Zobrazeno 1 - 5
of 5
pro vyhledávání: '"Yat T. Tang"'
Autor:
Veena Bhonagiri-Palsikar, Paul W. Sternberg, Shoba Ranganathan, Javier Sotillo, Robin B. Gasser, Jason Mulvenna, John Martin, Bruce A. Rosa, Soraya Gaze, Yat T. Tang, Xu Zhang, Wesley C. Warren, Makedonka Mitreva, Richard K. Wilson, Bin Zhan, Patrick Minx, Xin Gao, Esley M. Heizer, Alex Loukas, Sahar Abubucker, Peter J. Hotez, Jeffrey M. Bethony, Philip L. Felgner, John M. Hawdon, Élida Mara Leite Rabelo, Qi Wang, Kymberlie Hallsworth-Pepin, Annette M. Dougall, Rahul Tyagi
Publikováno v:
Nature genetics
The hookworm Necator americanus is the predominant soil-transmitted human parasite. Adult worms feed on blood in the small intestine, causing iron-deficiency anemia, malnutrition, growth and development stunting in children, and severe morbidity and
Autor:
Garland R. Marshall, James J. Havranek, Eduardo A. Groisman, Yat T. Tang, Ann M. Stock, Rong Gao
Publikováno v:
Chemical Biology & Drug Design
Two-component signal transduction (TCST) is the predominant signaling scheme used in bacteria to sense and respond to environmental changes in order to survive and thrive. A typical TCST system consists of a sensor histidine kinase to detect external
Autor:
Yat T, Tang, Garland R, Marshall
Publikováno v:
Methods in molecular biology (Clifton, N.J.). 716
The identification of small drug-like compounds that selectively inhibit the function of biological targets has historically been a major focus in the pharmaceutical industry, and in recent years, has generated much interest in academia as well. Drug
Autor:
Yat T. Tang, Garland R. Marshall
Publikováno v:
Journal of chemical information and modeling. 51(2)
Binding affinity prediction is one of the most critical components to computer-aided structure-based drug design. Despite advances in first-principle methods for predicting binding affinity, empirical scoring functions that are fast and only relative
Autor:
Yat T. Tang, Garland R. Marshall
Publikováno v:
Methods in Molecular Biology ISBN: 9781617790119
The identification of small drug-like compounds that selectively inhibit the function of biological targets has historically been a major focus in the pharmaceutical industry, and in recent years, has generated much interest in academia as well. Drug
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::5f38cac4923065aeaf987a2300464781
https://doi.org/10.1007/978-1-61779-012-6_1
https://doi.org/10.1007/978-1-61779-012-6_1