Multiple trichoepitheliomas--a novel mutation in the CYLD gene.
Amaro C, Freitas I, Lamarão P, Afonso A, Skrzypczak M, Heinritz W. J Eur Acad Dermatol Venereol.
J Eur Acad Dermatol Venereol. 2010 Jul;24(7):844-6
Publikacje
Publikacje pracowników w ePub
Genotoxicity assessment of chromium(III) propionate complex in the rat model using the comet assay.
Staniek H, Kostrzewska-Poczekaj M, Arndt M, Szyfter K, Krejpcio Z;
Food Chem Toxicol, 2010, 48 (1): 89-92.
HLA-DQA1*0505 sharing and killer immunoglobulin-like receptors in sub fertile couples: report from the 15th International Histocompatibility Workshop.
Varla-Leftherioti M, Keramitsoglou T, Parapanissiou E, Kurpisz M, Kontopoulou-Antonopoulou V, Tsekoura C, Kamieniczna M, Novokowska B, Paparistidis N, Vrani V, Daniilidis M, Spyropoulou-Vlachou M;
Tissue Antigens, 2010, 75 (6): 6686-72.
Self-incompatibility alleles in Polish wild pear (Pyrus pyraster (L.) Burgsd.): a preliminary analysis.
Wolko Ł, Antkowiak W, Sips M, Słomski R.
J Appl Genet. 2010;51(1):33-5.
Association of c.802C>T polymorphism of NOD2/CARD15 gene with the chronic gastritis and predisposition to cancer in H. pylori infected patients.
Hnatyszyn A, Szalata M, Stanczyk J, Cichy W, Slomski R.
Exp Mol Pathol. 2010 Jun;88(3):388-93.
Combined iPLEX and TaqMan assays to screen for 45 common mutations in Lynch syndrome and FAP patients.
Dymerska D, Serrano-Fernández P, Suchy J, Pławski A, Słomski R, Kaklewski K, Scott RJ, Gronwald J, Kładny J, Byrski T, Huzarski T, Lubiński J, Kurzawski G;
J Mol Diagn, 2010, 12 (1): 82-90.
SDF1-3' A gene polymorphism is associated with laryngeal cancer.
Kruszyna Ł, Lianeri M, Rydzanicz M, Szyfter K, Jagodziński PP;
Pathol Oncol Res, 2010, 16 (2): 223-227.
Megakaryocytic blast crisis in a chronic myeloid leukemia patient with a rare variant of Philadelphia rearrangement t(9;22;22) and a constitutional translocation t(3;7).
Jarmuz M, Kroll R, Przybyłowicz-Chalecka A, Ratajczak B, Gniot M, Szyfter K, Komarnicki M;
Cancer Genet Cytogenet, 2010, 199 (1): 45-47.
A simple method of investigating mutations in CHEK2 by DHPLC: a study of the German populations of Saxony, Saxony-Anhalt, and Thuringia.
Scharrer U, Skrzypczak-Zielinska M, Wituszynska W, Mierzejewski M, Krause K, Cybulski C, Froster UG;
Cancer Genet Cytogenet, 2010, 199 (1): 48-52.
A coding variant in NLRP1 is associated with autoimmune Addison's disease.
Zurawek M, Fichna M, Januszkiewicz-Lewandowska D, Gryczyńska M, Fichna P, Nowak J;
Hum Immunol, 2010, 7: 530-534.