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Journal Abstract Search

65 related items for PubMed ID: 8914639

  • 1. A novel AvaI polymorphism within exon 5 of the rhodopsin gene.
    Isashiki Y, Feng XM, Ohba N, Ozawa T, Izumo S.
    Jpn J Hum Genet; 1996 Mar; 41(1):221-3. PubMed ID: 8914639
    [Abstract] [Full Text] [Related]

  • 2. A Bsr BI polymorphism in exon 1C of the human interleukin-1 receptor type I (IL-1RI) gene.
    Sitara D, Wood N, Morse H, Keen L, Bidwell J.
    Genes Immun; 2000 Feb; 1(3):234-5. PubMed ID: 11196719
    [Abstract] [Full Text] [Related]

  • 3. Partial genomic structure of the bovine PIT1 gene and characterization of a HinfI transition polymorphism in exon 6.
    Dierkes B, Kriegesmann B, Baumgartner BG, Brenig B.
    Anim Genet; 1998 Oct; 29(5):405. PubMed ID: 9800338
    [No Abstract] [Full Text] [Related]

  • 4. [Genetic analysis of rhodopsin and peripherin genes in patients with autosomal dominant retinitis pigmentosa (adRP) in Polish families].
    Brzeziańska E, Zdzieszyńska M, Goś R, Lewiński A.
    Klin Oczna; 2004 Oct; 106(6):743-8. PubMed ID: 15787173
    [Abstract] [Full Text] [Related]

  • 5. An AvaII PCR/RFLP in an exon of the canine gene for the beta subunit of the amiloride-sensitive sodium channel (SCNN1B).
    Zhou T, Nonneman D, Shibuya H, Khan S, Liu PC, Johnson GS.
    Anim Genet; 1998 Jun; 29(3):239. PubMed ID: 9720188
    [No Abstract] [Full Text] [Related]

  • 6. An AvaII polymorphism in exon 5 of the human hepatic triglyceride lipase gene.
    Mori A, Takagi A, Ikeda Y, Ashida Y, Yamamoto A.
    Mol Cell Probes; 1996 Aug; 10(4):309-11. PubMed ID: 8865179
    [No Abstract] [Full Text] [Related]

  • 7. A novel donor splice site mutation in the glycogen debranching enzyme gene is associated with glycogen storage disease type III.
    Okubo M, Aoyama Y, Murase T.
    Biochem Biophys Res Commun; 1996 Jul 16; 224(2):493-9. PubMed ID: 8702417
    [Abstract] [Full Text] [Related]

  • 8. Identification of a BstNI polymorphism in exon 9 of the human hepatic triglyceride lipase gene.
    Takagi A, Ikeda Y, Mori A, Ashida Y, Yamamoto A.
    Mol Cell Probes; 1996 Aug 16; 10(4):313-4. PubMed ID: 8865180
    [No Abstract] [Full Text] [Related]

  • 9. AccII polymorphism of the p53 gene.
    de la Calle-Martín O, Fabregat V, Romero M, Soler J, Vives J, Yagüe J.
    Nucleic Acids Res; 1990 Aug 25; 18(16):4963. PubMed ID: 1975679
    [No Abstract] [Full Text] [Related]

  • 10. A common polymorphism in exon 40 of the human mannose 6-phosphate/insulin-like growth factor II receptor gene.
    Zhong X, Hemmi H, Shimatake H.
    Mol Cell Probes; 1999 Oct 25; 13(5):397-400. PubMed ID: 10508563
    [Abstract] [Full Text] [Related]

  • 11. Analysis of the PvuII restriction fragment-length polymorphism and exon structure of the estrogen receptor gene in breast cancer and peripheral blood.
    Yaich L, Dupont WD, Cavener DR, Parl FF.
    Cancer Res; 1992 Jan 01; 52(1):77-83. PubMed ID: 1345763
    [Abstract] [Full Text] [Related]

  • 12. A new XmnI polymorphism in the regulatory region of the corticotropin releasing hormone gene.
    Baerwald CG, Panayi GS, Lanchbury JS.
    Hum Genet; 1996 May 01; 97(5):697-8. PubMed ID: 8655158
    [Abstract] [Full Text] [Related]

  • 13. Reverse restriction fragment length polymorphism (RRFLP): A novel technique for genotyping infectious laryngotracheitis virus (ILTV) live attenuated vaccines.
    Callison SA, Riblet SM, Rodríguez-Avila A, García M.
    J Virol Methods; 2009 Sep 01; 160(1-2):119-24. PubMed ID: 19433109
    [Abstract] [Full Text] [Related]

  • 14. A BsmAI PCR/RFLP in the bovine microtubule-associated protein-5 (MAP1B)gene.
    Nonneman D, Shibuya H, Johnson GS.
    Anim Genet; 1996 Aug 01; 27(4):288-9. PubMed ID: 8856934
    [No Abstract] [Full Text] [Related]

  • 15. A novel Sac I RFLP in the 3' untranslated region of the myotonin protein kinase gene.
    Nakamura A, Minami N, Kamitani T, Kamakura K, Arahata K, Takeda S.
    J Hum Genet; 1999 Aug 01; 44(2):135-7. PubMed ID: 10083743
    [Abstract] [Full Text] [Related]

  • 16. A Dde I RFLP in exon 21 of human EL1 gene, encoding protein 4.1, detectable by SSCP.
    Maillet P, Dalla Venezia N, Bozon M, Vallier A, Delaunay J, Baklouti F.
    Hum Mutat; 1998 Aug 01; 11(4):342-3. PubMed ID: 9554757
    [Abstract] [Full Text] [Related]

  • 17. A novel PCR-RFLP assay for the detection of the single nucleotide polymorphism at position +1440 in the human CXCR2 gene.
    Viana AC, Kim YJ, Cirelli JA, Orrico SR, Curtis KC, Cano VS, Valentini SR, Scarel-Caminaga RM.
    Biochem Genet; 2007 Oct 01; 45(9-10):737-41. PubMed ID: 17939034
    [Abstract] [Full Text] [Related]

  • 18. A common polymorphism in exon 16 of the human insulin-like growth factor-1 receptor gene (IGF1R).
    Abu-Amero S, Preece M, Wakeling E, Moore G, Stanier P.
    Mol Cell Probes; 1997 Oct 01; 11(5):381-3. PubMed ID: 9375298
    [No Abstract] [Full Text] [Related]

  • 19. Genotype establishments for protein C deficiency by use of a DNA polymorphism in the gene.
    Yamamoto K, Tanimoto M, Matsushita T, Kagami K, Sugiura I, Hamaguchi M, Takamatsu J, Saito H.
    Blood; 1991 Jun 15; 77(12):2633-6. PubMed ID: 1675129
    [Abstract] [Full Text] [Related]

  • 20. A MseI polymorphism in exon 48 of the dystrophin gene.
    Yau SC, Roberts RG, Bentley DR, Mathew CG, Bobrow M.
    Nucleic Acids Res; 1991 Oct 25; 19(20):5803. PubMed ID: 1682892
    [No Abstract] [Full Text] [Related]

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