Lebl J - Search Results

1

Association between neuromedin U gene variants and overweight and obesity.

Hainerová I, Torekov SS, Ek J, Finková M, Borch-Johnsen K, Jørgensen T, Madsen OD, Lebl J, Hansen T, Pedersen O. Hainerová I, et al. Among authors: lebl j. J Clin Endocrinol Metab. 2006 Dec;91(12):5057-63. doi: 10.1210/jc.2006-1442. Epub 2006 Sep 19. J Clin Endocrinol Metab. 2006. PMID: 16984985

2

Genetic evidence that HNF-1alpha-dependent transcriptional control of HNF-4alpha is essential for human pancreatic beta cell function.

Hansen SK, Párrizas M, Jensen ML, Pruhova S, Ek J, Boj SF, Johansen A, Maestro MA, Rivera F, Eiberg H, Andel M, Lebl J, Pedersen O, Ferrer J, Hansen T. Hansen SK, et al. Among authors: lebl j. J Clin Invest. 2002 Sep;110(6):827-33. doi: 10.1172/JCI15085. J Clin Invest. 2002. PMID: 12235114 Free PMC article.

3

Genetic epidemiology of MODY in the Czech republic: new mutations in the MODY genes HNF-4alpha, GCK and HNF-1alpha.

Pruhova S, Ek J, Lebl J, Sumnik Z, Saudek F, Andel M, Pedersen O, Hansen T. Pruhova S, et al. Among authors: lebl j. Diabetologia. 2003 Feb;46(2):291-5. doi: 10.1007/s00125-002-1010-7. Epub 2003 Jan 8. Diabetologia. 2003. PMID: 12627330

4

Maturity-onset diabetes of the young with end-stage nephropathy: a new indication for simultaneous pancreas and kidney transplantation?

Saudek F, Průhová S, Boucek P, Lebl J, Adamec M, Ek J, Pedersen O, Hansen T. Saudek F, et al. Among authors: lebl j. Transplantation. 2004 Apr 27;77(8):1298-301. doi: 10.1097/01.tp.0000119721.35506.a7. Transplantation. 2004. PMID: 15114102

5

Molecular genetics and phenotypic characteristics of MODY caused by hepatocyte nuclear factor 4alpha mutations in a large European collection.

Pearson ER, Pruhova S, Tack CJ, Johansen A, Castleden HA, Lumb PJ, Wierzbicki AS, Clark PM, Lebl J, Pedersen O, Ellard S, Hansen T, Hattersley AT. Pearson ER, et al. Among authors: lebl j. Diabetologia. 2005 May;48(5):878-85. doi: 10.1007/s00125-005-1738-y. Epub 2005 Apr 14. Diabetologia. 2005. PMID: 15830177

6

Aetiological heterogeneity of asymptomatic hyperglycaemia in children and adolescents.

Feigerlová E, Pruhová S, Dittertová L, Lebl J, Pinterová D, Kolostová K, Cerná M, Pedersen O, Hansen T. Feigerlová E, et al. Among authors: lebl j. Eur J Pediatr. 2006 Jul;165(7):446-52. doi: 10.1007/s00431-006-0106-3. Epub 2006 Apr 7. Eur J Pediatr. 2006. PMID: 16602010

7

A novel -192c/g mutation in the proximal P2 promoter of the hepatocyte nuclear factor-4 alpha gene (HNF4A) associates with late-onset diabetes.

Ek J, Hansen SP, Lajer M, Nicot C, Boesgaard TW, Pruhova S, Johansen A, Albrechtsen A, Yderstraede K, Lauenborg J, Parrizas M, Boj SF, Jørgensen T, Borch-Johnsen K, Damm P, Ferrer J, Lebl J, Pedersen O, Hansen T. Ek J, et al. Among authors: lebl j. Diabetes. 2006 Jun;55(6):1869-73. doi: 10.2337/db05-1684. Diabetes. 2006. PMID: 16731855

8

Six novel mutations in the GCK gene in MODY patients.

Pinterova D, Ek J, Kolostova K, Pruhova S, Novota P, Romzova M, Feigerlova E, Cerna M, Lebl J, Pedersen O, Hansen T. Pinterova D, et al. Among authors: lebl j. Clin Genet. 2007 Jan;71(1):95-6. doi: 10.1111/j.1399-0004.2006.00729.x. Clin Genet. 2007. PMID: 17204055 No abstract available.

9

Melanocortin 4 receptor mutations in obese Czech children: studies of prevalence, phenotype development, weight reduction response, and functional analysis.

Hainerová I, Larsen LH, Holst B, Finková M, Hainer V, Lebl J, Hansen T, Pedersen O. Hainerová I, et al. Among authors: lebl j. J Clin Endocrinol Metab. 2007 Sep;92(9):3689-96. doi: 10.1210/jc.2007-0352. Epub 2007 Jun 19. J Clin Endocrinol Metab. 2007. PMID: 17579204

10

Autosomal inheritance of diabetes in two families characterized by obesity and a novel H241Q mutation in NEUROD1.

Gonsorcíková L, Průhová S, Cinek O, Ek J, Pelikánová T, Jørgensen T, Eiberg H, Pedersen O, Hansen T, Lebl J. Gonsorcíková L, et al. Among authors: lebl j. Pediatr Diabetes. 2008 Aug;9(4 Pt 2):367-72. doi: 10.1111/j.1399-5448.2008.00379.x. Epub 2008 Mar 5. Pediatr Diabetes. 2008. PMID: 18331410

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