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Items: 15

1.

The clinical course and genetic defect in the PCFT gene in a 27-year-old woman with hereditary folate malabsorption.

Min SH, Oh SY, Karp GI, Poncz M, Zhao R, Goldman ID.

J Pediatr. 2008 Sep;153(3):435-7. doi: 10.1016/j.jpeds.2008.04.009.

3.

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.

4.

[Two cases with generalized intracranial calcification due to hereditary folate malabsorption and literature review].

Zhang Y, Wang Q, Li DX, Liu YP, Song JQ, Li MQ, Qin YP, Yang YL.

Zhonghua Er Ke Za Zhi. 2016 Dec 2;54(12):931-935. doi: 10.3760/cma.j.issn.0578-1310.2016.12.012. Review. Chinese.

PMID:
27938595
5.

Molecular and functional characteristics of proton-coupled folate transporter.

Yuasa H, Inoue K, Hayashi Y.

J Pharm Sci. 2009 May;98(5):1608-16. doi: 10.1002/jps.21515. Review.

PMID:
18823045
7.

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

Zhao R, Goldman ID.

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

8.

Hereditary folate malabsorption: family report and review of the literature.

Geller J, Kronn D, Jayabose S, Sandoval C.

Medicine (Baltimore). 2002 Jan;81(1):51-68. Review. No abstract available.

9.

The proton-coupled folate transporter (PCFT-SLC46A1) and the syndrome of systemic and cerebral folate deficiency of infancy: Hereditary folate malabsorption.

Zhao R, Aluri S, Goldman ID.

Mol Aspects Med. 2017 Feb;53:57-72. doi: 10.1016/j.mam.2016.09.002. Epub 2016 Sep 21. Review.

PMID:
27664775
10.

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.

11.

Mechanisms of membrane transport of folates into cells and across epithelia.

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

Annu Rev Nutr. 2011 Aug 21;31:177-201. doi: 10.1146/annurev-nutr-072610-145133. Review.

12.

Membrane transporters and folate homeostasis: intestinal absorption and transport into systemic compartments and tissues.

Zhao R, Matherly LH, Goldman ID.

Expert Rev Mol Med. 2009 Jan 28;11:e4. doi: 10.1017/S1462399409000969. Review.

13.

Importance of vitamin B12 and folate metabolism in malabsorption.

Gallagher ND.

Clin Gastroenterol. 1983 May;12(2):437-41. Review.

PMID:
6347465
14.

Imerslund-Gräsbeck syndrome in a 25-month-old Italian girl caused by a homozygous mutation in AMN.

De Filippo G, Rendina D, Rocco V, Esposito T, Gianfrancesco F, Strazzullo P.

Ital J Pediatr. 2013 Sep 17;39:58. doi: 10.1186/1824-7288-39-58. Review.

15.

New perspectives on folate transport in relation to alcoholism-induced folate malabsorption--association with epigenome stability and cancer development.

Hamid A, Wani NA, Kaur J.

FEBS J. 2009 Apr;276(8):2175-91. doi: 10.1111/j.1742-4658.2009.06959.x. Epub 2009 Mar 9. Review.

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