Zobrazeno 1 - 5
of 5
pro vyhledávání: '"James R. O. Eaton"'
Autor:
Kamayani Singh, Graham Davies, Yara Alenazi, James R. O. Eaton, Akane Kawamura, Shoumo Bhattacharya
Publikováno v:
Scientific Reports, Vol 11, Iss 1, Pp 1-2 (2021)
Externí odkaz:
https://doaj.org/article/c6b106d446304fa1b2c20ab7c45a515c
Autor:
Kamayani Singh, Graham Davies, Yara Alenazi, James R. O. Eaton, Akane Kawamura, Shoumo Bhattacharya
Publikováno v:
Scientific Reports, Vol 7, Iss 1, Pp 1-15 (2017)
Abstract Chemokines function via G-protein coupled receptors in a robust network to recruit immune cells to sites of inflammation. Due to the complexity of this network, targeting single chemokines or receptors has not been successful in inflammatory
Externí odkaz:
https://doaj.org/article/b514a9c56ad24d53bfea2339ddae7894
Autor:
Shoumo Bhattacharya, James R. O. Eaton, Gopala K. Yakala, Lucía Geis-Asteggiante, Graham Davies, Benoit Darlot, Kalimuthu Karuppanan, Akane Kawamura, Carol V. Robinson
Publikováno v:
The Journal of Biological Chemistry
Chemokines mediate leucocyte migration and homeostasis, and are key targets in inflammatory diseases including atherosclerosis, cytokine storm and chronic auto-immune disease. Chemokine redundancy and ensuing network robustness has frustrated therape
Autor:
Shoumo Bhattacharya, Akane Kawamura, Kamayani Singh, James R. O. Eaton, Graham Davies, Yara Alenazi
Publikováno v:
Scientific Reports, Vol 11, Iss 1, Pp 1-2 (2021)
Scientific Reports
Scientific Reports
Chemokines function via G-protein coupled receptors in a robust network to recruit immune cells to sites of inflammation. Due to the complexity of this network, targeting single chemokines or receptors has not been successful in inflammatory disease.
Autor:
Eugenia Duodu, James R. O. Eaton, Dziyana Kraskouskaya, G. Andrés Cisneros, Steven K. Burger, Joel A. Drewry, Patrick T. Gunning
Publikováno v:
MedChemComm. 4:289-292
We herein explore the structural determinants of selective phosphopeptide recognition by employing novel bivalent, bis-(Zn2+-dipicolylamine)-based coordination complexes against a select library of model phosphoserine-containing peptides of varying a