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Fine-Scale Mapping at IGAD1 and Genome-Wide Genetic Linkage Analysis Implicate HLA-DQ/DR as a Major Susceptibility Locus in Selective IgA Deficiency and Common Variable Immunodeficiency

The Journal of immunology (1950), 2003-03, Vol.170 (5), p.2765-2775

2003

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Linkage of autosomal-dominant common variable immunodeficiency to chromosome 4q

European journal of human genetics : EJHG, 2006-07, Vol.14 (7), p.867-875

2006

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Role for Mannose Binding Lectin in the Prevention of Mycoplasma Infection

Infection and Immunity, 2005-08, Vol.73 (8), p.5238-5240

2005

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A 9-yr evaluation of carrier erythrocyte encapsulated adenosine deaminase (ADA) therapy in a patient with adult-type ADA deficiency

European journal of haematology, 2007-10, Vol.79 (4), p.338-348

2007

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Selective deficits in blood dendritic cell subsets in common variable immunodeficiency and X-linked agammaglobulinaemia but not specific polysaccharide antibody deficiency

Clinical immunology (Orlando, Fla.), 2008-04, Vol.127 (1), p.34-42

2008

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Analysis of families with common variable immunodeficiency (VID) and IgA deficiency suggests linkage of CVID to chromosome 16q

Human genetics, 2006-02, Vol.118 (6), p.725-729

2006

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Relevance of biallelic versus monoallelic TNFRSF13B mutations in distinguishing disease-causing from risk-increasing TNFRSF13B variants in antibody deficiency syndromes

Blood, 2009-02, Vol.113 (9), p.1967-1976

2009

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Effect of anti‐CD20 (rituximab) on resistant thrombocytopenia in autoimmune lymphoproliferative syndrome

British journal of haematology, 2002-09, Vol.118 (4), p.1078-1081

2002

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The immunocompromised patient: primary immunodeficiencies

Medicine (Abingdon. 1995, UK ed.), 2013-11, Vol.41 (11), p.619-623

Webster, A. David B

2013

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The immunocompromised patient: primary immunodeficiencies

Medicine (Abingdon. 1995, UK ed.), 2009-10, Vol.37 (10), p.518-521

Webster, A. David B

2009

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Up-Regulation of IL-12 in Monocytes: A Fundamental Defect in Common Variable Immunodeficiency

The Journal of immunology (1950), 2000-01, Vol.164 (1), p.488-494

2000

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ATM Mutations in cancer families

Cancer research (Chicago, Ill.), 1996-09, Vol.56 (18), p.4130-4133

1996

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Infection in patients with congenital immune deficiencies

Current opinion in infectious diseases, 1998-08, Vol.11 (4), p.419-424

1998

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Short tandem repeat (STR) haplotypes in HLA: an integrated 50-kb STR/linkage disequilibrium/gene map between the RING3 and HLA-B genes and identification of STR haplotype diversification in the class III region

European journal of human genetics : EJHG, 2001-08, Vol.9 (8), p.590-598

2001

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Ataxia-telangiectasia and T-cell leukemias : No evidence for somatic ATM mutation in sporadic T-ALL or for hypermethylation of the ATM-NPAT/E14 bidirectional promoter in T-PLL

Cancer research (Chicago, Ill.), 1998-06, Vol.58 (11), p.2293-2297

1998

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Structural Basis for Chromosome X-Linked Agammaglobulinemia: A Tyrosine Kinase Disease

Proceedings of the National Academy of Sciences - PNAS, 1994-12, Vol.91 (26), p.12803-12807

1994

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A Putative Susceptibility Locus on Chromosome 18 Is Not a Major Contributor to Human Selective IgA Deficiency: Evidence from Meiotic Mapping of 83 Multiple-Case Families

The Journal of immunology (1950), 1999-08, Vol.163 (4), p.2236-2242

1999

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Mutation pattern in the Bruton's tyrosine kinase gene in 26 unrelated patients with X-linked agammaglobulinemia

Human mutation, 1997, Vol.9 (5), p.418-425

1997

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Genetic Linkage of IgA Deficiency to the Major Histocompatibility Complex: Evidence for Allele Segregation Distortion, Parent-of-Origin Penetrance Differences, and the Role of Anti-IgA Antibodies in Disease Predisposition

American journal of human genetics, 1999-04, Vol.64 (4), p.1096-1109

1999

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Clustering of missense mutations in the ataxia-telangiectasia gene in a sporadic T-cell leukaemia

Nature genetics, 1997-09, Vol.17 (1), p.96-99

1997

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Fine mapping of IGAD1 in IgA deficiency and common variable immunodeficiency: identification and characterization of haplotypes shared by affected members of 101 multiple-case families

The Journal of immunology (1950), 2000-04, Vol.164 (8), p.4408-4416

2000

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The ATM gene and susceptibility to breast cancer : Analysis of 38 breast tumors reveals no evidence for mutation

Cancer research (Chicago, Ill.), 1996-06, Vol.56 (12), p.2726-2732

1996

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Clustering of missense mutations in the ataxia-telanglectasia gene in a sporadic T-cell leukaemia

Nature genetics, 1997-09, Vol.17 (1), p.96-99

1997

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Mutations in the DNA ligase I gene of an individual with immunodeficiencies and cellular hypersensitivity to DNA-damaging agents

Cell, 1992-05, Vol.69 (3), p.495-503

1992

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COMMON VARIABLE IMMUNODEFICIENCY

Immunology and allergy clinics of North America, 2001-02, Vol.21 (1), p.1-22

Webster, A. David B.

2001

Volltextzugriff (PDF)

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Fine-Scale Mapping at IGAD1 and Genome-Wide Genetic Linkage Analysis Implicate HLA-DQ/DR as a Major Susceptibility Locus in Selective IgA Deficiency and Common Variable Immunodeficiency

Linkage of autosomal-dominant common variable immunodeficiency to chromosome 4q

Role for Mannose Binding Lectin in the Prevention of Mycoplasma Infection

A 9-yr evaluation of carrier erythrocyte encapsulated adenosine deaminase (ADA) therapy in a patient with adult-type ADA deficiency

Selective deficits in blood dendritic cell subsets in common variable immunodeficiency and X-linked agammaglobulinaemia but not specific polysaccharide antibody deficiency

Analysis of families with common variable immunodeficiency (VID) and IgA deficiency suggests linkage of CVID to chromosome 16q

Relevance of biallelic versus monoallelic TNFRSF13B mutations in distinguishing disease-causing from risk-increasing TNFRSF13B variants in antibody deficiency syndromes

Effect of anti‐CD20 (rituximab) on resistant thrombocytopenia in autoimmune lymphoproliferative syndrome

The immunocompromised patient: primary immunodeficiencies

The immunocompromised patient: primary immunodeficiencies

Up-Regulation of IL-12 in Monocytes: A Fundamental Defect in Common Variable Immunodeficiency

ATM Mutations in cancer families

Infection in patients with congenital immune deficiencies

Short tandem repeat (STR) haplotypes in HLA: an integrated 50-kb STR/linkage disequilibrium/gene map between the RING3 and HLA-B genes and identification of STR haplotype diversification in the class III region

Ataxia-telangiectasia and T-cell leukemias : No evidence for somatic ATM mutation in sporadic T-ALL or for hypermethylation of the ATM-NPAT/E14 bidirectional promoter in T-PLL

Structural Basis for Chromosome X-Linked Agammaglobulinemia: A Tyrosine Kinase Disease

A Putative Susceptibility Locus on Chromosome 18 Is Not a Major Contributor to Human Selective IgA Deficiency: Evidence from Meiotic Mapping of 83 Multiple-Case Families

Mutation pattern in the Bruton's tyrosine kinase gene in 26 unrelated patients with X-linked agammaglobulinemia

Genetic Linkage of IgA Deficiency to the Major Histocompatibility Complex: Evidence for Allele Segregation Distortion, Parent-of-Origin Penetrance Differences, and the Role of Anti-IgA Antibodies in Disease Predisposition

Clustering of missense mutations in the ataxia-telangiectasia gene in a sporadic T-cell leukaemia

Fine mapping of IGAD1 in IgA deficiency and common variable immunodeficiency: identification and characterization of haplotypes shared by affected members of 101 multiple-case families

The ATM gene and susceptibility to breast cancer : Analysis of 38 breast tumors reveals no evidence for mutation

Clustering of missense mutations in the ataxia-telanglectasia gene in a sporadic T-cell leukaemia

Mutations in the DNA ligase I gene of an individual with immunodeficiencies and cellular hypersensitivity to DNA-damaging agents

COMMON VARIABLE IMMUNODEFICIENCY

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