Zobrazeno 1 - 10
of 349
pro vyhledávání: '"Farid, Boulad"'
Autor:
Susan E. Prockop, Aisha Hasan, Ekaterina Doubrovina, Parastoo B. Dahi, Irene Rodriguez-Sanchez, Michael Curry, Audrey Mauguen, Genovefa A. Papanicolaou, Yiqi Su, JinJuan Yao, Maria Arcila, Farid Boulad, Hugo Castro-Malaspina, Christina Cho, Kevin J. Curran, Sergio Giralt, Nancy A. Kernan, Guenther Koehne, Ann Jakubowski, Esperanza Papadopoulos, Miguel-Angel Perales, Ioannis Politikos, Keith Price, Annamalai Selvakumar, Craig S. Sauter, Roni Tamari, Teresa Vizconde, James W. Young, Richard J. O’Reilly
Publikováno v:
The Journal of Clinical Investigation, Vol 133, Iss 10 (2023)
Background Refractory CMV viremia and disease are associated with significant morbidity and mortality in recipients of hematopoietic stem cell transplant (HCT).Methods In phase I/II trials, we treated 67 subjects for CMV viremia or disease arising af
Externí odkaz:
https://doaj.org/article/c8bff7f8a061422b8ccb6a5d37b43f5a
Autor:
Chani Traube, Linda M. Gerber, Elizabeth A. Mauer, Keshia Small, Larisa Broglie, Yogi Raj Chopra, Christine N. Duncan, Christen L. Ebens, Julie C. Fitzgerald, Jason L. Freedman, Michelle P. Hudspeth, Caitlin Hurley, Kris M. Mahadeo, Jennifer McArthur, Miriam C. Shapiro, Matthew P. Sharron, Donna A. Wall, Matt S. Zinter, Bruce M. Greenwald, Gabrielle Silver, Farid Boulad
Publikováno v:
Frontiers in Oncology, Vol 11 (2021)
Introduction: Delirium occurs frequently in adults undergoing hematopoietic cell transplantation, with significant associated morbidity. Little is known about the burden of delirium in children in the peri-transplant period. This study was designed t
Externí odkaz:
https://doaj.org/article/4092fe23a114469190d477ee873c9361
Autor:
Elizabeth F. Stone, Scott T. Avecilla, David L. Wuest, Christine Lomas-Francis, Connie M. Westhoff, David L. Diuguid, Michel Sadelain, Farid Boulad, Patricia A. Shi
Publikováno v:
Haematologica, Vol 106, Iss 1 (2020)
Externí odkaz:
https://doaj.org/article/ef22411daaac4063b0fa39a4c25ffbd2
Autor:
Andrew L. H. Webster, Mathijs A. Sanders, Krupa Patel, Ralf Dietrich, Raymond J. Noonan, Francis P. Lach, Ryan R. White, Audrey Goldfarb, Kevin Hadi, Matthew M. Edwards, Frank X. Donovan, Remco M. Hoogenboezem, Moonjung Jung, Sunandini Sridhar, Tom F. Wiley, Olivier Fedrigo, Huasong Tian, Joel Rosiene, Thomas Heineman, Jennifer A. Kennedy, Lorenzo Bean, Rasim O. Rosti, Rebecca Tryon, Ashlyn-Maree Gonzalez, Allana Rosenberg, Ji-Dung Luo, Thomas S. Carroll, Sanjana Shroff, Michael Beaumont, Eunike Velleuer, Jeff C. Rastatter, Susanne I. Wells, Jordi Surrallés, Grover Bagby, Margaret L. MacMillan, John E. Wagner, Maria Cancio, Farid Boulad, Theresa Scognamiglio, Roger Vaughan, Kristin G. Beaumont, Amnon Koren, Marcin Imielinski, Settara C. Chandrasekharappa, Arleen D. Auerbach, Bhuvanesh Singh, David I. Kutler, Peter J. Campbell, Agata Smogorzewska
Publikováno v:
Nature, 612(7940), 495-502. Nature Publishing Group
Nature
Nature
Fanconi anaemia (FA), a model syndrome of genome instability, is caused by a deficiency in DNA interstrand crosslink repair resulting in chromosome breakage1–3. The FA repair pathway protects against endogenous and exogenous carcinogenic aldehydes4
Autor:
Farid Boulad, Aurelio Maggio, Xiuyan Wang, Paolo Moi, Santina Acuto, Friederike Kogel, Chayamon Takpradit, Susan Prockop, Jorge Mansilla-Soto, Annalisa Cabriolu, Ashlesha Odak, Jinrong Qu, Keyur Thummar, Fang Du, Lingbo Shen, Simona Raso, Rita Barone, Rosario Di Maggio, Lorella Pitrolo, Antonino Giambona, Maura Mingoia, John K. Everett, Pascha Hokama, Aoife M. Roche, Vito Adrian Cantu, Hriju Adhikari, Shantan Reddy, Eric Bouhassira, Narla Mohandas, Frederic D. Bushman, Isabelle Rivière, Michel Sadelain
Publikováno v:
Nature Medicine. 28:63-70
Autor:
Farid Boulad, Tsiporah Shore, Koen van Besien, Caterina Minniti, Mihaela Barbu-Stevanovic, Sylvie Wiener Fedus, Fabiana Perna, June Greenberg, Danielle Guarneri, Vijay Nandi, Audrey Mauguen, Karina Yazdanbakhsh, Michel Sadelain, Patricia A. Shi
Publikováno v:
Haematologica, Vol 103, Iss 9 (2018)
Externí odkaz:
https://doaj.org/article/a176e8ed3c684be4b5a469a875cb1b47
Autor:
Goby, Jean-Edouard
Publikováno v:
Bulletin de l'institut égyptien. 30:21-36
Goby Jean-Edouard. Farid Boulad Bey (1872-1947). In: Bulletin de l'Institut d'Egypte, tome 30, 1947. pp. 21-36.
Autor:
Parinda A. Mehta, Jamie Wilhelm, Thomas Leemhuis, K. Scott Baker, Farid Boulad, Kasiani Myers, Kanwaldeep Mallhi, Michelle Harris, Kaitlin Brooks, Robin Mueller, Erica Goodridge, Melissa Hunter, Adam Lane, Stella M. Davies
Publikováno v:
Transplantation and Cellular Therapy. 29:S90-S91
Autor:
Cassie Martinez, Stephen Gilheeney, Andrew L. Kung, Victoria Szenes, James Killinger, Mini Kamboj, Deborah Diotallevi, Giselle Melendez, Farid Boulad, Julia Glade Bender, Rachel Bright, Nicole Zakak, Stephen S. Roberts
Publikováno v:
J Pediatr Oncol Nurs
Background: Severe acute respiratory syndrome coronavirus-2 (SARS-CoV-2) first reached the United States in January 2020. Located in New York City (NYC), MSK Kids, at Memorial Sloan Kettering Cancer Center services, is one of the largest pediatric ca
Autor:
Andrew L. Webster, Mathijs A. Sanders, Krupa Patel, Ralf Dietrich, Raymond J. Noonan, Francis P. Lach, Ryan R. White, Audrey M. Goldfarb, Kevin Hadi, Matthew M. Edwards, Frank X. Donovan, Moonjung Jung, Sunandini Sridhar, Olivier Fedrigo, Huasong Tian, Joel Rosiene, Thomas Heineman, Jennifer Kennedy, Lorenzo Bean, Rasim O. Rosti, Rebecca Tryon, Ashlyn-Maree Gonzalez, Allana Rosenberg, Ji-Dung Luo, Thomas Carrol, Eunike Velleuer, Jeff C. Rastatter, Susanne I. Wells, Jordi Surrallés, Grover Bagby, Margaret L. MacMillan, John E. Wagner, Maria Cancio, Farid Boulad, Theresa Scognamiglio, Roger Vaughan, Amnon Koren, Marcin Imielinski, Settara Chandrasekharappa, Arleen D. Auerbach, Bhuvanesh Singh, David Kutler, Peter J. Campbell, Agata Smogorzewska
Publikováno v:
Cancer Research. 82:6196-6196
Fanconi anemia (FA), a model syndrome of genome instability, is caused by a deficiency in DNA interstrand crosslink (ICL) repair resulting in chromosome breakage. The FA repair pathway comprises at least 22 FANC proteins including BRCA1 and BRCA2 and