Hara M - Search Results

1

Missense mutation Gly574Ser in the transcription factor HNF-1alpha is a marker of atypical diabetes mellitus in African-American children.

Boutin P, Gresh L, Cisse A, Hara M, Bell G, Babu S, Eisenbarth G, Froguel P. Boutin P, et al. Among authors: hara m. Diabetologia. 1999 Mar;42(3):380-1. doi: 10.1007/s001250051166. Diabetologia. 1999. PMID: 10096793 No abstract available.

2

No diabetes-associated mutations in the coding region of the hepatocyte nuclear factor-4gamma gene (HNF4G) in Japanese patients with MODY.

Hara M, Wang X, Paz VP, Cox NJ, Iwasaki N, Ogata M, Iwamoto Y, Bell GI. Hara M, et al. Diabetologia. 2000 Aug;43(8):1064-9. doi: 10.1007/s001250051491. Diabetologia. 2000. PMID: 10990086

3

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

Iwasaki N, Oda N, Ogata M, Hara M, Hinokio Y, Oda Y, Yamagata K, Kanematsu S, Ohgawara H, Omori Y, Bell GI. Iwasaki N, et al. Among authors: hara m. Diabetes. 1997 Sep;46(9):1504-8. doi: 10.2337/diab.46.9.1504. Diabetes. 1997. PMID: 9287053

4

Mutation in hepatocyte nuclear factor-1 beta gene (TCF2) associated with MODY.

Horikawa Y, Iwasaki N, Hara M, Furuta H, Hinokio Y, Cockburn BN, Lindner T, Yamagata K, Ogata M, Tomonaga O, Kuroki H, Kasahara T, Iwamoto Y, Bell GI. Horikawa Y, et al. Among authors: hara m. Nat Genet. 1997 Dec;17(4):384-5. doi: 10.1038/ng1297-384. Nat Genet. 1997. PMID: 9398836 No abstract available.

5

Identification of three missense mutations in the peroxisome proliferator-activated receptor alpha gene in Japanese subjects with maturity-onset diabetes of the young.

Hara M, Wang X, Paz VP, Iwasaki N, Honda M, Iwamoto Y, Bell GI. Hara M, et al. J Hum Genet. 2001;46(5):285-8. doi: 10.1007/s100380170080. J Hum Genet. 2001. PMID: 11355020

6

Beta-cell transcription factors and diabetes: mutations in the coding region of the BETA2/NeuroD1 (NEUROD1) and Nkx2.2 (NKX2B) genes are not associated with maturity-onset diabetes of the young in Japanese.

Furuta H, Horikawa Y, Iwasaki N, Hara M, Sussel L, Le Beau MM, Davis EM, Ogata M, Iwamoto Y, German MS, Bell GI. Furuta H, et al. Among authors: hara m. Diabetes. 1998 Aug;47(8):1356-8. doi: 10.2337/diab.47.8.1356. Diabetes. 1998. PMID: 9703340 No abstract available.

7

Genetic variation in the gene encoding calpain-10 is associated with type 2 diabetes mellitus.

Horikawa Y, Oda N, Cox NJ, Li X, Orho-Melander M, Hara M, Hinokio Y, Lindner TH, Mashima H, Schwarz PE, del Bosque-Plata L, Horikawa Y, Oda Y, Yoshiuchi I, Colilla S, Polonsky KS, Wei S, Concannon P, Iwasaki N, Schulze J, Baier LJ, Bogardus C, Groop L, Boerwinkle E, Hanis CL, Bell GI. Horikawa Y, et al. Among authors: hara m. Nat Genet. 2000 Oct;26(2):163-75. doi: 10.1038/79876. Nat Genet. 2000. PMID: 11017071

8

Mutations in the coding region of the insulin promoter factor 1 gene are not a common cause of maturity-onset diabetes of the young in Japanese subjects.

Hara M, Lindner TH, Paz VP, Wang X, Iwasaki N, Ogata M, Iwamoto Y, Bell GI. Hara M, et al. Diabetes. 1998 May;47(5):845-6. doi: 10.2337/diabetes.47.5.845. Diabetes. 1998. PMID: 9588461 Clinical Trial. No abstract available.

9

Sustained expression of hepatocyte nuclear factor-6 leads to loss of pancreatic beta-cells by apoptosis.

Hara M, Shen J, Pugh W, Polonsky KS, Le Beau MM, Bell GI. Hara M, et al. Exp Clin Endocrinol Diabetes. 2007 Nov;115(10):654-61. doi: 10.1055/s-2007-982514. Exp Clin Endocrinol Diabetes. 2007. PMID: 18058600

10

Association of the (AU)AT-rich element polymorphism in PPP1R3 with hormonal and metabolic features of polycystic ovary syndrome.

Alcoser SY, Hara M, Bell GI, Ehrmann DA. Alcoser SY, et al. Among authors: hara m. J Clin Endocrinol Metab. 2004 Jun;89(6):2973-6. doi: 10.1210/jc.2003-031189. J Clin Endocrinol Metab. 2004. PMID: 15181086

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