Molecular and cellular pathogenesis of X-linked lymphoproliferative disease. - sprookjes - yvandenbroek - TriplyDB

Molecular and cellular pathogenesis of X-linked lymphoproliferative disease.

Molecular and cellular pathogenesis of X-linked lymphoproliferative disease.

http://www.wikidata.org/entity/Q36015040

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Selective generation of functional somatically mutated IgM+CD27+, but not Ig isotype-switched, memory B cells in X-linked lymphoproliferative disease Association between SAP and FynT: Inducible SH3 domain-mediated interaction controlled by engagement of the SLAM receptor Acute Epstein-Barr virus infection presenting as severe gastroenteritis without infectious mononucleosis-like manifestations.Signaling lymphocytic activation molecule (SLAM)/SLAM-associated protein pathway regulates human B-cell tolerance.A novel ICOS-independent, but CD28- and SAP-dependent, pathway of T cell-dependent, polysaccharide-specific humoral immunity in response to intact Streptococcus pneumoniae versus pneumococcal conjugate vaccine.The clinical utility of molecular diagnostic testing for primary immune deficiency disorders: a case based review.Molecular pathogenesis of EBV susceptibility in XLP as revealed by analysis of female carriers with heterozygous expression of SAP.The receptor Slamf1 on the surface of myeloid lineage cells controls susceptibility to infection by Trypanosoma cruzi A novel primary immunodeficiency with specific natural-killer cell deficiency maps to the centromeric region of chromosome 8.IL-2-inducible T-cell kinase deficiency: clinical presentation and therapeutic approach.Primary immunodeficiencies: a field in its infancy.CD48 on hematopoietic progenitors regulates stem cells and suppresses tumor formation.How I treat hemophagocytic lymphohistiocytosis.Expansion of somatically reverted memory CD8+ T cells in patients with X-linked lymphoproliferative disease caused by selective pressure from Epstein-Barr virus.X-linked lymphoproliferative disease due to SAP/SH2D1A deficiency: a multicenter study on the manifestations, management and outcome of the disease.Laboratory evaluation of primary immunodeficiencies Biochemical and genetic evidence for a SAP-PKC-theta interaction contributing to IL-4 regulation.SAP regulates T cell-mediated help for humoral immunity by a mechanism distinct from cytokine regulation.Characterization of a novel disease-causing mutation in exon 1 of SH2D1A gene through amplicon sequencing: a case report on HLH.Follicular B helper T cells in antibody responses and autoimmunity.Immune regulation by SLAM family receptors and SAP-related adaptors.NK cell regulation by SLAM family receptors and SAP-related adapters.Dissecting natural killer cell activation pathways through analysis of genetic mutations in human and mouse.Immunity to microbes: lessons from primary immunodeficiencies.Does the developmental status of Valpha14i NKT cells play a role in disease?Immunoglobulin replacement therapy in children.Genetic defects of apoptosis and primary immunodeficiency.IAPs: what's in a name?CD84 is a survival receptor for CLL cells.Innate immune responses against Epstein Barr virus infection Phenotypic differences between mice deficient in XIAP and SAP, two factors targeted in X-linked lymphoproliferative syndrome (XLP).Rheumatologic and autoimmune manifestations of primary immunodeficiency disorders.Restimulation-induced apoptosis of T cells is impaired in patients with X-linked lymphoproliferative disease caused by SAP deficiency.Signal transduction during activation and inhibition of natural killer cells.XIAP as a ubiquitin ligase in cellular signaling.Familial hemophagocytic lymphohistiocytosis: when rare diseases shed light on immune system functioning.Generating humoral immune memory following infection or vaccination.Familial haemophagocytic lymphohistiocytosis: advances in the genetic basis, diagnosis and management.The darker side of follicular helper T cells: from autoimmunity to immunodeficiency.Laboratory diagnosis of primary immunodeficiencies.

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Molecular and cellular pathogenesis of X-linked lymphoproliferative disease.

http://www.wikidata.org/entity/Q36015040

description

2005 nî lūn-bûn

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2005年の論文

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2005年学术文章

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2005年学术文章

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2005年学术文章

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2005年學術文章

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2005年學術文章

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2005年學術文章

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name

Molecular and cellular pathogenesis of X-linked lymphoproliferative disease.

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Molecular and cellular pathogenesis of X-linked lymphoproliferative disease.

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type

label

Molecular and cellular pathogenesis of X-linked lymphoproliferative disease.

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Molecular and cellular pathogenesis of X-linked lymphoproliferative disease.

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prefLabel

Molecular and cellular pathogenesis of X-linked lymphoproliferative disease.

@ast

Molecular and cellular pathogenesis of X-linked lymphoproliferative disease.

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J.0105-2896.2005.00230.X

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Immunological Reviews

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Molecular and cellular pathogenesis of X-linked lymphoproliferative disease.

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Cindy S Ma

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Jennifer L Cannons

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Kim E Nichols

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Pamela L Schwartzberg

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Stuart G Tangye

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P2860

ICOS is an inducible T-cell co-stimulator structurally and functionally related to CD28

The X-linked lymphoproliferative-disease gene product SAP regulates signals induced through the co-receptor SLAM

Direct interaction in T-cells between thetaPKC and the tyrosine kinase p59fyn

Crystal structures of the XLP protein SAP reveal a class of SH2 domains with extended, phosphotyrosine-independent sequence recognition

Epstein-Barr virus-negative boys with non-Hodgkin lymphoma are mutated in the SH2D1A gene, as are patients with X-linked lymphoproliferative disease (XLP)

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

Characterization of SH2D1A missense mutations identified in X-linked lymphoproliferative disease patients

Activation of NK cell-mediated cytotoxicity by a SAP-independent receptor of the CD2 family

Molecular dissection of the signaling and costimulatory functions of CD150 (SLAM): CD150/SAP binding and CD150-mediated costimulation

A "three-pronged" binding mechanism for the SAP/SH2D1A SH2 domain: structural basis and relevance to the XLP syndrome

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180-199

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10.1111/J.0105-2896.2005.00230.X

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2005-02-01T00:00:00Z

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15661030

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