M. Untrau

发表

Evaluation of human relevance of Nicofluprole-induced rat thyroid disruption

L. Richert, C. Parmentier, A. Baze, 2021, Toxicology and Applied Pharmacology.

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.

An unusually high substitution rate in transplant-associated BK polyomavirus in vivo is further concentrated in HLA-C-bound viral peptides

N. Paul, O. Kohlbacher, B. Schubert, 2018, PLoS pathogens.

Homozygous IL 36 RN mutation and NSD 1 duplication in a patient with severe pustular psoriasis and DITRA-unrelated symptoms

S. Barbarot, B. Isidor, S. Bahram, 2014 .

Polymorphisms in EGFR and IL28B are associated with spontaneous clearance in an HCV-infected iranian population

R. Malekzadeh, H. Poustchi, S. Merat, 2015, Genes and Immunity.

A new mutation in the C-SH2 domain of PTPN11 causes Noonan syndrome with multiple giant cell lesions

N. Paul, M. Heymann, B. Isidor, 2013, Journal of Human Genetics.

A new MHC‐linked susceptibility locus for primary Sjögren's syndrome: MICA

N. Paul, H. Inoko, B. Griffiths, 2017, Human molecular genetics.

Homozygous IL36RN mutation and NSD1 duplication in a patient with severe pustular psoriasis and symptoms unrelated to deficiency of interleukin‐36 receptor antagonist

S. Barbarot, C. Le Caignec, B. Isidor, 2015, The British journal of dermatology.

A de novo ADCY5 mutation causes early‐onset autosomal dominant chorea and dystonia

N. Paul, P. Damier, C. Le Caignec, 2015, Movement disorders : official journal of the Movement Disorder Society.

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

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

Performances of two rapid LAMP-based techniques for the intrapartum detection of Group B Streptococcus vaginal colonization

C. Poyart, M. Untrau, C. Plainvert, 2024, Annals of clinical microbiology and antimicrobials.