Literature DB >> 6617346

Human telomeric 6; 19 translocation chromosome with a tendency to break at the fusion point.

M E Drets, E Therman.   

Abstract

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Year:  1983        PMID： 6617346     DOI： 10.1007/bf00327334

Source DB:  PubMed          Journal:  Chromosoma        ISSN： 0009-5915            Impact factor:   4.316


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  16 in total

1.  Specific chromosome aberrations in senescent fibroblast cell lines derived from human embryos.

Authors:  P A Benn
Journal:  Am J Hum Genet       Date:  1976-09       Impact factor: 11.025

2.  Telomere replication, kinetochore organizers, and satellite DNA evolution.

Authors:  G P Holmquist; B Dancis
Journal:  Proc Natl Acad Sci U S A       Date:  1979-09       Impact factor: 11.205

3.  C-banding and non-homologous associations in Gyrllus argentinus.

Authors:  M E Drets; M Stoll
Journal:  Chromosoma       Date:  1974       Impact factor: 4.316

4.  Apparently isodicentric but functionally monocentric X chromosome in man.

Authors:  E Therman; G E Sarto; K Patau
Journal:  Am J Hum Genet       Date:  1974-01       Impact factor: 11.025

5.  New selective Giemsa technique for human chromosomes, Cd staining.

Authors:  H Eiberg
Journal:  Nature       Date:  1974-03-01       Impact factor: 49.962

6.  Palindromic base sequences and replication of eukaryote chromosome ends.

Authors:  T Cavalier-Smith
Journal:  Nature       Date:  1974-08-09       Impact factor: 49.962

7.  A woman with multiple congenital anomalies, mental retardation and mosaicism for an unusual translocation chromosome t(6;19).

Authors:  P D Pallister; K Patau; S L Inhorn; J M Opitz
Journal:  Clin Genet       Date:  1974       Impact factor: 4.438

8.  Replication and inactivation of a dicentric X formed by telomeric fusion.

Authors:  G E Sarto; E Therman
Journal:  Am J Obstet Gynecol       Date:  1980-04-01       Impact factor: 8.661

9.  Premature centromere division: a mechanism of non-disjunction causing X chromosome aneuploidy in somatic cells of man.

Authors:  P H Fitzgerald; A F Pickering; J M Mercer; P M Miethke
Journal:  Ann Hum Genet       Date:  1975-05       Impact factor: 1.670

10.  A boy with congenital malformations and chromosome breakage.

Authors:  G Daneshbod-Skibba; E Therman; N T Shahidi
Journal:  Am J Med Genet       Date:  1980
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  8 in total

1.  Alternate centromere inactivation in a pseudodicentric (15;20)(pter;pter) associated with a progressive neurological disorder.

Authors:  H Rivera; O Zuffardi; P Maraschio; A Caiulo; C Anichini; R Scarinci; R Vivarelli
Journal:  J Med Genet       Date:  1989-10       Impact factor: 6.318

2.  Origin of human chromosome 2: an ancestral telomere-telomere fusion.

Authors:  J W IJdo; A Baldini; D C Ward; S T Reeders; R A Wells
Journal:  Proc Natl Acad Sci U S A       Date:  1991-10-15       Impact factor: 11.205

3.  Dicentric chromosomes and the inactivation of the centromere.

Authors:  E Therman; C Trunca; E M Kuhn; G E Sarto
Journal:  Hum Genet       Date:  1986-03       Impact factor: 4.132

4.  Acquisition of telomere repeat sequences by transfected DNA integrated at the site of a chromosome break.

Authors:  J P Murnane; L C Yu
Journal:  Mol Cell Biol       Date:  1993-02       Impact factor: 4.272

5.  Comparative FISH mapping of the ancestral fusion point of human chromosome 2.

Authors:  F Kasai; E Takahashi; K Koyama; K Terao; Y Suto; K Tokunaga; Y Nakamura; M Hirai
Journal:  Chromosome Res       Date:  2000       Impact factor: 5.239

6.  Chromosome stability is maintained by short intercentromeric distance in functionally dicentric human Robertsonian translocations.

Authors:  S L Page; L G Shaffer
Journal:  Chromosome Res       Date:  1998-02       Impact factor: 5.239

7.  Types, stability, and phenotypic consequences of chromosome rearrangements leading to interstitial telomeric sequences.

Authors:  E Rossi; G Floridia; M Casali; C Danesino; G Chiumello; F Bernardi; I Magnani; L Papi; M Mura; O Zuffardi
Journal:  J Med Genet       Date:  1993-11       Impact factor: 6.318

8.  The role of dicentric chromosome formation and secondary centromere deletion in the evolution of myeloid malignancy.

Authors:  Ruth N Mackinnon; Lynda J Campbell
Journal:  Genet Res Int       Date:  2011-09-27
  8 in total

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