Zobrazeno 1 - 4
of 4
pro vyhledávání: '"Magdalena, Kuświk"'
Autor:
Beiping, Miao, Diamanto, Skopelitou, Aayushi, Srivastava, Sara, Giangiobbe, Dagmara, Dymerska, Nagarajan, Paramasivam, Abhishek, Kumar, Magdalena, Kuświk, Wojciech, Kluźniak, Katarzyna, Paszkowska-Szczur, Matthias, Schlesner, Jan, Lubinski, Kari, Hemminki, Asta, Försti, Obul Reddy, Bandapalli
Publikováno v:
International journal of molecular sciences. 23(3)
Colorectal cancer (CRC) is the third most frequently diagnosed malignancy worldwide. Only 5% of all CRC cases are due to germline mutations in known predisposition genes, and the remaining genetic burden still has to be discovered. In this study, we
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::81afa39d167e055c725cf8ceaf98440a
https://pubmed.ncbi.nlm.nih.gov/35163215
https://pubmed.ncbi.nlm.nih.gov/35163215
Autor:
Wojciech Marciniak, Tadeusz Dębniak, Piotr Baszuk, Susan M. Domchek, Angelo Paradiso, Arvids Irmejs, Jacek Gronwald, Cezary Cybulski, Anna Jakubowska, Jan Lubinski, Róża Derkacz, Marcin Lener, Joanne Kotsopoulos, Irita Roderte, Katherine Pullella, Tomasz Huzarski, Michał Falco, Magdalena Kuświk, Tomáš Matoušek, Margherita Patruno, Steven A. Narod
Publikováno v:
Cancers, Vol 13, Iss 3345, p 3345 (2021)
Cancers
Volume 13
Issue 13
Cancers
Volume 13
Issue 13
An important group of breast cancers is those associated with inherited susceptibility. In women, several predisposing mutations in genes involved in DNA repair have been discovered. Women with a germline pathogenic variant in BRCA1 have a lifetime c
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::279ffbe64a02cc8280217639e0a8be0b
https://www.mdpi.com/2072-6694/13/13/3345
https://www.mdpi.com/2072-6694/13/13/3345
Autor:
Beiping Miao, Jan Lubinski, Diamanto Skopelitou, Matthias Schlesner, Magdalena Kuświk, Nagarajan Paramasivam, Abhishek Kumar, Kari Hemminki, Asta Försti, Aayushi Srivastava, Obul Reddy Bandapalli, Dagmara Dymerska
Publikováno v:
Journal of Personalized Medicine
Volume 11
Issue 4
Volume 11
Issue 4
Colorectal cancer (CRC) shows one of the largest proportions of familial cases among different malignancies, but only 5–10% of all CRC cases are linked to mutations in established predisposition genes. Thus, familial CRC constitutes a promising tar
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::41e8afa3057f2a5d513e49588dbb205f
https://opus.bibliothek.uni-augsburg.de/opus4/frontdoor/index/index/docId/92391
https://opus.bibliothek.uni-augsburg.de/opus4/frontdoor/index/index/docId/92391
Autor:
Beata Kozak-Klonowska, Tomasz Byrski, Jan Lubinski, Tomasz Huzarski, Andrzej Pławski, Magdalena Kuświk, Monika Siołek, E. Kilar, Katarzyna Golebiewska, Pawel Borun, Rodney J. Scott, Raewyn Billings, Helena Rudnicka, Dagmara Dymerska, Marek Szwiec, Grzegorz Kurzawski
Publikováno v:
Clinical Genetics. 92:649-653
It is well known that founder mutations associated with cancer risk have useful implications for molecular diagnostics. We report the presence of a founder mutation in EPCAM involved in the etiology of Lynch syndrome (LS). The mutation extends nearly
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::6d86e05c1be7c69429ffc935627de0a1
https://doi.org/10.1111/cge.13026
https://doi.org/10.1111/cge.13026