Zobrazeno 1 - 7
of 7
pro vyhledávání: '"Nadia Zayed"'
Autor:
Thibaut S. Matis, Nadia Zayed, Bouchra Labraki, Manon de Ladurantaye, Théophane A. Matis, José Camacho Valenzuela, Nancy Hamel, Adrienne Atayan, Barbara Rivera, Yuval Tabach, Patricia N. Tonin, Alexandre Orthwein, Anne-Marie Mes-Masson, Zaki El Haffaf, William D. Foulkes, Paz Polak
Publikováno v:
npj Breast Cancer, Vol 7, Iss 1, Pp 1-7 (2021)
Abstract It was hypothesized that variants in underexplored homologous recombination repair (HR) genes could explain unsolved multiple-case breast cancer (BC) families. We investigated HR deficiency (HRD)-associated mutational signatures and second h
Externí odkaz:
https://doaj.org/article/cbb6acef8a0543f6b4e46805a7d21ec0
Autor:
Dominique Andre Behrends, Leticia Khendek, Chan Gao, Nadia Zayed, Janet Elizabeth Henderson, Paul Andre Martineau
Publikováno v:
Journal of Functional Biomaterials, Vol 6, Iss 2, Pp 407-421 (2015)
A fractured scaphoid is a common disabling injury that is frequently complicated by non-union. The treatment of non-union remains challenging because of the scaphoid’s small size and delicate blood supply. Large animal models are the most reliable
Externí odkaz:
https://doaj.org/article/e7033f236f934104ae262dc693975157
Autor:
Anne-Marie Mes-Masson, Alexandre Orthwein, Zaki El Haffaf, Bouchra Labraki, Patricia N. Tonin, Manon de Ladurantaye, José Camacho Valenzuela, Adrienne Atayan, Nadia Zayed, Yuval Tabach, William D. Foulkes, Thibaut S Matis, Nancy Hamel, Paz Polak, Barbara Rivera, Théophane A Matis
Publikováno v:
NPJ Breast Cancer
Dipòsit Digital de la UB
Universidad de Barcelona
npj Breast Cancer, Vol 7, Iss 1, Pp 1-7 (2021)
Dipòsit Digital de la UB
Universidad de Barcelona
npj Breast Cancer, Vol 7, Iss 1, Pp 1-7 (2021)
It was hypothesized that variants in underexplored homologous recombination repair (HR) genes could explain unsolved multiple-case breast cancer (BC) families. We investigated HR deficiency (HRD)-associated mutational signatures and second hits in tu
Autor:
Talia Boshari, Jorge S. Reis-Filho, Pedro Blecua, Nadia Zayed, Yanying Huo, William D. Foulkes, Marc Tischkowitz, Yuan Chun Ding, Britta Weigelt, Kathleen A. Burke, Samuel H. Berman, Bing Xia, Tzeh Keong Foo, Srilatha Simhadri, Susan L. Neuhausen, Nadeem Riaz
Publikováno v:
Oncogene
The major breast cancer suppressor proteins BRCA1 and BRCA2 play essential roles in homologous recombination (HR)-mediated DNA repair, which is thought to be critical for tumor suppression. The two BRCA proteins are linked by a third tumor suppressor
Autor:
Nadia Zayed, Chan Gao, Leticia Khendek, Janet E. Henderson, Paul A. Martineau, Dominique Behrends
Publikováno v:
Journal of Functional Biomaterials
Journal of Functional Biomaterials, Vol 6, Iss 2, Pp 407-421 (2015)
Volume 6
Issue 2
Pages 407-421
Journal of Functional Biomaterials, Vol 6, Iss 2, Pp 407-421 (2015)
Volume 6
Issue 2
Pages 407-421
A fractured scaphoid is a common disabling injury that is frequently complicated by non-union. The treatment of non-union remains challenging because of the scaphoid’s small size and delicate blood supply. Large animal models are the most reliable
Autor:
Marc Tischkowitz, Yuan Chun Ding, Jorge S. Reis-Filho, Kathleen A. Burke, William D. Foulkes, Samuel H. Berman, Britta Weigelt, Nadia Zayed, Bing Xia, Susan L. Neuhausen, Talia Boshari, Tzeh Keong Foo, Srilatha Simhadri
Publikováno v:
Cancer Research. 77:2470-2470
The major breast cancer suppressor proteins BRCA1 and BRCA2 play essential roles in homologous recombination (HR)-mediated DNA repair, which is thought to be critical for tumor suppression. The two BRCA proteins are physically and functionally linked
Autor:
G. B. Roby, Janet E. Henderson, Nadia Zayed, Chan Gao, Michael B. Sullivan, Michael H. Wang, Li Cheng, Domi A. Behrends, Paul A. Martineau
Publikováno v:
European Cells & Materials, Vol 28, Pp 209-222 (2014)
KitW-sh mice carry an inactivating mutation in the gene encoding the receptor for stem cell factor, which is expressed at high levels on the surface of haematopoietic precursor cells. The mutation results in mast cell deficiency, a variety of defects