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Andras Fiser

Showing results (51-60 of 107) with videos related to

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Progress in Retinal and Eye Research|July 11, 2022
Cell fate decisions, transcription factors and signaling during early retinal developmentRaven Diacou, Prithviraj Nandigrami, Andras Fiser, et al.
Structure (London, England : 1993)|April 16, 2013
Functional classification of immune regulatory proteinsRotem Rubinstein, Udupi A Ramagopal, Stanley G Nathenson, et al.
American Journal of Physiology. Cell Physiology|February 21, 2012
A P425R mutation of the proton-coupled folate transporter causing hereditary folate malabsorption produces a highly selective alteration in folate bindingDaniel Sanghoon Shin, Rongbao Zhao, Enghui H Yap, et al.
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.
Proteins|October 7, 2019
Assessing the accuracy of contact predictions in CASP13Rojan Shrestha, Eduardo Fajardo, Nelson Gil, et al.
The Journal of Biological Chemistry|March 13, 2019
Substitutions that lock and unlock the proton-coupled folate transporter (PCFT-SLC46A1) in an inward-open conformationSrinivas Aluri, Rongbao Zhao, Kai Lin, 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.
Proteomics|August 12, 2011
Photo-assisted peptide enrichment in protein complex cross-linking analysis of a model homodimeric protein using mass spectrometryFuning Yan, Fa-Yun Che, Edward Nieves, et al.
Blood|September 1, 2010
Functional roles of aspartate residues of the proton-coupled folate transporter (PCFT-SLC46A1); a D156Y mutation causing hereditary folate malabsorptionDaniel Sanghoon Shin, Sang Hee Min, Laura Russell, et al.
Pageof 11

Showing results (51-60 of 107) with videos related to

Sort By:
Pageof 11
Progress in Retinal and Eye Research|July 11, 2022
Cell fate decisions, transcription factors and signaling during early retinal developmentRaven Diacou, Prithviraj Nandigrami, Andras Fiser, et al.
Structure (London, England : 1993)|April 16, 2013
Functional classification of immune regulatory proteinsRotem Rubinstein, Udupi A Ramagopal, Stanley G Nathenson, et al.
American Journal of Physiology. Cell Physiology|February 21, 2012
A P425R mutation of the proton-coupled folate transporter causing hereditary folate malabsorption produces a highly selective alteration in folate bindingDaniel Sanghoon Shin, Rongbao Zhao, Enghui H Yap, et al.
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.
Proteins|October 7, 2019
Assessing the accuracy of contact predictions in CASP13Rojan Shrestha, Eduardo Fajardo, Nelson Gil, et al.
The Journal of Biological Chemistry|March 13, 2019
Substitutions that lock and unlock the proton-coupled folate transporter (PCFT-SLC46A1) in an inward-open conformationSrinivas Aluri, Rongbao Zhao, Kai Lin, 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.
Proteomics|August 12, 2011
Photo-assisted peptide enrichment in protein complex cross-linking analysis of a model homodimeric protein using mass spectrometryFuning Yan, Fa-Yun Che, Edward Nieves, et al.
Blood|September 1, 2010
Functional roles of aspartate residues of the proton-coupled folate transporter (PCFT-SLC46A1); a D156Y mutation causing hereditary folate malabsorptionDaniel Sanghoon Shin, Sang Hee Min, Laura Russell, et al.
Pageof 11