Literature DB >> 9096116

Identification and linkage mapping of Hst7, a new M. spretus/M. m. domesticus chromosome 17 hybrid sterility locus.

S H Pilder1.   

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Year:  1997        PMID： 9096116     DOI： 10.1007/s003359900415

Source DB:  PubMed          Journal:  Mamm Genome        ISSN： 0938-8990            Impact factor:   2.957


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  15 in total

Review 1.  Hybrid sterility in the mouse.

Authors:  J Forejt
Journal:  Trends Genet       Date:  1996-10       Impact factor: 11.639

2.  Evolution of mouse chromosome 17 and the origin of inversions associated with t haplotypes.

Authors:  M F Hammer; J Schimenti; L M Silver
Journal:  Proc Natl Acad Sci U S A       Date:  1989-05       Impact factor: 11.205

3.  Male sterility of the mouse t-complex is due to homozygosity of the distorter genes.

Authors:  M F Lyon
Journal:  Cell       Date:  1986-01-31       Impact factor: 41.582

4.  Molecular probes define different regions of the mouse t complex.

Authors:  H S Fox; G R Martin; M F Lyon; B Herrmann; A M Frischauf; H Lehrach; L M Silver
Journal:  Cell       Date:  1985-01       Impact factor: 41.582

5.  Cloning of the T gene required in mesoderm formation in the mouse.

Authors:  B G Herrmann; S Labeit; A Poustka; T R King; H Lehrach
Journal:  Nature       Date:  1990-02-15       Impact factor: 49.962

6.  Encyclopedia of the mouse genome V. Mouse chromosome 17.

Authors:  R Hamvas; Z Trachtulec; J Forejt; R W Williams; K Arzt; K Fischer-Lindahl; L M Silver
Journal:  Mamm Genome       Date:  1996       Impact factor: 2.957

7.  An alpha globin pseudogene is located within the mouse t complex.

Authors:  H S Fox; L M Silver; G R Martin
Journal:  Immunogenetics       Date:  1984       Impact factor: 2.846

8.  A novel mouse chromosome 17 hybrid sterility locus: implications for the origin of t haplotypes.

Authors:  S H Pilder; M F Hammer; L M Silver
Journal:  Genetics       Date:  1991-09       Impact factor: 4.562

9.  Genetic analysis of the proximal portion of the mouse t complex: evidence for a second inversion within t haplotypes.

Authors:  B Herrmann; M Bućan; P E Mains; A M Frischauf; L M Silver; H Lehrach
Journal:  Cell       Date:  1986-02-14       Impact factor: 41.582

10.  Nkx-2.5: a novel murine homeobox gene expressed in early heart progenitor cells and their myogenic descendants.

Authors:  T J Lints; L M Parsons; L Hartley; I Lyons; R P Harvey
Journal:  Development       Date:  1993-10       Impact factor: 6.868
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  3 in total

1.  Hybrid breakdown caused by substitution of the X chromosome between two mouse subspecies.

Authors:  Ayako Oka; Akihiko Mita; Noriko Sakurai-Yamatani; Hiromi Yamamoto; Nobuo Takagi; Toshiyuki Takano-Shimizu; Kiyotaka Toshimori; Kazuo Moriwaki; Toshihiko Shiroishi
Journal:  Genetics       Date:  2004-02       Impact factor: 4.562

2.  Disruption of genetic interaction between two autosomal regions and the X chromosome causes reproductive isolation between mouse strains derived from different subspecies.

Authors:  Ayako Oka; Toshihiro Aoto; Yoshikazu Totsuka; Riichi Takahashi; Masatsugu Ueda; Akihiko Mita; Noriko Sakurai-Yamatani; Hiromi Yamamoto; Satoshi Kuriki; Nobuo Takagi; Kazuo Moriwaki; Toshihiko Shiroishi
Journal:  Genetics       Date:  2006-10-22       Impact factor: 4.562

3.  Interspecific recombinant congenic strains between C57BL/6 and mice of the Mus spretus species: a powerful tool to dissect genetic control of complex traits.

Authors:  Gaëtan Burgio; Marek Szatanik; Jean-Louis Guénet; Maria-Rosa Arnau; Jean-Jacques Panthier; Xavier Montagutelli
Journal:  Genetics       Date:  2007-10-18       Impact factor: 4.562
  3 in total

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