Nagy N - Search Results

1

Somatic mosaicism of the PIK3CA gene identified in a Hungarian girl with macrodactyly and syndactyly.

Tripolszki K, Knox R, Parker V, Semple R, Farkas K, Sulák A, Horváth E, Széll M, Nagy N. Tripolszki K, et al. Among authors: nagy n. Eur J Med Genet. 2016 Apr;59(4):223-6. doi: 10.1016/j.ejmg.2016.02.002. Epub 2016 Feb 3. Eur J Med Genet. 2016. PMID: 26851524 Free article.

2

The expression of keratinocyte growth factor receptor (FGFR2-IIIb) correlates with the high proliferative rate of HaCaT keratinocytes.

Nagy N, Bata-Csörgo Z, Kopasz N, Szeg C, Pivarcsi A, Koreck A, Dobozy A, Kemény L, Széll M. Nagy N, et al. Exp Dermatol. 2006 Aug;15(8):596-605. doi: 10.1111/j.1600-0625.2006.00450.x. Exp Dermatol. 2006. PMID: 16842598

3

The Arg160Trp allele of melanocortin-1 receptor gene might protect against vitiligo.

Széll M, Baltás E, Bodai L, Bata-Csörgo Z, Nagy N, Dallos A, Pourfarzi R, Simics E, Kondorosi I, Szalai Z, Tóth GK, Hunyadi J, Dobozy A, Kemény L. Széll M, et al. Among authors: nagy n. Photochem Photobiol. 2008 May-Jun;84(3):565-71. doi: 10.1111/j.1751-1097.2008.00296.x. Epub 2008 Feb 11. Photochem Photobiol. 2008. PMID: 18282185

4

The altered expression of syndecan 4 in the uninvolved skin of venous leg ulcer patients may predispose to venous leg ulcer.

Nagy N, Németh IB, Szabad G, Szolnoky G, Belsõ N, Bata-Csörgõ Z, Dobozy A, Kemény L, Széll M. Nagy N, et al. Wound Repair Regen. 2008 Jul-Aug;16(4):495-502. doi: 10.1111/j.1524-475X.2008.00394.x. Wound Repair Regen. 2008. PMID: 18638267

5

The anti-apoptotic protein G1P3 is overexpressed in psoriasis and regulated by the non-coding RNA, PRINS.

Szegedi K, Sonkoly E, Nagy N, Németh IB, Bata-Csörgo Z, Kemény L, Dobozy A, Széll M. Szegedi K, et al. Among authors: nagy n. Exp Dermatol. 2010 Mar;19(3):269-78. doi: 10.1111/j.1600-0625.2010.01066.x. Exp Dermatol. 2010. PMID: 20377629

6

A newly identified missense mutation of the HR gene is associated with a novel, unusual phenotype of Marie Unna Hereditary Hypotrichosis 1 including limb deformities.

Farkas K, Nagy N, Kinyó A, Kemény L, Széll M. Farkas K, et al. Among authors: nagy n. Arch Dermatol Res. 2012 Oct;304(8):679-81. doi: 10.1007/s00403-012-1244-2. Epub 2012 May 15. Arch Dermatol Res. 2012. PMID: 22584530

7

A novel missense mutation of the CYLD gene identified in a Hungarian family with Brooke-Spiegler syndrome.

Nagy N, Farkas K, Kinyo A, Nemeth IB, Kis E, Varga J, Bata-Csorgo Z, Kemeny L, Szell M. Nagy N, et al. Exp Dermatol. 2012 Dec;21(12):967-9. doi: 10.1111/exd.12040. Exp Dermatol. 2012. PMID: 23171463

8

A novel seven-base deletion of the CTSC gene identified in a Hungarian family with Papillon-Lefèvre syndrome.

Farkas K, Paschali E, Papp F, Vályi P, Széll M, Kemény L, Nagy N, Csoma Z. Farkas K, et al. Among authors: nagy n. Arch Dermatol Res. 2013 Jul;305(5):453-5. doi: 10.1007/s00403-013-1323-z. Epub 2013 Feb 10. Arch Dermatol Res. 2013. PMID: 23397598 Free article.

9

A mutational hotspot in CYLD causing cylindromas: a comparison of phenotypes arising in different genetic backgrounds.

Nagy N, Rajan N, Farkas K, Kinyó A, Kemény L, Széll M. Nagy N, et al. Acta Derm Venereol. 2013 Nov;93(6):743-5. doi: 10.2340/00015555-1590. Acta Derm Venereol. 2013. PMID: 23584127 Free PMC article. No abstract available.

10

A newly identified missense mutation of the EDA1 gene in a Hungarian patient with Christ-Siemens-Touraine syndrome.

Kinyó A, Vályi P, Farkas K, Nagy N, Gergely B, Tripolszki K, Török D, Bata-Csörgő Z, Kemény L, Széll M. Kinyó A, et al. Among authors: nagy n. Arch Dermatol Res. 2014 Jan;306(1):97-100. doi: 10.1007/s00403-013-1408-8. Epub 2013 Aug 30. Arch Dermatol Res. 2014. PMID: 23989902

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