common variable immunodeficiency syndrome Alterations of the X-linked lymphoproliferative disease geneSH2D1A in

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• Publication year

  2013

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  Biology, Medicine

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  Open on Semantic Scholar

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  Semantic Scholar

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• Cell surface receptors Ly-9 and CD84 recruit the X-linked lymphoproliferative disease gene product SAP.

  2001cited by this paper
• X-linked lymphoproliferative disease: a progressive immunodeficiency.

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• Potential pathways for regulation of NK and T cell responses: differential X-linked lymphoproliferative syndrome gene product SAP interactions with SLAM and 2B4.

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• The CD2-subset of the Ig superfamily of cell surface molecules: receptor-ligand pairs expressed by NK cells and other immune cells.

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• SH2D1A and slam protein expression in human lymphocytes and derived cell lines

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• X-Linked Lymphoproliferative Disease

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• SLAM (CDw150) is a cellular receptor for measles virus

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• The gene defective in X-linked lymphoproliferative disease controls T cell dependent immune surveillance against Epstein-Barr virus.

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• Cutting Edge: Defective NK Cell Activation in X-Linked Lymphoproliferative Disease1

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

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• Diagnosis of X‐linked lymphoproliferative disease by analysis of SLAM‐associated protein expression

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• Recurrent B‐cell non‐Hodgkin's lymphoma in two brothers with X‐linked lymphoproliferative disease without evidence for Epstein–Barr virus infection

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• Cutting Edge: Functional Requirement for SAP in 2B4-Mediated Activation of Human Natural Killer Cells as Revealed by the X-Linked Lymphoproliferative Syndrome1

  2000cited by this paper
• Correlation of mutations of the SH2D1A gene and epstein-barr virus infection with clinical phenotype and outcome in X-linked lymphoproliferative disease.

  2000cited by this paper
• Common variable immunodeficiency: clinical and immunological features of 248 patients.

  1999cited by this paper
• Cutting edge: human 2B4, an activating NK cell receptor, recruits the protein tyrosine phosphatase SHP-2 and the adaptor signaling protein SAP.

  1999cited by this paper
• The abnormal gene in X-linked lymphoproliferative syndrome.

  1999cited by this paper
• Diagnostic Criteria for Primary Immunodeficiencies

  1999cited by this paper
• The X-linked lymphoproliferative-disease gene product SAP regulates signals induced through the co-receptor SLAM

  1998cited by this paper
• Inactivating mutations in an SH2 domain-encoding gene in X-linked lymphoproliferative syndrome.

  1998cited by this paper
• Host response to EBV infection in X-linked lymphoproliferative disease results from mutations in an SH2-domain encoding gene

  1998cited by this paper
• Epstein‐Barr virus‐infected B cells of males with the X‐linked lymphoproliferative syndrome stimulate and are susceptible to T‐cell‐mediated lysis

  1998cited by this paper
• Mutations in btk in patients with presumed X-linked agammaglobulinemia.

  1998cited by this paper
• Common variable immunodeficiency: how many diseases?

  1997cited by this paper
• Soluble and Membrane-bound Forms of Signaling Lymphocytic Activation Molecule (SLAM) Induce Proliferation and Ig Synthesis by Activated Human B Lymphocytes

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• EAT-2 is a novel SH2 domain containing protein that is up regulated by Ewing's sarcoma EWS/FLI1 fusion gene.

  1996cited by this paper
• X-Linked Lymphoproliferative Disease: Twenty-Five Years after the Discovery

  1995cited by this paper
• CD40 ligand expression is defective in a subset of patients with common variable immunodeficiency.

  1994cited by this paper
• A block in both early T lymphocyte and natural killer cell development in transgenic mice with high-copy numbers of the human CD3E gene.

  1994cited by this paper
• Immunoglobulin class and subclass deficiencies prior to Epstein-Barr virus infection in males with X-linked lymphoproliferative disease.

  1991cited by this paper
• Laboratory Test Handbook

  1990cited by this paper
• Studies of EBV-lymphoid cell interactions in two patients with the X-linked lymphoproliferative syndrome: normal EBV-specific HLA-restricted cytotoxicity.

  1986cited by this paper
• Delayed onset of infectious mononucleosis associated with acquired agammaglobulinemia and red cell aplasia.

  1984cited by this paper
• X-linked lymphoproliferative syndrome. Natural history of the immunodeficiency.

  1983cited by this paper
• Abnormal anti-Epstein Barr virus antibodies in carriers of the X-linked lymphoproliferative syndrome and in females at risk.

  1982cited by this paper
• Deficient natural killer cell activity in x-linked lymphoproliferative syndrome.

  1980cited by this paper
• X-linked lymphoproliferative syndrome registry report.

  1980cited by this paper
• X-linked recessive progressive combined variable immunodeficiency (Duncan's disease).

  1975cited by this paper
• Dysgammaglobulinaemia complicated by disseminated measles.

  1971cited by this paper
• Hereditary Alterations in the Immune Response: Coexistence of ‘Agammaglobulinemia', Acquired Hypogammaglobulinemia and Selective Immunoglobulin Deficiency in a Sibship

  1968cited by this paper
• Pathologic variants of congenital hypogamma-globulinemia: an analysis of 3 patients dying of measles.

  1967cited by this paper

• No citing papers are available for this paper.