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Nihon Rinsho. Japanese Journal of Clinical Medicine|July 26, 2002
[Genetics and genomics of long QT syndrome]Hiroyasu IwasaJournal of Human Genetics|August 9, 2002
Twenty single-nucleotide polymorphisms in four genes encoding cardiac ion channelsHiroyasu Iwasa, Masahiko Kurabayashi, Ryozo Nagai, et al.American Journal of Human Genetics|May 16, 2007
Homozygosity haplotype allows a genomewide search for the autosomal segments shared among patientsHitoshi Miyazawa, Masaaki Kato, Takuya Awata, et al.Neurology. Genetics|December 17, 2025
Identification of Intronic Variants in NDUFA3 as a Cause of Leigh Syndrome by Whole Genome Sequencing and RNA SequencingKohta Nakamura, Yoshihito Kishita, Ayumu Sugiura, et al.Brain & Development|December 4, 2014
Myocerebrohepatopathy spectrum disorder due to POLG mutations: A clinicopathological reportHesham Montassir, Yoshihiro Maegaki, Kei Murayama, et al.Pediatrics International : Official Journal of the Japan Pediatric Society|November 26, 2013
Molecular diagnosis of mitochondrial respiratory chain disorders in Japan: focusing on mitochondrial DNA depletion syndromeTaro Yamazaki, Kei Murayama, Alison G Compton, et al.Cancer Chemotherapy and Pharmacology|May 26, 2009
Association of UGT2B7 and ABCB1 genotypes with morphine-induced adverse drug reactions in Japanese patients with cancerKen-ichi Fujita, Yuichi Ando, Wataru Yamamoto, et al.Molecular Genetics and Metabolism|June 13, 2009
Fluctuating liver functions in siblings with MPV17 mutations and possible improvement associated with dietary and pharmaceutical treatments targeting respiratory chain complex IIShunsaku Kaji, Kei Murayama, Ikuo Nagata, et al.Plos Genetics|March 6, 2013
Tysnd1 deficiency in mice interferes with the peroxisomal localization of PTS2 enzymes, causing lipid metabolic abnormalities and male infertilityYumi Mizuno, Yuichi Ninomiya, Yutaka Nakachi, et al.Pageof 1