Minarik G - Search Results

1

Thiopurine S-Methyltransferase gene polymorphisms in a healthy Slovak population and pediatric patients with inflammatory bowel disease.

Chocholova A, Soltysova A, Minarik G, Cierna I, Sufliarska S, Mladosievicova B. Chocholova A, et al. Among authors: minarik g. Nucleosides Nucleotides Nucleic Acids. 2013;32(5):239-46. doi: 10.1080/15257770.2013.776685. Nucleosides Nucleotides Nucleic Acids. 2013. PMID: 23581716

2

Establishing the method of chimerism monitoring after allogeneic stem cell transplantation using multiplex polymerase chain reaction amplification of short tandem repeat markers and Amelogenin.

Sufliarska S, Minarik G, Horakova J, Bodova I, Bojtarova E, Czako B, Mistrik M, Drgona L, Demitrovicova M, Lakota J, Krivosikova M, Kovacs L. Sufliarska S, et al. Among authors: minarik g. Neoplasma. 2007;54(5):424-30. Neoplasma. 2007. PMID: 17688372

3

APEX microarray panel for genotyping polymorphisms in cancer chemotherapy and estimation frequencies in a Slovak population.

Soltysova A, Minarik G, Dzurenkova A, Sufliarska S, Kadasi L, Turna J, Mladosievicova B. Soltysova A, et al. Among authors: minarik g. Pharmacogenomics. 2011 Apr;12(4):577-92. doi: 10.2217/pgs.10.199. Pharmacogenomics. 2011. PMID: 21521029

4

Association of CD33 rs3865444:C˃A polymorphism with a reduced risk of late-onset Alzheimer's disease in Slovaks is limited to subjects carrying the APOE ε4 allele.

Javor J, Ďurmanová V, Párnická Z, Minárik G, Králová M, Pečeňák J, Vašečková B, Režnáková V, Šutovský S, Gmitterová K, Hromádka T, Peterajová Ľ, Shawkatová I. Javor J, et al. Among authors: minarik g. Int J Immunogenet. 2020 Oct;47(5):397-405. doi: 10.1111/iji.12489. Epub 2020 Apr 24. Int J Immunogenet. 2020. PMID: 32333488

5

Monosomy 3 Influences Epithelial-Mesenchymal Transition Gene Expression in Uveal Melanoma Patients; Consequences for Liquid Biopsy.

Soltysova A, Sedlackova T, Dvorska D, Jasek K, Chokhachi Baradaran P, Horvathova Kajabova V, Demkova L, Buocikova V, Kurucova T, Lyskova D, Furdova A, Minarik G, Babal P, Dankova Z, Smolkova B. Soltysova A, et al. Among authors: minarik g. Int J Mol Sci. 2020 Dec 17;21(24):9651. doi: 10.3390/ijms21249651. Int J Mol Sci. 2020. PMID: 33348918 Free PMC article.

6

Detection of His1069Gln mutation in Wilson disease by bidirectional PCR amplification of specific alleles (BI-PASA) test.

Poláková H, Katrincsáková B, Minárik G, Feráková E, Ficek A, Baldovic M, Kádasi L. Poláková H, et al. Among authors: minarik g. Gen Physiol Biophys. 2007 Jun;26(2):91-6. Gen Physiol Biophys. 2007. PMID: 17660582

7

Identification of the deletions in the UGT1A1 gene of the patients with Crigler-Najjar syndrome type I from Slovakia.

Zmetáková I, Ferák V, Minárik G, Ficek A, Poláková H, Feráková E, Kádasi L. Zmetáková I, et al. Among authors: minarik g. Gen Physiol Biophys. 2007 Dec;26(4):306-10. Gen Physiol Biophys. 2007. PMID: 18281749

8

Mutation analysis of the CFTR gene in Slovak cystic fibrosis patients by DHPLC and subsequent sequencing: identification of four novel mutations.

Kolesár P, Minárik G, Baldovic M, Ficek A, Kovács L, Kádasi L. Kolesár P, et al. Among authors: minarik g. Gen Physiol Biophys. 2008 Dec;27(4):299-305. Gen Physiol Biophys. 2008. PMID: 19202204

9

Prevalence of DFNB1 mutations in Slovak patients with non-syndromic hearing loss.

Minárik G, Tretinárová D, Szemes T, Kádasi L. Minárik G, et al. Int J Pediatr Otorhinolaryngol. 2012 Mar;76(3):400-3. doi: 10.1016/j.ijporl.2011.12.020. Epub 2012 Jan 26. Int J Pediatr Otorhinolaryngol. 2012. PMID: 22281373

10

Genetic polymorphisms related to testosterone metabolism in intellectually gifted boys.

Celec P, Tretinárová D, Minárik G, Ficek A, Szemes T, Lakatošová S, Schmidtová E, Turňa J, Kádaši Ľ, Ostatníková D. Celec P, et al. Among authors: minarik g. PLoS One. 2013;8(1):e54751. doi: 10.1371/journal.pone.0054751. Epub 2013 Jan 30. PLoS One. 2013. PMID: 23382957 Free PMC article.

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