Genetyczna różnorodność współczesnych populacji ludzkich.
Ziętkiewicz E;
W: Biologia molekularna w medycynie. Elementy genetyki klinicznej, (red. Bal J), Wydawnictwo Naukowe PWN, 2011, ISBN 978-83-01-16665-6: 50-67.
Publikacje
Publikacje pracowników w ePub
In vitro culturing of ciliary respiratory cells - a model for studies of genetic diseases.
Bukowy Z, Ziętkiewicz E, Witt M;
J Appl Genet, 2011, 52 (1): 39-51.
Weak association of anti-sperm antibodies and strong association of familial cryptorchidism/infertility with HLA-DRB1 polymorphisms in prepubertal Ukrainian boys.
Kurpisz M, Nakonechnyy A, Niepieklo-Miniewska W, Havrylyuk A, Kamieniczna M, Nowakowska B, Chopyak V, Kusnierczyk P;
Reprod Biol Endocrinol, 2011, 28 (9): 129.
NANOS1 and PUMILIO2 bind microRNA biogenesis factor GEMIN3, within chromatoid body in human germ cells.
Ginter-Matuszewska B, Kusz K, Spik A, Grzeszkowiak D, Rembiszewska A, Kupryjanczyk J, Jaruzelska J;
Histochem Cell Biol, 2011, 136 (3): 279-287.
Is the NBN gene mutation I171V a potential risk factor for malignant solid tumors in children?
Nowak J, Mosor M, Nowicka K, Rembowska J, Januszkiewicz D;
J Pediatr Hematol Oncol, 2011, 33 (6): e248-249.
Prevalence of the most frequent BRCA1 mutations in Polish population.
Brozek I, Cybulska C, Ratajska M, Piatkowska M, Kluska A, Balabas A, Dabrowska M, Nowakowska D, Niwinska A, Pamula-Pilat J, Tecza K, Pekala W, Rembowska J, Nowicka K, Mosor M, Januszkiewicz-Lewandowska D, Rachtan J, Grzybowska E, Nowak J, Steffen J, Limon J;
J Appl Genet, 2011, 52 (3): 325-330.
The prognosis of clinical course and the analysis of the frequency of the inflammation and dysplasia in the intestinal J-pouch at the patients after restorative proctocolectomy due to FAP.
Banasiewicz T, Marciniak R, Kaczmarek E, Krokowicz P, Paszkowski J, Lozynska-Nelke A, Gronek P, Plawski A, Drews M;
Int J Colorectal Dis, 2011, 26 (9): 1197-1203.
Pyrosequencing-based DNA methylation profiling of Fanconi anemia/BRCA pathway genes in laryngeal squamous cell carcinoma.
Szaumkessel M, Richter J, Giefing M, Jarmuz M, Kiwerska K, Tönnies H, Grenman R, Heidemann S, Szyfter K, Siebert R;
Int J Oncol, 201, 39 (2) :505-514.
Deletions and duplications of developmental pathway genes in 5q31 contribute to abnormal phenotypes.
Rosenfeld JA, Drautz JM, Clericuzio CL, Cushing T, Raskin S, Martin J, Tervo RC, Pitarque JA, Nowak DM, Karolak JA, Lamb AN, Schultz RA, Ballif BC, Bejjani BA, Gajecka M, Shaffer LG;
Am J Med Genet A, 2011, 155A (8): 1906-1916.
Activation of paired-homeobox gene PITX1 by del (5)(q31) in T-cell acute lymphoblastic leukemia.
Nagel S, Venturini L, Przybylski GK, Grabarczyk P, Schneider B, Meyer C, Kaufmann M, Schmidt ChA, Scherr M, Drexler HG, Macleod RAF;
Leuk Lymph, 2011, 52 (7): 1348-1359.