Zobrazeno 1 - 10
of 442
pro vyhledávání: '"T. Byrski"'
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:
T, Huzarski, T, Byrski, J, Gronwald, C, Cybulski, O, Oszurek, M, Szwiec, 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, P, Sun, J, Lubiński, S A, Narod, P, Wandzel
Publikováno v:
Breast Cancer Research and Treatment. 156:371-378
The aim of the study is to identify treatments which predict survival for women with a BRCA1 mutation, including oophorectomy and chemotherapy. 476 women with stage I to stage III breast cancer who carried a BRCA1 mutation were followed from diagnosi
Akademický článek
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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
Autor:
T, Huzarski, C, Cybulski, A, Jakubowska, T, Byrski, J, Gronwald, P, Domagała, M, Szwiec, D, Godlewski, E, Kilar, E, Marczyk, M, Siołek, B, Gorski, R, Wiśniowski, H, Janiszewska, D, Surdyka, R, Sibilski, P, Sun, S A, Narod, J, Lubiński, P, Wandzel
Publikováno v:
Breast Cancer Research and Treatment. 141:471-476
To identify characteristic features of breast cancers associated with an NBS1 mutation. To estimate and to compare 10-year survival rates for patients with early-onset breast cancer, with and without an NBS1 mutation. 4,566 women with stage I to stag
Autor:
D. Bazzacco, D. Mengoni, M. D. Salsac, A. Khouaja, S. M. Lenzi, E. Sahin, A. F. Lisetskiy, Kenia Teodoro Wiedemann, R. P. Singh, D. Curien, J. J. Valiente-Dobón, E. Fioretto, P. Mason, U. Datta Pramanik, A. Gottardo, J. Ollier, I. Stefan, R. Chapman, L. Corradi, F. Recchia, S. Courtin, R. Orlandi, G. Benzoni, B.J.P. Gall, S. Aydin, J. F. Smith, T. Byrski, K. Zuber, R. Moro, S. Erturk, Igor T. Čeliković, Predrag Ujić, Alejandro Algora, A. M. Stefanini, E. Farnea, M. Labiche, Dieter Ackermann, D. Verney, S. Leoni, G. Montagnoli, R. Silvestri, D. Lebhertz, P. T. Wady, F. Haas, G. Pollarolo, M. Yalcinkaya, A. Gadea, B. Mouginot, F. Ibrahim, O. Dorvaux, F. Azaiez, T. Faul, J. Robin, C. Michelagnoli, S. Franchoo, D. A. Torres, S. Szilner, David O'Donnell, C. A. Ur, Fernando Scarlassara, M. Trotta, A. Kusoglu, M. N. Erduran, B. Guiot, V. Modamio, K. Subotic, G. Duchêne, S. Lunardi, D. Montanari, G. de Angelis, F. Didierjean, M. Bostan, D. Tonev, D. R. Napoli, Elif Ince, J. R. B. Oliveira, G. La Rana
Publikováno v:
Nuclear Physics A. 893:1-12
The level structures of the N = 50 83As, 82Ge, and 81Ga isotones have been investigated by means of multi-nucleon transfer reactions. A first experiment was performed with the CLARA–PRISMA setup to identify these nuclei. A second experiment was car
Akademický článek
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Autor:
T, Byrski, J, Gronwald, T, Huzarski, E, Grzybowska, M, Budryk, M, Stawicka, T, Mierzwa, M, Szwiec, R, Wiśniowski, M, Siolek, S A, Narod, J, Lubinski, A, Kozłowski
Publikováno v:
Breast Cancer Research and Treatment. 108:289-296
There have been no studies to date which look at the relative effectiveness of different regimens of chemotherapy in women who have breast cancer and who carry a BRCA1 germ-line mutation. We wished to compare rates of response to neo-adjuvant chemoth
Autor:
C, Cybulski, J, Lubiński, D, Wokołorczyk, W, Kuźniak, A, Kashyap, V, Sopik, T, Huzarski, J, Gronwald, T, Byrski, M, Szwiec, A, Jakubowska, B, Górski, T, Dębniak, S A, Narod, M R, Akbari
Publikováno v:
Clinical genetics. 88(4)
A number of genes other than BRCA1 and BRCA2 have been associated with breast cancer predisposition, and extended genetic testing panels have been proposed. It is of interest to establish the full spectrum of deleterious mutations in women with famil
Autor:
M, Szwiec, A, Jakubowska, B, Górski, T, Huzarski, J, Tomiczek-Szwiec, J, Gronwald, T, Dębniak, T, Byrski, W, Kluźniak, D, Wokołorczyk, B, Birkenfeld, M R, Akbari, S A, Narod, J, Lubiński, C, Cybulski
Publikováno v:
Clinical genetics. 87(3)
Three founder alleles of BRCA1 (C61G, 4153delA, 5382insC) were reported in Poland in 2000, and these three mutations have comprised the standard testing panel used throughout the country. However, since 2000, other recurrent mutations of BRCA1 and BR