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Properties of the Arg376 residue of the proton-coupled folate transporter (PCFT-SLC46A1) and a glutamine mutant causing hereditary folate malabsorption.
Mahadeo K, Diop-Bove N, Shin D, Unal ES, Teo J, Zhao R, Chang MH, Fulterer A, Romero MF, Goldman ID. Mahadeo K, et al. Among authors: diop bove n. Am J Physiol Cell Physiol. 2010 Nov;299(5):C1153-61. doi: 10.1152/ajpcell.00113.2010. Epub 2010 Aug 4. Am J Physiol Cell Physiol. 2010. PMID: 20686069 Free PMC article.
Prevalence of a loss-of-function mutation in the proton-coupled folate transporter gene (PCFT-SLC46A1) causing hereditary folate malabsorption in Puerto Rico.
Mahadeo KM, Diop-Bove N, Ramirez SI, Cadilla CL, Rivera E, Martin M, Lerner NB, DiAntonio L, Duva S, Santiago-Borrero PJ, Goldman ID. Mahadeo KM, et al. Among authors: diop bove n. J Pediatr. 2011 Oct;159(4):623-7.e1. doi: 10.1016/j.jpeds.2011.03.005. Epub 2011 Apr 13. J Pediatr. 2011. PMID: 21489556 Free PMC article.
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.
Zhao R, Diop-Bove N, Goldman ID. Zhao R, et al. Among authors: diop bove n. Mol Pharmacol. 2014 Feb;85(2):310-21. doi: 10.1124/mol.113.089110. Epub 2013 Nov 18. Mol Pharmacol. 2014. PMID: 24249723 Free PMC article.
The intestinal absorption of folates.
Visentin M, Diop-Bove N, Zhao R, Goldman ID. Visentin M, et al. Among authors: diop bove n. Annu Rev Physiol. 2014;76:251-74. doi: 10.1146/annurev-physiol-020911-153251. Annu Rev Physiol. 2014. PMID: 24512081 Free PMC article. Review.