-
1
-
-
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
-
2
-
-
10344227150
-
Blood group terminology 2004: From the International Society of Blood Transfusion committee on terminology for red cell surface antigens
-
Daniels GL, Fletcher A, Garratty G, et al. Blood group terminology 2004: from the International Society of Blood Transfusion committee on terminology for red cell surface antigens. Vox Sang 2004 87 : 304 16.
-
(2004)
Vox Sang
, vol.87
, pp. 304-16
-
-
Daniels, G.L.1
Fletcher, A.2
Garratty, G.3
-
3
-
-
34250639586
-
Blood groups: Molecular genetic basis
-
In: Chichester, England: John Wiley & Sons Ltd.
-
Avent ND. Blood groups: molecular genetic basis. In : Encyclopedia of life sciences. Chichester, England : John Wiley & Sons Ltd.
-
Encyclopedia of Life Sciences
-
-
Avent, N.D.1
-
4
-
-
20544450099
-
The molecular genetics of blood group polymorphism
-
Daniels G. The molecular genetics of blood group polymorphism. Transpl Immunol 2005 14 : 143 53.
-
(2005)
Transpl Immunol
, vol.14
, pp. 143-53
-
-
Daniels, G.1
-
5
-
-
0028936247
-
Molecular basis of the Kell (K1) phenotype
-
Lee S, Wu X, Reid M, et al. Molecular basis of the Kell (K1) phenotype. Blood 1995 85 : 912 16.
-
(1995)
Blood
, vol.85
, pp. 912-16
-
-
Lee, S.1
Wu, X.2
Reid, M.3
-
6
-
-
0028923475
-
Molecular basis and PCR-DNA typing of the Fya/fyb blood group polymorphism
-
Tournamille C, Le Van Kim C, Gane P, et al. Molecular basis and PCR-DNA typing of the Fya/fyb blood group polymorphism. Hum Genet 1995 95 : 407 10.
-
(1995)
Hum Genet
, vol.95
, pp. 407-10
-
-
Tournamille, C.1
Le Van Kim, C.2
Gane, P.3
-
7
-
-
0027180212
-
Molecular genetic basis of the human Rhesus blood group system
-
Mouro I, Colin Y, Cherif-Zahar B, et al. Molecular genetic basis of the human Rhesus blood group system. Nat Genet 1993 5 : 62 5.
-
(1993)
Nat Genet
, vol.5
, pp. 62-5
-
-
Mouro, I.1
Colin, Y.2
Cherif-Zahar, B.3
-
8
-
-
0027965959
-
Sequence analysis of cDNA derived from reticulocyte mRNAs coding for Rh polypeptides and demonstration of E/e and C/c polymorphisms
-
Simsek S, de Jong CA, Cuijpers HT, et al. Sequence analysis of cDNA derived from reticulocyte mRNAs coding for Rh polypeptides and demonstration of E/e and C/c polymorphisms. Vox Sang 1994 67 : 203 9.
-
(1994)
Vox Sang
, vol.67
, pp. 203-9
-
-
Simsek, S.1
De Jong, C.A.2
Cuijpers, H.T.3
-
9
-
-
0034888213
-
Polymorphism and recombination events at the ABO locus: A major challenge for genomic ABO blood grouping strategies
-
Olsson ML, Chester MA. Polymorphism and recombination events at the ABO locus: a major challenge for genomic ABO blood grouping strategies. Transfus Med 2001 11 : 295 313.
-
(2001)
Transfus Med
, vol.11
, pp. 295-313
-
-
Olsson, M.L.1
Chester, M.A.2
-
10
-
-
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, et al. 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. 2747-52
-
-
Colin, Y.1
Cherif-Zahar, B.2
Le Van Kim, C.3
-
11
-
-
0033957696
-
The presence of an RHD pseudogene containing a 37 base pair duplication and a nonsense mutation in Africans with the Rh D-negative 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-negative blood group phenotype. Blood 2000 95 : 12 18.
-
(2000)
Blood
, vol.95
, pp. 12-18
-
-
Singleton, B.K.1
Green, C.A.2
Avent, N.D.3
-
13
-
-
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. 366-71
-
-
Avent, N.D.1
Jones, J.W.2
Liu, W.3
-
14
-
-
0029016552
-
Leu110Pro substitution in the RhD polypeptide is responsible for the DVII category blood group phenotype
-
Rouillac C, Le Van Kim C, Beolet M, et al. 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. 87-8
-
-
Rouillac, C.1
Le Van Kim, C.2
Beolet, M.3
-
16
-
-
0031034596
-
Molecular analysis of Rh transcripts and polypeptides from individuals expressing the DVI variant phenotype: An RHD gene deletion event does not generate All DVIccEe phenotypes
-
Avent ND, Liu W, Jones JW, et al. Molecular analysis of Rh transcripts and polypeptides from individuals expressing the DVI variant phenotype: an RHD gene deletion event does not generate All DVIccEe phenotypes. Blood 1997 89 : 1779 86.
-
(1997)
Blood
, vol.89
, pp. 1779-86
-
-
Avent, N.D.1
Liu, W.2
Jones, J.W.3
-
17
-
-
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. 1129-35
-
-
Mouro, I.1
Le Van Kim, C.2
Rouillac, C.3
-
18
-
-
0032521490
-
Three molecular structures cause rhesus D category VI phenotypes with distinct immunohematologic features
-
Wagner FF, Gassner C, Muller TH, et al. Three molecular structures cause rhesus D category VI phenotypes with distinct immunohematologic features. Blood 1998 91 : 2157 68.
-
(1998)
Blood
, vol.91
, pp. 2157-68
-
-
Wagner, F.F.1
Gassner, C.2
Muller, T.H.3
-
19
-
-
33645304041
-
The D category VI type 4 allele is prevalent in the Spanish population
-
Esteban R, Montero R, Flegel WA, et al. The D category VI type 4 allele is prevalent in the Spanish population. Transfusion 2006 46 : 616 23.
-
(2006)
Transfusion
, vol.46
, pp. 616-23
-
-
Esteban, R.1
Montero, R.2
Flegel, W.A.3
-
20
-
-
0032932817
-
Molecular basis of weak D phenotypes
-
Wagner FF, Gassner C, Muller TH, et al. Molecular basis of weak D phenotypes. Blood 1999 93 : 385 93.
-
(1999)
Blood
, vol.93
, pp. 385-93
-
-
Wagner, F.F.1
Gassner, C.2
Muller, T.H.3
-
21
-
-
33745039724
-
Molecular biology of Rh proteins and relevance to molecular medicine
-
Avent ND, Madgett TE, Lee ZE, et al. Molecular biology of Rh proteins and relevance to molecular medicine. Expert Rev Mol Med 2006 8 : 1 20.
-
(2006)
Expert Rev Mol Med
, vol.8
, pp. 1-20
-
-
Avent, N.D.1
Madgett, T.E.2
Lee, Z.E.3
-
22
-
-
17044380221
-
Anti-D immunization by del red blood cells
-
Wagner T, Kormoczi GF, Buchta C, et al. Anti-D immunization by DEL red blood cells. Transfusion 2005 45 : 520 6.
-
(2005)
Transfusion
, vol.45
, pp. 520-6
-
-
Wagner, T.1
Kormoczi, G.F.2
Buchta, C.3
-
23
-
-
0029001881
-
Disruption of a GATA motif in the Duffy gene promoter abolishes erythroid gene expression in Duffy-negative individuals
-
Tournamille C, Colin Y, Cartron JP, Le Van Kim C. Disruption of a GATA motif in the Duffy gene promoter abolishes erythroid gene expression in Duffy-negative individuals. Nat Genet 1995 10 : 224 8.
-
(1995)
Nat Genet
, vol.10
, pp. 224-8
-
-
Tournamille, C.1
Colin, Y.2
Cartron, J.P.3
Le Van Kim, C.4
-
24
-
-
0036176188
-
Molecular approaches to blood group identification
-
Reid ME, Lomas-Francis C. Molecular approaches to blood group identification. Curr Opin Hematol 2002 9 : 152 9.
-
(2002)
Curr Opin Hematol
, vol.9
, pp. 152-9
-
-
Reid, M.E.1
Lomas-Francis, C.2
-
25
-
-
4444364254
-
Molecular diagnostics in immunohaematology
-
van der Schoot CE. Molecular diagnostics in immunohaematology. Vox Sang 2004 87 (Suppl 2 189 92.
-
(2004)
Vox Sang
, vol.872
, pp. 189-92
-
-
Van Der Schoot, C.E.1
-
26
-
-
10344262881
-
Fetal blood group genotyping from DNA from maternal plasma: An important advance in the management and prevention of haemolytic disease of the fetus and newborn
-
Daniels G, Finning K, Martin P, Soothill P. Fetal blood group genotyping from DNA from maternal plasma: an important advance in the management and prevention of haemolytic disease of the fetus and newborn. Vox Sang 2004 87 : 225 32.
-
(2004)
Vox Sang
, vol.87
, pp. 225-32
-
-
Daniels, G.1
Finning, K.2
Martin, P.3
Soothill, P.4
-
27
-
-
0037225919
-
Prenatal typing of Rh and Kell blood group system antigens: The edge of a watershed
-
van der Schoot CE, Tax GH, Rijnders RJ, et al. Prenatal typing of Rh and Kell blood group system antigens: the edge of a watershed. Transfus Med Rev 2003 17 : 31 44.
-
(2003)
Transfus Med Rev
, vol.17
, pp. 31-44
-
-
Van Der Schoot, C.E.1
Tax, G.H.2
Rijnders, R.J.3
-
28
-
-
0032404119
-
Rh phenotype prediction by DNA typing and its application to practice
-
Flegel WA, Wagner FF, Muller TH, Gassner C. Rh phenotype prediction by DNA typing and its application to practice. Transfus Med 1998 8 : 281 302.
-
(1998)
Transfus Med
, vol.8
, pp. 281-302
-
-
Flegel, W.A.1
Wagner, F.F.2
Muller, T.H.3
Gassner, C.4
-
29
-
-
33745951429
-
Challenges of SNP genotyping and genetic variation: Its future role in diagnosis and treatment of cancer
-
Bernig T, Chanock SJ. Challenges of SNP genotyping and genetic variation: its future role in diagnosis and treatment of cancer. Expert Rev Mol Diagn 2006 6 : 319 31.
-
(2006)
Expert Rev Mol Diagn
, vol.6
, pp. 319-31
-
-
Bernig, T.1
Chanock, S.J.2
-
30
-
-
20044369371
-
Toward genome-wide SNP genotyping
-
Syvanen AC. Toward genome-wide SNP genotyping. Nat Genet 2005 37 (Suppl S5 10.
-
(2005)
Nat Genet
, vol.37
-
-
Syvanen, A.C.1
-
31
-
-
24044509819
-
Newborn screening - Setting evidence-based policy for protection
-
Natowicz M. Newborn screening - setting evidence-based policy for protection. N Engl J Med 2005 353 : 867 70.
-
(2005)
N Engl J Med
, vol.353
, pp. 867-70
-
-
Natowicz, M.1
-
32
-
-
7344259638
-
Shift from Rh-positive to Rh-negative phenotype caused by a somatic mutation within the RHD gene in a patient with chronic myelocytic leukaemia
-
Cherif-Zahar B, Bony V, Steffensen R, et al. Shift from Rh-positive to Rh-negative phenotype caused by a somatic mutation within the RHD gene in a patient with chronic myelocytic leukaemia. Br J Haematol 1998 102 : 1263 70.
-
(1998)
Br J Haematol
, vol.102
, pp. 1263-70
-
-
Cherif-Zahar, B.1
Bony, V.2
Steffensen, R.3
-
33
-
-
0343949989
-
Isolation and characterization of human glycophorin a cDNA clones by a synthetic oligonucleotide approach: Nucleotide sequence and mRNA structure
-
Siebert PD, Fukuda M. Isolation and characterization of human glycophorin A cDNA clones by a synthetic oligonucleotide approach: nucleotide sequence and mRNA structure. Proc Natl Acad Sci U S A 1986 83 : 1665 9.
-
(1986)
Proc Natl Acad Sci U S a
, vol.83
, pp. 1665-9
-
-
Siebert, P.D.1
Fukuda, M.2
-
34
-
-
0025270738
-
Molecular genetic basis of the histo-blood group ABO system
-
Yamamoto F, Clausen H, White T, et al. Molecular genetic basis of the histo-blood group ABO system. Nature 1990 345 : 229 33.
-
(1990)
Nature
, vol.345
, pp. 229-33
-
-
Yamamoto, F.1
Clausen, H.2
White, T.3
-
35
-
-
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 U S A 1990 87 : 6243 7.
-
(1990)
Proc Natl Acad Sci U S a
, vol.87
, pp. 6243-7
-
-
Cherif-Zahar, B.1
Bloy, C.2
Le Van Kim, C.3
-
36
-
-
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. 821-5
-
-
Avent, N.D.1
Ridgwell, K.2
Tanner, M.J.3
Anstee, D.J.4
-
37
-
-
29144444313
-
Blood transfusion in Europe - The White Book 2005: The patchwork of transfusion medicine in Europe
-
Mayr WR. Blood transfusion in Europe - The White Book 2005: the patchwork of transfusion medicine in Europe. Transfus Clin Biol 2005 12 : 357 8.
-
(2005)
Transfus Clin Biol
, vol.12
, pp. 357-8
-
-
Mayr, W.R.1
-
38
-
-
4043063528
-
The European Blood Directive: A new era of blood regulation has begun
-
Faber JC. The European Blood Directive: a new era of blood regulation has begun. Transfus Med 2004 14 : 257 73.
-
(2004)
Transfus Med
, vol.14
, pp. 257-73
-
-
Faber, J.C.1
-
39
-
-
0030945033
-
Evidence of genetic diversity underlying Rh D-, weak D (Du), and partial D phenotypes as determined by multiplex polymerase chain reaction analysis of the RHD gene
-
Avent ND, Martin PG, Armstrong-Fisher SS, et al. Evidence of genetic diversity underlying Rh D-, weak D (Du), and partial D phenotypes as determined by multiplex polymerase chain reaction analysis of the RHD gene. Blood 1997 89 : 2568 77.
-
(1997)
Blood
, vol.89
, pp. 2568-77
-
-
Avent, N.D.1
Martin, P.G.2
Armstrong-Fisher, S.S.3
-
40
-
-
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 30.
-
(1996)
Br J Haematol
, vol.93
, pp. 728-30
-
-
Avent, N.D.1
Martin, P.G.2
-
41
-
-
0029066655
-
Rapid Rh D genotyping by polymerase chain reaction-based amplification of DNA
-
Simsek S, Faas BH, Bleeker PM, et al. Rapid Rh D genotyping by polymerase chain reaction-based amplification of DNA. Blood 1995 85 : 2975 80.
-
(1995)
Blood
, vol.85
, pp. 2975-80
-
-
Simsek, S.1
Faas, B.H.2
Bleeker, P.M.3
-
42
-
-
0029821023
-
Evidence for a new type of O allele at the ABO locus, due to a combination of the A2 nucleotide deletion and the Ael nucleotide insertion
-
Olsson ML, Chester MA. Evidence for a new type of O allele at the ABO locus, due to a combination of the A2 nucleotide deletion and the Ael nucleotide insertion. Vox Sang 1996 71 : 113 17.
-
(1996)
Vox Sang
, vol.71
, pp. 113-17
-
-
Olsson, M.L.1
Chester, M.A.2
-
43
-
-
0032411624
-
The Fy(x) phenotype is associated with a missense mutation in the Fy(b) allele predicting Arg89Cys in the Duffy glycoprotein
-
Olsson ML, Smythe JS, Hansson C, et al. The Fy(x) phenotype is associated with a missense mutation in the Fy(b) allele predicting Arg89Cys in the Duffy glycoprotein. Br J Haematol 1998 103 : 1184 91.
-
(1998)
Br J Haematol
, vol.103
, pp. 1184-91
-
-
Olsson, M.L.1
Smythe, J.S.2
Hansson, C.3
-
44
-
-
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. 3662-8
-
-
Wagner, F.F.1
Flegel, W.A.2
-
45
-
-
0036659930
-
The DAU allele cluster of the RHD gene
-
Wagner FF, Ladewig B, Angert KS, et al. The DAU allele cluster of the RHD gene. Blood 2002 100 : 306 11.
-
(2002)
Blood
, vol.100
, pp. 306-11
-
-
Wagner, F.F.1
Ladewig, B.2
Angert, K.S.3
-
46
-
-
0037438591
-
Scianna antigens including Rd are expressed by ERMAP
-
Wagner FF, Poole J, Flegel WA. Scianna antigens including Rd are expressed by ERMAP. Blood 2003 101 : 752 7.
-
(2003)
Blood
, vol.101
, pp. 752-7
-
-
Wagner, F.F.1
Poole, J.2
Flegel, W.A.3
-
47
-
-
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. 951-8
-
-
Daniels, G.L.1
Faas, B.H.2
Green, C.A.3
-
48
-
-
0037591997
-
The molecular basis of the Lutheran blood group antigens
-
Daniels G, Crew V. The molecular basis of the Lutheran blood group antigens. Vox Sang 2002 83 (Suppl 1 189 92.
-
(2002)
Vox Sang
, vol.831
, pp. 189-92
-
-
Daniels, G.1
Crew, V.2
-
49
-
-
18544388692
-
Rapid genotyping of blood group antigens by multiplex polymerase chain reaction and DNA microarray hybridization
-
Beiboer SH, Wieringa-Jelsma T, Maaskant-Van Wijk PA, et al. Rapid genotyping of blood group antigens by multiplex polymerase chain reaction and DNA microarray hybridization. Transfusion 2005 45 : 667 79.
-
(2005)
Transfusion
, vol.45
, pp. 667-79
-
-
Beiboer, S.H.1
Wieringa-Jelsma, T.2
Maaskant-Van Wijk, P.A.3
-
50
-
-
23444435523
-
Reliable low-density DNA array based on allele-specific probes for detection of 118 mutations causing familial hypercholesterolemia
-
Tejedor D, Castillo S, Mozas P, et al. Reliable low-density DNA array based on allele-specific probes for detection of 118 mutations causing familial hypercholesterolemia. Clin Chem 2005 51 : 1137 44.
-
(2005)
Clin Chem
, vol.51
, pp. 1137-44
-
-
Tejedor, D.1
Castillo, S.2
Mozas, P.3
-
51
-
-
18544366423
-
Goodbye to agglutination and all that?
-
Anstee DJ. Goodbye to agglutination and all that? Transfusion 2005 45 (5 652 3.
-
(2005)
Transfusion
, vol.45
, Issue.5
, pp. 652-3
-
-
Anstee, D.J.1
-
52
-
-
27744509171
-
Partial D, weak D types, and novel RHD alleles among 33,864 multiethnic patients: Implications for anti-D alloimmunization and prevention
-
Denomme GA, Wagner FF, Fernandes BJ, et al. Partial D, weak D types, and novel RHD alleles among 33,864 multiethnic patients: implications for anti-D alloimmunization and prevention. Transfusion 2005 45 : 1554 60.
-
(2005)
Transfusion
, vol.45
, pp. 1554-60
-
-
Denomme, G.A.1
Wagner, F.F.2
Fernandes, B.J.3
-
54
-
-
17044365397
-
Homing in on D antigen immunogenicity
-
Flegel WA. Homing in on D antigen immunogenicity. Transfusion 2005 45 : 466 8.
-
(2005)
Transfusion
, vol.45
, pp. 466-8
-
-
Flegel, W.A.1
-
55
-
-
13244266816
-
Prenatal RHD testing of fetus and mother: Decision to administer anti-D prophylaxis
-
Ait Soussan ARD, Bonsel GJ, et al. Prenatal RHD testing of fetus and mother: decision to administer anti-D prophylaxis. Transfus Med Hemother 2004 31 (Suppl 3 50.
-
(2004)
Transfus Med Hemother
, vol.313
, pp. 50
-
-
Ait Soussan, A.R.D.1
Bonsel, G.J.2
-
57
-
-
18544388550
-
A flexible array format for large-scale, rapid blood group DNA typing
-
Hashmi G, Shariff T, Seul M, et al. A flexible array format for large-scale, rapid blood group DNA typing. Transfusion 2005 45 : 680 8.
-
(2005)
Transfusion
, vol.45
, pp. 680-8
-
-
Hashmi, G.1
Shariff, T.2
Seul, M.3
-
58
-
-
18544375772
-
High-throughput multiplex single-nucleotide polymorphism analysis for red cell and platelet antigen genotypes
-
Denomme GA, Van Oene M. High-throughput multiplex single-nucleotide polymorphism analysis for red cell and platelet antigen genotypes. Transfusion 2005 45 : 660 6.
-
(2005)
Transfusion
, vol.45
, pp. 660-6
-
-
Denomme, G.A.1
Van Oene, M.2
-
59
-
-
15244341802
-
Microarray-based genotyping for blood groups: Comparison of gene array and 5′-nuclease assay techniques with human platelet antigen as a model
-
Bugert P, McBride S, Smith G, et al. Microarray-based genotyping for blood groups: comparison of gene array and 5′-nuclease assay techniques with human platelet antigen as a model. Transfusion 2005 45 : 654 9.
-
(2005)
Transfusion
, vol.45
, pp. 654-9
-
-
Bugert, P.1
McBride, S.2
Smith, G.3
|