Zobrazeno 1 - 6
of 6
pro vyhledávání: '"John B. Jarman"'
Autor:
Kali M. Pruss, Haoqing Chen, Yuanyuan Liu, William Van Treuren, Steven K. Higginbottom, John B. Jarman, Curt R. Fischer, Justin Mak, Beverly Wong, Tina M. Cowan, Michael A. Fischbach, Justin L. Sonnenburg, Dylan Dodd
Publikováno v:
Nature Communications, Vol 14, Iss 1, Pp 1-12 (2023)
Here, using a mouse model, the authors report a previously undescribed role for medium-chain acyl-CoA dehydrogenase in host metabolism of gut microbiota metabolites, and show that circulating compounds, including the abundant organic acid hippurate,
Externí odkaz:
https://doaj.org/article/14334ccffc5848da904c149209a88138
Publikováno v:
PLoS ONE, Vol 9, Iss 6, p e100678 (2014)
Thrombosis is the cause of many cardiovascular syndromes and is a significant contributor to life-threatening diseases, such as myocardial infarction and stroke. Thrombus targeted imaging agents have the capability to provide molecular information ab
Externí odkaz:
https://doaj.org/article/e3afe9dfda6248c7b5f455ba607a03a1
Autor:
Dennis A. Dougherty, John B. Jarman
Publikováno v:
Chemical communications (Cambridge, England). 55(38)
A heptamethine-based charge-transfer dye was designed based on previous evidence of triplet state formation in orthogonal charge-transfer partners and calculations suggesting the formation of a charge-transfer state in heptamethine dye derivatives. A
Publikováno v:
Journal of the American Chemical Society
The synthetic modification of proteins plays an important role in chemical biology and biomaterials science. These fields provide a constant need for chemical tools that can introduce new functionality in specific locations on protein surfaces. In th
Autor:
Allie C. Obermeyer, John B. Jarman, Chawita Netirojjanakul, Kareem El Muslemany, Matthew B. Francis
Publikováno v:
Angewandte Chemie. 126:1075-1079
Autor:
Kareem M. El Muslemany, John B. Jarman, Chawita Netirojjanakul, Matthew B. Francis, Allie C. Obermeyer
Publikováno v:
Angewandte Chemie International Edition. 53:1057-1061
Using a small-molecule-based screen, ferricyanide was identified as a mild and efficient oxidant for the coupling of anilines and o-aminophenols on protein substrates. This reaction is compatible with thiols and 1,2-diols, allowing its use in the cre