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Progress in Retinal and Eye Research
|
July 11, 2022
Cell fate decisions, transcription factors and signaling during early retinal development
Raven Diacou, Prithviraj Nandigrami, Andras Fiser, et al.
Structure (London, England : 1993)
|
April 16, 2013
Functional classification of immune regulatory proteins
Rotem 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 binding
Daniel 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 isotypes
Chia-Ping Huang Yang, Eng-Hui Yap, Hui Xiao, et al.
Proteins
|
October 7, 2019
Assessing the accuracy of contact predictions in CASP13
Rojan 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 conformation
Srinivas Aluri, Rongbao Zhao, Kai Lin, et al.
Plos One
|
June 23, 2017
HIV-Tat regulates macrophage gene expression in the context of neuroAIDS
Loreto 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 spectrometry
Funing 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 malabsorption
Daniel Sanghoon Shin, Sang Hee Min, Laura Russell, et al.
Page
of 11
Search research articles
Search
Showing results (51-60 of 107) with videos related to
Sort By:
Page
of 11
Progress in Retinal and Eye Research
|
July 11, 2022
Cell fate decisions, transcription factors and signaling during early retinal development
Raven Diacou, Prithviraj Nandigrami, Andras Fiser, et al.
Structure (London, England : 1993)
|
April 16, 2013
Functional classification of immune regulatory proteins
Rotem 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 binding
Daniel 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 isotypes
Chia-Ping Huang Yang, Eng-Hui Yap, Hui Xiao, et al.
Proteins
|
October 7, 2019
Assessing the accuracy of contact predictions in CASP13
Rojan 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 conformation
Srinivas Aluri, Rongbao Zhao, Kai Lin, et al.
Plos One
|
June 23, 2017
HIV-Tat regulates macrophage gene expression in the context of neuroAIDS
Loreto 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 spectrometry
Funing 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 malabsorption
Daniel Sanghoon Shin, Sang Hee Min, Laura Russell, et al.
Page
of 11