Zobrazeno 1 - 6
of 6
pro vyhledávání: '"Samita Bhattacharya"'
Publikováno v:
Journal of Clinical Investigation. 111:553-559
Stat3 is the most pleiotropic member of the signal transducer and activator of transcription (STAT) family of transcription factors and mediates pivotal responses for the cytokine family. In resting cells, STATs, including Stat3, reside largely in th
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::cf667618adacc00ec93938da3f475143
https://doi.org/10.1172/jci15372
https://doi.org/10.1172/jci15372
Autor:
Joel Linden, Zhenhai Gao, Robin L. Woodard, Anna S. Robeva, Samita Bhattacharya, Xiaowei Jin, Diane L. Rosin, Heidi E. Taylor
Publikováno v:
Drug Development Research. 39:243-252
The four human adenosine receptors (ARs), A 1 , A 2A , A 2B , and A 3 , have been stably expressed in mammalian cells. Radioligand binding properties were examined for all four subtypes, including, for the first time the A 2B AR. The A 1 AR-selective
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::0b550079cbdaa9e6eea21c928f808c95
https://doi.org/10.1002/(sici)1098-2299(199611/12)39:3/4<243::aid-ddr3>3.0.co
https://doi.org/10.1002/(sici)1098-2299(199611/12)39:3/4<243::aid-ddr3>3.0.co
Autor:
Samita Bhattacharya, Joel Linden
Publikováno v:
Biochimica et Biophysica Acta (BBA) - Molecular Cell Research. 1265(1):15-21
2-Amino-3-benzoylthiophenes such as PD 81,273 (PD) have been shown to increase agonist, but not antagonist, radioligand binding and to enhance functional effects of A1 adenosine receptor (A1AR) activation in tissues derived from rats and guinea-pigs.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a9f03951980b4fe7ec01cdd859fa2328
Autor:
Samita Bhattacharya, Maria A. Burnatowska-Hledin, William L. Smith, David L. DeWitt, William S. Spielman
Publikováno v:
Gene. 128:285-288
A partial cDNA encoding the A1 adenosine receptor (A1AR), which lacks nucleotides coding for the first 74 amino acids (aa), was isolated from a rabbit kidney cDNA library. The missing 5' end sequence was obtained from an overlapping rabbit genomic cl
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::8f7787cda77f44a9aad01e20f1f30e81
https://doi.org/10.1016/0378-1119(93)90576-o
https://doi.org/10.1016/0378-1119(93)90576-o
Autor:
Kobina Ghartey, Samita Bhattacharya, Amy L. Tucker, Joel Linden, Rebecca Youkey, Matthew Leonard
PD81,723 {(2-amino-4,5-dimethyl-3-thienyl)-[3-(trifluromethyl)-phenyl]methanone} is a selective allosteric enhancer of the G(i)-coupled A1 AR (adenosine receptor) that is without effect on G(s)-coupled A2A ARs. PD81,723 elicits a decrease in the diss
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::418da1de6179ea750a8bca11c33dde22
https://europepmc.org/articles/PMC1449996/
https://europepmc.org/articles/PMC1449996/
Autor:
Hitoshi Takano, Xian Liang Tang, Zequan Yang, John A. Auchampach, Eitaro Kodani, Roberto Bolli, Samita Bhattacharya, Richard G. Black
Publikováno v:
Circulation research. 88(5)
Abstract —We investigated whether activation of A 1 or A 3 adenosine receptors (ARs) induces late preconditioning (PC) against infarction in conscious rabbits using the selective AR agonists 2-chloro- N 6 -cyclopentyladenosine (CCPA) and N 6 -3-iod
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f32be81474a662a334f03fcb456b8655
https://pubmed.ncbi.nlm.nih.gov/11249876
https://pubmed.ncbi.nlm.nih.gov/11249876