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Genomics|April 16, 1998

Human stanniocalcin (STC): genomic structure, chromosomal localization, and the presence of CAG trinucleotide repeatsA C Chang, K J Jeffrey, Y Tokutake, et al.

DNA Research : an International Journal for Rapid Publication of Reports on Genes and Genomes|July 29, 1998

Physical map of the human chromosome 8p12-p21 encompassing tumor suppressor and Werner's syndrome gene lociK Ichikawa, A Shimamoto, O Imamura, et al.

Gene|April 21, 1997

Cloning and characterization of a novel gene, WS-3, in human chromosome 8p11-p12K Ichikawa, Y Yamabe, O Imamura, et al.

Proceedings of the National Academy of Sciences of the United States of America|October 1, 1996

A unique human gene that spans over 230 kb in the human chromosome 8p11-12 and codes multiple family proteins sharing RNA-binding motifsA Shimamoto, S Kitao, K Ichikawa, et al.

Oncogene|October 14, 2000

Differential regulation of human RecQ family helicases in cell transformation and cell cycleT Kawabe, N Tsuyama, S Kitao, et al.

Human Genetics|July 1, 1997

Mutation and haplotype analyses of the Werner's syndrome gene based on its genomic structure: genetic epidemiology in the Japanese populationT Matsumoto, O Imamura, Y Yamabe, et al.

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Showing results (51-60 of 56) with videos related to

Sort By:

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You have reached the last page of results.This site can display upto 56 results.

Genomics|April 16, 1998

Human stanniocalcin (STC): genomic structure, chromosomal localization, and the presence of CAG trinucleotide repeatsA C Chang, K J Jeffrey, Y Tokutake, et al.

DNA Research : an International Journal for Rapid Publication of Reports on Genes and Genomes|July 29, 1998

Physical map of the human chromosome 8p12-p21 encompassing tumor suppressor and Werner's syndrome gene lociK Ichikawa, A Shimamoto, O Imamura, et al.

Gene|April 21, 1997

Cloning and characterization of a novel gene, WS-3, in human chromosome 8p11-p12K Ichikawa, Y Yamabe, O Imamura, et al.

Proceedings of the National Academy of Sciences of the United States of America|October 1, 1996

A unique human gene that spans over 230 kb in the human chromosome 8p11-12 and codes multiple family proteins sharing RNA-binding motifsA Shimamoto, S Kitao, K Ichikawa, et al.

Oncogene|October 14, 2000

Differential regulation of human RecQ family helicases in cell transformation and cell cycleT Kawabe, N Tsuyama, S Kitao, et al.

Human Genetics|July 1, 1997

Mutation and haplotype analyses of the Werner's syndrome gene based on its genomic structure: genetic epidemiology in the Japanese populationT Matsumoto, O Imamura, Y Yamabe, et al.

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