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Journal of Biochemistry|April 1, 1991
Effects of individual mutations in the P-450(C21) pseudogene on the P-450(C21) activity and their distribution in the patient genomes of congenital steroid 21-hydroxylase deficiencyY Higashi, T Hiromasa, A Tanae, et al.American Journal of Human Genetics|August 1, 1994
Linkage disequilibrium and haplotype studies of chromosome 8p 11.1-21.1 markers and Werner syndromeC E Yu, J Oshima, K A Goddard, et al.American Journal of Human Genetics|June 1, 1996
Toward localization of the Werner syndrome gene by linkage disequilibrium and ancestral haplotyping: lessons learned from analysis of 35 chromosome 8p11.1-21.1 markersK A Goddard, C E Yu, J Oshima, et al.Genomics|April 1, 1997
A high-density STS map based on a single contig of YAC and P1 clones in the chromosome 8p12-p21 regionN Mitsuda, J Nakura, L Ye, et al.Plant Molecular Biology|September 25, 1998
Identification of preferred binding sites of a light-inducible DNA-binding factor (MNF1) within 5'-upstream sequence of C4-type phosphoenolpyruvate carboxylase gene in maizeA MorishimaAmerican Journal of Medical Genetics|February 11, 1997
Association of a polymorphic variant of the Werner helicase gene with myocardial infarction in a Japanese populationL Ye, T Miki, J Nakura, et al.Genomics|October 1, 1994
Homozygosity mapping of the Werner syndrome locus (WRN)J Nakura, E M Wijsman, T Miki, et al.American Journal of Human Genetics|February 1, 1997
Mutations in the consensus helicase domains of the Werner syndrome gene. Werner's Syndrome Collaborative GroupC E Yu, J Oshima, E M Wijsman, et al.Journal of Cardiology. Supplement|January 1, 1988
[Mitral valve prolapse in patients with myocarditis and collagen diseases]T Miki, Y Yokota, T Miki, et al.Microbiology and Immunology|January 1, 1981
Electrochemical modification of vesicular stomatitis virus glycoprotein by host cell transformationT MikiPageof 94