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169 related items for PubMed ID: 8288249

  • 1. Assignment of the phosducin (PDC) gene to human chromosome 1q25-1q32.1 by somatic cell hybridization and in situ hybridization.
    Sparkes RS, Lee RH, Shinohara T, Craft CM, Kojis T, Klisak I, Heinzmann C, Bateman JB.
    Genomics; 1993 Nov; 18(2):426-8. PubMed ID: 8288249
    [Abstract] [Full Text] [Related]

  • 2. The sequence of the human phosducin gene (PDC) and its 5'-flanking region.
    Abe T, Kikuchi T, Shinohara T.
    Genomics; 1994 Jan 15; 19(2):369-72. PubMed ID: 8188267
    [Abstract] [Full Text] [Related]

  • 3. Radiation hybrid mapping of the genes for tenascin-R (TNR), phosducin (PDC), laminin C1 (LAMC1), and TAX in 1q25-q32.
    Williams H, Schachner M, Wang B, Kenwrick S.
    Genomics; 1997 Nov 15; 46(1):165-6. PubMed ID: 9403076
    [No Abstract] [Full Text] [Related]

  • 4. The gene for human phosducin (PDC), a soluble protein that binds G-protein beta gamma dimers, maps to 1q25-q31.1.
    Ding C, Li X, Griffin CA, Jabs EW, Hawkins AL, Levine MA.
    Genomics; 1993 Nov 15; 18(2):457-9. PubMed ID: 8288259
    [No Abstract] [Full Text] [Related]

  • 5. Regional mapping of the human renin gene to 1q32 by in situ hybridization.
    Cohen-Haguenauer O, Soubrier F, Van Cong N, Serero S, Turleau C, Jegou C, Gross MS, Corvol P, Frézal J.
    Ann Genet; 1989 Nov 15; 32(1):16-20. PubMed ID: 2665629
    [Abstract] [Full Text] [Related]

  • 6. Mutation screening of the phosducin gene PDC in patients with retinitis pigmentosa and allied diseases.
    Nishiguchi KM, Berson EL, Dryja TP.
    Mol Vis; 2004 Jan 26; 10():62-4. PubMed ID: 14758335
    [Abstract] [Full Text] [Related]

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  • 8. Reassignment of the human ARH9 RAS-related gene to chromosome 1p13-p21.
    Morris SW, Valentine MB, Kirstein MN, Huebner K.
    Genomics; 1993 Mar 26; 15(3):677-9. PubMed ID: 8468062
    [Abstract] [Full Text] [Related]

  • 9. Mapping of aldose reductase gene sequences to human chromosomes 1, 3, 7, 9, 11, and 13.
    Bateman JB, Kojis T, Heinzmann C, Klisak I, Diep A, Carper D, Nishimura C, Mohandas T, Sparkes RS.
    Genomics; 1993 Sep 26; 17(3):560-5. PubMed ID: 8244370
    [Abstract] [Full Text] [Related]

  • 10. Chromosomal assignment of the human gene for the cancer-associated retinopathy protein (recoverin) to chromosome 17p13.1.
    McGinnis JF, Austin B, Klisak I, Heinzmann C, Kojis T, Sparkes RS, Bateman JB, Lerious V.
    J Neurosci Res; 1995 Feb 01; 40(2):165-8. PubMed ID: 7745609
    [Abstract] [Full Text] [Related]

  • 11. Human retinal guanylate cyclase (GUC2D) maps to chromosome 17p13.1.
    Oliveira L, Miniou P, Viegas-Pequignot E, Rozet JM, Dollfus H, Pittler SJ.
    Genomics; 1994 Jul 15; 22(2):478-81. PubMed ID: 7806240
    [Abstract] [Full Text] [Related]

  • 12. Human TRK proto-oncogene maps to chromosome 1q32-q41.
    Miozzo M, Pierotti MA, Sozzi G, Radice P, Bongarzone I, Spurr NK, Della Porta G.
    Oncogene; 1990 Sep 15; 5(9):1411-4. PubMed ID: 2216464
    [Abstract] [Full Text] [Related]

  • 13. Localization of the human Ror1 gene (NTRKR1) to chromosome 1p31-p32 by fluorescence in situ hybridization and somatic cell hybrid analysis.
    Reddy UR, Phatak S, Allen C, Nycum LM, Sulman EP, White PS, Biegel JA.
    Genomics; 1997 Apr 15; 41(2):283-5. PubMed ID: 9143508
    [Abstract] [Full Text] [Related]

  • 14. The human tropomyosin gene involved in the generation of the TRK oncogene maps to chromosome 1q31.
    Radice P, Sozzi G, Miozzo M, De Benedetti V, Cariani T, Bongarzone I, Spurr NK, Pierotti MA, Della Porta G.
    Oncogene; 1991 Nov 15; 6(11):2145-8. PubMed ID: 1834975
    [Abstract] [Full Text] [Related]

  • 15. Isolation and investigation of canine phosducin as a candidate for canine generalized progressive retinal atrophies.
    Lin CT, Petersen-Jones SM, Sargan DR.
    Exp Eye Res; 1998 Oct 15; 67(4):473-80. PubMed ID: 9820795
    [Abstract] [Full Text] [Related]

  • 16. Assignment of the zeta-crystallin gene (CRYZ) to human chromosome 1p22-p31 and identification of restriction fragment length polymorphisms.
    Heinzmann C, Kojis TL, Gonzalez P, Rao PV, Zigler JS, Polymeropoulos MH, Klisak I, Sparkes RS, Mohandas T, Bateman JB.
    Genomics; 1994 Sep 15; 23(2):403-7. PubMed ID: 7835889
    [Abstract] [Full Text] [Related]

  • 17. Chromosome localization of human genes for clathrin adaptor polypeptides AP2 beta and AP50 and the clathrin-binding protein, VCP.
    Druck T, Gu Y, Prabhala G, Cannizzaro LA, Park SH, Huebner K, Keen JH.
    Genomics; 1995 Nov 01; 30(1):94-7. PubMed ID: 8595912
    [Abstract] [Full Text] [Related]

  • 18. Fine mapping of the autosomal recessive retinitis pigmentosa locus (RP12) on chromosome 1q; exclusion of the phosducin gene (PDC).
    van Soest S, te Nijenhuis S, van den Born LI, Bleeker-Wagemakers EM, Sharp E, Sandkuijl LA, Westerveld A, Bergen AA.
    Cytogenet Cell Genet; 1996 Nov 01; 73(1-2):81-5. PubMed ID: 8646891
    [Abstract] [Full Text] [Related]

  • 19. The gene for PAX7, a member of the paired-box-containing genes, is localized on human chromosome arm 1p36.
    Shapiro DN, Sublett JE, Li B, Valentine MB, Morris SW, Noll M.
    Genomics; 1993 Sep 01; 17(3):767-9. PubMed ID: 7902328
    [Abstract] [Full Text] [Related]

  • 20. The canine Phosducin gene: characterization of the exon-intron structure and exclusion as a candidate gene for generalized progressive retinal atrophy in 11 dog breeds.
    Dekomien G, Epplen JT.
    Mol Vis; 2002 Jun 07; 8():138-42. PubMed ID: 12091798
    [Abstract] [Full Text] [Related]

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