-
1
-
-
33748917315
-
Serious hazards of transfusion: A decade of hemovigilance in the UK
-
Stainsby D, Jones H, Asher D, Atterbury C, Boncinelli A, Brant L, Chapman CE, Davison K, Gerrard R, Gray A, Knowles S, Love EM, Milkins C, McClelland DB, Norfolk DR, Soldan K, Taylor C, Revill J, Williamson LM, Cohen H SHOT Steering Group. Serious hazards of transfusion: a decade of hemovigilance in the UK. Transfus Med Rev 2006 20 : 273 82.
-
(2006)
Transfus Med Rev
, vol.20
, pp. 273-82
-
-
Stainsby, D.1
Jones, H.2
Asher, D.3
Atterbury, C.4
Boncinelli, A.5
Brant, L.6
Chapman, C.E.7
Davison, K.8
Gerrard, R.9
Gray, A.10
Knowles, S.11
Love, E.M.12
Milkins, C.13
McClelland, D.B.14
Norfolk, D.R.15
Soldan, K.16
Taylor, C.17
Revill, J.18
Williamson, L.M.19
-
2
-
-
9644267431
-
Transfusion errors: Scope of the problem, consequences, and solutions
-
Sazama K. Transfusion errors: scope of the problem, consequences, and solutions. Curr Hematol Rep 2003 2 : 518 21.
-
(2003)
Curr Hematol Rep
, vol.2
, pp. 518-21
-
-
Sazama, K.1
-
4
-
-
0025101066
-
Cloning and characterization of DNA complementary to human UDP-GalNAc: Fuc-alpha1-2Gal alpha1-3GalNAc transferase (histo-blood group A transferase) mRNA
-
Yamamoto F, Marken J, Tsuji T, White T, Clausen H, Hakomori S. Cloning and characterization of DNA complementary to human UDP-GalNAc:Fuc-alpha1-2Gal alpha1-3GalNAc transferase (histo-blood group A transferase) mRNA. J Biol Chem 1990 265 : 1146 51.
-
(1990)
J Biol Chem
, vol.265
, pp. 1146-51
-
-
Yamamoto, F.1
Marken, J.2
Tsuji, T.3
White, T.4
Clausen, H.5
Hakomori, S.6
-
5
-
-
0034888001
-
The ABO blood group gene: A locus of considerable genetic diversity
-
Chester MA, Olsson ML. The ABO blood group gene: a locus of considerable genetic diversity. Transfus Med Rev 2001 15 : 177 200.
-
(2001)
Transfus Med Rev
, vol.15
, pp. 177-200
-
-
Chester, M.A.1
Olsson, M.L.2
-
6
-
-
17144474592
-
Molecular genetics of ABO
-
Yamamoto F. Molecular genetics of ABO. Vox Sang 2000 78 : 91 103.
-
(2000)
Vox Sang
, vol.78
, pp. 91-103
-
-
Yamamoto, F.1
-
7
-
-
0032170084
-
x allele: Genetic recombination of common alleles can result in the Ax phenotype
-
x allele: genetic recombination of common alleles can result in the Ax phenotype. Transfus Med 1998 8 : 231 8.
-
(1998)
Transfus Med
, vol.8
, pp. 231-8
-
-
Olsson, M.L.1
Chester, M.A.2
-
8
-
-
12444347830
-
New and unusual O alleles at the ABO locus are implicated in unexpected blood group phenotypes
-
Hosseini-Maaf B, Irshaid NM, Hellberg A, Wagner T, Levene C, Hustinx H, Steffensen R, Chester MA, Olsson ML. New and unusual O alleles at the ABO locus are implicated in unexpected blood group phenotypes. Transfusion 2005 45 : 70 81.
-
(2005)
Transfusion
, vol.45
, pp. 70-81
-
-
Hosseini-Maaf, B.1
Irshaid, N.M.2
Hellberg, A.3
Wagner, T.4
Levene, C.5
Hustinx, H.6
Steffensen, R.7
Chester, M.A.8
Olsson, M.L.9
-
11
-
-
0035383798
-
Loss of red cell A, B, and H antigens is frequent in myeloid malignancies
-
Bianco T, Farmer BJ, Sage RE, Dobrovic A. Loss of red cell A, B, and H antigens is frequent in myeloid malignancies. Blood 2001 97 : 3633 9.
-
(2001)
Blood
, vol.97
, pp. 3633-9
-
-
Bianco, T.1
Farmer, B.J.2
Sage, R.E.3
Dobrovic, A.4
-
12
-
-
0029892423
-
Fatal hemolytic transfusion reaction resulting from ABO mistyping of a patient with acquired B antigen detectable only by some monoclonal anti-B reagents
-
Garratty G, Arndt P, Co A, Rodberg K, Furmanski M. Fatal hemolytic transfusion reaction resulting from ABO mistyping of a patient with acquired B antigen detectable only by some monoclonal anti-B reagents. Transfusion 1996 36 : 351 7.
-
(1996)
Transfusion
, vol.36
, pp. 351-7
-
-
Garratty, G.1
Arndt, P.2
Co, A.3
Rodberg, K.4
Furmanski, M.5
-
13
-
-
0035469814
-
Genomic analysis of clinical samples with serologic ABO blood grouping discrepancies: Identification of 15 novel A and B subgroup alleles
-
Olsson ML, Irshaid NM, Hosseini-Maaf B, Hellberg A, Moulds MK, Sareneva H, Chester MA. Genomic analysis of clinical samples with serologic ABO blood grouping discrepancies: identification of 15 novel A and B subgroup alleles. Blood 2001 98 : 1585 93.
-
(2001)
Blood
, vol.98
, pp. 1585-93
-
-
Olsson, M.L.1
Irshaid, N.M.2
Hosseini-Maaf, B.3
Hellberg, A.4
Moulds, M.K.5
Sareneva, H.6
Chester, M.A.7
-
14
-
-
0346096786
-
Allelic genes of blood group antigens: A source of human mutations and cSNPs documented in the Blood Group Antigen Gene Mutation Database
-
Blumenfeld OO, Patnaik SK. Allelic genes of blood group antigens: a source of human mutations and cSNPs documented in the Blood Group Antigen Gene Mutation Database. Hum Mutat 2004 23 : 8 16.
-
(2004)
Hum Mutat
, vol.23
, pp. 8-16
-
-
Blumenfeld, O.O.1
Patnaik, S.K.2
-
15
-
-
0033572503
-
Applications of flow cytofluorometry to red blood cell immunology
-
Garratty G, Arndt PA. Applications of flow cytofluorometry to red blood cell immunology. Cytometry 1999 38 : 259 67.
-
(1999)
Cytometry
, vol.38
, pp. 259-67
-
-
Garratty, G.1
Arndt, P.A.2
-
16
-
-
0025830349
-
Quantitative flow cytometric analysis of ABO red cell antigens
-
Sharon R, Fibach E. Quantitative flow cytometric analysis of ABO red cell antigens. Cytometry 1991 12 : 545 9.
-
(1991)
Cytometry
, vol.12
, pp. 545-9
-
-
Sharon, R.1
Fibach, E.2
-
17
-
-
0026058908
-
Flow-cytometric analysis of erythrocytic blood group A antigen density profile
-
Berneman ZN, Van Bockstaele DR, Uyttenbroeck WM, Van Zaelen C, Cole-Dergent J, Muylle L, Peetermans ME. Flow-cytometric analysis of erythrocytic blood group A antigen density profile. Vox Sang 1991 61 : 265 74.
-
(1991)
Vox Sang
, vol.61
, pp. 265-74
-
-
Berneman, Z.N.1
Van Bockstaele, D.R.2
Uyttenbroeck, W.M.3
Van Zaelen, C.4
Cole-Dergent, J.5
Muylle, L.6
Peetermans, M.E.7
-
18
-
-
0028351203
-
Changes in ABH antigen expression on red cells during in vivo aging: A flow cytometric analysis
-
Fibach E, Sharon R. Changes in ABH antigen expression on red cells during in vivo aging: a flow cytometric analysis. Transfusion 1994 34 : 328 32.
-
(1994)
Transfusion
, vol.34
, pp. 328-32
-
-
Fibach, E.1
Sharon, R.2
-
19
-
-
62849092779
-
DNA methylation of the ABO promoter underlies loss of ABO allelic expression in a significant proportion of leukemic patients
-
Bianco-Miotto T, Hussey DJ, Day TK, O'Keefe DS, Dobrovic A. DNA methylation of the ABO promoter underlies loss of ABO allelic expression in a significant proportion of leukemic patients. PLoS ONE 2009 4 : e4788.
-
(2009)
PLoS ONE
, vol.4
, pp. 4788
-
-
Bianco-Miotto, T.1
Hussey, D.J.2
Day, T.K.3
O'Keefe, D.S.4
Dobrovic, A.5
-
20
-
-
34147142476
-
Bacterial glycosidases for the production of universal red blood cells
-
Liu QP, Sulzenbacher G, Yuan H, Bennett EP, Pietz G, Saunders K, Spence J, Nudelman E, Levery SB, White T, Neveu JM, Lane WS, Bourne Y, Olsson ML, Henrissat B, Clausen H. Bacterial glycosidases for the production of universal red blood cells. Nat Biotechnol 2007 25 : 454 64.
-
(2007)
Nat Biotechnol
, vol.25
, pp. 454-64
-
-
Liu, Q.P.1
Sulzenbacher, G.2
Yuan, H.3
Bennett, E.P.4
Pietz, G.5
Saunders, K.6
Spence, J.7
Nudelman, E.8
Levery, S.B.9
White, T.10
Neveu, J.M.11
Lane, W.S.12
Bourne, Y.13
Olsson, M.L.14
Henrissat, B.15
Clausen, H.16
-
21
-
-
0024396195
-
Further evidence for the presence of A antigen on group B erythrocytes through the use of specific exoglycosidases
-
Goldstein J, Lenny L, Davies D, Voak D. Further evidence for the presence of A antigen on group B erythrocytes through the use of specific exoglycosidases. Vox Sang 1989 57 : 142 6.
-
(1989)
Vox Sang
, vol.57
, pp. 142-6
-
-
Goldstein, J.1
Lenny, L.2
Davies, D.3
Voak, D.4
-
22
-
-
0024284028
-
A simple salting out procedure for extracting DNA from human nucleated cells
-
Miller SA, Dykes DD, Polesky HF. A simple salting out procedure for extracting DNA from human nucleated cells. Nucleic Acids Res 1988 16 : 1215.
-
(1988)
Nucleic Acids Res
, vol.16
, pp. 1215
-
-
Miller, S.A.1
Dykes, D.D.2
Polesky, H.F.3
-
23
-
-
0028844274
-
1 discriminating nucleotide substitution at the ABO locus
-
1 discriminating nucleotide substitution at the ABO locus. Vox Sang 1995 69 : 242 7.
-
(1995)
Vox Sang
, vol.69
, pp. 242-7
-
-
Olsson, M.L.1
Chester, M.A.2
-
24
-
-
0029939806
-
Polymorphisms at the ABO locus in subgroup A individuals
-
Olsson ML, Chester MA. Polymorphisms at the ABO locus in subgroup A individuals. Transfusion 1996 36 : 309 13.
-
(1996)
Transfusion
, vol.36
, pp. 309-13
-
-
Olsson, M.L.1
Chester, M.A.2
-
25
-
-
35448943597
-
An extensive PCR-ASP strategy for clinical ABO blood group genotyping that avoids potential errors caused by null, subgroup and hybrid alleles
-
Hosseini-Maaf B, Hellberg A, Chester MA, Olsson ML. An extensive PCR-ASP strategy for clinical ABO blood group genotyping that avoids potential errors caused by null, subgroup and hybrid alleles. Transfusion 2007 47 : 2110 25.
-
(2007)
Transfusion
, vol.47
, pp. 2110-25
-
-
Hosseini-Maaf, B.1
Hellberg, A.2
Chester, M.A.3
Olsson, M.L.4
-
26
-
-
0033198589
-
Allele-related variation in minisatellite repeats involved in the transcription of the blood group ABO gene
-
Irshaid NM, Chester MA, Olsson ML. Allele-related variation in minisatellite repeats involved in the transcription of the blood group ABO gene. Transfus Med 1999 9 : 219 26.
-
(1999)
Transfus Med
, vol.9
, pp. 219-26
-
-
Irshaid, N.M.1
Chester, M.A.2
Olsson, M.L.3
-
27
-
-
0027503637
-
Molecular genetic analysis of the ABO blood group system: 3. Ax and B(A) alleles
-
Yamamoto F, McNeill PD, Yamamoto M, Hakomori S, Harris T. Molecular genetic analysis of the ABO blood group system: 3. Ax and B(A) alleles. Vox Sang 1993 64 : 171 4.
-
(1993)
Vox Sang
, vol.64
, pp. 171-4
-
-
Yamamoto, F.1
McNeill, P.D.2
Yamamoto, M.3
Hakomori, S.4
Harris, T.5
-
28
-
-
0036517350
-
A weak blood group A phenotype caused by a new mutation at the ABO locus
-
Seltsam A, Hallensleben M, Eiz-Vesper B, Lenhard V, Heymann G, Blasczyk R. A weak blood group A phenotype caused by a new mutation at the ABO locus. Transfusion 2002 42 : 294 301.
-
(2002)
Transfusion
, vol.42
, pp. 294-301
-
-
Seltsam, A.1
Hallensleben, M.2
Eiz-Vesper, B.3
Lenhard, V.4
Heymann, G.5
Blasczyk, R.6
-
29
-
-
2442691614
-
ABO Exon and intron analysis in individuals with the AweakB phenotype reveals a novel O1v-A2 hybrid allele that causes four missense mutations in the A transferase
-
Hosseini-Maaf B, Hellberg A, Rodrigues MJ, Chester MA, Olsson ML. ABO Exon and intron analysis in individuals with the AweakB phenotype reveals a novel O1v-A2 hybrid allele that causes four missense mutations in the A transferase. BMC Genet 2003 4 : 17.
-
(2003)
BMC Genet
, vol.4
, pp. 17
-
-
Hosseini-Maaf, B.1
Hellberg, A.2
Rodrigues, M.J.3
Chester, M.A.4
Olsson, M.L.5
-
30
-
-
33644666696
-
A weak blood group A phenotype caused by a translation-initiator mutation in the ABO gene
-
Seltsam A, Das Gupta C, Bade-Doeding C, Blasczyk R. A weak blood group A phenotype caused by a translation-initiator mutation in the ABO gene. Transfusion 2006 46 : 434 40.
-
(2006)
Transfusion
, vol.46
, pp. 434-40
-
-
Seltsam, A.1
Das Gupta, C.2
Bade-Doeding, C.3
Blasczyk, R.4
-
31
-
-
18944402121
-
The Abantu phenotype in the ABO blood group system is due to a splice-site mutation in a hybrid between a new O1-like allelic lineage and the A2 allele
-
Hosseini-Maaf B, Smart E, Chester MA, Olsson ML. The Abantu phenotype in the ABO blood group system is due to a splice-site mutation in a hybrid between a new O1-like allelic lineage and the A2 allele. Vox Sang 2005 88 : 256 64.
-
(2005)
Vox Sang
, vol.88
, pp. 256-64
-
-
Hosseini-Maaf, B.1
Smart, E.2
Chester, M.A.3
Olsson, M.L.4
-
32
-
-
0028971174
-
el allele-specific nucleotide insertion at the blood group ABO locus and its detection using a sequence-specific polymerase chain reaction
-
el allele-specific nucleotide insertion at the blood group ABO locus and its detection using a sequence-specific polymerase chain reaction. Biochem Biophys Res Commun 1995 216 : 642 7.
-
(1995)
Biochem Biophys Res Commun
, vol.216
, pp. 642-7
-
-
Olsson, M.L.1
Thuresson, B.2
Chester, M.A.3
-
33
-
-
4243872835
-
A splice-site mutation defines the Afinn allele at the blood group ABO locus
-
Olsson ML, Irshaid NM, Kuosmanen M, Pirkola A, Chester MA. A splice-site mutation defines the Afinn allele at the blood group ABO locus. Transfusion 2000 40 (10S 13S.
-
(2000)
Transfusion
, vol.40
, Issue.10
-
-
Olsson, M.L.1
Irshaid, N.M.2
Kuosmanen, M.3
Pirkola, A.4
Chester, M.A.5
-
34
-
-
0027394938
-
Molecular genetic analysis of the ABO blood group system: 1. Weak subgroups: A3 and B3 alleles
-
Yamamoto F, McNeill PD, Yamamoto M, Hakomori S, Harris T, Judd WJ, Davenport RD. Molecular genetic analysis of the ABO blood group system: 1. Weak subgroups: A3 and B3 alleles. Vox Sang 1993 64 : 116 9.
-
(1993)
Vox Sang
, vol.64
, pp. 116-9
-
-
Yamamoto, F.1
McNeill, P.D.2
Yamamoto, M.3
Hakomori, S.4
Harris, T.5
Judd, W.J.6
Davenport, R.D.7
-
35
-
-
20544456881
-
Novel glycolipid variations revealed by monoclonal antibody immunochemical analysis of weak ABO subgroups of A
-
Svensson L, Rydberg L, Hellberg A, Gilliver LG, Olsson ML, Henry SM. Novel glycolipid variations revealed by monoclonal antibody immunochemical analysis of weak ABO subgroups of A. Vox Sang 2005 89 : 27 38.
-
(2005)
Vox Sang
, vol.89
, pp. 27-38
-
-
Svensson, L.1
Rydberg, L.2
Hellberg, A.3
Gilliver, L.G.4
Olsson, M.L.5
Henry, S.M.6
-
36
-
-
2442532037
-
A novel blood group B subgroup: Serological and genetic studies
-
Estalote AC, Palatnik M, Chester MA, Olsson ML, Sant'Anna Gomes BM. A novel blood group B subgroup: serological and genetic studies. Transfus Med 2004 14 : 173 80.
-
(2004)
Transfus Med
, vol.14
, pp. 173-80
-
-
Estalote, A.C.1
Palatnik, M.2
Chester, M.A.3
Olsson, M.L.4
Sant'Anna Gomes, B.M.5
-
37
-
-
23844518947
-
Identification of a novel B variant allele at the ABO locus in Chinese Han individuals with B subgroup
-
Deng ZH, Yu Q, Lian YL, Wu GG, Su YQ, Zhang X. Identification of a novel B variant allele at the ABO locus in Chinese Han individuals with B subgroup. Ann Clin Lab Sci 2005 35 : 265 9.
-
(2005)
Ann Clin Lab Sci
, vol.35
, pp. 265-9
-
-
Deng, Z.H.1
Yu, Q.2
Lian, Y.L.3
Wu, G.G.4
Su, Y.Q.5
Zhang, X.6
-
38
-
-
34247617415
-
Structural basis for red cell phenotypic changes in newly identified, naturally occurring subgroup mutants of the human blood group B glycosyltransferase
-
Hosseini-Maaf B, Letts JA, Persson M, Smart E, LePennec PY, Hustinx H, Zhao Z, Palcic MM, Evans SV, Chester MA, Olsson ML. Structural basis for red cell phenotypic changes in newly identified, naturally occurring subgroup mutants of the human blood group B glycosyltransferase. Transfusion 2007 47 : 864 75.
-
(2007)
Transfusion
, vol.47
, pp. 864-75
-
-
Hosseini-Maaf, B.1
Letts, J.A.2
Persson, M.3
Smart, E.4
Lepennec, P.Y.5
Hustinx, H.6
Zhao, Z.7
Palcic, M.M.8
Evans, S.V.9
Chester, M.A.10
Olsson, M.L.11
-
39
-
-
33644883923
-
Novel polymorphisms in exons 6 and 7 of A/B alleles detected by polymerase chain reaction-single strand conformation polymorphism
-
Chen YJ, Chen PS, Liu HM, Lyou JY, Hu HY, Lin JS, Tzeng CH. Novel polymorphisms in exons 6 and 7 of A/B alleles detected by polymerase chain reaction-single strand conformation polymorphism. Vox Sang 2006 90 : 119 27.
-
(2006)
Vox Sang
, vol.90
, pp. 119-27
-
-
Chen, Y.J.1
Chen, P.S.2
Liu, H.M.3
Lyou, J.Y.4
Hu, H.Y.5
Lin, J.S.6
Tzeng, C.H.7
-
40
-
-
0015622710
-
An inherited blood group A variant in the Finnish population. I. Basic characteristics
-
Mohn JF, Cunningham RK, Pirkola A, Furuhjelm U, Nevanlinna HR. An inherited blood group A variant in the Finnish population. I. Basic characteristics. Vox Sang 1973 24 : 385 403.
-
(1973)
Vox Sang
, vol.24
, pp. 385-403
-
-
Mohn, J.F.1
Cunningham, R.K.2
Pirkola, A.3
Furuhjelm, U.4
Nevanlinna, H.R.5
-
41
-
-
0006082275
-
Analysis of mutations in the blood-group H gene in donors with H-deficient phenotypes
-
Suppl
-
Johnson P. H., Mak M. K., Leong S., Broadberry R., Duraisamy G., Gooch A., Lin-Chu M., Makar Y., Okubo Y., Smart E., Koepsall E., Ewers M. Analysis of mutations in the blood-group H gene in donors with H-deficient phenotypes. Vox Sang 1994 67 Suppl 2 : 25.
-
(1994)
Vox Sang
, vol.67
, Issue.2
, pp. 25
-
-
Johnson, P.H.1
Mak, M.K.2
Leong, S.3
Broadberry, R.4
Duraisamy, G.5
Gooch, A.6
Lin-Chu, M.7
Makar, Y.8
Okubo, Y.9
Smart, E.10
Koepsall, E.11
Ewers, M.12
-
42
-
-
0031025282
-
Heterogeneity of the human H blood group alpha(1,2)fucosyltransferase gene among para-Bombay individuals
-
Yu LC, Yang YH, Broadberry RE, Chen YH, Lin M. Heterogeneity of the human H blood group alpha(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
-
43
-
-
33751378894
-
Identification of six new alleles at the FUT1 and FUT2 loci in ethnically diverse individuals with Bombay and Para-Bombay phenotypes
-
Storry JR, Johannesson JS, Poole J, Strindberg J, Rodrigues MJ, Yahalom V, Levene C, Fujita C, Castilho L, Hustinx H, Olsson ML. Identification of six new alleles at the FUT1 and FUT2 loci in ethnically diverse individuals with Bombay and Para-Bombay phenotypes. Transfusion 2006 46 : 2149 55.
-
(2006)
Transfusion
, vol.46
, pp. 2149-55
-
-
Storry, J.R.1
Johannesson, J.S.2
Poole, J.3
Strindberg, J.4
Rodrigues, M.J.5
Yahalom, V.6
Levene, C.7
Fujita, C.8
Castilho, L.9
Hustinx, H.10
Olsson, M.L.11
-
44
-
-
0021746878
-
A mouse monoclonal antibody with anti-A,(B) specificity which agglutinates Ax cells
-
Moore S, Chirnside A, Micklem LR, McClelland DB, James K. A mouse monoclonal antibody with anti-A,(B) specificity which agglutinates Ax cells. Vox Sang 1984 47 : 427 34.
-
(1984)
Vox Sang
, vol.47
, pp. 427-34
-
-
Moore, S.1
Chirnside, A.2
Micklem, L.R.3
McClelland, D.B.4
James, K.5
-
46
-
-
0025830776
-
A splice site mutation of the beta-spectrin gene causing exon skipping in hereditary elliptocytosis associated with a truncated beta-spectrin chain
-
Gallagher PG, Tse WT, Costa F, Scarpa A, Boivin P, Delaunay J, Forget BG. A splice site mutation of the beta-spectrin gene causing exon skipping in hereditary elliptocytosis associated with a truncated beta-spectrin chain. J Biol Chem 1991 266 : 15154 9.
-
(1991)
J Biol Chem
, vol.266
, pp. 15154-9
-
-
Gallagher, P.G.1
Tse, W.T.2
Costa, F.3
Scarpa, A.4
Boivin, P.5
Delaunay, J.6
Forget, B.G.7
-
47
-
-
0024209849
-
Different splice site utilization generates diversity between the rat and human pancreatic polypeptide precursors
-
Kopin AS, Toder AE, Leiter AB. Different splice site utilization generates diversity between the rat and human pancreatic polypeptide precursors. Arch Biochem Biophys 1988 267 : 742 8.
-
(1988)
Arch Biochem Biophys
, vol.267
, pp. 742-8
-
-
Kopin, A.S.1
Toder, A.E.2
Leiter, A.B.3
-
48
-
-
0015619039
-
An inherited blood group A variant in the Finnish population. II. Population studies
-
Nevanlinna HR, Pirkola A. An inherited blood group A variant in the Finnish population. II. Population studies. Vox Sang 1973 24 : 404 16.
-
(1973)
Vox Sang
, vol.24
, pp. 404-16
-
-
Nevanlinna, H.R.1
Pirkola, A.2
-
49
-
-
11344250009
-
The frequency and nature of blood group A3
-
Reed T. The frequency and nature of blood group A3. Transfusion 1964 4 : 457 60.
-
(1964)
Transfusion
, vol.4
, pp. 457-60
-
-
Reed, T.1
-
50
-
-
0033624752
-
Molecular heterogeneity of the A3 subgroup
-
Barjas-Castro ML, Carvalho MH, Locatelli MF, Bordin S, Saad ST. Molecular heterogeneity of the A3 subgroup. Clin Lab Haematol 2000 22 : 73 8.
-
(2000)
Clin Lab Haematol
, vol.22
, pp. 73-8
-
-
Barjas-Castro, M.L.1
Carvalho, M.H.2
Locatelli, M.F.3
Bordin, S.4
Saad, S.T.5
-
51
-
-
75749122973
-
-
Thesis, Nyt Nordisk Forlag, Copenhagen, Denmark. Translation in Camp FR Jr, Ellis, eds. Fort Knox, KY US Army Medical Research Laboratory
-
Gammelgaard A On rare, weak A antigens (A3, A4, A5 and Ax) in man Thesis, Nyt Nordisk Forlag, Copenhagen, Denmark. Translation in Camp FR Jr, Ellis, eds. Fort Knox, KY US Army Medical Research Laboratory 1966 : 126 36.
-
(1966)
On Rare, Weak A Antigens (A3, A4, A5 and Ax) in Man
, pp. 126-36
-
-
Gammelgaard, A.1
-
52
-
-
0035020152
-
Recombination and gene conversion-like events may contribute to ABO gene diversity causing various phenotypes
-
Ogasawara K, Yabe R, Uchikawa M, Nakata K, Watanabe J, Takahashi Y, Tokunaga K. Recombination and gene conversion-like events may contribute to ABO gene diversity causing various phenotypes. Immunogenetics 2001 53 : 190 9.
-
(2001)
Immunogenetics
, vol.53
, pp. 190-9
-
-
Ogasawara, K.1
Yabe, R.2
Uchikawa, M.3
Nakata, K.4
Watanabe, J.5
Takahashi, Y.6
Tokunaga, K.7
-
53
-
-
15244350749
-
Nondeletional ABO*O alleles express weak blood group a phenotypes
-
Seltsam A, Das Gupta C, Wagner FF, Blasczyk R. Nondeletional ABO*O alleles express weak blood group A phenotypes. Transfusion 2005 45 : 359 65.
-
(2005)
Transfusion
, vol.45
, pp. 359-65
-
-
Seltsam, A.1
Das Gupta, C.2
Wagner, F.F.3
Blasczyk, R.4
-
54
-
-
0022729857
-
UDP-N-acetyl-D-galactosamine as a donor substrate for the glycosyltransferase encoded by the B gene at the human blood group ABO locus
-
Greenwell P, Yates AD, Watkins WM. UDP-N-acetyl-D-galactosamine as a donor substrate for the glycosyltransferase encoded by the B gene at the human blood group ABO locus. Carbohydr Res 1986 149 : 149 70.
-
(1986)
Carbohydr Res
, vol.149
, pp. 149-70
-
-
Greenwell, P.1
Yates, A.D.2
Watkins, W.M.3
-
55
-
-
48249146230
-
Investigation into A antigen expression on O2 heterozygous group O-labeled red blood cell units
-
Yazer MH, Hult AK, Hellberg A, Hosseini-Maaf B, Palcic MM, Olsson ML. Investigation into A antigen expression on O2 heterozygous group O-labeled red blood cell units. Transfusion 2008 48 : 1650 7.
-
(2008)
Transfusion
, vol.48
, pp. 1650-7
-
-
Yazer, M.H.1
Hult, A.K.2
Hellberg, A.3
Hosseini-Maaf, B.4
Palcic, M.M.5
Olsson, M.L.6
-
56
-
-
12844268112
-
Structural basis for the inactivity of human blood group O2 glycosyltransferase
-
Lee HJ, Barry CH, Borisova SN, Seto NO, Zheng RB, Blancher A, Evans SV, Palcic MM. Structural basis for the inactivity of human blood group O2 glycosyltransferase. J Biol Chem 2005 280 : 525 9.
-
(2005)
J Biol Chem
, vol.280
, pp. 525-9
-
-
Lee, H.J.1
Barry, C.H.2
Borisova, S.N.3
Seto, N.O.4
Zheng, R.B.5
Blancher, A.6
Evans, S.V.7
Palcic, M.M.8
-
57
-
-
57749112102
-
Activation of beta1,3-N-acetylglucosaminyltransferase-2 (beta3Gn-T2) by beta3Gn-T8. Possible involvement of beta3Gn-T8 in increasing poly-N-acetyllactosamine chains in differentiated HL-60 cells
-
Seko A, Yamashita K. Activation of beta1,3-N- acetylglucosaminyltransferase-2 (beta3Gn-T2) by beta3Gn-T8. Possible involvement of beta3Gn-T8 in increasing poly-N-acetyllactosamine chains in differentiated HL-60 cells. J Biol Chem 2008 283 : 33094 100.
-
(2008)
J Biol Chem
, vol.283
, pp. 33094-100
-
-
Seko, A.1
Yamashita, K.2
-
60
-
-
4444255751
-
Uptake of A and B antigens by transfused group O erythrocytes
-
Renton PH, Hancock JA. Uptake of A and B antigens by transfused group O erythrocytes. Vox Sang 1962 7 : 33 8.
-
(1962)
Vox Sang
, vol.7
, pp. 33-8
-
-
Renton, P.H.1
Hancock, J.A.2
-
61
-
-
0023639542
-
ABH and Lewis antigen and antibody expression after bone marrow transplantation
-
Needs ME, McCarthy DM, Barrett J. ABH and Lewis antigen and antibody expression after bone marrow transplantation. Acta Haematol 1987 78 : 13 6.
-
(1987)
Acta Haematol
, vol.78
, pp. 13-6
-
-
Needs, M.E.1
McCarthy, D.M.2
Barrett, J.3
-
62
-
-
0016213249
-
In vitro transformation of group O red blood cells by A and B serum substances
-
Garretta M, Muller A, Courouce-Pauty AM, Moullec J. In vitro transformation of group O red blood cells by A and B serum substances. Biomedicine 1974 21 : 114 8.
-
(1974)
Biomedicine
, vol.21
, pp. 114-8
-
-
Garretta, M.1
Muller, A.2
Courouce-Pauty, A.M.3
Moullec, J.4
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