-
1
-
-
0028867451
-
Blood group terminology 1995. From the ISBT Working Party on Terminology for Red Cell Surface Antigens
-
Daniels GL, Anstee DJ, Cartron J-P, Dahr W, Issitt PD, Jorgensen J, Kornstad L, Lewis M, Levene C, Lomas-Francis C, et al.: Blood group terminology 1995. From the ISBT Working Party on Terminology for Red Cell Surface Antigens. Vox Sang 1995, 69:265-279.
-
(1995)
Vox Sang
, vol.69
, pp. 265-279
-
-
Daniels, G.L.1
Anstee, D.J.2
Cartron, J.-P.3
Dahr, W.4
Issitt, P.D.5
Jorgensen, J.6
Kornstad, L.7
Lewis, M.8
Levene, C.9
Lomas-Francis, C.10
-
2
-
-
0001062684
-
A critique of the theoretical hazard of inter vs. intra-racial transfusion
-
Giblett ER: A critique of the theoretical hazard of inter vs. intra-racial transfusion. Transfusion 1961, 1:233-238.
-
(1961)
Transfusion
, vol.1
, pp. 233-238
-
-
Giblett, E.R.1
-
3
-
-
0017657962
-
Blood group alloantibodies: An assessment of some laboratory practices
-
Giblett ER: Blood group alloantibodies: an assessment of some laboratory practices. Transfusion 1977, 4:299-308.
-
(1977)
Transfusion
, vol.4
, pp. 299-308
-
-
Giblett, E.R.1
-
4
-
-
0028876541
-
Multiple red cell transfusions and alloimmunization: Experience with 6996 antibodies detected in a total of 159,262 patients from 1985 to 1993
-
Hoettge GA, Domen RE, Rybicki LA, Schaffer PA: Multiple red cell transfusions and alloimmunization: experience with 6996 antibodies detected in a total of 159,262 patients from 1985 to 1993. Arch Pathol Lab Med 1995, 119:42-45.
-
(1995)
Arch Pathol Lab Med
, vol.119
, pp. 42-45
-
-
Hoettge, G.A.1
Domen, R.E.2
Rybicki, L.A.3
Schaffer, P.A.4
-
5
-
-
0031080817
-
Female alloimmunization with antibodies known to cause hemolytic disease
-
Geifman-Holtzman O, Wojtowycz M, Kosmas E, Artal R: Female alloimmunization with antibodies known to cause hemolytic disease. Obstet Gynecol 1997, 89:272-275.
-
(1997)
Obstet Gynecol
, vol.89
, pp. 272-275
-
-
Geifman-Holtzman, O.1
Wojtowycz, M.2
Kosmas, E.3
Artal, R.4
-
6
-
-
0025155469
-
Molecular cloning, sequence, and expression of a human GDP-L-fucose:beta-D-galactoside 2-alpha-L-fucosyltransferase cDNA that can form the H blood group antigen
-
Larsen RD, Ernst LK, Nair RP, Lowe JB: Molecular cloning, sequence, and expression of a human GDP-L-fucose:beta-D-galactoside 2-alpha-L-fucosyltransferase cDNA that can form the H blood group antigen. Proc Natl Acad Sci U S A 1990, 87:6674-6678.
-
(1990)
Proc Natl Acad Sci U S A
, vol.87
, pp. 6674-6678
-
-
Larsen, R.D.1
Ernst, L.K.2
Nair, R.P.3
Lowe, J.B.4
-
7
-
-
0031017961
-
Two missense mutations of H type α(1,2)fucosyltransferase gene (FUT1) responsible for para-Bombay phenotype
-
Wang BJ, Koda Y, Soejima M, Kimura H: Two missense mutations of H type α(1,2)fucosyltransferase gene (FUT1) responsible for para-Bombay phenotype. Vox Sang 1997, 72:31-35.
-
(1997)
Vox Sang
, vol.72
, pp. 31-35
-
-
Wang, B.J.1
Koda, Y.2
Soejima, M.3
Kimura, H.4
-
8
-
-
0031025282
-
Heterogeneity of the human H blood group α (1,2) fucosyltransferase gene among para-Bombay individuals
-
Yu L-C, Yang Y-H, Broadberry RE, Chen Y-H, Lin M: Heterogeneity of the human H blood group α (1,2) fucosyltransferase gene among para-Bombay individuals. Vox Sang 1997, 72:36-40.
-
(1997)
Vox Sang
, vol.72
, pp. 36-40
-
-
Yu, L.-C.1
Yang, Y.-H.2
Broadberry, R.E.3
Chen, Y.-H.4
Lin, M.5
-
9
-
-
0028935724
-
Molecular cloning of a human genomic region containing the H blood group α(1,2)fucosyltransferase gene and two H locus-related DNA restriction fragments
-
Rouquier S, Lowe JB, Kelly RJ, Fertitta AL, Lennon GG, Giorgi D: Molecular cloning of a human genomic region containing the H blood group α(1,2)fucosyltransferase gene and two H locus-related DNA restriction fragments. J Biol Chem 1995, 270:4632-4639.
-
(1995)
J Biol Chem
, vol.270
, pp. 4632-4639
-
-
Rouquier, S.1
Lowe, J.B.2
Kelly, R.J.3
Fertitta, A.L.4
Lennon, G.G.5
Giorgi, D.6
-
10
-
-
0028276829
-
Molecular basis for H blood group deficiency in Bombay (Oh) and para-Bombay Individuals
-
Kelly RJ, Ernst LK, Larsen RD, Bryant JG, Robinson JS, Lowe JB: Molecular basis for H blood group deficiency in Bombay (Oh) and para-Bombay Individuals. Proc Natl Acad Sci U S A 1994, 91:5843-5847.
-
(1994)
Proc Natl Acad Sci U S A
, vol.91
, pp. 5843-5847
-
-
Kelly, R.J.1
Ernst, L.K.2
Larsen, R.D.3
Bryant, J.G.4
Robinson, J.S.5
Lowe, J.B.6
-
11
-
-
0028965558
-
Sequence and expression of a candidate for the human secretor blood group α(1,2)fucosyltransferase gene (FUT2)
-
Kelly RJ, Rouquier S, Giorgi D, Lennon GG, Lowe JB: Sequence and expression of a candidate for the human secretor blood group α(1,2)fucosyltransferase gene (FUT2). J Biol Chem 1995, 270:4640-4649.
-
(1995)
J Biol Chem
, vol.270
, pp. 4640-4649
-
-
Kelly, R.J.1
Rouquier, S.2
Giorgi, D.3
Lennon, G.G.4
Lowe, J.B.5
-
12
-
-
0030016227
-
Characterization of the specificities of human blood group H gene-specified α1,2-L-fucosyltransferase toward sulfated/sialylated/fucosylated acceptors: Evidence for an inverse relationship between α1,2-L-fucosylation of Gal and α1,6-L-fucosylation of asparagine-linked GlcNAc
-
Chandrasekaran EV, Jain RK, Larsen RD, Wlasichuk K, Matta KL: Characterization of the specificities of human blood group H gene-specified α1,2-L-fucosyltransferase toward sulfated/sialylated/fucosylated acceptors: evidence for an inverse relationship between α1,2-L-fucosylation of Gal and α1,6-L-fucosylation of asparagine-linked GlcNAc. Biochemistry 1996, 35:8914-8924.
-
(1996)
Biochemistry
, vol.35
, pp. 8914-8924
-
-
Chandrasekaran, E.V.1
Jain, R.K.2
Larsen, R.D.3
Wlasichuk, K.4
Matta, K.L.5
-
13
-
-
0031019168
-
Expression of human H-type α1,2-fucosyl-transferase encoding for blood group H(O) antigen in Chinese hamster ovary cells-evidence for preferential fucosylation and truncation of polylactosamine sequences
-
Prieto PA, Larsen RD, Cho M, Rivera HN, Shilatifard A, Lowe JB, Cummings RD, Smith DF: Expression of human H-type α1,2-fucosyl-transferase encoding for blood group H(O) antigen in Chinese hamster ovary cells-evidence for preferential fucosylation and truncation of polylactosamine sequences. J Biol Chem 1997, 272:2089-2097.
-
(1997)
J Biol Chem
, vol.272
, pp. 2089-2097
-
-
Prieto, P.A.1
Larsen, R.D.2
Cho, M.3
Rivera, H.N.4
Shilatifard, A.5
Lowe, J.B.6
Cummings, R.D.7
Smith, D.F.8
-
14
-
-
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, 37:284-290.
-
(1997)
Transfusion
, vol.37
, pp. 284-290
-
-
Wagner, F.F.1
Flegel, W.A.2
-
15
-
-
0031589992
-
Molecular analysis of the O alleles at the blood group ABO locus in populations of different ethnic origin reveals novel crossing-over events and point mutations
-
Olsson ML, Guerreiro JF, Zago MA, Chester MA: Molecular analysis of the O alleles at the blood group ABO locus in populations of different ethnic origin reveals novel crossing-over events and point mutations. Biochem Biophys Res Commun 1997, 234:779-782.
-
(1997)
Biochem Biophys Res Commun
, vol.234
, pp. 779-782
-
-
Olsson, M.L.1
Guerreiro, J.F.2
Zago, M.A.3
Chester, M.A.4
-
16
-
-
0025270738
-
Molecular genetic basis of the histo-blood group ABO system
-
Yamamoto F-I, Clausen H, White T, Marken J, Hakomori S: Molecular genetic basis of the histo-blood group ABO system. Nature 1990, 345:229-235.
-
(1990)
Nature
, vol.345
, pp. 229-235
-
-
Yamamoto, F.-I.1
Clausen, H.2
White, T.3
Marken, J.4
Hakomori, S.5
-
17
-
-
0029792532
-
ABO glycosyl-transferase genotyping by polymerase chain reaction using sequence-specific primers
-
Gassner C, Schmarda A, Nussbaumer W, Schönitzer D: ABO glycosyl-transferase genotyping by polymerase chain reaction using sequence-specific primers. Blood 1996, 88:1852-1856.
-
(1996)
Blood
, vol.88
, pp. 1852-1856
-
-
Gassner, C.1
Schmarda, A.2
Nussbaumer, W.3
Schönitzer, D.4
-
19
-
-
10144246583
-
Molecular genetic analysis of variant phenotypes of the ABO blood group system
-
Ogasawara K, Yabe R, Uchikawa M, Saitou N, Bannai M, Nakata K, Takenaka M, Fujisawa K, Ishikawa Y, Juji T, et al.: Molecular genetic analysis of variant phenotypes of the ABO blood group system. Blood 1996, 88:2732-2737.
-
(1996)
Blood
, vol.88
, pp. 2732-2737
-
-
Ogasawara, K.1
Yabe, R.2
Uchikawa, M.3
Saitou, N.4
Bannai, M.5
Nakata, K.6
Takenaka, M.7
Fujisawa, K.8
Ishikawa, Y.9
Juji, T.10
-
20
-
-
15844366741
-
Extensive polymorphism of ABO blood group gene: Three major lineages of the alleles for the common ABO phenotypes
-
Ogasawara K, Bannai M, Saitou N, Yabe R, Nakata K, Takenaka M, Fujisawa K, Uchikawa M, Ishikawa Y, Juji T, et al.: Extensive polymorphism of ABO blood group gene: three major lineages of the alleles for the common ABO phenotypes. Hum Genet 1996, 97:777-783.
-
(1996)
Hum Genet
, vol.97
, pp. 777-783
-
-
Ogasawara, K.1
Bannai, M.2
Saitou, N.3
Yabe, R.4
Nakata, K.5
Takenaka, M.6
Fujisawa, K.7
Uchikawa, M.8
Ishikawa, Y.9
Juji, T.10
-
23
-
-
0028844274
-
2 discriminating nucleotide substitution at the ABO locus
-
2 discriminating nucleotide substitution at the ABO locus. Vox Sang 1995, 69:242-247.
-
(1995)
Vox Sang
, vol.69
, pp. 242-247
-
-
Olsson, M.L.1
Chester, M.A.2
-
24
-
-
0028889138
-
Determination of ABO glycosyltransferase genotypes by use of polymerase chain reaction and restriction enzymes
-
Stroncek DF, Konz R, Clay ME, Houchins JP, McCullough J: Determination of ABO glycosyltransferase genotypes by use of polymerase chain reaction and restriction enzymes. Transfusion 1995, 35:231-240.
-
(1995)
Transfusion
, vol.35
, pp. 231-240
-
-
Stroncek, D.F.1
Konz, R.2
Clay, M.E.3
Houchins, J.P.4
McCullough, J.5
-
25
-
-
0029031033
-
Molecular genetics of the ABO histo-blood group system
-
Yamamoto F: Molecular genetics of the ABO histo-blood group system. Vox Sang 1995, 69:1-7.
-
(1995)
Vox Sang
, vol.69
, pp. 1-7
-
-
Yamamoto, F.1
-
26
-
-
0031060667
-
Amplified product length polymorphism (APLP): A novel strategy for genotyplng the ABO blood group
-
Watanabe G, Umetsu K, Yuasa I, Suzuki T: Amplified product length polymorphism (APLP): a novel strategy for genotyplng the ABO blood group. Hum Genet 1997, 99:34-37.
-
(1997)
Hum Genet
, vol.99
, pp. 34-37
-
-
Watanabe, G.1
Umetsu, K.2
Yuasa, I.3
Suzuki, T.4
-
27
-
-
0030893812
-
A de novo recombination in the ABO blood group gene and evidence for the occurrence of recombination products
-
Suzuki K, Iwata M, Tsuji H, Takagi T, Tamura A, Ishimoto G, Ito S, Matsui K, Miyazaki T: A de novo recombination in the ABO blood group gene and evidence for the occurrence of recombination products. Hum Genet 1997, 99:454-461.
-
(1997)
Hum Genet
, vol.99
, pp. 454-461
-
-
Suzuki, K.1
Iwata, M.2
Tsuji, H.3
Takagi, T.4
Tamura, A.5
Ishimoto, G.6
Ito, S.7
Matsui, K.8
Miyazaki, T.9
-
28
-
-
0030927242
-
Evolution of the human RH (rhesus) blood group genes: A 50 year old prediction (partially) fulfilled
-
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, 6:843-850.
-
(1997)
Hum Mol Genet
, vol.6
, pp. 843-850
-
-
Carritt, B.1
Kemp, T.J.2
Poulter, M.3
-
29
-
-
0031006896
-
Molecular insights into the Rh protein family and associated antigens
-
Huang C-H: Molecular insights into the Rh protein family and associated antigens. Curr Opin Hematol 1997, 4:94-103.
-
(1997)
Curr Opin Hematol
, vol.4
, pp. 94-103
-
-
Huang, C.-H.1
-
30
-
-
0028578093
-
Defining the Rh blood group antigens: Biochemistry and molecular genetics
-
Cartron J-P: Defining the Rh blood group antigens: biochemistry and molecular genetics. Blood Rev 1994, 8:199-212.
-
(1994)
Blood Rev
, vol.8
, pp. 199-212
-
-
Cartron, J.-P.1
-
31
-
-
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, 70:123-131.
-
(1996)
Vox Sang
, vol.70
, pp. 123-131
-
-
Tippett, P.1
Lomas-Francis, C.2
Wallace, M.3
-
32
-
-
0030945033
-
u), and partial D phenotypes as determined by multiplex polymerase chain reaction analysis of the RHD gene
-
u), and partial D phenotypes as determined by multiplex polymerase chain reaction analysis of the RHD gene. Blood 1997, 89:2568-2577.
-
(1997)
Blood
, vol.89
, pp. 2568-2577
-
-
Avent, N.D.1
Martin, P.G.2
Armstrong-Fisher, S.S.3
Liu, W.4
Finning, K.M.5
Maddocks, D.6
Urbaniak, S.J.7
-
34
-
-
0030956120
-
Lower antigen site density and weak D immunogenicity cannot be explained by structural genomic abnormalities or regulatory defects of the RHD gene
-
Beckers EAM, Faas BH, Ligthart P, Overbeeke MA, von dem Borne AEGKr, van der Schoot CE, Van Rhenen DJ: Lower antigen site density and weak D immunogenicity cannot be explained by structural genomic abnormalities or regulatory defects of the RHD gene. Transfusion 1997, 37:616-623.
-
(1997)
Transfusion
, vol.37
, pp. 616-623
-
-
Beckers, E.A.M.1
Faas, B.H.2
Ligthart, P.3
Overbeeke, M.A.4
Von Dem Borne, A.E.G.Kr.5
Van Der Schoot, C.E.6
Van Rhenen, D.J.7
-
35
-
-
0030842967
-
A human monoclonal anti-D antibody which detects a nonconformation-dependent epitope on the RhD protein by immunoblotting
-
Apoil PA, Reid ME, Halverson G, Mouro I, Colin Y, Roubinet F, Cartron J-P, Blancher A: A human monoclonal anti-D antibody which detects a nonconformation-dependent epitope on the RhD protein by immunoblotting. Br J Hematol 1997, 98:365-374.
-
(1997)
Br J Hematol
, vol.98
, pp. 365-374
-
-
Apoil, P.A.1
Reid, M.E.2
Halverson, G.3
Mouro, I.4
Colin, Y.5
Roubinet, F.6
Cartron, J.-P.7
Blancher, A.8
-
36
-
-
0030610737
-
IIIa erythrocytes: RhD protein is associated with multiple dispersed amino acid variations
-
IIIa erythrocytes: RhD protein is associated with multiple dispersed amino acid variations. Am J Hematol 1997, 55:139-145.
-
(1997)
Am J Hematol
, vol.55
, pp. 139-145
-
-
Huang, C.-H.1
Chen, Y.2
Reid, M.3
-
37
-
-
15144346536
-
D category VI Type III: A D-Ce(3-6)-D hybrid protein with normal RHD antigen density on red cells [abstract]
-
Flegel WA, Müller TH, Schunter F, Gassner C, Schönitzer D, Wagner FF: D category VI Type III: A D-Ce(3-6)-D hybrid protein with normal RHD antigen density on red cells [abstract]. Transfusion 1997, 37(Suppl):101S.
-
(1997)
Transfusion
, vol.37
, Issue.SUPPL.
-
-
Flegel, W.A.1
Müller, T.H.2
Schunter, F.3
Gassner, C.4
Schönitzer, D.5
Wagner, F.F.6
-
38
-
-
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, Beolet M, D'Ambrosio A-M, Cartron J-P, Le Van Kim C: Transcript analysis of D category phenotypes predicts hybrid Rh D-CE-D proteins associated with alteration of D epitopes. Blood 1995, 85:2937-2944.
-
(1995)
Blood
, vol.85
, pp. 2937-2944
-
-
Rouillac, C.1
Colin, Y.2
Hughes-Jones, N.C.3
Beolet, M.4
D'Ambrosio, A.-M.5
Cartron, J.-P.6
Le Van Kim, C.7
-
39
-
-
0031034596
-
VIccEe phenotypes
-
VIccEe phenotypes. Blood 1997, 89:1779-1786.
-
(1997)
Blood
, vol.89
, pp. 1779-1786
-
-
Avent, N.D.1
Liu, W.2
Jones, J.W.3
Scott, M.L.4
Voak, D.5
Pisacka, M.6
Watt, J.7
Fletcher, A.8
-
40
-
-
0030614976
-
VI category erythrocytes: Correlation of the phenotype with a novel hybrid RhD-CE-D gene but not an internally deleted RhD gene
-
VI category erythrocytes: correlation of the phenotype with a novel hybrid RhD-CE-D gene but not an internally deleted RhD gene. Blood 1997, 89:1834-1835.
-
(1997)
Blood
, vol.89
, pp. 1834-1835
-
-
Huang, C.H.1
-
42
-
-
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
-
43
-
-
0029815713
-
W-red blood cells: Phenotypic homozygosity versus genotypic heterozygosity
-
W-red blood cells: phenotypic homozygosity versus genotypic heterozygosity. Blood 1996, 88:2326-2333.
-
(1996)
Blood
, vol.88
, pp. 2326-2333
-
-
Huang, C.-H.1
-
44
-
-
0030061717
-
Candidate gene acting as a suppressor of the RH locus in most cases of Rh-deficiency
-
Chérif-Zahar B, Raynal V, Gane P, Mattei MG, Bailly P, Gibbs B, Colin Y, Cartron JP: Candidate gene acting as a suppressor of the RH locus in most cases of Rh-deficiency. Nat Genet 1996, 12:168-173.
-
(1996)
Nat Genet
, vol.12
, pp. 168-173
-
-
Chérif-Zahar, B.1
Raynal, V.2
Gane, P.3
Mattei, M.G.4
Bailly, P.5
Gibbs, B.6
Colin, Y.7
Cartron, J.P.8
-
45
-
-
0030742588
-
The RHD gene is highly detectable in RhD-negative Japanese donors
-
Okuda H, Kawano M, Iwamoto S, Tanaka M, Seno T, Okubo Y, Kajii E: The RHD gene is highly detectable in RhD-negative Japanese donors. J Clin Invest 1997, 100:373-379.
-
(1997)
J Clin Invest
, vol.100
, pp. 373-379
-
-
Okuda, H.1
Kawano, M.2
Iwamoto, S.3
Tanaka, M.4
Seno, T.5
Okubo, Y.6
Kajii, E.7
-
46
-
-
0030982624
-
Prenatal analysis of rhesus CeDEe blood groups by heteroduplex generator
-
Rose NC, Hurwitz C, Silberstein L, Andovalu R, Stoerker J: Prenatal analysis of rhesus CeDEe blood groups by heteroduplex generator. Am J Obstet Gynecol 1997, 176:1084-1089.
-
(1997)
Am J Obstet Gynecol
, vol.176
, pp. 1084-1089
-
-
Rose, N.C.1
Hurwitz, C.2
Silberstein, L.3
Andovalu, R.4
Stoerker, J.5
-
47
-
-
8544236207
-
Specificity and sensitivity of RHD genotyping methods by PCR-based DNA amplification
-
Aubin JT, Kim CL, Mouro I, Colin Y, Bignozzi C, Brossard Y, Cartron JP: Specificity and sensitivity of RHD genotyping methods by PCR-based DNA amplification. Br J Haematol 1997, 98:356-364.
-
(1997)
Br J Haematol
, vol.98
, pp. 356-364
-
-
Aubin, J.T.1
Kim, C.L.2
Mouro, I.3
Colin, Y.4
Bignozzi, C.5
Brossard, Y.6
Cartron, J.P.7
-
48
-
-
0029883078
-
Denaturing gradient gel electrophoresis: A novel method for determining Rh phenotype from genomic DNA
-
Steers F, Wallace M, Johnson P, Carritt B, Daniels G: Denaturing gradient gel electrophoresis: a novel method for determining Rh phenotype from genomic DNA. Br J Haematol 1996, 94:417-421.
-
(1996)
Br J Haematol
, vol.94
, pp. 417-421
-
-
Steers, F.1
Wallace, M.2
Johnson, P.3
Carritt, B.4
Daniels, G.5
-
49
-
-
0030838226
-
RHD/CE typing by polymerase chain reaction using sequence-specific primers
-
Gassner C, Schmarda A, Kilga-Nogler S, Jenny-Feldkircher B, Rainer E, Müller TH, Wagner FF, Flegel WA, Schönitzer D: RHD/CE typing by polymerase chain reaction using sequence-specific primers. Transfusion 1997, 37:1020-1026.
-
(1997)
Transfusion
, vol.37
, pp. 1020-1026
-
-
Gassner, C.1
Schmarda, A.2
Kilga-Nogler, S.3
Jenny-Feldkircher, B.4
Rainer, E.5
Müller, T.H.6
Wagner, F.F.7
Flegel, W.A.8
Schönitzer, D.9
-
50
-
-
0030560729
-
Fetal RhD typing by polymerase chain reaction in pregnancies complicated by rhesus alloimmunization
-
Van den Veyver IB, Moise KJ Jr.: Fetal RhD typing by polymerase chain reaction in pregnancies complicated by rhesus alloimmunization. Obstet Gynecol 1996, 88:1061-1067.
-
(1996)
Obstet Gynecol
, vol.88
, pp. 1061-1067
-
-
Van Den Veyver, I.B.1
Moise Jr., K.J.2
-
51
-
-
0030853605
-
Differences between RhD-negative Africans and RhD-negative Europeans
-
Daniels G, Green C, Smart E: Differences between RhD-negative Africans and RhD-negative Europeans. Lancet 1997, 350:862-863.
-
(1997)
Lancet
, vol.350
, pp. 862-863
-
-
Daniels, G.1
Green, C.2
Smart, E.3
-
52
-
-
0031035263
-
Molecular background of VS and weak C expression in blacks
-
Faas BHW, Beckers EAM, Wildoer P, Ligthart PC, Overbeeke MAM, Zondervan HA, Von dem Borne AEGK, van der Schoot CE: 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.W.1
Beckers, E.A.M.2
Wildoer, P.3
Ligthart, P.C.4
Overbeeke, M.A.M.5
Zondervan, H.A.6
Von Dem Borne, A.E.G.K.7
Van Der Schoot, C.E.8
-
53
-
-
0031044711
-
Immunochemical analysis of the Kx protein from human red cells of different Kell phenotypes using antibodies raised against synthetic peptides
-
Carbonnet F, Hattab C, Collec E, Le Van Kim C, Cartron JP, Bertrand O: Immunochemical analysis of the Kx protein from human red cells of different Kell phenotypes using antibodies raised against synthetic peptides. Br J Haematol 1997, 96:857-863.
-
(1997)
Br J Haematol
, vol.96
, pp. 857-863
-
-
Carbonnet, F.1
Hattab, C.2
Collec, E.3
Le Van Kim, C.4
Cartron, J.P.5
Bertrand, O.6
-
55
-
-
0030845253
-
Review: Conditions causing weak expression of Kell system antigens
-
Oyen R, Halverson GR, Reid ME: Review: conditions causing weak expression of Kell system antigens. Immunohematology 1997, 13:75-79.
-
(1997)
Immunohematology
, vol.13
, pp. 75-79
-
-
Oyen, R.1
Halverson, G.R.2
Reid, M.E.3
-
56
-
-
0030820550
-
Molecular basis of Kell blood group phenotypes
-
Lee S: Molecular basis of Kell blood group phenotypes. Vox Sang 1997, 73:1-11.
-
(1997)
Vox Sang
, vol.73
, pp. 1-11
-
-
Lee, S.1
-
57
-
-
0028133343
-
Erythropoietic suppression in fetal anemia because of Kell alloimmunization
-
Vaughan JI, Warwick R, Letsky E, Nicolini U, Rodeck CH, Fisk NM: Erythropoietic suppression in fetal anemia because of Kell alloimmunization. Am J Obstet Gynec 1994, 171:247-252.
-
(1994)
Am J Obstet Gynec
, vol.171
, pp. 247-252
-
-
Vaughan, J.I.1
Warwick, R.2
Letsky, E.3
Nicolini, U.4
Rodeck, C.H.5
Fisk, N.M.6
-
58
-
-
0030043703
-
Decreased fetal erythropoiesis and hemolysis in Kell hemolytic anemia
-
Weiner CP, Widness JA: Decreased fetal erythropoiesis and hemolysis in Kell hemolytic anemia. Am J Obstet Gynecol 1996, 174:547-551.
-
(1996)
Am J Obstet Gynecol
, vol.174
, pp. 547-551
-
-
Weiner, C.P.1
Widness, J.A.2
-
59
-
-
0343113398
-
Hydrops fetalis with Kell isoimmunization
-
Parilla BV, Socol ML: Hydrops fetalis with Kell isoimmunization. Obstet Gynecol 1996, 88:730.
-
(1996)
Obstet Gynecol
, vol.88
, pp. 730
-
-
Parilla, B.V.1
Socol, M.L.2
-
60
-
-
15144357795
-
Inhibition of erythroid progenitor cell growth by anti-Kell: A mechanism for fetal anaemia in Kell-immunized pregnancies
-
Manning M, Warwick R, Vaughan J, Roberts IAG: Inhibition of erythroid progenitor cell growth by anti-Kell: a mechanism for fetal anaemia in Kell-immunized pregnancies [abstract]. Br J Haematol 1996, 93(Suppl 1):13.
-
(1996)
Br J Haematol
, vol.93
, Issue.1 SUPPL.
, pp. 13
-
-
Manning, M.1
Warwick, R.2
Vaughan, J.3
Roberts, I.A.G.4
-
61
-
-
0025971571
-
Anti-Kell in pregnancy
-
Leggat HM, Gibson JM, Barron SL, Reid MM: Anti-Kell in pregnancy. Br J Obstet Gynaecol 1991, 98:162-165.
-
(1991)
Br J Obstet Gynaecol
, vol.98
, pp. 162-165
-
-
Leggat, H.M.1
Gibson, J.M.2
Barron, S.L.3
Reid, M.M.4
-
62
-
-
0028500798
-
Monoclonal antibodies to high-incidence Kell epitopes: Characterization and application in automated screening of donor samples
-
Inglis G, Fraser RH, McTaggart S, Sheridan R, Forrest AH, Mitchell R: Monoclonal antibodies to high-incidence Kell epitopes: characterization and application in automated screening of donor samples. Transfus Med 1994, 4:209-212.
-
(1994)
Transfus Med
, vol.4
, pp. 209-212
-
-
Inglis, G.1
Fraser, R.H.2
McTaggart, S.3
Sheridan, R.4
Forrest, A.H.5
Mitchell, R.6
-
63
-
-
0029849311
-
Prenatal diagnosis of Kell blood group genotypes: KEL1 and KEL2
-
Lee SH, Bennett PR, Overton T, Warwick R, Wu X, Redman CM: Prenatal diagnosis of Kell blood group genotypes: KEL1 and KEL2. Am J Obstet Gynecol 1996, 175:455-459.
-
(1996)
Am J Obstet Gynecol
, vol.175
, pp. 455-459
-
-
Lee, S.H.1
Bennett, P.R.2
Overton, T.3
Warwick, R.4
Wu, X.5
Redman, C.M.6
-
64
-
-
0030986303
-
Use of the polymerase chain reaction sequence specific oligonucleotide technique for the detection of the K1/K2 polymorphism of the Kell blood group system
-
Mifsud NA, Haddad AP, Sparrow RL, Condon JA: Use of the polymerase chain reaction sequence specific oligonucleotide technique for the detection of the K1/K2 polymorphism of the Kell blood group system. Blood 1997, 89:4662-4663.
-
(1997)
Blood
, vol.89
, pp. 4662-4663
-
-
Mifsud, N.A.1
Haddad, A.P.2
Sparrow, R.L.3
Condon, J.A.4
-
65
-
-
0029949995
-
Kell typing by allele-specific PCR (ASP)
-
Avent ND, Martin PG: Kell typing by allele-specific PCR (ASP). Br J Haematol 1996, 93:728-730.
-
(1996)
Br J Haematol
, vol.93
, pp. 728-730
-
-
Avent, N.D.1
Martin, P.G.2
-
66
-
-
0030973219
-
Detection of Kell blood groups: Molecular methods in the diagnostic laboratory
-
Murphy MT, Fraser RH: Detection of Kell blood groups: molecular methods in the diagnostic laboratory. Blood Rev 1997, 11:8-15.
-
(1997)
Blood Rev
, vol.11
, pp. 8-15
-
-
Murphy, M.T.1
Fraser, R.H.2
-
67
-
-
0030787899
-
Prenatal determination of genotypes Kell and Cellano in at-risk pregnancies
-
Spence WC, Maddalena A, Demers DB, Bick DP: Prenatal determination of genotypes Kell and Cellano in at-risk pregnancies. J Reprod Med 1997, 42:353-357.
-
(1997)
J Reprod Med
, vol.42
, pp. 353-357
-
-
Spence, W.C.1
Maddalena, A.2
Demers, D.B.3
Bick, D.P.4
-
68
-
-
0028985434
-
The coding sequence of Duffy blood group gene in humans and simians: Restriction fragment length polymorphism, antibody and malarial parasite specificities, and expression in nonerythroid tissues in Duffy-negative individuals
-
Chaudhuri A, Polyakova J, Zbrzezna V, Pogo O: The coding sequence of Duffy blood group gene in humans and simians: restriction fragment length polymorphism, antibody and malarial parasite specificities, and expression in nonerythroid tissues in Duffy-negative individuals. Blood 1995, 85:615-621.
-
(1995)
Blood
, vol.85
, pp. 615-621
-
-
Chaudhuri, A.1
Polyakova, J.2
Zbrzezna, V.3
Pogo, O.4
-
70
-
-
0028928890
-
b alloantigen system is associated with a polymorphism at the 44-amino acid residue
-
b alloantigen system is associated with a polymorphism at the 44-amino acid residue. Blood 1995, 85:622-626.
-
(1995)
Blood
, vol.85
, pp. 622-626
-
-
Iwamoto, S.1
Omi, T.2
Kajii, E.3
Ikemoto, S.4
-
71
-
-
0029117030
-
b antigens and identification of a deletion in the Duffy gene of an apparently healthy individual with the Fy(a-b-) phenotype
-
b antigens and identification of a deletion in the Duffy gene of an apparently healthy individual with the Fy(a-b-) phenotype. Br J Haematol 1995, 90:823-829.
-
(1995)
Br J Haematol
, vol.90
, pp. 823-829
-
-
Mallinson, G.1
Soo, K.S.2
Schall, T.J.3
Pisacka, M.4
Anstee, D.J.5
-
72
-
-
0030917736
-
From malaria to chemokine receptor the emerging physiologic role of the duffy blood group antigen
-
Hadley TJ, Peiper SC: From malaria to chemokine receptor the emerging physiologic role of the duffy blood group antigen. Blood 1997, 89:3077-3091.
-
(1997)
Blood
, vol.89
, pp. 3077-3091
-
-
Hadley, T.J.1
Peiper, S.C.2
-
73
-
-
0029001881
-
Disruption of a GATA motif in the Duffy gene promoter abolishes erythroid gene expression in Duffy-negative individuals
-
Tournamille C, Colin Y, Cartron J-P, Le Van Kim C: Disruption of a GATA motif in the Duffy gene promoter abolishes erythroid gene expression in Duffy-negative individuals. Nature Genet 1995, 10:224-228.
-
(1995)
Nature Genet
, vol.10
, pp. 224-228
-
-
Tournamille, C.1
Colin, Y.2
Cartron, J.-P.3
Le Van Kim, C.4
-
74
-
-
0029946194
-
Characterization of the Duffy gene promotor: Evidence for tissue-specific abolishment of expression in Fy(a-b-) of black individuals
-
Iwamoto S, Li J, Sugimoto N, Okuda H, Kajii E: Characterization of the Duffy gene promotor: evidence for tissue-specific abolishment of expression in Fy(a-b-) of black individuals. Biochem Biophys Res Commun 1996, 222:852-859.
-
(1996)
Biochem Biophys Res Commun
, vol.222
, pp. 852-859
-
-
Iwamoto, S.1
Li, J.2
Sugimoto, N.3
Okuda, H.4
Kajii, E.5
-
75
-
-
0031035186
-
Detection of Duffy antigen in the plasma membranes and caveolae of vascular endothelial and epithelial cells of nonerythroid organs
-
Chaudhuri A, Nielsen S, Elkjaer ML, Zbrzezna V, Fang F, Pogo AO: Detection of Duffy antigen in the plasma membranes and caveolae of vascular endothelial and epithelial cells of nonerythroid organs. Blood 1997, 89:701-712.
-
(1997)
Blood
, vol.89
, pp. 701-712
-
-
Chaudhuri, A.1
Nielsen, S.2
Elkjaer, M.L.3
Zbrzezna, V.4
Fang, F.5
Pogo, A.O.6
-
77
-
-
0002131258
-
Molecular basis for blood groups and function of carrier proteins
-
Edited by Silberstein LE, Arlington, VA: American Association of Blood Banks
-
Reid ME: Molecular basis for blood groups and function of carrier proteins. In Molecular and Functional Aspects of Blood Group Antigens. Edited by Silberstein LE, Arlington, VA: American Association of Blood Banks; 1995:75-125.
-
(1995)
Molecular and Functional Aspects of Blood Group Antigens
, pp. 75-125
-
-
Reid, M.E.1
-
78
-
-
0029031584
-
Kidd blood group and urea transport function of human erythrocytes are carried by the same protein
-
Olivés B, Mattei M-G, Huet M, Neau P, Martial S, Cartron J-P, Bailly P: Kidd blood group and urea transport function of human erythrocytes are carried by the same protein. J Biol Chem 1995, 270:15607-15610.
-
(1995)
J Biol Chem
, vol.270
, pp. 15607-15610
-
-
Olivés, B.1
Mattei, M.-G.2
Huet, M.3
Neau, P.4
Martial, S.5
Cartron, J.-P.6
Bailly, P.7
-
79
-
-
0030750176
-
The molecular basis of the Kidd blood group polymorphism and its lack of association with type 1 diabetes susceptibility
-
Olivès B, Merriman M, Bailly P, Bain S, Barnett A, Todd J, Cartron J-P, Merriman T: The molecular basis of the Kidd blood group polymorphism and its lack of association with type 1 diabetes susceptibility. Hum Mol Genet 1997, 6:1017-1020.
-
(1997)
Hum Mol Genet
, vol.6
, pp. 1017-1020
-
-
Olivès, B.1
Merriman, M.2
Bailly, P.3
Bain, S.4
Barnett, A.5
Todd, J.6
Cartron, J.-P.7
Merriman, T.8
-
81
-
-
0028909047
-
Changes in the blood group Wright antigens are associated with a mutation at amino acid 658 in human erythrocyte band 3: A site of Interaction between band 3 and glycophorin A under certain conditions
-
Bruce LJ, Ring SM, Anstee DJ, Reid ME, Wilkinson S, Tanner MJA: Changes in the blood group Wright antigens are associated with a mutation at amino acid 658 in human erythrocyte band 3: a site of Interaction between band 3 and glycophorin A under certain conditions. Blood 1995, 85:541-547.
-
(1995)
Blood
, vol.85
, pp. 541-547
-
-
Bruce, L.J.1
Ring, S.M.2
Anstee, D.J.3
Reid, M.E.4
Wilkinson, S.5
Tanner, M.J.A.6
-
84
-
-
3542998263
-
Characterization of six low incidence blood group antigens carried by erythrocyte band 3
-
Jarolim P, Rubin HL, Reid M: Characterization of six low incidence blood group antigens carried by erythrocyte band 3 [abstract], Transfusion 1996, 36(suppl):49S.
-
(1996)
Transfusion
, vol.36
, Issue.SUPPL.
-
-
Jarolim, P.1
Rubin, H.L.2
Reid, M.3
-
85
-
-
10544253080
-
Characterization of 13 novel band 3 gene defects in hereditary spherocytosis with band 3 deficiency
-
Jarolim P, Murray JL, Rubin HL, Taylor WM, Prchal JT, Ballas SK, Snyder LM, Chrobak L, Melrose WD, Brabec V, et al.: Characterization of 13 novel band 3 gene defects in hereditary spherocytosis with band 3 deficiency. Blood 1996, 88:4366-4374.
-
(1996)
Blood
, vol.88
, pp. 4366-4374
-
-
Jarolim, P.1
Murray, J.L.2
Rubin, H.L.3
Taylor, W.M.4
Prchal, J.T.5
Ballas, S.K.6
Snyder, L.M.7
Chrobak, L.8
Melrose, W.D.9
Brabec, V.10
-
86
-
-
0027478159
-
Polymerase chain reaction-based detection of MN blood group-specific sequences in the human genome
-
Corfield VA, Moolman JC, Martell R, Brink PA: Polymerase chain reaction-based detection of MN blood group-specific sequences in the human genome. Transfusion 1993, 33:119-124.
-
(1993)
Transfusion
, vol.33
, pp. 119-124
-
-
Corfield, V.A.1
Moolman, J.C.2
Martell, R.3
Brink, P.A.4
-
87
-
-
0025962946
-
Typing of MNSs blood group specific sequences in the human genome and characterization of a restriction fragment tightly linked to S-s-alleles
-
Huang C-H, Guizzo ML, McCreary J, Leigh EM, Blumenfeld OO: Typing of MNSs blood group specific sequences In the human genome and characterization of a restriction fragment tightly linked to S-s-alleles. Blood 1991, 77:381-386.
-
(1991)
Blood
, vol.77
, pp. 381-386
-
-
Huang, C.-H.1
Guizzo, M.L.2
McCreary, J.3
Leigh, E.M.4
Blumenfeld, O.O.5
-
88
-
-
0028926499
-
Molecular characterization of glycophorin A transcripts in human erythroid cells using RT-PCR, allele-specific restriction, and sequencing
-
DuPont BR, Grant SG, Oto SH, Bigbee WL, Jensen RH, Langlois RG: Molecular characterization of glycophorin A transcripts in human erythroid cells using RT-PCR, allele-specific restriction, and sequencing. Vox Sang 1995, 68:121-129.
-
(1995)
Vox Sang
, vol.68
, pp. 121-129
-
-
DuPont, B.R.1
Grant, S.G.2
Oto, S.H.3
Bigbee, W.L.4
Jensen, R.H.5
Langlois, R.G.6
-
89
-
-
0023819221
-
An RFLP for glycoprotein A (MN) Is in linkage disequilibrium with MN and Ss
-
Murray JC, Buetow KH, Ferrell RE, Sieberg PD, Fukuda M: An RFLP for glycoprotein A (MN) Is In linkage disequilibrium with MN and Ss. Cytogenet Cell Genet 1988, 47:149-151.
-
(1988)
Cytogenet Cell Genet
, vol.47
, pp. 149-151
-
-
Murray, J.C.1
Buetow, K.H.2
Ferrell, R.E.3
Sieberg, P.D.4
Fukuda, M.5
-
90
-
-
0000466291
-
Use of hematopoietic cells and markers for the detection and quantitation of human in vivo somatic mutation
-
Edited by Garratty G. New York: Marcel Dekker
-
Grant SG, Jensen RH: Use of hematopoietic cells and markers for the detection and quantitation of human in vivo somatic mutation. In Immunobiology of Transfusion Medicine. Edited by Garratty G. New York: Marcel Dekker; 1994:299-323.
-
(1994)
Immunobiology of Transfusion Medicine
, pp. 299-323
-
-
Grant, S.G.1
Jensen, R.H.2
-
91
-
-
0028970067
-
Elevated frequency of glycophorin A mutations in erythrocytes from Chernobyl accident victims
-
Jensen RH, Langlois RG, Bigbee WL, Grant SG, Moore D, Pilinskaya M, Vorobtsova I, Pleshanov P: Elevated frequency of glycophorin A mutations in erythrocytes from Chernobyl accident victims. Radiat Res 1995, 141:129-135.
-
(1995)
Radiat Res
, vol.141
, pp. 129-135
-
-
Jensen, R.H.1
Langlois, R.G.2
Bigbee, W.L.3
Grant, S.G.4
Moore, D.5
Pilinskaya, M.6
Vorobtsova, I.7
Pleshanov, P.8
-
92
-
-
0029837485
-
Improved determination of variant erythrocytes at the glycophorin A (GPA) locus and variant frequency in patients treated with radioiodine for thyroid cancer
-
Schiwietz J, Lorenz R, Scheubeck M, Börner W, Hempel K: Improved determination of variant erythrocytes at the glycophorin A (GPA) locus and variant frequency in patients treated with radioiodine for thyroid cancer. Int J Radiat Biol 1996, 70:131-143.
-
(1996)
Int J Radiat Biol
, vol.70
, pp. 131-143
-
-
Schiwietz, J.1
Lorenz, R.2
Scheubeck, M.3
Börner, W.4
Hempel, K.5
-
93
-
-
0029957134
-
Somatic cell mutations at the glycophorin a locus in erythrocytes of atomic bomb survivors: Implications for radiation carcinogenesis
-
Kyoizumi S, Akiyama M, Cologne JB, Tanabe K, Nakamura N, Awa AA, Hirai Y, Kusunoki Y, Umeki S: Somatic cell mutations at the glycophorin a locus in erythrocytes of atomic bomb survivors: Implications for radiation carcinogenesis. Radiat Res 1996, 146:43-52.
-
(1996)
Radiat Res
, vol.146
, pp. 43-52
-
-
Kyoizumi, S.1
Akiyama, M.2
Cologne, J.B.3
Tanabe, K.4
Nakamura, N.5
Awa, A.A.6
Hirai, Y.7
Kusunoki, Y.8
Umeki, S.9
-
94
-
-
0030979873
-
Glycophorin A as a biological dosimeter for radiation dose to the bone marrow from iodine-131
-
Jensen RH, Reynolds JC, Robbins J, Bigbee WL, Grant SG, Langlois RG, Pineda JD, Lee TS, Barker C: Glycophorin A as a biological dosimeter for radiation dose to the bone marrow from iodine-131. Radiat Res 1997, 147:747-752.
-
(1997)
Radiat Res
, vol.147
, pp. 747-752
-
-
Jensen, R.H.1
Reynolds, J.C.2
Robbins, J.3
Bigbee, W.L.4
Grant, S.G.5
Langlois, R.G.6
Pineda, J.D.7
Lee, T.S.8
Barker, C.9
-
95
-
-
0031049912
-
Biodosimetry of Chemobyl cleanup workers from Estonia and Latvia using the glycophorin a in vivo somatic cell mutation assay
-
Bigbee WL, Jensen RH, Veidebaum T, Tekkel M, Rahu M, Stengrevics A, Auvinen A, Hakulinen T, Servomaa K, Rytömaa T, et al.: Biodosimetry of Chemobyl cleanup workers from Estonia and Latvia using the glycophorin a in vivo somatic cell mutation assay. Radiat Res 1997, 147:215-224.
-
(1997)
Radiat Res
, vol.147
, pp. 215-224
-
-
Bigbee, W.L.1
Jensen, R.H.2
Veidebaum, T.3
Tekkel, M.4
Rahu, M.5
Stengrevics, A.6
Auvinen, A.7
Hakulinen, T.8
Servomaa, K.9
Rytömaa, T.10
-
98
-
-
0027517150
-
Mutation at codon 322 in the human acetylcholinesterase (ACHE) gene accounts for YT blood group polymorphism
-
Bartels CF, Zelinski T, Lockridge O: Mutation at codon 322 in the human acetylcholinesterase (ACHE) gene accounts for YT blood group polymorphism. Am J Hum Genet 1993, 52:928-936.
-
(1993)
Am J Hum Genet
, vol.52
, pp. 928-936
-
-
Bartels, C.F.1
Zelinski, T.2
Lockridge, O.3
-
100
-
-
0027980902
-
Human red cell aquaporin CHIP. 1. Molecular characterization of ABH and Colton blood group antigens
-
Smith BL, Preston GM, Spring FA, Anstee DJ, Agre P: Human red cell aquaporin CHIP. 1. Molecular characterization of ABH and Colton blood group antigens. J Clin Invest 1994, 94:1043-1049.
-
(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
-
101
-
-
0029864568
-
A blood group related polymorphism of CD44 abolishes a hyaluronan binding consensus sequence without preventing hyaluronan binding
-
Telen MJ, Udani M, Washington MK, Levesque MC, Lloyd E, Rao N: A blood group related polymorphism of CD44 abolishes a hyaluronan binding consensus sequence without preventing hyaluronan binding. J Biol Chem 1996, 271:7147-7154.
-
(1996)
J Biol Chem
, vol.271
, pp. 7147-7154
-
-
Telen, M.J.1
Udani, M.2
Washington, M.K.3
Levesque, M.C.4
Lloyd, E.5
Rao, N.6
-
103
-
-
0030611739
-
a blood group antigen is a marker for the M6 leukocyte activation antigen, the human homolog of OX-47 antigen, basigin and neurothelin, an immunoglobulin superfamily molecule that is widely expressed in human cells and tissues
-
a blood group antigen is a marker for the M6 leukocyte activation antigen, the human homolog of OX-47 antigen, basigin and neurothelin, an immunoglobulin superfamily molecule that is widely expressed in human cells and tissues. Eur J Immunol 1997, 27:891-897.
-
(1997)
Eur J Immunol
, vol.27
, pp. 891-897
-
-
Spring, F.A.1
Holmes, C.H.2
Simpson, K.L.3
Mawby, W.J.4
Mattes, M.J.5
Okubo, Y.6
Parsons, S.F.7
-
104
-
-
0028449199
-
Molecular basis of glycophorin C variants and their associated blood group antigens
-
Reid ME, Spring FA: Molecular basis of glycophorin C variants and their associated blood group antigens. Transfus Med 1994, 4:139-149.
-
(1994)
Transfus Med
, vol.4
, pp. 139-149
-
-
Reid, M.E.1
Spring, F.A.2
-
105
-
-
0025909319
-
Identification of human erythrocyte blood group antigens on the C3b/C4b receptor
-
Rao N, Ferguson DJ, Lee SF, Telen MJ: Identification of human erythrocyte blood group antigens on the C3b/C4b receptor. J Immunol 1991, 146:3502-3507.
-
(1991)
J Immunol
, vol.146
, pp. 3502-3507
-
-
Rao, N.1
Ferguson, D.J.2
Lee, S.F.3
Telen, M.J.4
-
106
-
-
0025777768
-
The C3b/C4b receptor is recognized by the Knops, McCoy, Swain-langley, and York blood group antisera
-
Moulds JM, Nickells MW, Moulds JJ, Brown MC, Atkinson JP: The C3b/C4b receptor is recognized by the Knops, McCoy, Swain-langley, and York blood group antisera. J Exp Med 1991, 173:1159-1163.
-
(1991)
J Exp Med
, vol.173
, pp. 1159-1163
-
-
Moulds, J.M.1
Nickells, M.W.2
Moulds, J.J.3
Brown, M.C.4
Atkinson, J.P.5
-
107
-
-
0030017606
-
Neutralization of Knops system antibodies using soluble complement receptor 1
-
Moulds JM, Rowe KE: Neutralization of Knops system antibodies using soluble complement receptor 1. Transfusion 1996, 36:517-520.
-
(1996)
Transfusion
, vol.36
, pp. 517-520
-
-
Moulds, J.M.1
Rowe, K.E.2
-
108
-
-
1842403514
-
P-falciparum rosetting mediated by a parasite-variant erythrocyte membrane protein and complement-receptor 1
-
Rowe JA, Moulds JM, Newbold CI, Miller LH: P-falciparum rosetting mediated by a parasite-variant erythrocyte membrane protein and complement-receptor 1. Nature 1997, 388:292-295.
-
(1997)
Nature
, vol.388
, pp. 292-295
-
-
Rowe, J.A.1
Moulds, J.M.2
Newbold, C.I.3
Miller, L.H.4
-
109
-
-
0000973727
-
Sample suitability for the detection of minor leukocyte populations by polymerase chain reaction (PCR)
-
Reed W, Lee T-H, Busch MP, Vichinsky EP: Sample suitability for the detection of minor leukocyte populations by polymerase chain reaction (PCR) [abstract]. Transfusion 1997, 37(Suppl):107S.
-
(1997)
Transfusion
, vol.37
, Issue.SUPPL.
-
-
Reed, W.1
Lee, T.-H.2
Busch, M.P.3
Vichinsky, E.P.4
-
110
-
-
0030293185
-
Prenatal diagnosis of sickle cell anaemia and thalassaemia by analysis of fetal cells in maternal blood
-
Cheung M-C, Goldberg JD, Kan YW: Prenatal diagnosis of sickle cell anaemia and thalassaemia by analysis of fetal cells in maternal blood. Nat Genet 1996, 14:264-268.
-
(1996)
Nat Genet
, vol.14
, pp. 264-268
-
-
Cheung, M.-C.1
Goldberg, J.D.2
Kan, Y.W.3
-
111
-
-
0342618532
-
Presence of fetal DNA in maternal plasma and serum
-
Lo YMD, Corbetta N, Chamberlain PF, Rai V, Sargent IL, Redman CWG, Wainscoat JS: Presence of fetal DNA in maternal plasma and serum. Lancet 1997, 350:485-487.
-
(1997)
Lancet
, vol.350
, pp. 485-487
-
-
Lo, Y.M.D.1
Corbetta, N.2
Chamberlain, P.F.3
Rai, V.4
Sargent, I.L.5
Redman, C.W.G.6
Wainscoat, J.S.7
-
112
-
-
0008883517
-
Longterm multi-lineage chimerism of donor leukocytes in transfused trauma patients
-
Lee T-H, Paglieroni T, Ohro H, Holland PV, Busch MP: Longterm multi-lineage chimerism of donor leukocytes in transfused trauma patients [abstract]. Blood 1996, 88(Suppl 1):265a.
-
(1996)
Blood
, vol.88
, Issue.1 SUPPL.
-
-
Lee, T.-H.1
Paglieroni, T.2
Ohro, H.3
Holland, P.V.4
Busch, M.P.5
-
113
-
-
0029921113
-
Human red blood cell Wright antigens: A genetic and evolutionary perspective on glycophorin A-band 3 interaction
-
Huang C-H, Reid ME, Xie SS, Blumenfeld OO: Human red blood cell Wright antigens: a genetic and evolutionary perspective on glycophorin A-band 3 interaction. Blood 1996, 87:3942-3947.
-
(1996)
Blood
, vol.87
, pp. 3942-3947
-
-
Huang, C.-H.1
Reid, M.E.2
Xie, S.S.3
Blumenfeld, O.O.4
-
114
-
-
0030988964
-
Anti-D in a D-positive renal transplant patient
-
Saba NF, Sweeney JD, Penn LC, Lawton JC, Yankee RL, Huang CH, Schanfield MS: Anti-D in a D-positive renal transplant patient. Transfusion 1997, 37:321-324.
-
(1997)
Transfusion
, vol.37
, pp. 321-324
-
-
Saba, N.F.1
Sweeney, J.D.2
Penn, L.C.3
Lawton, J.C.4
Yankee, R.L.5
Huang, C.H.6
Schanfield, M.S.7
-
115
-
-
0031984056
-
DNA variation and the future of human genetics
-
Schafer AJ, Mawkins JR: DNA variation and the future of human genetics. Nat Biotechnol 1998, 16:33-39.
-
(1998)
Nat Biotechnol
, vol.16
, pp. 33-39
-
-
Schafer, A.J.1
Mawkins, J.R.2
-
117
-
-
0031444903
-
Involvement of Gly96 in the formation of the RH:26 epitope
-
Faas BHW, Ligthart PC, Lomas-Francis C, Overbeeke MAM, Von dem Borne AEGK, van der Schoot CE: Involvement of Gly96 in the formation of the RH:26 epitope. Transfusion 1997, 37:1123-1130.
-
(1997)
Transfusion
, vol.37
, pp. 1123-1130
-
-
Faas, B.H.W.1
Ligthart, P.C.2
Lomas-Francis, C.3
Overbeeke, M.A.M.4
Von Dem Borne, A.E.G.K.5
Van Der Schoot, C.E.6
-
118
-
-
0028936247
-
Molecular basis of the Kell (K1) phenotype
-
Lee S, Wu X, Reid ME, Zelinski T, Redman C: Molecular basis of the Kell (K1) phenotype. Blood 1995, 85:912-916.
-
(1995)
Blood
, vol.85
, pp. 912-916
-
-
Lee, S.1
Wu, X.2
Reid, M.E.3
Zelinski, T.4
Redman, C.5
-
119
-
-
0030036591
-
Point mutations characterize KEL10, the KEL3, KEL4, and KEL21 alleles, and the KEL17 and KEL11 alleles
-
Lee S, Wu X, Son S, Naime D, Reid M, Okudo Y, Sistonen P, Redman C: Point mutations characterize KEL10, the KEL3, KEL4, and KEL21 alleles, and the KEL17 and KEL11 alleles. Transfusion 1996, 36:490-494.
-
(1996)
Transfusion
, vol.36
, pp. 490-494
-
-
Lee, S.1
Wu, X.2
Son, S.3
Naime, D.4
Reid, M.5
Okudo, Y.6
Sistonen, P.7
Redman, C.8
-
120
-
-
0028889428
-
Molecular basis of the K:6,-7 [Js(a+b-)] phenotype in the Kell blood group system
-
Lee S, Wu X, Reid ME, Redman C: Molecular basis of the K:6,-7 [Js(a+b-)] phenotype in the Kell blood group system. Transfusion 1995, 35:822-825.
-
(1995)
Transfusion
, vol.35
, pp. 822-825
-
-
Lee, S.1
Wu, X.2
Reid, M.E.3
Redman, C.4
-
121
-
-
0030828097
-
The KEL24 and KEL14 alleles of the Kell blood group system
-
Lee S, Naime D, Reid M, Redman C: The KEL24 and KEL14 alleles of the Kell blood group system. Transfusion 1997, 37:1035-1038.
-
(1997)
Transfusion
, vol.37
, pp. 1035-1038
-
-
Lee, S.1
Naime, D.2
Reid, M.3
Redman, C.4
-
122
-
-
2442744729
-
Genotyping of Diego blood group system by use of polymerase chain reaction and Nae I restriction enzyme
-
Kim DA, Kim TY, Choi TY: Genotyping of Diego blood group system by use of polymerase chain reaction and Nae I restriction enzyme [abstract]. Transfusion 1997, 37(Suppl):33S.
-
(1997)
Transfusion
, vol.37
, Issue.SUPPL.
-
-
Kim, D.A.1
Kim, T.Y.2
Choi, T.Y.3
-
124
-
-
0006467635
-
A G→A mutation in the anion exchanger 1 gene (AE1) accounts for the Swann blood group polymorphism
-
Zelinski T, Rusnak A, McManus K, Coghlan G: A G→A mutation in the anion exchanger 1 gene (AE1) accounts for the Swann blood group polymorphism [abstract]. Transfusion 1997, 37(Suppl):89S.
-
(1997)
Transfusion
, vol.37
, Issue.SUPPL.
-
-
Zelinski, T.1
Rusnak, A.2
McManus, K.3
Coghlan, G.4
-
125
-
-
0030920024
-
SfaNI polymorphism distinguishes the alleles of the glycophorin A locus that determine the MN blood group
-
Leos SH, Bigbee WL, Jensen RH, Grant SG: SfaNI polymorphism distinguishes the alleles of the glycophorin A locus that determine the MN blood group. Acta Haematol 1997, 98:51-53.
-
(1997)
Acta Haematol
, vol.98
, pp. 51-53
-
-
Leos, S.H.1
Bigbee, W.L.2
Jensen, R.H.3
Grant, S.G.4
-
126
-
-
0000422982
-
MNSs blood groups and major glycophorins: Molecular basis for allelic variation
-
Edited by Cartron J-P, Rouger P. New York: Plenum Press
-
Huang C-H, Blumenfeld OO: MNSs blood groups and major glycophorins: molecular basis for allelic variation. In Molecular Basis of Major Human Blood Group Antigens. Edited by Cartron J-P, Rouger P. New York: Plenum Press; 1995:153-183.
-
(1995)
Molecular Basis of Major Human Blood Group Antigens
, pp. 153-183
-
-
Huang, C.-H.1
Blumenfeld, O.O.2
-
128
-
-
0027515173
-
a antigen on glycophorin D but not on glycophorin C: Further evidence that glycophorin D is a product of the GYPC gene
-
a antigen on glycophorin D but not on glycophorin C: further evidence that glycophorin D is a product of the GYPC gene. Blood 1993, 82:3198-3203.
-
(1993)
Blood
, vol.82
, pp. 3198-3203
-
-
Daniels, G.1
King, M.J.2
Avent, N.D.3
Khalid, G.4
Reid, M.5
Mallinson, G.6
Smythe, J.7
Cedergren, B.8
-
130
-
-
0028070786
-
Molecular basis of reduced or absent expression of decay-accelerating factor in Cromer blood group phenotypes
-
Lublin DM, Mallinson G, Poole J, Reid ME, Thompson ES, Ferdman BR, Telen MJ, Anstee DJ, Tanner MJ: Molecular basis of reduced or absent expression of decay-accelerating factor in Cromer blood group phenotypes. Blood 1994, 84:1276-1282.
-
(1994)
Blood
, vol.84
, pp. 1276-1282
-
-
Lublin, D.M.1
Mallinson, G.2
Poole, J.3
Reid, M.E.4
Thompson, E.S.5
Ferdman, B.R.6
Telen, M.J.7
Anstee, D.J.8
Tanner, M.J.9
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