Zobrazeno 1 - 10
of 47
pro vyhledávání: '"Magdalena M. Michalska"'
Autor:
Beata Smolarz, Dariusz Samulak, Krzysztof Szyłło, Marianna Makowska, Hanna Romanowicz, Zbigniew Kojs, Magdalena M. Michalska
Publikováno v:
Contemporary Oncology, Vol 23, Iss 2, Pp 92-95 (2019)
Externí odkaz:
https://doaj.org/article/859d900bd8bc4b3286effd558c191e4a
Publikováno v:
Advances in Medicine, Vol 2015 (2015)
Aim. The aim of this study was to evaluate the role of the Lys751Gln (rs13181) ERCC2 gene polymorphism in clinical parameters and the risk for development of ovarian cancer. Material and Methods. The study consisted of 430 patients with ovarian cance
Externí odkaz:
https://doaj.org/article/92c34b5119d14f3db84c4bf4cefa0fca
Autor:
Bogdan Zięba, Jakub Borycki, Iwona Bojar, Radosław Kołaciński, Dariusz Samulak, Stefan Brandl, Magdalena M. Michalska
Publikováno v:
Annals of Agricultural and Environmental Medicine, Vol 27, Iss 4, Pp 717-720 (2020)
Inversion of the uterus is defined as the turning inside out of the fundus into the uterine cavity. According to the literature, uterine inversion occurs in 1/20,000 or even 1/1,584 deliveries. Mortality rates following acute uterine inversion were r
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::87d57a6da66710f6709b33842239cbd3
https://doi.org/10.26444/aaem/130512
https://doi.org/10.26444/aaem/130512
Autor:
Tomasz Szaflik, Hanna Romanowicz, Krzysztof Szyłło, Radosław Kołaciński, Magdalena M. Michalska, Dariusz Samulak, Beata Smolarz
Publikováno v:
International Journal of Molecular Sciences; Volume 23; Issue 19; Pages: 11583
Endometriosis is a disease of complex etiology. Hormonal, immunological, and environmental factors are involved in its formation. In recent years, special attention has been paid to genetic mechanisms that can have a significant impact on the increas
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8e7edf820c3f391ae0c04cfedcd716fb
https://doi.org/10.3390/ijms231911583
https://doi.org/10.3390/ijms231911583
Publikováno v:
Pathology Oncology Research
Ovarian cancer is one of the most common types of cancer in women. The repair system via homologous recombination repairs double-strand breaks (DSB) of DNA, which are the most mortal for cell, out of all DNA damages. The genes, which encode the doubl
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::668785d1bbbe00e009c9244c1b3ff177
https://doi.org/10.1007/s12253-019-00604-5
https://doi.org/10.1007/s12253-019-00604-5
Publikováno v:
Oncotarget
Aim The aim of the study was to determine the relationship between single nucleotide polymorphisms (SNPs) of DNA repair genes and modulation of the risk of breast cancer. The following SNPs were analysed: XRCC1-Arg399Gln (rs25487), hMSH2-Gly322Asp (r
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::47c51a9623cb4c1f50f07ace7fcf419c
https://doi.org/10.18632/oncotarget.26568
https://doi.org/10.18632/oncotarget.26568
Autor:
Dariusz Samulak, Hanna Romanowicz, Krzysztof Szyłło, Beata Smolarz, Zbigniew Kojs, Magdalena M. Michalska, Marianna Makowska
Publikováno v:
Contemporary Oncology
Contemporary Oncology, Vol 23, Iss 2, Pp 92-95 (2019)
Contemporary Oncology, Vol 23, Iss 2, Pp 92-95 (2019)
Introduction Long-term infection with human papillomavirus (HPV) is the cause of cervical cancer and its precursor - cervical intraepithelial neoplasia (CIN). The presence of HPV infection can be presumed in more than 99% of cases of cervical cancer
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e90653e6f0e5451fbbc7c775397f07a8
https://doi.org/10.5114/wo.2019.85880
https://doi.org/10.5114/wo.2019.85880
Autor:
Jan Bieńkiewicz, Hanna Romanowicz, Dariusz Samulak, Jakub Malinowski, Tomasz Szaflik, Magdalena M. Michalska, Beata Smolarz
Publikováno v:
European Journal of Obstetrics & Gynecology and Reproductive Biology. 208:36-40
The reported study was designed to explore associations between the ERCC2- R156R gene single nucleotide polymorphism (SNP) and the risk of ovarian cancer.The R156R (C to A, rs238406) polymorphism of ERCC2 gene was investigated by the PCR-RFLP techniq
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2d2fa853ec14715325729dba62f55680
https://doi.org/10.1016/j.ejogrb.2016.11.012
https://doi.org/10.1016/j.ejogrb.2016.11.012
Publikováno v:
Experimental and Molecular Pathology. 100:243-247
The variability, perceived in DNA repair genes, may be of clinical importance for evaluation of the risk of occurrence of a given type of cancer, its prophylactics and therapy. The aim of the present work was to evaluate associations between the risk
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a62b4d1cf4ac50736aee5f1f95007a0a
https://doi.org/10.1016/j.yexmp.2016.01.007
https://doi.org/10.1016/j.yexmp.2016.01.007
Publikováno v:
Anticancer research. 38(9)
AIM The goals of this study included an analysis of the incidence of single nucleotide polymorphisms (SNPs) genotypes and alleles in DNA repair genes and evaluation of the effects by which this genetic variability may influence the risk for endometri
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::858a425f0ffd3c75b5af142eea443a75
https://pubmed.ncbi.nlm.nih.gov/30194171
https://pubmed.ncbi.nlm.nih.gov/30194171