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87 related items for PubMed ID: 9339382

  • 1. Mapping of the gene (NRAP) encoding N-RAP in the mouse and human genomes.
    Luo G, Leroy E, Kozak CA, Polymeropoulos MH, Horowits R.
    Genomics; 1997 Oct 01; 45(1):229-32. PubMed ID: 9339382
    [Abstract] [Full Text] [Related]

  • 2. Complete cDNA sequence and tissue localization of N-RAP, a novel nebulin-related protein of striated muscle.
    Luo G, Zhang JQ, Nguyen TP, Herrera AH, Paterson B, Horowits R.
    Cell Motil Cytoskeleton; 1997 Oct 01; 38(1):75-90. PubMed ID: 9295142
    [Abstract] [Full Text] [Related]

  • 3. Structure of the human gene (COX6A2) for the heart/muscle isoform of cytochrome c oxidase subunit VIa and its chromosomal location in humans, mice, and cattle.
    Bachman NJ, Riggs PK, Siddiqui N, Makris GJ, Womack JE, Lomax MI.
    Genomics; 1997 May 15; 42(1):146-51. PubMed ID: 9177785
    [Abstract] [Full Text] [Related]

  • 4. Genomic organization, alternative splicing, and expression of human and mouse N-RAP, a nebulin-related LIM protein of striated muscle.
    Mohiddin SA, Lu S, Cardoso JP, Carroll S, Jha S, Horowits R, Fananapazir L.
    Cell Motil Cytoskeleton; 2003 Jul 15; 55(3):200-12. PubMed ID: 12789664
    [Abstract] [Full Text] [Related]

  • 5. Mapping of the KHSRP gene to a region of conserved synteny on human chromosome 19p13.3 and mouse chromosome 17.
    Ring HZ, Vameghi-Meyers V, Nikolic JM, Min H, Black DL, Francke U.
    Genomics; 1999 Mar 15; 56(3):350-2. PubMed ID: 10087204
    [Abstract] [Full Text] [Related]

  • 6. Mapping of the ARIX homeodomain gene to mouse chromosome 7 and human chromosome 11q13.
    Johnson KR, Smith L, Johnson DK, Rhodes J, Rinchik EM, Thayer M, Lewis EJ.
    Genomics; 1996 May 01; 33(3):527-31. PubMed ID: 8661014
    [Abstract] [Full Text] [Related]

  • 7. Characterization of nebulette and nebulin and emerging concepts of their roles for vertebrate Z-discs.
    Millevoi S, Trombitas K, Kolmerer B, Kostin S, Schaper J, Pelin K, Granzier H, Labeit S.
    J Mol Biol; 1998 Sep 11; 282(1):111-23. PubMed ID: 9733644
    [Abstract] [Full Text] [Related]

  • 8. Terminal regions of mouse nebulin: sequence analysis and complementary localization with N-RAP.
    Herrera AH, Elzey B, Law DJ, Horowits R.
    Cell Motil Cytoskeleton; 2000 Mar 11; 45(3):211-22. PubMed ID: 10706776
    [Abstract] [Full Text] [Related]

  • 9. Molecular interactions of N-RAP, a nebulin-related protein of striated muscle myotendon junctions and intercalated disks.
    Luo G, Herrera AH, Horowits R.
    Biochemistry; 1999 May 11; 38(19):6135-43. PubMed ID: 10320340
    [Abstract] [Full Text] [Related]

  • 10. Cloning of cDNA encoding human rapsyn and mapping of the RAPSN gene locus to chromosome 11p11.2-p11.1.
    Buckel A, Beeson D, James M, Vincent A.
    Genomics; 1996 Aug 01; 35(3):613-6. PubMed ID: 8812503
    [Abstract] [Full Text] [Related]

  • 11. Comparative mapping of human chromosome 10 to pig chromosomes 10 and 14.
    Nonneman D, Rohrer GA.
    Anim Genet; 2004 Aug 01; 35(4):338-43. PubMed ID: 15265077
    [Abstract] [Full Text] [Related]

  • 12. The murine Bin1 gene functions early in myogenesis and defines a new region of synteny between mouse chromosome 18 and human chromosome 2.
    Mao NC, Steingrimsson E, DuHadaway J, Wasserman W, Ruiz JC, Copeland NG, Jenkins NA, Prendergast GC.
    Genomics; 1999 Feb 15; 56(1):51-8. PubMed ID: 10036185
    [Abstract] [Full Text] [Related]

  • 13. Characterization of the gene encoding human sarcolipin (SLN), a proteolipid associated with SERCA1: absence of structural mutations in five patients with Brody disease.
    Odermatt A, Taschner PE, Scherer SW, Beatty B, Khanna VK, Cornblath DR, Chaudhry V, Yee WC, Schrank B, Karpati G, Breuning MH, Knoers N, MacLennan DH.
    Genomics; 1997 Nov 01; 45(3):541-53. PubMed ID: 9367679
    [Abstract] [Full Text] [Related]

  • 14. Paralogous sm22alpha (Tagln) genes map to mouse chromosomes 1 and 9: further evidence for a paralogous relationship.
    Stanier P, Abu-Hayyeh S, Murdoch JN, Eddleston J, Copp AJ.
    Genomics; 1998 Jul 01; 51(1):144-7. PubMed ID: 9693045
    [Abstract] [Full Text] [Related]

  • 15. Two novel mouse genes--Nubp2, mapped to the t-complex on chromosome 17, and Nubp1, mapped to chromosome 16--establish a new gene family of nucleotide-binding proteins in eukaryotes.
    Nakashima H, Grahovac MJ, Mazzarella R, Fujiwara H, Kitchen JR, Threat TA, Ko MS.
    Genomics; 1999 Sep 01; 60(2):152-60. PubMed ID: 10486206
    [Abstract] [Full Text] [Related]

  • 16. Genetic structure and chromosomal mapping of MyD88.
    Hardiman G, Jenkins NA, Copeland NG, Gilbert DJ, Garcia DK, Naylor SL, Kastelein RA, Bazan JF.
    Genomics; 1997 Oct 15; 45(2):332-9. PubMed ID: 9344657
    [Abstract] [Full Text] [Related]

  • 17. The mouse Psma1 gene coding for the alpha-type C2 proteasome subunit: structural and functional analysis, mapping, and colocalization with Pde3b on mouse chromosome 7.
    Hopitzan A, Himmelbauer H, Spevak W, Castanon MJ.
    Genomics; 2000 Jun 15; 66(3):313-23. PubMed ID: 10873386
    [Abstract] [Full Text] [Related]

  • 18. Identification and characterization of a new human gene encoding a small protein with high homology to the proline-rich region of the SH3BGR gene.
    Egeo A, Mazzocco M, Arrigo P, Vidal-Taboada JM, Oliva R, Pirola B, Giglio S, Rasore-Quartino A, Scartezzini P.
    Biochem Biophys Res Commun; 1998 Jun 18; 247(2):302-6. PubMed ID: 9642120
    [Abstract] [Full Text] [Related]

  • 19. The human glutamate receptor delta 2 gene (GRID2) maps to chromosome 4q22.
    Hu W, Zuo J, De Jager PL, Heintz N.
    Genomics; 1998 Jan 01; 47(1):143-5. PubMed ID: 9465309
    [Abstract] [Full Text] [Related]

  • 20. 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]

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