Lista de obras - Nathalie Lambert - Dominio Público Uruguay

A RAB27A duplication in several cases of Griscelli syndrome type 2: An explanation for cases lacking a genetic diagnosis

artículo científico publicado en 2017

A Variety of Alu-Mediated Copy Number Variations Can Underlie IL-12Rβ1 Deficiency

A large multicentre analysis of CTGF -945 promoter polymorphism does not confirm association with systemic sclerosis susceptibility or phenotype

artículo científico publicado en 2008

A newly identified isoform of Slp2a associates with Rab27a in cytotoxic T cells and participates to cytotoxic granule secretion

artículo científico publicado en 2008

An in vivo genetic reversion highlights the crucial role of Myb-Like, SWIRM, and MPN domains 1 (MYSM1) in human hematopoiesis and lymphocyte differentiation

artículo científico publicado en 2015

Analyzing HLA-G polymorphisms in children from women with scleroderma.

artículo científico publicado en 2012

Anti-Ephrin Type-B Receptor 2 (EphB2) and Anti-Three Prime Histone mRNA EXonuclease 1 (THEX1) Autoantibodies in Scleroderma and Lupus

artículo científico publicado en 2016

Autosomal dominant STAT3 deficiency and hyper-IgE syndrome: molecular, cellular, and clinical features from a French national survey

artículo científico publicado en 2012

CD21 deficiency in 2 siblings with recurrent respiratory infections and hypogammaglobulinemia

artículo científico publicado en 2017

Cells from a vanished twin as a source of microchimerism 40 years later

artículo científico publicado en 2010

Characterization of Crohn disease in X-linked inhibitor of apoptosis-deficient male patients and female symptomatic carriers.

artículo científico publicado en 2014

Chimerism in women with end stage renal diseases: Who's who?

artículo científico publicado en 2012

Chronic Intestinal Pseudo-Obstruction and Lymphoproliferative Syndrome as a Novel Phenotype Associated With Tetratricopeptide Repeat Domain 7A Deficiency

artículo científico publicado en 2019

Clinical similarities and differences of patients with X-linked lymphoproliferative syndrome type 1 (XLP-1/SAP deficiency) versus type 2 (XLP-2/XIAP deficiency).

artículo científico publicado en 2010

Comparing HLA shared epitopes in French Caucasian patients with scleroderma

artículo científico publicado en 2012

Defective NKT cell development in mice and humans lacking the adapter SAP, the X-linked lymphoproliferative syndrome gene product

artículo científico publicado en 2005

Dynamic changes in fetal microchimerism in maternal peripheral blood mononuclear cells, CD4+ and CD8+ cells in normal pregnancy

artículo científico publicado en 2010

Evaluation of X Chromosome Inactivation with Respect to HLA Genetic Susceptibility in Rheumatoid Arthritis and Systemic Sclerosis

artículo científico publicado en 2016

Genotype, phenotype, and outcomes of nine patients with T-B+NK+ SCID

artículo científico publicado en 2011

Griscelli syndrome types 1 and 3: analysis of four new cases and long-term evaluation of previously diagnosed patients.

artículo científico publicado en 2012

HLA allelic variants encoding DR11 in diffuse and limited systemic sclerosis in Caucasian women

artículo científico publicado en 2004

HLA-DRB1 genotypes and the risk of developing anti citrullinated protein antibody (ACPA) positive rheumatoid arthritis

artículo científico publicado en 2013

How microchimerism can impart HLA susceptibility in patients with rheumatoid arthritis

artículo científico publicado en 2010

Improving the diagnostic efficiency of primary immunodeficiencies with targeted next-generation sequencing

artículo científico publicado en 2020

Male DNA in female donor apheresis and CD34-enriched products

artículo científico publicado en 2003

Male microchimerism and HLA compatibility in French women with sclerodema: a different profile in limited and diffuse subset

artículo científico publicado en 2009

Male microchimerism in healthy women and women with scleroderma: cells or circulating DNA? A quantitative answer

artículo científico publicado en 2002

Male microchimerism in women with systemic sclerosis and healthy women who have never given birth to a son.

artículo científico publicado en 2004

Male microchimerism in women without sons: quantitative assessment and correlation with pregnancy history

artículo científico publicado en 2005

Maternal HLA class II compatibility in men with systemic lupus erythematosus

artículo científico publicado en 2005

Maternal and sibling microchimerism in twins and triplets discordant for neonatal lupus syndrome-congenital heart block

artículo científico publicado en 2004

Maternal microchimerism in healthy adults in lymphocytes, monocyte/macrophages and NK cells

artículo científico publicado en 2006

Maternal microchimerism in peripheral blood in type 1 diabetes and pancreatic islet beta cell microchimerism.

artículo científico publicado en 2007

Microchimeric cells: guardians or actors of immunity in scleroderma?

scientific article published on 23 November 2006

Microchimerism and rheumatic diseases

scientific article published on 07 November 2012

Microchimerism in autoimmune disease: more questions than answers?

artículo científico publicado en 2003

Microchimérisme dans la sclérodermie : dix ans après

scientific article published on 15 April 2010

Munc13-4 is essential for cytolytic granules fusion and is mutated in a form of familial hemophagocytic lymphohistiocytosis (FHL3).

artículo científico publicado en 2003

New autoantibodies in early rheumatoid arthritis

artículo científico publicado en 2013

New autoantigens in rheumatoid arthritis (RA): screening 8268 protein arrays with sera from patients with RA.

artículo científico publicado en 2008

Newly Identified BRAF Mutation in Rheumatoid Arthritis

artículo científico publicado en 2016

Patients with ankylosing spondylitis have been breast fed less often than healthy controls: a case-control retrospective study

artículo científico publicado en 2015

Pregnancy, microchimerism, and the maternal grandmother

artículo científico publicado en 2011

Primary T-cell immunodeficiency with immunodysregulation caused by autosomal recessive LCK deficiency

artículo científico publicado en 2012

Prospective study of fetal DNA in serum and disease activity during pregnancy in women with inflammatory arthritis

artículo científico publicado en 2006

Quantification of maternal microchimerism by HLA-specific real-time polymerase chain reaction: studies of healthy women and women with scleroderma

artículo científico publicado en 2004

Rheumatoid arthritis: Forward and reverse inheritance - the yin and the yang

artículo científico publicado en 2017

SYK expression endows human ZAP70-deficient CD8 T cells with residual TCR signaling

artículo científico publicado en 2015

T-cell receptor variable region of the beta-chain gene use in peripheral blood and multiple synovial membranes during rheumatoid arthritis

artículo científico publicado en 1995

TTC7A mutations disrupt intestinal epithelial apicobasal polarity

artículo científico publicado en 2014

Transfer of the shared epitope through microchimerism in women with rheumatoid arthritis.

artículo científico publicado en 2009

Use of T-Cell Receptor V? Genes in Synovial Membrane in Rheumatoid Arthritis

article

X-linked primary immunodeficiency associated with hemizygous mutations in the moesin (MSN) gene

scientific journal article

XIAP deficiency in humans causes an X-linked lymphoproliferative syndrome

artículo científico publicado en 2006

Lista de obras de Nathalie Lambert

A RAB27A duplication in several cases of Griscelli syndrome type 2: An explanation for cases lacking a genetic diagnosis

A Variety of Alu-Mediated Copy Number Variations Can Underlie IL-12Rβ1 Deficiency

A large multicentre analysis of CTGF -945 promoter polymorphism does not confirm association with systemic sclerosis susceptibility or phenotype

A newly identified isoform of Slp2a associates with Rab27a in cytotoxic T cells and participates to cytotoxic granule secretion

An in vivo genetic reversion highlights the crucial role of Myb-Like, SWIRM, and MPN domains 1 (MYSM1) in human hematopoiesis and lymphocyte differentiation

Analyzing HLA-G polymorphisms in children from women with scleroderma.

Anti-Ephrin Type-B Receptor 2 (EphB2) and Anti-Three Prime Histone mRNA EXonuclease 1 (THEX1) Autoantibodies in Scleroderma and Lupus

Autosomal dominant STAT3 deficiency and hyper-IgE syndrome: molecular, cellular, and clinical features from a French national survey

CD21 deficiency in 2 siblings with recurrent respiratory infections and hypogammaglobulinemia

Cells from a vanished twin as a source of microchimerism 40 years later

Characterization of Crohn disease in X-linked inhibitor of apoptosis-deficient male patients and female symptomatic carriers.

Chimerism in women with end stage renal diseases: Who's who?

Chronic Intestinal Pseudo-Obstruction and Lymphoproliferative Syndrome as a Novel Phenotype Associated With Tetratricopeptide Repeat Domain 7A Deficiency

Clinical similarities and differences of patients with X-linked lymphoproliferative syndrome type 1 (XLP-1/SAP deficiency) versus type 2 (XLP-2/XIAP deficiency).

Comparing HLA shared epitopes in French Caucasian patients with scleroderma

Defective NKT cell development in mice and humans lacking the adapter SAP, the X-linked lymphoproliferative syndrome gene product

Dynamic changes in fetal microchimerism in maternal peripheral blood mononuclear cells, CD4+ and CD8+ cells in normal pregnancy

Evaluation of X Chromosome Inactivation with Respect to HLA Genetic Susceptibility in Rheumatoid Arthritis and Systemic Sclerosis

Genotype, phenotype, and outcomes of nine patients with T-B+NK+ SCID

Griscelli syndrome types 1 and 3: analysis of four new cases and long-term evaluation of previously diagnosed patients.

HLA allelic variants encoding DR11 in diffuse and limited systemic sclerosis in Caucasian women

HLA-DRB1 genotypes and the risk of developing anti citrullinated protein antibody (ACPA) positive rheumatoid arthritis

How microchimerism can impart HLA susceptibility in patients with rheumatoid arthritis

Improving the diagnostic efficiency of primary immunodeficiencies with targeted next-generation sequencing

Male DNA in female donor apheresis and CD34-enriched products

Male microchimerism and HLA compatibility in French women with sclerodema: a different profile in limited and diffuse subset

Male microchimerism in healthy women and women with scleroderma: cells or circulating DNA? A quantitative answer

Male microchimerism in women with systemic sclerosis and healthy women who have never given birth to a son.

Male microchimerism in women without sons: quantitative assessment and correlation with pregnancy history

Maternal HLA class II compatibility in men with systemic lupus erythematosus

Maternal and sibling microchimerism in twins and triplets discordant for neonatal lupus syndrome-congenital heart block

Maternal microchimerism in healthy adults in lymphocytes, monocyte/macrophages and NK cells

Maternal microchimerism in peripheral blood in type 1 diabetes and pancreatic islet beta cell microchimerism.

Microchimeric cells: guardians or actors of immunity in scleroderma?

Microchimerism and rheumatic diseases

Microchimerism in autoimmune disease: more questions than answers?

Microchimérisme dans la sclérodermie : dix ans après

Munc13-4 is essential for cytolytic granules fusion and is mutated in a form of familial hemophagocytic lymphohistiocytosis (FHL3).

New autoantibodies in early rheumatoid arthritis

New autoantigens in rheumatoid arthritis (RA): screening 8268 protein arrays with sera from patients with RA.

Newly Identified BRAF Mutation in Rheumatoid Arthritis

Patients with ankylosing spondylitis have been breast fed less often than healthy controls: a case-control retrospective study

Pregnancy, microchimerism, and the maternal grandmother

Primary T-cell immunodeficiency with immunodysregulation caused by autosomal recessive LCK deficiency

Prospective study of fetal DNA in serum and disease activity during pregnancy in women with inflammatory arthritis

Quantification of maternal microchimerism by HLA-specific real-time polymerase chain reaction: studies of healthy women and women with scleroderma

Rheumatoid arthritis: Forward and reverse inheritance - the yin and the yang

SYK expression endows human ZAP70-deficient CD8 T cells with residual TCR signaling

T-cell receptor variable region of the beta-chain gene use in peripheral blood and multiple synovial membranes during rheumatoid arthritis

TTC7A mutations disrupt intestinal epithelial apicobasal polarity

Transfer of the shared epitope through microchimerism in women with rheumatoid arthritis.

Use of T-Cell Receptor V? Genes in Synovial Membrane in Rheumatoid Arthritis

X-linked primary immunodeficiency associated with hemizygous mutations in the moesin (MSN) gene

XIAP deficiency in humans causes an X-linked lymphoproliferative syndrome