Literature DB >> 8601494

Molecular analysis of 36 mutations at the mouse pink-eyed dilution (p) locus.

D K Johnson1, L J Stubbs, C T Culiat, C S Montgomery, L B Russell, E M Rinchik.   

Abstract

Thirty-six radiation- or chemically induced homozygous-lethal mutations at the p locus in mouse chromosome 7 have been analyzed at 17 loci defined by molecular probes to determine the types of lesions, numbers of p-region markers deleted or rearranged, regions of overlap of deletion mutations, and genetic distances between loci. A linear deletion map of the [Myod1, Ldh3]-[Snrpn, Znf127] region has been constructed from the molecular analyses of the p-locus deletions. The utility of these deletions as tools for the isolation and characterization of the genes specifying the neurological, reproductive, and developmental phenotypes genetically mapped to this region will grow as more detailed molecular analyses continue.

Entities:  

Mesh:

Substances:

Year:  1995        PMID: 8601494      PMCID: PMC1206887     

Source DB:  PubMed          Journal:  Genetics        ISSN: 0016-6731            Impact factor:   4.562


  40 in total

1.  Physical analysis of murine albino deletions that disrupt liver-specific gene regulation or mesoderm development.

Authors:  M L Klebig; B S Kwon; E M Rinchik
Journal:  Mamm Genome       Date:  1992       Impact factor: 2.957

2.  The albino-deletion complex of the mouse: molecular mapping of deletion breakpoints that define regions necessary for development of the embryonic and extraembryonic ectoderm.

Authors:  S K Sharan; B Holdener-Kenny; S Ruppert; A Schedl; G Kelsey; E M Rinchik; T Magnuson
Journal:  Genetics       Date:  1991-11       Impact factor: 4.562

3.  The Position of ru-2 and qv with Respect to the FLECKED Translocation in the Mouse.

Authors:  E M Eicher
Journal:  Genetics       Date:  1970-03       Impact factor: 4.562

4.  The location of Cattanach's translocation in the X-chromosome linkage map of the mouse.

Authors:  B M Cattanach
Journal:  Genet Res       Date:  1966-10       Impact factor: 1.588

5.  A putative gene family in 15q11-13 and 16p11.2: possible implications for Prader-Willi and Angelman syndromes.

Authors:  K Buiting; V Greger; B H Brownstein; R M Mohr; I Voiculescu; A Winterpacht; B Zabel; B Horsthemke
Journal:  Proc Natl Acad Sci U S A       Date:  1992-06-15       Impact factor: 11.205

6.  A cluster of three GABAA receptor subunit genes is deleted in a neurological mutant of the mouse p locus.

Authors:  Y Nakatsu; R F Tyndale; T M DeLorey; D Durham-Pierre; J M Gardner; H J McDanel; Q Nguyen; J Wagstaff; M Lalande; J M Sikela
Journal:  Nature       Date:  1993-07-29       Impact factor: 49.962

7.  Evaluation of potential models for imprinted and nonimprinted components of human chromosome 15q11-q13 syndromes by fine-structure homology mapping in the mouse.

Authors:  R D Nicholls; W Gottlieb; L B Russell; M Davda; B Horsthemke; E M Rinchik
Journal:  Proc Natl Acad Sci U S A       Date:  1993-03-01       Impact factor: 11.205

8.  N-ethyl-N-nitrosourea-induced prenatally lethal mutations define at least two complementation groups within the embryonic ectoderm development (eed) locus in mouse chromosome 7.

Authors:  E M Rinchik; D A Carpenter
Journal:  Mamm Genome       Date:  1993       Impact factor: 2.957

9.  Microdissection of the Prader-Willi syndrome chromosome region and identification of potential gene sequences.

Authors:  K Buiting; M Neumann; H J Lüdecke; G Senger; U Claussen; J Antich; E Passarge; B Horsthemke
Journal:  Genomics       Date:  1990-03       Impact factor: 5.736

10.  Organization and sequence of the human P gene and identification of a new family of transport proteins.

Authors:  S T Lee; R D Nicholls; M T Jong; K Fukai; R A Spritz
Journal:  Genomics       Date:  1995-03-20       Impact factor: 5.736

View more
  22 in total

Review 1.  Genetics of Angelman syndrome.

Authors:  Y Jiang; E Lev-Lehman; J Bressler; T F Tsai; A L Beaudet
Journal:  Am J Hum Genet       Date:  1999-07       Impact factor: 11.025

2.  Comparison of the genetic effects of equimolar doses of ENU and MNU: while the chemicals differ dramatically in their mutagenicity in stem-cell spermatogonia, both elicit very high mutation rates in differentiating spermatogonia.

Authors:  Liane B Russell; Patricia R Hunsicker; William L Russell
Journal:  Mutat Res       Date:  2006-12-14       Impact factor: 2.433

3.  A microsatellite map of the pink-eyed dilution (p) deletion complex in mouse chromosome 7.

Authors:  M S Dhar; D K Johnson
Journal:  Mamm Genome       Date:  1997-02       Impact factor: 2.957

4.  Molecular and functional mapping of the piebald deletion complex on mouse chromosome 14.

Authors:  J J Roix; A Hagge-Greenberg; D M Bissonnette; S Rodick; L B Russell; T P O'Brien
Journal:  Genetics       Date:  2001-02       Impact factor: 4.562

5.  Differential response of mouse male germ-cell stages to radiation-induced specific-locus and dominant mutations.

Authors:  W L Russell; J W Bangham; L B Russell
Journal:  Genetics       Date:  1998-04       Impact factor: 4.562

6.  Distinct phenotypes distinguish the molecular classes of Angelman syndrome.

Authors:  A C Lossie; M M Whitney; D Amidon; H J Dong; P Chen; D Theriaque; A Hutson; R D Nicholls; R T Zori; C A Williams; D J Driscoll
Journal:  J Med Genet       Date:  2001-12       Impact factor: 6.318

Review 7.  Mouse chromosome engineering for modeling human disease.

Authors:  Louise van der Weyden; Allan Bradley
Journal:  Annu Rev Genomics Hum Genet       Date:  2006       Impact factor: 8.929

8.  Hypopigmentation in the Prader-Willi syndrome correlates with P gene deletion but not with haplotype of the hemizygous P allele.

Authors:  R A Spritz; T Bailin; R D Nicholls; S T Lee; S K Park; M J Mascari; M G Butler
Journal:  Am J Med Genet       Date:  1997-07-11

9.  Lack of Pwcr1/MBII-85 snoRNA is critical for neonatal lethality in Prader-Willi syndrome mouse models.

Authors:  Feng Ding; Yelena Prints; Madhu S Dhar; Dabney K Johnson; Carmen Garnacho-Montero; Robert D Nicholls; Uta Francke
Journal:  Mamm Genome       Date:  2005-06       Impact factor: 2.957

10.  Cloning, functional study and comparative mapping of Luzp2 to mouse chromosome 7 and human chromosome 11p13-11p14.

Authors:  Min Wu; Edward J Michaud; Dabney K Johnson
Journal:  Mamm Genome       Date:  2003-05       Impact factor: 2.957

View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.