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Issei Imoto

Showing results (71-80 of 241) with videos related to

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Hepatology (Baltimore, Md.)|May 25, 2002
TFDP1, CUL4A, and CDC16 identified as targets for amplification at 13q34 in hepatocellular carcinomasKohichiroh Yasui, Shigeki Arii, Chen Zhao, et al.
American Journal of Physiology. Gastrointestinal and Liver Physiology|January 24, 2002
Stimulatory effects of bilirubin on amylase release from isolated rat pancreatic aciniYoshihide Hirohata, Masatoshi Fujii, Yoshinori Okabayashi, et al.
Human Genome Variation|February 2, 2017
Genome-first approach diagnosed Cabezas syndrome via novel <i>CUL4B</i> mutation detectionNobuhiko Okamoto, Miki Watanabe, Takuya Naruto, et al.
Brain & Development|July 30, 2019
A 16q22.2-q23.1 deletion identified in a male infant with West syndromeTatsuo Mori, Aya Goji, Yoshihiro Toda, et al.
Human Psychopharmacology|May 27, 2015
No association between the COMT Val158Met polymorphism and the long-term clinical response in obsessive-compulsive disorder in the Japanese populationHidehiro Umehara, Shusuke Numata, Atsushi Tajima, et al.
American Journal of Medical Genetics. Part A|July 17, 2008
The CASK gene harbored in a deletion detected by array-CGH as a potential candidate for a gene causative of X-linked dominant mental retardationShin Hayashi, Seiji Mizuno, Ohsuke Migita, et al.
The American Journal of Pathology|June 25, 2004
Overexpression of PDZK1 within the 1q12-q22 amplicon is likely to be associated with drug-resistance phenotype in multiple myelomaJun Inoue, Takemi Otsuki, Akira Hirasawa, et al.
Journal of Human Genetics|May 2, 2009
Molecular cloning of t(2;7)(p24.3;p14.2), a novel chromosomal translocation in myelodysplastic syndrome-derived acute myeloid leukemiaKazuhiro Fujita, Masashi Sanada, Hiroshi Harada, et al.
Human Genetics|July 8, 2011
Novel intragenic duplications and mutations of CASK in patients with mental retardation and microcephaly with pontine and cerebellar hypoplasia (MICPCH)Shin Hayashi, Nobuhiko Okamoto, Yasutsugu Chinen, et al.
Biochemical and Biophysical Research Communications|March 21, 2020
The C-terminal region including the MH6 domain of Msx1 regulates skeletal developmentAki Ichihara, Akihiro Yasue, Silvia Naomi Mitsui, et al.
Pageof 25

Showing results (71-80 of 241) with videos related to

Sort By:
Pageof 25
Hepatology (Baltimore, Md.)|May 25, 2002
TFDP1, CUL4A, and CDC16 identified as targets for amplification at 13q34 in hepatocellular carcinomasKohichiroh Yasui, Shigeki Arii, Chen Zhao, et al.
American Journal of Physiology. Gastrointestinal and Liver Physiology|January 24, 2002
Stimulatory effects of bilirubin on amylase release from isolated rat pancreatic aciniYoshihide Hirohata, Masatoshi Fujii, Yoshinori Okabayashi, et al.
Human Genome Variation|February 2, 2017
Genome-first approach diagnosed Cabezas syndrome via novel <i>CUL4B</i> mutation detectionNobuhiko Okamoto, Miki Watanabe, Takuya Naruto, et al.
Brain & Development|July 30, 2019
A 16q22.2-q23.1 deletion identified in a male infant with West syndromeTatsuo Mori, Aya Goji, Yoshihiro Toda, et al.
Human Psychopharmacology|May 27, 2015
No association between the COMT Val158Met polymorphism and the long-term clinical response in obsessive-compulsive disorder in the Japanese populationHidehiro Umehara, Shusuke Numata, Atsushi Tajima, et al.
American Journal of Medical Genetics. Part A|July 17, 2008
The CASK gene harbored in a deletion detected by array-CGH as a potential candidate for a gene causative of X-linked dominant mental retardationShin Hayashi, Seiji Mizuno, Ohsuke Migita, et al.
The American Journal of Pathology|June 25, 2004
Overexpression of PDZK1 within the 1q12-q22 amplicon is likely to be associated with drug-resistance phenotype in multiple myelomaJun Inoue, Takemi Otsuki, Akira Hirasawa, et al.
Journal of Human Genetics|May 2, 2009
Molecular cloning of t(2;7)(p24.3;p14.2), a novel chromosomal translocation in myelodysplastic syndrome-derived acute myeloid leukemiaKazuhiro Fujita, Masashi Sanada, Hiroshi Harada, et al.
Human Genetics|July 8, 2011
Novel intragenic duplications and mutations of CASK in patients with mental retardation and microcephaly with pontine and cerebellar hypoplasia (MICPCH)Shin Hayashi, Nobuhiko Okamoto, Yasutsugu Chinen, et al.
Biochemical and Biophysical Research Communications|March 21, 2020
The C-terminal region including the MH6 domain of Msx1 regulates skeletal developmentAki Ichihara, Akihiro Yasue, Silvia Naomi Mitsui, et al.
Pageof 25