Lista de obras - Marie-Claude Stolzenberg

A survey of 90 patients with autoimmune lymphoproliferative syndrome related to TNFRSF6 mutation

artículo científico publicado en 2011

Alteration of HLA-B27 peptide presentation after infection of transfected murine L cells by Shigella flexneri.

artículo científico publicado en 1998

Autoimmune lymphoproliferative syndrome caused by a homozygous null FAS ligand (FASLG) mutation

artículo científico publicado en 2012

Autoimmune lymphoproliferative syndrome with somatic Fas mutations

artículo científico publicado en 2004

Constitutive expression of MHC class II genes in melanoma cell lines results from the transcription of class II transactivator abnormally initiated from its B cell-specific promoter

scientific article published on 01 July 2001

Defective anti-polysaccharide response and splenic marginal zone disorganization in ALPS patients

artículo científico publicado en 2014

Deficiency in Mucosa-associated Lymphoid Tissue Lymphoma Translocation 1: A Novel Cause of IPEX-Like Syndrome

artículo científico publicado en 2016

Differential sensitivity of Jurkat and primary T cells to caspase-independent cell death triggered upon Fas stimulation

artículo científico publicado en 2002

FAS-L, IL-10, and double-negative CD4- CD8- TCR alpha/beta+ T cells are reliable markers of autoimmune lymphoproliferative syndrome (ALPS) associated with FAS loss of function

artículo científico publicado en 2009

Germ-line exclusion of a single p53 allele by premature termination of translation in a Li-Fraumeni syndrome family

scientific article published on 01 October 1994

Hypomorphic mutation of ZAP70 in human results in a late onset immunodeficiency and no autoimmunity.

artículo científico publicado en 2009

Inherited STING-activating mutation underlies a familial inflammatory syndrome with lupus-like manifestations ⬇️

artículo científico publicado en 2014

Intrinsic antiproliferative activity of the innate sensor STING in T lymphocytes

artículo científico publicado en 2017

Isolation, sequencing and expression of RED, a novel human gene encoding an acidic-basic dipeptide repeat.

artículo científico publicado en 1999

LRBA deficiency with autoimmunity and early onset chronic erosive polyarthritis

artículo científico publicado en 2016

Onset of autoimmune lymphoproliferative syndrome (ALPS) in humans as a consequence of genetic defect accumulation

artículo científico publicado en 2010

Perforin-dependent apoptosis functionally compensates Fas deficiency in activation-induced cell death of human T lymphocytes

artículo científico publicado en 2007

RAS-associated lymphoproliferative disease evolves into severe juvenile myelo-monocytic leukemia

artículo científico publicado en 2014

Reduced expression of FOXP3 and regulatory T-cell function in severe forms of early-onset autoimmune enteropathy

artículo científico publicado en 2010

Relationship between antibody production to Epstein-Barr virus (EBV) early antigens and various EBV-related diseases ⬇️

artículo científico publicado el 1 de enero de 1991

Lista de obras de Marie-Claude Stolzenberg

A survey of 90 patients with autoimmune lymphoproliferative syndrome related to TNFRSF6 mutation

Alteration of HLA-B27 peptide presentation after infection of transfected murine L cells by Shigella flexneri.

Autoimmune lymphoproliferative syndrome caused by a homozygous null FAS ligand (FASLG) mutation

Autoimmune lymphoproliferative syndrome with somatic Fas mutations

Constitutive expression of MHC class II genes in melanoma cell lines results from the transcription of class II transactivator abnormally initiated from its B cell-specific promoter

Defective anti-polysaccharide response and splenic marginal zone disorganization in ALPS patients

Deficiency in Mucosa-associated Lymphoid Tissue Lymphoma Translocation 1: A Novel Cause of IPEX-Like Syndrome

Differential sensitivity of Jurkat and primary T cells to caspase-independent cell death triggered upon Fas stimulation

FAS-L, IL-10, and double-negative CD4- CD8- TCR alpha/beta+ T cells are reliable markers of autoimmune lymphoproliferative syndrome (ALPS) associated with FAS loss of function

Germ-line exclusion of a single p53 allele by premature termination of translation in a Li-Fraumeni syndrome family

Hypomorphic mutation of ZAP70 in human results in a late onset immunodeficiency and no autoimmunity.

Inherited STING-activating mutation underlies a familial inflammatory syndrome with lupus-like manifestations ⬇️

Intrinsic antiproliferative activity of the innate sensor STING in T lymphocytes

Isolation, sequencing and expression of RED, a novel human gene encoding an acidic-basic dipeptide repeat.

LRBA deficiency with autoimmunity and early onset chronic erosive polyarthritis

Onset of autoimmune lymphoproliferative syndrome (ALPS) in humans as a consequence of genetic defect accumulation

Perforin-dependent apoptosis functionally compensates Fas deficiency in activation-induced cell death of human T lymphocytes

RAS-associated lymphoproliferative disease evolves into severe juvenile myelo-monocytic leukemia

Reduced expression of FOXP3 and regulatory T-cell function in severe forms of early-onset autoimmune enteropathy

Relationship between antibody production to Epstein-Barr virus (EBV) early antigens and various EBV-related diseases ⬇️