Zobrazeno 1 - 6
of 6
pro vyhledávání: '"Katarzyna, Gliniewicz"'
Autor:
Cybulski, Katarzyna Gliniewicz, Wojciech Kluźniak, Dominika Wokołorczyk, Tomasz Huzarski, Klaudia Stempa, Helena Rudnicka, Anna Jakubowska, Marek Szwiec, Joanna Jarkiewicz-Tretyn, Mariusz Naczk, Tomasz Kluz, Tadeusz Dębniak, Jacek Gronwald, Jan Lubiński, Steven A. Narod, Mohammad R. Akbari, Cezary
Publikováno v:
Genes; Volume 14; Issue 7; Pages: 1329
The APOBEC3B gene belongs to a cluster of DNA-editing enzymes on chromosome 22 and encodes an activation-induced cytidine deaminase. A large deletion of APOBEC3B was associated with increased breast cancer risk, but the evidence is inconclusive. To i
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=multidiscipl::fbf6761a074c3052ca7ebae008b84995
Autor:
Sylwia Morawska, Pawel Domagala, Marek Szwiec, Steven A. Narod, Tomasz Huzarski, Aniruddh Kashyap, Jacek Gronwald, Jan Lubinski, Cezary Cybulski, Dominika Wokołorczyk, Katarzyna Gliniewicz, Anna Jakubowska, Wojciech Kluźniak, Mohammad R. Akbari, Agata Szymiczek, Klaudia Stempa, Tadeusz Dębniak, Bogna Rusak
Publikováno v:
International Journal of Cancer. 147:2793-2800
In designing national strategies for genetic testing, it is important to define the full spectrum of pathogenic mutations in prostate cancer (PCa) susceptibility genes. To investigate the frequency of mutations in PCa susceptibility genes in Polish f
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::2e48dd0a8589572b876a560e8eb35c98
https://doi.org/10.1002/ijc.33272
https://doi.org/10.1002/ijc.33272
Autor:
Helena Rudnicka, Klaudia Stempa, Mariusz Naczk, Wojciech Kluźniak, Karolina Malińska, Cezary Cybulski, Anna Jakubowska, Emilia Rogoża-Janiszewska, Joanna Tomiczek-Szwiec, Piotr Kozlowski, Tomasz Huzarski, Marcin Lener, Katarzyna Gliniewicz, Malwina Suszynska, Tomasz Kluz, Tadeusz Dębniak, Jacek Gronwald, Pawel Domagala, Mohammad R. Akbari, Steven A. Narod, Jan Lubinski, Dominika Wokołorczyk
Publikováno v:
Cancers
Volume 13
Issue 21
Cancers, Vol 13, Iss 5464, p 5464 (2021)
Volume 13
Issue 21
Cancers, Vol 13, Iss 5464, p 5464 (2021)
Simple Summary Current cancer testing gene panels tend to be comprehensive. One of the genes commonly included in the testing panels is BARD1. To establish whether BARD1 mutations predispose to prostate cancer, we sequenced BARD1 in 390 hereditary pr
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d8dd34bbb3e25ccb29162a1a1aa4982e
https://pubmed.ncbi.nlm.nih.gov/34771627
https://pubmed.ncbi.nlm.nih.gov/34771627
Autor:
Wojciech Kluźniak, Jacek Gronwald, Aniruddh Kashyap, Anna Jakubowska, Steven A. Narod, Katarzyna Gliniewicz, Dominika Wokołorczyk, Klaudia Stempa, Bogna Rusak, Mohammad R. Akbari, Sylwia Morawska, Pawel Domagala, Marek Szwiec, Tadeusz Dębniak, Jan Lubinski, Tomasz Huzarski, Cezary Cybulski
Publikováno v:
Br J Cancer
BACKGROUND: The objective of this study was to establish the contribution of PALB2 mutations to prostate cancer risk and to estimate survival among PALB2 carriers. METHODS: We genotyped 5472 unselected men with prostate cancer and 8016 controls for t
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1f73ff1bc09171971f29e00c7a0e157d
https://pubmed.ncbi.nlm.nih.gov/34006922
https://pubmed.ncbi.nlm.nih.gov/34006922
Autor:
Dominika, Wokołorczyk, Wojciech, Kluźniak, Tomasz, Huzarski, Jacek, Gronwald, Agata, Szymiczek, Bogna, Rusak, Klaudia, Stempa, Katarzyna, Gliniewicz, Aniruddh, Kashyap, Sylwia, Morawska, Tadeusz, Dębniak, Anna, Jakubowska, Marek, Szwiec, Paweł, Domagała, Jan, Lubiński, Steven A, Narod, Mohammad R, Akbari, Cezary, Cybulski
Publikováno v:
International journal of cancerREFERENCES. 147(10)
In designing national strategies for genetic testing, it is important to define the full spectrum of pathogenic mutations in prostate cancer (PCa) susceptibility genes. To investigate the frequency of mutations in PCa susceptibility genes in Polish f
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::4fcad72e129bcb2399e8a203d36b71b6
https://pubmed.ncbi.nlm.nih.gov/32875559
https://pubmed.ncbi.nlm.nih.gov/32875559
Autor:
Dominika Wokołorczyk, Jacek Gronwald, Klaudia Stempa, Mohammad R. Akbari, Jan Lubinski, Cezary Cybulski, Bogna Rusak, Steven A. Narod, Sylwia Morawska, Aniruddh Kashyap, Tomasz Huzarski, Małgorzata Stawicka, Helena Rudnicka, Marek Szwiec, Anna Jakubowska, Magdalena Cechowska, Wojciech Kluźniak, Joanna Jarkiewicz-Tretyn, Pawel Domagala, Karina Mordak, Marcin Lener, Katarzyna Gliniewicz, Tadeusz Dębniak
Publikováno v:
Cancers
Volume 11
Issue 10
Cancers, Vol 11, Iss 10, p 1548 (2019)
Volume 11
Issue 10
Cancers, Vol 11, Iss 10, p 1548 (2019)
Bloom Syndrome is a rare recessive disease which includes a susceptibility to various cancers. It is caused by homozygous mutations of the BLM gene. To investigate whether heterozygous carriers of a BLM mutation are predisposed to breast cancer, we s
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c6ad944061ee3cfe132bc144a4b2f3d4