Literature DB >> 11807405

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

James Geller1, David Kronn, Somasundaram Jayabose, Claudio Sandoval.   

Abstract

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Year:  2002        PMID： 11807405     DOI： 10.1097/00005792-200201000-00004

Source DB:  PubMed          Journal:  Medicine (Baltimore)        ISSN： 0025-7974            Impact factor:   1.889


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  45 in total

1.  Effect of chronic alcohol exposure on folate uptake by liver mitochondria.

Authors:  Arundhati Biswas; Sundar Rajan Senthilkumar; Hamid M Said
Journal:  Am J Physiol Cell Physiol       Date:  2011-09-28       Impact factor: 4.249

2.  The obligatory intestinal folate transporter PCFT (SLC46A1) is regulated by nuclear respiratory factor 1.

Authors:  Nitzan Gonen; Yehuda G Assaraf
Journal:  J Biol Chem       Date:  2010-08-19       Impact factor: 5.157

3.  CSF 5-Methyltetrahydrofolate Serial Monitoring to Guide Treatment of Congenital Folate Malabsorption Due to Proton-Coupled Folate Transporter (PCFT) Deficiency.

Authors:  A Torres; S A Newton; B Crompton; A Borzutzky; E J Neufeld; L Notarangelo; G T Berry
Journal:  JIMD Rep       Date:  2015-05-26

Review 4.  Mechanisms of membrane transport of folates into cells and across epithelia.

Authors:  Rongbao Zhao; Ndeye Diop-Bove; Michele Visentin; I David Goldman
Journal:  Annu Rev Nutr       Date:  2011-08-21       Impact factor: 11.848

5.  Prevalence of a loss-of-function mutation in the proton-coupled folate transporter gene (PCFT-SLC46A1) causing hereditary folate malabsorption in Puerto Rico.

Authors:  Kris M Mahadeo; Ndeye Diop-Bove; Sonia I Ramirez; Carmen L Cadilla; Enid Rivera; Madelena Martin; Norma B Lerner; Lisa DiAntonio; Salvatore Duva; Pedro J Santiago-Borrero; I David Goldman
Journal:  J Pediatr       Date:  2011-04-13       Impact factor: 4.406

Review 6.  Membrane transporters and folate homeostasis: intestinal absorption and transport into systemic compartments and tissues.

Authors:  Rongbao Zhao; Larry H Matherly; I David Goldman
Journal:  Expert Rev Mol Med       Date:  2009-01-28       Impact factor: 5.600

7.  A role for the proton-coupled folate transporter (PCFT-SLC46A1) in folate receptor-mediated endocytosis.

Authors:  Rongbao Zhao; Sang Hee Min; Yanhua Wang; Estela Campanella; Philip S Low; I David Goldman
Journal:  J Biol Chem       Date:  2008-12-11       Impact factor: 5.157

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

Authors:  Daniel Sanghoon Shin; Rongbao Zhao; Andras Fiser; David I Goldman
Journal:  Am J Physiol Cell Physiol       Date:  2012-07-25       Impact factor: 4.249

9.  A novel PCFT gene mutation (p.Cys66LeufsX99) causing hereditary folate malabsorption.

Authors:  Esther Meyer; Manju A Kurian; Shanaz Pasha; Richard C Trembath; Trevor Cole; Eamonn R Maher
Journal:  Mol Genet Metab       Date:  2009-11-16       Impact factor: 4.797

10.  N-linked glycosylation and its impact on the electrophoretic mobility and function of the human proton-coupled folate transporter (HsPCFT).

Authors:  Ersin Selcuk Unal; Rongbao Zhao; Andong Qiu; I David Goldman
Journal:  Biochim Biophys Acta       Date:  2008-03-20
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