Zobrazeno 1 - 10
of 25
pro vyhledávání: '"P G, Febbo"'
Autor:
Michael S Leapman, Antonio C Westphalen, Niloufar Ameli, H Jeffrey Lawrence, Phillip G Febbo, Matthew R Cooperberg, Peter R Carroll
Publikováno v:
PLoS ONE, Vol 12, Iss 10, p e0185535 (2017)
We aimed to directly compare results from multi-parametric prostate MRI (mpMRI) and a biopsy-based 17-gene RT-PCR assay providing a Genomic Prostate Score (GPS) among individuals who were candidates for active surveillance with low and intermediate r
Externí odkaz:
https://doaj.org/article/8a760b025e2d486fb847de4c34c0cd3e
Autor:
Tarek A. Bismar, Francesca Demichelis, Alberto Riva, Robert Kim, Sooryanarayana Varambally, Le He, Jeff Kutok, Jonathan C. Aster, Jeffery Tang, Rainer Kuefer, Matthias D. Hofer, Phillip G. Febbo, Arul M. Chinnaiyan, Mark A. Rubin
Publikováno v:
Neoplasia: An International Journal for Oncology Research, Vol 8, Iss 1, Pp 59-68 (2006)
The critical clinical question in prostate cancer research is: How do we develop means of distinguishing aggressive disease from indolent disease? Using a combination of proteomic and expression array data, we identified a set of 36 genes with concor
Externí odkaz:
https://doaj.org/article/8b145fd24fe745d391e7c8c88a42d0ad
Publikováno v:
PLoS Computational Biology, Vol 4, Iss 2, p e28 (2008)
Cancer is a heterogeneous disease often requiring a complexity of alterations to drive a normal cell to a malignancy and ultimately to a metastatic state. Certain genetic perturbations have been implicated for initiation and progression. However, to
Externí odkaz:
https://doaj.org/article/0bf4b488409945e58ec6c24335bba782
Autor:
Eric J. Small, Lawrence Fong, Karen E. Knudsen, Brad Sickler, Robert E. Reiter, Charles J. Ryan, Theodore C. Goldstein, Tomasz M. Beer, Martin E. Gleave, Rahul Aggarwal, Julian S. Gehring, Rajdeep Das, John Shon, Scott M. Dehm, Alan Ashworth, David A. Quigley, Ha X. Dang, Terence W. Friedlander, R. Keira Cheetham, Denise Playdle, Paul Lloyd, Serafim Batzoglou, Jack F. Youngren, Jin Zhang, Nathan A. Lack, Adam Foye, Felix Y. Feng, Jörg Hakenberg, Adina M. Bailey, Owen N. Witte, Abhijit Parolia, Scott A. Tomlins, Travis J. Barnard, Donavan T. Cheng, Jiaoti Huang, Li Zhang, P. G. Febbo, Alexander W. Wyatt, Kim N. Chi, Matthew Rettig, Vishal Kothari, Daniel E. Spratt, Housheng Hansen He, Haolong Li, George Thomas, Arnold Liao, Shuang G. Zhao, Hui Li, Joshua M. Stuart, Won Kim, Primo N. Lara, Christopher G. Maher, Jonathan Chou, Joshi J. Alumkal, Amina Zoubeidi, Marc D. Perry, Ruhollah Moussavi-Baygi, Luke A. Gilbert, Arul M. Chinnaiyan, Christopher P. Evans, Hani Goodarzi, Marcin Cieslik, Kyle Kai-How Farh
Publikováno v:
Cell, vol 174, iss 3
Quigley, DA; Dang, HX; Zhao, SG; Lloyd, P; Aggarwal, R; Alumkal, JJ; et al.(2018). Genomic Hallmarks and Structural Variation in Metastatic Prostate Cancer. Cell, 174(3), 758-769.e9. doi: 10.1016/j.cell.2018.06.039. UC Davis: Retrieved from: http://www.escholarship.org/uc/item/796124qb
Quigley, DA; Dang, HX; Zhao, SG; Lloyd, P; Aggarwal, R; Alumkal, JJ; et al.(2018). Genomic Hallmarks and Structural Variation in Metastatic Prostate Cancer. Cell, 174(3), 758-769.e9. doi: 10.1016/j.cell.2018.06.039. UC Davis: Retrieved from: http://www.escholarship.org/uc/item/796124qb
© 2018 Elsevier Inc. While mutations affecting protein-coding regions have been examined across many cancers, structural variants at the genome-wide level are still poorly defined. Through integrative deep whole-genome and -transcriptome analysis of
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1928a409b1341bcafb393804416865b5
https://escholarship.org/uc/item/796124qb
https://escholarship.org/uc/item/796124qb
Autor:
Xiao Yi Yang, Katherine A. Tsamis, Mickey K. Kim, David S. Hsu, Jennifer A. Freedman, P. G. Febbo, Timothy M. Clay, Takuya Osada, Michael A. Morse, Michael B. Datto, H. Kim Lyerly, Bryan M. Clary, William T. Barry
Publikováno v:
Molecular Cancer Therapeutics. 11:1500-1509
Despite advances in contemporary chemotherapeutic strategies, long-term survival still remains elusive for patients with metastatic colorectal cancer. A better understanding of the molecular markers of drug sensitivity to match therapy with patient i
Autor:
Ben Herman, Celestia S. Higano, Fenghai Duan, Bennett B. Chin, Donna Hartfeil, P. G. Febbo, Robert K. Doot, David A. Mankoff, Mark Muzi, Mary-Ellen Taplin, Evan Y. Yu, Jina M. Taub, Xuan Deng, Joshi J. Alumkal
(18)F-fluoride PET quantitatively images bone metabolism and may serve as a pharmacodynamic assessment for systemic therapy such as dasatinib, a potent SRC kinase inhibitor, with activity in bone.This was an imaging companion trial (American College
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3136a51e54090b4bcdfd7f67f5f024b3
https://europepmc.org/articles/PMC4410847/
https://europepmc.org/articles/PMC4410847/
Autor:
David F. McDermott, Amanda Youmans, Meredith M. Regan, Mirna Lechpammer, Michael B. Atkins, Melissa P. Upton, James W. Mier, P. G. Febbo, Sabina Signoretti, Eric J. Stanbridge
Publikováno v:
Clinical Cancer Research. 11:3714-3721
Purpose: Renal cancer response to interleukin 2 (IL-2) therapy and patient survival has been correlated with tumor histology and carbonic anhydrase IX (CAIX) expression. In an effort to confirm and expand these observations, we examined CAIX expressi
Autor:
Judith Manola, Donald S. Kaufman, Meredith M. Regan, Daniel J. George, Miah-Hiang Tay, Philip W. Kantoff, William Oh, Irving D. Kaplan, Stacey B Leibowitz, Matthew R. Smith, P. G. Febbo
Publikováno v:
Annals of Oncology. 15:974-978
Medical or surgical castration is effective in advanced prostate cancer but with profound side-effects, particularly on sexual function. Effective, less toxic therapies are needed. This study examined whether the addition of finasteride to high-dose
Autor:
Philip W. Kantoff, Judith Prisby, P. G. Febbo, William Oh, Judith Manola, Donald S. Kaufman, Irving D. Kaplan
Publikováno v:
American Journal of Clinical Oncology. 26:312-316
Patients with clinical T3 or T4 prostate cancer or with elevated serum prostate-specific antigen (PSA) levels greater than 40 ng/ml are at high risk of failure with primary treatment. Chemotherapy administered at the time of diagnosis may decrease th
Publikováno v:
Minerva urologica e nefrologica = The Italian journal of urology and nephrology. 59(1)
Systemic therapy beyond hormonal therapy for advanced prostate cancer includes chemotherapy, antiangiogenic therapy, signal transduction inhibitors, immunomodulatory therapy, and other experimental therapeutics. This review will discuss the state of