Zobrazeno 1 - 10
of 69
pro vyhledávání: '"Marc B, Cox"'
Autor:
Robert A Hiatt, Yazmin P Carrasco, Alan L Paciorek, Lauren Kaplan, Marc B Cox, Carlos J Crespo, Andrew Feig, Karsten Hueffer, Harris McFerrin, Keith Norris, Elizabeth Roberts-Kirchhoff, Carrie L Saetermoe, Gillian Beth Silver, Katherine Snyder, Arturo R Zavala, Audrey G Parangan-Smith, Diversity Program Consortium
Publikováno v:
PLoS ONE, Vol 17, Iss 9, p e0274100 (2022)
BackgroundThe lack of race/ethnic and gender diversity in grants funded by the National Institutes of Health (NIH) is a persistent challenge related to career advancement and the quality and relevance of health research. We describe pilot programs at
Externí odkaz:
https://doaj.org/article/da39c65205594ab69a83253e3b4423dd
Autor:
Timothy W. Collins, Stephen B. Aley, Thomas Boland, Guadalupe Corral, Marc B. Cox, Lourdes E. Echegoyen, Sara E. Grineski, Osvaldo F. Morera, Homer Nazeran
Publikováno v:
BMC Proceedings, Vol 11, Iss S12, Pp 117-131 (2017)
Abstract Background and purpose With funding from the National Institutes of Health, BUILDing SCHOLARS was established at The University of Texas at El Paso with the goal of implementing, evaluating and sustaining a suite of institutional, faculty an
Externí odkaz:
https://doaj.org/article/ede20f73867347528fe7e2b73bba5d69
Autor:
Olga B. Soto, Christian S. Ramirez, Rina Koyani, Isela A. Rodriguez‐Palomares, Jessica R. Dirmeyer, Brian Grajeda, Sourav Roy, Marc B. Cox
Publikováno v:
Journal of Cellular Biochemistry.
Autor:
Nina R. Ortiz, Naihsuan Guy, Yenni A. Garcia, Jeffrey C. Sivils, Mario D. Galigniana, Marc B. Cox
Publikováno v:
Subcellular Biochemistry ISBN: 9783031147395
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::a4b09892f2b77ae7c0faa2f009173286
https://doi.org/10.1007/978-3-031-14740-1_2
https://doi.org/10.1007/978-3-031-14740-1_2
Autor:
Nina R, Ortiz, Naihsuan, Guy, Yenni A, Garcia, Jeffrey C, Sivils, Mario D, Galigniana, Marc B, Cox
Publikováno v:
Sub-cellular biochemistry. 101
The Hsp90 chaperone is known to interact with a diverse array of client proteins. However, in every case examined, Hsp90 is also accompanied by a single or several co-chaperone proteins. One class of co-chaperone contains a tetratricopeptide repeat (
Autor:
Oscar Ekpenyong, Candace Cooper, Jing Ma, Naihsuan C. Guy, Ashley N. Payan, Fuqiang Ban, Artem Cherkasov, Marc B. Cox, Dong Liang, Huan Xie
Publikováno v:
Pharmaceuticals, Vol 13, Iss 11, p 386 (2020)
Background: GMC1 (2-(1H-benzimidazol-2-ylsulfanyl)-N-[(Z)-(4-methoxyphenyl) methylideneamino] acetamide) effectively inhibits androgen receptor function by binding directly to FKBP52. This is a novel mechanism for the treatment of castration resistan
Externí odkaz:
https://doaj.org/article/2618ea822bf5400b9641607a3a58a63b
Autor:
Robert A, Hiatt, Yazmin P, Carrasco, Alan L, Paciorek, Lauren, Kaplan, Marc B, Cox, Carlos J, Crespo, Andrew, Feig, Karsten, Hueffer, Harris, McFerrin, Keith, Norris, Elizabeth, Roberts-Kirchhoff, Carrie L, Saetermoe, Gillian Beth, Silver, Katherine, Snyder, Arturo R, Zavala, Audrey G, Parangan-Smith
Publikováno v:
PloS one. 17(9)
Background The lack of race/ethnic and gender diversity in grants funded by the National Institutes of Health (NIH) is a persistent challenge related to career advancement and the quality and relevance of health research. We describe pilot programs a
Autor:
Ji Ho Suh, Arundhati Chattopadhyay, Douglas H Sieglaff, Cheryl Storer Samaniego, Marc B Cox, Paul Webb
Publikováno v:
PLoS ONE, Vol 10, Iss 9, p e0137103 (2015)
The androgen receptor (AR) surface-directed antagonist MJC13 inhibits AR function and proliferation of prostate cancer (PC) cells. These effects are related to arrest of an AR/chaperone complex in the cytoplasm. Here, we compared MJC13 and classic AR
Externí odkaz:
https://doaj.org/article/7d9ea420c30e452c91eaf1d8600be977
Autor:
Cheryl Storer Samaniego, Ji Ho Suh, Arundhati Chattopadhyay, Karen Olivares, Naihsuan Guy, Jeffrey C Sivils, Prasenjit Dey, Fumiaki Yumoto, Robert J Fletterick, Anders M Strom, Jan-Åke Gustafsson, Paul Webb, Marc B Cox
Publikováno v:
PLoS ONE, Vol 10, Iss 7, p e0134015 (2015)
FKBP52 and β-catenin have emerged in recent years as attractive targets for prostate cancer treatment. β-catenin interacts directly with the androgen receptor (AR) and has been characterized as a co-activator of AR-mediated transcription. FKBP52 is
Externí odkaz:
https://doaj.org/article/36f3df2021f144458e404729f6693ced
Publikováno v:
Cancer Research. 82:LB038-LB038
Background: Prostate cancer (PCa) is the most common non-cutaneous cancer afflicting men, both in the United States and worldwide. Aberrant molecular signaling mechanisms mediated by the Androgen Receptor (AR) are attributed as the main culprits for