Słomski R - Search Results

1

Two coexisting heterozygous frameshift mutations in PROP1 are responsible for a different phenotype of combined pituitary hormone deficiency.

Ziemnicka K, Budny B, Drobnik K, Baszko-Błaszyk D, Stajgis M, Katulska K, Waśko R, Wrotkowska E, Słomski R, Ruchała M. Ziemnicka K, et al. Among authors: slomski r. J Appl Genet. 2016 Aug;57(3):373-81. doi: 10.1007/s13353-015-0328-z. Epub 2015 Nov 25. J Appl Genet. 2016. PMID: 26608600 Free PMC article.

2

[Transferase S-glutathione class pi gene (GSTP1) polymorphism in thyroid cancer patients].

Marciniak P, Drobnik K, Ziemnicka K, Gut P, Słomski R, Sowiński J. Marciniak P, et al. Among authors: slomski r. Endokrynol Pol. 2006 Sep-Oct;57(5):509-15. Endokrynol Pol. 2006. PMID: 17133316 Polish.

3

Association analysis of vitamin D receptor gene polymorphisms with bone mineral density in young women with Graves' disease.

Horst-Sikorska W, Ignaszak-Szczepaniak M, Marcinkowska M, Kaczmarek M, Stajgis M, Slomski R. Horst-Sikorska W, et al. Among authors: slomski r. Acta Biochim Pol. 2008;55(2):371-80. Epub 2008 May 26. Acta Biochim Pol. 2008. PMID: 18506225

4

APC gene mutations causing familial adenomatous polyposis in Polish patients.

Plawski A, Slomski R. Plawski A, et al. Among authors: slomski r. J Appl Genet. 2008;49(4):407-14. doi: 10.1007/BF03195640. J Appl Genet. 2008. PMID: 19029688

5

Association between estrogen receptor alpha gene polymorphisms and bone mineral density in Polish female patients with Graves' disease.

Ignaszak-Szczepaniak M, Horst-Sikorska W, Dytfeld J, Gowin E, Słomski R, Stajgis M. Ignaszak-Szczepaniak M, et al. Among authors: slomski r. Acta Biochim Pol. 2011;58(1):101-9. Epub 2011 Mar 21. Acta Biochim Pol. 2011. PMID: 21423915

6

Expression of human growth hormone in the milk of transgenic rabbits with transgene mapped to the telomere region of chromosome 7q.

Lipinski D, Zeyland J, Szalata M, Plawski A, Jarmuz M, Jura J, Korcz A, Smorag Z, Pienkowski M, Slomski R. Lipinski D, et al. Among authors: slomski r. J Appl Genet. 2012 Nov;53(4):435-42. doi: 10.1007/s13353-012-0110-4. Epub 2012 Aug 17. J Appl Genet. 2012. PMID: 22898896 Free PMC article.

7

CCND1 gene polymorphic variants in patients with differentiated thyroid carcinoma.

Hryhorowicz S, Ziemnicka K, Kaczmarek-Ryś M, Hoppe-Gołębiewska J, Pławski A, Skrzypczak-Zielińska M, Szkudlarek M, Gołąb M, Budny B, Ruchała M, Słomski R. Hryhorowicz S, et al. Among authors: slomski r. Oncol Lett. 2015 Jan;9(1):442-448. doi: 10.3892/ol.2014.2617. Epub 2014 Oct 15. Oncol Lett. 2015. PMID: 25436006 Free PMC article.

8

The c.470 T > C CHEK2 missense variant increases the risk of differentiated thyroid carcinoma in the Great Poland population.

Kaczmarek-Ryś M, Ziemnicka K, Hryhorowicz ST, Górczak K, Hoppe-Gołębiewska J, Skrzypczak-Zielińska M, Tomys M, Gołąb M, Szkudlarek M, Budny B, Siatkowski I, Gut P, Ruchała M, Słomski R, Pławski A. Kaczmarek-Ryś M, et al. Among authors: slomski r. Hered Cancer Clin Pract. 2015 Mar 1;13(1):8. doi: 10.1186/s13053-015-0030-5. eCollection 2015. Hered Cancer Clin Pract. 2015. PMID: 25798211 Free PMC article.

9

Modifying impact of RET gene haplotypes on medullary thyroid carcinoma clinical course.

Kaczmarek-Ryś M, Ziemnicka K, Pławski A, Budny B, Michalak M, Hryhorowicz S, Hoppe-Gołębiewska J, Boruń P, Gołąb M, Czetwertyńska M, Sromek M, Szalata M, Ruchała M, Słomski R. Kaczmarek-Ryś M, et al. Among authors: slomski r. Endocr Relat Cancer. 2018 Apr;25(4):421-436. doi: 10.1530/ERC-17-0452. Epub 2018 Jan 31. Endocr Relat Cancer. 2018. PMID: 29386230

10

CFTR transcripts are undetectable in lymphocytes and respiratory epithelial cells of a CF patient homozygous for the nonsense mutation R553X.

Will K, Reiss J, Dean M, Schlösser M, Slomski R, Schmidtke J, Stuhrmann M. Will K, et al. Among authors: slomski r. J Med Genet. 1993 Oct;30(10):833-7. doi: 10.1136/jmg.30.10.833. J Med Genet. 1993. PMID: 7693946 Free PMC article.

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