المؤلفون: Shun Watanabe, Takaaki Abe, Hisato Shima, Masaaki Toyomizu, Shigeo Kure, Satoru Nagatoishi, Teruyuki Yanagisawa, Shin Ichiro Kanno, Yuki Ohba, Daisuke Saigusa, Joseph V. Bonventre, Sadayoshi Ito, Motoi Kikusato, Kazuto Nakada, Eikan Mishima, Hitoshi Osaka, Hiroaki Yamaguchi, Miyuki Yokoro, Yoshihisa Tomioka, Ken Ichi Hayashi, Takaharu Ichimura, Nobuyoshi Mori, Yasutoshi Akiyama, Akihiro Matsuo, Nariyasu Mano, Kohei Tsumoto, Hiroko Shinbo, Masahiro Kohzuki, Tetsuro Matsuhashi, Kazutaka Murayama, Yoichi Takeuchi, Akinori Yuri, Chitose Suzuki, Osamu Hashizume, Koichi Kikuchi, Jun Ichi Anzai, Daichi Minaki, Takehiro Suzuki, Tai Kudo, Takeya Sato, Takafumi Toyohara

المصدر: Journal of the American Society of Nephrology : JASN. 27(7)

مصطلحات موضوعية: 0301 basic medicine, Male, Mitochondrial DNA, Mitochondrial disease, Myocytes, Smooth Muscle, Oxidative phosphorylation, Mitochondrion, Pharmacology, Kidney, medicine.disease_cause, Phenylbutyrate, Rats, Sprague-Dawley, 03 medical and health sciences, Mice, Up Front Matters, medicine, Animals, Myocytes, Cardiac, chemistry.chemical_classification, Reactive oxygen species, ATP synthase, biology, Indoleacetic Acids, Chemistry, General Medicine, Acute Kidney Injury, medicine.disease, Phenylbutyrates, Mitochondria, Mice, Inbred C57BL, 030104 developmental biology, Kidney Tubules, Nephrology, Reperfusion Injury, biology.protein, Brief Communications, Oxidative stress, Power Plants

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::45fe914f54798368fe8d88d5d61aa957
https://pubmed.ncbi.nlm.nih.gov/26744487

المؤلفون: Hitoshi Osaka, Mizue Iai, Atsushi Takagi, Kenji Kurosawa, Hiroko Shinbo, Kiyoko Sameshima, Sumimasa Yamashita, Megumi Tsuji, Noritaka Furuya

المصدر: Braindevelopment. 33(6)

مصطلحات موضوعية: medicine.medical_specialty, Methylenetetrahydrofolate reductase deficiency, Molecular Sequence Data, Mutation, Missense, Reductase, Asymptomatic, chemistry.chemical_compound, Exon, Polyneuropathies, Developmental Neuroscience, Asian People, Internal medicine, medicine, Missense mutation, Animals, Humans, Amino Acid Sequence, Methylenetetrahydrofolate Reductase (NADPH2), Tetrahydrofolates, Genetics, Methionine, biology, business.industry, Brain, Infant, General Medicine, Microcephalus, biology.organism_classification, medicine.disease, Magnetic Resonance Imaging, digestive system diseases, Endocrinology, chemistry, Psychotic Disorders, Muscle Spasticity, Methylenetetrahydrofolate reductase, Pediatrics, Perinatology and Child Health, biology.protein, Homocystinuria, Neurology (clinical), medicine.symptom, business, Sequence Alignment

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b8d781fed9cb10ae2f4e492b8248cda6
https://pubmed.ncbi.nlm.nih.gov/20850942