-between-mtdna-amount-and-methylation-levels-cpg-island-exon-2-wild-type-and-mutant2020-04-01T14:19Znever https://www.institutimagine.org/fr/fdxr-mutations-cause-sensorial-neuropathies-and-expand-spectrum-mitochondrial-fe-s-synthesis-7292020-04-01T14:18Znever https://www.institutimagine.org/fr/genetic-diagnosis-mendelian-disorders-rna-sequencing-7302020-03-30T14:58Znever https://www.institutimagine.org/fr/biallelic-mutations-lipt2-cause-mitochondrial-lipoylation-defect-associated-severe-neonatal-7312020-04-01T14:16Znever https://www.institutimagine.org/fr/mutations-mdh2-encoding-krebs-cycle-enzyme-cause-early-onset-severe-encephalopathy-7322020-04-01T14:15Znever https://www.institutimagine.org/fr/segregation-mitochondrial-dna-mutations-human-placenta-implication-prenatal-diagnosis-mtdna-7332020-04-01T14:14Znever https://www.institutimagine.org/fr/inhibition-mitochondrial-translation-fibroblasts-patient-expressing-kars-ppro228leu-variant-and-7342020-04-01T14:13Znever https://www.institutimagine.org/fr/ndufb8-mutations-cause-mitochondrial-complex-i-deficiency-individuals-leigh-encephalomyopathy-7352020-04-01T14:13Znever https://www.institutimagine.org/fr/biallelic-mutations-mrps34-lead-instability-small-mitoribosomal-subunit-and-leigh-syndrome-7362020-04-01T14:12Znever https://www.institutimagine.org/fr/bi-allelic-mutations-mitochondrial-ribosomal-protein-mrps2-cause-sensorineural-hearing-loss-7372020-04-01T14:11Znever https://www.institutimagine.org/fr/mitochondrial-double-stranded-rna-triggers-antiviral-signalling-humans-7382020-04-01T14:09Znever https://www.institutimagine.org/fr/impaired-transferrin-receptor-palmitoylation-and-recycling-neurodegeneration-brain-iron2020-04-01T14:09Znever https://www.institutimagine.org/fr/mutations-mrps28-gene-encoding-small-mitoribosomal-subunit-protein-bs1m-patient-intrauterine-growth2020-04-01T14:07Znever https://www.institutimagine.org/fr/clinical-neuroimaging-and-biochemical-findings-patients-and-patient-fibroblasts-expressing-ten2020-04-01T14:05Znever https://www.institutimagine.org/fr/efficacy-ruxolitinib-subcutaneous-panniculitis-t-cell-lymphoma-and-hemophagocytic-7462020-04-15T12:18Znever https://www.institutimagine.org/fr/kinesin-1-regulates-antigen-cross-presentation-through-scission-tubulations-early-endosomes-7472020-07-22T16:47Znever https://www.institutimagine.org/fr/clonal-tracking-gene-therapy-patients-reveals-diversity-human-hematopoietic-differentiation2020-07-10T07:51Znever https://www.institutimagine.org/fr/gain-function-rac2-mutation-associated-bone-marrow-hypoplasia-and-autosomal-dominant-form-severe2020-04-21T08:31Znever https://www.institutimagine.org/fr/neural-basis-interindividual-variability-social-perception-typically-developing-children-and-7552025-03-24T11:12Zyearly https://www.institutimagine.org/fr/homozygous-nlrp1-gain-function-mutation-siblings-syndromic-form-recurrent-respiratory-02020-07-23T09:31Znever https://www.institutimagine.org/fr/developmental-cell-death-regulates-lineage-related-interneuron-oligodendroglia-functional-clusters2020-05-05T19:25Znever https://www.institutimagine.org/fr/reallocation-olfactory-cajal-retzius-cells-shapes-neocortex-architecture-7662020-05-05T19:23Znever https://www.institutimagine.org/fr/recurrent-rttn-mutation-leading-severe-microcephaly-polymicrogyria-and-growth-restriction-7672020-05-05T20:29Znever https://www.institutimagine.org/fr/mutations-tbr1-gene-leads-cortical-malformations-and-intellectual-disability-7682020-05-05T20:29Znever https://www.institutimagine.org/fr/further-refinement-col4a1-and-col4a2-related-cortical-malformations-7692020-05-05T20:26Znever https://www.institutimagine.org/fr/mutations-mast1-cause-mega-corpus-callosum-syndrome-cerebellar-hypoplasia-and-cortical2020-05-05T20:27Znever https://www.institutimagine.org/fr/delineating-foxg1-syndrome-congenital-microcephaly-hyperkinetic-encephalopathy-7712020-05-05T20:29Znever https://www.institutimagine.org/fr/heterogeneous-clinical-phenotypes-and-cerebral-malformations-reflected-rotatin-cellular-dynamics2020-05-05T20:27Znever https://www.institutimagine.org/fr/inherited-human-ifn-g-deficiency-underlies-mycobacterial-disease-7772020-07-10T07:51Znever https://www.institutimagine.org/fr/bi-allelic-variations-smo-humans-cause-broad-spectrum-developmental-anomalies-due-abnormal-hedgehog2022-01-13T16:50Znever https://www.institutimagine.org/fr/new-publication-7812020-05-18T15:37Znever https://www.institutimagine.org/fr/common-homozygosity-predicted-loss-function-variants-reveals-both-redundant-and-advantageous2021-04-29T05:13Znever https://www.institutimagine.org/fr/editing-g-globin-repressor-binding-site-restores-fetal-hemoglobin-synthesis-and-corrects-sickle2020-06-04T21:41Znever https://www.institutimagine.org/fr/dysgammaglobulinemia-autosomal-dominant-activation-induced-cytidine-deaminase-deficiency-unraveling2020-07-10T07:50Znever https://www.institutimagine.org/fr/clinician-friendly-data-warehouse-oriented-toward-narrative-reports-dr-warehouse-8182020-07-23T09:10Znever https://www.institutimagine.org/fr/next-generation-phenotyping-using-narrative-reports-rare-disease-clinical-data-warehouse-8192020-06-30T21:10Znever https://www.institutimagine.org/fr/finding-patients-using-similarity-measures-rare-diseases-oriented-clinical-data-warehouse-dr-8202020-06-30T21:13Znever https://www.institutimagine.org/fr/impaired-type-i-interferon-activity-and-inflammatory-responses-severe-covid-19-patients-8272020-09-28T14:44Znever https://www.institutimagine.org/fr/loss-function-rims2-causes-syndromic-congenital-cone-rod-synaptic-disease-neurodevelopmental-and2020-07-17T16:28Znever https://www.institutimagine.org/fr/def6-deficiency-mendelian-susceptibility-ebv-infection-lymphoma-and-autoimmunity-8312020-07-21T14:41Znever https://www.institutimagine.org/fr/impaired-lymphocyte-function-and-differentiation-ctps1-deficient-patients-result-hypomorphic-8322020-07-21T14:42Znever https://www.institutimagine.org/fr/primary-immunodeficiencies-reveal-molecular-requirements-effective-host-defense-against-ebv-8332020-07-21T14:42Znever https://www.institutimagine.org/fr/concomitant-pik3cd-and-tnfrsf9-deficiencies-cause-chronic-active-epstein-barr-virus-infection-t-8342020-07-21T14:43Znever https://www.institutimagine.org/fr/signaling-pathways-involved-t-cell-mediated-immunity-against-epstein-barr-virus-lessons-genetic-8352020-07-21T14:44Znever https://www.institutimagine.org/fr/fgfr3-positive-regulator-osteoblast-expansion-and-differentiation-during-zebrafish-skull-vault-8372020-07-23T12:53Znever https://www.institutimagine.org/fr/animal-models-craniosynostosis-8382020-07-23T11:51Znever https://www.institutimagine.org/fr/constitutively-active-fgfr3-disrupts-primary-cilium-length-and-ift20-trafficking-various2020-07-23T11:53Znever https://www.institutimagine.org/fr/achondroplasia-development-pathogenesis-and-therapy-8402020-07-23T11:54Znever https://www.institutimagine.org/fr/homozygous-loss-function-mutations-ccdc134-are-responsible-severe-form-osteogenesis-imperfecta-8412020-07-23T11:55Znever https://www.institutimagine.org/fr/biallelic-variants-kynu-cause-multisystemic-syndrome-hand-hyperphalangism-8422022-11-25T21:37Znever https://www.institutimagine.org/fr/absence-gp130-cytokine-receptor-signaling-causes-extended-stuve-wiedemann-syndrome-8432020-07-23T11:58Znever https://www.institutimagine.org/fr/dendritic-cell-maturation-regulates-tspan7-function-hiv-1-transfer-cd4-t-lymphocytes-8442020-07-23T12:52Znever https://www.institutimagine.org/fr/tspan7-effector-actin-nucleation-required-dendritic-cell-mediated-transfer-hiv-1-t-cells-8452020-07-23T12:54Znever https://www.institutimagine.org/fr/actin-nucleation-and-hiv-transfer-dendritic-cells-t-lymphocytes-8462020-07-23T12:55Znever https://www.institutimagine.org/fr/actin-dynamics-regulates-dendritic-cell-mediated-transfer-hiv-1-t-cells-8472020-07-23T12:55Znever https://www.institutimagine.org/fr/targeted-deep-sequencing-reveals-clonal-and-subclonal-mutational-signatures-adult-t-cell-8482020-07-23T13:12Znever https://www.institutimagine.org/fr/novel-treatments-adult-t-cell-leukemia-lymphoma-8492020-07-23T13:12Znever https://www.institutimagine.org/fr/recent-advances-understanding-and-therapeutic-management-mastocytosis-8502020-07-23T13:13Znever https://www.institutimagine.org/fr/neuroinflammatory-disorders-and-mastocytosis-possible-association-8512020-07-23T13:15Znever https://www.institutimagine.org/fr/lessons-learn-low-dose-cyclosporin-new-approach-unexpected-clinical-applications-8532020-07-23T14:57Znever https://www.institutimagine.org/fr/omalizumab-therapy-mast-cell-mediator-symptoms-patients-ism-cm-mmas-and-mcas-8542020-07-23T13:18Znever https://www.institutimagine.org/fr/impaired-type-i-interferon-activity-and-inflammatory-responses-severe-covid-19-patients-8582020-07-30T14:38Znever https://www.institutimagine.org/fr/copa-syndrome-novel-autosomal-dominant-immune-dysregulatory-disease-8592020-07-31T08:46Znever https://www.institutimagine.org/fr/mutations-copa-lead-abnormal-trafficking-sting-golgi-and-interferon-signaling-8612021-09-10T09:14Znever https://www.institutimagine.org/fr/standardised-imaging-pipeline-phenotyping-mouse-laterality-defects-and-associated-heart-8692020-09-14T08:16Znever https://www.institutimagine.org/fr/deployment-cell-lineages-form-mammalian-heart-8702020-09-14T08:17Znever https://www.institutimagine.org/fr/deployment-cell-lineages-form-mammalian-heart-8712020-09-14T08:17Znever https://www.institutimagine.org/fr/standardised-imaging-pipeline-phenotyping-mouse-laterality-defects-and-associated-heart-8722020-09-14T08:47Znever https://www.institutimagine.org/fr/deployment-cell-lineages-form-mammalian-heart-8732020-09-14T08:48Znever https://www.institutimagine.org/fr/left-right-asymmetry-heart-development-and-disease-forming-right-loop-8742020-09-14T08:50Znever https://www.institutimagine.org/fr/amotl1-mediates-sequestration-hippo-effector-yap1-downstream-fat4-restrict-heart-growth-8752020-09-14T08:52Znever https://www.institutimagine.org/fr/deployment-cell-lineages-form-mammalian-heart-8762020-09-14T08:53Znever https://www.institutimagine.org/fr/predictive-model-asymmetric-morphogenesis-3d-reconstructions-mouse-heart-looping-dynamics-8772020-09-14T08:54Znever https://www.institutimagine.org/fr/mutations-greb1l-cause-bilateral-kidney-agenesis-humans-and-mice-8782020-09-14T08:55Znever https://www.institutimagine.org/fr/amotl1-mediates-sequestration-hippo-effector-yap1-downstream-fat4-restrict-heart-growth-8792020-09-14T08:56Znever https://www.institutimagine.org/fr/imaging-and-analyzing-primary-cilia-cardiac-cells-8802020-09-14T08:58Znever https://www.institutimagine.org/fr/integrating-multi-scale-knowledge-cardiac-development-computational-model-ventricular-02020-09-14T09:01Znever https://www.institutimagine.org/fr/cardiac-cell-lineages-form-heart-8822020-09-14T09:02Znever https://www.institutimagine.org/fr/more-we-know-more-we-have-discover-exciting-future-understanding-cilia-and-ciliopathies-8832020-09-14T09:03Znever https://www.institutimagine.org/fr/cilia-and-heart-morphogenesis-8842020-09-14T09:04Znever https://www.institutimagine.org/fr/imaging-and-analyzing-primary-cilia-cardiac-cells-8852020-09-14T09:05Znever https://www.institutimagine.org/fr/integrating-multi-scale-knowledge-cardiac-development-computational-model-ventricular-trabeculation2020-09-14T09:05Znever https://www.institutimagine.org/fr/resolving-cell-lineage-contributions-ventricular-conduction-system-cx40-gfp-allele-dual2020-09-14T09:07Znever https://www.institutimagine.org/fr/quantitative-analysis-polarity-3d-reveals-local-cell-coordination-embryonic-mouse-heart-8882020-09-14T09:08Znever https://www.institutimagine.org/fr/cell-lineages-growth-and-repair-mouse-heart-8892020-09-14T09:09Znever https://www.institutimagine.org/fr/asymmetric-fate-posterior-part-second-heart-field-results-unexpected-leftright-contributions-both2020-09-14T09:10Znever https://www.institutimagine.org/fr/cell-lineages-growth-and-repair-mouse-heart-8912020-09-14T09:11Znever https://www.institutimagine.org/fr/tracing-cells-tracking-cell-lineage-and-clonal-behavior-8922020-09-14T09:11Znever https://www.institutimagine.org/fr/clonal-analysis-reveals-common-lineage-relationships-between-head-muscles-and-second-heart-field2020-09-14T09:12Znever https://www.institutimagine.org/fr/biphasic-development-mammalian-ventricular-conduction-system-8942020-09-14T09:13Znever https://www.institutimagine.org/fr/active-cell-movements-coupled-positional-induction-are-involved-lineage-segregation-mouse2020-09-14T09:14Znever https://www.institutimagine.org/fr/landmarks-and-lineages-developing-heart-8962020-09-14T09:15Znever https://www.institutimagine.org/fr/myocardium-base-aorta-and-pulmonary-trunk-prefigured-outflow-tract-heart-and-subdomains-second2020-09-14T09:16Znever https://www.institutimagine.org/fr/anterior-visceral-endoderm-mouse-embryo-established-both-preimplantation-precursor-cells-and-de2020-09-14T09:17Znever https://www.institutimagine.org/fr/left-and-right-ventricular-contributions-formation-interventricular-septum-mouse-heart-8992020-09-14T09:18Znever https://www.institutimagine.org/fr/smooth-muscle-dorsal-aorta-shares-common-clonal-origin-skeletal-muscle-myotome-9002020-09-14T09:19Znever https://www.institutimagine.org/fr/building-mammalian-heart-two-sources-myocardial-cells-9012020-09-14T09:20Znever https://www.institutimagine.org/fr/oriented-clonal-cell-growth-developing-mouse-myocardium-underlies-cardiac-morphogenesis-9022020-09-14T09:21Znever https://www.institutimagine.org/fr/clonal-origin-myocardial-cells-different-regions-embryonic-mouse-heart-9032020-09-14T09:23Znever https://www.institutimagine.org/fr/retrospective-clonal-analysis-myocardium-reveals-two-phases-clonal-growth-developing-mouse-heart2020-09-14T09:24Znever https://www.institutimagine.org/fr/oriented-clonal-cell-growth-developing-mouse-myocardium-underlies-cardiac-morphogenesis-9052020-09-14T09:24Znever https://www.institutimagine.org/fr/lineage-tree-venous-pole-heart-clonal-analysis-clarifies-controversial-genealogy-based-genetic-9062020-09-14T09:48Znever https://www.institutimagine.org/fr/pseudouridylation-defect-due-and-mutations-causes-nephrotic-syndrome-cataracts-hearing-impairment2020-09-16T09:36Znever https://www.institutimagine.org/fr/autoantibodies-against-type-i-ifns-patients-life-threatening-covid-19-9102020-09-28T14:43Znever https://www.institutimagine.org/fr/inborn-errors-type-i-ifn-immunity-patients-life-threatening-covid-19-9112020-09-28T14:42Znever https://www.institutimagine.org/fr/novel-therapeutic-approaches-treatment-achondroplasia-9172022-11-25T21:19Znever https://www.institutimagine.org/fr/fgfr3-periosteal-cells-drives-cartilage-bone-transformation-bone-repair-9182020-10-05T12:24Znever https://www.institutimagine.org/fr/animal-models-craniosynostosis-9192020-10-05T12:24Znever https://www.institutimagine.org/fr/electronic-health-records-diagnosis-rare-diseases-9212020-10-05T12:54Znever https://www.institutimagine.org/fr/slc10a7-mutations-cause-skeletal-dysplasia-amelogenesis-imperfecta-mediated-gag-biosynthesis2022-11-28T09:03Znever https://www.institutimagine.org/fr/slc10a7-mutations-cause-skeletal-dysplasia-amelogenesis-imperfecta-mediated-gag-biosynthesis-02022-01-13T16:55Znever https://www.institutimagine.org/fr/xylt1-mutations-desbuquois-dysplasia-type-2-9262020-10-13T12:58Znever https://www.institutimagine.org/fr/mutations-are-responsible-autosomal-recessive-osteogenesis-imperfecta-9272022-11-28T09:02Znever 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