Application of proteomic methods for identification of sperm immunogenic antigens.
Domagała A, Pulido S, Kurpisz M, Herr JC;
Molecular Human Reproduction, 2007, 13 (7): 437-444.
Publikacje
Publikacje pracowników w ePub
Different chromosomal breakpoints impact the level of LMO2 expression in T-ALL.
Dik WA, Nadel B, Przybylski GK, Asnafi V, Grabarczyk P, Navarro JM, Verhaaf B, Schmidt ChA, Macintyre EA, van Dongen JJM, Langerak AW;
Blood, 2007, 110, 1: 388-392.
I171V germline mutation in the NBS1 gene significantly increases.
Rożnowski K, Januszkiewicz-Lewandowska D, Mosor M, Pernak M, Litwiniuk M, Nowak J;
Breast Cancer Res Treat, 2007, 110 (2): 343-348.
Polymorphisms of the human PUMILIO2 gene and male sterility.
Kusz K, Ginter-Matuszewska B, Ziolkowska K, Spik A, Bierla J, Jedrzejczak P, Latos-Bielenska A, Pawelczyk L, Jaruzelska J;
Mol Reprod Dev, 2007, 74 (6): 795-799.
Inhibition of BCL11B expression leads to apoptosis of malignant but not normal mature T cells.
Grabarczyk P, Przybylski GK, Depke M, Volker U, Bahr J, Assmus K, Broker BM, Walther R, Schmidt CA;
Oncogene, 26 (26): 3797-3810.
Effects of age and gender on micronucleus and chromosome nondisjunction frequencies in centenarians and younger subjects.
Wojda A, Ziętkiewicz E, Witt M;
Mutagenesis, 2007, 22 (3): 195-200.
Polymorphisms in base-excision repair and nucleotide-excision repair genes in relation to lung cancer risk.
De Ruyck K, Szaumkessel M, De Rudder I, Dehoorne A, Vral A, Claes K, Velghe A, Van Meerbeeck J, Thierens H;
Mutat Res, 2007,, 631 (2): 101-110.
The AAPC case, with an early onset of colorectal cancer.
Plawski A, Nowakowska D, Podralska M, Lipinski D, Steffen J, Slomski R;
Int J Colorectal Dis, 2007, 22 (4): 449-451.
The effect of novel recombination between gene NKX2-5 and the TRD locus in T-cell acute lymphoblastic leukemia on activation of the NKX2-5 gene.
Przybylski GK, Dik WA, Grabarczyk P, Wanzeck J, Chudobska P, Jankowski K, von Bergh A, van Dongen JJM, Schmidt ChA, Langerak AW;
Haematologica, 2006, 91 (3): 317-321.
The analysis of meiotic segregation patterns and aneuploidy in the spermatozoa of father and son with translocation t(4;5)(p15.1;p12) and the prediction of the individual probability rate for unbalanced progeny at birth.
Wiland E, Midro AT, Panasiuk B, Kurpisz M;
J Androl. 2007, 28 (2): 262-272.