-
1
-
-
0037398141
-
International Society of Blood Transfusion Committee on terminology for red cell surface antigens: Vancouver Report
-
Daniels GL, Cartron JP, Fletcher A, et al. International Society of Blood Transfusion Committee on terminology for red cell surface antigens: Vancouver Report. Vox Sang 2003;84:244-7.
-
(2003)
Vox Sang
, vol.84
, pp. 244-247
-
-
Daniels, G.L.1
Cartron, J.P.2
Fletcher, A.3
-
2
-
-
0030346980
-
Rh serology - Coordinator's report
-
Scott M. Rh serology - coordinator's report. Transfus Clin Biol 1996;3:333-7.
-
(1996)
Transfus Clin Biol
, vol.3
, pp. 333-337
-
-
Scott, M.1
-
3
-
-
0036177943
-
Section 1A: Rh serology. Coordinator's report
-
Scott M. Section 1A: Rh serology. Coordinator's report. Transfus Clin Biol 2002;9:23-9.
-
(2002)
Transfus Clin Biol
, vol.9
, pp. 23-29
-
-
Scott, M.1
-
4
-
-
0005382020
-
Observations on subdivisions of the Rh antigen D
-
Tippett P, Sanger R. Observations on subdivisions of the Rh antigen D. Vox Sang 1962;7:9-13.
-
(1962)
Vox Sang
, vol.7
, pp. 9-13
-
-
Tippett, P.1
Sanger, R.2
-
5
-
-
0026495861
-
Molecular cloning and primary structure of the human blood group RhD polypeptide
-
Le van Kim C, Mouro I, Cherif-Zahar B, et al. Molecular cloning and primary structure of the human blood group RhD polypeptide. Proc Natl Acad Sci USA 1992;89:10925-9.
-
(1992)
Proc Natl Acad Sci USA
, vol.89
, pp. 10925-10929
-
-
Le Van Kim, C.1
Mouro, I.2
Cherif-Zahar, B.3
-
6
-
-
0027293541
-
Molecular cloning of RhD cDNA derived from a gene present in RhD-positive, but not RhD-negative individuals
-
Arce MA, Thompson ES, Wagner S, Coyne KE, Ferdman BA, Lublin DM. Molecular cloning of RhD cDNA derived from a gene present in RhD-positive, but not RhD-negative individuals. Blood 1993;82:651-655
-
(1993)
Blood
, vol.82
, pp. 651-655
-
-
Arce, M.A.1
Thompson, E.S.2
Wagner, S.3
Coyne, K.E.4
Ferdman, B.A.5
Lublin, D.M.6
-
7
-
-
0025024967
-
Molecular cloning and protein structure of a human blood group Rh polypeptide
-
Cherif-Zahar B, Bloy C, Le Van Kim C, et al. Molecular cloning and protein structure of a human blood group Rh polypeptide. Proc Natl Acad Sci USA 1990;87:6243-7.
-
(1990)
Proc Natl Acad Sci USA
, vol.87
, pp. 6243-6247
-
-
Cherif-Zahar, B.1
Bloy, C.2
Le Van Kim, C.3
-
8
-
-
0025167261
-
cDNA cloning of a 30 kDa erythrocyte membrane protein associated with Rh (Rhesus)-blood-group-antigen expression
-
Avent ND, Ridgwell K, Tanner MJ, Anstee DJ. cDNA cloning of a 30 kDa erythrocyte membrane protein associated with Rh (Rhesus)-blood-group-antigen expression. Biochem J 1990;271:821-5.
-
(1990)
Biochem J
, vol.271
, pp. 821-825
-
-
Avent, N.D.1
Ridgwell, K.2
Tanner, M.J.3
Anstee, D.J.4
-
9
-
-
0032932817
-
Molecular basis of weak D phenotypes
-
Wagner FF, Gassner C, Müller TH, Schönitzer D, Schunter F, Flegel WA. Molecular basis of weak D phenotypes. Blood 1999;93:385-93.
-
(1999)
Blood
, vol.93
, pp. 385-393
-
-
Wagner, F.F.1
Gassner, C.2
Müller, T.H.3
Schönitzer, D.4
Schunter, F.5
Flegel, W.A.6
-
10
-
-
0026808712
-
Isolation of cDNA clones for a 50 kDa glycoprotein of the human erythrocyte membrane associated with Rh (rhesus) blood-group antigen expression
-
Ridgwell K, Spurr NK, Laguda B, MacGeoch C, Avent ND, Tanner MJ. Isolation of cDNA clones for a 50 kDa glycoprotein of the human erythrocyte membrane associated with Rh (rhesus) blood-group antigen expression. Biochem J 1992;287:223-8.
-
(1992)
Biochem J
, vol.287
, pp. 223-228
-
-
Ridgwell, K.1
Spurr, N.K.2
Laguda, B.3
MacGeoch, C.4
Avent, N.D.5
Tanner, M.J.6
-
11
-
-
0038491423
-
Rh-RhAG/ankyrin-R, a new interaction site between the membrane bilayer and the red cell skeleton, is impaired by Rh(null)-associated mutation
-
Nicolas V, Le Van Kim C, Gane P, et al. Rh-RhAG/ankyrin-R, a new interaction site between the membrane bilayer and the red cell skeleton, is impaired by Rh(null)-associated mutation. J Biol Chem 2003;278:25526-33.
-
(2003)
J Biol Chem
, vol.278
, pp. 25526-25533
-
-
Nicolas, V.1
Le Van Kim, C.2
Gane, P.3
-
12
-
-
0030061717
-
Candidate gene acting as a suppressor of the RH locus in most cases of Rh-deficiency
-
Cherif-Zahar B, Raynal V, Gane P, et al. Candidate gene acting as a suppressor of the RH locus in most cases of Rh-deficiency. Nat Genet 1996;12:168-73.
-
(1996)
Nat Genet
, vol.12
, pp. 168-173
-
-
Cherif-Zahar, B.1
Raynal, V.2
Gane, P.3
-
13
-
-
0033757434
-
The human Rhesus-associated RhAG protein and a kidney homologue promote ammonium transport in yeast
-
Marini AM, Matassi G, Raynal V, Andre B, Cartron JP, Cherif-Zahar B.The human Rhesus-associated RhAG protein and a kidney homologue promote ammonium transport in yeast. Nat Genet 2000;26:341-4.
-
(2000)
Nat Genet
, vol.26
, pp. 341-344
-
-
Marini, A.M.1
Matassi, G.2
Raynal, V.3
Andre, B.4
Cartron, J.P.5
Cherif-Zahar, B.6
-
14
-
-
0037066722
-
Identification of the erythrocyte Rh blood group glycoprotein as a mammalian ammonium transporter
-
Westhoff CM, Ferreri-Jacobia M, Mak DO, Foskett JK. Identification of the erythrocyte Rh blood group glycoprotein as a mammalian ammonium transporter. J Biol Chem 2002;277:12499-502.
-
(2002)
J Biol Chem
, vol.277
, pp. 12499-12502
-
-
Westhoff, C.M.1
Ferreri-Jacobia, M.2
Mak, D.O.3
Foskett, J.K.4
-
15
-
-
0038486939
-
The Rh complex exports ammonium from human red blood cells
-
Hemker MB, Cheroutre G, van Zwieten R, et al. The Rh complex exports ammonium from human red blood cells. Br J Haematol 2003;122:333-40.
-
(2003)
Br J Haematol
, vol.122
, pp. 333-340
-
-
Hemker, M.B.1
Cheroutre, G.2
Van Zwieten, R.3
-
16
-
-
0037188490
-
Rhesus expression in a green alga is regulated by CO(2)
-
Soupene E, King N, Feild E, et al. Rhesus expression in a green alga is regulated by CO(2). Proc Natl Acad Sci USA 2002;99:7769-73.
-
(2002)
Proc Natl Acad Sci USA
, vol.99
, pp. 7769-7773
-
-
Soupene, E.1
King, N.2
Feild, E.3
-
17
-
-
0028012272
-
Organization of the gene (RHCE) encoding the human blood group RhCcEe antigens and characterization of the promoter region
-
Cherif-Zahar B, Le Van Kim C, Rouillac C, Raynal V, Cartron JP, Colin Y. Organization of the gene (RHCE) encoding the human blood group RhCcEe antigens and characterization of the promoter region. Genomics 1994;19:68-74.
-
(1994)
Genomics
, vol.19
, pp. 68-74
-
-
Cherif-Zahar, B.1
Le Van Kim, C.2
Rouillac, C.3
Raynal, V.4
Cartron, J.P.5
Colin, Y.6
-
18
-
-
0034659823
-
RHD gene deletion occurred in the Rhesus box
-
Wagner FF, Flegel WA. RHD gene deletion occurred in the Rhesus box. Blood 2000;95:3662-8.
-
(2000)
Blood
, vol.95
, pp. 3662-3668
-
-
Wagner, F.F.1
Flegel, W.A.2
-
19
-
-
0034114775
-
Gene organization and rearrangements at the human Rhesus blood group locus revealed by fiber-FISH analysis
-
Suto Y, Ishikawa Y, Hyodo H, Uchikawa M, Juji T. Gene organization and rearrangements at the human Rhesus blood group locus revealed by fiber-FISH analysis. Hum Genet 2000;106:164-71.
-
(2000)
Hum Genet
, vol.106
, pp. 164-171
-
-
Suto, Y.1
Ishikawa, Y.2
Hyodo, H.3
Uchikawa, M.4
Juji, T.5
-
20
-
-
0037085782
-
RHCE represents the ancestral RH position, while RHD is the duplicated gene
-
Wagner FF, Flegel WA. RHCE represents the ancestral RH position, while RHD is the duplicated gene. Blood 2002;99:2272-3.
-
(2002)
Blood
, vol.99
, pp. 2272-2273
-
-
Wagner, F.F.1
Flegel, W.A.2
-
21
-
-
0037121069
-
Entire sequence of a mouse chromosomal segment containing the gene Rhced and a comparative analysis of the homologous human sequence
-
Kumada M, Iwamoto S, Kamesaki T, Okuda H, Kajii E. Entire sequence of a mouse chromosomal segment containing the gene Rhced and a comparative analysis of the homologous human sequence. Gene 2002;299:165-72.
-
(2002)
Gene
, vol.299
, pp. 165-172
-
-
Kumada, M.1
Iwamoto, S.2
Kamesaki, T.3
Okuda, H.4
Kajii, E.5
-
22
-
-
0025723965
-
Genetic basis of the RhD-positive and RhD-negative blood group polymorphism as determined by Southern analysis
-
Colin Y, Cherif-Zahar B, Le Van Kim C, Raynal V, Van Huffel V, Cartron JP. Genetic basis of the RhD-positive and RhD-negative blood group polymorphism as determined by Southern analysis. Blood 1991;78:2747-52.
-
(1991)
Blood
, vol.78
, pp. 2747-2752
-
-
Colin, Y.1
Cherif-Zahar, B.2
Le Van Kim, C.3
Raynal, V.4
Van Huffel, V.5
Cartron, J.P.6
-
23
-
-
0035057567
-
Determination of RhD zygosity: Comparison of a double amplification refractory mutation system approach and a multiplex real-time quantitative PCR approach
-
Chiu RW, Murphy MF, Fidler C, Zee BC, Wainscoat JS, Lo YM. Determination of RhD zygosity: comparison of a double amplification refractory mutation system approach and a multiplex real-time quantitative PCR approach. Clin Chem 2001;47:667-72.
-
(2001)
Clin Chem
, vol.47
, pp. 667-672
-
-
Chiu, R.W.1
Murphy, M.F.2
Fidler, C.3
Zee, B.C.4
Wainscoat, J.S.5
Lo, Y.M.6
-
24
-
-
0036560615
-
Novel 3'Rhesus box sequences confound RHD zygosity assignment
-
Matheson KA, Denomme GA. Novel 3'Rhesus box sequences confound RHD zygosity assignment. Transfusion 2002;42:645-50.
-
(2002)
Transfusion
, vol.42
, pp. 645-650
-
-
Matheson, K.A.1
Denomme, G.A.2
-
25
-
-
1442293220
-
RHD allele distribution in Africans of Mali
-
Wagner FF, Moulds JM, Tounkara A, Kouriba B, Flegel WA. RHD allele distribution in Africans of Mali. BMC Genet 2003;4:14.
-
(2003)
BMC Genet
, vol.4
, pp. 14
-
-
Wagner, F.F.1
Moulds, J.M.2
Tounkara, A.3
Kouriba, B.4
Flegel, W.A.5
-
27
-
-
0029815713
-
W- red blood cells: Phenotypic homozygosity versus genotypic heterozygosity
-
W- red blood cells: phenotypic homozygosity versus genotypic heterozygosity. Blood 1996;88:2326-33.
-
(1996)
Blood
, vol.88
, pp. 2326-2333
-
-
Huang, C.H.1
-
28
-
-
0035191966
-
E variants found in Japanese and c antigenicity alteration without substitution in the second extracellular loop
-
Kashiwase K, Ishikawa Y, Hyodo H, et al. E variants found in Japanese and c antigenicity alteration without substitution in the second extracellular loop. Transfusion 2001;41:1408-12.
-
(2001)
Transfusion
, vol.41
, pp. 1408-1412
-
-
Kashiwase, K.1
Ishikawa, Y.2
Hyodo, H.3
-
29
-
-
0034053829
-
Evans antigen: A new hybrid structure occurring on background of D·· and D- Rh complexes
-
Cheng GJ, Chen Y, Reid ME, Huang CH. Evans antigen: a new hybrid structure occurring on background of D·· and D- Rh complexes. Vox Sang 2000;78:44-51.
-
(2000)
Vox Sang
, vol.78
, pp. 44-51
-
-
Cheng, G.J.1
Chen, Y.2
Reid, M.E.3
Huang, C.H.4
-
30
-
-
0024369405
-
Demonstration of seven epitopes on the Rh antigen D using human monoclonal anti-D antibodies and red cells from D categories
-
Lomas C, Tippett P, Thompson KM, Melamed MD, Hughes-Jones NC. Demonstration of seven epitopes on the Rh antigen D using human monoclonal anti-D antibodies and red cells from D categories. Vox Sang 1989;57:261-4.
-
(1989)
Vox Sang
, vol.57
, pp. 261-264
-
-
Lomas, C.1
Tippett, P.2
Thompson, K.M.3
Melamed, M.D.4
Hughes-Jones, N.C.5
-
32
-
-
0042334906
-
The RHCE allele ceRT: D epitope 6 expression does not require D-specific amíno amino acids
-
Wagner FF, Ladewig B, Flegel WA. The RHCE allele ceRT: D epitope 6 expression does not require D-specific amíno amino acids. Transfusion 2003;43:1248-54.
-
(2003)
Transfusion
, vol.43
, pp. 1248-1254
-
-
Wagner, F.F.1
Ladewig, B.2
Flegel, W.A.3
-
33
-
-
0032762793
-
Molecular configuration of Rh D epitopes as defined by site-directed mutagenesis and expression of mutant Rh constructs in K562 erythroleukemia cells
-
Liu W, Avent ND, Jones JW Scott ML, Voak D. Molecular configuration of Rh D epitopes as defined by site-directed mutagenesis and expression of mutant Rh constructs in K562 erythroleukemia cells. Blood 1999;94:3986-96.
-
(1999)
Blood
, vol.94
, pp. 3986-3996
-
-
Liu, W.1
Avent, N.D.2
Jones, J.W.3
Scott, M.L.4
Voak, D.5
-
34
-
-
0031001398
-
Polymorphism of the h allele and the population frequency of sporadic nonfunctional alleles
-
Wagner FF, Flegel WA. Polymorphism of the h allele and the population frequency of sporadic nonfunctional alleles. Transfusion 1997;37:284-90.
-
(1997)
Transfusion
, vol.37
, pp. 284-290
-
-
Wagner, F.F.1
Flegel, W.A.2
-
35
-
-
0033957696
-
The presence of an RHD pseudogene containing a 37 base-pair duplication and a nonsense mutation in Africans with the Rh D- blood group phenotype
-
Singleton BK, Green CA, Avent ND, et al. The presence of an RHD pseudogene containing a 37 base-pair duplication and a nonsense mutation in Africans with the Rh D- blood group phenotype. Blood 2000;95:12-8.
-
(2000)
Blood
, vol.95
, pp. 12-18
-
-
Singleton, B.K.1
Green, C.A.2
Avent, N.D.3
-
36
-
-
0012514010
-
Molecular background of Rh D-positive, D-negative, D(el) and weak D phenotypes in Chinese
-
Shao CP, Maas JH, Su YQ, Kohler M, Legler TJ. Molecular background of Rh D-positive, D-negative, D(el) and weak D phenotypes in Chinese. Vox Sang 2002;83:156-61.
-
(2002)
Vox Sang
, vol.83
, pp. 156-161
-
-
Shao, C.P.1
Maas, J.H.2
Su, Y.Q.3
Kohler, M.4
Legler, T.J.5
-
37
-
-
0031035263
-
Molecular background of VS and weak C expression in blacks
-
Faas BH, Beckers EA, Wildoer P, et al. Molecular background of VS and weak C expression in blacks. Transfusion 1997;37:38-44.
-
(1997)
Transfusion
, vol.37
, pp. 38-44
-
-
Faas, B.H.1
Beckers, E.A.2
Wildoer, P.3
-
38
-
-
0027993037
-
Serotype switching in a partially deleted RHD gene
-
Blunt T, Daniels G, Carritt B. Serotype switching in a partially deleted RHD gene. Vox Sang 1994;67:397-401.
-
(1994)
Vox Sang
, vol.67
, pp. 397-401
-
-
Blunt, T.1
Daniels, G.2
Carritt, B.3
-
39
-
-
0035432989
-
A D(V)-like phenotype is obliterated by A226P in the partial D DBS
-
Wagner FF, Ernst M, Sonneborn HH, Flegel WA. A D(V)-like phenotype is obliterated by A226P in the partial D DBS. Transfusion 2001;41:1052-8.
-
(2001)
Transfusion
, vol.41
, pp. 1052-1058
-
-
Wagner, F.F.1
Ernst, M.2
Sonneborn, H.H.3
Flegel, W.A.4
-
40
-
-
0032521490
-
Three molecular structures cause Rhesus D category VI phenotypes with distinct immunohematologic features
-
Wagner FF, Gassner C, Müller TH, Schönitzer D, Schunter F, Flegel WA. Three molecular structures cause Rhesus D category VI phenotypes with distinct immunohematologic features. Blood 1998;91:2157-68.
-
(1998)
Blood
, vol.91
, pp. 2157-2168
-
-
Wagner, F.F.1
Gassner, C.2
Müller, T.H.3
Schönitzer, D.4
Schunter, F.5
Flegel, W.A.6
-
41
-
-
0033970308
-
Detection of Rh23 in the partial D phenotype associated with the D(Va) category
-
Omi T, Okuda H, Iwamoto S, et al. Detection of Rh23 in the partial D phenotype associated with the D(Va) category. Transfusion 2000;40:256-8.
-
(2000)
Transfusion
, vol.40
, pp. 256-258
-
-
Omi, T.1
Okuda, H.2
Iwamoto, S.3
-
42
-
-
0027958599
-
Rearrangements of the blood group RhD gene associated with the DVI category phenotype
-
Mouro I, Le Van Kim C, Rouillac C, et al. Rearrangements of the blood group RhD gene associated with the DVI category phenotype. Blood 1994;83:1129-35.
-
(1994)
Blood
, vol.83
, pp. 1129-1135
-
-
Mouro, I.1
Le Van Kim, C.2
Rouillac, C.3
-
43
-
-
0029059940
-
Transcript analysis of D category phenotypes predicts hybrid Rh D-CE-D proteins associated with alteration of D epitopes
-
Rouillac C, Colin Y, Hughes-Jones NC, et al. Transcript analysis of D category phenotypes predicts hybrid Rh D-CE-D proteins associated with alteration of D epitopes. Blood 1995;85:2937-44.
-
(1995)
Blood
, vol.85
, pp. 2937-2944
-
-
Rouillac, C.1
Colin, Y.2
Hughes-Jones, N.C.3
-
44
-
-
0029938326
-
The genetic basis of a new partial D antigen: DDBT
-
Beckers EA, Faas BH, Simsek S, et al. The genetic basis of a new partial D antigen: DDBT. Br J Haematol 1996;93:720-7.
-
(1996)
Br J Haematol
, vol.93
, pp. 720-727
-
-
Beckers, E.A.1
Faas, B.H.2
Simsek, S.3
-
45
-
-
0028070857
-
FPTT is a low-incidence Rh antigen associated with a "new" partial Rh D phenotype, DFR
-
Lomas C, Grassmann W, Ford D, et al. FPTT is a low-incidence Rh antigen associated with a "new" partial Rh D phenotype, DFR. Transfusion 1994;34:612-6.
-
(1994)
Transfusion
, vol.34
, pp. 612-616
-
-
Lomas, C.1
Grassmann, W.2
Ford, D.3
-
46
-
-
0030009496
-
The Rh antigen D: Partial D antigens and associated low incidence antigens
-
Tippett P, Lomas-Francis C, Wallace M. The Rh antigen D: partial D antigens and associated low incidence antigens. Vox Sang 1996;70(3):123-31.
-
(1996)
Vox Sang
, vol.70
, Issue.3
, pp. 123-131
-
-
Tippett, P.1
Lomas-Francis, C.2
Wallace, M.3
-
47
-
-
0028963904
-
Lack of G blood group antigen in DIIIb erythrocytes is associated with segmental DNA exchange between RH genes
-
Rouillac C, Le Van Kim C, Blancher A, Roubinet F, Cartron JP, Colin Y. Lack of G blood group antigen in DIIIb erythrocytes is associated with segmental DNA exchange between RH genes. Br J Haematol 1995;89:424-6.
-
(1995)
Br J Haematol
, vol.89
, pp. 424-426
-
-
Rouillac, C.1
Le Van Kim, C.2
Blancher, A.3
Roubinet, F.4
Cartron, J.P.5
Colin, Y.6
-
48
-
-
0030057292
-
Characterization of the hybrid RHD gene leading to the partial D category IIIc phenotype
-
Beckers EA, Faas BH, Ligthart P, et al. Characterization of the hybrid RHD gene leading to the partial D category IIIc phenotype. Transfusion 1996;36:567-74.
-
(1996)
Transfusion
, vol.36
, pp. 567-574
-
-
Beckers, E.A.1
Faas, B.H.2
Ligthart, P.3
-
50
-
-
0037105381
-
DNB: A partial D with anti-D frequent in Central Europe
-
Wagner FF, Eicher NI, Jorgensen JR, Lonicer CB, Flegel WA. DNB: a partial D with anti-D frequent in Central Europe. Blood 2002;100:2253-6.
-
(2002)
Blood
, vol.100
, pp. 2253-2256
-
-
Wagner, F.F.1
Eicher, N.I.2
Jorgensen, J.R.3
Lonicer, C.B.4
Flegel, W.A.5
-
51
-
-
0029016552
-
Leu110Pro substitution in the RhD polypeptide is responsible for the DVII category blood group phenotype
-
Rouillac C, Le Van Kim C, Beolet M, Cartron JP, Colin Y. Leu110Pro substitution in the RhD polypeptide is responsible for the DVII category blood group phenotype. Am J Hematol 1995;49:87-8.
-
(1995)
Am J Hematol
, vol.49
, pp. 87-88
-
-
Rouillac, C.1
Le Van Kim, C.2
Beolet, M.3
Cartron, J.P.4
Colin, Y.5
-
52
-
-
0034656006
-
Weak D alleles express distinct phenotypes
-
Wagner FF, Frohmajer A, Ladewig B, et al. Weak D alleles express distinct phenotypes. Blood 2000;95:2699-708.
-
(2000)
Blood
, vol.95
, pp. 2699-2708
-
-
Wagner, F.F.1
Frohmajer, A.2
Ladewig, B.3
-
53
-
-
0035125518
-
PCR screening for common weak D types shows different distributions in three Central European populations
-
Müller TH, Wagner FF, Trockenbacher A, et al. PCR screening for common weak D types shows different distributions in three Central European populations. Transfusion 2001;41:45-52.
-
(2001)
Transfusion
, vol.41
, pp. 45-52
-
-
Müller, T.H.1
Wagner, F.F.2
Trockenbacher, A.3
-
54
-
-
0034509717
-
RHD gene mutations and the weak D phenotype: An Australian blood donor study
-
Cowley NM, Saul A, Hyland CA. RHD gene mutations and the weak D phenotype: an Australian blood donor study. Vox Sang 2000;79:251-2.
-
(2000)
Vox Sang
, vol.79
, pp. 251-252
-
-
Cowley, N.M.1
Saul, A.2
Hyland, C.A.3
-
55
-
-
2342600875
-
Molecular genetic RHD characterization of 577 cases with serologic suspect for weak D
-
Döscher A, Ladewig B, Das Gupta C, et al. Molecular genetic RHD characterization of 577 cases with serologic suspect for weak D (abstract). Transfus Med Hemother 2003;30S1:B2.03.
-
(2003)
Transfus Med Hemother
, vol.30 S1
-
-
Döscher, A.1
Ladewig, B.2
Das Gupta, C.3
-
56
-
-
0035522352
-
Molecular characterization of weak D phenotypes by site-directed mutagenesis and expression of mutant Rh-green fluorescence protein fusions in K562 cells
-
Kamesaki T, Iwamoto S, Kumada M, et al. Molecular characterization of weak D phenotypes by site-directed mutagenesis and expression of mutant Rh-green fluorescence protein fusions in K562 cells. Vox Sang 2001;81:254-8.
-
(2001)
Vox Sang
, vol.81
, pp. 254-258
-
-
Kamesaki, T.1
Iwamoto, S.2
Kumada, M.3
-
58
-
-
0030610737
-
Human D(IIIa) erythrocytes: RhD protein is associated with multiple dispersed amino acid variations
-
Huang CH, Chen Y, Reid M. Human D(IIIa) erythrocytes: RhD protein is associated with multiple dispersed amino acid variations. Am J Hematol 1997;55:139-45.
-
(1997)
Am J Hematol
, vol.55
, pp. 139-145
-
-
Huang, C.H.1
Chen, Y.2
Reid, M.3
-
59
-
-
0032762182
-
DAR, a new RhD variant involving exons 4, 5, and 7, often in linkage with ceAR, a new rhce variant frequently found in African blacks
-
Hemker MB, Ligthart PC, Berger L, van Rhenen DJ, van der Schoot CE, Wijk PA. DAR, a new RhD variant involving exons 4, 5, and 7, often in linkage with ceAR, a new rhce variant frequently found in African blacks. Blood 1999;94:4337-42.
-
(1999)
Blood
, vol.94
, pp. 4337-4342
-
-
Hemker, M.B.1
Ligthart, P.C.2
Berger, L.3
Van Rhenen, D.J.4
Van Der Schoot, C.E.5
Wijk, P.A.6
-
60
-
-
0036659930
-
The DAU allele cluster of the RHD gene
-
Wagner FF, Ladewig B, Angert KS, Heymann GA, Eicher NI, Flegel WA. The DAU allele cluster of the RHD gene. Blood 2002;100:306-11.
-
(2002)
Blood
, vol.100
, pp. 306-311
-
-
Wagner, F.F.1
Ladewig, B.2
Angert, K.S.3
Heymann, G.A.4
Eicher, N.I.5
Flegel, W.A.6
-
61
-
-
0027180212
-
Molecular genetic basis of the human Rhesus blood group system
-
Mouro I, Colin Y, Cherif-Zahar B, Cartron JP, Le Van Kim C. Molecular genetic basis of the human Rhesus blood group system. Nat Genet 1993;5:62-5.
-
(1993)
Nat Genet
, vol.5
, pp. 62-65
-
-
Mouro, I.1
Colin, Y.2
Cherif-Zahar, B.3
Cartron, J.P.4
Le Van Kim, C.5
-
62
-
-
0034844215
-
Partial expression of RHc on the RHD polypeptide
-
Faas BH, Beuling EA, Ligthart PC, van Rhenen DJ, van der Schoot CE. Partial expression of RHc on the RHD polypeptide. Transfusion 2001;41:1136-42.
-
(2001)
Transfusion
, vol.41
, pp. 1136-1142
-
-
Faas, B.H.1
Beuling, E.A.2
Ligthart, P.C.3
Van Rhenen, D.J.4
Van Der Schoot, C.E.5
-
63
-
-
0030017665
-
Involvement of Serl03 of the Rh polypeptides in G epitope formation
-
Faas BH, Beckers EA, Simsek S, et al. Involvement of Serl03 of the Rh polypeptides in G epitope formation. Transfusion 1996;36:506-11.
-
(1996)
Transfusion
, vol.36
, pp. 506-511
-
-
Faas, B.H.1
Beckers, E.A.2
Simsek, S.3
-
64
-
-
0038052865
-
RHCE-D-CE hybrid genes can cause false-negative DNA typing of the Rh e antigen
-
Oct
-
Hundhausen T, Petershofen EK, Doescher A, Bauerfeind U, Muller TH, Schunter F. RHCE-D-CE hybrid genes can cause false-negative DNA typing of the Rh e antigen. Vox Sang 2002 Oct;83(3):268-72.
-
(2002)
Vox Sang
, vol.83
, Issue.3
, pp. 268-272
-
-
Hundhausen, T.1
Petershofen, E.K.2
Doescher, A.3
Bauerfeind, U.4
Muller, T.H.5
Schunter, F.6
-
65
-
-
0030927242
-
Evolution of the human RH (rhesus) blood group genes: A 50 year old prediction (partially) fulfilled
-
Jun
-
Carritt B, Kemp TJ, Poulter M. Evolution of the human RH (rhesus) blood group genes: a 50 year old prediction (partially) fulfilled. Hum Mol Genet 1997 Jun;6(6):843-50.
-
(1997)
Hum Mol Genet
, vol.6
, Issue.6
, pp. 843-850
-
-
Carritt, B.1
Kemp, T.J.2
Poulter, M.3
-
66
-
-
0029967852
-
DNA-based Rhesus typing: Simultaneous determination of RHC and RHD status using the polymerase chain reaction
-
Poulter M, Kemp TJ, Carritt B. DNA-based Rhesus typing: simultaneous determination of RHC and RHD status using the polymerase chain reaction. Vox Sang 1996;7:164-8.
-
(1996)
Vox Sang
, vol.7
, pp. 164-168
-
-
Poulter, M.1
Kemp, T.J.2
Carritt, B.3
-
67
-
-
0029980771
-
Molecular analysis of blood group Rh transcripts from a rGr variant
-
Mouro I, Colin Y, Gane P, et al. Molecular analysis of blood group Rh transcripts from a rGr variant. Br J Haematol 1996;93:472-4.
-
(1996)
Br J Haematol
, vol.93
, pp. 472-474
-
-
Mouro, I.1
Colin, Y.2
Gane, P.3
-
68
-
-
0028332774
-
Refining the DNA polymorphisms that associate with the rhesus c phenotype
-
Wolter LC, Hyland CA, Saul A. Refining the DNA polymorphisms that associate with the rhesus c phenotype. Blood 1994;84:985-6.
-
(1994)
Blood
, vol.84
, pp. 985-986
-
-
Wolter, L.C.1
Hyland, C.A.2
Saul, A.3
-
69
-
-
0030838226
-
RHD/CE typing by polymerase chain reaction using sequence-specific primers
-
Gassner C, Schmarda A, Kilga-Nogler S, et al. RHD/CE typing by polymerase chain reaction using sequence-specific primers. Transfusion 1997;37:1020-6.
-
(1997)
Transfusion
, vol.37
, pp. 1020-1026
-
-
Gassner, C.1
Schmarda, A.2
Kilga-Nogler, S.3
-
70
-
-
0031671377
-
The VS and V blood group polymorphisms in Africans: A serologic and molecular analysis
-
Daniels GL, Faas BH, Green CA, et al. The VS and V blood group polymorphisms in Africans: a serologic and molecular analysis. Transfusion 1998;38:951-8.
-
(1998)
Transfusion
, vol.38
, pp. 951-958
-
-
Daniels, G.L.1
Faas, B.H.2
Green, C.A.3
-
71
-
-
0034651012
-
The Rh blood group system: A review
-
Avent ND, Reid ME. The Rh blood group system: a review. Blood 2000;95:375-87.
-
(2000)
Blood
, vol.95
, pp. 375-387
-
-
Avent, N.D.1
Reid, M.E.2
-
73
-
-
0029042196
-
Identification of a partial internal deletion in the RH locus causing the human erythrocyte D-phenotype
-
Huang CH, Reid ME, Chen Y. Identification of a partial internal deletion in the RH locus causing the human erythrocyte D- phenotype. Blood 1995;86:784-90.
-
(1995)
Blood
, vol.86
, pp. 784-790
-
-
Huang, C.H.1
Reid, M.E.2
Chen, Y.3
-
74
-
-
0029847269
-
Lack of RHCE-encoded proteins in the D-phenotype may result from homologous recombination between the two RH genes
-
Cherif-Zahar B, Raynal V, Cartron JP. Lack of RHCE-encoded proteins in the D- phenotype may result from homologous recombination between the two RH genes. Blood 1996;88:1518-20.
-
(1996)
Blood
, vol.88
, pp. 1518-1520
-
-
Cherif-Zahar, B.1
Raynal, V.2
Cartron, J.P.3
-
75
-
-
0029839979
-
Genetic recombination at the human RH locus: A family study of the red-cell Evans phenotype reveals a transfer of exons 2-6 from the RHD to the RHCE gene
-
Huang CH, Chen Y, Reid M, Ghosh S. Genetic recombination at the human RH locus: a family study of the red-cell Evans phenotype reveals a transfer of exons 2-6 from the RHD to the RHCE gene. Am J Hum Genet 1996;59:825-33.
-
(1996)
Am J Hum Genet
, vol.59
, pp. 825-833
-
-
Huang, C.H.1
Chen, Y.2
Reid, M.3
Ghosh, S.4
-
76
-
-
0042839561
-
A Dc-phenotype encoded by an RHCE-D(5-7/8)-CE hybrid allele
-
Cotorruelo CM, Biondi CS, Borras SE, Di Monaco RA, Racca A. A Dc- phenotype encoded by an RHCE-D(5-7/8)-CE hybrid allele. Vox Sang 2003;85:102-8.
-
(2003)
Vox Sang
, vol.85
, pp. 102-108
-
-
Cotorruelo, C.M.1
Biondi, C.S.2
Borras, S.E.3
Di Monaco, R.A.4
Racca, A.5
-
77
-
-
0028076934
-
Molecular analysis of the structure and expression of the RH locus in individuals with D-, Dc-, and DCw- gene complexes
-
Cherif-Zahar B, Raynal V, D'Ambrosio AM, Cartron JP, Colin Y. Molecular analysis of the structure and expression of the RH locus in individuals with D-, Dc-, and DCw- gene complexes. Blood 1994;84:4354-60.
-
(1994)
Blood
, vol.84
, pp. 4354-4360
-
-
Cherif-Zahar, B.1
Raynal, V.2
D'Ambrosio, A.M.3
Cartron, J.P.4
Colin, Y.5
-
78
-
-
0036892762
-
Rare RHCE phenotypes in Black individuals of Afro-Caribbean origin: Identification and transfusion safety
-
Noizat-Pirenne F, Lee K, Pennec PY, et al. Rare RHCE phenotypes in Black individuals of Afro-Caribbean origin: identification and transfusion safety. Blood 2002;100:4223-31.
-
(2002)
Blood
, vol.100
, pp. 4223-4231
-
-
Noizat-Pirenne, F.1
Lee, K.2
Pennec, P.Y.3
-
79
-
-
0032527131
-
null disease: The amorph type results from a novel double mutation in RhCe gene on D-negative background
-
null disease: the amorph type results from a novel double mutation in RhCe gene on D-negative background. Blood 1998;92:664-71.
-
(1998)
Blood
, vol.92
, pp. 664-671
-
-
Huang, C.H.1
Chen, Y.2
Reid, M.E.3
Seidl, C.4
-
80
-
-
2642672673
-
Molecular defects of the RHCE gene in Rh-deficient individuals of the amorph type
-
Cherif-Zahar B, Matassi G, Raynal V, et al. Molecular defects of the RHCE gene in Rh-deficient individuals of the amorph type. Blood 1998;92:639-46.
-
(1998)
Blood
, vol.92
, pp. 639-646
-
-
Cherif-Zahar, B.1
Matassi, G.2
Raynal, V.3
-
81
-
-
0010770884
-
Studies of two partial Ds: DMH and DOL
-
Avent ND, Poole J, Singleton B, et al. Studies of two partial Ds: DMH and DOL (abstract). Transfus Med 9, 1999;33(suppl):33.
-
(1999)
Transfus Med 9
, vol.33
, Issue.SUPPL.
, pp. 33
-
-
Avent, N.D.1
Poole, J.2
Singleton, B.3
-
82
-
-
0008148199
-
Characterization of D category IV type IV, DFW, and DNB
-
Wagner FF, Gassner C, Eicher NI, Lonicer C, Flegel WA. Characterization of D category IV type IV, DFW, and DNB (abstract). Transfusion 1998;38(suppl):63S.
-
(1998)
Transfusion
, vol.38
, Issue.SUPPL.
-
-
Wagner, F.F.1
Gassner, C.2
Eicher, N.I.3
Lonicer, C.4
Flegel, W.A.5
-
83
-
-
0030716461
-
The serological profile and molecular basis of a new partial D phenotype, DHR
-
Jones JW, Finning K, Mattock R, et al. The serological profile and molecular basis of a new partial D phenotype, DHR. Vox Sang 1997;73:252-6.
-
(1997)
Vox Sang
, vol.73
, pp. 252-256
-
-
Jones, J.W.1
Finning, K.2
Mattock, R.3
-
84
-
-
0013477007
-
Molecular analysis of two D-variants, DHMi and DHMii
-
Liu W, Jones JW, Scott ML, Voak D, Avent ND. Molecular analysis of two D-variants, DHMi and DHMii (abstract). Transfus Med 6, 1996;21(suppl):21.
-
(1996)
Transfus Med 6
, vol.21
, Issue.SUPPL.
, pp. 21
-
-
Liu, W.1
Jones, J.W.2
Scott, M.L.3
Voak, D.4
Avent, N.D.5
-
85
-
-
25044446166
-
Six new RHD-alleles with previously unknown polymorphisms
-
Döscher A, Ladewig B, Gerdes I, et al. Six new RHD-alleles with previously unknown polymorphisms (abstract). Transfus Med Hemother 2003;30(suppl 1):B2.04.
-
(2003)
Transfus Med Hemother
, vol.30
, Issue.SUPPL. 1
-
-
Döscher, A.1
Ladewig, B.2
Gerdes, I.3
-
86
-
-
0030923358
-
Molecular basis of the D variant phenotypes DNU and DII allows localization of critical amino acids required for expression of Rh D epitopes epD3, 4 and 9 to the sixth external domain of the Rh D protein
-
Avent ND, Jones JW, Liu W, et al. Molecular basis of the D variant phenotypes DNU and DII allows localization of critical amino acids required for expression of Rh D epitopes epD3, 4 and 9 to the sixth external domain of the Rh D protein. Br J Haematol 1997;97:366-71.
-
(1997)
Br J Haematol
, vol.97
, pp. 366-371
-
-
Avent, N.D.1
Jones, J.W.2
Liu, W.3
-
87
-
-
25044453973
-
A novel partial RhD with highly retained epitope composition in an individual with alloanti-D
-
Körmöczi GF, Legler TJ, Daniels GL, et al. A novel partial RhD with highly retained epitope composition in an individual with alloanti-D (abstract). Transfus Med Hemother 2003;30(suppl 1):B2.07.
-
(2003)
Transfus Med Hemother
, vol.30
, Issue.SUPPL. 1
-
-
Körmöczi, G.F.1
Legler, T.J.2
Daniels, G.L.3
-
89
-
-
0031755001
-
Heterogeneity of blood group RhE variants revealed by serological analysis and molecular alteration of the RHCE gene and transcript
-
Noizat-Pirenne F, Mouro I, Gane P, et al. Heterogeneity of blood group RhE variants revealed by serological analysis and molecular alteration of the RHCE gene and transcript. Br J Haematol 1998;103:429-36.
-
(1998)
Br J Haematol
, vol.103
, pp. 429-436
-
-
Noizat-Pirenne, F.1
Mouro, I.2
Gane, P.3
-
90
-
-
0029984078
-
Molecular basis of the altered antigenic expression of RhD in weak D(Du) and RhC/e in Rh phenotypes
-
Rouillac C, Gane P, Cartron J, Le Pennec PY, Cartron JP, Colin Y. Molecular basis of the altered antigenic expression of RhD in weak D(Du) and RhC/e in Rh phenotypes. Blood 1996;87:4853-61.
-
(1996)
Blood
, vol.87
, pp. 4853-4861
-
-
Rouillac, C.1
Gane, P.2
Cartron, J.3
Le Pennec, P.Y.4
Cartron, J.P.5
Colin, Y.6
-
91
-
-
19044367183
-
Molecular background of D(C)(e) haplotypes within the white population
-
Noizat-Pirenne F, Le Pennec PY, Mouro I, et al. Molecular background of D(C)(e) haplotypes within the white population. Transfusion 2002;42:627-33.
-
(2002)
Transfusion
, vol.42
, pp. 627-633
-
-
Noizat-Pirenne, F.1
Le Pennec, P.Y.2
Mouro, I.3
-
93
-
-
0031444903
-
Involvement of Gly96 in the formation of the Rh26 epitope
-
Faas BH, Ligthart PC, Lomas-Francis C, Overbeeke MA, von dem Borne AE, van der Schoot CE. Involvement of Gly96 in the formation of the Rh26 epitope. Transfusion 1997;37:1123-30.
-
(1997)
Transfusion
, vol.37
, pp. 1123-1130
-
-
Faas, B.H.1
Ligthart, P.C.2
Lomas-Francis, C.3
Overbeeke, M.A.4
Von Dem Borne, A.E.5
Van Der Schoot, C.E.6
-
94
-
-
0034992295
-
16Cys encoded by the RHce gene is associated with altered expression of the e antigen and is frequent in the RO haplotype
-
Westhoff CM, Silberstein LE, Wylie DE, Skavdahl M, Reid ME. 16Cys encoded by the RHce gene is associated with altered expression of the e antigen and is frequent in the RO haplotype. Br J Haematol 2001;113:666-71.
-
(2001)
Br J Haematol
, vol.113
, pp. 666-671
-
-
Westhoff, C.M.1
Silberstein, L.E.2
Wylie, D.E.3
Skavdahl, M.4
Reid, M.E.5
-
95
-
-
2142748281
-
Deletion of Arg 229 in RhCE polypeptide alters expression of Rhe and ce-associated Rh6 antigen
-
Huang CH, Reid ME, Chen Y, Novaretti M. Deletion of Arg 229 in RhCE polypeptide alters expression of Rhe and ce-associated Rh6 antigen (abstract). Blood 1992;90(suppl):272a.
-
(1992)
Blood
, vol.90
, Issue.SUPPL.
-
-
Huang, C.H.1
Reid, M.E.2
Chen, Y.3
Novaretti, M.4
-
96
-
-
0034983363
-
Two new alleles of the RHCE gene in Black individuals: The RHce allele ceMO and the RHcE allele cEMI
-
Noizat-Pirenne F, Mouro I, Le Pennec PY, et al. Two new alleles of the RHCE gene in Black individuals: the RHce allele ceMO and the RHcE allele cEMI. Br J Haematol 2001;113:672-9.
-
(2001)
Br J Haematol
, vol.113
, pp. 672-679
-
-
Noizat-Pirenne, F.1
Mouro, I.2
Le Pennec, P.Y.3
-
97
-
-
25044481117
-
Crawford (Rh43), a low-incidence antigen, is associated with a novel RHCE variant RHce allele, ceCF
-
Schlanser G, Moulds MK, Flegel WA, Wagner FF, Frame T. Crawford (Rh43), a low-incidence antigen, is associated with a novel RHCE variant RHce allele, ceCF (abstract). Transfusion 2003;43(suppl):35A.
-
(2003)
Transfusion
, vol.43
, Issue.SUPPL.
-
-
Schlanser, G.1
Moulds, M.K.2
Flegel, W.A.3
Wagner, F.F.4
Frame, T.5
|