Zobrazeno 1 - 10
of 14
pro vyhledávání: '"Sumiko Nissato"'
Autor:
Takehito Sugasawa, Naoki Mukai, Kyoko Tamura, Taiko Tamba, Shintaro Mori, Yuki Miyashiro, Mami Yamaguchi, Norihiko Moriyama, Sumiko Nissato, Song G. Ra, Yasuko Yoshida, Yasushi Kawakami, Kazuhiro Takekoshi
Publikováno v:
Gazzetta Medica Italiana Archivio per le Scienze Mediche. 176
Autor:
M. Hoshino, Takehito Sugasawa, M. Yamaguchi, T. Tamba, Hajime Ohmori, Sumiko Nissato, Yasushi Kawakami, S. Mori, Kazuhiro Takekoshi, Sg. Ra, K. Tamura, N. Mukai, Yasuko Yoshida, Y. Miyashiro
Publikováno v:
International journal of sports medicine. 37(10)
We aimed to clarify the effects of cold stimulation at various temperatures on mitochondrial activity and vascular endothelial growth factor (VEGF) expression in vitro. Human fibroblast, human mesenchymal stem cell, and rat skeletal muscle myoblast c
Autor:
Yasushi Kawakami, Kazumasa Isobe, Hitomi Kodama, Takahiro Okamoto, Kazuhiro Takekoshi, Sumiko Nissato, Masatoshi Iihara
Publikováno v:
Endocrine Journal. 57:351-356
Recently, mutations in nuclear genes encoding two mitochondrial complex II subunit proteins, Succinate dehydrogenase D (SDHD) and SDHB, have been found to be associated with the development of familial pheochromocytomas and paragangliomas (hereditary
Autor:
Kazuhiro Takekoshi, Hitoshi Shimano, Ling Fu, Sumiko Nissato, Kazumi Suzukawa, Hideto Takahashi, Toru Yashiro, Yasushi Kawakami, Ichirou Tatsuno, Kazumasa Isobe, Hisato Hara
Publikováno v:
Journal of Atherosclerosis and Thrombosis. 16:442-447
Aim: Recent studies have demonstrated that serum adiponectin and its receptors in adipose and muscle tissues are suppressed in diabetic or obese individuals. Patients with pheochromocytoma are frequently diabetic.Methods: Using real-time PCR, we exam
Autor:
Shigeru Minowada, Kazumasa Isobe, Toru Yashiro, Hisato Hara, Ichiro Tatsuno, Yasushi Kawakami, Sumiko Nissato, Kazuhiro Takekoshi, Toru Nanmoku, Kazumi Suzukawa
Publikováno v:
Hormone Research in Paediatrics. 68:68-71
The SDHA, SDHB, SDHC, and SDHD genes code for subunits of succinate dehydrogenase (SDH), which forms part of the mitochondrial respiratory chain. Germline mutations in the genes encoding SDHB and SDHD have been reported in familial paragangliomas/phe
Publikováno v:
Journal of the Neurological Sciences. 195:129-138
Little information is available on molecular defects involved in adult Sandhoff disease presenting as motor neuron disease phenotype. We studied enzyme activities of beta-hexosaminidase (Hex) and the HEXB gene encoding the beta-subunit of Hex in a fa
Autor:
Hiroaki Suzuki, Nobuhiro Yamada, Yasushi Kawakami, Kazuhiro Takekoshi, Kazumasa Isobe, Sumiko Nissato, Koichi Kawai
Publikováno v:
Endocrine journal. 55(2)
Recently, nuclear genes encoding two mitochondrial complex II subunit proteins, SDHD and SDHB, have been found to be associated with the development of familial pheochromocytomas and paragangliomas (hereditary pheochromocytoma/paraganglioma syndrome:
Autor:
Ichiro Tatsuno, Toru Yashiro, Kazuhiro Takekoshi, Sumiko Nissato, Yasushi Kawakami, Kazumasa Isobe
Publikováno v:
Annals of the New York Academy of Sciences. 1073
Mutations in the genes encoding succinate dehydrogenase (SDH) have been associated with susceptibility to pheochromocytoma. However, few reports have examined the level of SDH mRNAs expression. In this study, we examined the level of expression of mR
Autor:
Kazumasa, Isobe, Shigeru, Minowada, Ichiro, Tatsuno, Kazumi, Suzukawa, Sumiko, Nissato, Toru, Nanmoku, Hisato, Hara, Toru, Yashiro, Yasushi, Kawakami, Kazuhiro, Takekoshi
Publikováno v:
Hormone research. 68(2)
The SDHA, SDHB, SDHC, and SDHD genes code for subunits of succinate dehydrogenase (SDH), which forms part of the mitochondrial respiratory chain. Germline mutations in the genes encoding SDHB and SDHD have been reported in familial paragangliomas/phe
Autor:
Kazumasa Isobe, Hajime Ohmori, Michiko Fukuhara, Sumiko Nissato, Zeng Quin, Kazuhiro Takekoshi, Yasushi Kawakami
Publikováno v:
Metabolism: clinical and experimental. 55(8)
Adenosine monophosphate-activated protein kinase (AMPK) is activated in response to adenosine triphosphate depletion caused by the metabolic and nutritional state. Mammalian AMPK is a heterotrimeric enzyme composed of a catalytic alpha subunit and 2