0 results match your search.
-
Laurent GUILLEMOT
Source :
Nat Commun2017 Feb 27Pmid / DOI:
28239148 -
Frédéric Rieux-Laucat, Sylvain Latour, Alain Fischer, Jean-Laurent CASANOVA , Anne DURANDY, Despina Moshous, Sven KRACKER
Source :
J Allergy Clin Immunol2017 Feb 1Pmid / DOI:
27555459 -
Whole-exome sequencing to analyze population structure, parental inbreeding, and familial linkage.
Jacinta Bustamante
Source :
Proc. Natl. Acad. Sci. U.S.A.2017 Jan 26Pmid / DOI:
27247391 -
Gene Therapy with Hematopoietic Stem Cells: The Diseased Bone Marrow's Point of View.
Marina Cavazzana, Chantal LAGRESLE-PEYROU
Source :
Stem Cells Dev2017 Jan 15Pmid / DOI:
27750026 -
Dynamic Transcriptional and Epigenetic Regulation of Human Epidermal Keratinocyte Differentiation.
Annarita Miccio
Source :
Stem Cell Reports2017 Jan 11Pmid / DOI:
27050947 -
Primary immunodeficiencies suggest redundancy within the human immune system
Source :
Science Immunology2016 Dec 23Pmid / DOI:
-
[Actin nucleation and HIV transfer from dendritic cells to T lymphocytes].
Mickaël Ménager
Source :
Med Sci (Paris)2016 Dec 1Pmid / DOI:
28044965 -
A mutation in VPS15 (PIK3R4) causes a ciliopathy and affects IFT20 release from the cis-Golgi.
Isabelle PERRAULT
Source :
Nat Commun2016 Nov 24Pmid / DOI:
27882921 -
Gene Therapy for X-Linked Severe Combined Immunodeficiency: Where Do We Stand?
Marina Cavazzana, Emmanuelle SIX, Chantal LAGRESLE-PEYROU, Isabelle André
Source :
Hum. Gene Ther.2016 Nov 4Pmid / DOI:
26790362 -
Sven KRACKER, Anne DURANDY
Source :
J Allergy Clin Immunol. 20182016 Oct 16Pmid / DOI:
27555459 -
Kremen1 and Dickkopf1 control cell survival in a Wnt-independent manner.
Frédéric Causeret, Alessandra Pierani
Source :
Cell Death Differ.2016 Oct 14Pmid / DOI:
26206087 -
Spontaneous and electric field-controlled front-rear polarization of human keratinocytes.
Matias Simons
Source :
Mol. Biol. Cell2016 Oct 11Pmid / DOI:
26424799 -
Alessandra Pierani, Lisa Vigier, Frédéric Causeret
Source :
Curr. Biol.2016 Aug 22Pmid / DOI:
26387718 -
Alessandra Pierani, Frédéric Causeret
Source :
Evodevo2016 Aug 15Pmid / DOI:
27525057 -
Novel NEK8 Mutations Cause Severe Syndromic Renal Cystic Dysplasia through YAP Dysregulation.
Sophie Saunier
Source :
PLoS Genet.2016 Aug 9Pmid / DOI:
26967905