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Naoya Hosono

Showing results (11-20 of 52) with videos related to

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Journal of Human Genetics|March 30, 2012
Genetic differences in the two main groups of the Japanese population based on autosomal SNPs and haplotypesYumi Yamaguchi-Kabata, Tatsuhiko Tsunoda, Natsuhiko Kumasaka, et al.
Cancer Science|February 26, 2008
Impact of CYP2D6*10 on recurrence-free survival in breast cancer patients receiving adjuvant tamoxifen therapyKazuma Kiyotani, Taisei Mushiroda, Mitsunori Sasa, et al.
Forensic Science International. Genetics|April 22, 2014
Development of a SNP set for human identification: A set with high powers of discrimination which yields high genetic information from naturally degraded DNA samples in the Thai populationHathaichanoke Boonyarit, Surakameth Mahasirimongkol, Nuttama Chavalvechakul, et al.
Legal Medicine (Tokyo, Japan)|March 13, 2009
Automated SNPs typing system based on the Invader assayHiroaki Nakahara, Naoya Hosono, Tetsushi Kitayama, et al.
Breast Cancer Research and Treatment|September 28, 2011
Dose-adjustment study of tamoxifen based on CYP2D6 genotypes in Japanese breast cancer patientsKazuma Kiyotani, Taisei Mushiroda, Chiyo K Imamura, et al.
Journal of Human Genetics|January 14, 2011
Impact of LIMK1, MMP2 and TNF-α variations for intracranial aneurysm in Japanese populationSiew-Kee Low, Hitoshi Zembutsu, Atsushi Takahashi, et al.
Pharmacogenetics and Genomics|August 4, 2010
Development of new HLA-B*3505 genotyping method using Invader assayNaoya Hosono, Soranun Chantarangsu, Kazuma Kiyotani, et al.
Nature Genetics|August 17, 2010
A genome-wide association study identifies four susceptibility loci for keloid in the Japanese populationMitsuko Nakashima, Suyoun Chung, Atsushi Takahashi, et al.
Human Molecular Genetics|August 19, 2010
A functional variant in NKX3.1 associated with prostate cancer susceptibility down-regulates NKX3.1 expressionShusuke Akamatsu, Ryo Takata, Kyota Ashikawa, et al.
Neurobiology of Aging|March 10, 2012
Novel deletion mutations of OPTN in amyotrophic lateral sclerosis in JapaneseAritoshi Iida, Naoya Hosono, Motoki Sano, et al.
Pageof 6

Showing results (11-20 of 52) with videos related to

Sort By:
Pageof 6
Journal of Human Genetics|March 30, 2012
Genetic differences in the two main groups of the Japanese population based on autosomal SNPs and haplotypesYumi Yamaguchi-Kabata, Tatsuhiko Tsunoda, Natsuhiko Kumasaka, et al.
Cancer Science|February 26, 2008
Impact of CYP2D6*10 on recurrence-free survival in breast cancer patients receiving adjuvant tamoxifen therapyKazuma Kiyotani, Taisei Mushiroda, Mitsunori Sasa, et al.
Forensic Science International. Genetics|April 22, 2014
Development of a SNP set for human identification: A set with high powers of discrimination which yields high genetic information from naturally degraded DNA samples in the Thai populationHathaichanoke Boonyarit, Surakameth Mahasirimongkol, Nuttama Chavalvechakul, et al.
Legal Medicine (Tokyo, Japan)|March 13, 2009
Automated SNPs typing system based on the Invader assayHiroaki Nakahara, Naoya Hosono, Tetsushi Kitayama, et al.
Breast Cancer Research and Treatment|September 28, 2011
Dose-adjustment study of tamoxifen based on CYP2D6 genotypes in Japanese breast cancer patientsKazuma Kiyotani, Taisei Mushiroda, Chiyo K Imamura, et al.
Journal of Human Genetics|January 14, 2011
Impact of LIMK1, MMP2 and TNF-α variations for intracranial aneurysm in Japanese populationSiew-Kee Low, Hitoshi Zembutsu, Atsushi Takahashi, et al.
Pharmacogenetics and Genomics|August 4, 2010
Development of new HLA-B*3505 genotyping method using Invader assayNaoya Hosono, Soranun Chantarangsu, Kazuma Kiyotani, et al.
Nature Genetics|August 17, 2010
A genome-wide association study identifies four susceptibility loci for keloid in the Japanese populationMitsuko Nakashima, Suyoun Chung, Atsushi Takahashi, et al.
Human Molecular Genetics|August 19, 2010
A functional variant in NKX3.1 associated with prostate cancer susceptibility down-regulates NKX3.1 expressionShusuke Akamatsu, Ryo Takata, Kyota Ashikawa, et al.
Neurobiology of Aging|March 10, 2012
Novel deletion mutations of OPTN in amyotrophic lateral sclerosis in JapaneseAritoshi Iida, Naoya Hosono, Motoki Sano, et al.
Pageof 6