Combined immunodeficiency with life-threatening EBV-associated lymphoproliferative disorder in patients lacking functional CD27. - Wikidata - wikimedia - TriplyDB

Combined immunodeficiency with life-threatening EBV-associated lymphoproliferative disorder in patients lacking functional CD27.

Combined immunodeficiency with life-threatening EBV-associated lymphoproliferative disorder in patients lacking functional CD27.

http://www.wikidata.org/entity/Q36862306

about

JAGN1 deficiency causes aberrant myeloid cell homeostasis and congenital neutropenia International Consensus Document (ICON): Common Variable Immunodeficiency Disorders Three-stage quality control strategies for DNA re-sequencing data NK Cell Influence on the Outcome of Primary Epstein-Barr Virus Infection Targeting the T-cell co-stimulatory CD27/CD70 pathway in cancer immunotherapy: rationale and potential Autoimmune and other cytopenias in primary immunodeficiencies: pathomechanisms, novel differential diagnoses, and treatment Clinical and Molecular Heterogeneity of RTEL1 Deficiency Interleukin-2-inducible T-cell kinase (ITK) deficiency - clinical and molecular aspects.Combined immunodeficiency evolving into predominant CD4+ lymphopenia caused by somatic chimerism in JAK3 B-cell subpopulations in children: National reference values Biallelic loss-of-function mutation in NIK causes a primary immunodeficiency with multifaceted aberrant lymphoid immunity.A review of the diverse genetic disorders in the Lebanese population: highlighting the urgency for community genetic services.The syndrome of hemophagocytic lymphohistiocytosis in primary immunodeficiencies: implications for differential diagnosis and pathogenesis.Utility of next generation sequencing in clinical primary immunodeficiencies.Application of whole genome and RNA sequencing to investigate the genomic landscape of common variable immunodeficiency disorders.Mutations in GATA2 cause human NK cell deficiency with specific loss of the CD56(bright) subset.B-cell deficiency and severe autoimmunity caused by deficiency of protein kinase C δ.Investigating the specific core genetic-and-epigenetic networks of cellular mechanisms involved in human aging in peripheral blood mononuclear cells.A Systematic Review and Network Meta-Analysis to Evaluate the Comparative Efficacy of Interventions for Unfit Patients with Chronic Lymphocytic Leukemia.Dual T cell- and B cell-intrinsic deficiency in humans with biallelic RLTPR mutations.Inherited CD70 deficiency in humans reveals a critical role for the CD70-CD27 pathway in immunity to Epstein-Barr virus infection.Combined immunodeficiency and Epstein-Barr virus-induced B cell malignancy in humans with inherited CD70 deficiency A novel immunodeficiency syndrome associated with partial trisomy 19p13.Primary antibody deficiencies.The contextual role of TNFR family members in CD8(+) T-cell control of viral infections.The importance of co-stimulation in the orchestration of T helper cell differentiation.ATVB Distinguished Scientist Award: How Costimulatory and Coinhibitory Pathways Shape Atherosclerosis.Genes associated with common variable immunodeficiency: one diagnosis to rule them all?Severe Epstein-Barr virus infection in primary immunodeficiency and the normal host.Human immunity against EBV-lessons from the clinic.Fatal Lymphoproliferative Disease in Two Siblings Lacking Functional FAAP24.NF-κB1 Haploinsufficiency Causing Immunodeficiency and EBV-Driven Lymphoproliferation.Activating PI3Kδ mutations in a cohort of 669 patients with primary immunodeficiency.High incidence of Epstein-Barr virus (EBV)-positive Hodgkin lymphoma and Hodgkin lymphoma-like B-cell lymphoproliferations with EBV latency profile 2 in children with interleukin-2-inducible T-cell kinase deficiency.Epstein-Barr virus infection transforms CD25+ B cells into antibody-secreting cells in rheumatoid arthritis patients.Long-term remission after allogeneic hematopoietic stem cell transplantation in LPS-responsive beige-like anchor (LRBA) deficiency Epstein-Barr Virus-Specific Immune Control by Innate Lymphocytes.Signaling by the Epstein-Barr virus LMP1 protein induces potent cytotoxic CD4+ and CD8+ T cell responses.CD27-Mediated Regulatory T Cell Depletion and Effector T Cell Costimulation Both Contribute to Antitumor Efficacy.Epstein-Barr Virus and Hemophagocytic Lymphohistiocytosis.

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Combined immunodeficiency with life-threatening EBV-associated lymphoproliferative disorder in patients lacking functional CD27.

http://www.wikidata.org/entity/Q36862306

description

2012 nî lūn-bûn

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2012年の論文

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2012年論文

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2012年論文

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2012年论文

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2012年论文

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Arndt Borkhardt

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Elisabeth Förster-Waldl

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Elisabeth Salzer

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Elisangela Santos-Valente

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Gerhard Fritsch

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Kaan Boztug

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Kirsten Bienemann

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Markus G Seidel

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Martina Schwendinger

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Michael Gombert

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P2860

PLINK: a tool set for whole-genome association and population-based linkage analyses

A method and server for predicting damaging missense mutations

XIAP deficiency in humans causes an X-linked lymphoproliferative syndrome

The TNF receptor family member CD27 signals to Jun N-terminal kinase via Traf-2

The T cell activation antigen CD27 is a member of the nerve growth factor/tumor necrosis factor receptor gene family

Fast and accurate long-read alignment with Burrows-Wheeler transform

Predicting the effects of coding non-synonymous variants on protein function using the SIFT algorithm

A framework for variation discovery and genotyping using next-generation DNA sequencing data

CD27 sustains survival of CTLs in virus-infected nonlymphoid tissue in mice by inducing autocrine IL-2 production.

CD27 is required for generation and long-term maintenance of T cell immunity.

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98

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22801960

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