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Insulin sensitivity in patients with NIDDM and the A-to-G mutation at nucleotide 3,243 of the mitochondrial tRNALeu(UUR) gene.
Published in:
1995
By:
- Iwasaki, Naoko;
- Wasada, Taro;
- Takahashi, Yoshiatsu;
- Babazono, Tetsuya;
- Ohgawara, Hisako;
- Omori, Yasue;
- Iwasaki, N;
- Wasada, T;
- Takahashi, Y;
- Babazono, T;
- Ohgawara, H;
- Omori, Y
Publication type:
Letter
Familial hyperproinsulinemia associated with NIDDM. A case study.
Published in:
1993
By:
- Oohashi, H;
- Ohgawara, H;
- Nanjo, K;
- Tasaka, Y;
- Cao, Q P;
- Chan, S J;
- Rubenstein, A H;
- Steiner, D F;
- Omori, Y
Publication type:
journal article
Increased plasma endothelin in NIDDM patients with retinopathy.
Published in:
1992
By:
- Kawamura, Makiko;
- Ohgawara, Hisako;
- Naruse, Mitsuhide;
- Suzuki, Nobuhiro;
- Iwasaki, Naoko;
- Naruse, Kiyoko;
- Hori, Sadao;
- Demura, Hiroshi;
- Omori, Yasue;
- Kawamura, M;
- Ohgawara, H;
- Naruse, M;
- Suzuki, N;
- Iwasaki, N;
- Naruse, K;
- Hori, S;
- Demura, H;
- Omori, Y
Publication type:
journal article
Association studies of variants in the genes involved in pancreatic beta-cell function in type 2 diabetes in Japanese subjects.
Published in:
2006
By:
- Yokoi N;
- Kanamori M;
- Horikawa Y;
- Takeda J;
- Sanke T;
- Furuta H;
- Nanjo K;
- Mori H;
- Kasuga M;
- Hara K;
- Kadowaki T;
- Tanizawa Y;
- Oka Y;
- Iwami Y;
- Ohgawara H;
- Yamada Y;
- Seino Y;
- Yano H;
- Cox NJ;
- Seino S
Publication type:
journal article
Mutations in the hepatocyte nuclear factor-1alpha/MODY3 gene in Japanese subjects with early- and late-onset NIDDM.
Published in:
1997
By:
- Iwasaki, Naoko;
- Oda, Naohisa;
- Ogata, Makiko;
- Hara, Manami;
- Hinokio, Yoshinori;
- Oda, Yukie;
- Yamagata, Kazuya;
- Kanematsu, Sachiko;
- Ohgawara, Hisako;
- Omori, Yasue;
- Bell, Graeme I.;
- Iwasaki, N;
- Oda, N;
- Ogata, M;
- Hara, M;
- Hinokio, Y;
- Oda, Y;
- Yamagata, K;
- Kanematsu, S;
- Ohgawara, H
Publication type:
journal article
Identification of microsatellite markers near the human genes encoding the beta-cell ATP-sensitive K+ channel and linkage studies with NIDDM in Japanese.
Published in:
1996
By:
- Iwasaki, Naoko;
- Kawamura, Makiko;
- Yamagata, Kazuya;
- Cox, Nancy J.;
- Karibe, Sachiyo;
- Ohgawara, Hisako;
- Inagaki, Nobuya;
- Seino, Susumu;
- Bell, Graeme I.;
- Omori, Yasue;
- Iwasaki, N;
- Kawamura, M;
- Yamagata, K;
- Cox, N J;
- Karibe, S;
- Ohgawara, H;
- Inagaki, N;
- Seino, S;
- Bell, G I;
- Omori, Y
Publication type:
journal article

Found: 6

Insulin sensitivity in patients with NIDDM and the A-to-G mutation at nucleotide 3,243 of the mitochondrial tRNALeu(UUR) gene.

Familial hyperproinsulinemia associated with NIDDM. A case study.

Increased plasma endothelin in NIDDM patients with retinopathy.

Association studies of variants in the genes involved in pancreatic beta-cell function in type 2 diabetes in Japanese subjects.

Mutations in the hepatocyte nuclear factor-1alpha/MODY3 gene in Japanese subjects with early- and late-onset NIDDM.

Identification of microsatellite markers near the human genes encoding the beta-cell ATP-sensitive K+ channel and linkage studies with NIDDM in Japanese.