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Yoko Aoki

Showing results (141-150 of 255) with videos related to

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Human Molecular Genetics|October 17, 2015
Adult mice expressing a Braf Q241R mutation on an ICR/CD-1 background exhibit a cardio-facio-cutaneous syndrome phenotypeMitsuji Moriya, Shin-Ichi Inoue, Sachiko Miyagawa-Tomita, et al.
Human Molecular Genetics|July 19, 2014
New BRAF knockin mice provide a pathogenetic mechanism of developmental defects and a therapeutic approach in cardio-facio-cutaneous syndromeShin-Ichi Inoue, Mitsuji Moriya, Yusuke Watanabe, et al.
Japanese Journal of Infectious Diseases|May 27, 2008
Analysis of monthly isolation of respiratory viruses from children by cell culture using a microplate method: a two-year study from 2004 to 2005 in yamagata, JapanKatsumi Mizuta, Chieko Abiko, Yoko Aoki, et al.
Clinical Pediatric Endocrinology : Case Reports and Clinical Investigations : Official Journal of the Japanese Society for Pediatric Endocrinology|April 4, 2024
Genetic backgrounds and genotype-phenotype relationships in anthropometric parameters of 116 Japanese individuals with Noonan syndromeYasuko Shoji, Ayaha Hata, Takatoshi Maeyama, et al.
Orphanet Journal of Rare Diseases|September 13, 2019
Detection of NRAS mutation in cell-free DNA biological fluids from patients with kaposiform lymphangiomatosisMichio Ozeki, Yoko Aoki, Akifumi Nozawa, et al.
Plos One|March 19, 2014
TBX1 mutation identified by exome sequencing in a Japanese family with 22q11.2 deletion syndrome-like craniofacial features and hypocalcemiaTsutomu Ogata, Tetsuya Niihori, Noriko Tanaka, et al.
Medicina Clinica|September 8, 2014
[Cardiofaciocutaneous syndrome, a Noonan syndrome related disorder: clinical and molecular findings in 11 patients]Atilano Carcavilla, Sixto García-Miñaúr, Antonio Pérez-Aytés, et al.
Human Molecular Genetics|April 18, 2003
Transgenic expression of a dominant-negative connexin26 causes degeneration of the organ of Corti and non-syndromic deafnessTakayuki Kudo, Shigeo Kure, Katsuhisa Ikeda, et al.
Annals of Neurology|October 29, 2002
Heterozygous GLDC and GCSH gene mutations in transient neonatal hyperglycinemiaShigeo Kure, Kanako Kojima, Akiko Ichinohe, et al.
Journal of Human Genetics|September 28, 2022
Comprehensive targeted next-generation sequencing in patients with slow-flow vascular malformationsAkifumi Nozawa, Akihiro Fujino, Shunsuke Yuzuriha, et al.
Pageof 26

Showing results (141-150 of 255) with videos related to

Sort By:
Pageof 26
Human Molecular Genetics|October 17, 2015
Adult mice expressing a Braf Q241R mutation on an ICR/CD-1 background exhibit a cardio-facio-cutaneous syndrome phenotypeMitsuji Moriya, Shin-Ichi Inoue, Sachiko Miyagawa-Tomita, et al.
Human Molecular Genetics|July 19, 2014
New BRAF knockin mice provide a pathogenetic mechanism of developmental defects and a therapeutic approach in cardio-facio-cutaneous syndromeShin-Ichi Inoue, Mitsuji Moriya, Yusuke Watanabe, et al.
Japanese Journal of Infectious Diseases|May 27, 2008
Analysis of monthly isolation of respiratory viruses from children by cell culture using a microplate method: a two-year study from 2004 to 2005 in yamagata, JapanKatsumi Mizuta, Chieko Abiko, Yoko Aoki, et al.
Clinical Pediatric Endocrinology : Case Reports and Clinical Investigations : Official Journal of the Japanese Society for Pediatric Endocrinology|April 4, 2024
Genetic backgrounds and genotype-phenotype relationships in anthropometric parameters of 116 Japanese individuals with Noonan syndromeYasuko Shoji, Ayaha Hata, Takatoshi Maeyama, et al.
Orphanet Journal of Rare Diseases|September 13, 2019
Detection of NRAS mutation in cell-free DNA biological fluids from patients with kaposiform lymphangiomatosisMichio Ozeki, Yoko Aoki, Akifumi Nozawa, et al.
Plos One|March 19, 2014
TBX1 mutation identified by exome sequencing in a Japanese family with 22q11.2 deletion syndrome-like craniofacial features and hypocalcemiaTsutomu Ogata, Tetsuya Niihori, Noriko Tanaka, et al.
Medicina Clinica|September 8, 2014
[Cardiofaciocutaneous syndrome, a Noonan syndrome related disorder: clinical and molecular findings in 11 patients]Atilano Carcavilla, Sixto García-Miñaúr, Antonio Pérez-Aytés, et al.
Human Molecular Genetics|April 18, 2003
Transgenic expression of a dominant-negative connexin26 causes degeneration of the organ of Corti and non-syndromic deafnessTakayuki Kudo, Shigeo Kure, Katsuhisa Ikeda, et al.
Annals of Neurology|October 29, 2002
Heterozygous GLDC and GCSH gene mutations in transient neonatal hyperglycinemiaShigeo Kure, Kanako Kojima, Akiko Ichinohe, et al.
Journal of Human Genetics|September 28, 2022
Comprehensive targeted next-generation sequencing in patients with slow-flow vascular malformationsAkifumi Nozawa, Akihiro Fujino, Shunsuke Yuzuriha, et al.
Pageof 26