Patrick Revy
Patrick Revy
Imagine Institute, "Genome Dynamics in the Immune System" Laboratory
Verified email at inserm.fr
Title
Cited by
Cited by
Year
Activation-induced cytidine deaminase (AID) deficiency causes the autosomal recessive form of the Hyper-IgM syndrome (HIGM2)
P Revy, T Muto, Y Levy, F Geissmann, A Plebani, O Sanal, N Catalan, ...
Cell 102 (5), 565-575, 2000
17852000
Interferon-γ–receptor deficiency in an infant with fatal bacille Calmette–Guérin infection
E Jouanguy, F Altare, S Lamhamedi, P Revy, JF Emile, M Newport, ...
New England Journal of Medicine 335 (26), 1956-1962, 1996
10261996
Cernunnos, a novel nonhomologous end-joining factor, is mutated in human immunodeficiency with microcephaly
D Buck, L Malivert, R de Chasseval, A Barraud, MC Fondanèche, O Sanal, ...
Cell 124 (2), 287-299, 2006
7602006
XIAP deficiency in humans causes an X-linked lymphoproliferative syndrome
S Rigaud, MC Fondaneche, N Lambert, B Pasquier, V Mateo, P Soulas, ...
Nature 444 (7115), 110-114, 2006
6862006
Human uracil–DNA glycosylase deficiency associated with profoundly impaired immunoglobulin class-switch recombination
K Imai, G Slupphaug, WI Lee, P Revy, S Nonoyama, N Catalan, L Yel, ...
Nature immunology 4 (10), 1023-1028, 2003
6692003
TGF-β1 prevents the noncognate maturation of human dendritic Langerhans cells
F Geissmann, P Revy, A Regnault, Y Lepelletier, M Dy, N Brousse, ...
The Journal of Immunology 162 (8), 4567-4575, 1999
4901999
Inherited interleukin 12 deficiency in a child with bacille Calmette-Guérin and Salmonella enteritidis disseminated infection.
F Altare, D Lammas, P Revy, E Jouanguy, R Döffinger, S Lamhamedi, ...
The Journal of clinical investigation 102 (12), 2035-2040, 1998
4741998
Functional antigen-independent synapses formed between T cells and dendritic cells
P Revy, M Sospedra, B Barbour, A Trautmann
Nature immunology 2 (10), 925-931, 2001
3482001
Retinoids regulate survival and antigen presentation by immature dendritic cells
F Geissmann, P Revy, N Brousse, Y Lepelletier, C Folli, A Durandy, ...
Journal of Experimental Medicine 198 (4), 623-634, 2003
2192003
V (D) J and immunoglobulin class switch recombinations: a paradigm to study the regulation of DNA end-joining
P Soulas-Sprauel, P Rivera-Munoz, L Malivert, G Le Guyader, ...
Oncogene 26 (56), 7780-7791, 2007
1772007
Hyper-IgM syndrome type 4 with a B lymphocyte–intrinsic selective deficiency in Ig class-switch recombination
K Imai, N Catalan, A Plebani, L Maródi, Ö Sanal, S Kumaki, V Nagendran, ...
The Journal of clinical investigation 112 (1), 136-142, 2003
1472003
Human RTEL1 deficiency causes Hoyeraal–Hreidarsson syndrome with short telomeres and genome instability
T Le Guen, L Jullien, F Touzot, M Schertzer, L Gaillard, M Perderiset, ...
Human molecular genetics 22 (16), 3239-3249, 2013
1442013
Cernunnos interacts with the XRCC4· DNA-ligase IV complex and is homologous to the yeast nonhomologous end-joining factor Nej1
I Callebaut, L Malivert, A Fischer, JP Mornon, P Revy, JP De Villartay
Journal of Biological Chemistry 281 (20), 13857-13860, 2006
1432006
Whole-exome sequencing identifies Coronin-1A deficiency in 3 siblings with immunodeficiency and EBV-associated B-cell lymphoproliferation
D Moshous, E Martin, W Carpentier, A Lim, I Callebaut, D Canioni, ...
Journal of allergy and clinical immunology 131 (6), 1594-1603. e9, 2013
1362013
Structural characterization of filaments formed by human Xrcc4–Cernunnos/XLF complex involved in nonhomologous DNA end-joining
V Ropars, P Drevet, P Legrand, S Baconnais, J Amram, G Faure, ...
Proceedings of the National Academy of Sciences 108 (31), 12663-12668, 2011
1362011
Heterozygous RTEL1 mutations are associated with familial pulmonary fibrosis
C Kannengiesser, R Borie, C Ménard, M Réocreux, P Nitschké, S Gazal, ...
European Respiratory Journal 46 (2), 474-485, 2015
1192015
A homozygous mucosa-associated lymphoid tissue 1 (MALT1) mutation in a family with combined immunodeficiency
HH Jabara, T Ohsumi, J Chou, MJ Massaad, H Benson, A Megarbane, ...
Journal of allergy and clinical immunology 132 (1), 151-158, 2013
1162013
Mutations in KEOPS-complex genes cause nephrotic syndrome with primary microcephaly
DA Braun, J Rao, G Mollet, D Schapiro, MC Daugeron, W Tan, ...
Nature genetics 49 (10), 1529-1538, 2017
1122017
Analysis of class switch recombination and somatic hypermutation in patients affected with autosomal dominant hyper-IgM syndrome type 2
K Imai, Y Zhu, P Revy, T Morio, S Mizutani, A Fischer, S Nonoyama, ...
Clinical immunology 115 (3), 277-285, 2005
1092005
Hyper‐immunoglobulin M syndromes caused by intrinsic B‐lymphocyte defects
A Durandy, P Revy, K Imai, A Fischer
Immunological reviews 203 (1), 67-79, 2005
1042005
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