Yamada S - Search Results

1

Molecular cloning of a novel brain-type Na(+)-dependent inorganic phosphate cotransporter.

Aihara Y, Mashima H, Onda H, Hisano S, Kasuya H, Hori T, Yamada S, Tomura H, Yamada Y, Inoue I, Kojima I, Takeda J. Aihara Y, et al. Among authors: yamada y, yamada s. J Neurochem. 2000 Jun;74(6):2622-5. doi: 10.1046/j.1471-4159.2000.0742622.x. J Neurochem. 2000. PMID: 10820226 Free article.

2

Identification and characterization of the gene encoding a second proteolipid subunit of human vacuolar H(+)-ATPase (ATP6F).

Nishigori H, Yamada S, Tomura H, Fernald AA, Le Beau MM, Takeuchi T, Takeda J. Nishigori H, et al. Among authors: yamada s. Genomics. 1998 Jun 1;50(2):222-8. doi: 10.1006/geno.1998.5310. Genomics. 1998. PMID: 9653649

3

Genes expressed during the differentiation of pancreatic AR42J cells into insulin-secreting cells.

Mashima H, Yamada S, Tajima T, Seno M, Yamada H, Takeda J, Kojima I. Mashima H, et al. Among authors: yamada h, yamada s. Diabetes. 1999 Feb;48(2):304-9. doi: 10.2337/diabetes.48.2.304. Diabetes. 1999. PMID: 10334306

4

Cloning of cDNA and the gene encoding human hepatocyte nuclear factor (HNF)-3 beta and mutation screening in Japanese subjects with maturity-onset diabetes of the young.

Yamada S, Zhu Q, Aihara Y, Onda H, Zhang Z, Yu L, Jin L, Si YJ, Nishigori H, Tomura H, Inoue I, Morikawa A, Yamagata K, Hanafusa T, Matsuzawa Y, Takeda J. Yamada S, et al. Diabetologia. 2000 Jan;43(1):121-4. doi: 10.1007/s001250050016. Diabetologia. 2000. PMID: 10672453

5

Mutations in the small heterodimer partner gene are associated with mild obesity in Japanese subjects.

Nishigori H, Tomura H, Tonooka N, Kanamori M, Yamada S, Sho K, Inoue I, Kikuchi N, Onigata K, Kojima I, Kohama T, Yamagata K, Yang Q, Matsuzawa Y, Miki T, Seino S, Kim MY, Choi HS, Lee YK, Moore DD, Takeda J. Nishigori H, et al. Among authors: yamada s. Proc Natl Acad Sci U S A. 2001 Jan 16;98(2):575-80. doi: 10.1073/pnas.98.2.575. Epub 2001 Jan 2. Proc Natl Acad Sci U S A. 2001. PMID: 11136233 Free PMC article.

6

Identification of mutations in the hepatocyte nuclear factor-1alpha gene in Japanese subjects with early-onset NIDDM and functional analysis of the mutant proteins.

Yamada S, Tomura H, Nishigori H, Sho K, Mabe H, Iwatani N, Takumi T, Kito Y, Moriya N, Muroya K, Ogata T, Onigata K, Morikawa A, Inoue I, Takeda J. Yamada S, et al. Diabetes. 1999 Mar;48(3):645-8. doi: 10.2337/diabetes.48.3.645. Diabetes. 1999. PMID: 10078571 No abstract available.

7

Mutations in the hepatocyte nuclear factor-1alpha gene (MODY3) are not a major cause of late-onset NIDDM in Japanese subjects.

Yamada S, Nishigori H, Onda H, Takahashi K, Kitano N, Morikawa A, Takeuchi T, Takeda J. Yamada S, et al. Diabetes. 1997 Sep;46(9):1512-3. doi: 10.2337/diab.46.9.1512. Diabetes. 1997. PMID: 9287055 No abstract available.

8

Frameshift mutation, A263fsinsGG, in the hepatocyte nuclear factor-1beta gene associated with diabetes and renal dysfunction.

Nishigori H, Yamada S, Kohama T, Tomura H, Sho K, Horikawa Y, Bell GI, Takeuchi T, Takeda J. Nishigori H, et al. Among authors: yamada s. Diabetes. 1998 Aug;47(8):1354-5. doi: 10.2337/diab.47.8.1354. Diabetes. 1998. PMID: 9703339 No abstract available.

9

Gene expression profile in rat pancreatic islet and RINm5F cells.

Wang H, Horikawa Y, Jin L, Narita T, Yamada S, Shihara N, Tatemoto K, Muramatsu M, Mune T, Takeda J. Wang H, et al. Among authors: yamada s. J Mol Endocrinol. 2005 Aug;35(1):1-12. doi: 10.1677/jme.1.01738. J Mol Endocrinol. 2005. PMID: 16087717

10

Identification of mutations in the hepatocyte nuclear factor (HNF)-1 alpha gene in Japanese subjects with IDDM.

Yamada S, Nishigori H, Onda H, Utsugi T, Yanagawa T, Maruyama T, Onigata K, Nagashima K, Nagai R, Morikawa A, Takeuchi T, Takeda J. Yamada S, et al. Diabetes. 1997 Oct;46(10):1643-7. doi: 10.2337/diacare.46.10.1643. Diabetes. 1997. PMID: 9313763

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