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Role of the tryptophan residues in proton-coupled folate transporter (PCFT-SLC46A1) function.

Najmi M, Zhao R, Fiser A, Goldman ID.

Am J Physiol Cell Physiol. 2016 Jul 1;311(1):C150-7. doi: 10.1152/ajpcell.00084.2016. Epub 2016 Jun 1.


Hereditary folate malabsorption with extensive intracranial calcification.

Ahmad I, Mukhtar G, Iqbal J, Ali SW.

Indian Pediatr. 2015 Jan;52(1):67-8.


Identification of Tyr residues that enhance folate substrate binding and constrain oscillation of the proton-coupled folate transporter (PCFT-SLC46A1).

Visentin M, Unal ES, Najmi M, Fiser A, Zhao R, Goldman ID.

Am J Physiol Cell Physiol. 2015 Apr 15;308(8):C631-41. doi: 10.1152/ajpcell.00238.2014. Epub 2015 Jan 21.


Reversible pancytopenia and immunodeficiency in a patient with hereditary folate malabsorption.

Erlacher M, Grünert SC, Cseh A, Steinfeld R, Salzer U, Lausch E, Nosswitz U, Dückers G, Niehues T, Ehl S, Niemeyer CM, Speckmann C.

Pediatr Blood Cancer. 2015 Jun;62(6):1091-4. doi: 10.1002/pbc.25364. Epub 2014 Dec 11.


Biology of the major facilitative folate transporters SLC19A1 and SLC46A1.

Hou Z, Matherly LH.

Curr Top Membr. 2014;73:175-204. doi: 10.1016/B978-0-12-800223-0.00004-9. Review.


Impact of folate therapy on combined immunodeficiency secondary to hereditary folate malabsorption.

Kishimoto K, Kobayashi R, Sano H, Suzuki D, Maruoka H, Yasuda K, Chida N, Yamada M, Kobayashi K.

Clin Immunol. 2014 Jul;153(1):17-22. doi: 10.1016/j.clim.2014.03.014. Epub 2014 Mar 29.


The first Chinese case report of hereditary folate malabsorption with a novel mutation on SLC46A1.

Wang Q, Li X, Ding Y, Liu Y, Qin Y, Yang Y.

Brain Dev. 2015 Jan;37(1):163-7. doi: 10.1016/j.braindev.2014.01.010. Epub 2014 Feb 15.


The intestinal absorption of folates.

Visentin M, Diop-Bove N, Zhao R, Goldman ID.

Annu Rev Physiol. 2014;76:251-74. doi: 10.1146/annurev-physiol-020911-153251. Review.


The major facilitative folate transporters solute carrier 19A1 and solute carrier 46A1: biology and role in antifolate chemotherapy of cancer.

Matherly LH, Wilson MR, Hou Z.

Drug Metab Dispos. 2014 Apr;42(4):632-49. doi: 10.1124/dmd.113.055723. Epub 2014 Jan 6. Review.


The proton-coupled folate transporter: physiological and pharmacological roles.

Zhao R, Goldman ID.

Curr Opin Pharmacol. 2013 Dec;13(6):875-80. Review.


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

Diop-Bove N, Jain M, Scaglia F, Goldman ID.

Gene. 2013 Sep 25;527(2):673-4. doi: 10.1016/j.gene.2013.06.039. Epub 2013 Jun 28.


Inhibition of the proton-coupled folate transporter (PCFT-SLC46A1) by bicarbonate and other anions.

Zhao R, Visentin M, Suadicani SO, Goldman ID.

Mol Pharmacol. 2013 Jul;84(1):95-103. doi: 10.1124/mol.113.085605. Epub 2013 Apr 22.


Role of the fourth transmembrane domain in proton-coupled folate transporter function as assessed by the substituted cysteine accessibility method.

Shin DS, Zhao R, Fiser A, Goldman ID.

Am J Physiol Cell Physiol. 2013 Jun 15;304(12):C1159-67. doi: 10.1152/ajpcell.00353.2012. Epub 2013 Apr 3.


Folate and thiamine transporters mediated by facilitative carriers (SLC19A1-3 and SLC46A1) and folate receptors.

Zhao R, Goldman ID.

Mol Aspects Med. 2013 Apr-Jun;34(2-3):373-85. doi: 10.1016/j.mam.2012.07.006. Review.


The human proton-coupled folate transporter: Biology and therapeutic applications to cancer.

Desmoulin SK, Hou Z, Gangjee A, Matherly LH.

Cancer Biol Ther. 2012 Dec;13(14):1355-73. doi: 10.4161/cbt.22020. Epub 2012 Sep 6. Review.


Functional roles of the A335 and G338 residues of the proton-coupled folate transporter (PCFT-SLC46A1) mutated in hereditary folate malabsorption.

Shin DS, Zhao R, Fiser A, Goldman DI.

Am J Physiol Cell Physiol. 2012 Oct 15;303(8):C834-42. doi: 10.1152/ajpcell.00171.2012. Epub 2012 Jul 25.


Identification of a functionally critical GXXG motif and its relationship to the folate binding site of the proton-coupled folate transporter (PCFT-SLC46A1).

Zhao R, Shin DS, Fiser A, Goldman ID.

Am J Physiol Cell Physiol. 2012 Sep 15;303(6):C673-81. doi: 10.1152/ajpcell.00123.2012. Epub 2012 Jul 11.


A P425R mutation of the proton-coupled folate transporter causing hereditary folate malabsorption produces a highly selective alteration in folate binding.

Shin DS, Zhao R, Yap EH, Fiser A, Goldman ID.

Am J Physiol Cell Physiol. 2012 May 1;302(9):C1405-12. doi: 10.1152/ajpcell.00435.2011. Epub 2012 Feb 15.


Identification and functional impact of homo-oligomers of the human proton-coupled folate transporter.

Hou Z, Kugel Desmoulin S, Etnyre E, Olive M, Hsiung B, Cherian C, Wloszczynski PA, Moin K, Matherly LH.

J Biol Chem. 2012 Feb 10;287(7):4982-95. doi: 10.1074/jbc.M111.306860. Epub 2011 Dec 16.


Update and new concepts in vitamin responsive disorders of folate transport and metabolism.

Watkins D, Rosenblatt DS.

J Inherit Metab Dis. 2012 Jul;35(4):665-70. doi: 10.1007/s10545-011-9418-1. Epub 2011 Nov 23. Review.


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