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Yoichi Matsubara

Showing results (121-130 of 165) with videos related to

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Japanese Journal of Ophthalmology|August 19, 2024
Mutations of CYP1B1 and FOXC1 genes for childhood glaucoma in Japanese individualsNobuo Fuse, Masae Kimura, Ai Shimizu, et al.
Journal of Hypertension|November 15, 2008
Seasonal trends of blood pressure during pregnancy in Japan: the babies and their parents' longitudinal observation in Suzuki Memorial Hospital in Intrauterine Period studyHirohito Metoki, Takayoshi Ohkubo, Yumiko Watanabe, et al.
Pediatric Blood & Cancer|January 23, 2018
Somatic MECOM mosaicism in a patient with congenital bone marrow failure without a radial abnormalityTomoo Osumi, Shin-Ichi Tsujimoto, Kazuhiko Nakabayashi, et al.
American Journal of Human Genetics|November 20, 2015
Mutations in MECOM, Encoding Oncoprotein EVI1, Cause Radioulnar Synostosis with Amegakaryocytic ThrombocytopeniaTetsuya Niihori, Meri Ouchi-Uchiyama, Yoji Sasahara, et al.
Clinical and Experimental Hypertension (New York, N.Y. : 1993)|May 15, 2012
Daily serial hemodynamic data during pregnancy and seasonal variation: the BOSHI studyHirohito Metoki, Takayoshi Ohkubo, Taku Obara, et al.
Molecular Genetics & Genomic Medicine|January 8, 2016
Testicular dysgenesis/regression without campomelic dysplasia in patients carrying missense mutations and upstream deletion of SOX9Yuko Katoh-Fukui, Maki Igarashi, Keisuke Nagasaki, et al.
Cancer Science|March 16, 2017
Exome sequencing deciphers a germline MET mutation in familial epidermal growth factor receptor-mutant lung cancerNaoki Tode, Toshiaki Kikuchi, Tomohiro Sakakibara, et al.
Journal of Human Genetics|November 5, 2010
A genome-wide association study identifies RNF213 as the first Moyamoya disease geneFumiaki Kamada, Yoko Aoki, Ayumi Narisawa, et al.
Molecular Genetics and Metabolism|April 3, 2004
Genetic testing of glycogen storage disease type Ib in Japan: five novel G6PT1 mutations and a rapid detection method for a prevalent mutation W118RKanako Kojima, Shigeo Kure, Fumiaki Kamada, et al.
Journal of Human Genetics|April 19, 2005
Functional analysis of PTPN11/SHP-2 mutants identified in Noonan syndrome and childhood leukemiaTetsuya Niihori, Yoko Aoki, Hirofumi Ohashi, et al.
Pageof 17

Showing results (121-130 of 165) with videos related to

Sort By:
Pageof 17
Japanese Journal of Ophthalmology|August 19, 2024
Mutations of CYP1B1 and FOXC1 genes for childhood glaucoma in Japanese individualsNobuo Fuse, Masae Kimura, Ai Shimizu, et al.
Journal of Hypertension|November 15, 2008
Seasonal trends of blood pressure during pregnancy in Japan: the babies and their parents' longitudinal observation in Suzuki Memorial Hospital in Intrauterine Period studyHirohito Metoki, Takayoshi Ohkubo, Yumiko Watanabe, et al.
Pediatric Blood & Cancer|January 23, 2018
Somatic MECOM mosaicism in a patient with congenital bone marrow failure without a radial abnormalityTomoo Osumi, Shin-Ichi Tsujimoto, Kazuhiko Nakabayashi, et al.
American Journal of Human Genetics|November 20, 2015
Mutations in MECOM, Encoding Oncoprotein EVI1, Cause Radioulnar Synostosis with Amegakaryocytic ThrombocytopeniaTetsuya Niihori, Meri Ouchi-Uchiyama, Yoji Sasahara, et al.
Clinical and Experimental Hypertension (New York, N.Y. : 1993)|May 15, 2012
Daily serial hemodynamic data during pregnancy and seasonal variation: the BOSHI studyHirohito Metoki, Takayoshi Ohkubo, Taku Obara, et al.
Molecular Genetics & Genomic Medicine|January 8, 2016
Testicular dysgenesis/regression without campomelic dysplasia in patients carrying missense mutations and upstream deletion of SOX9Yuko Katoh-Fukui, Maki Igarashi, Keisuke Nagasaki, et al.
Cancer Science|March 16, 2017
Exome sequencing deciphers a germline MET mutation in familial epidermal growth factor receptor-mutant lung cancerNaoki Tode, Toshiaki Kikuchi, Tomohiro Sakakibara, et al.
Journal of Human Genetics|November 5, 2010
A genome-wide association study identifies RNF213 as the first Moyamoya disease geneFumiaki Kamada, Yoko Aoki, Ayumi Narisawa, et al.
Molecular Genetics and Metabolism|April 3, 2004
Genetic testing of glycogen storage disease type Ib in Japan: five novel G6PT1 mutations and a rapid detection method for a prevalent mutation W118RKanako Kojima, Shigeo Kure, Fumiaki Kamada, et al.
Journal of Human Genetics|April 19, 2005
Functional analysis of PTPN11/SHP-2 mutants identified in Noonan syndrome and childhood leukemiaTetsuya Niihori, Yoko Aoki, Hirofumi Ohashi, et al.
Pageof 17