Zobrazeno 1 - 10
of 10
pro vyhledávání: '"Katarina Zavodna"'
Autor:
Vanda Repiská, Behulova R, Katarina Zavodna, Katarína Fabišíková, Petra Priscakova, Olívia Hamidová
Publikováno v:
Frontiers in Genetics
Frontiers in Genetics, Vol 11 (2020)
Frontiers in Genetics, Vol 11 (2020)
MUTYH-associated polyposis (MAP) is a rare hereditary condition caused by the biallelic mutation in the MUTYH gene encoding MUTYH glycosylase. This enzyme is a key member of the base excision repair (BER) pathway responsible for the repair of DNA les
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3bf47c0b816a53c5297223e725c724f6
http://europepmc.org/articles/PMC7770176
http://europepmc.org/articles/PMC7770176
Autor:
D Keder, M Vizvaryova, Katarina Zavodna, J Benuska, K Mlada, Z Ferancikova, M Konecny, Vanda Repiská, L Masak, Weismann P, J Kausitz, E Weismanova
Publikováno v:
Neoplasma. 56:230-238
The aim of this study was to establish the sensitive, specific and clinically acceptable method for detection of tumor cells (TCs) circulating in peripheral blood (PB) of cervical cancer patients without the clinically detectable risk of disease prog
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::76b0e8db54f1d34a86d592cd9131c578
https://doi.org/10.4149/neo_2009_03_230
https://doi.org/10.4149/neo_2009_03_230
Autor:
Iveta Mlkva, Miriam Vizvaryova, Michal Konecny, Vladimíra Vranová, Juraj Kausitz, Zdena Bartosova, Petr Kuglík, Eva Weismanova, Katarina Zavodna
Publikováno v:
Breast Cancer Research and Treatment. 109:581-583
The Large genomic rearrangements (LGR) in BRCA1/2 represent a substantial proportion of disease-causing changes. In our pilot study we demonstrate the specific case of the Slovak breast/ovarian cancer family, where BRCA1 analysis revealed the discrep
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d79800fc518494ebbfe98c987fa10690
https://doi.org/10.1007/s10549-007-9670-0
https://doi.org/10.1007/s10549-007-9670-0
Autor:
Zdena Bartosova, Juraj Kausitz, Miriam Milly, Iveta Mlkva, Eva Weismanova, Jaroslava Gregorova, Katarina Zavodna, Denisa Ilencikova, Michal Konecny
Publikováno v:
Breast cancer research and treatment. 126(1)
Germline mutations in the BRCA1/2 genes account for the majority of hereditary breast ovarian cancer (HBOC). Identification of causal mutations may have significant impact on clinical management of such families. Despite high mutation detection rate,
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f08e7598676b4f9d9c57355a96867a77
https://pubmed.ncbi.nlm.nih.gov/21203900
https://pubmed.ncbi.nlm.nih.gov/21203900
Autor:
Tomas Slamka, Zdena Bartosova, Bujalkova M, Tomas Krivulcik, David Martinicky, Denisa Ilencikova, Katarina Zavodna
Publikováno v:
BMC Cancer, Vol 9, Iss 1, p 405 (2009)
BMC Cancer
BMC Cancer
Background Depending on the population studied, large genomic rearrangements (LGRs) of the mismatch repair (MMR) genes constitute various proportions of the germline mutations that predispose to hereditary non-polyposis colorectal cancer (HNPCC). It
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2afc68d21bf2c5543c5db12149655318
https://doi.org/10.1186/1471-2407-9-405
https://doi.org/10.1186/1471-2407-9-405
Autor:
R Behulova, Katarina Zavodna, S Spanik, J Kausitz, S Galbavy, E Weismanova, Tomas Krivulcik, M Vizvaryova, M Konecny
Publikováno v:
Neoplasma. 56(3)
Colorectal carcinoma (CRC) represents a serious problem worldwide: in the Slovak republic are diagnosed about 2600 new CRC cases annually and its incidence is increasing. Colorectal cancer patients may succumb to the disease because of local recurren
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::fb2adeed0cf17fd82a5a5380b4f553a3
https://pubmed.ncbi.nlm.nih.gov/19309232
https://pubmed.ncbi.nlm.nih.gov/19309232
Autor:
Katarina Zavodna, Michal Konecny, Juraj Kausitz, Frantisek Cisarik, Miriam Vizvaryova, Bujalkova M, Behulova R, Eva Weismanova, Tomas Krivulcik
Publikováno v:
Breast cancer research and treatment. 119(1)
Mutations in the BRCA1 and BRCA2 genes account for the majority of hereditary breast ovarian cancer (HBOC) cases. However, after BRCA1 and BRCA2 screening still the most HBOC cases remain negative for any mutational event. Accordingly, in these cases
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3be28ea5ce69c0538b9be25c4c8f7b3c
https://pubmed.ncbi.nlm.nih.gov/19011960
https://pubmed.ncbi.nlm.nih.gov/19011960
Autor:
Giancarlo Marra, Josef Jiricny, Denisa Ilencikova, Tomas Krivulcik, Bujalkova M, Brigitte Wolf, Karl Heinimann, Katarina Zavodna, Zdena Bartosova, Michal Kovac, Judith Karner-Hanusch
Publikováno v:
Clinical chemistry. 54(11)
Background: In the workup of patients with suspected hereditary nonpolyposis colorectal cancer (HNPCC), detection of loss of heterozygosity (LOH) could help pinpoint the mismatch-repair (MMR) gene carrying the germline mutation, but analysis of micro
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::510f107bbe4cd97a30686e41edb50808
https://pubmed.ncbi.nlm.nih.gov/18772310
https://pubmed.ncbi.nlm.nih.gov/18772310
Autor:
Katarína Fabišíková, Olívia Hamidová, Regína Lohajová Behulová, Katarína Závodná, Petra Priščáková, Vanda Repiská
Publikováno v:
Frontiers in Genetics, Vol 11 (2020)
MUTYH-associated polyposis (MAP) is a rare hereditary condition caused by the biallelic mutation in the MUTYH gene encoding MUTYH glycosylase. This enzyme is a key member of the base excision repair (BER) pathway responsible for the repair of DNA les
Externí odkaz:
https://doaj.org/article/700a8d7817384124922f9cb01fff68d2
Autor:
Michal Konecny, Katarina Zavodna, Vladimira Vranova, Miriam Vizvaryova, Eva Weismanova, Iveta Mlkva, Petr Kuglik, Juraj Kausitz, Zdena Bartosova
Publikováno v:
Breast Cancer Research & Treatment; Jun2008, Vol. 109 Issue 3, p581-583, 3p, 1 Diagram, 1 Chart