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Journal Abstract Search


122 related items for PubMed ID: 10425213

  • 21. Exon/intron boundaries, novel polymorphisms, and association analysis with schizophrenia of the human synaptic vesicle monoamine transporter (SVMT) gene.
    Kunugi H, Ishida S, Akahane A, Nanko S.
    Mol Psychiatry; 2001 Jul; 6(4):456-60. PubMed ID: 11443533
    [Abstract] [Full Text] [Related]

  • 22. [Cloning, genomic organization and promoter activity of the mouse zinc finger protein gene ZF-12].
    Li JZ, Chen X, Wang SL, Sun X, Zhang YZ, Yu L, Fu JL.
    Yi Chuan Xue Bao; 2003 Apr; 30(4):311-6. PubMed ID: 12812053
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  • 23. Genomic sequences and structural organization of the human nidogen gene (NID).
    Zimmermann K, Hoischen S, Hafner M, Nischt R.
    Genomics; 1995 May 20; 27(2):245-50. PubMed ID: 7557988
    [Abstract] [Full Text] [Related]

  • 24. Genomic organization and expression of the mouse equilibrative, nitrobenzylthioinosine-sensitive nucleoside transporter 1 (ENT1) gene.
    Choi DS, Handa M, Young H, Gordon AS, Diamond I, Messing RO.
    Biochem Biophys Res Commun; 2000 Oct 14; 277(1):200-8. PubMed ID: 11027664
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  • 25. Genomic organization of the mouse AZ1 gene that encodes the protein localized to preacrosomes of spermatids.
    Aoto H, Miyake Y, Nakamura M, Tajima S.
    Genomics; 1997 Feb 15; 40(1):138-41. PubMed ID: 9070930
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  • 26. Genomic Organization of the ATM gene.
    Uziel T, Savitsky K, Platzer M, Ziv Y, Helbitz T, Nehls M, Boehm T, Rosenthal A, Shiloh Y, Rotman G.
    Genomics; 1996 Apr 15; 33(2):317-20. PubMed ID: 8660985
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  • 27. Genomic organization and polymorphisms detected by denaturing high-performance liquid chromatography of porcine SLC11A1 gene.
    Wu ZF, Luo WH, Yang GF, Zhang XQ.
    DNA Seq; 2007 Oct 15; 18(5):327-33. PubMed ID: 17654007
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  • 28. Chromosomal organization and localization of the novel class IV human histone deacetylase 11 gene.
    Voelter-Mahlknecht S, Ho AD, Mahlknecht U.
    Int J Mol Med; 2005 Oct 15; 16(4):589-98. PubMed ID: 16142391
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  • 29. Full-length cDNA cloning and genomic organization of the mouse liver-specific organic anion transporter-1 (lst-1).
    Ogura K, Choudhuri S, Klaassen CD.
    Biochem Biophys Res Commun; 2000 Jun 07; 272(2):563-70. PubMed ID: 10833452
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  • 30. Mutations in NPC1 highlight a conserved NPC1-specific cysteine-rich domain.
    Greer WL, Dobson MJ, Girouard GS, Byers DM, Riddell DC, Neumann PE.
    Am J Hum Genet; 1999 Nov 07; 65(5):1252-60. PubMed ID: 10521290
    [Abstract] [Full Text] [Related]

  • 31. Morquio A syndrome: cloning, sequence, and structure of the human N-acetylgalactosamine 6-sulfatase (GALNS) gene.
    Morris CP, Guo XH, Apostolou S, Hopwood JJ, Scott HS.
    Genomics; 1994 Aug 07; 22(3):652-4. PubMed ID: 8001980
    [Abstract] [Full Text] [Related]

  • 32. Molecular characterization of the porcine deleted in malignant brain tumors 1 gene (DMBT1).
    Haase B, Humphray SJ, Lyer S, Renner M, Poustka A, Mollenhauer J, Leeb T.
    Gene; 2006 Jul 19; 376(2):184-91. PubMed ID: 16624504
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  • 33. The human RAP250 gene: genomic structure and promoter analysis.
    Antonson P, Al-Beidh F, Matthews J, Gustafsson JA.
    Gene; 2004 Mar 03; 327(2):233-8. PubMed ID: 14980720
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  • 34. Genomic organization and linkage via a bidirectional promoter of the AP-3 (adaptor protein-3) mu3A and AK (adenosine kinase) genes: deletion mutants of AK in Chinese hamster cells extend into the AP-3 mu3A gene.
    Singh B, Gupta RS.
    Biochem J; 2004 Mar 01; 378(Pt 2):519-28. PubMed ID: 14575525
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  • 35. Genomic organization and complete nucleotide sequence of the human PWP2 gene on chromosome 21.
    Nagamine K, Kudoh J, Minoshima S, Kawasaki K, Asakawa S, Ito F, Shimizu N.
    Genomics; 1997 Jun 15; 42(3):528-31. PubMed ID: 9205129
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  • 36. Characterisation of two deletions involving NPC1 and flanking genes in Niemann-Pick type C disease patients.
    Rodríguez-Pascau L, Toma C, Macías-Vidal J, Cozar M, Cormand B, Lykopoulou L, Coll MJ, Grinberg D, Vilageliu L.
    Mol Genet Metab; 2012 Dec 15; 107(4):716-20. PubMed ID: 23142039
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  • 37. NPC1: Complete genomic sequence, mutation analysis, and characterization of haplotypes.
    Bauer P, Knoblich R, Bauer C, Finckh U, Hufen A, Kropp J, Braun S, Kustermann-Kuhn B, Schmidt D, Harzer K, Rolfs A.
    Hum Mutat; 2002 Jan 15; 19(1):30-8. PubMed ID: 11754101
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  • 38. Structure and polymorphism of the mouse myelin/oligodendrocyte glycoprotein gene.
    Daubas P, Pham-Dinh D, Dautigny A.
    Genomics; 1994 Sep 01; 23(1):36-41. PubMed ID: 7829100
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  • 39. Niemann-Pick C1 disease gene: homology to mediators of cholesterol homeostasis.
    Carstea ED, Morris JA, Coleman KG, Loftus SK, Zhang D, Cummings C, Gu J, Rosenfeld MA, Pavan WJ, Krizman DB, Nagle J, Polymeropoulos MH, Sturley SL, Ioannou YA, Higgins ME, Comly M, Cooney A, Brown A, Kaneski CR, Blanchette-Mackie EJ, Dwyer NK, Neufeld EB, Chang TY, Liscum L, Strauss JF, Ohno K, Zeigler M, Carmi R, Sokol J, Markie D, O'Neill RR, van Diggelen OP, Elleder M, Patterson MC, Brady RO, Vanier MT, Pentchev PG, Tagle DA.
    Science; 1997 Jul 11; 277(5323):228-31. PubMed ID: 9211849
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  • 40. Niemann-Pick type C disease: mutations of NPC1 gene and evidence of abnormal expression of some mutant alleles in fibroblasts.
    Tarugi P, Ballarini G, Bembi B, Battisti C, Palmeri S, Panzani F, Di Leo E, Martini C, Federico A, Calandra S.
    J Lipid Res; 2002 Nov 11; 43(11):1908-19. PubMed ID: 12401890
    [Abstract] [Full Text] [Related]


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