Adrianna Mostowska
Department of Biochemistry and Molecular Biology
Poznan University of Medical Sciences
Poznan
Poland
Name/email consistency: high
- Association of DVL2 and AXIN2 gene polymorphisms with cleft lip with or without cleft palate in a polish population. Mostowska, A., Hozyasz, K.K., Wójcicki, P., Lasota, A., Dunin-Wilczyńska, I., Jagodziński, P.P. Birth Defects Res. Part A Clin. Mol. Teratol. (2012)
- Polymorphisms of stress-related genes and the risk of nonsyndromic cleft lip with or without cleft palate. Mostowska, A., Hozyasz, K.K., Wojcicka, K., Lianeri, M., Jagodzinski, P.P. Birth Defects Res. Part A Clin. Mol. Teratol. (2011)
- Polymorphisms in CHDH gene and the risk of tooth agenesis. Mostowska, A., Biedziak, B., Dunin-Wilczynska, I., Komorowska, A., Jagodzinski, P.P. Birth Defects Res. Part A Clin. Mol. Teratol. (2011)
- Association between genetic variants of reported candidate genes or regions and risk of cleft lip with or without cleft palate in the polish population. Mostowska, A., Hozyasz, K.K., Wojcicki, P., Biedziak, B., Paradowska, P., Jagodzinski, P.P. Birth Defects Res. Part A Clin. Mol. Teratol. (2010)
- Polymorphisms located in the region containing BHMT and BHMT2 genes as maternal protective factors for orofacial clefts. Mostowska, A., Hozyasz, K.K., Biedziak, B., Misiak, J., Jagodzinski, P.P. Eur. J. Oral Sci. (2010)
- Associations of folate and choline metabolism gene polymorphisms with orofacial clefts. Mostowska, A., Hozyasz, K.K., Wojcicki, P., Dziegelewska, M., Jagodzinski, P.P. J. Med. Genet. (2010)
- Polymorphic variants of genes encoding main antioxidant enzymes and the risk of CL/P-affected pregnancies. Mostowska, A., Hozyasz, K.K., Lianeri, M., Piwowar, W., Jagodzinski, P.P. Clin. Biochem. (2007)
- A novel mutation in PAX9 causes familial form of molar oligodontia. Mostowska, A., Biedziak, B., Trzeciak, W.H. Eur. J. Hum. Genet. (2006)
- Axis inhibition protein 2 (AXIN2) polymorphisms may be a risk factor for selective tooth agenesis. Mostowska, A., Biedziak, B., Jagodzinski, P.P. J. Hum. Genet. (2006)
- A novel c.581C>T transition localized in a highly conserved homeobox sequence of MSX1: is it responsible for oligodontia?. Mostowska, A., Biedziak, B., Trzeciak, W.H. J. Appl. Genet. (2006)
- Maternal MTR genotype contributes to the risk of non-syndromic cleft lip and palate in the Polish population. Mostowska, A., Hozyasz, K.K., Jagodzinski, P.P. Clin. Genet. (2006)
- Gene symbol: IRF6. Disease: Van der Woude syndrome. Mostowska, A., Wójcicki, P., Kobus, K., Trzeciak, W.H. Hum. Genet. (2005)









