Výsledky vyhledávání - "Oyama, Chikako"

ACID SPHINGOMYELINASE IS ESSENTIAL FOR CHOLESTEROLREDUCING AGENTS TO POSITIVELY AFFECT ACCUMULATED FREE CHOLESTEROL IN NIEMANN-PICK DISEASE TYPE C FIBROBLASTS

Autor: HIRAYAMA, Masashi, NOGUCHI, Atsuko, OYAMA, Chikako, HIRAI, Daishi, TAKAHASHI, Tsutomu

Publikováno v: 秋田医学. 42(3/4):137-146

Niemann-Pick disease (NP) is a group of lipid storage disorders that includes three types of diseases.While NP type A (NP-A) and NP type B (NP-B) are caused by a lysosomal acid sphingomyelinase(ASM) deficiency, NP type C (NP-C) is a neurovisceral dis

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=jairo_______::b799369cee94b4be8689dae6f6a0ef86
http://hdl.handle.net/10295/3138

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HYPOXIC-ISCHEMIC BRAIN INJURY IN NEWBORN RAT : NEUROPROTECTIVE EFFECTS OF ACETAMINOPHEN AND THE INVOLVEMENT OF ACID SPHINGOMYELINASE ACTIVATION

Autor: Oguma, Rena, Ishida-Nakajima, Wako, Kawamura, Masanari, Miura, Shinobu, Oyama, Chikako, Sato, Yoko, Arai, Hirokazu, Takahashi, Tsutomu

Publikováno v: 秋田医学. 39(3/4):109-118

Acetaminophen is widely used as an analgesic and antipyretic medication. Recently, acetaminophen has been shown as effective against neuronal cell death through its antioxidant and anti-inflammatory properties. In this study, we used the Rice-Vannucc

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=jairo_______::1cf9435cca35270137430d61bd4cefa5
http://hdl.handle.net/10295/2160

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BUTYRATE REDUCES FREE CHOLESTEROL ACCUMULATION IN NIEMANN-PICK DISEASE TYPE C1 CELLS (NOVA SCOTIA FORM) THROUGH THE INDUCTION OF ACID SPHINGOMYELINASE

Autor: Oyama, Chikako, Hirayama, Masashi, Noguchi, Atsuko, Arai, Hirokazu, Takahashi, Tsutomu

Publikováno v: 秋田医学. 38(3/4):111-119

Niemann-Pick disease type C (NPC) is an inherited disorder caused by mutations in either the NPC1 or the NPC2 gene that affect intracellular free cholesterol trafficking. Most cases of NPC have mutations in the NPC1 gene. Acid sphingomyelinase (ASM)

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=jairo_______::2ae532c4d773aff8b17e17231d5b9a1d
http://hdl.handle.net/10295/1883

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SECONDARY IMPAIRMENT OF INTRACELLULAR CHOLESTEROL TRANSPORT IN CELLS WITH NIEMANN-PICK DISEASE TYPE C

Autor: Oyama, Katsuyuki, Oyama, Chikako, Takahashi, Tsutomu

Publikováno v: 秋田医学. 37(3/4):153-162

Niemann-Pick disease type C (NPC) is an autosomal recessive lipidosis resulting from mutations of the NPC1 or NPC2 gene, clinically characterized by hepatosplenomegaly and progressive neurological symptoms including vertical supranuclear ophthalmople

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=jairo_______::26d1c7cf2f958b5dc758f27a8853ce66
http://hdl.handle.net/10295/1813

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Akademický článek

Novel mutation of methylmalonyl-CoA mutase gene causing the mut ⁰ form of methylmalonic acidemia in a Japanese girl.

Autor: Oyama, Chikako, Takahashi, Tsutomu, Matsumori, Mika, Shoji, Yutaka, Tajima, Gou, Sakura, Nobuo, Hasegawa, Yuki, Yamaguchi, Seiji, Kakinuma, Hiroaki, Takada, Goro

Publikováno v: Pediatrics International; Apr2007, Vol. 49 Issue 2, p232-234, 3p, 1 Diagram

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Report

A novel S269C mutation in fibroblast growth factor receptor 3 in a Japanese child with hypochondroplasia.

Autor: Takahashi I; Department of Pediatrics, Akita University Graduate School of Medicine, Akita, Japan., Kondo D; Department of Pediatrics, Akita University Graduate School of Medicine, Akita, Japan., Oyama C; Department of Pediatrics, Akita University Graduate School of Medicine, Akita, Japan., Yano T; Department of Pediatrics, Akita University Graduate School of Medicine, Akita, Japan., Tamura H; Department of Pediatrics, Akita University Graduate School of Medicine, Akita, Japan., Noguchi A; Department of Pediatrics, Akita University Graduate School of Medicine, Akita, Japan., Takahashi T; Department of Pediatrics, Akita University Graduate School of Medicine, Akita, Japan.

Publikováno v: Human genome variation [Hum Genome Var] 2018 Apr 12; Vol. 5, pp. 1. Date of Electronic Publication: 2018 Apr 12 (Print Publication: 2018).

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