-
1
-
-
0027980902
-
Human red cell aquaporin CHIP.I. Molecular characteriza- tion of ABH and Colton blood group antigens
-
Smith BL, Preston GM, Spring FA, Anstee DJ, Agre P. Human red cell aquaporin CHIP. I. Molecular characteriza- tion of ABH and Colton blood group antigens. J Clin Invest 1994;94:1043-9.
-
(1994)
J Clin Invest
, vol.94
, pp. 1043-1049
-
-
Smith, B.L.1
Preston, G.M.2
Spring, F.A.3
Anstee, D.J.4
Agre, P.5
-
3
-
-
0033153117
-
A single mutation inside the NPA motif of Aquaporin-1 found in a Colton-null phenotype
-
Chretien S, Cartron JP. A single mutation inside the NPA motif of Aquaporin-1 found in a Colton-null phenotype. Blood 1999;93:4021-3.
-
(1999)
Blood
, vol.93
, pp. 4021-4023
-
-
Chretien, S.1
Cartron, J.P.2
-
4
-
-
0034777978
-
An AQP1 null allele in an Indian woman with Co(a-b-) phenotype and high-titer anti-Co3 associated with mild HDN
-
Joshi SR, Wagner FF, Vasantha K, Panjwani SR, Flegel WA. An AQP1 null allele in an Indian woman with Co(a-b-) phenotype and high-titer anti-Co3 associated with mild HDN. Transfusion 2001;41:1273-8.
-
(2001)
Transfusion
, vol.41
, pp. 1273-1278
-
-
Joshi, S.R.1
Wagner, F.F.2
Vasantha, K.3
Panjwani, S.R.4
Flegel, W.A.5
-
5
-
-
0028088012
-
Mutations in Aquaporin-1 in phenotypically normal humans without functional CHIP water channels
-
Preston GM, Smith BL, Zeidel ML, Moulds JJ, Agre P. Mutations in Aquaporin-1 in phenotypically normal humans without functional CHIP water channels. Science 1994;265: 1585-7.
-
(1994)
Science
, vol.265
, pp. 1585-1587
-
-
Preston, G.M.1
Smith, B.L.2
Zeidel, M.L.3
Moulds, J.J.4
Agre, P.5
-
6
-
-
0030066779
-
Functional analysis of Aquaporin-1-deficient red cells. The Colton-null phenotype
-
Mathai JC, Mori S, Smith BL, Preston GM, Mohandas N, Collins M, van Zijl PC, Zeidel ML, Agre P. Functional analysis of Aquaporin-1-deficient red cells. The Colton-null phenotype. J Biol Chem 1996;271:1309-13.
-
(1996)
J Biol Chem
, vol.271
, pp. 1309-1313
-
-
Mathai, J.C.1
Mori, S.2
Smith, B.L.3
Preston, G.M.4
Mohandas, N.5
Collins, M.6
Van Zijl, P.C.7
Zeidel, M.L.8
Agre, P.9
-
8
-
-
0027980006
-
A novel form of congenital dyserythropoietic anemia associated with deficiency of erythroid CD44 and a unique blood group phenotype [In(a-b-),Co(a-b-)
-
Parsons SF, Jones J, Anstee DJ, Judson PA, Gardner B, Wiener E, Poole J, Illum N, Wickramasinghe SN. A novel form of congenital dyserythropoietic anemia associated with deficiency of erythroid CD44 and a unique blood group phenotype [In(a-b-), Co(a-b-)]. Blood 1994;83:860-8.
-
(1994)
Blood
, vol.83
, pp. 860-868
-
-
Parsons, S.F.1
Jones, J.2
Anstee, D.J.3
Judson, P.A.4
Gardner, B.5
Wiener, E.6
Poole, J.7
Illum, N.8
Wickramasinghe, S.N.9
-
9
-
-
0035913207
-
Defective urinary-concentrating ability due to a complete deficiency of Aquaporin-1
-
King LS, Choi M, Fernandez PC, Cartron JP, Agre P. Defective urinary-concentrating ability due to a complete deficiency of Aquaporin-1. N Engl J Med 2001;345:175-9.
-
(2001)
N Engl J Med
, vol.345
, pp. 175-179
-
-
King, L.S.1
Choi, M.2
Fernandez, P.C.3
Cartron, J.P.4
Agre, P.5
-
10
-
-
0037154182
-
Decreased pulmonary vascular permeability in Aquaporin-1-null humans
-
King LS, Nielsen S, Agre P, Brown RH. Decreased pulmonary vascular permeability in Aquaporin-1-null humans. Proc Natl Acad Sci USA 2002;99:1059-63.
-
(2002)
Proc Natl Acad Sci USA
, vol.99
, pp. 1059-1063
-
-
King, L.S.1
Nielsen, S.2
Agre, P.3
Brown, R.H.4
-
11
-
-
0023239372
-
Studies on the blood of a Co(a-b-) proposita and her family
-
Lacey PA, Robinson J, Collins ML, Bailey DG, Evans CC, Moulds JJ, Daniels GL. Studies on the blood of a Co(a-b-) proposita and her family. Transfusion 1987;27:268-71.
-
(1987)
Transfusion
, vol.27
, pp. 268-271
-
-
Lacey, P.A.1
Robinson, J.2
Collins, M.L.3
Bailey, D.G.4
Evans, C.C.5
Moulds, J.J.6
Daniels, G.L.7
-
13
-
-
0032478806
-
Evidence for the presence of Aquaporin-3 in human red blood cells
-
Roudier N, Verbavatz JM, Maurel C, Ripoche P, Tacnet F. Evidence for the presence of Aquaporin-3 in human red blood cells. J Biol Chem 1998;273:8407-12.
-
(1998)
J Biol Chem
, vol.273
, pp. 8407-8412
-
-
Roudier, N.1
Verbavatz, J.M.2
Maurel, C.3
Ripoche, P.4
Tacnet, F.5
-
14
-
-
60149102569
-
Identification and characterization of a novel XK splice site mutation in a patient with McLeod syndrome
-
Arnaud L, Salachas F, Lucien N, Maisonobe T, Le Pennec PY, Babinet J, Cartron JP. Identification and characterization of a novel XK splice site mutation in a patient with McLeod syndrome. Transfusion 2009;49:479-84.
-
(2009)
Transfusion
, vol.49
, pp. 479-484
-
-
Arnaud, L.1
Salachas, F.2
Lucien, N.3
Maisonobe, T.4
Le Pennec, P.Y.5
Babinet, J.6
Cartron, J.P.7
-
15
-
-
0032957639
-
Two-stage PCR protocol allowing introduction of multiple mutations, deletions and insertions using QuikChange site-directed mutagenesis
-
Wang W, Malcolm BA. Two-stage PCR protocol allowing introduction of multiple mutations, deletions and insertions using QuikChange site-directed mutagenesis. Biotechniques 1999;26:680-2.
-
(1999)
Biotechniques
, vol.26
, pp. 680-682
-
-
Wang, W.1
Malcolm, B.A.2
-
16
-
-
0032006158
-
Isolation of the human Aquaporin-1 promoter and functional characterization in human erythroleukemia cell lines
-
Umenishi F, Verkman AS. Isolation of the human Aquaporin-1 promoter and functional characterization in human erythroleukemia cell lines. Genomics 1998;47: 341-9.
-
(1998)
Genomics
, vol.47
, pp. 341-349
-
-
Umenishi, F.1
Verkman, A.S.2
-
17
-
-
78649470313
-
A clinically relevant Co(a)-like allele encoded by AQP1 (Q47R)
-
Wagner FF, Flegel WA. A clinically relevant Co(a)-like allele encoded by AQP1 (Q47R). Infus Ther Transfus Med 2002; 29:(Sonderheft 1):5.
-
(2002)
Infus Ther Transfus Med
, vol.29
, pp. 5
-
-
Wagner, F.F.1
Flegel, W.A.2
-
18
-
-
77954752254
-
A clinically relevant Co(a)-like allele encoded by AQP1 (Q47R
-
Wagner FF, Flegel WA. A clinically relevant Co(a)-like allele encoded by AQP1 (Q47R). Transfusion 2002;42:24S.
-
(2002)
Transfusion
, vol.42
-
-
Wagner, F.F.1
Flegel, W.A.2
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