Effect of exposure to non-esterified fatty acid on progressive deterioration of insulin secretion in patients with Type 2 diabetes: a long-term follow-up study von Morita, S., Shimajiri, Y., Sakagashira, S., Furuta, M., Sanke, T.

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Podocalyxin expression in undifferentiated thyroid carcinomas von Yasuoka, H, Tsujimoto, M, Hirokawa, M, Tori, M, Nakahara, M, Miyauchi, A, Kodama, R, Sanke, T, Nakamura, Y

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Nonsense mutation of islet-1 gene (Q310X) found in a type 2 diabetic patient with a strong family history von SHIMOMURA, H, SANKE, T, HANABUSA, T, TSUNODA, K, FURUTA, H, NANJO, K

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Single nucleotide polymorphism (D68D, T to C) in the syntaxin 1A gene correlates to age at onset and insulin requirement in Type II diabetic patients von TSUNODA, K, SANKE, T, NAKAGAWA, T, FURUTA, H, NANJO, K

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Functional Variants in the Glutathione Peroxidase-1 (GPx-1) Gene Are Associated With Increased Intima-Media Thickness of Carotid Arteries and Risk of Macrovascular Diseases in Japa... von Hamanishi, Tohru, Furuta, Hiroto, Kato, Hisako, Doi, Asako, Tamai, Masanori, Shimomura, Hiroko, Sakagashira, Setsuya, Nishi, Masahiro, Sasaki, Hideyuki, Sanke, Tokio, Nanjo, Kishio

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An islet amyloid peptide is derived from an 89-amino acid precursor by proteolytic processing von Sanke, T, Bell, G I, Sample, C, Rubenstein, A H, Steiner, D F

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Organization of the human carboxypeptidase E gene and molecular scanning for mutations in Japanese subjects with NIDDM or obesity von UTSUNOMIYA, N, OHAGI, S, SANKE, T, TATSUTA, H, HANABUSA, T, NANJO, K

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Enhanced in vitro production of amyloid-like fibrils from mutant (S20G) islet amyloid polypeptide von Ma, Z., Westermark, G. T., Sakagashira, S., Sanke, T., Gustavsson, Å., Sakamoto, H., Engström, U., Nanjo, K., Westermark, P.

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Plasma islet amyloid polypeptide (Amylin) levels and their responses to oral glucose in type 2 (non-insulin-dependent) diabetic patients von Sanke, T, Hanabusa, T, Nakano, Y, Oki, C, Okai, K, Nishimura, S, Kondo, M, Nanjo, K

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A missense mutation of the muscle glycogen synthase gene (M416V) is associated with insulin resistance in the Japanese population von SHIMOMURA, H, SANKE, T, UEDA, K, HANABUSA, T, SAKAGASHIRA, S, NANJO, K

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Molecular scanning for mutations in the melanocortin-4 receptor gene in obese/diabetic Japanese von Ohshiro, Y, Sanke, T, Ueda, K, Shimajiri, Y, Nakagawa, T, Tsunoda, K, Nishi, M, Sasaki, H, Takasu, N, Nanjo, K

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Contrast-Enhanced Ultrasonography in the Diagnosis of Solid Renal Tumors von Tamai, Hideyuki, Takiguchi, Yoshie, Oka, Masashi, Shingaki, Naoki, Enomoto, Shotaro, Shiraki, Tatsuya, Furuta, Machi, Inoue, Izumi, Iguchi, Mikitaka, Yanaoka, Kimihiko, Arii, Kenji, Shimizu, Yasuhito, Nakata, Hiroya, Shinka, Toshiaki, Sanke, Tokio, Ichinose, Masao

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Islet amyloid polypeptide amide causes peripheral insulin resistance in vivo in dogs von SOWA, R, SANKE, T, HIRAYAMA, J, TABATA, H, FURUTA, H, NISHIMURA, S, NANJO, K

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Molecular scanning for mutations in the melanocortin-4 receptor gene in obese/diabetic Japanese von OHSHIRO, Y., SANKE, T., UEDA, K., SHIMAJIRI, Y., NAKAGAWA, T., TSUNODA, K., NISHI, M., SASAKI, H., TAKASU, N., NANJO, K.

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Simple tandem repeat DNA polymorphism in the human glycogen synthase gene is associated with NIDDM in Japanese subjects von KUROYAMA, H, SANKE, T, OHAGI, S, FURUTA, M, FURUTA, H, NANJO, K

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S20G Mutant Amylin Exhibits Increased in Vitro Amyloidogenicity and Increased Intracellular Cytotoxicity Compared to Wild-Type Amylin von Sakagashira, Setsuya, Hiddinga, Henry J., Tateishi, Kayoko, Sanke, Tokio, Hanabusa, Tadashi, Nanjo, Kishio, Eberhardt, Norman L.

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Cloning of mouse islet amyloid polypeptide gene and characterization of its promoter von Ekawa, K, Nishi, M, Ohagi, S, Sanke, T, Nanjo, K

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A Missense Mutation of Pax4 Gene (R121W) Is Associated With Type 2 Diabetes in Japanese von SHIMAJIRI, Yoshinori, SANKE, Tokio, FURUTA, Hiroto, HANABUSA, Tadashi, NAKAGAWA, Takayuki, FUJITANI, Yoshio, KAJIMOTO, Yoshitaka, TAKASU, Nobuyuki, NANJO, Kishio

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Genetics of type 2 diabetes mellitus von So, W Y, Ng, M C, Lee, S C, Sanke, T, Lee, H K, Chan, J C

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Clinical features of diabetes mellitus with the mitochondrial DNA 3243 (A–G) mutation in Japanese: Maternal inheritance and mitochondria-related complications von Suzuki, Susumu, Oka, Yoshitomo, Kadowaki, Takashi, Kanatsuka, Azuma, Kuzuya, Takeshi, Kobayashi, Masashi, Sanke, Tokio, Seino, Yutaka, Nanjo, Kishio

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