X-linked lymphoproliferative syndrome: a genetic condition typified by the triad of infection, immunodeficiency and lymphoma.
about
Mg2+ regulates cytotoxic functions of NK and CD8 T cells in chronic EBV infection through NKG2DImmunodeficiency and autoimmunity: lessons from systemic lupus erythematosusSAP-mediated inhibition of diacylglycerol kinase α regulates TCR-induced diacylglycerol signaling.Tailored immune responses: novel effector helper T cell subsets in protective immunity.CD27 deficiency is associated with combined immunodeficiency and persistent symptomatic EBV viremiaTargeted sequencing identifies a novel SH2D1A pathogenic variant in a Chinese family: Carrier screening and prenatal genetic testing.Retrospective TREC testing of newborns with Severe Combined Immunodeficiency and other primary immunodeficiency diseases.Familial hemophagocytic lymphohistiocytosis: when rare diseases shed light on immune system functioning.Ten warning signs of primary immunodeficiency: a new paradigm is needed for the 21st century.The demographics of primary immunodeficiency diseases across the unique ethnic groups in Iran, and approaches to diagnosis and treatment.Primary immunodeficiency associated with defects in CD1 and CD1-restricted T cells.Diagnostic evaluation of patients with suspected haemophagocytic lymphohistiocytosis.Modes of infection and oncogenesis by the Epstein-Barr virus.Clinical utility of natural killer cells in cancer therapy and transplantation.XLP: clinical features and molecular etiology due to mutations in SH2D1A encoding SAP.Very early-onset inflammatory bowel disease: gaining insight through focused discovery.How genetic testing can lead to targeted management of XIAP deficiency-related inflammatory bowel disease.Primary hemophagocytic lymphohistiocytosis in Iran: report from a single referral center.Two Unrelated Burkitt Lymphomas Seven Years Apart in a Patient With X-Linked Lymphoproliferative Disease Type 1 (XLP1).A mutation in caspase-9 decreases the expression of BAFFR and ICOS in patients with immunodeficiency and lymphoproliferation.Clinical and molecular characteristics of Chinese patients with X-linked lymphoproliferative syndrome type 1.XLP1 inhibitory effect by 2B4 does not affect DNAM-1 and NKG2D activating pathways in NK cells.Clinical and genetic features of 5 Chinese patients with X-linked lymphoproliferative syndrome.Lymphoma and cerebral vasculitis in association with X-linked lymphoproliferative disease.The value of DNA storage and pedigree analysis in rare diseases: a 17-year-old boy with X-linked lymphoproliferative disease (XLP) caused by a de novo SH2D1A mutation.Hematopoietic Stem Cell Transplantation for XIAP Deficiency in Japan.Hematopoietic cell transplantation for asymptomatic X-linked lymphoproliferative syndrome type 1
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X-linked lymphoproliferative syndrome: a genetic condition typified by the triad of infection, immunodeficiency and lymphoma.
description
2010 nî lūn-bûn
@nan
2010年の論文
@ja
2010年学术文章
@wuu
2010年学术文章
@zh-cn
2010年学术文章
@zh-hans
2010年学术文章
@zh-my
2010年学术文章
@zh-sg
2010年學術文章
@yue
2010年學術文章
@zh
2010年學術文章
@zh-hant
name
X-linked lymphoproliferative s ...... immunodeficiency and lymphoma.
@en
X-linked lymphoproliferative s ...... immunodeficiency and lymphoma.
@nl
type
label
X-linked lymphoproliferative s ...... immunodeficiency and lymphoma.
@en
X-linked lymphoproliferative s ...... immunodeficiency and lymphoma.
@nl
prefLabel
X-linked lymphoproliferative s ...... immunodeficiency and lymphoma.
@en
X-linked lymphoproliferative s ...... immunodeficiency and lymphoma.
@nl
P2860
P50
P1476
X-linked lymphoproliferative s ...... immunodeficiency and lymphoma
@en
P2093
Kim E Nichols
Rupali Das
P2860
P356
10.1111/J.1365-2141.2010.08442.X
P407
P577
2010-11-18T00:00:00Z