Škereňová M - Search Results

1

Low Variability and Stable Frequency of Common Haplotypes of the TP53 Gene Region in Colorectal Cancer Patients in a Slovak Population.

Škereňová M, Halašová E, Matáková T, Jesenská Ľ, Jurečeková J, Šarlinová M, Čierny D, Dobrota D. Škereňová M, et al. Anticancer Res. 2017 Apr;37(4):1901-1907. doi: 10.21873/anticanres.11528. Anticancer Res. 2017. PMID: 28373458

2

Variability of GP6 gene in patients with sticky platelet syndrome and deep venous thrombosis and/or pulmonary embolism.

Kotuličová D, Chudý P, Škereňová M, Ivanková J, Dobrotová M, Kubisz P. Kotuličová D, et al. Among authors: skerenova m. Blood Coagul Fibrinolysis. 2012 Sep;23(6):543-7. doi: 10.1097/MBC.0b013e328355a808. Blood Coagul Fibrinolysis. 2012. PMID: 22821001

3

Platelet aggregation abnormalities in patients with fetal losses: the GP6 gene polymorphism.

Sokol J, Biringer K, Skerenova M, Hasko M, Bartosova L, Stasko J, Danko J, Kubisz P. Sokol J, et al. Among authors: skerenova m. Fertil Steril. 2012 Nov;98(5):1170-4. doi: 10.1016/j.fertnstert.2012.07.1108. Epub 2012 Aug 14. Fertil Steril. 2012. PMID: 22901851 Free article.

4

The prevalence of the platelet glycoprotein VI polymorphisms in patients with sticky platelet syndrome and ischemic stroke.

Kubisz P, Ivanková J, Škereňová M, Staško J, Hollý P. Kubisz P, et al. Among authors: skerenova m. Hematology. 2012 Nov;17(6):355-62. doi: 10.1179/1024533212Z.000000000142. Hematology. 2012. PMID: 23168074 Free article.

5

Association of specific diplotypes defined by common rs1800682 and rare rs34995925 single nucleotide polymorphisms within the STAT1 transcription binding site of the FAS gene promoter with preeclampsia.

Lasabova Z, Zigo I, Svecova I, Szabo G, Stanclova A, Skerenova M, Zubor P, Biskupska-Bodova K, Rigo J, Nagy B, Danko J. Lasabova Z, et al. Among authors: skerenova m. Gen Physiol Biophys. 2014;33(2):199-204. doi: 10.4149/gpb_2013081. Epub 2014 Jan 22. Gen Physiol Biophys. 2014. PMID: 24448373

6

Mismatch repair gene polymorphisms and association with lung cancer development.

Slováková P, Majerová L, Matáková T, Skereňová M, Kavcová E, Halašová E. Slováková P, et al. Among authors: skerenova m. Adv Exp Med Biol. 2015;833:15-22. doi: 10.1007/5584_2014_83. Adv Exp Med Biol. 2015. PMID: 25252909

7

Polymorphisms of DNA repair genes and lung cancer in chromium exposure.

Sarlinova M, Majerova L, Matakova T, Musak L, Slovakova P, Skereňová M, Kavcová E, Halašová E. Sarlinova M, et al. Among authors: skerenova m. Adv Exp Med Biol. 2015;833:1-8. doi: 10.1007/5584_2014_82. Adv Exp Med Biol. 2015. PMID: 25300687

8

Genetic variants in interleukin 7 receptor α chain (IL-7Ra) are associated with multiple sclerosis risk and disability progression in Central European Slovak population.

Čierny D, Hányšová S, Michalik J, Kantorová E, Kurča E, Škereňová M, Lehotský J. Čierny D, et al. Among authors: skerenova m. J Neuroimmunol. 2015 May 15;282:80-4. doi: 10.1016/j.jneuroim.2015.03.010. Epub 2015 Mar 18. J Neuroimmunol. 2015. PMID: 25903732

9

Associations of CYP1A2 Polymorphisms with the Risk Haplotypes in Lung Cancer in the Slovak Population.

Matakova T, Halasova E, Dzian A, Hruby R, Halasa M, Javorka K, Skerenova M. Matakova T, et al. Among authors: skerenova m. Adv Exp Med Biol. 2016;911:23-32. doi: 10.1007/5584_2016_220. Adv Exp Med Biol. 2016. PMID: 26987327

10

Polymorphisms of Selected DNA Repair Genes and Lung Cancer in Chromium Exposure.

Halasova E, Matakova T, Skerenova M, Krutakova M, Slovakova P, Dzian A, Javorkova S, Pec M, Kypusova K, Hamzik J. Halasova E, et al. Among authors: skerenova m. Adv Exp Med Biol. 2016;911:17-22. doi: 10.1007/5584_2016_218. Adv Exp Med Biol. 2016. PMID: 26987333

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