Publications and ressources

The human CIB1-EVER1-EVER2 complex governs keratinocyte-intrinsic immunity to β-papillomaviruses.

Jean-Laurent CASANOVA

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Cilia in hereditary cerebral anomalies.

Alexandre Benmerah

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Signaling pathways involved in the T-cell-mediated immunity against Epstein-Barr virus: Lessons from genetic diseases.

Sylvain Latour, Alain Fischer

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Cilia in hereditary cerebral anomalies.

Sophie Thomas, Lucile Boutaud, Alexandre Benmerah

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De novo SCAMP5 mutation causes a neurodevelopmental disorder with autistic features and seizures.

Claude Besmond, Matias Simons, Stanislas Lyonnet, Arnold Munnich, Nathalie Boddaert, Marlène Rio

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Effectiveness and safety of the tri-iodothyronine analogue Triac in children and adults with MCT8 deficiency: an international, single-arm, open-label, phase 2 trial.

Michel Polak, Athanasia Stoupa

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NKp46 is a diagnostic biomarker and may be a therapeutic target in gastrointestinal T-cell lymphoproliferative diseases: a CELAC study.

Olivier Hermine

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A deep intronic splice mutation of STAT3 underlies hyper IgE syndrome by negative dominance.

Jean-Laurent CASANOVA

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PAXX and Xlf interplay revealed by impaired CNS development and immunodeficiency of double KO mice.

Jean-Pierre De Villartay

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Prevalence and risk factors for latent tuberculosis infection among healthcare workers in Morocco.

Laurent Abel , Aurélie Cobat, Jocelyn Quistrebert

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New Publication

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Modulation of the gut microbiota to improve innate resistance.

Nadine CERF-BENSUSSAN

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Pleiotropic effects for Parkin and LRRK2 in leprosy type-1 reactions and Parkinson's disease.

Laurent Abel , Aurélie Cobat, Alexandre Alcaïs

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Mutations in MAST1 Cause Mega-Corpus-Callosum Syndrome with Cerebellar Hypoplasia and Cortical Malformations.

Lydie Burglen, Nadia Bahi-Buisson

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Ex vivo generated human T-lymphoid progenitors as a tool to accelerate immune reconstitution after partially HLA compatible hematopoietic stem cell transplantation or after gene therapy.

Isabelle André, Laura SIMONS, Kuiying MA, Marina Cavazzana

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