Literature DB >> 2916166

Regional localization of CCG1 gene which complements hamster cell cycle mutation BN462 to Xq11-Xq13.

C J Brown1, T Sekiguchi, T Nishimoto, H F Willard.   

Abstract

The human CCG1 gene, which complements the temperature-sensitive hamster cell cycle mutations BN462 and ts13, has recently been cloned and shown to be located on the X chromosome. We have used somatic cell hybrids segregating portions of multiple X--autosome translocations to localize this gene to the Xq11 to Xq13 region of the human X chromosome.

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Year:  1989        PMID: 2916166     DOI: 10.1007/BF01534674

Source DB:  PubMed          Journal:  Somat Cell Mol Genet        ISSN: 0740-7750


  3 in total

1.  The human CCG1 gene, essential for progression of the G1 phase, encodes a 210-kilodalton nuclear DNA-binding protein.

Authors:  T Sekiguchi; Y Nohiro; Y Nakamura; N Hisamoto; T Nishimoto
Journal:  Mol Cell Biol       Date:  1991-06       Impact factor: 4.272

2.  Two unrelated patients with inversions of the X chromosome and non-specific mental retardation: physical and transcriptional mapping of their common breakpoint region in Xq13.1.

Authors:  L Villard; S Briault; A M Lossi; C Paringaux; J Belougne; L Colleaux; D R Pincus; E Woollatt; J Lespinasse; A Munnich; C Moraine; M Fontès; J Gecz
Journal:  J Med Genet       Date:  1999-10       Impact factor: 6.318

3.  X linked Charcot-Marie-Tooth disease (CMTX1): a study of 15 families with 12 highly informative polymorphisms.

Authors:  S Cochrane; J Bergoffen; N D Fairweather; E Müller; M L Mostacciuolo; A P Monaco; K H Fischbeck; N E Haites
Journal:  J Med Genet       Date:  1994-03       Impact factor: 6.318

  3 in total

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