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Journal Abstract Search

101 related items for PubMed ID: 8432538

  • 1.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 2. Cloning, structural analysis, and chromosomal localization of the human CSRP2 gene encoding the LIM domain protein CRP2.
    Weiskirchen R, Erdel M, Utermann G, Bister K.
    Genomics; 1997 Aug 15; 44(1):83-93. PubMed ID: 9286703
    [Abstract] [Full Text] [Related]

  • 3. 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]

  • 4. Localization of the gene encoding the human heat shock cognate protein, HSP73, to chromosome 11.
    Tavaria M, Gabriele T, Anderson RL, Mirault ME, Baker E, Sutherland G, Kola I.
    Genomics; 1995 Sep 01; 29(1):266-8. PubMed ID: 8530083
    [Abstract] [Full Text] [Related]

  • 5. cDNA cloning, tissue distribution, and chromosomal localization of myelodysplasia/myeloid leukemia factor 2 (MLF2).
    Kuefer MU, Look AT, Williams DC, Valentine V, Naeve CW, Behm FG, Mullersman JE, Yoneda-Kato N, Montgomery K, Kucherlapati R, Morris SW.
    Genomics; 1996 Jul 15; 35(2):392-6. PubMed ID: 8661158
    [Abstract] [Full Text] [Related]

  • 6. cDNA cloning and gene structure of a novel water channel expressed exclusively in human kidney: evidence for a gene cluster of aquaporins at chromosome locus 12q13.
    Ma T, Yang B, Kuo WL, Verkman AS.
    Genomics; 1996 Aug 01; 35(3):543-50. PubMed ID: 8812490
    [Abstract] [Full Text] [Related]

  • 7. Human ESP1/CRP2, a member of the LIM domain protein family: characterization of the cDNA and assignment of the gene locus to chromosome 14q32.3.
    Karim MA, Ohta K, Egashira M, Jinno Y, Niikawa N, Matsuda I, Indo Y.
    Genomics; 1996 Jan 15; 31(2):167-76. PubMed ID: 8824798
    [Abstract] [Full Text] [Related]

  • 8. Genomic structure and chromosomal localization of the gene encoding TRAX, a Translin-associated factor X.
    Meng G, Aoki K, Tokura K, Nakahara K, Inazawa J, Kasai M.
    J Hum Genet; 2000 Jan 15; 45(5):305-8. PubMed ID: 11043515
    [Abstract] [Full Text] [Related]

  • 9. FISH identifies different types of duplications with 12q13-15 as the commonly involved segment in B-cell lymphoproliferative malignancies characterized by partial trisomy 12.
    Dierlamm J, Wlodarska I, Michaux L, Vermeesch JR, Meeus P, Stul M, Criel A, Verhoef G, Thomas J, Delannoy A, Louwagie A, Cassiman JJ, Mecucci C, Hagemeijer A, Van den Berghe H.
    Genes Chromosomes Cancer; 1997 Oct 15; 20(2):155-66. PubMed ID: 9331566
    [Abstract] [Full Text] [Related]

  • 10. A novel human amino acid transporter, hNAT3: cDNA cloning, chromosomal mapping, genomic structure, expression, and functional characterization.
    Gu S, Adan-Rice D, Leach RJ, Jiang JX.
    Genomics; 2001 Jun 15; 74(3):262-72. PubMed ID: 11414754
    [Abstract] [Full Text] [Related]

  • 11. Cytogenetic and radiation hybrid mapping of human arachidonate 5-lipoxygenase-activating protein (ALOX5AP) to chromosome 13q12.
    Yandava CN, Kennedy BP, Pillari A, Duncan AM, Drazen JM.
    Genomics; 1999 Feb 15; 56(1):131-3. PubMed ID: 10036194
    [Abstract] [Full Text] [Related]

  • 12. LPP, the preferred fusion partner gene of HMGIC in lipomas, is a novel member of the LIM protein gene family.
    Petit MM, Mols R, Schoenmakers EF, Mandahl N, Van de Ven WJ.
    Genomics; 1996 Aug 15; 36(1):118-29. PubMed ID: 8812423
    [Abstract] [Full Text] [Related]

  • 13. Regional chromosomal assignments for four members of the MADS domain transcription enhancer factor 2 (MEF2) gene family to human chromosomes 15q26, 19p12, 5q14, and 1q12-q23.
    Hobson GM, Krahe R, Garcia E, Siciliano MJ, Funanage VL.
    Genomics; 1995 Oct 10; 29(3):704-11. PubMed ID: 8575763
    [Abstract] [Full Text] [Related]

  • 14.
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  • 15. Genomic cloning and chromosomal assignment of the E2F dimerization partner TFDP gene family.
    Zhang Y, Venkatraj VS, Fischer SG, Warburton D, Chellappan SP.
    Genomics; 1997 Jan 01; 39(1):95-8. PubMed ID: 9027491
    [Abstract] [Full Text] [Related]

  • 16. Genomic organization and mutation analysis of the gene encoding lecithin retinol acyltransferase in human retinal pigment epithelium.
    Ruiz A, Kuehn MH, Andorf JL, Stone E, Hageman GS, Bok D.
    Invest Ophthalmol Vis Sci; 2001 Jan 01; 42(1):31-7. PubMed ID: 11133845
    [Abstract] [Full Text] [Related]

  • 17.
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  • 18. Molecular cloning, structure, expression, and chromosomal localization of the human Osterix (SP7) gene.
    Gao Y, Jheon A, Nourkeyhani H, Kobayashi H, Ganss B.
    Gene; 2004 Oct 27; 341():101-10. PubMed ID: 15474293
    [Abstract] [Full Text] [Related]

  • 19. Chromosomal mapping of the human and murine orphan receptors ERRalpha (ESRRA) and ERRbeta (ESRRB) and identification of a novel human ERRalpha-related pseudogene.
    Sladek R, Beatty B, Squire J, Copeland NG, Gilbert DJ, Jenkins NA, Giguère V.
    Genomics; 1997 Oct 15; 45(2):320-6. PubMed ID: 9344655
    [Abstract] [Full Text] [Related]

  • 20. Chromosomal aberrations evaluated by CGH, FISH and GTG-banding in a case of AIDS-related Burkitt's lymphoma.
    Zunino A, Viaggi S, Ottaggio L, Fronza G, Schenone A, Roncella S, Abbondandolo A.
    Haematologica; 2000 Mar 15; 85(3):250-5. PubMed ID: 10702812
    [Abstract] [Full Text] [Related]

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