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170 related items for PubMed ID: 9420147

  • 1. The fifth allele of the human deoxyribonuclease I (DNase I) polymorphism.
    Iida R, Yasuda T, Aoyama M, Tsubota E, Kobayashi M, Yuasa I, Matsuki T, Kishi K.
    Electrophoresis; 1997 Oct; 18(11):1936-9. PubMed ID: 9420147
    [Abstract] [Full Text] [Related]

  • 2. A new allele, DNASE1*6, of human deoxyribonuclease I polymorphism encodes an Arg to Cys substitution responsible for its instability.
    Yasuda T, Takeshita H, Iida R, Kogure S, Kishi K.
    Biochem Biophys Res Commun; 1999 Jun 24; 260(1):280-3. PubMed ID: 10381379
    [Abstract] [Full Text] [Related]

  • 3. Genotyping of human deoxyribonuclease I polymorphism by the polymerase chain reaction.
    Yasuda T, Nadano D, Tenjo E, Takeshita H, Sawazaki K, Nakanaga M, Kishi K.
    Electrophoresis; 1995 Oct 24; 16(10):1889-93. PubMed ID: 8586059
    [Abstract] [Full Text] [Related]

  • 4. Overestimated frequency of a possible emphysema-susceptibility allele when microsomal epoxide hydrolase is genotyped by the conventional polymerase chain reaction-based method.
    Keicho N, Emi M, Kajita M, Matsushita I, Nakata K, Azuma A, Ohishi N, Kudoh S.
    J Hum Genet; 2001 Oct 24; 46(2):96-8. PubMed ID: 11281420
    [Abstract] [Full Text] [Related]

  • 5. Identification of the nucleotide substitution that generates the fourth polymorphic site in human deoxyribonuclease I (DNase I).
    Iida R, Yasuda T, Takeshita H, Tsubota E, Yuasa I, Nakajima T, Kishi K.
    Hum Genet; 1996 Oct 24; 98(4):415-8. PubMed ID: 8792814
    [Abstract] [Full Text] [Related]

  • 6. PCR-based genotyping of MNSs blood group: subtyping of M allele to MG and MT.
    Akane A, Kobayashi T, Li ZX, Yoshimura S, Okii Y, Yoshida M, Tokiyasu T, Watabiki T.
    Jpn J Hum Genet; 1997 Dec 24; 42(4):489-98. PubMed ID: 9560948
    [Abstract] [Full Text] [Related]

  • 7. The DNA-binding capacity of genetic variants of the bovine STAT5A transcription factor.
    Flisikowski K, Szymanowska M, Zwierzchowski L.
    Cell Mol Biol Lett; 2003 Dec 24; 8(3):831-40. PubMed ID: 12949622
    [Abstract] [Full Text] [Related]

  • 8. Detection of known and new mutations in the thiopurine S-methyltransferase gene by single-strand conformation polymorphism analysis.
    Spire-Vayron de la Moureyre C, Debuysère H, Sabbagh N, Marez D, Vinner E, Chevalier ED, Lo Guidice JM, Broly F.
    Hum Mutat; 1998 Dec 24; 12(3):177-85. PubMed ID: 9711875
    [Abstract] [Full Text] [Related]

  • 9. Structure of the human deoxyribonuclease I (DNase I) gene: identification of the nucleotide substitution that generates its classical genetic polymorphism.
    Yasuda T, Kishi K, Yanagawa Y, Yoshida A.
    Ann Hum Genet; 1995 Jan 24; 59(1):1-15. PubMed ID: 7762978
    [Abstract] [Full Text] [Related]

  • 10. Detection of catechol-O-methyltransferase Val158Met polymorphism by a simple one-step tetra-primer amplification refractory mutation system-PCR.
    Ruiz-Sanz JI, Aurrekoetxea I, Ruiz del Agua A, Ruiz-Larrea MB.
    Mol Cell Probes; 2007 Jun 24; 21(3):202-7. PubMed ID: 17337160
    [Abstract] [Full Text] [Related]

  • 11. [Analysis on FUT1 and FUT2 gene of 10 para-Bombay individuals in China].
    Guo ZH, Xiang D, Zhu ZY, Wang JL, Zhang JM, Liu X, Shen W, Chen HP.
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2004 Oct 24; 21(5):417-21. PubMed ID: 15476160
    [Abstract] [Full Text] [Related]

  • 12. Molecular analysis of the third allele of human deoxyribonuclease I polymorphism.
    Yasuda T, Nadano D, Takeshita H, Tenjo E, Kishi K.
    Ann Hum Genet; 1995 Apr 24; 59(2):139-47. PubMed ID: 7625762
    [Abstract] [Full Text] [Related]

  • 13. First-trimester prenatal molecular diagnosis of infantile hypophosphatasia in a Japanese family.
    Orimo H, Nakajima E, Hayashi Z, Kijima K, Watanabe A, Tenjin H, Araki T, Shimada T.
    Prenat Diagn; 1996 Jun 24; 16(6):559-63. PubMed ID: 8809899
    [Abstract] [Full Text] [Related]

  • 14. A convenient method for genotyping of human O6-methylguanine-DNA methyltransferase polymorphism.
    Abe M, Inoue R, Suzuki T.
    Jpn J Hum Genet; 1997 Sep 24; 42(3):425-8. PubMed ID: 12503189
    [Abstract] [Full Text] [Related]

  • 15. The molecular basis for genetic polymorphism of human deoxyribonuclease I: identification of the nucleotide substitution that generates the fourth allele.
    Yasuda T, Nadano D, Takeshita H, Tenjo E, Sawazaki K, Ootani M, Kishi K.
    FEBS Lett; 1995 Feb 13; 359(2-3):211-4. PubMed ID: 7867802
    [Abstract] [Full Text] [Related]

  • 16. Mutation analysis of Taiwanese Wilson disease patients.
    Wan L, Tsai CH, Tsai Y, Hsu CM, Lee CC, Tsai FJ.
    Biochem Biophys Res Commun; 2006 Jun 30; 345(2):734-8. PubMed ID: 16696937
    [Abstract] [Full Text] [Related]

  • 17. A novel catalase mutation detected by polymerase chain reaction-single strand conformation polymorphism, nucleotide sequencing, and western blot analyses is responsible for the type C of Hungarian acatalasemia.
    Góth L, Rass P, Madarasi I.
    Electrophoresis; 2001 Jan 30; 22(1):49-51. PubMed ID: 11197178
    [Abstract] [Full Text] [Related]

  • 18. Polymorphism of human complement component C6: an amino acid substitution (Glu/Ala) within the second thrombospondin repeat differentiates between the two common allotypes C6 A and C6 B.
    Dewald G, Nöthen MM, Cichon S.
    Biochem Biophys Res Commun; 1993 Jul 15; 194(1):458-64. PubMed ID: 8101442
    [Abstract] [Full Text] [Related]

  • 19. Herpes simplex virus genotyping: multiple optional PCR-based RFLP systems and a non-isotopic single-strand conformation polymorphism method.
    Abba MC, Golijow CD.
    J Virol Methods; 2004 Jun 01; 118(1):73-6. PubMed ID: 15158071
    [Abstract] [Full Text] [Related]

  • 20. A restriction fragment length polymorphism results in a nonconservative amino acid substitution encoded within the first exon of the human lysyl oxidase gene.
    Csiszar K, Mariani TJ, Gosin JS, Deak SB, Boyd CD.
    Genomics; 1993 May 01; 16(2):401-6. PubMed ID: 8100215
    [Abstract] [Full Text] [Related]

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