C. Macquin

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.

A mouse model of MSU-induced acute inflammation in vivo suggests imiquimod-dependent targeting of Il-1β as relevant therapy for gout patients

N. Paul, J. Armspach, J. Sibilia, 2020, Theranostics.

NLRP3- and AIM2-autonomy in a mouse model of MSU crystal-induced acute inflammation in vivo highlights imiquimod-dependent targeting of Il-1β expression as relevant therapy for gout patients

N. Paul, J. Armspach, J. Sibilia, 2019, bioRxiv.

NKG2D ligands in inflammatory joint diseases: analysis in human samples and mouse models.

L. Punzi, J. Sibilia, P. Georgel, 2020, Clinical and experimental rheumatology.

Deregulation of Type I IFN-Dependent Genes Correlates with Increased Susceptibility to Cytomegalovirus Acute Infection of Dicer Mutant Mice

S. Pfeffer, P. Georgel, S. Bahram, 2012, PloS one.

The non-conventional MHC class I MR1 molecule controls infection by Klebsiella pneumoniae in mice.

P. Georgel, S. Bahram, C. Macquin, 2011, Molecular immunology.

Increased Viral Dissemination in the Brain and Lethality in MCMV-Infected, Dicer-Deficient Neonates

P. Georgel, W. Krężel, S. Bahram, 2015, Viruses.

Lipolysis is altered in MHC class I zinc-alpha(2)-glycoprotein deficient mice.

I. Castan-Laurell, P. Valet, S. Bahram, 2007, FEBS letters.

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.

Rapid Evolution of Major Histocompatibility Complex Class I Genes in Primates Generates New Disease Alleles in Humans via Hitchhiking Diversity

Kazuho Ikeo, Takashi Gojobori, Katsushi Tokunaga, 2006, Genetics.

Identification of driver genes for critical forms of COVID-19 in a deeply phenotyped young patient cohort

Daniel M. Lidar, J. Gulcher, J. Casanova, 2021, Science Translational Medicine.

Identification of driver genes for severe forms of COVID-19 in a deeply phenotyped young patient cohort

J. Gulcher, J. Casanova, S. Mayeur, 2021, medRxiv.

The Heterogeneous Allelic Repertoire of Human Toll-Like Receptor (TLR) Genes

P. Georgel, S. Bahram, C. Macquin, 2009, PloS one.

Lipolysis is altered in MHC class I zinc‐α2‐glycoprotein deficient mice

I. Castan-Laurell, P. Valet, S. Bahram, 2007 .

Contrasting role of NLRP12 in autoinflammation: evidence from a case report and mouse models

D. Levy, F. Maurier, P. Georgel, 2021, RMD Open.

Use of in vivo imaging to monitor the progression of experimental mouse cytomegalovirus infection in neonates.

P. Georgel, S. Bahram, E. Ostermann, 2013, Journal of visualized experiments : JoVE.