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Journal Abstract Search

77 related items for PubMed ID: 9554757

  • 1. 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; 11(4):342-3. PubMed ID: 9554757
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  • 2. The DNA-binding capacity of genetic variants of the bovine STAT5A transcription factor.
    Flisikowski K, Szymanowska M, Zwierzchowski L.
    Cell Mol Biol Lett; 2003; 8(3):831-40. PubMed ID: 12949622
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  • 9. 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
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  • 10. 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
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  • 11. Optimization of the MhcOvar-DRB1 gene typing.
    Arrieta-Aguirre I, García-Etxebarria K, Jugo BM.
    Tissue Antigens; 2006 Mar; 67(3):222-8. PubMed ID: 16573559
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  • 12. [Analysis, identification and correction of some errors of model refseqs appeared in NCBI Human Gene Database by in silico cloning and experimental verification of novel human genes].
    Zhang DL, Ji L, Li YD.
    Yi Chuan Xue Bao; 2004 May; 31(5):431-43. PubMed ID: 15478601
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  • 13. Genetic variation in the kappa-casein gene (CSN3) of Chinese yak (Bos grunniens) and phylogenetic analysis of CSN3 sequences in the genus Bos.
    Prinzenberg EM, Jianlin H, Erhardt G.
    J Dairy Sci; 2008 Mar; 91(3):1198-203. PubMed ID: 18292276
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  • 14. 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 Mar; 46(2):96-8. PubMed ID: 11281420
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  • 15. Rapid assignment of the swine major histocompatibility complex (SLA) class I and II genotypes in Clawn miniature swine using PCR-SSP and PCR-RFLP methods.
    Ando A, Ota M, Sada M, Katsuyama Y, Goto R, Shigenari A, Kawata H, Anzai T, Iwanaga T, Miyoshi Y, Fujimura N, Inoko H.
    Xenotransplantation; 2005 Mar; 12(2):121-6. PubMed ID: 15693842
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  • 16. 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; 42(4):489-98. PubMed ID: 9560948
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  • 17. The human Nramp2 gene: characterization of the gene structure, alternative splicing, promoter region and polymorphisms.
    Lee PL, Gelbart T, West C, Halloran C, Beutler E.
    Blood Cells Mol Dis; 1998 Jun; 24(2):199-215. PubMed ID: 9642100
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  • 18. Sequence and exon-intron organization of the DNA encoding the alpha I domain of human spectrin. Application to the study of mutations causing hereditary elliptocytosis.
    Sahr KE, Tobe T, Scarpa A, Laughinghouse K, Marchesi SL, Agre P, Linnenbach AJ, Marchesi VT, Forget BG.
    J Clin Invest; 1989 Oct; 84(4):1243-52. PubMed ID: 2794061
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  • 19. Detection of heterozygous mutations in the RB1 gene in retinoblastoma patients using single-strand conformation polymorphism analysis and polymerase chain reaction sequencing.
    Hogg A, Onadim Z, Baird PN, Cowell JK.
    Oncogene; 1992 Jul; 7(7):1445-51. PubMed ID: 1352398
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  • 20. Organization of the murine Cd22 locus. Mapping to chromosome 7 and characterization of two alleles.
    Law CL, Torres RM, Sundberg HA, Parkhouse RM, Brannan CI, Copeland NG, Jenkins NA, Clark EA.
    J Immunol; 1993 Jul 01; 151(1):175-87. PubMed ID: 8100843
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