Familial adenomatous polyposis: age of onset and association with mutations oft the APC gene in patients from West Ukraine.
Lozynska MR, Lozynskyy YS, Plawski A, Pinyazhko RO, Prokopchuk NM, Fedota OM;
Biopolymers and Cell, 2017, 33 (2): 102-115.
Publikacje
Publikacje pracowników w ePub
Cryptorchidism and varicocele: another look at the reasons for launching autoaggression.
Havrylyuk AM, Chopyak VV, Nakonechnyi IA, Fraczek M, Kurpisz M
Paediatric Surgery, 2017; 3(56):75-83.
Distribution of polymorphisms rs12979860, rs8099917 and rs12980275 IL28B in patients with chronic hepatitis C.
Wysocka-Leszczyńska J, Kałużna E, Świątek-Kościelna B, Gowin E, Nowak J, Bereszyńska I, Mozer-Lisewska I, Wysocki J, Januszkiewicz-Lewandowska D;
Adv Clin Exp Med (Wrocław), 2017, 26 (8): 1257-1261.
Translocation t(8;14)(q24;q11) with concurrent PTEN alterations and deletions of STIL/TAL1 and CDKN2A/B in a pediatric case of acute T-lymphoblastic leukemia: A genetic profile associated with adverse prognosis.
Skalska-Sadowska J, Dawidowska M, Szarzyńska-Zawadzka B, Jarmuż-Szymczak M, Czerwińska-Rybak J, Machowska L, Derwich K;
Pediatr Blood Cancer. 2017 Apr;64(4). doi: 10.1002/pbc.26266. Epub 2016 Oct 19.
Cost-effective screening of DNMT3A coding sequence identifies somatic mutation in pediatric T-cell acute lymphoblastic leukemia.
Szarzyńska-Zawadzka B, Kosmalska M, Sędek Ł, Sonsala A, Twardoch M, Kowalczyk JR, Szczepański T, Witt M, Dawidowska M
Eur J Haematol., 2017, 99 (6): 514-519.
Genetic factors influencingthe reduction of central corneal thickness in disorders affecting the eye.
Świerkowska J, Gajęcka M;
Ophthalmic Genetics, 2017, 38 (6): 501-510,
Longrange PCR-based next-generation sequencing in pharmacokinetics and pharmacodynamics study of propofol among patients under general anaesthesia.
Zakerska-Banaszak O, Skrzypczak-Zielińska M, Tamowicz B, Mikstacki A, Walczak M, Prendecki M, Doroszewska J, Pollak A, Lechowicz U, Oldak M, Huminska-Lisowska K, Molinska-Glura M, Szalata M, Słomski R;
Scientific Report, 2017, Nov 13; 7(1):15399. doi: 10.1038/s41598-017-15657-2.
New EPCAM founder deletion in Polish population.
4. Dymerska D, Gołębiewska K, Kuświk M, Rudnicka H, Scott RJ, Billings R, Pławski A, Boruń P, Siołek M, Kozak-Klonowska B, Szwiec M, Kilar E, Huzarski T, Byrski T, Lubinski J, Kurzawski;
Clin Genet, 2017, 92 (6): 649-653.
The Gene-Diet Associations in Postmenopausal Women with Newly Diagnosed Dyslipidemia.
6. Grygiel-Górniak B, Kaczmarek E, Mosor M, Przysławski J, Nowak J;
J Nutr Health Aging, 2017; 21(9):1031-1037.