Zobrazeno 1 - 6
of 6
pro vyhledávání: '"Abbie M. Frederick"'
Autor:
Alex Toker, Abbie M. Frederick, Alex H. Ramos, Kristian Cibulskis, Nam Pho, Verónica Bautista-Piña, Valeria Quintanar-Jurado, Eric S. Lander, Kornelia Polyak, Claudia Rangel-Escareño, Sergio Rodriguez-Cuevas, José Baselga, Kristin K. Brown, Sandra Romero-Cordoba, Antonio Maffuz-Aziz, Shouyong Peng, Jorge Melendez-Zajgla, Rameen Beroukhim, Michael S. Lawrence, Alfredo Hidalgo-Miranda, Stacey Gabriel, Dennis C. Sgroi, Gerardo Jimenez-Sanchez, Andrea L. Richardson, Daniel Auclair, Gad Getz, Nicolas Stransky, Andrey Sivachenko, Rosa Rebollar-Vega, Fujiko Duke, Melissa Parkin, Todd R. Golub, Levi A. Garraway, Juan Carlos Fernández-López, Maria L. Cortes, Lihua Zou, Joonil Jung, Robert C. Onofrio, Laura Uribe-Figueroa, Kristin G. Ardlie, Kristin Thompson, Shantanu Banerji, Scott L. Carter, Joshua M. Francis, Matthew Meyerson, Carrie Sougnez, Steven E. Schumacher
Publikováno v:
Nature. 486:405-409
Breast carcinoma is the leading cause of cancer-related mortality in women worldwide with an estimated 1.38 million new cases and 458,000 deaths in 2008 alone1. This malignancy represents a heterogeneous group of tumours with characteristic molecular
Publikováno v:
Biochemical and Biophysical Research Communications. 378:419-423
The antineoplastic prodrug Cloretazine exerts its cytotoxicity via a synergism between 2-chloroethylating and carbamoylating activities that are cogenerated upon activation in situ. Cloretazine is reported here to inhibit the nucleotidyl-transferase
Autor:
Ece D. Gamsiz, Eric M. Morrow, Stephen Sanders, Bernie Devlin, Michael Schmidt, Elizabeth W. Triche, Shailender Nagpal, Edwin H. Cook, Michael T. Murtha, Daniel H. Geschwind, Sorin Istrail, Emma W. Viscidi, Matthew W. State, Abbie M. Frederick
Publikováno v:
American journal of human genetics, vol 93, iss 1
Intellectual disability (ID), often attributed to autosomal-recessive mutations, occurs in 40% of autism spectrum disorders (ASDs). For this reason, we conducted a genome-wide analysis of runs of homozygosity (ROH) in simplex ASD-affected families co
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::be23562f4666b144736178187de0892e
https://escholarship.org/uc/item/2cr2b10z
https://escholarship.org/uc/item/2cr2b10z
Autor:
Andrey Sivachenko, Juan Carlos Fernández-López, Carrie Sougnez, Antonio Maffuz-Aziz, Jorge Melendez-Zajgla, Nam Pho, Rosa Rebollar-Vega, Lihua Zou, Valeria Quintanar-Jurado, Eric S. Lander, Kristin G. Ardlie, Joonil Jung, Verónica Bautista-Piña, Fujiko Duke, Shantanu Banerji, Sergio Rodriguez-Cuevas, Andrea L. Richardson, Stacey Gabriel, Kornelia Polyak, Gad Getz, Matthew Meyerson, Melissa Parkin, Kristin K. Brown, Sandra Romero-Cordoba, Kristian Cibulskis, Robert C. Onofrio, Shouyong Peng, Abbie M. Frederick, Kristin Thompson, Scott L. Carter, Dennis C. Sgroi, Joshua M. Francis, Nicolas Stransky, Daniel Auclair, Claudia Rangel-Escareño, José Baselga, Laura Uribe-Figueroa, Steven E. Schumacher, Alex H. Ramos, Alex Toker, Rameen Beroukhim, Michael S. Lawrence, Alfredo Hidalgo-Miranda, Gerardo Jimenez-Sanchez, Levi A. Garraway, Todd R. Golub, Maria L. Cortes
Publikováno v:
Cancer Epidemiology, Biomarkers & Prevention. 21:PL07-01
Today, more than 55% of the world's breast cancer cases are diagnosed in low and middle-income countries and in 2020, more that 70% of the cases will come from the developing nations. In Mexico, breast cancer-specific mortality doubled during the pas
Autor:
Michael Okamoto, Barbara A. Weir, Aimee M. Crago, Samuel Singer, Shantanu Banerji, Marc Ladanyi, Matthew Meyerson, Jordi Barretina, Abbie M. Frederick, David E. Root, Glenn S. Cowley
Publikováno v:
Cancer Research. 71:4972-4972
We previously profiled several adult soft-tissue sarcoma subtypes using sequencing, copy number analysis, and gene expression arrays. This high-throughput genetic profiling revealed dozens of candidate genes deserving of further functional validation
Autor:
David M. Bodine, Elliott H. Margulies, Patrick G. Gallagher, Andre M. Pilon, Dewang Zhou, Hatice Ozel Abaan, Tim M. Townes, Abbie M. Frederick, Amy Werner Allen
Publikováno v:
Blood. 112:283-283
Erythroid Kruppel-Like Factor (EKLF; KLF1) is the founding member of the Kruppel family of transcription factors, with 3 C2H2 zinc-fingers that bind a 9-base consensus sequence (NCNCNCCCN). The functions of EKLF, first identified as an activator of t