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Yoichi Matsubara

Showing results (51-60 of 165) with videos related to

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Ebiomedicine|December 20, 2017
Mice with an Oncogenic HRAS Mutation are Resistant to High-Fat Diet-Induced Obesity and Exhibit Impaired Hepatic Energy HomeostasisDaiju Oba, Shin-Ichi Inoue, Sachiko Miyagawa-Tomita, et al.
The European Journal of Neuroscience|May 7, 2004
Glycine cleavage system in neurogenic regionsAkiko Ichinohe, Shigeo Kure, Sumiko Mikawa, et al.
JMA Journal|November 23, 2020
Research and Development Strategy for Future Embryonic Stem Cell-Based Therapy in JapanAkihiro Umezawa, Yoji Sato, Shinji Kusakawa, et al.
The Journal of Dermatology|March 16, 2017
Somatic HRAS p.G12S mosaic mutation causes unilaterally distributed epidermal nevi, woolly hair and palmoplantar keratosisAki Honda, Noriko Umegaki-Arao, Takashi Sasaki, et al.
American Journal of Medical Genetics. Part A|January 5, 2011
Implications of prenatal diagnosis of the fetus with both interstitial deletion and a small marker ring originating from chromosome 5Hiroyasu Ohashi, Kaoru Suzumori, Yasushi Chisaka, et al.
Breast Cancer (Tokyo, Japan)|January 14, 2004
Collaboration of breast cancer clinic and genetic counseling division for BRCA1 and BRCA2 mutation family in JapanMotohiro Takeda, Takanori Ishida, Kohji Ohnuki, et al.
Drug Metabolism and Pharmacokinetics|May 25, 2011
Novel single nucleotide polymorphism of the CYP2A13 gene in Japanese individualsYuichiro Tamaki, Masashi Honda, Yuka Muroi, et al.
Ebiomedicine|March 23, 2019
New Noonan syndrome model mice with RIT1 mutation exhibit cardiac hypertrophy and susceptibility to β-adrenergic stimulation-induced cardiac fibrosisShingo Takahara, Shin-Ichi Inoue, Sachiko Miyagawa-Tomita, et al.
Journal of Human Genetics|February 10, 2023
Biallelic CC2D2A variants, SNV and LINE-1 insertion simultaneously identified in siblings using long-read whole-genome sequencing and haplotype phasingKumiko Yanagi, Jonathan Coker, Kaori Miyana, et al.
American Journal of Medical Genetics. Part A|September 13, 2011
Implantable cardioverter defibrillator for progressive hypertrophic cardiomyopathy in a patient with LEOPARD syndrome and a novel PTPN11 mutation Gln510HisYasushi Wakabayashi, Kyohei Yamazaki, Yoko Narumi, et al.
Pageof 17

Showing results (51-60 of 165) with videos related to

Sort By:
Pageof 17
Ebiomedicine|December 20, 2017
Mice with an Oncogenic HRAS Mutation are Resistant to High-Fat Diet-Induced Obesity and Exhibit Impaired Hepatic Energy HomeostasisDaiju Oba, Shin-Ichi Inoue, Sachiko Miyagawa-Tomita, et al.
The European Journal of Neuroscience|May 7, 2004
Glycine cleavage system in neurogenic regionsAkiko Ichinohe, Shigeo Kure, Sumiko Mikawa, et al.
JMA Journal|November 23, 2020
Research and Development Strategy for Future Embryonic Stem Cell-Based Therapy in JapanAkihiro Umezawa, Yoji Sato, Shinji Kusakawa, et al.
The Journal of Dermatology|March 16, 2017
Somatic HRAS p.G12S mosaic mutation causes unilaterally distributed epidermal nevi, woolly hair and palmoplantar keratosisAki Honda, Noriko Umegaki-Arao, Takashi Sasaki, et al.
American Journal of Medical Genetics. Part A|January 5, 2011
Implications of prenatal diagnosis of the fetus with both interstitial deletion and a small marker ring originating from chromosome 5Hiroyasu Ohashi, Kaoru Suzumori, Yasushi Chisaka, et al.
Breast Cancer (Tokyo, Japan)|January 14, 2004
Collaboration of breast cancer clinic and genetic counseling division for BRCA1 and BRCA2 mutation family in JapanMotohiro Takeda, Takanori Ishida, Kohji Ohnuki, et al.
Drug Metabolism and Pharmacokinetics|May 25, 2011
Novel single nucleotide polymorphism of the CYP2A13 gene in Japanese individualsYuichiro Tamaki, Masashi Honda, Yuka Muroi, et al.
Ebiomedicine|March 23, 2019
New Noonan syndrome model mice with RIT1 mutation exhibit cardiac hypertrophy and susceptibility to β-adrenergic stimulation-induced cardiac fibrosisShingo Takahara, Shin-Ichi Inoue, Sachiko Miyagawa-Tomita, et al.
Journal of Human Genetics|February 10, 2023
Biallelic CC2D2A variants, SNV and LINE-1 insertion simultaneously identified in siblings using long-read whole-genome sequencing and haplotype phasingKumiko Yanagi, Jonathan Coker, Kaori Miyana, et al.
American Journal of Medical Genetics. Part A|September 13, 2011
Implantable cardioverter defibrillator for progressive hypertrophic cardiomyopathy in a patient with LEOPARD syndrome and a novel PTPN11 mutation Gln510HisYasushi Wakabayashi, Kyohei Yamazaki, Yoko Narumi, et al.
Pageof 17