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Proceedings of the National Academy of Sciences of the United States of America|March 20, 2003
The LIM-only protein FHL2 is a serum-inducible transcriptional coactivator of AP-1Aurore Morlon, Paolo Sassone-CorsiHuman Molecular Genetics|October 28, 2005
TAB2, TRAF6 and TAK1 are involved in NF-kappaB activation induced by the TNF-receptor, Edar and its adaptator EdaraddAurore Morlon, Arnold Munnich, Asma SmahiAnnals of the Rheumatic Diseases|July 22, 2018
Multi-OMICS analyses unveil STAT1 as a potential modifier gene in mevalonate kinase deficiencyRaphael Carapito, Christine Carapito, Aurore Morlon, et al.Nature Medicine|March 15, 2022
The MHC class I MICA gene is a histocompatibility antigen in kidney transplantationRaphael Carapito, Ismail Aouadi, Martin Verniquet, et al.Bone Marrow Transplantation|April 15, 2020
Compatibility at amino acid position 98 of MICB reduces the incidence of graft-versus-host disease in conjunction with the CMV statusRaphael Carapito, Ismail Aouadi, Angélique Pichot, et al.The Journal of Clinical Investigation|October 4, 2017
Mutations in signal recognition particle SRP54 cause syndromic neutropenia with Shwachman-Diamond-like featuresRaphael Carapito, Martina Konantz, Catherine Paillard, et al.Blood|August 24, 2016
Matching for the nonconventional MHC-I MICA gene significantly reduces the incidence of acute and chronic GVHDRaphael Carapito, Nicolas Jung, Marius Kwemou, et al.American Journal of Human Genetics|January 15, 2019
ZMIZ1 Variants Cause a Syndromic Neurodevelopmental DisorderRaphael Carapito, Ekaterina L Ivanova, Aurore Morlon, et al.Pageof 1