Lebl J - Search Results

1

Homozygous carriers of the G allele of rs4664447 of the glucagon gene (GCG) are characterised by decreased fasting and stimulated levels of insulin, glucagon and glucagon-like peptide (GLP)-1.

Torekov SS, Ma L, Grarup N, Hartmann B, Hainerová IA, Kielgast U, Kissow H, Rosenkilde M; GIANT Consortium; Lebl J, Witte DR, Jørgensen T, Sandbaek A, Lauritzen T, Madsen OD, Wang J, Linneberg A, Madsbad S, Holst JJ, Hansen T, Pedersen O. Torekov SS, et al. Among authors: lebl j. Diabetologia. 2011 Nov;54(11):2820-31. doi: 10.1007/s00125-011-2265-7. Epub 2011 Aug 7. Diabetologia. 2011. PMID: 21822931

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

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

5

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

6

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

7

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

8

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

9

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

10

Further evidence that mutations in INS can be a rare cause of Maturity-Onset Diabetes of the Young (MODY).

Boesgaard TW, Pruhova S, Andersson EA, Cinek O, Obermannova B, Lauenborg J, Damm P, Bergholdt R, Pociot F, Pisinger C, Barbetti F, Lebl J, Pedersen O, Hansen T. Boesgaard TW, et al. Among authors: lebl j. BMC Med Genet. 2010 Mar 12;11:42. doi: 10.1186/1471-2350-11-42. BMC Med Genet. 2010. PMID: 20226046 Free PMC article.

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