荏原徹 (Tetsu Ebara) - マイポータル

Severe hypertriglyceridemia in Japan: Differences in causes and therapeutic responses

Toshio Murase, Minoru Okubo, Tetsu Ebara, Yasumichi Mori

JOURNAL OF CLINICAL LIPIDOLOGY 11(6) 1383-1392 2017年12月査読有り

Apolipoprotein C-IITuzla: A novel large deletion in APOC2 caused by Alu-Alu homologous recombination in an infant with apolipoprotein C-II deficiency

Minoru Okubo, Alma Toromanovic, Tetsu Ebara, Toshio Murase

CLINICA CHIMICA ACTA 438 148-153 2015年1月査読有り

Hypertriglyceridemia and pancreatitis in a patient with apolipoprotein E7 (p.[E244K; E245K])/E4

Makoto Arai, Akihiro Nishimura, Yasumichi Mori, Tetsu Ebara, Minoru Okubo

CLINICA CHIMICA ACTA 436 188-192 2014年9月査読有り

Lipoprotein lipase activity in heterozygotes for lipoprotein lipase gene mutations reveals a gender bias

Toshio Murase, Tetsu Ebara, Minoru Okubo

ANNALS OF CLINICAL BIOCHEMISTRY 51(2) 294-297 2014年3月査読有り

Hepatic lipase activity is decreased in Japanese patients with type III hyperlipoproteinemia

Toshio Murase, Tetsu Ebara, Minoru Okubo

CLINICA CHIMICA ACTA 414 185-187 2012年12月査読有り

Reduced plasma apolipoprotein A-V concentrations in two lecithin: cholesterol acyltransferase deficient patients

Tetsu Ebara, Hiroaki Hattori, Toshio Murase, Minoru Okubo

CLINICAL CHEMISTRY AND LABORATORY MEDICINE 48(9) 1359-1360 2010年9月査読有り

Serum aspirin esterase is strongly associated with glucose and lipids in healthy subjects: different association patterns in subjects with type 2 diabetes mellitus

Kazuhiko Kotani, Satoshi Kimura, Tetsu Ebara, Russell Caccavello, Alejandro Gugliucci

DIABETOLOGY & METABOLIC SYNDROME 2 50 2010年7月査読有り

Novel AGL mutation in a Turkish patient with glycogen storage disease type IIIa

Yoshiko Aoyama, Yoriko Endo, Tetsu Ebara, Toshio Murase, Yoon S. Shin, Teodor Podskarbi, Isil Ozer, Muebeccel Demirkol, Guelden Goekcay, Minoru Okubo

PEDIATRICS INTERNATIONAL 52(1) 145-147 2010年2月査読有り

A novel APOA5 splicing mutation IVS2+1g > a in a Japanese chylomicronemia patient

Minoru Okubo, Mitsuaki Ishihara, Tadao Iwasaki, Tetsu Ebara, Yoshiko Aoyama, Toshio Murase, Hiroaki Hattori

ATHEROSCLEROSIS 207(1) 24-25 2009年11月査読有り

Molecular features of 23 patients with glycogen storage disease type III in Turkey: a novel mutation p.R1147G associated with isolated glucosidase deficiency, along with 9 AGL mutations

Yoshiko Aoyama, Isil Ozer, Mubeccel Demirkol, Tetsu Ebara, Toshio Murase, Teodor Podskarbi, Yoon S. Shin, Gulden Gokcay, Minoru Okubo

JOURNAL OF HUMAN GENETICS 54(11) 681-686 2009年11月査読有り

Egyptian glycogen storage disease type III - identification of six novel AGL mutations, including a large 1.5 kb deletion and a missense mutation p.L620P with subtype IIId

Yoriko Endo, Ekram Fateen, Mortada El Shabrawy, Yoshiko Aoyama, Tetsu Ebara, Toshio Murase, Teodor Podskarbi, Yoon S. Shin, Minoru Okubo

CLINICAL CHEMISTRY AND LABORATORY MEDICINE 47(10) 1233-1238 2009年10月査読有り

Pancreatitis Caused by Hypertriglyceridemia in a Patient Compound Heterozygous for Leu334Phe and-514C -> T in the Hepatic Lipase Gene

Tetsu Ebara, Toshio Murase, Minoru Okubo

PANCREAS 38(2) 233-235 2009年3月査読有り

Impact of elevated serum lipoprotein (a) concentrations on the risk of coronary heart disease in patients with type 2 diabetes mellitus

Toshio Murase, Minoru Okubo, Michiyo Amemiya-Kudo, Tetsu Ebara, Yasumichi Mori

METABOLISM-CLINICAL AND EXPERIMENTAL 57(6) 791-795 2008年6月査読有り

Is LPL deficiency atherogenic?

Ebara T, Murase T, Okubo M

Circulation research 102(11) e118; author reply e119 2008年6月査読有り

A novel complex deletion-insertion mutation mediated by Alu repetitive elements leads to lipoprotein lipase deficiency

Minoru Okubo, Asako Horinishi, VMieko Saito, Tetsu Ebara, Yoriko Endo, Kohei Kaku, Toshio Murase, Masaaki Eto

MOLECULAR GENETICS AND METABOLISM 92(3) 229-233 2007年11月査読有り

A 60-y-old chylomicronemia patient homozygous for missense mutation (G188E) in the lipoprotein lipase gene showed no accelerated atherosclerosis

Tetsu Ebara, Yoriko Endo, Shouichi Yoshiike, Masatomi Tsuji, Susumu Taguchi, Toshio Murase, Minoru Okubo

CLINICA CHIMICA ACTA 386(1-2) 100-104 2007年11月査読有り

A Japanese patient with cardiomyopathy caused by a novel mutation R285X in the AGL gene.

Ogimoto A, Okubo M, Okayama H, Shin YS, Endo Y, Ebara T, Inoue K, Ohtsuka T, Tahara H, Murase T …

Circulation journal : official journal of the Japanese Circulation Society 71(10) 1653-1656 2007年10月査読有り

Molecular analysis of the AGL gene: heterogeneity of mutations in patients with glycogen storage disease type III from Germany, Canada, Afghanistan, Iran, and Turkey

Yoriko Endo, Asako Horinishi, Matthias Vorgerd, Yoshiko Aoyama, Tetsu Ebara, Toshio Murase, Masato Odawara, Teodor Podskarbi, Yoon S. Shin, Minoru Okubo

JOURNAL OF HUMAN GENETICS 51(11) 958-963 2006年査読有り

Molecular characterization of Egyptian patients with glycogen storage disease type IIIa

Yoriko Endo, Ekram Fateen, Yoshiko Aoyama, Asako Horinishi, Tetsu Ebara, Toshio Murase, Yoon S. Shin, Minoru Okubo

Journal of Human Genetics 50(10) 538-542 2005年10月査読有り

Lipoprotein lipase mRNA in white adipose tissue but not in skeletal muscle is increased by pioglitazone through PPAR-gamma

H Kageyama, T Hirano, K Okada, T Ebara, A Kageyama, T Murakami, S Shioda, M Adachi

BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS 305(1) 22-27 2003年5月査読有り

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