Zobrazeno 1 - 8
of 8
pro vyhledávání: '"Fumihisa Soga"'
Autor:
Yoshinaga Saeki, Yoshitaka Nagai, Fumihisa Soga, Takehiko Yanagihara, Satoshi Ueno, M. Hirano
Publikováno v:
Neurology. 46:791-795
We investigated the dopamine receptor (DAR) mRNA expression in peripheral blood lymphocytes from 45 patients with Parkinson's disease (PD) and 21 age-matched controls using the quantitative reverse transcription and polymerase chain reaction method.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b56bdaadd9353cc1e67cc0485d975e52
https://doi.org/10.1212/wnl.46.3.791
https://doi.org/10.1212/wnl.46.3.791
Autor:
Yoichi, Makari, Hirotsugu, Nagase, Shohei, Iijima, Masaaki, Miyo, Takuya, Sakamoto, Takashi, Doi, Minako, Hoshi, Yasuhiro, Miyake, Satoshi, Oshima, Kimimasa, Ikeda, Kazuya, Yamashita, Fumihisa, Soga, Eiji, Kurokawa, Nobuteru, Kikkawa
Publikováno v:
Gan to kagaku ryoho. Cancerchemotherapy. 39(12)
A 60-year-old man showed symptoms associated with pulmonary embolism and anemia in June 2011, and was subsequently diagnosed with stage IV gastric cancer. Following frequent multiple cerebral infarctions and the development of symptoms, the patient w
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::cfcf41608552f2bcd87ac50d3bb1a109
https://pubmed.ncbi.nlm.nih.gov/23268078
https://pubmed.ncbi.nlm.nih.gov/23268078
Publikováno v:
Biochemical and Biophysical Research Communications. 194:368-374
The sequential reverse transcription and polymerase chain reaction amplified the mRNA coding for the D3 dopamine receptor (D3R) in human peripheral blood lymphocytes. Pharmacological analysis confirmed the binding of the D3R specific ligand to the ly
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::922833f41c3074e9b1be469f40e5895b
https://doi.org/10.1006/bbrc.1993.1829
https://doi.org/10.1006/bbrc.1993.1829
Autor:
Shiro Yorifuji, H Imanishi, Hideki Yoshikawa, Misako Kaido, Koji Inui, Fumihisa Soga, Keiko Toyooka, T Higashi, Nishimura T, Harutoshi Fujimura, Takehiko Yanagihara
Publikováno v:
Acta neuropathologica. 92(3)
A 53-year-old Japanese woman with a point mutation in mitochondrial DNA (tRNALeu(UUR), nt3243) consistent with mitochondrial myopathy, encephalopathy, lactic acidosis and stroke-like episodes (MELAS) and Alzheimer-type brain pathology is reported. Th
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e3c994d7726a55e61397f6839a1732fe
https://pubmed.ncbi.nlm.nih.gov/8870835
https://pubmed.ncbi.nlm.nih.gov/8870835
Autor:
Tomoyuki Uemichi, Nobuyuki Takahashi, Fumihisa Soga, Seiichiro Tarui, Shiro Yorifuji, S. Ueno
Publikováno v:
Amyloid and Amyloidosis 1990 ISBN: 9789401054508
We identified three novel variants of transthyretin (TTR), TTR-Cys 114, TTR-Gly 42, and TTR-Arg 50, in three Japanese kindreds with familial amyloidotic polyneuropathy. Amyloid deposits reacted with anti-TTR serum. Amino acid mutations were deduced f
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::5bba4fd8bbac413c5892d23bf35c1c1c
https://doi.org/10.1007/978-94-011-3284-8_153
https://doi.org/10.1007/978-94-011-3284-8_153
Autor:
Nobuyuki Takahashi, Seiichiro Tarui, Fumihisa Soga, Tomoyuki Uemichi, Satoshi Ueno, Shiro Yorifuji
Publikováno v:
Biochemical and biophysical research communications. 169(3)
Two mutant genes coding for two different variants of transthyretin were identified in two independent kindreds with familial amyloidotic polyneuropathy. A single base change from A to G was identified in exon 2 of transthyretin gene in two brothers
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c8cb3adf8bd67a368a35c4120d5c820b
https://pubmed.ncbi.nlm.nih.gov/2363717
https://pubmed.ncbi.nlm.nih.gov/2363717
Publikováno v:
FEBS Letters. (1):35-37
DNA sequence polymorphisms in transthyretin (TrR) genes were investigated by single-strand conformation polymorphism (SSCP) analysis of polymerase chain reaction products. The amplified DNA fragments that encode each exon of the normal TTR gene showe
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::29438b8f2f0bf0363f78e6bf564c714c
Autor:
Saburo Ogasahara, Yusaku Nakamura, Norio Kono, Fumihisa Soga, Mitsuo Takahashi, Shigeo Hashimoto, Yoshiro Nishikawa, Shiro Yorifuji, Seiichiro Tarui
Publikováno v:
Neurology. 36(1)
We studied the metabolism of coenzyme Q10 (CoQ) and the effects of CoQ therapy in five patients with Kearns-Sayre syndrome (KSS). Although the mitochondrial fraction was increased in muscles from KSS patients, CoQ content was slightly low. CoQ synthe
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::76a75b2aee822bf1993894de680cf366
https://pubmed.ncbi.nlm.nih.gov/3941783
https://pubmed.ncbi.nlm.nih.gov/3941783