Zobrazeno 1 - 4
of 4
pro vyhledávání: '"Max C. Caccese"'
Autor:
Joseph I. Kliegman, Dorothea Fiedler, Colm J. Ryan, Yi-Fan Xu, Xiao-yang Su, David Thomas, Max C. Caccese, Ada Cheng, Michael Shales, Joshua D. Rabinowitz, Nevan J. Krogan, Kevan M. Shokat
Publikováno v:
Cell Reports, Vol 5, Iss 6, Pp 1725-1736 (2013)
Current approaches for identifying synergistic targets use cell culture models to see if the combined effect of clinically available drugs is better than predicted by their individual efficacy. New techniques are needed to systematically and rational
Externí odkaz:
https://doaj.org/article/6e8a50a061a746a3bc5414fd47db57d1
Autor:
Theodore C. Chan, Gary M. Vilke, Max C. Caccese, Jesse J. Brennan, Allyson A. Kreshak, Vaishal M. Tolia, Edward M. Castillo
Publikováno v:
The Journal of Emergency Medicine. 55:620-626
Background A recent hepatitis A virus (HAV) outbreak in San Diego, California represents one of the largest HAV outbreaks in the United States. The County of San Diego Health and Human Services Agency identified homelessness and illicit or injection
Autor:
Giuseppe Condomitti, John R. Yates, Joris de Wit, Kristel M. Vennekens, Jeffrey N. Savas, Anirvan Ghosh, Max C. Caccese, Matthew L. O'Sullivan
Publikováno v:
Neuron
Leucine-rich repeat (LRR) proteins have recently been identified as important regulators of synapse development and function, but for many LRR proteins the ligand-receptor interactions are not known. Here we identify the heparan sulfate (HS) proteogl
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b1260980e030b92a246c0f011838d947
https://europepmc.org/articles/PMC4003527/
https://europepmc.org/articles/PMC4003527/
Autor:
Ada Cheng, Max C. Caccese, Joseph I. Kliegman, Michael Shales, Dorothea Fiedler, David Thomas, Nevan J. Krogan, Colm J. Ryan, Xiaoyang Su, Yi-Fan Xu, Joshua D. Rabinowitz, Kevan M. Shokat
Publikováno v:
Cell reports, vol 5, iss 6
Cell Reports, Vol 5, Iss 6, Pp 1725-1736 (2013)
Cell Reports, Vol 5, Iss 6, Pp 1725-1736 (2013)
Current approaches for identifying synergistic targets use cell culture models with combinations of clinically available drugs to see if the combined effect of the combination is better than predicted by their individual efficacy. New techniques are