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Journal Abstract Search


98 related items for PubMed ID: 9177773

  • 1. Genomic localization of the human gene for KCNA10, a cGMP-activated K channel.
    Orias M, Bray-Ward P, Curran ME, Keating MT, Desir GV.
    Genomics; 1997 May 15; 42(1):33-7. PubMed ID: 9177773
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  • 2. Regulation of the voltage-gated K+ channel KCNA10 by KCNA4B, a novel beta-subunit.
    Tian S, Liu W, Wu Y, Rafi H, Segal AS, Desir GV.
    Am J Physiol Renal Physiol; 2002 Jul 15; 283(1):F142-9. PubMed ID: 12060596
    [Abstract] [Full Text] [Related]

  • 3. 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
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  • 4. Characterisation of the human voltage-gated potassium channel gene, KCNA7, a candidate gene for inherited cardiac disorders, and its exclusion as cause of progressive familial heart block I (PFHBI).
    Bardien-Kruger S, Wulff H, Arieff Z, Brink P, Chandy KG, Corfield V.
    Eur J Hum Genet; 2002 Jan 01; 10(1):36-43. PubMed ID: 11896454
    [Abstract] [Full Text] [Related]

  • 5. Mapping human YAC clones by fluorescence in situ hybridization using Alu-PCR from single yeast colonies.
    Baldini A, Lindsay EA.
    Methods Mol Biol; 1994 Jan 01; 33():75-84. PubMed ID: 7894594
    [No Abstract] [Full Text] [Related]

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  • 7. 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
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  • 9. Molecular cloning of a human cDNA IGSF3 encoding an immunoglobulin-like membrane protein: expression and mapping to chromosome band 1p13.
    Saupe S, Roizès G, Peter M, Boyle S, Gardiner K, De Sario A.
    Genomics; 1998 Sep 15; 52(3):305-11. PubMed ID: 9790749
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  • 10. A pore mutation in a novel KQT-like potassium channel gene in an idiopathic epilepsy family.
    Charlier C, Singh NA, Ryan SG, Lewis TB, Reus BE, Leach RJ, Leppert M.
    Nat Genet; 1998 Jan 15; 18(1):53-5. PubMed ID: 9425900
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  • 11. 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
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  • 15. Structure of the human type I iodothyronine 5'-deiodinase gene and localization to chromosome 1p32-p33.
    Jakobs TC, Koehler MR, Schmutzler C, Glaser F, Schmid M, Köhrle J.
    Genomics; 1997 Jun 01; 42(2):361-3. PubMed ID: 9192862
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  • 16. Human rod monochromacy: linkage analysis and mapping of a cone photoreceptor expressed candidate gene on chromosome 2q11.
    Wissinger B, Jägle H, Kohl S, Broghammer M, Baumann B, Hanna DB, Hedels C, Apfelstedt-Sylla E, Randazzo G, Jacobson SG, Zrenner E, Sharpe LT.
    Genomics; 1998 Aug 01; 51(3):325-31. PubMed ID: 9721202
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  • 17. FISH of Alu-PCR-amplified YAC clones and applications in tumor cytogenetics.
    Lengauer C, Speicher MR, Cremer T.
    Methods Mol Biol; 1994 Aug 01; 33():85-94. PubMed ID: 7894595
    [No Abstract] [Full Text] [Related]

  • 18. Molecular characterization and refined genomic localization of three human potassium ion channel genes.
    Landes GM, Curran ME, Keating MT.
    Cytogenet Cell Genet; 1995 Aug 01; 70(3-4):280-4. PubMed ID: 7789190
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  • 19. Partial gene structure and assignment to chromosome 2q37 of the human inwardly rectifying K+ channel (Kir7.1) gene (KCNJ13).
    Derst C, Döring F, Preisig-Müller R, Daut J, Karschin A, Jeck N, Weber S, Engel H, Grzeschik KH.
    Genomics; 1998 Dec 15; 54(3):560-3. PubMed ID: 9878260
    [Abstract] [Full Text] [Related]

  • 20. Positional cloning of novel skin-specific genes from the human epidermal differentiation complex.
    Zhao XP, Elder JT.
    Genomics; 1997 Oct 15; 45(2):250-8. PubMed ID: 9344646
    [Abstract] [Full Text] [Related]


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