(Q40638236)

22 September 2017

Primary immunodeficiency diseases: dissectors of the immune system (English)

1 reference

22 September 2017

Rebecca H Buckley

1

1 reference

22 September 2017

1 July 2002

1 reference

22 September 2017

Immunological Reviews

1 reference

22 September 2017

185

1 reference

22 September 2017

206-219

1 reference

IMMUNOLOGICAL FUNCTION OF THE THYMUS

22 September 2017

1 reference

https://api.crossref.org/works/10.1034%2FJ.1600-065X.2002.18517.X

The role of the thymus in development of immunologic capacity in rabbits and mice

21 January 2018

1 reference

https://api.crossref.org/works/10.1034%2FJ.1600-065X.2002.18517.X

The Bursa of Fabricius and Antibody Production

21 January 2018

1 reference

https://api.crossref.org/works/10.1034%2FJ.1600-065X.2002.18517.X

Role of the thymus and other central lymphoid tissues in immunological disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1034%2FJ.1600-065X.2002.18517.X

Protection of phagocytized bacteria from the killing action of antibiotics.

21 January 2018

1 reference

https://api.crossref.org/works/10.1034%2FJ.1600-065X.2002.18517.X

Immunodeficiency diseases caused by defects in phagocytes

21 January 2018

1 reference

https://api.crossref.org/works/10.1034%2FJ.1600-065X.2002.18517.X

21 January 2018

The hyper-IgE syndrome

1 reference

https://api.crossref.org/works/10.1034%2FJ.1600-065X.2002.18517.X

Hyper-IgE syndrome with recurrent infections--an autosomal dominant multisystem disorder

21 January 2018

1 reference

https://api.crossref.org/works/10.1034%2FJ.1600-065X.2002.18517.X

Immunoglobulin spots on the surface of rabbit lymphocytes

21 January 2018

1 reference

https://api.crossref.org/works/10.1034%2FJ.1600-065X.2002.18517.X

Continuous cultures of fused cells secreting antibody of predefined specificity

21 January 2018

1 reference

https://api.crossref.org/works/10.1034%2FJ.1600-065X.2002.18517.X

Delayed separation of the umbilical cord, widespread infections, and defective neutrophil mobility

21 January 2018

1 reference

https://api.crossref.org/works/10.1034%2FJ.1600-065X.2002.18517.X

Inherited deficiency of the Mac-1, LFA-1, p150,95 glycoprotein family and its molecular basis

21 January 2018

1 reference

https://api.crossref.org/works/10.1034%2FJ.1600-065X.2002.18517.X

Primary immunodeficiency diseases due to defects in lymphocytes

21 January 2018

1 reference

https://api.crossref.org/works/10.1034%2FJ.1600-065X.2002.18517.X

Searching for genes involved in the pathogenesis of primary immunodeficiency diseases: lessons from mouse knockouts

21 January 2018

1 reference

https://api.crossref.org/works/10.1034%2FJ.1600-065X.2002.18517.X

The glycoprotein encoded by the X-linked chronic granulomatous disease locus is a component of the neutrophil cytochrome b complex

21 January 2018

1 reference

https://api.crossref.org/works/10.1034%2FJ.1600-065X.2002.18517.X

Sequence-based analysis of properdin deficiency: identification of point mutations in two phenotypic forms of an X-linked immunodeficiency

21 January 2018

1 reference

https://api.crossref.org/works/10.1034%2FJ.1600-065X.2002.18517.X

IPEX is a unique X-linked syndrome characterized by immune dysfunction, polyendocrinopathy, enteropathy, and a variety of autoimmune phenomena

21 January 2018

1 reference

https://api.crossref.org/works/10.1034%2FJ.1600-065X.2002.18517.X

JM2, encoding a fork head-related protein, is mutated in X-linked autoimmunity-allergic disregulation syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1034%2FJ.1600-065X.2002.18517.X

A single ataxia telangiectasia gene with a product similar to PI-3 kinase

21 January 2018

1 reference

https://api.crossref.org/works/10.1034%2FJ.1600-065X.2002.18517.X

Cloning a balanced translocation associated with DiGeorge syndrome and identification of a disrupted candidate gene

21 January 2018

1 reference

https://api.crossref.org/works/10.1034%2FJ.1600-065X.2002.18517.X

A common region of 10p deleted in DiGeorge and velocardiofacial syndromes

21 January 2018

1 reference

https://api.crossref.org/works/10.1034%2FJ.1600-065X.2002.18517.X

A transcription map of the DiGeorge and velo-cardio-facial syndrome minimal critical region on 22q11.

21 January 2018

1 reference

https://api.crossref.org/works/10.1034%2FJ.1600-065X.2002.18517.X

A gene encoding a novel RFX-associated transactivator is mutated in the majority of MHC class II deficiency patients

21 January 2018

1 reference

https://api.crossref.org/works/10.1034%2FJ.1600-065X.2002.18517.X

Severe combined immunodeficiency due to a defect in the tyrosine kinase ZAP-70.

21 January 2018

1 reference

https://api.crossref.org/works/10.1034%2FJ.1600-065X.2002.18517.X

Mutation of Jak3 in a patient with SCID: essential role of Jak3 in lymphoid development.

21 January 2018

1 reference

https://api.crossref.org/works/10.1034%2FJ.1600-065X.2002.18517.X

Defective IL7R expression in T(-)B(+)NK(+) severe combined immunodeficiency

21 January 2018

1 reference

https://api.crossref.org/works/10.1034%2FJ.1600-065X.2002.18517.X

A new gene involved in DNA double-strand break repair and V(D)J recombination is located on human chromosome 10p

21 January 2018

1 reference

https://api.crossref.org/works/10.1034%2FJ.1600-065X.2002.18517.X

Activation-induced cytidine deaminase (AID) deficiency causes the autosomal recessive form of the Hyper-IgM syndrome (HIGM2)

21 January 2018

1 reference

https://api.crossref.org/works/10.1034%2FJ.1600-065X.2002.18517.X

Mutations in activation-induced cytidine deaminase in patients with hyper IgM syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1034%2FJ.1600-065X.2002.18517.X

Interferon-gamma-receptor deficiency in an infant with fatal bacille Calmette-Guérin infection

21 January 2018

1 reference

https://api.crossref.org/works/10.1034%2FJ.1600-065X.2002.18517.X

A mutation in the interferon-gamma-receptor gene and susceptibility to mycobacterial infection

21 January 2018

1 reference

https://api.crossref.org/works/10.1034%2FJ.1600-065X.2002.18517.X

Hereditary alterations in the immune response: coexistence of "agammaglobulinemia", acquired hypogammaglobulinemia and selective immunoglobulin deficiency in a sibship

21 January 2018

1 reference

https://api.crossref.org/works/10.1034%2FJ.1600-065X.2002.18517.X

HLA antigens in primary immunodeficiency diseases

21 January 2018

1 reference

https://api.crossref.org/works/10.1034%2FJ.1600-065X.2002.18517.X

Individuals with IgA deficiency and common variable immunodeficiency share polymorphisms of major histocompatibility complex class III genes

21 January 2018

1 reference

https://api.crossref.org/works/10.1034%2FJ.1600-065X.2002.18517.X

Mapping of the X-linked form of hyper-IgM syndrome (HIGM1) to Xq26 by close linkage to HPRT

21 January 2018

1 reference

https://api.crossref.org/works/10.1034%2FJ.1600-065X.2002.18517.X

A 39-kDa protein on activated helper T cells binds CD40 and transduces the signal for cognate activation of B cells

21 January 2018

1 reference

https://api.crossref.org/works/10.1034%2FJ.1600-065X.2002.18517.X

Specific missense mutations in NEMO result in hyper-IgM syndrome with hypohydrotic ectodermal dysplasia

21 January 2018

1 reference

https://api.crossref.org/works/10.1034%2FJ.1600-065X.2002.18517.X

Hyper IgM syndrome associated with defective CD40-mediated B cell activation

21 January 2018

1 reference

https://api.crossref.org/works/10.1034%2FJ.1600-065X.2002.18517.X

Mutations of CD40 gene cause an autosomal recessive form of immunodeficiency with hyper IgM.

21 January 2018

1 reference

https://api.crossref.org/works/10.1034%2FJ.1600-065X.2002.18517.X

Hematopoietic stem-cell transplantation for the treatment of severe combined immunodeficiency.

21 January 2018

1 reference

https://api.crossref.org/works/10.1034%2FJ.1600-065X.2002.18517.X

A severe combined immunodeficiency mutation in the mouse

21 January 2018

1 reference

https://api.crossref.org/works/10.1034%2FJ.1600-065X.2002.18517.X

Interleukin-2 receptor gamma chain mutation results in X-linked severe combined immunodeficiency in humans

21 January 2018

1 reference

https://api.crossref.org/works/10.1034%2FJ.1600-065X.2002.18517.X

The interleukin-2 receptor gamma chain maps to Xq13.1 and is mutated in X-linked severe combined immunodeficiency, SCIDX1.

21 January 2018

1 reference

https://api.crossref.org/works/10.1034%2FJ.1600-065X.2002.18517.X

Severe combined immunodeficiency: a retrospective single-center study of clinical presentation and outcome in 117 patients

21 January 2018

1 reference

https://api.crossref.org/works/10.1034%2FJ.1600-065X.2002.18517.X

Natural and engineered disorders of lymphocyte development

21 January 2018

1 reference

https://api.crossref.org/works/10.1034%2FJ.1600-065X.2002.18517.X

Adenosine deaminase deficiency: molecular basis and recent developments

21 January 2018

1 reference

https://api.crossref.org/works/10.1034%2FJ.1600-065X.2002.18517.X

Interleukin-2 receptor gamma chain: a functional component of the interleukin-7 receptor

21 January 2018

1 reference

https://api.crossref.org/works/10.1034%2FJ.1600-065X.2002.18517.X

RAG mutations in human B cell-negative SCID.

21 January 2018

1 reference

https://api.crossref.org/works/10.1034%2FJ.1600-065X.2002.18517.X

The interleukin-2 receptor gamma chain: its role in the multiple cytokine receptor complexes and T cell development in XSCID

21 January 2018

1 reference

https://api.crossref.org/works/10.1034%2FJ.1600-065X.2002.18517.X

Cutting edge: the common gamma-chain is an indispensable subunit of the IL-21 receptor complex

21 January 2018

1 reference

https://api.crossref.org/works/10.1034%2FJ.1600-065X.2002.18517.X

Interleukin-2 receptor gamma chain: a functional component of the interleukin-4 receptor

21 January 2018

1 reference

https://api.crossref.org/works/10.1034%2FJ.1600-065X.2002.18517.X

Mutations of Jak-3 gene in patients with autosomal severe combined immune deficiency (SCID)

21 January 2018

1 reference

https://api.crossref.org/works/10.1034%2FJ.1600-065X.2002.18517.X

Of genes and phenotypes: the immunological and molecular spectrum of combined immune deficiency. Defects of the gamma(c)-JAK3 signaling pathway as a model

21 January 2018

1 reference

https://api.crossref.org/works/10.1034%2FJ.1600-065X.2002.18517.X

Partial V(D)J recombination activity leads to Omenn syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1034%2FJ.1600-065X.2002.18517.X

Highly restricted human T cell repertoire in peripheral blood and tissue-infiltrating lymphocytes in Omenn's syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1034%2FJ.1600-065X.2002.18517.X

A human severe combined immunodeficiency (SCID) condition with increased sensitivity to ionizing radiations and impaired V(D)J rearrangements defines a new DNA recombination/repair deficiency

21 January 2018

1 reference

https://api.crossref.org/works/10.1034%2FJ.1600-065X.2002.18517.X

The use of intravenous immune globulin in immunodeficiency diseases

21 January 2018

1 reference

https://api.crossref.org/works/10.1034%2FJ.1600-065X.2002.18517.X

Hu-1: Major Histocompatibility Locus in Man

21 January 2018

1 reference

https://api.crossref.org/works/10.1034%2FJ.1600-065X.2002.18517.X

Hemopoietic stem cell transplantation using mouse bone marrow and spleen cells fractionated by lectins

21 January 2018

1 reference

https://api.crossref.org/works/10.1034%2FJ.1600-065X.2002.18517.X

Advances in the understanding and treatment of human severe combined immunodeficiency

21 January 2018

1 reference

https://api.crossref.org/works/10.1034%2FJ.1600-065X.2002.18517.X

Neonatal bone marrow transplantation for severe combined immunodeficiency

21 January 2018

1 reference

https://api.crossref.org/works/10.1034%2FJ.1600-065X.2002.18517.X

Gene therapy for immunodeficiency

21 January 2018

1 reference

https://api.crossref.org/works/10.1034%2FJ.1600-065X.2002.18517.X

The potential for therapy of immune disorders with gene therapy

21 January 2018

1 reference

https://api.crossref.org/works/10.1034%2FJ.1600-065X.2002.18517.X

Gene therapy for human severe combined immunodeficiencies

21 January 2018

1 reference

https://api.crossref.org/works/10.1034%2FJ.1600-065X.2002.18517.X

Sustained correction of X-linked severe combined immunodeficiency by ex vivo gene therapy

21 January 2018

1 reference

https://api.crossref.org/works/10.1034%2FJ.1600-065X.2002.18517.X

Gene therapy of human severe combined immunodeficiency (SCID)-X1 disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1034%2FJ.1600-065X.2002.18517.X

CD40 ligand mutations in X-linked immunodeficiency with hyper-IgM

21 January 2018

1 reference

https://api.crossref.org/works/10.1034%2FJ.1600-065X.2002.18517.X

Delineation of the Thymic and Bursal Lymphoid Systems in the Chicken

21 January 2018

1 reference

https://api.crossref.org/works/10.1034%2FJ.1600-065X.2002.18517.X

Defective expression of T-cell CD40 ligand causes X-linked immunodeficiency with hyper-IgM

21 January 2018

1 reference

https://api.crossref.org/works/10.1034%2FJ.1600-065X.2002.18517.X

Classification of Primary Immunodeficiencies

21 January 2018

1 reference

https://api.crossref.org/works/10.1034%2FJ.1600-065X.2002.18517.X

7 January 2021

The modulation of B7.2 and B7.1 on B cells by immunosuppressive agents

1 reference

https://api.crossref.org/works/10.1034%2FJ.1600-065X.2002.18517.X

7 January 2021

Adhesion molecule deficiencies and their clinical significance

1 reference

https://api.crossref.org/works/10.1034%2FJ.1600-065X.2002.18517.X

7 January 2021

4 Primary immunodeficiency mutation databases

1 reference

https://api.crossref.org/works/10.1034%2FJ.1600-065X.2002.18517.X

7 January 2021

Alterations of the X-linked lymphoproliferative disease gene SH2D1A in common variable immunodeficiency syndrome

1 reference

https://api.crossref.org/works/10.1034%2FJ.1600-065X.2002.18517.X

7 January 2021

Evidence for a defect in "switch" T cells in patients with immunodeficiency and hyperimmunoglobulinemia M

1 reference

https://api.crossref.org/works/10.1034%2FJ.1600-065X.2002.18517.X

7 January 2021

CD40 ligand gene defects responsible for X-linked hyper-IgM syndrome

1 reference

https://api.crossref.org/works/10.1034%2FJ.1600-065X.2002.18517.X

7 January 2021

The CD40 ligand, gp39, is defective in activated T cells from patients with X-linked hyper-IgM syndrome

1 reference

https://api.crossref.org/works/10.1034%2FJ.1600-065X.2002.18517.X

7 January 2021

Immunodeficiency with hyperimmunoglobulinemia M in two female patients is not associated with abnormalities of CD40 or CD40 ligand expression

1 reference

https://api.crossref.org/works/10.1034%2FJ.1600-065X.2002.18517.X

7 January 2021

Human severe combined immunodeficiency: genetic, phenotypic, and functional diversity in one hundred eight infants

1 reference

https://api.crossref.org/works/10.1034%2FJ.1600-065X.2002.18517.X

7 January 2021

Adenosine-deaminase deficiency in two patients with severely impaired cellular immunity

1 reference

https://api.crossref.org/works/10.1034%2FJ.1600-065X.2002.18517.X

7 January 2021

Thymic function after hematopoietic stem-cell transplantation for the treatment of severe combined immunodeficiency

1 reference

https://api.crossref.org/works/10.1034%2FJ.1600-065X.2002.18517.X

7 January 2021

Hematopoietic stem cell transplantation for severe combined immunodeficiency in the neonatal period leads to superior thymic output and improved survival

1 reference

https://api.crossref.org/works/10.1034%2FJ.1600-065X.2002.18517.X

7 January 2021

Mutations in the tyrosine phosphatase CD45 gene in a child with severe combined immunodeficiency disease

1 reference

https://api.crossref.org/works/10.1034%2FJ.1600-065X.2002.18517.X

7 January 2021

Atypical X-Linked Severe Combined Immunodeficiency Due to Possible Spontaneous Reversion of the Genetic Defect in T Cells

1 reference

https://api.crossref.org/works/10.1034%2FJ.1600-065X.2002.18517.X

7 January 2021

The lymph node pathology of Omenn's syndrome.

1 reference

https://api.crossref.org/works/10.1034%2FJ.1600-065X.2002.18517.X

7 January 2021

Use of intravenous gamma-globulin in antibody immunodeficiency: results of a multicenter controlled trial

1 reference

https://api.crossref.org/works/10.1034%2FJ.1600-065X.2002.18517.X

7 January 2021

Immunological reconstitution of sex-linked lymphopenic immunological deficiency

1 reference

https://api.crossref.org/works/10.1034%2FJ.1600-065X.2002.18517.X

7 January 2021

Bone-marrow transplantation in a patient with the Wiskott-Aldrich syndrome

1 reference

https://api.crossref.org/works/10.1034%2FJ.1600-065X.2002.18517.X

7 January 2021

10.1034/J.1600-065X.2002.18517.X

Identifiers

DOI

1 reference

22 September 2017

1 reference

PubMed ID

12190932