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Journal Abstract Search

71 related items for PubMed ID: 8432548

  • 1. Localization of a potassium channel gene (KCNE1) to 21q22.1-q22.2 by in situ hybridization and somatic cell hybridization.
    Chevillard C, Attali B, Lesage F, Fontes M, Barhanin J, Lazdunski M, Mattei MG.
    Genomics; 1993 Jan; 15(1):243-5. PubMed ID: 8432548
    [No Abstract] [Full Text] [Related]

  • 2. Confirmation of the assignment of the gene encoding Kv1.3, a voltage-gated potassium channel (KCNA3) to the proximal short arm of human chromosome 1.
    Folander K, Douglass J, Swanson R.
    Genomics; 1994 Sep 01; 23(1):295-6. PubMed ID: 7829094
    [No Abstract] [Full Text] [Related]

  • 3. Human G-protein-coupled inwardly rectifying potassium channel (GIRK1) gene (KCNJ3): localization to chromosome 2 and identification of a simple tandem repeat polymorphism.
    Stoffel M, Espinosa R, Powell KL, Philipson LH, Le Beau MM, Bell GI.
    Genomics; 1994 May 01; 21(1):254-6. PubMed ID: 8088798
    [Abstract] [Full Text] [Related]

  • 4. Localization of the gene encoding the alpha 2/delta subunit (CACNL2A) of the human skeletal muscle voltage-dependent Ca2+ channel to chromosome 7q21-q22 by somatic cell hybrid analysis.
    Powers PA, Scherer SW, Tsui LC, Gregg RG, Hogan K.
    Genomics; 1994 Jan 01; 19(1):192-3. PubMed ID: 8188232
    [No Abstract] [Full Text] [Related]

  • 5. Localization of two potassium channel beta subunit genes, KCNA1B and KCNA2B.
    Schultz D, Litt M, Smith L, Thayer M, McCormack K.
    Genomics; 1996 Feb 01; 31(3):389-91. PubMed ID: 8838324
    [Abstract] [Full Text] [Related]

  • 6. Localization of the human tripeptidyl peptidase II gene (TPP2) to 13q32-q33 by nonradioactive in situ hybridization and somatic cell hybrids.
    Martinsson T, Vujic M, Tomkinson B.
    Genomics; 1993 Aug 01; 17(2):493-5. PubMed ID: 8406500
    [Abstract] [Full Text] [Related]

  • 7. Gene assignment by polymerase chain reaction: localization of the human potassium channel IsK gene to the Down's syndrome region of chromosome 21q22.1-q22.2.
    Malo MS, Srivastava K, Ingram VM.
    Gene; 1995 Jul 04; 159(2):273-5. PubMed ID: 7622063
    [Abstract] [Full Text] [Related]

  • 8. Assignment of human glutaryl-CoA dehydrogenase gene (GCDH) to the short arm of chromosome 19 (19p13.2) by in situ hybridization and somatic cell hybrid analysis.
    Greenberg CR, Duncan AM, Gregory CA, Singal R, Goodman SI.
    Genomics; 1994 May 01; 21(1):289-90. PubMed ID: 8088809
    [No Abstract] [Full Text] [Related]

  • 9. Localization of cDNAs to a region poorly represented in the CEPH chromosome 21 YAC contig: candidate genes for genetic diseases mapped to 21q22.3.
    Gardiner K, Ichikawa H, Ohki M, Patterson D, Cheng JF.
    Genomics; 1995 Nov 20; 30(2):376-9. PubMed ID: 8586445
    [Abstract] [Full Text] [Related]

  • 10. Assignment of human potassium channel gene KCNA4 (Kv1.4, PCN2) to chromosome 11q13.4-->q14.1.
    Philipson LH, Eddy RL, Shows TB, Bell GI.
    Genomics; 1993 Feb 20; 15(2):463-4. PubMed ID: 8449523
    [No Abstract] [Full Text] [Related]

  • 11. Localization of the human glucosidase I gene to chromosome 2p12-p13 by fluorescence in situ hybridization and PCR analysis of somatic cell hybrids.
    Kalz-Füller B, Heidrich-Kaul C, Nöthen M, Bause E, Schwanitz G.
    Genomics; 1996 Jun 15; 34(3):442-3. PubMed ID: 8786151
    [No Abstract] [Full Text] [Related]

  • 12. Assignment of electron transfer flavoprotein-ubiquinone oxidoreductase (ETF-QO) to human chromosome 4q33 by fluorescence in situ hybridization and somatic cell hybridization.
    Spector EB, Seltzer WK, Goodman SI.
    Mol Genet Metab; 1999 Aug 15; 67(4):364-7. PubMed ID: 10444348
    [Abstract] [Full Text] [Related]

  • 13. [Identification of the breakpoint-flanking markers on chromosomes 1 and 17 of a constitutional translocation T(1;17)(P36;Q12-21) in a patient with neuroblastoma].
    Laureys GG.
    Verh K Acad Geneeskd Belg; 1995 Aug 15; 57(5):389-422. PubMed ID: 8571670
    [Abstract] [Full Text] [Related]

  • 14. 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]

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

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  • 17. Assignment of DNA cytosine-5-methyltransferase 1 (DNMT1) gene to porcine chromosome 2q21-->q22 by somatic cell and radiation hybrid panel mapping.
    Bosak N, Fujisaki S, Kiuchi S, Hiraiwa H, Yasue H.
    Cytogenet Genome Res; 2003 Mar 15; 101(2):178. PubMed ID: 14619887
    [No Abstract] [Full Text] [Related]

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  • 19. Localization of the gene (TAF2D) encoding the 100-kDa subunit (hTAFII100) of the human TFIID complex to chromosome 10 band q24-q25.2.
    Dubrovskaya V, Mattei MG, Tora L.
    Genomics; 1996 Sep 15; 36(3):556-7. PubMed ID: 8884287
    [No Abstract] [Full Text] [Related]

  • 20. The human inward rectifying K+ channel Kir 2.2 (KCNJ12) gene: gene structure, assignment to chromosome 17p11.1, and identification of a simple tandem repeat polymorphism.
    Hugnot JP, Pedeutour F, Le Calvez C, Grosgeorge J, Passage E, Fontes M, Lazdunski M.
    Genomics; 1997 Jan 01; 39(1):113-6. PubMed ID: 9027495
    [Abstract] [Full Text] [Related]

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