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J Nakura

Showing results (51-60 of 59) with videos related to

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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.
Human Genetics|May 1, 1994
Evidence against DNA polymerase beta as a candidate gene for Werner syndromeM Chang, G C Burmer, J Sweasy, et al.
American 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.
Science (New York, N.Y.)|April 12, 1996
Positional cloning of the Werner's syndrome geneC E Yu, J Oshima, Y H Fu, et al.
Genomics|August 15, 1996
Narrowing the position of the Werner syndrome locus by homozygosity analysis-extension of homozygosity analysisJ Nakura, T Miki, L Ye, et al.
Human Molecular Genetics|December 1, 1996
Homozygous and compound heterozygous mutations at the Werner syndrome locusJ Oshima, C E Yu, C Piussan, et al.
Pageof 6

Showing results (51-60 of 59) with videos related to

Sort By:
Pageof 6
You have reached the last page of results.This site can display upto 59 results.
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.
Human Genetics|May 1, 1994
Evidence against DNA polymerase beta as a candidate gene for Werner syndromeM Chang, G C Burmer, J Sweasy, et al.
American 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.
Science (New York, N.Y.)|April 12, 1996
Positional cloning of the Werner's syndrome geneC E Yu, J Oshima, Y H Fu, et al.
Genomics|August 15, 1996
Narrowing the position of the Werner syndrome locus by homozygosity analysis-extension of homozygosity analysisJ Nakura, T Miki, L Ye, et al.
Human Molecular Genetics|December 1, 1996
Homozygous and compound heterozygous mutations at the Werner syndrome locusJ Oshima, C E Yu, C Piussan, et al.
Pageof 6