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Yoko Aoki

Showing results (111-120 of 255) with videos related to

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Microbiology and Immunology|December 15, 2010
Endemicity of human metapneumovirus subgenogroups A2 and B2 in Yamagata, Japan, between 2004 and 2009Katsumi Mizuta, Chieko Abiko, Yoko Aoki, et al.
Scientific Reports|April 30, 2025
Missense and truncated variants in ERF in individuals with a Noonan-like phenotype without craniosynostosisYusuke Goto, Tetsuya Niihori, Seiji Mizuno, et al.
Japanese Journal of Infectious Diseases|March 22, 2013
Seasonal patterns of respiratory syncytial virus, influenza A virus, human metapneumovirus, and parainfluenza virus type 3 infections on the basis of virus isolation data between 2004 and 2011 in Yamagata, JapanKatsumi Mizuta, Chieko Abiko, Yoko Aoki, et al.
Molecular Genetics and Metabolism|August 17, 2004
Mutation analysis of the MMAA and MMAB genes in Japanese patients with vitamin B(12)-responsive methylmalonic acidemia: identification of a prevalent MMAA mutationXue Yang, Osamu Sakamoto, Yoichi Matsubara, et al.
Nature Genetics|September 20, 2005
Germline mutations in HRAS proto-oncogene cause Costello syndromeYoko Aoki, Tetsuya Niihori, Hiroshi Kawame, et al.
Microbiology and Immunology|May 15, 2013
Molecular epidemiology of Coxsackievirus A16 strains isolated from children in Yamagata, Japan between 1988 and 2011Katsumi Mizuta, Chieko Abiko, Yoko Aoki, et al.
Microbiology and Immunology|September 6, 2012
Epidemiology of parainfluenza virus types 1, 2 and 3 infections based on virus isolation between 2002 and 2011 in Yamagata, JapanKatsumi Mizuta, Chieko Abiko, Yoko Aoki, et al.
American Journal of Medical Genetics. Part A|March 26, 2014
Identification of a novel missense mutation of MAF in a Japanese family with congenital cataract by whole exome sequencing: a clinical report and review of literatureYoko Narumi, Sachiko Nishina, Motoharu Tokimitsu, et al.
Journal of Human Genetics|November 18, 2003
Novel IRF6 mutations in Japanese patients with Van der Woude syndrome: two missense mutations (R45Q and P396S) and a 17-kb deletionShuji Kayano, Shigeo Kure, Yoichi Suzuki, et al.
Neurology. Genetics|November 6, 2024
Updated Genetic Analysis of Japanese Familial ALS Patients Carrying <i>SOD1</i> Variants Revealed Phenotypic Differences for Common VariantsAyumi Nishiyama, Tetsuya Niihori, Naoki Suzuki, et al.
Pageof 26

Showing results (111-120 of 255) with videos related to

Sort By:
Pageof 26
Microbiology and Immunology|December 15, 2010
Endemicity of human metapneumovirus subgenogroups A2 and B2 in Yamagata, Japan, between 2004 and 2009Katsumi Mizuta, Chieko Abiko, Yoko Aoki, et al.
Scientific Reports|April 30, 2025
Missense and truncated variants in ERF in individuals with a Noonan-like phenotype without craniosynostosisYusuke Goto, Tetsuya Niihori, Seiji Mizuno, et al.
Japanese Journal of Infectious Diseases|March 22, 2013
Seasonal patterns of respiratory syncytial virus, influenza A virus, human metapneumovirus, and parainfluenza virus type 3 infections on the basis of virus isolation data between 2004 and 2011 in Yamagata, JapanKatsumi Mizuta, Chieko Abiko, Yoko Aoki, et al.
Molecular Genetics and Metabolism|August 17, 2004
Mutation analysis of the MMAA and MMAB genes in Japanese patients with vitamin B(12)-responsive methylmalonic acidemia: identification of a prevalent MMAA mutationXue Yang, Osamu Sakamoto, Yoichi Matsubara, et al.
Nature Genetics|September 20, 2005
Germline mutations in HRAS proto-oncogene cause Costello syndromeYoko Aoki, Tetsuya Niihori, Hiroshi Kawame, et al.
Microbiology and Immunology|May 15, 2013
Molecular epidemiology of Coxsackievirus A16 strains isolated from children in Yamagata, Japan between 1988 and 2011Katsumi Mizuta, Chieko Abiko, Yoko Aoki, et al.
Microbiology and Immunology|September 6, 2012
Epidemiology of parainfluenza virus types 1, 2 and 3 infections based on virus isolation between 2002 and 2011 in Yamagata, JapanKatsumi Mizuta, Chieko Abiko, Yoko Aoki, et al.
American Journal of Medical Genetics. Part A|March 26, 2014
Identification of a novel missense mutation of MAF in a Japanese family with congenital cataract by whole exome sequencing: a clinical report and review of literatureYoko Narumi, Sachiko Nishina, Motoharu Tokimitsu, et al.
Journal of Human Genetics|November 18, 2003
Novel IRF6 mutations in Japanese patients with Van der Woude syndrome: two missense mutations (R45Q and P396S) and a 17-kb deletionShuji Kayano, Shigeo Kure, Yoichi Suzuki, et al.
Neurology. Genetics|November 6, 2024
Updated Genetic Analysis of Japanese Familial ALS Patients Carrying <i>SOD1</i> Variants Revealed Phenotypic Differences for Common VariantsAyumi Nishiyama, Tetsuya Niihori, Naoki Suzuki, et al.
Pageof 26