BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

129 related articles for article (PubMed ID: 8088814)

  • 1. Linkage analysis of the whirler deafness gene on mouse chromosome 4.
    Fleming J; Rogers MJ; Brown SD; Steel KP
    Genomics; 1994 May; 21(1):42-8. PubMed ID: 8088814
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Fine mapping of the circling (cir) gene on the distal portion of mouse chromosome 9.
    Cho KI; Lee JW; Kim KS; Lee EJ; Suh JG; Lee HJ; Kim HT; Hong SH; Chung WH; Chang KT; Hyun BH; Oh YS; Ryoo ZY
    Comp Med; 2003 Dec; 53(6):642-8. PubMed ID: 14727813
    [TBL] [Abstract][Full Text] [Related]  

  • 3. DFNB31, a recessive form of sensorineural hearing loss, maps to chromosome 9q32-34.
    Mustapha M; Chouery E; Chardenoux S; Naboulsi M; Paronnaud J; Lemainque A; Mégarbané A; Loiselet J; Weil D; Lathrop M; Petit C
    Eur J Hum Genet; 2002 Mar; 10(3):210-2. PubMed ID: 11973626
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Elongation of hair cell stereocilia is defective in the mouse mutant whirler.
    Holme RH; Kiernan BW; Brown SD; Steel KP
    J Comp Neurol; 2002 Aug; 450(1):94-102. PubMed ID: 12124769
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Fine genetic and comparative mapping of the deafness mutation Ames waltzer on mouse chromosome 10.
    Zobeley E; Sufalko DK; Adkins S; Burmeister M
    Genomics; 1998 Jun; 50(2):260-6. PubMed ID: 9653653
    [TBL] [Abstract][Full Text] [Related]  

  • 6. A gene for congenital, recessive deafness DFNB3 maps to the pericentromeric region of chromosome 17.
    Friedman TB; Liang Y; Weber JL; Hinnant JT; Barber TD; Winata S; Arhya IN; Asher JH
    Nat Genet; 1995 Jan; 9(1):86-91. PubMed ID: 7704031
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Genetic mapping of the whirler mutation.
    Rogers MJ; Fleming J; Kiernan BW; Mburu P; Varela A; Brown SD; Steel KP
    Mamm Genome; 1999 May; 10(5):513-9. PubMed ID: 10337627
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Genetic and physical maps of the stargazer locus on mouse chromosome 15.
    Letts VA; Valenzuela A; Kirley JP; Sweet HO; Davisson MT; Frankel WN
    Genomics; 1997 Jul; 43(1):62-8. PubMed ID: 9226373
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Reverse genetics in the mouse and its application to the study of deafness.
    Rinchik EM; Johnson DK; Margolis FL; Jackson IJ; Russell LB; Carpenter DA
    Ann N Y Acad Sci; 1991; 630():80-92. PubMed ID: 1952626
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Genetic linkage analysis of the Ak1, Col5a1, Epb7.2, Fpgs, Grp78, Pbx3, and Notch1 genes in the region of mouse chromosome 2 homologous to human chromosome 9q.
    Pilz A; Prohaska R; Peters J; Abbott C
    Genomics; 1994 May; 21(1):104-9. PubMed ID: 8088777
    [TBL] [Abstract][Full Text] [Related]  

  • 11. The deafness locus (dn) maps to mouse chromosome 19.
    Keats BJ; Nouri N; Huang JM; Money M; Webster DB; Berlin CI
    Mamm Genome; 1995 Jan; 6(1):8-10. PubMed ID: 7719036
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Vestibular dysfunction in the epistatic circler mouse is caused by phenotypic interaction of one recessive gene and three modifier genes.
    Cryns K; Van Spaendonck MP; Flothmann K; van Alphen AM; Van De Heyning PH; Timmermans JP; De Zeeuw CI; Van Camp G
    Genome Res; 2002 Apr; 12(4):613-7. PubMed ID: 11932245
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Genetic and physical delineation of the region of the mouse deafness mutation shaker-2.
    Wakabayashi Y; Kikkawa Y; Matsumoto Y; Shinbo T; Kosugi S; Chou D; Furuya M; Jishage K; Noda T; Yonekawa H; Kominami R
    Biochem Biophys Res Commun; 1997 May; 234(1):107-10. PubMed ID: 9168970
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Linkage mapping around the ragged (Ra) and wasted (wst) loci on distal mouse chromosome 2.
    Abbott C; Malas S; Pilz A; Pate L; Ali R; Peters J
    Genomics; 1994 Mar; 20(1):94-8. PubMed ID: 8020960
    [TBL] [Abstract][Full Text] [Related]  

  • 15. The mapping of a cDNA from the human X-linked Duchenne muscular dystrophy gene to the mouse X chromosome.
    Brockdorff N; Cross GS; Cavanna JS; Fisher EM; Lyon MF; Davies KE; Brown SD
    Nature; 1987 Jul 9-15; 328(6126):166-8. PubMed ID: 3600793
    [TBL] [Abstract][Full Text] [Related]  

  • 16. A curly-tail modifier locus, mct1, on mouse chromosome 17.
    Letts VA; Schork NJ; Copp AJ; Bernfield M; Frankel WN
    Genomics; 1995 Oct; 29(3):719-24. PubMed ID: 8575765
    [TBL] [Abstract][Full Text] [Related]  

  • 17. The mouse mutation progressive motor neuronopathy (pmn) maps to chromosome 13.
    Brunialti AL; Poirier C; Schmalbruch H; Guénet JL
    Genomics; 1995 Sep; 29(1):131-5. PubMed ID: 8530062
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Assignment of the protein kinase C delta polypeptide gene (PRKCD) to human chromosome 3 and mouse chromosome 14.
    Huppi K; Siwarski D; Goodnight J; Mischak H
    Genomics; 1994 Jan; 19(1):161-2. PubMed ID: 8188219
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Physical and genetic maps of the deafwaddler region on distal mouse Chr 6.
    McKee-Johnson JW; Street VA; Erford SK; Robinson LC; Tempel BL
    Genomics; 1998 May; 49(3):371-7. PubMed ID: 9615221
    [TBL] [Abstract][Full Text] [Related]  

  • 20. A non-syndrome form of neurosensory, recessive deafness maps to the pericentromeric region of chromosome 13q.
    Guilford P; Ben Arab S; Blanchard S; Levilliers J; Weissenbach J; Belkahia A; Petit C
    Nat Genet; 1994 Jan; 6(1):24-8. PubMed ID: 8136828
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 7.