Ołdak M - Search Results

1

Isolation and culture of human primary keratinocytes-a methods review.

Ścieżyńska A, Nogowska A, Sikorska M, Konys J, Karpińska A, Komorowski M, Ołdak M, Malejczyk J. Ścieżyńska A, et al. Among authors: oldak m. Exp Dermatol. 2019 Feb;28(2):107-112. doi: 10.1111/exd.13860. Epub 2019 Jan 14. Exp Dermatol. 2019. PMID: 30548893 Review.

2

[Signal transduction mechanisms induced by epidermal growth factor receptor (EGFR) and their role in apoptosis regulation].

Ołdak M, Malejczyk J. Ołdak M, et al. Postepy Hig Med Dosw. 1999;53(2):315-29. Postepy Hig Med Dosw. 1999. PMID: 10355296 Review. Polish.

3

Clinical aspects of disrupted Hedgehog signaling (Review).

Oldak M, Grzela T, Lazarczyk M, Malejczyk J, Skopinski P. Oldak M, et al. Int J Mol Med. 2001 Oct;8(4):445-52. Int J Mol Med. 2001. PMID: 11562786 Review.

4

Natural cell-mediated cytotoxicity of peripheral blood lymphocytes against target cells transfected with epidermodysplasia verruciformis-specific human papillomavirus type 8 L1 DNA sequences.

Oldak M, Majewski S, Grzela T, Stark S, Malejczyk M, Osiecka-Iwan A, Fuchs PG, Jablonska S, Pfister HJ, Malejczyk J. Oldak M, et al. Int J Mol Med. 2004 Jan;13(1):187-91. Int J Mol Med. 2004. PMID: 14654993

5

Human papillomavirus type 8 E2 protein unravels JunB/Fra-1 as an activator of the beta4-integrin gene in human keratinocytes.

Oldak M, Maksym RB, Sperling T, Yaniv M, Smola H, Pfister HJ, Malejczyk J, Smola S. Oldak M, et al. J Virol. 2010 Feb;84(3):1376-86. doi: 10.1128/JVI.01220-09. Epub 2009 Nov 18. J Virol. 2010. PMID: 19923172 Free PMC article.

6

Association of UDP-glucuronosyltransferase 1A9 (UGT1A9) gene polymorphism with kidney allograft function.

Pazik J, Ołdak M, Dąbrowski M, Lewandowski Z, Sitarek E, Podgórska M, Ważna E, Płoski R, Szmidt J, Chmura A, Durlik M, Malejczyk J. Pazik J, et al. Among authors: oldak m. Ann Transplant. 2011 Oct-Dec;16(4):69-73. doi: 10.12659/aot.882221. Ann Transplant. 2011. PMID: 22210424

7

Late-onset lattice corneal dystrophy without typical lattice lines caused by a novel mutation in the TGFBI gene.

Ołdak M, Szaflik JP, Ścieżyńska A, Udziela M, Maksym RB, Rymgayłło-Jankowska B, Hofmann-Rummelt C, Menzel-Severing J, Płoski R, Żarnowski T, Kruse FE, Szaflik J. Ołdak M, et al. Cornea. 2014 Mar;33(3):294-9. doi: 10.1097/ICO.0000000000000062. Cornea. 2014. PMID: 24473223

8

Evidence against RAB40AL being the locus for Martin-Probst X-linked deafness-intellectual disability syndrome.

Ołdak M, Ścieżyńska A, Młynarski W, Borowiec M, Ruszkowska E, Szulborski K, Pollak A, Kosińska J, Mueller-Malesińska M, Stawiński P, Szaflik JP, Płoski R. Ołdak M, et al. Hum Mutat. 2014 Oct;35(10):1171-4. doi: 10.1002/humu.22620. Epub 2014 Aug 7. Hum Mutat. 2014. PMID: 25044830

9

Recipient uridine 5'-diphospho-glucuronosyltransferase UGT1A9 c.98T>C variant determines transplanted kidney filtration rate.

Pazik J, Ołdak M, Lewandowski Z, Dąbrowski M, Podgórska M, Sitarek E, Malejczyk J, Płoski R, Durlik M. Pazik J, et al. Among authors: oldak m. Transplant Proc. 2014 Oct;46(8):2678-82. doi: 10.1016/j.transproceed.2014.09.077. Transplant Proc. 2014. PMID: 25380893

10

Fuchs Endothelial Corneal Dystrophy: Strong Association with rs613872 Not Paralleled by Changes in Corneal Endothelial TCF4 mRNA Level.

Ołdak M, Ruszkowska E, Udziela M, Oziębło D, Bińczyk E, Ścieżyńska A, Płoski R, Szaflik JP. Ołdak M, et al. Biomed Res Int. 2015;2015:640234. doi: 10.1155/2015/640234. Epub 2015 Sep 16. Biomed Res Int. 2015. PMID: 26451375 Free PMC article.

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