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Ndeye Diop-Bove

Showing results (1-10 of 8) with videos related to

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Molecular Pharmacology|November 20, 2013
Enhanced receptor-mediated endocytosis and cytotoxicity of a folic acid-desacetylvinblastine monohydrazide conjugate in a pemetrexed-resistant cell line lacking folate-specific facilitative carriers but with increased folate receptor expressionRongbao Zhao, Ndeye Diop-Bove, I David Goldman
Annual Review of Nutrition|May 17, 2011
Mechanisms of membrane transport of folates into cells and across epitheliaRongbao Zhao, Ndeye Diop-Bove, Michele Visentin, et al.
Annual Review of Physiology|February 12, 2014
The intestinal absorption of folatesMichele Visentin, Ndeye Diop-Bove, Rongbao Zhao, et al.
The Journal of Biological Chemistry|May 24, 2011
Random mutagenesis of the proton-coupled folate transporter (SLC46A1), clustering of mutations, and the bases for associated losses of functionRongbao Zhao, Daniel Sanghoon Shin, Ndeye Diop-Bove, et al.
Pediatric Hematology and Oncology|August 28, 2010
Mutation of the proton-coupled folate transporter gene (PCFT-SLC46A1) in Turkish siblings with hereditary folate malabsorptionBerna Atabay, Meral Turker, Esra Arun Ozer, et al.
Molecular Genetics and Metabolism|February 22, 2011
Identification of novel mutations in the proton-coupled folate transporter (PCFT-SLC46A1) associated with hereditary folate malabsorptionDaniel Sanghoon Shin, Kris Mahadeo, Sang Hee Min, et al.
American Journal of Physiology. Cell Physiology|August 6, 2010
Properties of the Arg376 residue of the proton-coupled folate transporter (PCFT-SLC46A1) and a glutamine mutant causing hereditary folate malabsorptionKris Mahadeo, Ndeye Diop-Bove, Daniel Shin, et al.
The Journal of Pediatrics|April 15, 2011
Prevalence of a loss-of-function mutation in the proton-coupled folate transporter gene (PCFT-SLC46A1) causing hereditary folate malabsorption in Puerto RicoKris M Mahadeo, Ndeye Diop-Bove, Sonia I Ramirez, et al.
Pageof 1

Showing results (1-10 of 8) with videos related to

Sort By:
Pageof 1
Molecular Pharmacology|November 20, 2013
Enhanced receptor-mediated endocytosis and cytotoxicity of a folic acid-desacetylvinblastine monohydrazide conjugate in a pemetrexed-resistant cell line lacking folate-specific facilitative carriers but with increased folate receptor expressionRongbao Zhao, Ndeye Diop-Bove, I David Goldman
Annual Review of Nutrition|May 17, 2011
Mechanisms of membrane transport of folates into cells and across epitheliaRongbao Zhao, Ndeye Diop-Bove, Michele Visentin, et al.
Annual Review of Physiology|February 12, 2014
The intestinal absorption of folatesMichele Visentin, Ndeye Diop-Bove, Rongbao Zhao, et al.
The Journal of Biological Chemistry|May 24, 2011
Random mutagenesis of the proton-coupled folate transporter (SLC46A1), clustering of mutations, and the bases for associated losses of functionRongbao Zhao, Daniel Sanghoon Shin, Ndeye Diop-Bove, et al.
Pediatric Hematology and Oncology|August 28, 2010
Mutation of the proton-coupled folate transporter gene (PCFT-SLC46A1) in Turkish siblings with hereditary folate malabsorptionBerna Atabay, Meral Turker, Esra Arun Ozer, et al.
Molecular Genetics and Metabolism|February 22, 2011
Identification of novel mutations in the proton-coupled folate transporter (PCFT-SLC46A1) associated with hereditary folate malabsorptionDaniel Sanghoon Shin, Kris Mahadeo, Sang Hee Min, et al.
American Journal of Physiology. Cell Physiology|August 6, 2010
Properties of the Arg376 residue of the proton-coupled folate transporter (PCFT-SLC46A1) and a glutamine mutant causing hereditary folate malabsorptionKris Mahadeo, Ndeye Diop-Bove, Daniel Shin, et al.
The Journal of Pediatrics|April 15, 2011
Prevalence of a loss-of-function mutation in the proton-coupled folate transporter gene (PCFT-SLC46A1) causing hereditary folate malabsorption in Puerto RicoKris M Mahadeo, Ndeye Diop-Bove, Sonia I Ramirez, et al.
Pageof 1