A. Morlon

发表

Matching for the nonconventional MHC-I MICA gene significantly reduces the incidence of acute and chronic GVHD.

H. Inoko, M. Labopin, I. Yakoub-Agha, 2016, Blood.

Transcriptional cascades during spermatogenesis: pivotal role of CREM and ACT

P. Sassone-Corsi, G. Fimia, Betina Macho, 2001, Molecular and Cellular Endocrinology.

Routes of Transcriptional Activation in the Testis: CREM and its Co-Activator ACT

P. Sassone-Corsi, G. Fimia, A. Morlon, 2000 .

Multi-OMICS analyses unveil STAT1 as a potential modifier gene in mevalonate kinase deficiency

Alvaro Sebastian Vaca Jacome, N. Paul, F. Delalande, 2018, Annals of the rheumatic diseases.

Compatibility at amino acid position 98 of MICB reduces the incidence of graft-versus-host disease in conjunction with the CMV status

I. Yakoub-Agha, D. Blaise, M. Mohty, 2020, Bone Marrow Transplantation.

Mutations in signal recognition particle SRP54 cause syndromic neutropenia with Shwachman-Diamond–like features

Magalie S Leduc, M. Konantz, C. Lengerke, 2017, The Journal of clinical investigation.

ZMIZ1 Variants Cause a Syndromic Neurodevelopmental Disorder.

H. Mefford, G. Cooper, N. Paul, 2019, American journal of human genetics.

TAB2, TRAF6 and TAK1 are involved in NF-kappaB activation induced by the TNF-receptor, Edar and its adaptator Edaradd.

Arnold Munnich, A. Smahi, A. Munnich, 2005, Human molecular genetics.

Transcription factor TEAD4 regulates expression of Myogenin and the unfolded protein response genes during C2C12 cell differentiation

T. Ye, B. Jost, A. Benhaddou, 2011, Cell Death and Differentiation.

The LIM-only protein FHL2 is a serum-inducible transcriptional coactivator of AP-1

P. Sassone-Corsi, A. Morlon, Aurore Morlon, 2003, Proceedings of the National Academy of Sciences of the United States of America.

The MHC class I MICA gene is a histocompatibility antigen in kidney transplantation

A. Blancher, N. Kamar, S. Bahram, 2022, Nature Medicine.