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Yoichi Matsubara

Showing results (61-70 of 165) with videos related to

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Journal of Biochemical and Biophysical Methods|March 21, 2006
Competitive allele-specific short oligonucleotide hybridization (CASSOH) with enzyme-linked immunosorbent assay (ELISA) for the detection of pharmacogenetic single nucleotide polymorphisms (SNPs)Masahiro Hiratsuka, Aiko Ebisawa, Kanako Sakuyama, et al.
Pediatric Diabetes|May 25, 2019
KLF11 variant in a family clinically diagnosed with early childhood-onset type 1B diabetesKikumi Ushijima, Satoshi Narumi, Tsutomu Ogata, et al.
Hepatology Research : the Official Journal of the Japan Society of Hepatology|May 25, 2013
Sequential analysis of amino acid substitutions with hepatitis B virus in association with nucleoside/nucleotide analog treatment detected by deep sequencingMasashi Ninomiya, Yasuteru Kondo, Tetsuya Niihori, et al.
Drug Metabolism and Disposition: the Biological Fate of Chemicals|July 13, 2011
Functional characterization of CYP2B6 allelic variants in demethylation of antimalarial artemetherMasashi Honda, Yuka Muroi, Yuichiro Tamaki, et al.
Journal of Human Genetics|September 12, 2025
Functional analysis of novel and recurrent RINT1 variants in patients with infantile liver dysfunctionTaiga Aoki, Ayano Inui, Yoshiyasu Ogata, et al.
Endocrine Journal|February 22, 2019
Dihydrotestosterone induces minor transcriptional alterations in genital skin fibroblasts of children with and without androgen insensitivityKanako Tanase-Nakao, Kentaro Mizuno, Yutaro Hayashi, et al.
Journal of Human Genetics|June 20, 2024
A novel homozygous variant of the PIGK gene caused by paternal disomy in a patient with neurodevelopmental disorder, cerebellar atrophy, and seizuresKenichiro Sadamitsu, Kumiko Yanagi, Yuiko Hasegawa, et al.
BMC Medical Genomics|May 30, 2019
Transient multifocal genomic crisis creating chromothriptic and non-chromothriptic rearrangements in prezygotic testicular germ cellsAtsushi Hattori, Kohji Okamura, Yumiko Terada, 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.
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.
Pageof 17

Showing results (61-70 of 165) with videos related to

Sort By:
Pageof 17
Journal of Biochemical and Biophysical Methods|March 21, 2006
Competitive allele-specific short oligonucleotide hybridization (CASSOH) with enzyme-linked immunosorbent assay (ELISA) for the detection of pharmacogenetic single nucleotide polymorphisms (SNPs)Masahiro Hiratsuka, Aiko Ebisawa, Kanako Sakuyama, et al.
Pediatric Diabetes|May 25, 2019
KLF11 variant in a family clinically diagnosed with early childhood-onset type 1B diabetesKikumi Ushijima, Satoshi Narumi, Tsutomu Ogata, et al.
Hepatology Research : the Official Journal of the Japan Society of Hepatology|May 25, 2013
Sequential analysis of amino acid substitutions with hepatitis B virus in association with nucleoside/nucleotide analog treatment detected by deep sequencingMasashi Ninomiya, Yasuteru Kondo, Tetsuya Niihori, et al.
Drug Metabolism and Disposition: the Biological Fate of Chemicals|July 13, 2011
Functional characterization of CYP2B6 allelic variants in demethylation of antimalarial artemetherMasashi Honda, Yuka Muroi, Yuichiro Tamaki, et al.
Journal of Human Genetics|September 12, 2025
Functional analysis of novel and recurrent RINT1 variants in patients with infantile liver dysfunctionTaiga Aoki, Ayano Inui, Yoshiyasu Ogata, et al.
Endocrine Journal|February 22, 2019
Dihydrotestosterone induces minor transcriptional alterations in genital skin fibroblasts of children with and without androgen insensitivityKanako Tanase-Nakao, Kentaro Mizuno, Yutaro Hayashi, et al.
Journal of Human Genetics|June 20, 2024
A novel homozygous variant of the PIGK gene caused by paternal disomy in a patient with neurodevelopmental disorder, cerebellar atrophy, and seizuresKenichiro Sadamitsu, Kumiko Yanagi, Yuiko Hasegawa, et al.
BMC Medical Genomics|May 30, 2019
Transient multifocal genomic crisis creating chromothriptic and non-chromothriptic rearrangements in prezygotic testicular germ cellsAtsushi Hattori, Kohji Okamura, Yumiko Terada, 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.
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.
Pageof 17