Author

Ndeye Diop-Bove

Observed names: N. Diop-Bove, Ndeye Khady Diop-Bove

Observed institutions: Ningbo University, Albert Einstein College of Medicine, Wayne State University, Yeshiva University, The Barbara Ann Karmanos Cancer Institute

OpenAlex ID: A5016105341

Mechanisms of Membrane Transport of Folates into Cells and Across Epithelia

2011 · Rongbao Zhao, Ndeye Diop-Bove, et al. · Annual Review of Nutrition · 365

The Intestinal Absorption of Folates

2011 · Michele Visentin, Ndeye Diop-Bove, et al. · Annual Review of Physiology · 222

Hypermethylation of the human proton-coupled folate transporter (SLC46A1) minimal trancriptional regulatory region in an antifolate-resistant HeLa cell line

2009 · Ndeye Khady Diop-Bove, Julia Wu, et al. · Molecular Cancer Therapeutics · 56

Identification of novel mutations in the proton-coupled folate transporter (PCFT-SLC46A1) associated with hereditary folate malabsorption

2011 · Daniel Sanghoon Shin, Kris Mahadeo, et al. · Molecular Genetics and Metabolism · 46

Properties of the Arg376 residue of the proton-coupled folate transporter (PCFT-SLC46A1) and a glutamine mutant causing hereditary folate malabsorption

2010 · Kris Mahadeo, Ndeye Diop-Bove, et al. · American Journal of Physiology-Cell Physiology · 42

Mutation of the Proton-coupled Folate Transporter Gene (pcft-slc46a1) in Turkish Siblings With Hereditary Folate Malabsorption

2010 · Berna Atabay, Meral Turker, et al. · Pediatric Hematology and Oncology · 28

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 Expression

2013 · Rongbao Zhao, Ndeye Diop-Bove, et al. · Molecular Pharmacology · 23

Prevalence of a Loss-of-Function Mutation in the Proton-Coupled Folate Transporter Gene (PCFT-SLC46A1) Causing Hereditary Folate Malabsorption in Puerto Rico

2011 · Kris M. Mahadeo, Ndeye Diop-Bove, et al. · The Journal of Pediatrics · 22

Random Mutagenesis of the Proton-coupled Folate Transporter (SLC46A1), Clustering of Mutations, and the Bases for Associated Losses of Function

2011 · Rongbao Zhao, Daniel Sanghoon Shin, et al. · Journal of Biological Chemistry · 19

A novel deletion mutation in the proton-coupled folate transporter (PCFT; SLC46A1) in a Nicaraguan child with hereditary folate malabsorption

2013 · N. Diop-Bove, M. Jain, et al. · Gene · 13

Biological Role, Properties, and Therapeutic Applications of the Reduced Folate Carrier (RFC-SLC19A1) and the Proton-Coupled Folate Transporter (PCFT-SLC46A1)

2011 · Larry H. Matherly, Ndeye Diop-Bove, et al. · Springer eBooks · 5

Table 1. [Summary of Molecular Genetic Testing Used in Hereditary Folate Malabsorption].

2014 · Ndeye Diop-Bove, David Kronn, et al.

Table 2. [Selected SLC46A1 Pathogenic Variants].

2014 · Ndeye Diop-Bove, David Kronn, et al.

Works count: 13

Citation count: 841

H-index: 10

I10-index: 10