Mapping of the X-linked agammaglobulinemia locus by use of restriction fragment-length polymorphism
about
Analysis of clinical presentations of Bruton disease: a review of 20 years of accumulated data from pediatric patients at Severance HospitalBTKbase, mutation database for X-linked agammaglobulinemia (XLA)BTKbase, mutation database for X-linked agammaglobulinemia (XLA).Deletion within the Src homology domain 3 of Bruton's tyrosine kinase resulting in X-linked agammaglobulinemia (XLA)Discordant phenotype in siblings with X-linked agammaglobulinemia.Genomic organization and structure of Bruton agammaglobulinemia tyrosine kinase: localization of mutations associated with varied clinical presentations and course in X chromosome-linked agammaglobulinemia.Comparative genomics and host resistance against infectious diseasesIdentification of novel Bruton's tyrosine kinase mutations in 10 unrelated subjects with X linked agammaglobulinaemiaShared pathways to infectious disease susceptibility?Methylation of HpaII and HhaI sites near the polymorphic CAG repeat in the human androgen-receptor gene correlates with X chromosome inactivation.A novel X-linked combined immunodeficiency disease.Close linkage of the locus for X chromosome-linked severe combined immunodeficiency to polymorphic DNA markers in Xq11-q13.Linkage of the Wiskott-Aldrich syndrome with polymorphic DNA sequences from the human X chromosome.Atypical X-linked agammaglobulinaemia caused by a novel BTK mutation in a selective immunoglobulin M deficiency patient.X-linked severe combined immunodeficiency: localization within the region Xq13.1-q21.1 by linkage and deletion analysis.B lymphocytes from X-linked agammaglobulinemia. Delayed expression of light chain and demonstration of Lyonization in carriers.Application of carrier testing to genetic counseling for X-linked agammaglobulinemiaPrimary immunodeficiencies: milestones in the history of pediatric immunology.BTK Signaling in B Cell Differentiation and Autoimmunity.Definition of the gene loci in X-linked immunodeficiencies.Evaluation of immunity.X-linked mental retardation syndrome with seizures, hypogammaglobulinemia, and progressive gait disturbance is regionally mapped between xq21.33 and Xq23.
P2860
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P2860
Mapping of the X-linked agammaglobulinemia locus by use of restriction fragment-length polymorphism
description
1986 nî lūn-bûn
@nan
1986 թուականի Փետրուարին հրատարակուած գիտական յօդուած
@hyw
1986 թվականի փետրվարին հրատարակված գիտական հոդված
@hy
1986年の論文
@ja
1986年論文
@yue
1986年論文
@zh-hant
1986年論文
@zh-hk
1986年論文
@zh-mo
1986年論文
@zh-tw
1986年论文
@wuu
name
Mapping of the X-linked agamma ...... n fragment-length polymorphism
@ast
Mapping of the X-linked agamma ...... n fragment-length polymorphism
@en
Mapping of the X-linked agamma ...... n fragment-length polymorphism
@nl
type
label
Mapping of the X-linked agamma ...... n fragment-length polymorphism
@ast
Mapping of the X-linked agamma ...... n fragment-length polymorphism
@en
Mapping of the X-linked agamma ...... n fragment-length polymorphism
@nl
prefLabel
Mapping of the X-linked agamma ...... n fragment-length polymorphism
@ast
Mapping of the X-linked agamma ...... n fragment-length polymorphism
@en
Mapping of the X-linked agamma ...... n fragment-length polymorphism
@nl
P2093
P2860
P356
P1476
Mapping of the X-linked agamma ...... n fragment-length polymorphism
@en
P2093
P2860
P304
P356
10.1172/JCI112351
P407
P577
1986-02-01T00:00:00Z