XIAP deficiency in humans causes an X-linked lymphoproliferative syndrome
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XIAP deficiency: a unique primary immunodeficiency best classified as X-linked familial hemophagocytic lymphohistiocytosis and not as X-linked lymphoproliferative diseasePrimary immunodeficiency diseases: an update from the International Union of Immunological Societies Primary Immunodeficiency Diseases Classification CommitteeCould the eIF2α-Independent Translation Be the Achilles Heel of Cancer?Severe infectious diseases of childhood as monogenic inborn errors of immunityCytotoxic granule secretion by lymphocytes and its link to immune homeostasisRegulation of Cell Death by IAPs and Their AntagonistsInfectious MononucleosisT-regulatory cells in primary immune deficienciesThe diagnostic approach to monogenic very early onset inflammatory bowel diseaseSystematic review: macrophage activation syndrome in inflammatory bowel diseaseXIAP regulates cytosol-specific innate immunity to Listeria infectionX-linked lymphoproliferative syndromes: brothers or distant cousins?Infectious mononucleosis.Making a definitive diagnosis: successful clinical application of whole exome sequencing in a child with intractable inflammatory bowel diseaseGenetic variation in IBD: progress, clues to pathogenesis and possible clinical utilityIdentification of an Xiap-like pseudogene on mouse chromosome 7Herpes-virus infection in patients with Langerhans cell histiocytosis: a case-controlled sero-epidemiological study, and in situ analysis.Common variable immunodeficiency: etiological and treatment issues.SLAM-family receptors: immune regulators with or without SAP-family adaptors.Cutaneous granulomatosis and combined immunodeficiency revealing Ataxia-Telangiectasia: a case reportOvercoming chemotherapy drug resistance by targeting inhibitors of apoptosis proteins (IAPs)Hemophagocytic Syndrome and Critical Illness: New Insights into Diagnosis and Management.The clinical utility of molecular diagnostic testing for primary immune deficiency disorders: a case based review.Primary deficiency of microsomal triglyceride transfer protein in human abetalipoproteinemia is associated with loss of CD1 function.Distinct 5' UTRs regulate XIAP expression under normal growth conditions and during cellular stressMolecular pathogenesis of EBV susceptibility in XLP as revealed by analysis of female carriers with heterozygous expression of SAP.A timely arrival for genomic medicine.IAP inhibitors enhance co-stimulation to promote tumor immunity.Genetic features of late onset primary hemophagocytic lymphohistiocytosis in adolescence or adulthoodGenetic resistance to rhabdovirus infection in teleost fish is paralleled to the derived cell resistance status.Using flow cytometry to screen patients for X-linked lymphoproliferative disease due to SAP deficiency and XIAP deficiencyXIAP impairs Smac release from the mitochondria during apoptosis.IL-2-inducible T-cell kinase deficiency: clinical presentation and therapeutic approach.BID-dependent release of mitochondrial SMAC dampens XIAP-mediated immunity against Shigella.X-Linked Lymphoproliferative Syndrome and Common Variable Immunodeficiency May Not Be Differentiated by SH2D1A and XIAP/BIRC4 Genes Sequence Analysis.Immunologic difference between hypersensitivity to mosquito bite and hemophagocytic lymphohistiocytosis associated with Epstein-Barr virus infectionDetection of chromosomal breakpoints in patients with developmental delay and speech disordersA detrimental role for invariant natural killer T cells in the pathogenesis of experimental dengue virus infection.Severe viral infections and primary immunodeficiencies.Chemoimmunotherapy for hemophagocytic lymphohistiocytosis: long-term results of the HLH-94 treatment protocol
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P2860
XIAP deficiency in humans causes an X-linked lymphoproliferative syndrome
description
2006 nî lūn-bûn
@nan
2006 թուականի Նոյեմբերին հրատարակուած գիտական յօդուած
@hyw
2006 թվականի նոյեմբերին հրատարակված գիտական հոդված
@hy
2006年の論文
@ja
2006年論文
@yue
2006年論文
@zh-hant
2006年論文
@zh-hk
2006年論文
@zh-mo
2006年論文
@zh-tw
2006年论文
@wuu
name
XIAP deficiency in humans causes an X-linked lymphoproliferative syndrome
@ast
XIAP deficiency in humans causes an X-linked lymphoproliferative syndrome
@en
XIAP deficiency in humans causes an X-linked lymphoproliferative syndrome
@nl
type
label
XIAP deficiency in humans causes an X-linked lymphoproliferative syndrome
@ast
XIAP deficiency in humans causes an X-linked lymphoproliferative syndrome
@en
XIAP deficiency in humans causes an X-linked lymphoproliferative syndrome
@nl
prefLabel
XIAP deficiency in humans causes an X-linked lymphoproliferative syndrome
@ast
XIAP deficiency in humans causes an X-linked lymphoproliferative syndrome
@en
XIAP deficiency in humans causes an X-linked lymphoproliferative syndrome
@nl
P2093
P50
P3181
P356
P1433
P1476
XIAP deficiency in humans causes an X-linked lymphoproliferative syndrome
@en
P2093
Benoit Pasquier
Lionel Galicier
Marie-Claude Fondanèche
Nathalie Lambert
Pauline Soulas
Stéphanie Rigaud
P2888
P3181
P356
10.1038/NATURE05257
P407
P50
P577
2006-11-02T00:00:00Z
P5875
P6179
1047162408