Dzieciuchowicz Ł, Tomczak J, Strauss E, Oszkinis G
Ann Vascular Surgery, 2018,52 (October): 49-56, Epub 2018 May 14 DOI: https://doi.org/10.1016/j.avsg.2018.02.032, IF-1,363, MNiSW-20.
New publication
New publication: Associations and interactions between variants in selenoprotein genes, selenoprotein levels and the development of abdominal aortic aneurysm, peripheral arterial disease, and heart failure.
Strauss E, Tomczak J, Staniszewski R, Oszkinis G
PLOS One, 2018,Sep 6; 13 (9):e0203350. doi: 10.1371/journal.pone.0203350. eCollection 2018, IF-2,766, MNiSW-40.
New publication: MicroRNA High Throughput Loss-of-Function Screening Reveals an Oncogenic Role for miR-21-5p in Hodgkin Lymphoma.
Yuan Y, Niu F, Nolte IM, Koerts J, de Jong D, Rutgers B, Osinga J, Azkanaz M, Terpstra M, Bystrykh L, Diepstra A, Visser L, Dzikiewicz-Krawczyk A, Kok K, Kluiver J, van den Berg A
J Cell Physiol Biochem, 2018, 49 (1): 144-159, doi: 10.1159/000492850. Epub 2018 Sep 5, IF-5,500, MNiSW-50.
New publication: Sperm mitochondrial dysfunction and oxidative stress as possible reasons for isolated asthenozoospermia.
Nowicka-Bauer K., Lepczyński A, Ozgo M, Kamieniczna M, Frączek M, Stański L, Olszewska M, Malcher A, Skrzypczak W, Kurpisz M
J Physiol Pharmacol, 2018, 69 (3), 15 stron, IF-2,478, MNiSW-25.
New publication: SPIN1 is a proto-oncogene and SPIN3 is a tumor suppressor in human seminoma.
Janecki DM, Sajek M, Śmiałek MJ, Kotecki M, Ginter-Matuszewska B, Kuczyńska B, Spik A, Kolanowski T, Katazawa R, Kurpisz M, Jaruzelska J
Oncotarget, 2018, 9 (65): 32466-77, MNiSW-40.
New publication: Single nucleotide polymorhism rs1164913 associated with CC genotype in miR-196a2 is overrepresented in laryngeal squamous cell carcinoma, but not in salivary gland tumors in Polish patients.
Skalski M, Ustaszewski A, Jaśkiewicz K, Kiwerska K, Wierzbicka M, Grenman R, Giefing M
J Applied Genetics, 2018, 59 (3): 301-304, Epub 2018 April 1, IF-1,756, MNiSW-20.
New publication: Analysis of the Seasonality of Births in a Large Cohort of Patients with Thyroid Hemiagenesis – A Preliminary Study.
Szczepanek-Parulska E, Zybek-Kocik A, Fichna M, Niedziela M, Czarnywojtek A, Fularz P, Michalak M, Moczko J and Ruchala
Iranian Journal of Pediatrics, 2018, 28 (4): e61373, Epub June 25, DOI: 10.5812/ijp.61373., IF-0,902, MNiSW-15.
New publication: Transcriptomic population markers for human population discrimination.
Daca-Roszak P, Świerniak M, Jaksik R, Tyszkiewicz T, Oczko-Wojciechowska M, Żebracka-Gala J, Jarzab, B, Witt M, Zietkiewicz E
BMC Genetics, 2018, 19, e54 (11 stron), https://doi.org/10.1186/s12863-018-0663-2., IF-2,469, MNiSW-25.
New publication: A case of two sisters suffering from 46,XY gonadal dysgenesis and carrying a mutation of a novel candidate sex-determining gene STARD8 on the X chromosome.
Ilaslan E, Calvel P, Nowak D, Szarras-Czapnik M, Slowikowska-Hilczer J, Spik A, Sararols P, Nef S, Jaruzelska J, Kusz-Zamelczyk K
Sex Dev, 2018, 12 (4): 191-195, IF-1,913, MNiSW-20.
New publication: Downregulation of CEACAM6 gene expression in laryngeal squamous cel carcinoma i san effect of DNA hypermethylation and correlates with disease progression.
Bednarek K, Kostrzewska-Poczekaj M, Szaumkessel M, Kiwerska K, Paczkowska J, Byzia E, Ustaszewski A, Janiszewska J, Bartochowska A, Grenmann R, Wierzbicka M, Szyfter K, Giefing M, Jarmuż-Szymczak M
Am J Cancer Res, 2018, 8 (7): 1249-1261, IF-3,998, MNiSW-35.