Zobrazeno 1 - 10
of 54
pro vyhledávání: '"Masayo, Yamazaki"'
Publikováno v:
Clinical Pediatric Endocrinology
Congenital central hypothyroidism (C-CH) is defined as hypothyroidism due to a lack of stimulation of the normal thyroid gland (1, 2). C-CH is caused by anatomical or functional impairments in neurons that secrete hypothalamic-thyrotropin releasing h
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::61d99cdaa4a6b881fff4e8460708e341
http://europepmc.org/articles/PMC6646241
http://europepmc.org/articles/PMC6646241
Autor:
Masayo Yamazaki, Takanori Yamagata, Hiroko Shimbo, Makiko Tajika, Ayako Ueda, Takahiro Ikeda, Kei Murayama, Hitoshi Osaka
Publikováno v:
Human Genome Variation, Vol 5, Iss 1, Pp 1-4 (2018)
Human Genome Variation
Human Genome Variation
Approximately 80% of cases of mitochondrial myopathy, encephalopathy, lactic acidosis, and stroke-like episodes (MELAS) harbor a heteroplasmic m.3243A>G transition in the tRNALeu (UUR) (MTTL1) gene. We report a MELAS case with a rare heteroplasmic m.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f0b2bce3c5c5022d5a2931f76f69c64d
http://link.springer.com/article/10.1038/s41439-018-0026-6
http://link.springer.com/article/10.1038/s41439-018-0026-6
Autor:
Koji Yokoyama, Masayo Yamazaki, Mizuki Kobayashi, Takanori Yamagata, Makiko Oguma, Toshihiro Tajima, Shuntaro Morikawa, Takeshi Yamaguchi
Publikováno v:
Clinical Pediatric Endocrinology. 27:95-100
Genetic defects in the immunoglobulin superfamily member 1(IGSF1) protein are the cause of congenital central hypothyroidism (C-CH). Here we report two Japanese siblings with C-CH due to a novel IGSF1 mutation. The youngest brother showed a failure t
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::ea8fec49c5565b07e64161a38b6ebe80
https://doi.org/10.1297/cpe.27.95
https://doi.org/10.1297/cpe.27.95
Autor:
Masayo Yamazaki1, Hideo Sugie2, Makiko Oguma1,3, Tohru Yorifuji4, Toshihiro Tajima1, Takanori Yamagata1 r0845mh@jichi.ac.jp
Publikováno v:
Clinical Pediatric Endocrinology. 2017, Vol. 26 Issue 3, p165-169. 5p. 1 Diagram, 1 Graph.
Autor:
Makiko, Oguma, Mizuki, Kobayashi, Masayo, Yamazaki, Koji, Yokoyama, Shuntaro, Morikawa, Takeshi, Yamaguchi, Takanori, Yamagata, Toshihiro, Tajima
Publikováno v:
Clinical Pediatric Endocrinology
Genetic defects in the immunoglobulin superfamily member 1(IGSF1) protein are the cause of congenital central hypothyroidism (C-CH). Here we report two Japanese siblings with C-CH due to a novel IGSF1 mutation. The youngest brother showed a failure t
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::1b8a866a8e4323490ec3f048e6bf4593
https://pubmed.ncbi.nlm.nih.gov/29662269
https://pubmed.ncbi.nlm.nih.gov/29662269
Autor:
Tohru Yorifuji, Toshihiro Tajima, Makiko Oguma, Takanori Yamagata, Masayo Yamazaki, Hideo Sugie
Publikováno v:
Clinical Pediatric Endocrinology
Neonatal diabetes mellitus (NDM) is an insulin-requiring monogenic form of diabetes that generally presents before six months of age. The following two types of NDM are known: transient NDM (TNDM) and permanent NDM (PNDM). Here we report on an infant
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b15073a8e22d21f222f17de9732e1f14
https://pubmed.ncbi.nlm.nih.gov/28804207
https://pubmed.ncbi.nlm.nih.gov/28804207
Autor:
Jerome H. Hochman, Edward J. Carlini, Roy Eisenhandler, Bing Li, Qin Mei, Masayo Yamazaki, Brenda F. Leake, Steven W. Louie, Catherine Booth-Genthe, Thomas H. Rushmore, Richard B. Kim
Publikováno v:
Journal of Pharmacological and Toxicological Methods. 54:78-89
Introduction P-glycoprotein is localized in numerous tissues throughout the body and plays an important role in the disposition of many xenobiotics. The contribution of P-glycoprotein-mediated drug transport is being evaluated in early drug discovery
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b8d2c6a0561758da15dc277affbe69f1
https://doi.org/10.1016/j.vascn.2005.12.004
https://doi.org/10.1016/j.vascn.2005.12.004
Publikováno v:
Clinical Pediatric Endocrinology; Jul2019, Vol. 28 Issue 3, p69-79, 11p
Autor:
Masayo Yamazaki, Julie A. Stone, Punam Sandhu, Richard B. Kim, Brenda F. Leake, Paul G. Pearson, Xin Xu, Wooin Lee, Jiunn H. Lin
Publikováno v:
Drug Metabolism and Disposition. 33:676-682
Caspofungin (CANCIDAS, a registered trademark of Merck & Co., Inc.) is a novel echinocandin antifungal agent used in the treatment of esophageal and invasive candidiases, invasive aspergillosis, and neutropenia. Available data suggest that the liver
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7e6ceed928e75e1bed5ce9ab024822c3
https://doi.org/10.1124/dmd.104.003244
https://doi.org/10.1124/dmd.104.003244
Autor:
Masahiko Sato, Tomoyuki Ohe, Akio Kanatani, Naoko Fujino, Yoshihiro Shibata, Mikiko Hata, Sachiko Tanaka, Masayo Yamazaki, Masato Chiba, Yasuyuki Ishii, Takehiro Fukami
Publikováno v:
Drug Metabolism and Disposition. 31:1251-1254
The ratio of drug levels in cerebrospinal fluid (CSF) to plasma (CSF/plasma) at equilibrium has been viewed as in vivo free fraction (fp) in plasma [CSF/plasma = fp], if no active transport is involved in brain penetration. We determined the CSF/plas
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8e2da61e318c4c6a7a91e8926accf3dc
https://doi.org/10.1124/dmd.31.10.1251
https://doi.org/10.1124/dmd.31.10.1251