BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

517 related articles for article (PubMed ID: 17129779)

  • 1. Identification of an intestinal folate transporter and the molecular basis for hereditary folate malabsorption.
    Qiu A; Jansen M; Sakaris A; Min SH; Chattopadhyay S; Tsai E; Sandoval C; Zhao R; Akabas MH; Goldman ID
    Cell; 2006 Dec; 127(5):917-28. PubMed ID: 17129779
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Identification of proton-coupled high-affinity human intestinal folate transporter mutated in human hereditary familial folate malabsorption.
    Wolf G
    Nutr Rev; 2007 Dec; 65(12 Pt 1):554-7. PubMed ID: 18236695
    [TBL] [Abstract][Full Text] [Related]  

  • 3. The molecular identity and characterization of a Proton-coupled Folate Transporter--PCFT; biological ramifications and impact on the activity of pemetrexed.
    Zhao R; Goldman ID
    Cancer Metastasis Rev; 2007 Mar; 26(1):129-39. PubMed ID: 17340171
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Functional characterization of PCFT/HCP1 as the molecular entity of the carrier-mediated intestinal folate transport system in the rat model.
    Inoue K; Nakai Y; Ueda S; Kamigaso S; Ohta KY; Hatakeyama M; Hayashi Y; Otagiri M; Yuasa H
    Am J Physiol Gastrointest Liver Physiol; 2008 Mar; 294(3):G660-8. PubMed ID: 18174275
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Functional characterization of human proton-coupled folate transporter/heme carrier protein 1 heterologously expressed in mammalian cells as a folate transporter.
    Nakai Y; Inoue K; Abe N; Hatakeyama M; Ohta KY; Otagiri M; Hayashi Y; Yuasa H
    J Pharmacol Exp Ther; 2007 Aug; 322(2):469-76. PubMed ID: 17475902
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Hereditary folate malabsorption: a positively charged amino acid at position 113 of the proton-coupled folate transporter (PCFT/SLC46A1) is required for folic acid binding.
    Lasry I; Berman B; Glaser F; Jansen G; Assaraf YG
    Biochem Biophys Res Commun; 2009 Aug; 386(3):426-31. PubMed ID: 19508863
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Down-regulation of reduced folate carrier may result in folate malabsorption across intestinal brush border membrane during experimental alcoholism.
    Hamid A; Wani NA; Rana S; Vaiphei K; Mahmood A; Kaur J
    FEBS J; 2007 Dec; 274(24):6317-28. PubMed ID: 18005257
    [TBL] [Abstract][Full Text] [Related]  

  • 8. 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. PubMed ID: 19292860
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Vitamin D3 and its nuclear receptor increase the expression and activity of the human proton-coupled folate transporter.
    Eloranta JJ; Zaïr ZM; Hiller C; Häusler S; Stieger B; Kullak-Ublick GA
    Mol Pharmacol; 2009 Nov; 76(5):1062-71. PubMed ID: 19666701
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Rodent intestinal folate transporters (SLC46A1): secondary structure, functional properties, and response to dietary folate restriction.
    Qiu A; Min SH; Jansen M; Malhotra U; Tsai E; Cabelof DC; Matherly LH; Zhao R; Akabas MH; Goldman ID
    Am J Physiol Cell Physiol; 2007 Nov; 293(5):C1669-78. PubMed ID: 17898134
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Characterization of a folate transporter in HeLa cells with a low pH optimum and high affinity for pemetrexed distinct from the reduced folate carrier.
    Wang Y; Zhao R; Goldman ID
    Clin Cancer Res; 2004 Sep; 10(18 Pt 1):6256-64. PubMed ID: 15448015
    [TBL] [Abstract][Full Text] [Related]  

  • 12. 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; 527(2):673-4. PubMed ID: 23816405
    [TBL] [Abstract][Full Text] [Related]  

  • 13. A role for the proton-coupled folate transporter (PCFT-SLC46A1) in folate receptor-mediated endocytosis.
    Zhao R; Min SH; Wang Y; Campanella E; Low PS; Goldman ID
    J Biol Chem; 2009 Feb; 284(7):4267-74. PubMed ID: 19074442
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Molecular and functional characteristics of proton-coupled folate transporter.
    Yuasa H; Inoue K; Hayashi Y
    J Pharm Sci; 2009 May; 98(5):1608-16. PubMed ID: 18823045
    [TBL] [Abstract][Full Text] [Related]  

  • 15. The human proton-coupled folate transporter (hPCFT): modulation of intestinal expression and function by drugs.
    Urquhart BL; Gregor JC; Chande N; Knauer MJ; Tirona RG; Kim RB
    Am J Physiol Gastrointest Liver Physiol; 2010 Feb; 298(2):G248-54. PubMed ID: 19762432
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Haem and folate transport by proton-coupled folate transporter/haem carrier protein 1 (SLC46A1).
    Laftah AH; Latunde-Dada GO; Fakih S; Hider RC; Simpson RJ; McKie AT
    Br J Nutr; 2009 Apr; 101(8):1150-6. PubMed ID: 18782461
    [TBL] [Abstract][Full Text] [Related]  

  • 17. The functional roles of the His247 and His281 residues in folate and proton translocation mediated by the human proton-coupled folate transporter SLC46A1.
    Unal ES; Zhao R; Chang MH; Fiser A; Romero MF; Goldman ID
    J Biol Chem; 2009 Jun; 284(26):17846-57. PubMed ID: 19389703
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Absorption and malabsorption of folates.
    Rosenberg IH
    Clin Haematol; 1976 Oct; 5(3):589-618. PubMed ID: 10121
    [TBL] [Abstract][Full Text] [Related]  

  • 19. 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
    Am J Physiol Cell Physiol; 2010 Nov; 299(5):C1153-61. PubMed ID: 20686069
    [TBL] [Abstract][Full Text] [Related]  

  • 20. The spectrum of mutations in the PCFT gene, coding for an intestinal folate transporter, that are the basis for hereditary folate malabsorption.
    Zhao R; Min SH; Qiu A; Sakaris A; Goldberg GL; Sandoval C; Malatack JJ; Rosenblatt DS; Goldman ID
    Blood; 2007 Aug; 110(4):1147-52. PubMed ID: 17446347
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 26.