Zobrazeno 1 - 5
of 5
pro vyhledávání: '"Gopa Dhar"'
Autor:
Ananya, Roy, Oishika, Chatterjee, Nilanjan, Banerjee, Tanaya, Roychowdhury, Gopa, Dhar, Gopeswar, Mukherjee, Subhrangsu, Chatterjee
Publikováno v:
Journal of biomolecular structuredynamics.
Autor:
Oishika Chatterjee, Gopeswar Mukherjee, Nilanjan Banerjee, Ananya Roy, Subhrangsu Chatterjee, Gopa Dhar, Tanaya Roychowdhury
c-MYC is deregulated in triple negative breast cancer (TNBC) pointing to be a promising biomarker for breast cancer treatment. Precise level of MYC expression is important in the control of cellular growth and proliferation. Designing of c-MYC-target
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0d56e6bb74cd9af8e8979e546225328b
Autor:
Gopa Dhar, Pinak Chakrabarti, Avadhesha Surolia, Asim Poddar, Vishnu Dwivedi, Bhabatarak Bhattacharyya, Gopal Chakraborti, Gautam Basu, Soumyananda Chakraborti, Amlan Das
Publikováno v:
Biochemistry. 52:7449-7460
Curcumin has shown promising therapeutic utilities for many diseases, including cancer; however, its clinical application is severely limited because of its poor stability under physiological conditions. Here we find that curcumin also loses its acti
Autor:
Asim Poddar, Gopa Dhar, Devlina Chakravarty, Joyita Hazra, Mahadeb Pal, Jesmita Dhar, Pinak Chakrabarti, Bhabatarak Bhattacharyya, Avadhesha Surolia
Publikováno v:
Biochemistry. 54(4)
Curcumin, derived from rhizomes of the Curcuma longa plant, is known to possess a wide range of medicinal properties. We have examined the interaction of curcumin with actin and determined their binding and thermodynamic parameters using isothermal t
Autor:
Pinak Chakrabarti, Bhabatarak Bhattacharyya, Shubhra Ghosh Dastidar, Asim Poddar, Soumyananda Chakraborti, Suvroma Gupta, Gopa Dhar, Dulal Panda, Devlina Chakravarty, Biswa Prasun Chatterji
Publikováno v:
IndraStra Global.
Tubulin, an alpha,beta heterodimer, has four distinct ligand binding sites (for paclitaxel, peloruside/laulimalide, via, and colchicine). The site where colchicine binds is a promising drug target for arresting cell division and has been observed to