About: Sylvain Latour

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An Entity of Type : foaf:Person, within Data Space : data.idref.fr associated with source document(s)

Attributes	Values
type	Person
sameAs	Latour, Sylvain Latour, Sylvain Latour, Sylvain
preferred label	Latour, Sylvain
name	Sylvain Latour
Language	http://lexvo.org/id/iso639-3/fra
isni:identifierValid	000000013921475X
Given name	Sylvain
familyName	Latour
has biographical i...tion (Deprecated)	Chercheur au CNRS et à l'unité INSERM 768 \"développement normal et pathologique du système immunitaire\". Directeur de thèse à l'Université de Paris 6 en 2007. Chercheur à l'Institut Imagine - INSERM U1163 (IMAGINE) (en 2019)
gender	male
ORCID iD	0000-0001-8238-4391
Scopus ID	57207543202
is sameAs of	Latour, Sylvain Latour, Sylvain
is Thesis advisor of	http://www.sudoc.fr/174751990/id http://www.sudoc.fr/124023088/id http://www.sudoc.fr/117714518/id http://www.sudoc.fr/165580321/id http://www.sudoc.fr/165888172/id http://www.sudoc.fr/144397056/id http://www.sudoc.fr/243037538/id http://www.sudoc.fr/229622577/id http://www.sudoc.fr/270538011/id http://www.sudoc.fr/247037125/id Caractérisation moléculaire et fonctionnelle de la signalisation de Ly-9, un récepteur de la famille SLAM, régulation par l'adaptateur SAP, produit du gène du syndrome de Purtilo Identification et caractérisation d'un nouveau syndrome lymphoprolifératif lié à l'X causé par des mutations dans le gènes BIRC4 codant la molécule anti-apoptopique XIAP http://www.sudoc.fr/236201549/id http://www.sudoc.fr/261847368/id http://www.sudoc.fr/246984759/id Activation et inhibition de la réponse cytotoxique des cellules NK par le récepteur 2B4, rôle de l'adaptateur SAP http://www.sudoc.fr/247171530/id
is Praeses of	http://www.sudoc.fr/270539387/id http://www.sudoc.fr/273125087/id http://www.sudoc.fr/281237298/id http://www.sudoc.fr/281032009/id
is Author of	http://www.sudoc.fr/043675670/id http://www.sudoc.fr/245714235/id Diagnostic Yield of Next-Generation Sequencing in Very Early-Onset Inflammatory Bowel Diseases: A Multicenter Study LES RECEPTEURS DE FAIBLE AFFINITE POUR LA PORTION FC DES IGG, IDENTIFICATION ET ANALYSE MOLECULAIRE DES PROPRIETES ACTIVATRICES ET REGULATRICES DES RFCGII ET RFCGIII MURINS Identification, in mouse macrophages and in serum, of a soluble receptor for the Fc portion of IgG (FcγR) encoded by an alternatively spliced transcript of the FcγRII gene Intestinal dysbiosis in Inflammatory Bowel Disease associated with primary immunodeficiency. Inherited CD70 deficiency in humans reveals a critical role for the CD70–CD27 pathway in immunity to Epstein-Barr virus infection Concomitant PIK3CD and TNFRSF9 deficiencies cause chronic active Epstein-Barr virus infection of T cells Aggressive large B‐cell lymphoma triggered by a parvovirus B19 infection in a previously healthy child Corrigendum to: Diagnostic Yield of Next-Generation Sequencing in Very Early-Onset Inflammatory Bowel Diseases: A Multicenter Study http://hub.abes.fr/edp/periodical/medsci/2007/volume_23/issue_3/medsci2007233p235/w Epstein-Barr Virus Genome Deletions in Epstein-Barr Virus-Positive T/NK Cell Lymphoproliferative Diseases Inherited immunodeficiencies associated with proximal and distal defects in T cell receptor signaling and co-signaling Dominant-negative IKZF1 mutations cause a T, B, and myeloid cell combined immunodeficiency https://hal.archives-ouvertes.fr/hal-02343581#id Clinical similarities and differences of patients with X-linked lymphoproliferative syndrome type 1 (XLP-1/SAP deficiency) versus type 2 (XLP-2/XIAP deficiency). TLR-induced cytokines promote effective proinflammatory natural Th17 cell responses. Impaired lymphocyte function and differentiation in CTPS1-deficient patients result from a hypomorphic homozygous mutation Stepwise development of MAIT cells in mouse and human. Transient mTOR inhibition rescues 4-1BB CAR-Tregs from tonic signal-induced dysfunction Contribution of rare and predicted pathogenic gene variants to childhood-onset lupus: a large, genetic panel analysis of British and French cohorts https://hal.archives-ouvertes.fr/hal-02391943#id Loss of RASGRP 1 in humans impairs T‐cell expansion leading to Epstein‐Barr virus susceptibility Whole-exome sequencing identifies Coronin-1A deficiency in 3 siblings with immunodeficiency and EBV-associated B-cell lymphoproliferation Primary T-cell immunodeficiency with immunodysregulation caused by autosomal recessive LCK deficiency SLAM-associated protein favors the development of iNKT2 over iNKT17 cells. Distinct intracytoplasmic sequences are required for endocytosis and phagocytosis via murine FcγRII in mast cells CTP synthase 1 deficiency in humans reveals its central role in lymphocyte proliferation TCR density in early iNKT cell precursors regulates agonist selection and subset differentiation in mice https://archive-ouverte.unige.ch/unige:2378#id Inherited defects causing hemophagocytic lymphohistiocytic syndrome Munc18-2 deficiency causes familial hemophagocytic lymphohistiocytosis type 5 and impairs cytotoxic granule exocytosis in patient NK cells Inherited TNFSF9 deficiency causes broad Epstein–Barr virus infection with EBV+ smooth muscle tumors Late-Onset Progressive Multifocal Leukoencephalopathy (PML) and Lymphoma in a 65-Year-Old Patient with XIAP Deficiency Identification of Germline Non-coding Deletions in XIAP Gene Causing XIAP Deficiency Reveals a Key Promoter Sequence
is primary topic of	http://www.idref.fr/117717886
is Opponent of	http://www.sudoc.fr/167019104/id http://www.sudoc.fr/18816197X/id http://www.sudoc.fr/240459075/id http://www.sudoc.fr/265756316/id http://www.sudoc.fr/269982809/id http://www.sudoc.fr/275804275/id http://www.sudoc.fr/274027240/id
is Thesis referee of	http://www.sudoc.fr/220991596/id http://www.sudoc.fr/167529706/id http://www.sudoc.fr/261051873/id http://www.sudoc.fr/244390878/id http://www.sudoc.fr/223463973/id

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