Zobrazeno 1 - 10 of 188 pro vyhledávání: '"S, Miyabayashi"'
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Apple chlorotic leaf spot virus 50 kDa protein is targeted to plasmodesmata and accumulates in sieve elements in transgenic plant leaves
Autor: Nobuyuki Yoshikawa, S. Oogake, K. Ogawa, S. Miyabayashi, Tsuyoshi Takahashi, Y. Ikeda, M. Terada
Publikováno v: Archives of Virology. 144:2475-2483
We investigated the in situ localization of the 50 kDa protein encoded by ORF2 of Apple chlorotic leaf spot virus (ACLSV) genome which is thought to be a movement protein. In immunogold electron microscopy of ACLSV-infected Chenopodium quinoa leaves,
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::14bc55c28eaae6dab3b7f60c56edecf2
https://doi.org/10.1007/s007050050660
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3
Mitochondrial deoxyribonucleic acid 3256C-T mutation in a Japanese family with noninsulin-dependent diabetes mellitus
Autor: M, Hirai, S, Suzuki, M, Onoda, Y, Hinokio, A, Hirai, M, Ohtomo, M, Chiba, S, Kasuga, S, Hirai, Y, Satoh, H, Akai, S, Miyabayashi, T, Toyota
Publikováno v: The Journal of clinical endocrinology and metabolism. 83(3)
Accumulating reports indicate a relationship between mitochondrial DNA mutation and impaired glucose-induced insulin secretion leading to a subtype of noninsulin-dependent diabetes mellitus. DNA from a 45-yr-old Japanese woman with noninsulin-depende
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=pmid________::717c17e0f60516f598dc3f35e92891bc
https://pubmed.ncbi.nlm.nih.gov/9506761
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4
[Leigh syndrome: serial CT and MR imaging findings]
Autor: H, Ariga, S, Takahashi, S, Miyabayashi, A, Ohnuma, S, Higano, N, Kurihara, K, Sakamoto
Publikováno v: Nihon Igaku Hoshasen Gakkai zasshi. Nippon acta radiologica. 56(12)
Serial CT and MRI findings in five patients (two boys and three girls) with Leigh syndrome were retrospectively reviewed in a follow-up period lasting from six months to 10 years. The two boys were found to have cytochrome c oxidase deficiency and on
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=pmid________::cabfbb42ec6439d882c087f5bfa44ade
https://pubmed.ncbi.nlm.nih.gov/8940814
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7
[A study of myocardial disorders in an autopsy case of mitochondrial encephalomyopathy]
Autor: Y, Hiruta, M, Muto, T, Ichihara, K, Uruga, M, Mochizuki, E, Wachi, S, Miyabayashi, F, Mayumi, K, Adachi, H, Toshima
Publikováno v: Kokyu to junkan. Respirationcirculation. 41(3)
We report an autopsy case of a 19 year-old man with MELAS (mitochondrial myopathy, encephalopathy, lactic acidosis, and stroke-like episodes) a subgroup of mitochondrial encephalomyopathy presenting cardiomyopathy. He had repeatedly suffered from tra
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=pmid________::d083a01cea9ffc71ad17c5a494d1a385
https://pubmed.ncbi.nlm.nih.gov/8469836
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8
[Prenatal diagnosis of carbamyl phosphate synthetase deficiency by fetal liver biopsy]
Autor: J, Murotsuki, S, Uehara, K, Okamura, A, Yajima, M, Kikuchi, T, Oura, S, Miyabayashi
Publikováno v: Nihon Sanka Fujinka Gakkai zasshi. 43(12)
Carbamyl phosphate synthetase deficiency (CPSD) is one of the enzyme defects of the urea cycle and inherited as an autosomal recessive. A definitive enzymatic diagnosis of CPSD can be made by biochemical assay of liver biopsy material, but not of cul
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=pmid________::6f80056b689e1bd7ac24fc4045f85d76
https://pubmed.ncbi.nlm.nih.gov/1744457
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10
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Plný text Recenzováno Digitální knihovna AV ČR
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