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Issei Imoto

Showing results (131-140 of 241) with videos related to

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Psychiatry Research|November 5, 2016
Cumulative effect of the plasma total homocysteine-related genetic variants on schizophrenia riskMakoto Kinoshita, Shusuke Numata, Atsushi Tajima, et al.
Carcinogenesis|November 30, 2010
YAP is a candidate oncogene for esophageal squamous cell carcinomaTomoki Muramatsu, Issei Imoto, Takeshi Matsui, et al.
Plos One|November 7, 2015
Simultaneous Detection of Both Single Nucleotide Variations and Copy Number Alterations by Next-Generation Sequencing in Gorlin SyndromeKei-ichi Morita, Takuya Naruto, Kousuke Tanimoto, et al.
Human Genome Variation|April 16, 2016
A novel COL11A1 missense mutation in siblings with non-ocular Stickler syndromeTomohiro Kohmoto, Atsumi Tsuji, Kei-Ichi Morita, et al.
Human Genome Variation|November 22, 2016
Exome-first approach identified a novel gloss deletion associated with Lowe syndromeMiki Watanabe, Ryuji Nakagawa, Tomohiro Kohmoto, et al.
Oncogene|October 7, 2004
Involvement of overexpressed wild-type BRAF in the growth of malignant melanoma cell linesHideaki Tanami, Issei Imoto, Akira Hirasawa, et al.
Carcinogenesis|December 24, 2010
Copy number alterations in urothelial carcinomas: their clinicopathological significance and correlation with DNA methylation alterationsNaotaka Nishiyama, Eri Arai, Ryo Nagashio, et al.
Journal of Human Genetics|January 20, 2012
Deletion at chromosome 10p11.23-p12.1 defines characteristic phenotypes with marked midface retrusionNana Okamoto, Shin Hayashi, Ayako Masui, et al.
Human Genome Variation|April 22, 2017
Detection of 1p36 deletion by clinical exome-first diagnostic approachMiki Watanabe, Yasunobu Hayabuchi, Akemi Ono, et al.
Annals of Surgical Oncology|July 5, 2014
Hypomethylation of long interspersed nuclear element-1 (LINE-1) is associated with poor prognosis via activation of c-MET in hepatocellular carcinomaChengzhan Zhu, Tohru Utsunomiya, Tetsuya Ikemoto, et al.
Pageof 25

Showing results (131-140 of 241) with videos related to

Sort By:
Pageof 25
Psychiatry Research|November 5, 2016
Cumulative effect of the plasma total homocysteine-related genetic variants on schizophrenia riskMakoto Kinoshita, Shusuke Numata, Atsushi Tajima, et al.
Carcinogenesis|November 30, 2010
YAP is a candidate oncogene for esophageal squamous cell carcinomaTomoki Muramatsu, Issei Imoto, Takeshi Matsui, et al.
Plos One|November 7, 2015
Simultaneous Detection of Both Single Nucleotide Variations and Copy Number Alterations by Next-Generation Sequencing in Gorlin SyndromeKei-ichi Morita, Takuya Naruto, Kousuke Tanimoto, et al.
Human Genome Variation|April 16, 2016
A novel COL11A1 missense mutation in siblings with non-ocular Stickler syndromeTomohiro Kohmoto, Atsumi Tsuji, Kei-Ichi Morita, et al.
Human Genome Variation|November 22, 2016
Exome-first approach identified a novel gloss deletion associated with Lowe syndromeMiki Watanabe, Ryuji Nakagawa, Tomohiro Kohmoto, et al.
Oncogene|October 7, 2004
Involvement of overexpressed wild-type BRAF in the growth of malignant melanoma cell linesHideaki Tanami, Issei Imoto, Akira Hirasawa, et al.
Carcinogenesis|December 24, 2010
Copy number alterations in urothelial carcinomas: their clinicopathological significance and correlation with DNA methylation alterationsNaotaka Nishiyama, Eri Arai, Ryo Nagashio, et al.
Journal of Human Genetics|January 20, 2012
Deletion at chromosome 10p11.23-p12.1 defines characteristic phenotypes with marked midface retrusionNana Okamoto, Shin Hayashi, Ayako Masui, et al.
Human Genome Variation|April 22, 2017
Detection of 1p36 deletion by clinical exome-first diagnostic approachMiki Watanabe, Yasunobu Hayabuchi, Akemi Ono, et al.
Annals of Surgical Oncology|July 5, 2014
Hypomethylation of long interspersed nuclear element-1 (LINE-1) is associated with poor prognosis via activation of c-MET in hepatocellular carcinomaChengzhan Zhu, Tohru Utsunomiya, Tetsuya Ikemoto, et al.
Pageof 25