These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


PUBMED FOR HANDHELDS

Journal Abstract Search


133 related items for PubMed ID: 8034307

  • 1. Voltage-gated potassium channel genes are clustered in paralogous regions of the mouse genome.
    Lock LF, Gilbert DJ, Street VA, Migeon MB, Jenkins NA, Copeland NG, Tempel BL.
    Genomics; 1994 Apr; 20(3):354-62. PubMed ID: 8034307
    [Abstract] [Full Text] [Related]

  • 2. Cloning of a human cDNA expressing a high voltage-activating, TEA-sensitive, type-A K+ channel which maps to chromosome 1 band p21.
    Rudy B, Sen K, Vega-Saenz de Miera E, Lau D, Ried T, Ward DC.
    J Neurosci Res; 1991 Jul; 29(3):401-12. PubMed ID: 1920536
    [Abstract] [Full Text] [Related]

  • 3.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 4.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 5.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 6.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 7. Molecular genetic analysis of distal mouse chromosome 6 defines gene order and positions of the deafwaddler and opisthotonos mutations.
    Street VA, Robinson LC, Erford SK, Tempel BL.
    Genomics; 1995 Sep 01; 29(1):123-30. PubMed ID: 8530061
    [Abstract] [Full Text] [Related]

  • 8. Chromosomal mapping of the potassium channel genes Kcnq2 and Kcnq3 in mouse.
    McCormack T, Rudy B, Seldin MF.
    Genomics; 1999 Mar 15; 56(3):360-1. PubMed ID: 10087209
    [No Abstract] [Full Text] [Related]

  • 9.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 10. Fine-scale comparative mapping of the human 7q11.23 region and the orthologous region on mouse chromosome 5G: the low-copy repeats that flank the Williams-Beuren syndrome deletion arose at breakpoint sites of an evolutionary inversion(s).
    Valero MC, de Luis O, Cruces J, Pérez Jurado LA.
    Genomics; 2000 Oct 01; 69(1):1-13. PubMed ID: 11013070
    [Abstract] [Full Text] [Related]

  • 11. 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]

  • 12.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 13. Isolation, characterization, and mapping of the mouse and human Fgd2 genes, faciogenital dysplasia (FGD1; Aarskog syndrome) gene homologues.
    Pasteris NG, Gorski JL.
    Genomics; 1999 Aug 15; 60(1):57-66. PubMed ID: 10458911
    [Abstract] [Full Text] [Related]

  • 14. Mapping of murine fibroblast growth factor receptors refines regions of homology between mouse and human chromosomes.
    Avraham KB, Givol D, Avivi A, Yayon A, Copeland NG, Jenkins NA.
    Genomics; 1994 Jun 15; 21(3):656-8. PubMed ID: 7959747
    [Abstract] [Full Text] [Related]

  • 15.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 16. Mouse-human orthology relationships in an olfactory receptor gene cluster.
    Lapidot M, Pilpel Y, Gilad Y, Falcovitz A, Sharon D, Haaf T, Lancet D.
    Genomics; 2001 Feb 01; 71(3):296-306. PubMed ID: 11170746
    [Abstract] [Full Text] [Related]

  • 17. Gene structures and expression profiles of three human KCND (Kv4) potassium channels mediating A-type currents I(TO) and I(SA).
    Isbrandt D, Leicher T, Waldschütz R, Zhu X, Luhmann U, Michel U, Sauter K, Pongs O.
    Genomics; 2000 Mar 01; 64(2):144-54. PubMed ID: 10729221
    [Abstract] [Full Text] [Related]

  • 18.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 19. Evolutionarily plastic regions at human 3p21.3 coincide with tumor breakpoints identified by the "elimination test".
    Darai E, Kost-Alimova M, Kiss H, Kansoul H, Klein G, Imreh S.
    Genomics; 2005 Jul 01; 86(1):1-12. PubMed ID: 15913951
    [Abstract] [Full Text] [Related]

  • 20. Molecular diversity of the SCG10/stathmin gene family in the mouse.
    Okazaki T, Yoshida BN, Avraham KB, Wang H, Wuenschell CW, Jenkins NA, Copeland NG, Anderson DJ, Mori N.
    Genomics; 1993 Nov 01; 18(2):360-73. PubMed ID: 8288240
    [Abstract] [Full Text] [Related]


    Page: [Next] [New Search]
    of 7.