Literature DB >> 8597630

A high-resolution genetic map of mouse chromosome 15 encompassing the Dominant megacolon (Dom) locus.

A Puliti1, M O Prehu, D Simon-Chazottes, L Ferkdadji, M Peuchmaur, M Goossens, J L Guénet.   

Abstract

Dominant megacolon (Dom) is one of four mutations in the mouse that can produce a phenotype similar to Hirschsprung disease in human. The Dom gene product is not known, and no candidate region has been defined for a possible human homolog. In this publication we report mapping the Dom locus with high definition, using several intra-and interspecific crosses and a set of 16 Chr 15-specific microsatellites flanking this locus.

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Year:  1995        PMID: 8597630     DOI: 10.1007/bf00539000

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


  21 in total

1.  GENE-LINK: a program in PASCAL for backcross genetic analysis.

Authors:  X Montagutelli
Journal:  J Hered       Date:  1990 Nov-Dec       Impact factor: 2.645

2.  Concurrent de novo interstitial deletion of band 2p22 and reciprocal translocation (3;7)(p21;q22).

Authors:  G C Webb; C G Keith; N T Campbell
Journal:  J Med Genet       Date:  1988-02       Impact factor: 6.318

3.  Phenotypic diversity, allelic series and modifier genes.

Authors:  G Romeo; V A McKusick
Journal:  Nat Genet       Date:  1994-08       Impact factor: 38.330

4.  Chromosomal localization of the human homolog (c-sis) of the simian sarcoma virus onc gene.

Authors:  R Dalla-Favera; R C Gallo; A Giallongo; C M Croce
Journal:  Science       Date:  1982-11-12       Impact factor: 47.728

5.  The association of Waardenburg syndrome and Hirschsprung megacolon.

Authors:  G S Omenn; V A McKusick
Journal:  Am J Med Genet       Date:  1979

6.  Gene for human CD59 (likely Ly-6 homologue) is located on the short arm of chromosome 11.

Authors:  U H Forsberg; V Bazil; I Stefanová; J Schröder
Journal:  Immunogenetics       Date:  1989       Impact factor: 2.846

7.  The use of acetylcholinesterase (AChE) in the diagnosis of Hirschsprung's disease and intestinal neuronal dysplasia.

Authors:  B D Lake; M T Malone; R A Risdon
Journal:  Pediatr Pathol       Date:  1989

8.  Waardenburg syndrome and Hirschsprung disease: evidence for pleiotropic effects of a single dominant gene.

Authors:  J A Badner; A Chakravarti
Journal:  Am J Med Genet       Date:  1990-01

9.  Mice deficient for PDGF B show renal, cardiovascular, and hematological abnormalities.

Authors:  P Levéen; M Pekny; S Gebre-Medhin; B Swolin; E Larsson; C Betsholtz
Journal:  Genes Dev       Date:  1994-08-15       Impact factor: 11.361

10.  A missense mutation of the endothelin-B receptor gene in multigenic Hirschsprung's disease.

Authors:  E G Puffenberger; K Hosoda; S S Washington; K Nakao; D deWit; M Yanagisawa; A Chakravart
Journal:  Cell       Date:  1994-12-30       Impact factor: 41.582

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  2 in total

1.  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

2.  Mutation of the Sry-related Sox10 gene in Dominant megacolon, a mouse model for human Hirschsprung disease.

Authors:  B Herbarth; V Pingault; N Bondurand; K Kuhlbrodt; I Hermans-Borgmeyer; A Puliti; N Lemort; M Goossens; M Wegner
Journal:  Proc Natl Acad Sci U S A       Date:  1998-04-28       Impact factor: 11.205

  2 in total

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