Schioth HB - Search Results

1

The role of common and rare MC4R variants and FTO polymorphisms in extreme form of obesity.

Rovite V, Petrovska R, Vaivade I, Kalnina I, Fridmanis D, Zaharenko L, Peculis R, Pirags V, Schioth HB, Klovins J. Rovite V, et al. Among authors: schioth hb. Mol Biol Rep. 2014 Mar;41(3):1491-500. doi: 10.1007/s11033-013-2994-4. Epub 2014 Jan 3. Mol Biol Rep. 2014. PMID: 24385306

2

Association between a rare SNP in the second intron of human Agouti related protein gene and increased BMI.

Kalnina I, Kapa I, Pirags V, Ignatovica V, Schiöth HB, Klovins J. Kalnina I, et al. Among authors: schioth hb. BMC Med Genet. 2009 Jul 14;10:63. doi: 10.1186/1471-2350-10-63. BMC Med Genet. 2009. PMID: 19602223 Free PMC article.

3

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: schioth hb. 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

4

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: schioth hb. Gene. 2013 Sep 25;527(2):462-8. doi: 10.1016/j.gene.2013.06.079. Epub 2013 Jul 13. Gene. 2013. PMID: 23860325

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. Among authors: schioth hb. 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

Identification of somatostatin receptor type 5 gene polymorphisms associated with acromegaly.

Ciganoka D, Balcere I, Kapa I, Peculis R, Valtere A, Nikitina-Zake L, Lase I, Schiöth HB, Pirags V, Klovins J. Ciganoka D, et al. Among authors: schioth hb. Eur J Endocrinol. 2011 Oct;165(4):517-25. doi: 10.1530/EJE-11-0416. Epub 2011 Aug 2. Eur J Endocrinol. 2011. PMID: 21810856 Free PMC article.

7

Genome-wide analysis reveals DNA methylation markers that vary with both age and obesity.

Almén MS, Nilsson EK, Jacobsson JA, Kalnina I, Klovins J, Fredriksson R, Schiöth HB. Almén MS, et al. Among authors: schioth hb. Gene. 2014 Sep 10;548(1):61-7. doi: 10.1016/j.gene.2014.07.009. Epub 2014 Jul 8. Gene. 2014. PMID: 25010727 Free article.

8

Replacement of short segments within transmembrane domains of MC2R disrupts retention signal.

Fridmanis D, Petrovska R, Pjanova D, Schiöth HB, Klovins J. Fridmanis D, et al. Among authors: schioth hb. J Mol Endocrinol. 2014 Oct;53(2):201-15. doi: 10.1530/JME-14-0169. Epub 2014 Jul 29. J Mol Endocrinol. 2014. PMID: 25074265

9

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. Among authors: schioth hb. 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

10

Significantly altered peripheral blood cell DNA methylation profile as a result of immediate effect of metformin use in healthy individuals.

Elbere I, Silamikelis I, Ustinova M, Kalnina I, Zaharenko L, Peculis R, Konrade I, Ciuculete DM, Zhukovsky C, Gudra D, Radovica-Spalvina I, Fridmanis D, Pirags V, Schiöth HB, Klovins J. Elbere I, et al. Among authors: schioth hb. Clin Epigenetics. 2018 Dec 13;10(1):156. doi: 10.1186/s13148-018-0593-x. Clin Epigenetics. 2018. PMID: 30545422 Free PMC article. Clinical Trial.

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