Grolmusz VK - Search Results

1

Is HLA type a possible cancer risk modifier in Lynch syndrome?

Ahadova A, Witt J, Haupt S, Gallon R, Hüneburg R, Nattermann J, Ten Broeke S, Bohaumilitzky L, Hernandez-Sanchez A, Santibanez-Koref M, Jackson MS, Ahtiainen M, Pylvänäinen K, Andini K, Grolmusz VK, Möslein G, Dominguez-Valentin M, Møller P, Fürst D, Sijmons R, Borthwick GM, Burn J, Mecklin JP, Heuveline V, von Knebel Doeberitz M, Seppälä T, Kloor M. Ahadova A, et al. Among authors: grolmusz vk. Int J Cancer. 2023 May 15;152(10):2024-2031. doi: 10.1002/ijc.34312. Epub 2022 Oct 14. Int J Cancer. 2023. PMID: 36214792 Free article. Review.

2

A common genetic variation in GZMB may associate with cancer risk in patients with Lynch syndrome.

Grolmusz VK, Nagy P, Likó I, Butz H, Pócza T, Bozsik A, Papp J, Oláh E, Patócs A. Grolmusz VK, et al. Front Oncol. 2023 Feb 20;13:1005066. doi: 10.3389/fonc.2023.1005066. eCollection 2023. Front Oncol. 2023. PMID: 36890824 Free PMC article.

3

Reclassification of Five BRCA1/2 Variants with Unknown Significance Using Complex Functional Study.

Bozsik A, Papp J, Grolmusz VK, Patócs A, Oláh E, Butz H. Bozsik A, et al. Among authors: grolmusz vk. Cancer Res Treat. 2022 Oct;54(4):970-984. doi: 10.4143/crt.2021.1078. Epub 2022 Feb 8. Cancer Res Treat. 2022. PMID: 35167739 Free PMC article.

4

Germline Structural Variations in Cancer Predisposition Genes.

Pócza T, Grolmusz VK, Papp J, Butz H, Patócs A, Bozsik A. Pócza T, et al. Among authors: grolmusz vk. Front Genet. 2021 Apr 14;12:634217. doi: 10.3389/fgene.2021.634217. eCollection 2021. Front Genet. 2021. PMID: 33936164 Free PMC article. Review.

5

Cell cycle dependent RRM2 may serve as proliferation marker and pharmaceutical target in adrenocortical cancer.

Grolmusz VK, Karászi K, Micsik T, Tóth EA, Mészáros K, Karvaly G, Barna G, Szabó PM, Baghy K, Matkó J, Kovalszky I, Tóth M, Rácz K, Igaz P, Patócs A. Grolmusz VK, et al. Am J Cancer Res. 2016 Sep 1;6(9):2041-2053. eCollection 2016. Am J Cancer Res. 2016. PMID: 27725909 Free PMC article.

6

PALB2 Variants Extend the Mutational Profile of Hungarian Patients with Breast and Ovarian Cancer.

Butz H, Nagy P, Papp J, Bozsik A, Grolmusz VK, Pócza T, Oláh E, Patócs A. Butz H, et al. Among authors: grolmusz vk. Cancers (Basel). 2023 Aug 31;15(17):4350. doi: 10.3390/cancers15174350. Cancers (Basel). 2023. PMID: 37686625 Free PMC article.

7

Lack of association between C385A functional polymorphism of the fatty acid amide hydrolase gene and polycystic ovary syndrome.

Grolmusz VK, Stenczer B, Fekete T, Szendei G, Patócs A, Rácz K, Reismann P. Grolmusz VK, et al. Exp Clin Endocrinol Diabetes. 2013 Jun;121(6):338-42. doi: 10.1055/s-0033-1337941. Epub 2013 Apr 24. Exp Clin Endocrinol Diabetes. 2013. PMID: 23616186 Clinical Trial.

8

The rs4844880 polymorphism in the promoter region of the HSD11B1 gene associates with bone mineral density in healthy and postmenopausal osteoporotic women.

Feldman K, Szappanos A, Butz H, Grolmusz V, Majnik J, Likó I, Kriszt B, Lakatos P, Tóth M, Rácz K, Patócs A. Feldman K, et al. Steroids. 2012 Nov;77(13):1345-51. doi: 10.1016/j.steroids.2012.08.014. Epub 2012 Sep 14. Steroids. 2012. PMID: 22986073

9

[Importance of the 11β-hydroxysteroid dehydrogenase enzyme in clinical disorders].

Feldman K, Likó I, Nagy Z, Szappanos A, Grolmusz VK, Tóth M, Rácz K, Patócs A. Feldman K, et al. Among authors: grolmusz vk. Orv Hetil. 2013 Feb 24;154(8):283-93. doi: 10.1556/OH.2013.29558. Orv Hetil. 2013. PMID: 23419529 Review. Hungarian.

10

Genetic variants of the HSD11B1 gene promoter may be protective against polycystic ovary syndrome.

Grolmusz VK, Acs OD, Feldman-Kovács K, Szappanos Á, Stenczer B, Fekete T, Szendei G, Reismann P, Rácz K, Patócs A. Grolmusz VK, et al. Mol Biol Rep. 2014 Sep;41(9):5961-9. doi: 10.1007/s11033-014-3473-2. Epub 2014 Jun 27. Mol Biol Rep. 2014. PMID: 24969481

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