The molecular background of autoimmune endocrine disorders.
Fichna M, Zurawek M;
Adv Clin Exp Med, 2007; 16: 549-559.
Publikacje
Publikacje pracowników w ePub
GCK and HNF1alpha mutations and polymorphisms in Polish women with gestational diabetes.
Zurawek M, Wender-Ozegowska E, Januszkiewicz-Lewandowska D, Zawiejska A, Nowak J;
Diabetes Res Clin Pract, 2007; 76 (1): 157-158.
Identification of cryptic imbalance in phenotypically normal and abnormal translocation carriers.
Gajęcka M, Glotzbach CD, Jarmuż M, Ballif BC, Shaffer LG;
Eur J Hum Genet, 2006, 14 (12): 1255-1262.
Myoblast preparation for transplantation into injured myocardium.
Seidel M, Rozwadowska N, Tomczak K, Kurpisz M;
European Heart Journal, 2006, 8, suppl. H: H8-H15.
The effect of aryl hydrocarbon receptor ligands on the expression of AhR, ahRR, ARNT, Hiflalfa, CYP1A1 and NQO1 genes in rat liver.
Brauze D, Widerak M, Cwykiel M, Szyfter K, Baer-Dubowska W;
Toxicol Lett, 2006, 167: 3: 212-220.
Podstawy badania genetycznego w andrologii i poradnictwie.
Wiland E, Midro AT, Kurpisz M;
In: "Andrologia" PZWL, W-wa, wyd. II, 2006 (red. M. Semczuk, M. Kurpisz): 204-214.
Regional distribution of heterozygous 657del5 mutation carriers of the NBS1 gene in Wielkopolska province (Poland).
Ziółkowska I, Mosor M, Nowak J;
J Appl Genet, 2006, 47 (3): 269-272.
Molekularne metody diagnostyki i oceny efektywności terapii we współczesnej hematoonkologii pediatrycznej.
Dawidowska M, Wachowiak J, Witt M;
Post Bioch, 2006; 52: 408-416.
Identification of sequence motifs at the breakpoint junctions in three t(1:9)(p36.3;q34) and delineation of mechanisms involved in generating balanced translocations.
Gajęcka M, Pavlicek A, Glotzbach CD, Ballif BC, Jarmuż M, Jurka J, Shaffer LG;
Hum Genet, 2006, 120 (4): 519-526.
Evidence for involvement of TRE-2 (USP6) oncogene, low-copy repeat and acrocentric heterochromatin in two families with chromosomal translocations.
Ou Z, Jarmuż M, Sparagana SP, Michaud J, Decarie JC, Yatsenko SA, Nowakowska B, Furman P, Shaw CA, Shaffer LG, Lupski JR, Chinault AC, Cheung, SW, Stankiewicz P;
Hum Genet, 2006, 120 (2): 227-237.