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You are here: Home › Publikacje › Page 161

Publications

Publikacje pracowników w ePub

Identification of a novel polymorphism - the duplication of the NPHP1 (nephronophthisis 1) gene.

Baris H, Bejjani BA, Tan WH, Coulter DL, Martin JA, Storm AL, Burton BK, Saitta SC, Gajęcka M, Ballif BC, Irons MB, Shaffer LG, Kimonis VE;

Am J Med Genet, 2006, 140A: 1876-1879.

Amplification of hTERT and hTERC genes in leukemic cells with high expression and activity of telomerase.

Nowak T, Januszkiewicz D, Zawada M, Pernak M, Lewandowski K, Rembowska J, Nowicka K, Mańkowski P, Nowak J;

Oncol Rep, 2006, 16 (2): 301-305.

The influence of environmental exposure to complex mixtures including PAHs and lead on genotoxic effects in children living in Upper Silesia, Poland.

Mielżyńska D, Siwińska E, Kapka L, Szyfter K, Knudsen LE, Merlo DF;

Mutagenesis, 2006, 21 (5): 295-304.

Pattern of immunoglobulin and T-cell receptor (Ig/TCR) gene rearrangements in Polish pediatric acute lymphoblastic leukemia patients - implications for RQ-PCR-based assessment of minimal residual disease.

Dawidowska M, Derwich K, Szczepański T, Jółkowska J, van der Velden VHJ, Wachowiak J, Witt M;

Leukemia, 2006, 30: 1119-1125.

Transferase S-glutathione class pi gene (GSTP1) polymorphism in thyroid cancer patients.

Marciniak P, Drobnik K, Ziemnicka K, Gut P, Słomski R, Sowiński J;

Endokrynol Pol, 2006, 57 (5): 509-515.

Does loss of heterozygosity in critical genome regions predict a local relapse in patients after laryngectomy?

Szukała K, Sowińska A, Wierzbicka M, Biczysko W, Szyfter W, Szyfter K;

Mutat Res, 2006, 30; 60 0(1-2): 67-76.

Loop formation by the transgene WAP:6xHishGH in transgenic rabbit fibroblasts, revealed by fluorescence in situ hybridization to nuclear halos.

Michalak E, Lipiński D, Słomski R;

J Appl Genet, 2006, 47 (3): 24724-9.

Association of the heterozygous germline I171V mutation of the NBS1 gene with childhood acute lymphoblastic leukemia.

Mosor M, Ziółkowska I, Pernak-Schwarz M, Januszkiewicz-Lewandowska D, Nowak J;

Leukemia, 2006, 20 (8): 1454-1456.

Two novel preselenin 1 gene mutations connected with frontotemporal dementia-like clinical phenotype: genetic and bioinformatic assessment.

Zekanowski C, Golan MP, Krzyśko KA, Lipczyńska-Łojkowska W, Filipek S, Kowalska A, Rossa G, Pepłońska B, Styczyńska M, Maruszak A, Religa D, Wender M, Kulczycki J, Barcikowska M, Kuźnicki J;

Exp Neurol, 2006, 200: 82-88.

Chromosomal rearrangements involving the BCL3 locus are recurrent in classical Hodgkin and peripheral T-cell lymphoma.

Martin-Subero JI, Włodarska I, Bastard Ch, Picquenot M, Hoppner J, Giefing M, Klapper W, Siebert R;

Blood, 2006, 106, 1: 401-402.

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