Zobrazeno 1 - 10
of 215
pro vyhledávání: '"G, Kurzawski"'
Autor:
C. Cybulski, W. Kluźniak, T. Huzarski, D. Wokołorczyk, A. Kashyap, A. Jakubowska, M. Szwiec, T. Byrski, T. Dębniak, B. Górski, V. Sopik, M. R. Akbari, P. Sun, J. Gronwald, S. A. Narod, J. Lubiński, D. Dymerska, G. Kurzawski, K. Tutlewska, M. Kuswik, H. Rudnicka, R. J. Scott, R. Billings, A. Pławski, J. Lubinski, T. Gromowski, K. Kąklewski, W. Marciniak, K. Durda, M. Lener, G. Sukiennicki, K. Kaczmarek, K. Jaworska-Bieniek, K. Paszkowska-Szczur, P. Waloszczyk, K. Hemminki, A. Försti, O. Oszurek, K. Gugała, M. Stawicka, Z. Morawiec, T. Mierzwa, M. Falco, H. Janiszewska, E. Kilar, E. Marczyk, B. Kozak-Klonowska, M. Siołek, D. Surdyka, R. Wiśniowski, M. Posmyk, P. Domagała, Polish Breast Cancer Consortium, E. N. Imyanitov, M. Muszyńska, K. Prajzendanc, N. Peruga, A. Morawski, M. R. Lener, P. Baszuk, A. Wiechowska-Kozłowska, J. Kładny, S. Pietrzak, A. Soluch, A. Plawski, U. R. Rashid, H. Naeemi, N. Muhammad, A. Loya, M. A. Yusuf, A. Savanevich, O. Aszurek, A. Mathe, M. Wong-Brown, W. Locke, C. Stirzaker, S. G. Braye, J. F. Forbes, S. Clark, K. Avery-Kiejda, J. Tomiczek-Szwiec, J. Jakubowicz, R. Sibilski, R. Posmyk
Publikováno v:
Hereditary Cancer in Clinical Practice, Vol 15, Iss S2, Pp 1-6 (2017)
Externí odkaz:
https://doaj.org/article/a2b9ebb454084ff9ad1608367602a071
Autor:
D, Dymerska, K, Gołębiewska, M, Kuświk, H, Rudnicka, R J, Scott, R, Billings, A, Pławski, P, Boruń, M, Siołek, B, Kozak-Klonowska, M, Szwiec, E, Kilar, T, Huzarski, T, Byrski, J, Lubiński, G, Kurzawski
Publikováno v:
Clinical genetics. 92(6)
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=pmid________::715657be5500bd16a9b0cffce7310238
https://pubmed.ncbi.nlm.nih.gov/28369810
https://pubmed.ncbi.nlm.nih.gov/28369810
Autor:
A, Kurlapska, P, Serrano-Fernández, P, Baszuk, S, Gupta, T, Starzyńska, E, Małecka-Panas, A, Dabrowski, T, Dębniak, G, Kurzawski, J, Suchy, W, Rogoza-Mateja, R J, Scott, J, Lubiński
Publikováno v:
Clinical genetics. 88(3)
Genetic markers associated with colorectal cancer may be used in population screening for the early identification of patients at elevated risk of disease. We genotyped 3059 individuals with no cancer family history for eight markers previously assoc
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::25822f8ea143a6eec5d5dc8906c5d3bd
https://pubmed.ncbi.nlm.nih.gov/25117299
https://pubmed.ncbi.nlm.nih.gov/25117299
Autor:
G, Kurzawski, J, Suchy, M, Lener, E, Kłujszo-Grabowska, J, Kładny, K, Safranow, K, Jakubowska, A, Jakubowska, T, Huzarski, T, Byrski, T, Debniak, C, Cybulski, J, Gronwald, O, Oszurek, D, Oszutowska, E, Kowalska, S, Góźdź, S, Niepsuj, R, Słomski, A, Pławski, A, Łacka-Wojciechowska, A, Rozmiarek, Ł, Fiszer-Maliszewska, M, Bebenek, D, Sorokin, M M, Sasiadek, A, Stembalska, Z, Grzebieniak, E, Kilar, M, Stawicka, D, Godlewski, P, Richter, I, Brozek, B, Wysocka, J, Limon, A, Jawień, Z, Banaszkiewicz, H, Janiszewska, J, Kowalczyk, D, Czudowska, R J, Scott, J, Lubiński
Publikováno v:
Clinical genetics. 69(1)
Germline mutations in the DNA mismatch repair genes MSH2 and MLH1 account for a significant proportion of hereditary non-polyposis colorectal cancer (HNPCC) families. One approach by which development of an efficient DNA-testing procedure can be impl
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::818007c27c3913726d88a4776a84d2c8
https://pubmed.ncbi.nlm.nih.gov/16451135
https://pubmed.ncbi.nlm.nih.gov/16451135
Akademický článek
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Publikováno v:
Journal of applied genetics. 42(3)
Analysis of significance of age at cancer diagnosis as a factor allowing identification of a subgroup of patients with a high frequency of hMSH2 and hMLH1 mutations among families that fulfil suspected HNPCC criteria was performed. DNA from thirty-on
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::dccacd3cf0612be1c6eba407bbf8ba01
https://pubmed.ncbi.nlm.nih.gov/14564042
https://pubmed.ncbi.nlm.nih.gov/14564042
Publikováno v:
Polish journal of pathology : official journal of the Polish Society of Pathologists. 52(3)
The majority of hereditary nonpolyposis colorectal cancer (HNPCC) is caused by mutations in DNA mismatch repair genes, especially in MLH1 and MSH2. Tumours in such patients also show microsatellite instability characteristic for DNA repair defects. T
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::53726704f2b0b7ae78c74950423daa40
https://pubmed.ncbi.nlm.nih.gov/11769399
https://pubmed.ncbi.nlm.nih.gov/11769399
Akademický článek
Tento výsledek nelze pro nepřihlášené uživatele zobrazit.
K zobrazení výsledku je třeba se přihlásit.
K zobrazení výsledku je třeba se přihlásit.
Publikováno v:
Endocrine regulations. 33(3)
To evaluate the detection possibility of TSH receptor gene mutation within the third cytoplasmic loop and the sixth transmembrane domain in the cytological material obtained by means of fine needle biopsy of autonomous and non-autonomous nodules.The
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::d06559cf4f5c9e2cf7d327ab63503892
https://pubmed.ncbi.nlm.nih.gov/10571960
https://pubmed.ncbi.nlm.nih.gov/10571960
Autor:
G. Kurzawski, A. Vanags, M. Bitina, Arvids Irmejs, Andris Gardovskis, Viktors Borosenko, Bohdan Górski, Janis Gardovskis, I. Melbarde-Gorkusa, Edvins Miklasevics
Publikováno v:
European Journal of Cancer Supplements. 5:242-243
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::5575413c7c51ec2e6827a54b720de66f
https://doi.org/10.1016/s1359-6349(07)70952-7
https://doi.org/10.1016/s1359-6349(07)70952-7