Loss of B Cells in Patients with Heterozygous Mutations in IKAROS.
about
Co-existence of IL7R high and SH2B3 low expression distinguishes a novel high-risk acute lymphoblastic leukemia with Ikaros dysfunctionCommon Variable Immunodeficiency Caused by FANC Mutations.Genetic Diagnosis Using Whole Exome Sequencing in Common Variable Immunodeficiency.Studying human immunodeficiencies in humans: advances in fundamental concepts and therapeutic interventions.Indications to Epigenetic Dysfunction in the Pathogenesis of Common Variable Immunodeficiency.Genes associated with common variable immunodeficiency: one diagnosis to rule them all?Dendritic cell analysis in primary immunodeficiencyPrimary immunodeficiency diseases: Genomic approaches delineate heterogeneous Mendelian disorders.Novel nonsense gain-of-function NFKB2 mutations associated with a combined immunodeficiency phenotype.The immunophenotypic fingerprint of patients with primary antibody deficiencies is partially present in their asymptomatic first-degree relatives.Normal hematologic parameters and fetal hemoglobin silencing with heterozygous IKZF1 mutationsGenetic heterogeneity of uncharacterized childhood autoimmune diseases with lymphoproliferation.Germline IKAROS mutation associated with primary immunodeficiency that progressed to T-cell acute lymphoblastic leukemia.Phenotypic characterization of patients with rheumatologic manifestations of common variable immunodeficiency.Dried Blood Spots, an Affordable Tool to Collect, Ship, and Sequence gDNA from Patients with an X-Linked Agammaglobulinemia Phenotype Residing in a Developing Country.Loss-of-function nuclear factor κB subunit 1 (NFKB1) variants are the most common monogenic cause of common variable immunodeficiency in Europeans.Germline Genetic IKZF1 Variation and Predisposition to Childhood Acute Lymphoblastic Leukemia.Ikaros family zinc finger 1 regulates dendritic cell development and function in humans.Childhood cancer predisposition syndromes-A concise review and recommendations by the Cancer Predisposition Working Group of the Society for Pediatric Oncology and Hematology.CDG: An Online Server for Detecting Biologically Closest Disease-Causing Genes and its Application to Primary Immunodeficiency.
P2860
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P2860
Loss of B Cells in Patients with Heterozygous Mutations in IKAROS.
description
2016 nî lūn-bûn
@nan
2016 թուականի Մարտին հրատարակուած գիտական յօդուած
@hyw
2016 թվականի մարտին հրատարակված գիտական հոդված
@hy
2016年の論文
@ja
2016年論文
@yue
2016年論文
@zh-hant
2016年論文
@zh-hk
2016年論文
@zh-mo
2016年論文
@zh-tw
2016年论文
@wuu
name
Loss of B Cells in Patients with Heterozygous Mutations in IKAROS.
@ast
Loss of B Cells in Patients with Heterozygous Mutations in IKAROS.
@en
type
label
Loss of B Cells in Patients with Heterozygous Mutations in IKAROS.
@ast
Loss of B Cells in Patients with Heterozygous Mutations in IKAROS.
@en
prefLabel
Loss of B Cells in Patients with Heterozygous Mutations in IKAROS.
@ast
Loss of B Cells in Patients with Heterozygous Mutations in IKAROS.
@en
P2093
P2860
P50
P356
P1476
Loss of B Cells in Patients with Heterozygous Mutations in IKAROS.
@en
P2093
A Kumánovics
A Stray-Pedersen
E W Gelfand
J E Niemela
J K Abbott
P2860
P304
P356
10.1056/NEJMOA1512234
P407
P577
2016-03-01T00:00:00Z