Literature DB >> 3258841

Molecular characterization of ataxia telangiectasia T cell clones. II. The clonal inv(14) in ataxia telangiectasia differs from the inv(14) in T cell lymphoma.

F Zhang1, M H Stern, G Thomas, A Aurias.   

Abstract

We compared inversions of chromosome 14 in an ataxia telangiectasia clone and in a malignant T cell line (SUP-T1). The R-banding chromosome analysis showed a clear difference between the distal breakpoint of the two inversions. Fine mapping of the distal breakpoint in the ataxia telangiectasia inv(14) was performed by in situ hybridization. We conclude that this breakpoint is centromeric to the immunoglobulin heavy chain locus and to the D14S1 anonymous locus. Our results favor the existence of an unknown oncogene in band 14q32.1.

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Year:  1988        PMID: 3258841     DOI: 10.1007/bf00291726

Source DB:  PubMed          Journal:  Hum Genet        ISSN: 0340-6717            Impact factor:   4.132


  31 in total

1.  Specific chromosome aberrations in ataxia telangiectasia.

Authors:  J M Oxford; D G Harnden; J M Parrington; J D Delhanty
Journal:  J Med Genet       Date:  1975-09       Impact factor: 6.318

2.  Abnormalities of chromosome 14 at band 14q11 in Japanese patients with adult T-cell leukemia.

Authors:  N Sadamori; M Kusano; K Nishino; M Tagawa; E Yao; Y Yamada; T Amagasaki; K Kinoshita; M Ichimaru
Journal:  Cancer Genet Cytogenet       Date:  1985-07

3.  Cytogenetic study of patients with ataxia-telangiectasia.

Authors:  N P Bochkov; Y M Lopukhin; N P Kuleshov; L V Kovalchuk
Journal:  Humangenetik       Date:  1974

4.  Distinguishing the Philadelphia chromosome of acute lymphoblastic leukemia from its counterpart in chronic myelogenous leukemia.

Authors:  S Rodenhuis; L A Smets; R M Slater; H Behrendt; A J Veerman
Journal:  N Engl J Med       Date:  1985-07-04       Impact factor: 91.245

5.  Localization of the restriction fragment length polymorphism D14S1 (pAW-101) to chromosome 14q32.1 leads to 32.2 by in situ hybridization.

Authors:  T A Donlon; M Litt; S R Newcom; R E Magenis
Journal:  Am J Hum Genet       Date:  1983-11       Impact factor: 11.025

6.  High frequencies of inversions and translocations of chromosomes 7 and 14 in ataxia telangiectasia.

Authors:  A Aurias; B Dutrillaux; D Buriot; J Lejeune
Journal:  Mutat Res       Date:  1980-02       Impact factor: 2.433

7.  A chromosome 14 inversion in a T-cell lymphoma is caused by site-specific recombination between immunoglobulin and T-cell receptor loci.

Authors:  C T Denny; Y Yoshikai; T W Mak; S D Smith; G F Hollis; I R Kirsch
Journal:  Nature       Date:  1986 Apr 10-16       Impact factor: 49.962

8.  Common region on chromosome 14 in T-cell leukemia and lymphoma.

Authors:  F Hecht; R Morgan; B K Hecht; S D Smith
Journal:  Science       Date:  1984-12-21       Impact factor: 47.728

9.  The chromosome breakpoint at 14q32 in an ataxia telangiectasia t(14;14) T cell clone is different from the 14q32 breakpoint in Burkitts and an inv(14) T cell lymphoma.

Authors:  A A Kennaugh; S V Butterworth; R Hollis; R Baer; T H Rabbitts; A M Taylor
Journal:  Hum Genet       Date:  1986-07       Impact factor: 4.132

10.  Gene for alpha-chain of human T-cell receptor: location on chromosome 14 region involved in T-cell neoplasms.

Authors:  C M Croce; M Isobe; A Palumbo; J Puck; J Ming; D Tweardy; J Erikson; M Davis; G Rovera
Journal:  Science       Date:  1985-03-01       Impact factor: 47.728

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  4 in total

1.  Molecular analysis of a t(14;14) translocation in leukemic T-cells of an ataxia telangiectasia patient.

Authors:  G Russo; M Isobe; R Gatti; J Finan; O Batuman; K Huebner; P C Nowell; C M Croce
Journal:  Proc Natl Acad Sci U S A       Date:  1989-01       Impact factor: 11.205

2.  Molecular characterization of ataxia telangiectasia T cell clones. III. Mapping the 14q32.1 distal breakpoint.

Authors:  M H Stern; F R Zhang; G Thomas; C Griscelli; A Aurias
Journal:  Hum Genet       Date:  1988-12       Impact factor: 4.132

3.  Inv(14) with distal breakpoint in 14q32.1 in three cases of T cell lymphoma.

Authors:  B Schlegelberger; A C Feller; H H Wacker; J Lohmeyer; W Grote
Journal:  Hum Genet       Date:  1990-06       Impact factor: 4.132

4.  De novo microdeletion on an inherited Robertsonian translocation chromosome: a cause for dysmorphism in the apparently balanced translocation carrier.

Authors:  D T Bonthron; S J Smith; J Fantes; C M Gosden
Journal:  Am J Hum Genet       Date:  1993-09       Impact factor: 11.025

  4 in total

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