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Journal Abstract Search

98 related items for PubMed ID: 7945295

  • 21. Assignment of tear lipocalin gene to human chromosome 9q34-9qter.
    Glasgow BJ, Heinzmann C, Kojis T, Sparkes RS, Mohandas T, Bateman JB.
    Curr Eye Res; 1993 Nov; 12(11):1019-23. PubMed ID: 8306712
    [Abstract] [Full Text] [Related]

  • 22. Localization of human phosphoribosylpyrophosphate synthetase subunit I and II genes (PRPS1 and PRPS2) to different regions of the X chromosome and assignment of two PRPS1-related genes to autosomes.
    Taira M, Kudoh J, Minoshima S, Iizasa T, Shimada H, Shimizu Y, Tatibana M, Shimizu N.
    Somat Cell Mol Genet; 1989 Jan; 15(1):29-37. PubMed ID: 2536962
    [Abstract] [Full Text] [Related]

  • 23. Isolation and mapping of human T-cell protein tyrosine phosphatase sequences: localization of genes and pseudogenes discriminated using fluorescence hybridization with genomic versus cDNA probes.
    Johnson CV, Cool DE, Glaccum MB, Green N, Fischer EH, Bruskin A, Hill DE, Lawrence JB.
    Genomics; 1993 Jun; 16(3):619-29. PubMed ID: 8325634
    [Abstract] [Full Text] [Related]

  • 24. Assignment of the gene for human tenascin to the region q32-q34 of chromosome 9.
    Rocchi M, Archidiacono N, Romeo G, Saginati M, Zardi L.
    Hum Genet; 1991 Apr; 86(6):621-3. PubMed ID: 1709136
    [Abstract] [Full Text] [Related]

  • 25. The prostate-specific antigen gene and the human glandular kallikrein-1 gene are tandemly located on chromosome 19.
    Riegman PH, Vlietstra RJ, Klaassen P, van der Korput JA, Geurts van Kessel A, Romijn JC, Trapman J.
    FEBS Lett; 1989 Apr 10; 247(1):123-6. PubMed ID: 2468530
    [Abstract] [Full Text] [Related]

  • 26. Cystatin C (CST3), the candidate gene for hereditary cystatin C amyloid angiopathy (HCCAA), and other members of the cystatin gene family are clustered on chromosome 20p11.2.
    Schnittger S, Rao VV, Abrahamson M, Hansmann I.
    Genomics; 1993 Apr 10; 16(1):50-5. PubMed ID: 8486384
    [Abstract] [Full Text] [Related]

  • 27. Mapping of the genes encoding human inducible and endothelial nitric oxide synthase (NOS2 and NOS3) to the pericentric region of chromosome 17 and to chromosome 7, respectively.
    Xu W, Charles IG, Moncada S, Gorman P, Sheer D, Liu L, Emson P.
    Genomics; 1994 May 15; 21(2):419-22. PubMed ID: 7522210
    [Abstract] [Full Text] [Related]

  • 28. The glycine cleavage system: structure of a cDNA encoding human H-protein, and partial characterization of its gene in patients with hyperglycinemias.
    Koyata H, Hiraga K.
    Am J Hum Genet; 1991 Feb 15; 48(2):351-61. PubMed ID: 1671321
    [Abstract] [Full Text] [Related]

  • 29. Non-ketotic hyperglycinemia: an aim of the second generation of studies on pathogenesis.
    Hiraga K, Koyata H, Sakakibara T, Ishiguro Y, Matsui C.
    Mol Biol Med; 1991 Feb 15; 8(1):65-79. PubMed ID: 1943691
    [Abstract] [Full Text] [Related]

  • 30. Assignment of human thyrotropin-releasing hormone (TRH) receptor gene to chromosome 8.
    Yamada M, Monden T, Konaka S, Mori M.
    Somat Cell Mol Genet; 1993 Nov 15; 19(6):577-80. PubMed ID: 8128317
    [Abstract] [Full Text] [Related]

  • 31. Chromosome assignment of the murine Hox-4.1 gene.
    Pravtcheva D, Newman M, Hunihan L, Lonai P, Ruddle FH.
    Genomics; 1989 Oct 15; 5(3):541-5. PubMed ID: 2575585
    [Abstract] [Full Text] [Related]

  • 32. Localization of brain nitric oxide synthase (NOS) to human chromosome 12.
    Kishimoto J, Spurr N, Liao M, Lizhi L, Emson P, Xu W.
    Genomics; 1992 Nov 15; 14(3):802-4. PubMed ID: 1385308
    [Abstract] [Full Text] [Related]

  • 33. Human dopa decarboxylase: localization to human chromosome 7p11 and characterization of hepatic cDNAs.
    Scherer LJ, McPherson JD, Wasmuth JJ, Marsh JL.
    Genomics; 1992 Jun 15; 13(2):469-71. PubMed ID: 1612608
    [Abstract] [Full Text] [Related]

  • 34. Mapping of human lactate dehydrogenase-A, -B, and -C genes and their related sequences: the gene for LDHC is located with that for LDHA on chromosome 11.
    Li SS, Luedemann M, Sharief FS, Takano T, Deaven LL.
    Cytogenet Cell Genet; 1988 Jun 15; 48(1):16-8. PubMed ID: 3180843
    [Abstract] [Full Text] [Related]

  • 35. The gene for the iron sulfur protein of succinate dehydrogenase (SDH-IP) maps to human chromosome 1p35-36.1.
    Leckschat S, Ream-Robinson D, Scheffler IE.
    Somat Cell Mol Genet; 1993 Sep 15; 19(5):505-11. PubMed ID: 8291026
    [Abstract] [Full Text] [Related]

  • 36. Gene for selenium-dependent glutathione peroxidase maps to human chromosomes 3, 21 and X.
    McBride OW, Mitchell A, Lee BJ, Mullenbach G, Hatfield D.
    Biofactors; 1988 Dec 15; 1(4):285-92. PubMed ID: 3255357
    [Abstract] [Full Text] [Related]

  • 37. The gene for human glutaredoxin (GLRX) is localized to human chromosome 5q14.
    Padilla CA, Bajalica S, Lagercrantz J, Holmgren A.
    Genomics; 1996 Mar 15; 32(3):455-7. PubMed ID: 8838810
    [Abstract] [Full Text] [Related]

  • 38. The human Hb (mu) class glutathione S-transferases are encoded by a dispersed gene family.
    DeJong JL, Mohandas T, Tu CP.
    Biochem Biophys Res Commun; 1991 Oct 15; 180(1):15-22. PubMed ID: 1930212
    [Abstract] [Full Text] [Related]

  • 39. Mapping the human CAS2 gene, the homologue of the mouse brown (b) locus, to human chromosome 9p22-pter.
    Chintamaneni CD, Ramsay M, Colman MA, Fox MF, Pickard RT, Kwon BS.
    Biochem Biophys Res Commun; 1991 Jul 15; 178(1):227-35. PubMed ID: 1906272
    [Abstract] [Full Text] [Related]

  • 40. Sublocalization of the synovial sarcoma-associated t(X;18) chromosomal breakpoint in Xp11.2 using cosmid cloning and fluorescence in situ hybridization.
    de Leeuw B, Suijkerbuijk RF, Balemans M, Sinke RJ, de Jong B, Molenaar WM, Meloni AM, Sandberg AA, Geraghty M, Hofker M.
    Oncogene; 1993 Jun 15; 8(6):1457-63. PubMed ID: 8389029
    [Abstract] [Full Text] [Related]

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