Lista de obras - Sophie Caillat-Zucman - Dominio Público Uruguay

21-Hydroxylase epitopes are targeted by CD8 T cells in autoimmune Addison’s disease

artículo científico publicado en 2010

35th Annual Meeting of the European Association for the Study of Diabetes

artículo científico

35th Annual Meeting of the European Association for the Study of Diabetes : Brussels, Belgium, 28 September-2 October 1999

article

A Common Stromal Cell-Derived Factor-1 Chemokine Gene Variant is Associated With the Early Onset of Type 1 Diabetes

article

A dinucleotide repeat polymorphism at the poly(ADP-ribose) polymerase gene is not associated with predisposition to type 1 diabetes in French Caucasians

artículo científico publicado en 2001

A direct role for NKG2D/MICA interaction in villous atrophy during celiac disease.

artículo científico publicado en 2004

Absence of functional relevance of human transporter associated with antigen processing polymorphism for peptide selection ⬇️

artículo científico publicado el 1 de septiembre de 1997

Absence of primary association between DM gene polymorphism and insulin-dependent diabetes mellitus or celiac disease

article

Adenovirally transduced dendritic cells induce bispecific cytotoxic T lymphocyte responses against adenovirus and cytomegalovirus pp65 or against adenovirus and Epstein-Barr virus EBNA3C protein: a novel approach for immunotherapy

artículo científico publicado en 2002

Adult celiac disease with severe or partial villous atrophy: a comparative study

artículo científico publicado en 2008

Adulthood-Onset Celiac Disease Is Associated with Intercellular Adhesion Molecule-1 (ICAM-1) Gene Polymorphism

article

Age-dependent HLA genetic heterogeneity of type 1 insulin-dependent diabetes mellitus ⬇️

artículo científico publicado el 1 de diciembre de 1992

Anti-bovine serum albumin antibodies: genetic heterogeneity and clinical relevance in adult-onset IDDM.

artículo científico publicado en 1995

Anticardiolipin antibodies in patients with multiple sclerosis do not represent a subgroup of patients according to clinical, familial, and biological characteristics.

artículo científico publicado en 2002

Antigen crosspresentation by human plasmacytoid dendritic cells.

artículo científico publicado en 2007

Association of PTPN22+1858C/T polymorphism with Type 1 diabetes in the North Indian population

artículo científico publicado en 2014

Association of the AChRα-subunit Gene (CHRNA), DQA1*0101, and the DR3 Haplotype in Myasthenia Gravis. Evidence for a Three-gene Disease Model in a Subgroup of Patients

article

Association of the R92QTNFRSF1Amutation and extracranial deep vein thrombosis in patients with Behçet's disease

scientific article published on 01 February 2005

Associations of MHC ancestral haplotypes with resistance/susceptibility to AIDS disease development

artículo científico publicado en 2003

Automation of large-scale HLA oligotyping using a robotic workstation.

artículo científico publicado en 1993

BCR/ABL promotes dendritic cell-mediated natural killer cell activation

artículo científico publicado en 2005

Bidirectional intragraft alloreactivity drives the repopulation of human intestinal allografts and correlates with clinical outcome.

artículo científico publicado en 2016

Blood transfusions under cyclosporine coverage before renal transplantation in children

artículo científico publicado en 1995

CD4+CD25+ regulatory T cells inhibit natural killer cell functions in a transforming growth factor-beta-dependent manner

artículo científico publicado en 2005

CD4+NKG2D+ T Cells in Crohn’s Disease Mediate Inflammatory and Cytotoxic Responses Through MICA Interactions

article

CTLA-4 gene polymorphism is associated with predisposition to IDDM in a population from central Poland.

artículo científico publicado en 1998

CTLA-4/CD 28 region polymorphisms in children from families with autoimmune hepatitis ⬇️

artículo científico publicado el 1 de diciembre de 2001

Cellular expression, trafficking, and function of two isoforms of human ULBP5/RAET1G.

artículo científico publicado en 2009

Characteristics of Vogt-Koyanagi-Harada disease in a French cohort: ethnicity, systemic manifestations, and HLA genotype data

artículo científico publicado en 2008

Circulating regulatory anti-T cell receptor antibodies in patients with myasthenia gravis

artículo científico publicado en 2003

Clinical characteristics of type 2 diabetes in patients with mutations of HFE

artículo científico publicado en 2000

Clinicopathological significance of major histocompatibility complex class I-related chain a and B expression in thyroid cancer

artículo científico publicado en 2006

Comparative analysis of human NK cell activation induced by NKG2D and natural cytotoxicity receptors

artículo científico publicado en 2004

Contribution of DRB1*04 Variants to Predisposition to or Protection from Insulin Dependent Diabetes Mellitus is Independent of DQ

artículo científico publicado en 1996

Controversies about the histological features of chronic HCV patients with persistently normal alanine transaminase levels: what can be done about the present definition?

artículo científico publicado en 2002

Correction of Fas (CD95) deficiency by haploidentical bone marrow transplantation.

artículo científico publicado en 1997

Correction: Cellular Expression, Trafficking, and Function of Two Isoforms of Human ULBP5/RAET1G

artículo científico publicado en 2009

Correction: Cellular Expression, Trafficking, and Function of Two Isoforms of Human ULBP5/RAET1G.

artículo científico publicado en 2009

Crohn’s disease associated CARD15 (NOD2) variants are not involved in the susceptibility to type 1 diabetes

Ctla-4 blockade confers lymphocyte resistance to regulatory T-cells in advanced melanoma: surrogate marker of efficacy of tremelimumab?

artículo científico publicado en 2008

Delineation of Late Onset Hypoventilation Associated with Hypothalamic Dysfunction Syndrome

Dendritic cell-derived exosomes promote natural killer cell activation and proliferation: a role for NKG2D ligands and IL-15Ralpha

artículo científico publicado en 2009

Dermatite herpétiforme survenant chez des patients atteints de maladie cœliaque dans l'enfance

scientific article published on 01 June 1996

Diabetes mellitus after abdominal radiation therapy

artículo científico publicado en 1995

Differences in the frequency and function of HHV8-specific CD8 T cells between asymptomatic HHV8 infection and Kaposi sarcoma

artículo científico publicado en 2006

Differential in situ expression of cytokines in renal allograft rejection

artículo científico publicado en 1991

Distinct HLA class II alleles determine antibody response to vaccination with hepatitis B surface antigen

artículo científico publicado en 1998

Distinctive effects of CCR5, CCR2, and SDF1 genetic polymorphisms in AIDS progression

artículo científico publicado en 1998

Distribution of HLA-DRB1 alleles in a mixed population with insulin-dependent diabetes mellitus from the southeast of Brazil

artículo científico publicado en 1998

Does haploidentical transplantation in children with primary immunodeficiencies have the potential to exploit donor NK cell alloreactivity?

artículo científico publicado en 2004

Donor-Specific Anti-HLA Antibodies in Allogeneic Hematopoietic Stem Cell Transplantation

artículo científico publicado en 2016

Early posttransplantation donor-derived invariant natural killer T-cell recovery predicts the occurrence of acute graft-versus-host disease and overall survival

artículo científico publicado en 2012

Enhanced prevalence of plasmatic soluble MHC class I chain-related molecule in vascular pregnancy diseases

artículo científico publicado en 2014

Evidence after imputation for a role of MICA variants in nonprogression and elite control of HIV type 1 infection

artículo científico publicado en 2014

Ex vivo characterization of multiepitopic tumor-specific CD8 T cells in patients with chronic myeloid leukemia: implications for vaccine development and adoptive cellular immunotherapy

artículo científico publicado en 2005

Excessive interleukin-15 transpresentation endows NKG2D+CD4+ T cells with innate-like capacity to lyse vascular endothelium in granulomatosis with polyangiitis (Wegener's)

artículo científico publicado en 2011

Expression of Major Histocompatibility Complex Class I Chain–Related Molecule A, NKG2D, and Transforming Growth Factor–β in the Liver of Humans with Alveolar Echinococcosis: New Actors in the Tolerance to Parasites?

scientific article published on 01 May 2008

Expression of NKG2D and CD107 in CD8(+) effector memory lymphocytes in Churg-Strauss syndrome

artículo científico publicado en 2012

FCRL3 −169CT functional polymorphism in type 1 diabetes and autoimmunity traits

artículo científico publicado en 2007

Factors associated with the presence of glutamic acid decarboxylase and islet antigen-2 autoantibodies in patients with long-standing type 1 diabetes

artículo científico publicado en 2013

Family study of linkage disequilibrium between TAP2 transporter and HLA class II genes. Absence of TAP2 contribution to association with insulin-dependent diabetes mellitus.

artículo científico publicado en 1995

Family-based association of HLA class II alleles and haplotypes with type I diabetes in Brazilians reveals some characteristics of a highly diversified population

artículo científico publicado en 2001

Feto-maternal microchimerism in connective tissue diseases

artículo científico publicado en 2002

Focal segmental glomerulosclerosis associated with mitochondrial cytopathy

artículo científico publicado en 2000

Genetic predisposition to IDDM.

artículo científico publicado en 2000

Genetic predisposition to autoimmune endocrine diseases.

artículo científico publicado en 1999

Genetics of autoimmune endocrine diseases

artículo científico publicado en 1993

HIV-1 virological remission lasting more than 12 years after interruption of early antiretroviral therapy in a perinatally infected teenager enrolled in the French ANRS EPF-CO10 paediatric cohort: a case report

artículo científico publicado en 2015

HLA class I polymorphism in a Moroccan population from Casablanca.

artículo científico publicado en 2002

HLA class II DNA polymorphism in a Moroccan population from the Souss, Agadir area

artículo científico publicado en 1998

HLA class II allele and haplotype distribution in a population from central Poland

artículo científico publicado en 1998

HLA class II-associated predisposition to insulin-dependent diabetes mellitus in a Polish population

artículo científico publicado en 1998

HLA genetic heterogeneity of hepatitis B vaccine response in hemodialyzed patients

artículo científico publicado en 1993

HLA-Associated Heterogeneity of the Humoral Response to Islet Antigens in Insulin-dependent Diabetes

artículo científico publicado en 1995

HLA-B phenotype modifies the course of Behçet's disease in Moroccan patients.

artículo científico publicado en 2003

Hepatitis C virus (HCV) evades NKG2D-dependent NK cell responses through NS5A-mediated imbalance of inflammatory cytokines.

artículo científico publicado en 2010

How NKG2D ligands trigger autoimmunity?

artículo científico publicado en 2006

Human Herpesvirus 8 (HHV8) sequentially shapes the NK cell repertoire during the course of asymptomatic infection and Kaposi sarcoma

artículo científico publicado en 2012

Human leukocyte antigen class II alleles may contribute to the severity of hepatitis C virus-related liver disease

artículo científico publicado en 2002

Identification by genomic typing of non-DR3 HLA class II genes associated with myasthenia gravis

artículo científico publicado en 1993

Identification of peptides from autoantigens GAD65 and IA-2 that bind to HLA class II molecules predisposing to or protecting from type 1 diabetes

artículo científico publicado en 1999

Impact of HLA matching on outcome of hematopoietic stem cell transplantation in children with inherited diseases: a single-center comparative analysis of genoidentical, haploidentical or unrelated donors

article

In situ antigenic modulation of human graft-infiltrating T cells is induced by OKT3 treatment

artículo científico publicado en 1990

Induction of NKG2D ligands by gamma radiation and tumor necrosis factor-alpha may participate in the tissue damage during acute graft-versus-host disease

artículo científico publicado en 2008

Influence of HLA-DR phenotype on the risk of hepatitis C virus-associated mixed cryoglobulinemia

artículo científico publicado en 2001

Insulin-Dependent Diabetes Mellitus in Non-DR3/Non-DR4 Subjects

artículo científico publicado en 1997

Insulin-dependent diabetes and human leucocyte antigens

artículo científico publicado en 1997

Interleukin-15 activates human natural killer cells to clear the intestinal protozoan cryptosporidium.

artículo científico publicado en 2005

Intrahepatic virus-specific IL-10-producing CD8 T cells prevent liver damage during chronic hepatitis C virus infection

artículo científico publicado en 2006

Is there any impact of HLA-DPB1 disparity in 10/10 HLA-matched unrelated hematopoietic SCT? Results of a French multicentric retrospective study.

artículo científico publicado en 2014

Islet cell antibody heterogeneity among type 1 (insulin-dependent) diabetic patients

artículo científico publicado el 1 de agosto de 1992

Lack of evidence of a specific role for C4A gene deficiency in determining disease susceptibility among C4-deficient patients with systemic lupus erythematosus (SLE).

artículo científico publicado en 2001

Linkage analyses of chromosome 6 loci, including HLA, in familial aggregations of Crohn disease

artículo científico publicado en 1994

Linkage and association study of the CTLA-4 region in coeliac disease for Italian and Tunisian populations.

artículo científico publicado en 1999

Linkage disequilibrium between HLA class II (DR, DQ, DP) and antigen processing (LMP, TAP, DM) genes of the major histocompatibility complex.

artículo científico publicado en 1996

Linkage disequilibrium between HLA class II region and autoimmune hepatitis in pediatric patients

artículo científico publicado en 2004

Long-term T-cell reconstitution after hematopoietic stem-cell transplantation in primary T-cell-immunodeficient patients is associated with myeloid chimerism and possibly the primary disease phenotype

scientific article published on 01 February 2007

Long-term follow-up of 61 coeliac patients diagnosed in childhood: evolution toward latency is possible on a normal diet

artículo científico publicado en 2007

MHC Class I Chain-Related Gene A Diversity in Head and Neck Squamous Cell Carcinoma

article

Major histocompatibility class II genes polymorphism in insulin dependent diabetes mellitus with or without associated thyroid autoimmunity.

artículo científico publicado en 1998

Maternally inherited diabetes and deafness: a multicenter study

artículo científico publicado en 2001

Mechanisms and significance of HLA type I diabetes association

artículo científico publicado en 1991

Microchimerism frequency two to thirty years after cadaveric kidney transplantation

scientific article published on 01 September 1994

Molecular mechanisms of HLA association with autoimmune diseases.

artículo científico publicado en 2008

Mutations in HFE, the hemochromatosis candidate gene, in patients with NIDDM.

artículo científico publicado en 1998

NCR3/NKp30 contributes to pathogenesis in primary Sjogren's syndrome

artículo científico publicado en 2013

NKG2D expression on HIV-specific CD8+ T cells is reduced in viremic HIV-1-infected patients but maintained in HIV controllers

artículo científico publicado en 2013

NKp30 isoforms and NKp30 ligands are predictive biomarkers of response to imatinib mesylate in metastatic GIST patients

artículo científico publicado en 2016

New class I and II HLA alleles strongly associated with opposite patterns of progression to AIDS.

artículo científico publicado en 1999

New insights into the understanding of MHC associations with immune-mediated disorders

artículo científico publicado en 2017

No association between the Friedreich's ataxia gene and NIDDM in the French population

article

No major role for the CTLA-4 gene in the association of autoimmune thyroid disease with IDDM

artículo científico publicado en 1998

Ontogeny of human mucosal-associated invariant T cells and related T cell subsets

artículo científico publicado en 2018

PD-1 mediates functional exhaustion of activated NK cells in patients with Kaposi sarcoma

artículo científico publicado en 2016

PTPN22 R620W Functional Variant in Type 1 Diabetes and Autoimmunity Related Traits

artículo científico publicado en 2007

Peripheral microchimerism in long-term cadaveric-kidney allograft recipients

scientific article published in The Lancet

Physiopathologie de la maladie de Behçet

artículo científico publicado en 2006

Polymorphism of antigen processing (TAP, LMP) and HLA class II genes in celiac disease

article

Polymorphism of the HLA-DMA and DMB genes in Rheumatoid Arthritis

article

Potential role of NKG2D/MHC class I-related chain A interaction in intrathymic maturation of single-positive CD8 T cells

artículo científico publicado en 2003

Prevalence of macular pattern dystrophy in maternally inherited diabetes and deafness

scientific article published on 01 September 1999

Protection from insulin-dependent diabetes mellitus is linked to a peptide transporter gene

article

Rationale for a T Cell Receptor Peptide Therapy in Myasthenia Gravis

artículo científico publicado en 2003

Recognition of a subregion of human proinsulin by class I-restricted T cells in type 1 diabetic patients

artículo científico publicado en 2005

Recognition of human proinsulin leader sequence by class I-restricted T-cells in HLA-A*0201 transgenic mice and in human type 1 diabetes

artículo científico publicado en 2008

Reevaluation of the relative risk for susceptibility to celiac disease of HLA-DRB1, -DQA1, -DQB1, -DPB1, and -TAP2 alleles in a French population

artículo científico publicado en 1995

Regulation of CD4(+)NKG2D(+) Th1 cells in patients with metastatic melanoma treated with sorafenib: role of IL-15Rα and NKG2D triggering

artículo científico publicado en 2013

Relationship between peptide selectivities of human transporters associated with antigen processing and HLA class I molecules ⬇️

artículo científico publicado el 15 de julio de 1998

Relationship of HLA-DQ8 and severity of celiac disease: comparison of New York and Parisian cohorts

artículo científico publicado en 2004

Severe cutaneous papillomavirus disease after haemopoietic stem-cell transplantation in patients with severe combined immune deficiency caused by common gammac cytokine receptor subunit or JAK-3 deficiency

artículo científico publicado en 2004

Sjogren syndrome: an unexpected disease occurring fourteen years after oligoarticular onset juvenile idiopathic arthritis

scientific article published on 01 October 2002

Soluble MHC Class I chain-related molecule serum levels are predictive markers of implantation failure and successful term pregnancies following IVF

artículo científico publicado en 2007

Structural analysis of two HLA-DR-presented autoantigenic epitopes: crucial role of peripheral but not central peptide residues for T-cell receptor recognition

artículo científico publicado en 2000

Substrate selection by transporters associated with antigen processing occurs during peptide binding to TAP.

artículo científico publicado en 1998

Systemic chimerism in cadaveric kidney allograft recipients

scientific article published on 01 February 1995

T-cell-depleted HLA non-identical bone marrow transplantation in the child: prevention of graft-versus-host reaction by administration of donor T lymphocytes alloreactive against the recipient

artículo científico publicado en 2001

TAP1 and TAP2 transporter genes and predisposition to insulin dependent diabetes mellitus

artículo científico publicado el 1 de enero de 1992

The decreased susceptibility of Bcr/Abl targets to NK cell-mediated lysis in response to imatinib mesylate involves modulation of NKG2D ligands, GM1 expression, and synapse formation

artículo científico publicado en 2006

Tissue-specific microvascular endothelial cells show distinct capacity to activate NK cells: implications for the pathophysiology of granulomatosis with polyangiitis

artículo científico publicado en 2014

Transfer of Symptomatic Peanut Allergy to the Recipient of a Combined Liver-And-Kidney Transplant

scientific article published on 01 September 1997

Transient familial haemophagocytic lymphohistiocytosis reactivation post-CD34 haematopoietic stem cell transplantation

artículo científico publicado en 2005

Use of Single-Antigen Flow Beads Assays to Assess Anti-HLA Donor-Specific Antibody Strength

artículo científico publicado en 2015

Xenotransplantation: baboons as potential liver donors? Scientific and ethical issues

artículo científico publicado en 1993

[Recent findings on the genetics of Behçet's disease]

artículo científico publicado en 1999

[Routine application of HLA class II oligotyping. Value of automatization]

artículo científico publicado en 1992

[Screening of pre-diabetes type I: possibilities and limits]

artículo científico publicado en 1992

Lista de obras de Sophie Caillat-Zucman

21-Hydroxylase epitopes are targeted by CD8 T cells in autoimmune Addison’s disease

35th Annual Meeting of the European Association for the Study of Diabetes

35th Annual Meeting of the European Association for the Study of Diabetes : Brussels, Belgium, 28 September-2 October 1999

A Common Stromal Cell-Derived Factor-1 Chemokine Gene Variant is Associated With the Early Onset of Type 1 Diabetes

A dinucleotide repeat polymorphism at the poly(ADP-ribose) polymerase gene is not associated with predisposition to type 1 diabetes in French Caucasians

A direct role for NKG2D/MICA interaction in villous atrophy during celiac disease.

Absence of functional relevance of human transporter associated with antigen processing polymorphism for peptide selection ⬇️

Absence of primary association between DM gene polymorphism and insulin-dependent diabetes mellitus or celiac disease

Adenovirally transduced dendritic cells induce bispecific cytotoxic T lymphocyte responses against adenovirus and cytomegalovirus pp65 or against adenovirus and Epstein-Barr virus EBNA3C protein: a novel approach for immunotherapy

Adult celiac disease with severe or partial villous atrophy: a comparative study

Adulthood-Onset Celiac Disease Is Associated with Intercellular Adhesion Molecule-1 (ICAM-1) Gene Polymorphism

Age-dependent HLA genetic heterogeneity of type 1 insulin-dependent diabetes mellitus ⬇️

Anti-bovine serum albumin antibodies: genetic heterogeneity and clinical relevance in adult-onset IDDM.

Anticardiolipin antibodies in patients with multiple sclerosis do not represent a subgroup of patients according to clinical, familial, and biological characteristics.

Antigen crosspresentation by human plasmacytoid dendritic cells.

Association of PTPN22+1858C/T polymorphism with Type 1 diabetes in the North Indian population

Association of the AChRα-subunit Gene (CHRNA), DQA1*0101, and the DR3 Haplotype in Myasthenia Gravis. Evidence for a Three-gene Disease Model in a Subgroup of Patients

Association of the R92QTNFRSF1Amutation and extracranial deep vein thrombosis in patients with Behçet's disease

Associations of MHC ancestral haplotypes with resistance/susceptibility to AIDS disease development

Automation of large-scale HLA oligotyping using a robotic workstation.

BCR/ABL promotes dendritic cell-mediated natural killer cell activation

Bidirectional intragraft alloreactivity drives the repopulation of human intestinal allografts and correlates with clinical outcome.

Blood transfusions under cyclosporine coverage before renal transplantation in children

CD4+CD25+ regulatory T cells inhibit natural killer cell functions in a transforming growth factor-beta-dependent manner

CD4+NKG2D+ T Cells in Crohn’s Disease Mediate Inflammatory and Cytotoxic Responses Through MICA Interactions

CTLA-4 gene polymorphism is associated with predisposition to IDDM in a population from central Poland.

CTLA-4/CD 28 region polymorphisms in children from families with autoimmune hepatitis ⬇️

Cellular expression, trafficking, and function of two isoforms of human ULBP5/RAET1G.

Characteristics of Vogt-Koyanagi-Harada disease in a French cohort: ethnicity, systemic manifestations, and HLA genotype data

Circulating regulatory anti-T cell receptor antibodies in patients with myasthenia gravis

Clinical characteristics of type 2 diabetes in patients with mutations of HFE

Clinicopathological significance of major histocompatibility complex class I-related chain a and B expression in thyroid cancer

Comparative analysis of human NK cell activation induced by NKG2D and natural cytotoxicity receptors

Contribution of DRB1*04 Variants to Predisposition to or Protection from Insulin Dependent Diabetes Mellitus is Independent of DQ

Controversies about the histological features of chronic HCV patients with persistently normal alanine transaminase levels: what can be done about the present definition?

Correction of Fas (CD95) deficiency by haploidentical bone marrow transplantation.

Correction: Cellular Expression, Trafficking, and Function of Two Isoforms of Human ULBP5/RAET1G

Correction: Cellular Expression, Trafficking, and Function of Two Isoforms of Human ULBP5/RAET1G.

Crohn’s disease associated CARD15 (NOD2) variants are not involved in the susceptibility to type 1 diabetes

Ctla-4 blockade confers lymphocyte resistance to regulatory T-cells in advanced melanoma: surrogate marker of efficacy of tremelimumab?

Delineation of Late Onset Hypoventilation Associated with Hypothalamic Dysfunction Syndrome

Dendritic cell-derived exosomes promote natural killer cell activation and proliferation: a role for NKG2D ligands and IL-15Ralpha

Dermatite herpétiforme survenant chez des patients atteints de maladie cœliaque dans l'enfance

Diabetes mellitus after abdominal radiation therapy

Differences in the frequency and function of HHV8-specific CD8 T cells between asymptomatic HHV8 infection and Kaposi sarcoma

Differential in situ expression of cytokines in renal allograft rejection

Distinct HLA class II alleles determine antibody response to vaccination with hepatitis B surface antigen

Distinctive effects of CCR5, CCR2, and SDF1 genetic polymorphisms in AIDS progression

Distribution of HLA-DRB1 alleles in a mixed population with insulin-dependent diabetes mellitus from the southeast of Brazil

Does haploidentical transplantation in children with primary immunodeficiencies have the potential to exploit donor NK cell alloreactivity?

Donor-Specific Anti-HLA Antibodies in Allogeneic Hematopoietic Stem Cell Transplantation

Early posttransplantation donor-derived invariant natural killer T-cell recovery predicts the occurrence of acute graft-versus-host disease and overall survival

Enhanced prevalence of plasmatic soluble MHC class I chain-related molecule in vascular pregnancy diseases

Evidence after imputation for a role of MICA variants in nonprogression and elite control of HIV type 1 infection

Ex vivo characterization of multiepitopic tumor-specific CD8 T cells in patients with chronic myeloid leukemia: implications for vaccine development and adoptive cellular immunotherapy

Excessive interleukin-15 transpresentation endows NKG2D+CD4+ T cells with innate-like capacity to lyse vascular endothelium in granulomatosis with polyangiitis (Wegener's)

Expression of Major Histocompatibility Complex Class I Chain–Related Molecule A, NKG2D, and Transforming Growth Factor–β in the Liver of Humans with Alveolar Echinococcosis: New Actors in the Tolerance to Parasites?

Expression of NKG2D and CD107 in CD8(+) effector memory lymphocytes in Churg-Strauss syndrome

FCRL3 −169CT functional polymorphism in type 1 diabetes and autoimmunity traits

Factors associated with the presence of glutamic acid decarboxylase and islet antigen-2 autoantibodies in patients with long-standing type 1 diabetes

Family study of linkage disequilibrium between TAP2 transporter and HLA class II genes. Absence of TAP2 contribution to association with insulin-dependent diabetes mellitus.

Family-based association of HLA class II alleles and haplotypes with type I diabetes in Brazilians reveals some characteristics of a highly diversified population

Feto-maternal microchimerism in connective tissue diseases

Focal segmental glomerulosclerosis associated with mitochondrial cytopathy

Genetic predisposition to IDDM.

Genetic predisposition to autoimmune endocrine diseases.

Genetics of autoimmune endocrine diseases

HIV-1 virological remission lasting more than 12 years after interruption of early antiretroviral therapy in a perinatally infected teenager enrolled in the French ANRS EPF-CO10 paediatric cohort: a case report

HLA class I polymorphism in a Moroccan population from Casablanca.

HLA class II DNA polymorphism in a Moroccan population from the Souss, Agadir area

HLA class II allele and haplotype distribution in a population from central Poland

HLA class II-associated predisposition to insulin-dependent diabetes mellitus in a Polish population

HLA genetic heterogeneity of hepatitis B vaccine response in hemodialyzed patients

HLA-Associated Heterogeneity of the Humoral Response to Islet Antigens in Insulin-dependent Diabetes

HLA-B phenotype modifies the course of Behçet's disease in Moroccan patients.

Hepatitis C virus (HCV) evades NKG2D-dependent NK cell responses through NS5A-mediated imbalance of inflammatory cytokines.

How NKG2D ligands trigger autoimmunity?

Human Herpesvirus 8 (HHV8) sequentially shapes the NK cell repertoire during the course of asymptomatic infection and Kaposi sarcoma

Human leukocyte antigen class II alleles may contribute to the severity of hepatitis C virus-related liver disease