Carrier detection in X-linked agammaglobulinemia by analysis of X-chromosome inactivation.
about
Isolation of the defective gene in X linked agammaglobulinaemia.Is skewed X inactivation responsible for symptoms in female carriers for adrenoleucodystrophy?Early B cell defects.BTK inhibitors in chronic lymphocytic leukemia: a glimpse to the future.Molecular pathogenesis of EBV susceptibility in XLP as revealed by analysis of female carriers with heterozygous expression of SAP.Methylation of HpaII and HhaI sites near the polymorphic CAG repeat in the human androgen-receptor gene correlates with X chromosome inactivation.Evidence for failure of V(D)J recombination in bone marrow pre-B cells from X-linked agammaglobulinemia.Mutations in btk in patients with presumed X-linked agammaglobulinemia.Nonrandom X chromosome DNA methylation patterns in hemophiliac females.Prenatal diagnosis and carrier detection in primary immunodeficiency disordersIdentification 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 immunodeficiencyBrother/sister pairs affected with early-onset, progressive muscular dystrophy: molecular studies reveal etiologic heterogeneity.Noninactivation of a selectable human X-linked gene that complements a murine temperature-sensitive cell cycle defect.Unusual patterns of exon skipping in Bruton tyrosine kinase are associated with mutations involving the intron 17 3' splice site.Selection against lethal alleles in females heterozygous for incontinentia pigmentiPathogenesis-based therapy reverses cutaneous abnormalities in an inherited disorder of distal cholesterol metabolismGenetic study of a new X-linked recessive immunodeficiency syndromeB 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 agammaglobulinemiaAn X chromosome gene regulates hematopoietic stem cell kinetics.Sequence analysis and expression of an X-linked, lymphocyte-regulated gene family (XLR)Clonal diversity in the B cell repertoire of patients with X-linked agammaglobulinemia.First among equals: competition between genetically identical cells.Genetics of human X-linked immunodeficiency diseases.Sex-biased chromatin and regulatory cross-talk between sex chromosomes, autosomes, and mitochondria.BTK Signaling in B Cell Differentiation and Autoimmunity.Definition of the gene loci in X-linked immunodeficiencies.Evaluation of immunity.Role of Bruton's tyrosine kinase in B cells and malignancies.
P2860
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P2860
Carrier detection in X-linked agammaglobulinemia by analysis of X-chromosome inactivation.
description
1987 nî lūn-bûn
@nan
1987年の論文
@ja
1987年論文
@yue
1987年論文
@zh-hant
1987年論文
@zh-hk
1987年論文
@zh-mo
1987年論文
@zh-tw
1987年论文
@wuu
1987年论文
@zh
1987年论文
@zh-cn
name
Carrier detection in X-linked ...... of X-chromosome inactivation.
@en
type
label
Carrier detection in X-linked ...... of X-chromosome inactivation.
@en
prefLabel
Carrier detection in X-linked ...... of X-chromosome inactivation.
@en
P2093
P1476
Carrier detection in X-linked ...... of X-chromosome inactivation.
@en
P2093
Pardoll DM
Winkelstein JA
P304
P356
10.1056/NEJM198702193160802
P407
P577
1987-02-01T00:00:00Z