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
Aoyama, Yoshiko, Ozer, Isil, Demirkol, Mubeccel, Ebara, Tetsu, Murase, Toshio, Podskarbi, Teodor, Shin, Yoon S, Gokcay, Gulden, Okubo, Minoru
Published in Journal of human genetics (01.11.2009)
Published in Journal of human genetics (01.11.2009)
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Molecular analysis of the AGL gene: heterogeneity of mutations in patients with glycogen storage disease type III from Germany, Canada, Afghanistan, Iran, and Turkey
Endo, Yoriko, Horinishi, Asako, Vorgerd, Matthias, Aoyama, Yoshiko, Ebara, Tetsu, Murase, Toshio, Odawara, Masato, Podskarbi, Teodor, Shin, Yoon S, Okubo, Minoru
Published in Journal of human genetics (01.11.2006)
Published in Journal of human genetics (01.11.2006)
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Serum aspirin esterase is strongly associated with glucose and lipids in healthy subjects: different association patterns in subjects with type 2 diabetes mellitus
Kotani, Kazuhiko, Kimura, Satoshi, Ebara, Tetsu, Caccavello, Russell, Gugliucci, Alejandro
Published in Diabetology and metabolic syndrome (27.07.2010)
Published in Diabetology and metabolic syndrome (27.07.2010)
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Delayed catabolism of apoB-48 lipoproteins due to decreased heparan sulfate proteoglycan production in diabetic mice
Ebara, T, Conde, K, Kako, Y, Liu, Y, Xu, Y, Ramakrishnan, R, Goldberg, I J, Shachter, N S
Published in The Journal of clinical investigation (15.06.2000)
Published in The Journal of clinical investigation (15.06.2000)
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Novel AGL mutation in a Turkish patient with glycogen storage disease type IIIa
Aoyama, Yoshiko, Endo, Yoriko, Ebara, Tetsu, Murase, Toshio, Shin, Yoon S., Podskarbi, Teodor, Ozer, Isil, Demirkol, Mübeccel, Gökçay, Gülden, Okubo, Minoru
Published in Pediatrics international (01.02.2010)
Published in Pediatrics international (01.02.2010)
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A Japanese Patient With Cardiomyopathy Caused by a Novel Mutation R285X in the AGL Gene
Ogimoto, Akiyoshi, Okubo, Minoru, Okayama, Hideki, Shin, Yoon S., Endo, Yoriko, Ebara, Tetsu, Inoue, Katsuji, Ohtsuka, Tomoaki, Tahara, Hideki, Murase, Toshio, Higaki, Jistuo
Published in Circulation Journal (2007)
Published in Circulation Journal (2007)
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BACTERIAL SPECIES AND ANTIMICROBIAL SUSCEPTIBILITY OF WOUND CULTURE OBTAINED FROM DIABETIC GANGRENE PATIENTS WHO UNDERWENT LIMB AMPUTATION AT A JAPANESE UNIVERSITY HOSPITAL
YAMAGUCHI, Hayato, FUKUOKA, Seiji, NAKAMURA, Masanori, EBARA, Tetsu, KIMURA, Satoshi
Published in Journal of The Showa University Society (2014)
Published in Journal of The Showa University Society (2014)
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Molecular characterization of Egyptian patients with glycogen storage disease type IIIa
Endo, Yoriko, Fateen, Ekram, Aoyama, Yoshiko, Horinishi, Asako, Ebara, Tetsu, Murase, Toshio, Shin, Yoon S, Okubo, Minoru
Published in Journal of human genetics (01.10.2005)
Published in Journal of human genetics (01.10.2005)
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Hypertriglyceridemia and pancreatitis in a patient with apolipoprotein E7 (p.[E244K; E245K])/E4
Arai, Makoto, Nishimura, Akihiro, Mori, Yasumichi, Ebara, Tetsu, Okubo, Minoru
Published in Clinica chimica acta (25.09.2014)
Published in Clinica chimica acta (25.09.2014)
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Hyperlipidemia in streptozocin-diabetic hamsters as a model for human insulin-deficient diabetes: comparison to streptozocin-diabetic rats
Ebara, T, Hirano, T, Mamo, J.C.L, Sakamaki, R, Furukawa, S, Nagano, S, Takahashi, T
Published in Metabolism, clinical and experimental (01.03.1994)
Published in Metabolism, clinical and experimental (01.03.1994)
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A novel APOA5 splicing mutation IVS2+1g>a in a Japanese chylomicronemia patient
Okubo, Minoru, Ishihara, Mitsuaki, Iwasaki, Tadao, Ebara, Tetsu, Aoyama, Yoshiko, Murase, Toshio, Hattori, Hiroaki
Published in Atherosclerosis (01.11.2009)
Published in Atherosclerosis (01.11.2009)
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Severe hypertriglyceridemia in Japan: Differences in causes and therapeutic responses
Murase, Toshio, Okubo, Minoru, Ebara, Tetsu, Mori, Yasumichi
Published in Journal of clinical lipidology (01.11.2017)
Published in Journal of clinical lipidology (01.11.2017)
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A novel complex deletion–insertion mutation mediated by Alu repetitive elements leads to lipoprotein lipase deficiency
Okubo, Minoru, Horinishi, Asako, Saito, Mieko, Ebara, Tetsu, Endo, Yoriko, Kaku, Kohei, Murase, Toshio, Eto, Masaaki
Published in Molecular genetics and metabolism (01.11.2007)
Published in Molecular genetics and metabolism (01.11.2007)
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