Zobrazeno 1 - 10
of 161
pro vyhledávání: '"Robert L, Reddick"'
Autor:
Heather F Pidcoke, Wilfred Delacruz, Maryanne C Herzig, Beverly S Schaffer, Sahar T Leazer, Chriselda G Fedyk, Robbie K Montogomery, Nicolas J Prat, Bijaya K Parida, James K Aden, Michael R Scherer, Robert L Reddick, Robert E Shade, Andrew P Cap
Publikováno v:
PLoS ONE, Vol 17, Iss 12, p e0279694 (2022)
A perfluorocarbon (PFC) investigated for treatment of traumatic brain injury (TBI) delivers oxygen to support brain function, but causes transient thrombocytopenia. TBI can cause acute inflammation with resulting thrombocytopenia; an interaction betw
Externí odkaz:
https://doaj.org/article/ecc3faad40b14eefb38de77adbf4c278
Autor:
Subramanya Srikantan, Yilun Deng, Zi-Ming Cheng, Anqi Luo, Yuejuan Qin, Qing Gao, Glaiza-Mae Sande-Docor, Sifan Tao, Xingyu Zhang, Nathan Harper, Chris E. Shannon, Marcel Fourcaudot, Zhi Li, Balakuntalam S. Kasinath, Stephen Harrison, Sunil Ahuja, Robert L. Reddick, Lily Q. Dong, Muhammad Abdul-Ghani, Luke Norton, Ricardo C. T. Aguiar, Patricia L. M. Dahia
Publikováno v:
Nature Communications, Vol 10, Iss 1, Pp 1-17 (2019)
TMEM127 is a tumor suppressor protein, loss of which predisposes to catecholamine-secreting tumors. Here the authors show that TMEM127 expression is modulated by nutritional status and that it has a role in regulating organismal insulin sensitivity.
Externí odkaz:
https://doaj.org/article/759408e47c5a4d35885debb0d56f6eb3
Autor:
Addanki P. Kumar, Rita Ghosh, Robert L. Reddick, Dinesh Thapa, Roble Bedolla, Paul Rivas, Guiming Li
PDF file - 79KB, Effect of RES on the protein levels of p4E-BP1 and FOXO-3 in prostate cancer cells
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::169179a73543f6622300373dec04aaf4
https://doi.org/10.1158/1940-6207.22524432.v1
https://doi.org/10.1158/1940-6207.22524432.v1
Autor:
Addanki P. Kumar, Rita Ghosh, Robert L. Reddick, Dinesh Thapa, Roble Bedolla, Paul Rivas, Guiming Li
PDF file - 94KB, Effect of RES on body weight and food consumption in PTEN knockout mice
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::705572fa611859be87e41d79a8bc9494
https://doi.org/10.1158/1940-6207.22524429
https://doi.org/10.1158/1940-6207.22524429
Autor:
Addanki P. Kumar, Rita Ghosh, Robert L. Reddick, Dinesh Thapa, Roble Bedolla, Paul Rivas, Guiming Li
PDF file - 60KB, Apoptosis in SIRT1 knockdown DU145 cells
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4fa75f50b2b3acba99d47757091dad46
https://doi.org/10.1158/1940-6207.22524435.v1
https://doi.org/10.1158/1940-6207.22524435.v1
Autor:
Shih‐Bo Huang, Paul Rivas, Xiaoyu Yang, Zhao Lai, Yidong Chen, Keri L. Schadler, Ming Hu, Robert L. Reddick, Rita Ghosh, Addanki P. Kumar
Publikováno v:
Mol Carcinog
Emerging evidence suggests an important role for SIRT1, a nicotinamide adenine dinucleotide (NAD)-dependent deacetylase in cancer development, progression and therapeutic resistance; making it a viable therapeutic target. Here, we examined the impact
Autor:
Patricia L.M. Dahia, Ricardo C.T. Aguiar, Yidong Chen, Robert L. Reddick, Jan Bruder, Marta Barontini, Neil Aronin, Sarika Rao, I. Tolgay Ocal, Manju L. Prasad, Gustavo M. Silva, Shintaro Iwata, Qing Gao, Zi-Ming Cheng, Yuejuan Qin, Rodrigo A. Toledo
Supplementary Appendix: List of all supplementary data files; Supplemental Methods: Additional clinical details of Samples, and details of whole exome sequencing, targeted sequencing and in silico structure modeling not included in main article
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::62fadc0665be6fa207fdff19736c5c9c
https://doi.org/10.1158/1078-0432.22457802.v1
https://doi.org/10.1158/1078-0432.22457802.v1
Autor:
Patricia L.M. Dahia, Ricardo C.T. Aguiar, Yidong Chen, Robert L. Reddick, Jan Bruder, Marta Barontini, Neil Aronin, Sarika Rao, I. Tolgay Ocal, Manju L. Prasad, Gustavo M. Silva, Shintaro Iwata, Qing Gao, Zi-Ming Cheng, Yuejuan Qin, Rodrigo A. Toledo
Purpose: Pheochromocytomas and paragangliomas (PPGL) are genetically heterogeneous tumors of neural crest origin, but the molecular basis of most PPGLs is unknown.Experimental Design: We performed exome or transcriptome sequencing of 43 samples from
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3c258e7c083018896e91674880a4ec87
https://doi.org/10.1158/1078-0432.c.6523701.v1
https://doi.org/10.1158/1078-0432.c.6523701.v1
Autor:
Patricia L.M. Dahia, Ricardo C.T. Aguiar, Yidong Chen, Robert L. Reddick, Jan Bruder, Marta Barontini, Neil Aronin, Sarika Rao, I. Tolgay Ocal, Manju L. Prasad, Gustavo M. Silva, Shintaro Iwata, Qing Gao, Zi-Ming Cheng, Yuejuan Qin, Rodrigo A. Toledo
Supplemental Figure 1: Alternative views of Figure 1 displaying mutations in our cohort; Supplemental Figure 2: Histone 3.3 G34W mutation in patient samples; Supplemental Figure 3: In silico analysis of histone 3.3 and G34W mutant; Supplemental Figur
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9c9318cf4ace5911fb2633c48d842a6d
https://doi.org/10.1158/1078-0432.22457808
https://doi.org/10.1158/1078-0432.22457808