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American Journal of Physiology. Cell Physiology|January 23, 2015
Identification of Tyr residues that enhance folate substrate binding and constrain oscillation of the proton-coupled folate transporter (PCFT-SLC46A1)Michele Visentin, Ersin Selcuk Unal, Mitra Najmi, et al.
Proceedings of the National Academy of Sciences of the United States of America|September 22, 2016
2-(m-Azidobenzoyl)taxol binds differentially to distinct β-tubulin isotypesChia-Ping Huang Yang, Eng-Hui Yap, Hui Xiao, et al.
Plos One|June 23, 2017
HIV-Tat regulates macrophage gene expression in the context of neuroAIDSLoreto Carvallo, Lillie Lopez, Jorge E Fajardo, et al.
Blood Advances|January 19, 2018
Hereditary folate malabsorption due to a mutation in the external gate of the proton-coupled folate transporter SLC46A1Srinivas Aluri, Rongbao Zhao, Charlotte Lubout, et al.
The Journal of Biological Chemistry|September 7, 2020
A proton-coupled folate transporter mutation causing hereditary folate malabsorption locks the protein in an inward-open conformationHe-Qin Zhan, Mitra Najmi, Kai Lin, et al.
The Journal of Biological Chemistry|April 25, 2009
The functional roles of the His247 and His281 residues in folate and proton translocation mediated by the human proton-coupled folate transporter SLC46A1Ersin Selcuk Unal, Rongbao Zhao, Min-Hwang Chang, et al.
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