Somatic rearrangement of chromosome 14 in human lymphocytes.
about
Molecular analysis of a t(14;14) translocation in leukemic T-cells of an ataxia telangiectasia patientA new chromosomal instability disorder: the Nijmegen breakage syndromeGenetics of neoplasia--impact of ecogenetics on oncogenesis. A review.Juxtaposition of the T-cell receptor alpha-chain locus (14q11) and a region (14q32) of potential importance in leukemogenesis by a 14;14 translocation in a patient with T-cell chronic lymphocytic leukemia and ataxia-telangiectasiaGenetic and biochemical studies with ataxia telangiectasia. A review.Molecular cloning of a DNA fragment from human chromosome 14(14q11) involved in T-cell malignancies.The breakpoint of an inversion of chromosome 14 in a T-cell leukemia: sequences downstream of the immunoglobulin heavy chain locus are implicated in tumorigenesis.Mapping of human chromosomal regions related to neoplasia: evidence from chromosomes 1 and 17New translocations in human lymphocytes: a mutagen monitoring systemT-lymphocytes with 7;14 translocations: frequency of occurrence, breakpoints, and clinical and biological significance.Specific chromosome aberrations in senescent fibroblast cell lines derived from human embryosDisorders of B cells and helper T cells in the pathogenesis of the immunoglobulin deficiency of patients with ataxia telangiectasia.Chromosome abnormalities and predisposition towards cancer.Cytogenetics of malignant epithelial cells and lymphoblastoid cell lines from nasopharyngeal carcinoma.Surface phenotyping, histology and the nature of non-Hodgkin lymphoma in 157 patients.Highly polymorphic DNA site D14S1 maps to the region of Burkitt lymphoma translocation and is closely linked to the heavy chain gamma 1 immunoglobulin locus.Hybrid T cell receptor genes formed by interlocus recombination in normal and ataxia-telangiectasis lymphocytes.Lymphoma development in mice and humans: diversity of initiation is followed by convergent cytogenetic evolution.Genomic constitution of an H-2:Tla variant leukemia.Epstein-Barr virus-associated malignancies.Preleukemia. Cytogenetic clues in some confusing disorders.Consistent chromosome abnormalities in human leukemia and lymphoma.Ocular manifestations of the neurocutaneous syndromes.Chromosome changes in acute leukaemia.Human T-cell tumours containing chromosome 14 inversion or translocation with breakpoints proximal to immunoglobulin joining regions at 14q32.Ataxia telangiectasia genes and predisposition to leukaemia, lymphoma and breast cancer.A bidirectional promoter connects the poly(ADP-ribose) polymerase 2 (PARP-2) gene to the gene for RNase P RNA. structure and expression of the mouse PARP-2 gene.Three consecutive primary malignancies in one patient during childhood.
P2860
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P2860
Somatic rearrangement of chromosome 14 in human lymphocytes.
description
1975 nî lūn-bûn
@nan
1975 թուականի Յունիսին հրատարակուած գիտական յօդուած
@hyw
1975 թվականի հունիսին հրատարակված գիտական հոդված
@hy
1975年の論文
@ja
1975年論文
@yue
1975年論文
@zh-hant
1975年論文
@zh-hk
1975年論文
@zh-mo
1975年論文
@zh-tw
1975年论文
@wuu
name
Somatic rearrangement of chromosome 14 in human lymphocytes.
@ast
Somatic rearrangement of chromosome 14 in human lymphocytes.
@en
type
label
Somatic rearrangement of chromosome 14 in human lymphocytes.
@ast
Somatic rearrangement of chromosome 14 in human lymphocytes.
@en
prefLabel
Somatic rearrangement of chromosome 14 in human lymphocytes.
@ast
Somatic rearrangement of chromosome 14 in human lymphocytes.
@en
P2093
P2860
P356
P1476
Somatic rearrangement of chromosome 14 in human lymphocytes.
@en
P2093
P2860
P304
P356
10.1073/PNAS.72.6.2071
P407
P577
1975-06-01T00:00:00Z