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Volumn 117, Issue 16, 2011, Pages 4397-4398

Investigation of the ABC transporter MRP1 in selected patients with presumed defects in vitamin B12 absorption

Author keywords

[No Author keywords available]

Indexed keywords

ABC TRANSPORTER; CYANOCOBALAMIN; GENOMIC DNA; INTRINSIC FACTOR; MULTIDRUG RESISTANCE PROTEIN 1;

EID: 79955953549     PISSN: 00064971     EISSN: 15280020     Source Type: Journal    
DOI: 10.1182/blood-2010-12-322750     Document Type: Letter
Times cited : (12)

References (10)
  • 1
    • 77949904065 scopus 로고    scopus 로고
    • Identification of multidrug resistance protein 1 (MRP1/ABCC1) as a molecular gate for cellular export of cobalamin
    • Beedholm-Ebsen R, van deWetering K, Hardlei T, Nexo E, Borst P, Moestrup SK. Identification of multidrug resistance protein 1 (MRP1/ABCC1) as a molecular gate for cellular export of cobalamin. Blood. 2010;115(8):1632-1639.
    • (2010) Blood , vol.115 , Issue.8 , pp. 1632-1639
    • Beedholm-Ebsen, R.1    Van DeWetering, K.2    Hardlei, T.3    Nexo, E.4    Borst, P.5    Moestrup, S.K.6
  • 2
    • 8344273321 scopus 로고    scopus 로고
    • Cobalamin transport proteins and their cell-surface receptors
    • Seetharam B, Yammani RR. Cobalamin transport proteins and their cell-surface receptors. Expert Rev Mol Med. 2003;5(18):1-18.
    • (2003) Expert Rev Mol Med , vol.5 , Issue.18 , pp. 1-18
    • Seetharam, B.1    Yammani, R.R.2
  • 5
    • 34248165629 scopus 로고    scopus 로고
    • Imerslund-Gräsbeck syndrome (selective vitamin B12 malabsorption with proteinuria)
    • Gräsbeck R. Imerslund-Gräsbeck syndrome (selective vitamin B12 malabsorption with proteinuria). Orphanet J Rare Dis. 2006;1:17.
    • (2006) Orphanet J Rare Dis , vol.1 , pp. 17
    • Gräsbeck, R.1
  • 9
    • 0842307311 scopus 로고    scopus 로고
    • Identification of a 4-base deletion in the gene in inherited intrinsic factor deficiency
    • DOI 10.1182/blood-2003-07-2239
    • Yassin F, Rothenberg SP, Rao S, Gordon MM, Alpers DH, Quadros EV. Identification of a 4-base deletion in the gene in inherited intrinsic factor deficiency. Blood. 2004;103(4):1515-1517. (Pubitemid 38168671)
    • (2004) Blood , vol.103 , Issue.4 , pp. 1515-1517
    • Yassin, F.1    Rothenberg, S.P.2    Rao, S.3    Gordon, M.M.4    Alpers, D.H.5    Quadros, E.V.6


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.