Møller AM - Search Results

1

A prevalent amino acid polymorphism at codon 98 in the hepatocyte nuclear factor-1alpha gene is associated with reduced serum C-peptide and insulin responses to an oral glucose challenge.

Urhammer SA, Fridberg M, Hansen T, Rasmussen SK, Møller AM, Clausen JO, Pedersen O. Urhammer SA, et al. Among authors: moller am. Diabetes. 1997 May;46(5):912-6. doi: 10.2337/diab.46.5.912. Diabetes. 1997. PMID: 9133564

2

Novel MODY3 mutations in the hepatocyte nuclear factor-1alpha gene: evidence for a hyperexcitability of pancreatic beta-cells to intravenous secretagogues in a glucose-tolerant carrier of a P447L mutation.

Hansen T, Eiberg H, Rouard M, Vaxillaire M, Møller AM, Rasmussen SK, Fridberg M, Urhammer SA, Holst JJ, Almind K, Echwald SM, Hansen L, Bell GI, Pedersen O. Hansen T, et al. Among authors: moller am. Diabetes. 1997 Apr;46(4):726-30. doi: 10.2337/diab.46.4.726. Diabetes. 1997. PMID: 9075819

3

Genetic variation in the hepatocyte nuclear factor-1 alpha gene in Danish Caucasians with late-onset NIDDM.

Urhammer SA, Rasmussen SK, Kaisaki PJ, Oda N, Yamagata K, Møller AM, Fridberg M, Hansen L, Hansen T, Bell GI, Pedersen O. Urhammer SA, et al. Among authors: moller am. Diabetologia. 1997 Apr;40(4):473-5. doi: 10.1007/s001250050703. Diabetologia. 1997. PMID: 9112026

4

Chromosomal mapping and mutational analysis of the coding region of the glycogen synthase kinase-3alpha and beta isoforms in patients with NIDDM.

Hansen L, Arden KC, Rasmussen SB, Viars CS, Vestergaard H, Hansen T, Møller AM, Woodgett JR, Pedersen O. Hansen L, et al. Among authors: moller am. Diabetologia. 1997 Aug;40(8):940-6. doi: 10.1007/s001250050771. Diabetologia. 1997. PMID: 9267989

5

Studies of the genetic variability of the coding region of the hepatocyte nuclear factor-4alpha in Caucasians with maturity onset NIDDM.

Møller AM, Urhammer SA, Dalgaard LT, Reneland R, Berglund L, Hansen T, Clausen JO, Lithell H, Pedersen O. Møller AM, et al. Diabetologia. 1997 Aug;40(8):980-3. doi: 10.1007/s001250050778. Diabetologia. 1997. PMID: 9267996

6

Mutational analysis of the coding region of the uncoupling protein 2 gene in obese NIDDM patients: impact of a common amino acid polymorphism on juvenile and maturity onset forms of obesity and insulin resistance.

Urhammer SA, Dalgaard LT, Sørensen TI, Møller AM, Andersen T, Tybjaerg-Hansen A, Hansen T, Clausen JO, Vestergaard H, Pedersen O. Urhammer SA, et al. Among authors: moller am. Diabetologia. 1997 Oct;40(10):1227-30. doi: 10.1007/s001250050811. Diabetologia. 1997. PMID: 9349606

7

Decreased tolbutamide-stimulated insulin secretion in healthy subjects with sequence variants in the high-affinity sulfonylurea receptor gene.

Hansen T, Echwald SM, Hansen L, Møller AM, Almind K, Clausen JO, Urhammer SA, Inoue H, Ferrer J, Bryan J, Aguilar-Bryan L, Permutt MA, Pedersen O. Hansen T, et al. Among authors: moller am. Diabetes. 1998 Apr;47(4):598-605. doi: 10.2337/diabetes.47.4.598. Diabetes. 1998. PMID: 9568693 Clinical Trial.

8

The effect of two frequent amino acid variants of the hepatocyte nuclear factor-1alpha gene on estimates of the pancreatic beta-cell function in Caucasian glucose-tolerant first-degree relatives of type 2 diabetic patients.

Urhammer SA, Møller AM, Nyholm B, Ekstrøm CT, Eiberg H, Clausen JO, Hansen T, Pedersen O, Schmitz O. Urhammer SA, et al. Among authors: moller am. J Clin Endocrinol Metab. 1998 Nov;83(11):3992-5. doi: 10.1210/jcem.83.11.5228. J Clin Endocrinol Metab. 1998. PMID: 9814481

9

Mutations in the hepatocyte nuclear factor-1alpha gene in Caucasian families originally classified as having Type I diabetes.

Møller AM, Dalgaard LT, Pociot F, Nerup J, Hansen T, Pedersen O. Møller AM, et al. Diabetologia. 1998 Dec;41(12):1528-31. doi: 10.1007/s001250051101. Diabetologia. 1998. PMID: 9867222

10

A novel Phe75fsdelT mutation in the hepatocyte nuclear factor-4alpha gene in a Danish pedigree with maturity-onset diabetes of the young.

Møller AM, Dalgaard LT, Ambye L, Hansen L, Schmitz O, Hansen T, Pedersen O. Møller AM, et al. J Clin Endocrinol Metab. 1999 Jan;84(1):367-9. doi: 10.1210/jcem.84.1.5396. J Clin Endocrinol Metab. 1999. PMID: 9920109

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