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Publikováno v:
Journal of Molecular Endocrinology. 48:1-9
DHCR24encodes 3β-hydroxysteroid-Δ24 reductase, catalyzing the conversion of desmosterol to cholesterol. Our previous study demonstrated that DHCR24 exerts an anti-apoptotic function as a reactive oxygen species (ROS) scavenger, for which it needs i
Publikováno v:
Journal of Bone and Mineral Metabolism. 30:144-153
Desmosterolosis is an autosomal recessive disease caused by mutations in the 3β-hydroxysterol-Delta24 reductase (DHCR24) gene, with severe developmental anomalies including short limbs. We utilized DHCR24 knockout (KO) mice to study the underlying b
Autor:
Refetoff, Samuel, Murata, Yoshiharu
Publikováno v:
Endocrine Journal; 2016, Vol. 63 Issue 11, p941-941, 1p
Publikováno v:
Biochemical Journal. 424:201-209
We have reported previously a non-genomic action of T3 (3,3',5-tri-iodothyronine), which stimulates the PI3K (phosphoinositide 3-kinase)/Akt pathway via p85alpha, the regulatory subunit of PI3K, in human skin fibroblasts. The aim of the present study
Publikováno v:
Molecular Endocrinology. 22:893-903
AMP-activated protein kinase (AMPK) is a key regulator of glucose and fatty acid homeostasis. In muscle cells, AMPK stimulates mitochondrial fatty acid oxidation and ATP production. The thyroid hormone T3 increases cellular oxygen consumption and is
Autor:
Hisao Seo, K. Maki, Takahide Kaji, Rusella Mirza, Yoshiharu Murata, Shizu Hayasaka, Fukushi Kambe
Publikováno v:
British Journal of Dermatology. 158:679-684
Summary Background The DHCR24 (3β-hydroxysterol-Δ24 reductase) gene encodes an enzyme catalysing conversion of desmosterol to cholesterol. Desmosterolosis is an autosomal recessive disease due to mutation in the DHCR24 gene, with low cholesterol an
Publikováno v:
Endocrinology. 149:3267-3273
3beta-Hydroxysteroid-Delta24 reductase (DHCR24) is an endoplasmic reticulum-resident, multifunctional enzyme that possesses antiapoptotic and cholesterol-synthesizing activities. To clarify the molecular basis of the former activity, we investigated
Autor:
Yoshiharu Murata, Masamichi Ogawa, John A. Phillips, Yoshitaka Hayashi, Hisao Seo, Takashi Kamijo, Michiyo Yamamoto
Publikováno v:
Growth Hormone & IGF Research. 17:249-253
Objective To characterize the cause of a sporadic isolated growth hormone deficiency in a single patient. Methods Genomic DNA was extracted from blood samples of the patient and his family. Exons and exon–intron junctions of the GH-1 gene were ampl
Autor:
Yutaka Ishihara, Takami Inoue, Naohito Yamamoto, Yutaka Tomoda, Nobuo Matsui, Fumitaka Kikkawa, Tetsuya Mizutani, Hisao Seo, Osamu Narita, Nobuhiko Suganuma, Hisanori Oguri
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::113976b960a309b153e507bb19337cb6
https://doi.org/10.1159/000416258
https://doi.org/10.1159/000416258