Fridmanis D - Search Results

1

Polymorphisms in FTO and near TMEM18 associate with type 2 diabetes and predispose to younger age at diagnosis of diabetes.

Kalnina I, Zaharenko L, Vaivade I, Rovite V, Nikitina-Zake L, Peculis R, Fridmanis D, Geldnere K, Jacobsson JA, Almen MS, Pirags V, Schiöth HB, Klovins J. Kalnina I, et al. Among authors: fridmanis d. Gene. 2013 Sep 25;527(2):462-8. doi: 10.1016/j.gene.2013.06.079. Epub 2013 Jul 13. Gene. 2013. PMID: 23860325

2

High affinity agonistic metal ion binding sites within the melanocortin 4 receptor illustrate conformational change of transmembrane region 3.

Lagerström MC, Klovins J, Fredriksson R, Fridmanis D, Haitina T, Ling MK, Berglund MM, Schiöth HB. Lagerström MC, et al. Among authors: fridmanis d. J Biol Chem. 2003 Dec 19;278(51):51521-6. doi: 10.1074/jbc.M307683200. Epub 2003 Sep 30. J Biol Chem. 2003. PMID: 14523020 Free article.

3

Unusual genomic structure: melanocortin receptors in Fugu.

Schiöth HB, Haitina T, Fridmanis D, Klovins J. Schiöth HB, et al. Among authors: fridmanis d. Ann N Y Acad Sci. 2005 Apr;1040:460-3. doi: 10.1196/annals.1327.090. Ann N Y Acad Sci. 2005. PMID: 15891089 Review.

4

Formation of new genes explains lower intron density in mammalian Rhodopsin G protein-coupled receptors.

Fridmanis D, Fredriksson R, Kapa I, Schiöth HB, Klovins J. Fridmanis D, et al. Mol Phylogenet Evol. 2007 Jun;43(3):864-80. doi: 10.1016/j.ympev.2006.11.007. Epub 2006 Nov 17. Mol Phylogenet Evol. 2007. PMID: 17188520

5

Identification of domains responsible for specific membrane transport and ligand specificity of the ACTH receptor (MC2R).

Fridmanis D, Petrovska R, Kalnina I, Slaidina M, Peculis R, Schiöth HB, Klovins J. Fridmanis D, et al. Mol Cell Endocrinol. 2010 Jun 10;321(2):175-83. doi: 10.1016/j.mce.2010.02.032. Epub 2010 Mar 3. Mol Cell Endocrinol. 2010. PMID: 20206229

6

Single nucleotide polymorphisms of the purinergic 1 receptor are not associated with myocardial infarction in a Latvian population.

Ignatovica V, Latkovskis G, Peculis R, Megnis K, Schioth HB, Vaivade I, Fridmanis D, Pirags V, Erglis A, Klovins J. Ignatovica V, et al. Among authors: fridmanis d. Mol Biol Rep. 2012 Feb;39(2):1917-25. doi: 10.1007/s11033-011-0938-4. Epub 2011 Jun 4. Mol Biol Rep. 2012. PMID: 21643756

7

Stronger association of common variants in TCF7L2 gene with nonobese type 2 diabetes in the Latvian population.

Kalnina I, Geldnere K, Tarasova L, Nikitina-Zake L, Peculis R, Fridmanis D, Pirags V, Klovins J. Kalnina I, et al. Among authors: fridmanis d. Exp Clin Endocrinol Diabetes. 2012 Sep;120(8):466-8. doi: 10.1055/s-0032-1306298. Epub 2012 Mar 22. Exp Clin Endocrinol Diabetes. 2012. PMID: 22441719

8

Association of genetic variation in the organic cation transporters OCT1, OCT2 and multidrug and toxin extrusion 1 transporter protein genes with the gastrointestinal side effects and lower BMI in metformin-treated type 2 diabetes patients.

Tarasova L, Kalnina I, Geldnere K, Bumbure A, Ritenberga R, Nikitina-Zake L, Fridmanis D, Vaivade I, Pirags V, Klovins J. Tarasova L, et al. Among authors: fridmanis d. Pharmacogenet Genomics. 2012 Sep;22(9):659-66. doi: 10.1097/FPC.0b013e3283561666. Pharmacogenet Genomics. 2012. PMID: 22735389

9

Identification of glyoxalase 1 polymorphisms associated with enzyme activity.

Peculis R, Konrade I, Skapare E, Fridmanis D, Nikitina-Zake L, Lejnieks A, Pirags V, Dambrova M, Klovins J. Peculis R, et al. Among authors: fridmanis d. Gene. 2013 Feb 15;515(1):140-3. doi: 10.1016/j.gene.2012.11.009. Epub 2012 Nov 29. Gene. 2013. PMID: 23201419

10

The association of common SNPs and haplotypes in CETP gene with HDL cholesterol levels in Latvian population.

Radovica I, Fridmanis D, Vaivade I, Nikitina-Zake L, Klovins J. Radovica I, et al. Among authors: fridmanis d. PLoS One. 2013 May 13;8(5):e64191. doi: 10.1371/journal.pone.0064191. Print 2013. PLoS One. 2013. PMID: 23675527 Free PMC article.

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