-
1
-
-
77949904065
-
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
-
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
-
3
-
-
2942545500
-
Update on cobalamin, folate, and homocysteine
-
Carmel R, Green R, Rosenblatt DS, Watkins D. Update on cobalamin, folate, and homocysteine. Hematology Am Soc Hematol Educ Program. 2003:62-81.
-
(2003)
Hematology Am Soc Hematol Educ Program
, pp. 62-81
-
-
Carmel, R.1
Green, R.2
Rosenblatt, D.S.3
Watkins, D.4
-
4
-
-
1442357042
-
12)-intrinsic factor receptor is a novel complex of cubilin and amnionless
-
DOI 10.1182/blood-2003-08-2852
-
Fyfe JC, Madsen M, Hojrup P, et al. The functional cobalamin (vitamin B12)-intrinsic factor receptor is a novel complex of cubilin and amnionless. Blood. 2004;103(5):1573-1579. (Pubitemid 38268944)
-
(2004)
Blood
, vol.103
, Issue.5
, pp. 1573-1579
-
-
Fyfe, J.C.1
Madsen, M.2
Hojrup, P.3
Christensen, E.I.4
Tanner, S.M.5
De La, C.A.6
He, Q.7
Moestrup, S..K.8
-
5
-
-
34248165629
-
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
-
6
-
-
0037371866
-
Amnionless, essential for mouse gastrulation, is mutated in recessive hereditary megaloblastic anemia
-
DOI 10.1038/ng1098
-
Tanner SM, Aminoff M, Wright FA, et al. Amnionless, essential for mouse gastrulation, is mutated in recessive hereditary megaloblastic anemia. Nat Genet. 2003;33(3):426-429. (Pubitemid 36278863)
-
(2003)
Nature Genetics
, vol.33
, Issue.3
, pp. 426-429
-
-
Tanner, S.M.1
Aminoff, M.2
Wright, F.A.3
Liyanarachchi, S.4
Kuronen, M.5
Saarinen, A.6
Massika, O.7
Mandel, H.8
Broch, H.9
De La, C.A.10
-
7
-
-
11144354849
-
12: Founder Effects, Consanguinity, and High Clinical Awareness Explain Aggregations in Scandinavia and the Middle East
-
DOI 10.1002/humu.20014
-
Tanner SM, Li Z, Bisson R, et al. Genetically heterogeneous selective intestinal malabsorption of vitamin B12: founder effects, consanguinity, and high clinical awareness explain aggregations in Scandinavia and the Middle East. Hum Mutat. 2004;23(4):327-333. (Pubitemid 38461514)
-
(2004)
Human Mutation
, vol.23
, Issue.4
, pp. 327-333
-
-
Tanner, S.M.1
Li, Z.2
Bisson, R.3
Acar, C.4
Oner, C.5
Oner, R.6
Cetin, M.7
Abdelaal, M.A.8
Ismail, E.A.9
Lissens, W.10
Krahe, R.11
Broch, H.12
Grasbeck, R.13
De La, C.A.14
-
8
-
-
20144372885
-
Hereditary juvenile cobalamin deficiency caused by mutations in the intrinsic factor gene
-
DOI 10.1073/pnas.0500517102
-
Tanner SM, Li Z, Perko JD, et al. Hereditary juvenile cobalamin deficiency caused by mutations in the intrinsic factor gene. Proc Natl Acad Sci U S A. 2005;102(11):4130-4133. (Pubitemid 40388567)
-
(2005)
Proceedings of the National Academy of Sciences of the United States of America
, vol.102
, Issue.11
, pp. 4130-4133
-
-
Tanner, S.M.1
Li, Z.2
Perko, J.D.3
Oner, C.4
Cetin, M.5
Altay, C.6
Yurtsever, Z.7
David, K.L.8
Faivre, L.9
Ismail, E.A.10
Grasbeck, R.11
De La, C.A.12
-
9
-
-
0842307311
-
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
-
10
-
-
0035065591
-
The amnionless gene, essential for mouse gastrulation, encodes a visceral-endoderm-specific protein with an extracellular cysteine-rich domain
-
DOI 10.1038/86912
-
Kalantry S, Manning S, Haub O, et al. The amnionless gene, essential for mouse gastrulation, encodes a visceral-endoderm-specific protein with an extracellular cysteine-rich domain. Nat Genet. 2001;27(4):412-416. (Pubitemid 32268422)
-
(2001)
Nature Genetics
, vol.27
, Issue.4
, pp. 412-416
-
-
Kalantry, S.1
Manning, S.2
Haub, O.3
Tomihara-Newberger, C.4
Lee, H.-G.5
Fangman, J.6
Disteche, C.M.7
Manova, K.8
Lacy, E.9
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