Characterization of homozygous deletions in laryngeal squamous cell carcinoma cell lines.
Giefing M, Martin-Subero JI, Kiwerska K, Jarmuz M, Grenman R, Siebert R, Szyfter K;
Cancer Genet Cytogenet, 2008, 18 4(1): 38-43.
Publications
Publikacje pracowników w ePub
Consistent chromosome abnormalities identify novel polymicrogyria loci in 1p36.3, 2p16-p23.1, 4q21.21-q22.1, 6q26-q27 and 21q2.
Dobnys WB, Mirzaa G, Christian SL, Petras K, Roseberry J, Clark GD, Curry CJR, McDonald-McGinn D, Medne L, Zackai E, Parsons J, Zand DJ, Hisama FM, Wals ChA, Leventer RJ, Martin ChL, Gajęcka M, Shaffer LG;
Am J Med Genet A, 2008, 146A: 1637-1654.
Interactions among activity of glucose-6-phosphate dehydrogenase in immature oocytes, expression of apoptosis-related genes Bcl-2 and Bax, and developmental competence following IVP in cattle.
Opiela J, Katska-Ksiazkiewicz L, Lipiński D, Słomski R, Bzowska M, Ryńska B;
Theriogenology, 2008, 69(5): 546-555.
Heterozygous carriers of the I171V mutation of the NBS1 gene have a significantly increased risk of solid malignant tumours.
Nowak J, Mosor M, Ziółkowska I, Wierzbicka M, Pernak-Schwarz M, Przyborska M, Roznowski K, Pławski A, Słomski R, Januszkiewicz D;
Eur J Cancer, 2008, 44 (4): 627-630.
Thyroid cancer in two siblings with FAP syndrome and APC mutation.
Brozek I, Plawski A, Podralska M, Kanka C, Slomski R, Limon J;
Int J Colorectal Dis, 2008, 23 (3): 331-332.
Sequence analysis of 21 genes located in the Kartagener syndrome linkage region on chromosome 15q.
Geremek M, Schoenmaker F, Zietkiewicz E, Pogorzelski A, Diehl S, Wijmenga C, Witt M;
Eur J Hum Genet, 2008, 16 (6): 688-695.
Successful pregnancy after preimplantation genetic diagnosis for carrier of t(2;7)(p11.2;q22) with high rates of unbalanced sperm and embryos: a case report.
Wiland E, Hobel CJ, Hill D, Kurpisz M;
Prenat Diagn, 2008, 28 (1): 36-41.
Proinflammatory cytokines as an intermediate factor enhancing lipid sperm membrane peroxidation in in vitro conditions.
Fraczek M, Sanocka D, Kamieniczna M, Kurpisz M;
J Androl, 2008, 29 (1): 85-92.
The role of genetic factor in etiopathogenesis of squamous cell carcinoma of the head and neck in young adults.
Gawecki W, Kostrzewska-Poczekaj M, Gajecka M, Milecki P, Szyfter K, Szyfter W;
Eur Arch Otorhinolaryngol, 2007, 264 (12): 1459-1465.
Recurrent APC gene mutations in Polish FAP families.
Pławski A, Podralska M, Słomski R;
Hered Cancer Clin Pract, 2007, 5 (4): 195-198