Nonrandom X chromosome inactivation in B cells from carriers of X chromosome-linked severe combined immunodeficiency.
about
Missense mutation in exon 7 of the common gamma chain gene causes a moderate form of X-linked combined immunodeficiencyInterleukin-21: a modulator of lymphoid proliferation, apoptosis and differentiationSevere combined immunodeficiencies (SCID)B cell-intrinsic signaling through IL-21 receptor and STAT3 is required for establishing long-lived antibody responses in humans.Increased radiosensitivity of granulocyte macrophage colony-forming units and skin fibroblasts in human autosomal recessive severe combined immunodeficiencyImmunodeficiency due to a unique protracted developmental delay in the B-cell lineageThe random inactivation of the X chromosome carrying the defective gene responsible for X-linked hyper IgM syndrome (X-HIM) in female carriers of HIGM1.Blockade of T- and B-lymphocyte development by antibody to the gamma c subunit of the receptors for interleukins 2, 4, and 7X-linked severe combined immunodeficiency. Diagnosis in males with sporadic severe combined immunodeficiency and clarification of clinical findings.Nonrandom X chromosome DNA methylation patterns in hemophiliac females.Virus-specific immunity after gene therapy in a murine model of severe combined immunodeficiency.Refinement of linkage of human severe combined immunodeficiency (SCIDX1) to polymorphic markers in Xq13.Identification of novel RFLPs in the vicinity of CpG islands in Xq28: application to the analysis of the pattern of X chromosome inactivation.Maximum-likelihood analysis of human T-cell X chromosome inactivation patterns: normal women versus carriers of X-linked severe combined immunodeficiencyX-linked severe combined immunodeficiency disease and the gamma c receptor component: prospects for molecular diagnosis.X-linked severe combined immunodeficiency: localization within the region Xq13.1-q21.1 by linkage and deletion analysis.Genetic study of a new X-linked recessive immunodeficiency syndromeApplication of carrier testing to genetic counseling for X-linked agammaglobulinemiaIL-21 is the primary common γ chain-binding cytokine required for human B-cell differentiation in vivo.An X chromosome gene regulates hematopoietic stem cell kinetics.DNA-based HLA typing of nonhematopoietic tissue used to select the marrow transplant donor for successful treatment of transfusion-associated graft-versus-host diseaseXLP: clinical features and molecular etiology due to mutations in SH2D1A encoding SAP.Definition of the gene loci in X-linked immunodeficiencies.Mutation analysis by a non-radioactive single-strand conformation polymorphism assay in nine families with X-linked severe combined immunodeficiency (SCIDX1).The role of common gamma chain in human monocytes in vivo; evaluation from the studies of X-linked severe combined immunodeficiency (X-SCID) carriers and X-SCID patients who underwent cord blood stem cell transplantation.Reduced memory B-cell populations in boys with B-cell dysfunction after bone marrow transplantation for X-linked severe combined immunodeficiency.
P2860
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P2860
Nonrandom X chromosome inactivation in B cells from carriers of X chromosome-linked severe combined immunodeficiency.
description
1988 nî lūn-bûn
@nan
1988 թուականի Մայիսին հրատարակուած գիտական յօդուած
@hyw
1988 թվականի մայիսին հրատարակված գիտական հոդված
@hy
1988年の論文
@ja
1988年論文
@yue
1988年論文
@zh-hant
1988年論文
@zh-hk
1988年論文
@zh-mo
1988年論文
@zh-tw
1988年论文
@wuu
name
Nonrandom X chromosome inactiv ...... ere combined immunodeficiency.
@ast
Nonrandom X chromosome inactiv ...... ere combined immunodeficiency.
@en
Nonrandom X chromosome inactiv ...... ere combined immunodeficiency.
@nl
type
label
Nonrandom X chromosome inactiv ...... ere combined immunodeficiency.
@ast
Nonrandom X chromosome inactiv ...... ere combined immunodeficiency.
@en
Nonrandom X chromosome inactiv ...... ere combined immunodeficiency.
@nl
prefLabel
Nonrandom X chromosome inactiv ...... ere combined immunodeficiency.
@ast
Nonrandom X chromosome inactiv ...... ere combined immunodeficiency.
@en
Nonrandom X chromosome inactiv ...... ere combined immunodeficiency.
@nl
P2093
P2860
P356
P1476
Nonrandom X chromosome inactiv ...... ere combined immunodeficiency.
@en
P2093
P2860
P304
P356
10.1073/PNAS.85.9.3090
P407
P577
1988-05-01T00:00:00Z