-
1
-
-
4644325805
-
Genetic basis of blood group diversity
-
Storry J.R., Olsson M.L. Genetic basis of blood group diversity. Br J Haematol 2004, 126:759-771.
-
(2004)
Br J Haematol
, vol.126
, pp. 759-771
-
-
Storry, J.R.1
Olsson, M.L.2
-
2
-
-
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. Nat Genet 1995, 10:224-228.
-
(1995)
Nat Genet
, vol.10
, pp. 224-228
-
-
Tournamille, C.1
Colin, Y.2
Cartron, J.P.3
Le Van Kim, C.4
-
3
-
-
0033970708
-
Genomic characterization of the kidd blood group gene: different molecular basis of the Jk(a-b-) phenotype in Polynesians and Finns
-
Irshaid N.M., Henry S.M., Olsson M.L. Genomic characterization of the kidd blood group gene: different molecular basis of the Jk(a-b-) phenotype in Polynesians and Finns. Transfusion 2000, 40:69-74.
-
(2000)
Transfusion
, vol.40
, pp. 69-74
-
-
Irshaid, N.M.1
Henry, S.M.2
Olsson, M.L.3
-
4
-
-
0344303481
-
Mutations in GYPB exon 5 drive the S-s-U+(var) phenotype in persons of African descent: implications for transfusion
-
Storry J.R., Reid M.E., Fetics S., Huang C.H. Mutations in GYPB exon 5 drive the S-s-U+(var) phenotype in persons of African descent: implications for transfusion. Transfusion 2003, 43:1738-1747.
-
(2003)
Transfusion
, vol.43
, pp. 1738-1747
-
-
Storry, J.R.1
Reid, M.E.2
Fetics, S.3
Huang, C.H.4
-
5
-
-
0032932817
-
Molecular basis of weak D phenotypes
-
Wagner F.F., Gassner C., Muller T.H., Schonitzer D., Schunter F., Flegel W.A. Molecular basis of weak D phenotypes. Blood 1999, 93:385-393.
-
(1999)
Blood
, vol.93
, pp. 385-393
-
-
Wagner, F.F.1
Gassner, C.2
Muller, T.H.3
Schonitzer, D.4
Schunter, F.5
Flegel, W.A.6
-
6
-
-
0037105381
-
DNB: a partial D with anti-D frequent in central Europe
-
Wagner F.F., Eicher N.I., Jorgensen J.R., Lonicer C.B., Flegel W.A. DNB: a partial D with anti-D frequent in central Europe. Blood 2002, 100:2253-2256.
-
(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
-
7
-
-
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 M.B., Ligthart P.C., Berger L., van Rhenen D.J., van der Schoot C.E., Wijk P.A. 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, 94:4337-4342.
-
(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
-
8
-
-
0025270738
-
Molecular genetic basis of the histo-blood group ABO system
-
Yamamoto F., Clausen H., White T., Marken J., Hakomori S. Molecular genetic basis of the histo-blood group ABO system. Nature 1990, 345:229-233.
-
(1990)
Nature
, vol.345
, pp. 229-233
-
-
Yamamoto, F.1
Clausen, H.2
White, T.3
Marken, J.4
Hakomori, S.5
-
9
-
-
0028088012
-
Mutations in aquaporin-1 in phenotypically normal humans without functional CHIP water channels
-
Preston G.M., Smith B.L., Zeidel M.L., Moulds J.J., Agre P. Mutations in aquaporin-1 in phenotypically normal humans without functional CHIP water channels. Science 1994, 265:1585-1587.
-
(1994)
Science
, vol.265
, pp. 1585-1587
-
-
Preston, G.M.1
Smith, B.L.2
Zeidel, M.L.3
Moulds, J.J.4
Agre, P.5
-
10
-
-
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 B.K., Green C.A., Avent N.D., Martin P.G., Smart E., Daka A., 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
Martin, P.G.4
Smart, E.5
Daka, A.6
-
11
-
-
79955013437
-
The Rh and RhAG blood group systems
-
Chou S.T., Westhoff C.M. The Rh and RhAG blood group systems. Immunohematology 2010, 26:178-186.
-
(2010)
Immunohematology
, vol.26
, pp. 178-186
-
-
Chou, S.T.1
Westhoff, C.M.2
-
12
-
-
77649154817
-
MNS blood group system: a review
-
Reid M.E. MNS blood group system: a review. Immunohematology 2009, 25:95-101.
-
(2009)
Immunohematology
, vol.25
, pp. 95-101
-
-
Reid, M.E.1
-
13
-
-
0022372670
-
Enzymatic amplification of beta-globin genomic sequences and restriction site analysis for diagnosis of sickle cell anemia
-
Saiki R.K., Scharf S., Faloona F., Mullis K.B., Horn G.T., Erlich H.A., et al. Enzymatic amplification of beta-globin genomic sequences and restriction site analysis for diagnosis of sickle cell anemia. Science 1985, 230:1350-1354.
-
(1985)
Science
, vol.230
, pp. 1350-1354
-
-
Saiki, R.K.1
Scharf, S.2
Faloona, F.3
Mullis, K.B.4
Horn, G.T.5
Erlich, H.A.6
-
14
-
-
0028923475
-
Molecular basis and PCR-DNA typing of the Fya/fyb blood group polymorphism
-
Tournamille C., Le Van Kim C., Gane P., Cartron J.P., Colin Y. Molecular basis and PCR-DNA typing of the Fya/fyb blood group polymorphism. Hum Genet 1995, 95:407-410.
-
(1995)
Hum Genet
, vol.95
, pp. 407-410
-
-
Tournamille, C.1
Le Van Kim, C.2
Gane, P.3
Cartron, J.P.4
Colin, Y.5
-
15
-
-
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 non-erythroid tissues in Duffy-negative individuals
-
Chaudhuri A., Polyakova J., Zbrzezna V., Pogo A.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 non-erythroid 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, A.O.4
-
16
-
-
0032411624
-
The Fy(x) phenotype is associated with a missense mutation in the Fy(b) allele predicting Arg89Cys in the Duffy glycoprotein
-
Olsson M.L., Smythe J.S., Hansson C., Poole J., Mallinson G., Jones J., 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, 103:1184-1191.
-
(1998)
Br J Haematol
, vol.103
, pp. 1184-1191
-
-
Olsson, M.L.1
Smythe, J.S.2
Hansson, C.3
Poole, J.4
Mallinson, G.5
Jones, J.6
-
17
-
-
28544449472
-
The use of real-time PCR methods in DNA sequence variation analysis
-
Gibson N.J. The use of real-time PCR methods in DNA sequence variation analysis. Clin Chim Acta 2006, 363:32-47.
-
(2006)
Clin Chim Acta
, vol.363
, pp. 32-47
-
-
Gibson, N.J.1
-
18
-
-
17044442211
-
Real-time PCR Genotyping using displacing probes
-
Cheng J., Zhang Y., Li Q., Real-time PCR genotyping using displacing probes. Nucleic Acids Res 2004, 32:e61.
-
(2004)
Nucleic Acids Res
, vol.32
-
-
Cheng, J.1
Zhang, Y.2
Li, Q.3
-
19
-
-
73649103469
-
Partial C antigen in sickle cell disease patients: clinical relevance and prevention of alloimmunization
-
Tournamille C., Meunier-Costes N., Costes B., Martret J., Barrault A., Gauthier P., et al. Partial C antigen in sickle cell disease patients: clinical relevance and prevention of alloimmunization. Transfusion 2010, 50:13-19.
-
(2010)
Transfusion
, vol.50
, pp. 13-19
-
-
Tournamille, C.1
Meunier-Costes, N.2
Costes, B.3
Martret, J.4
Barrault, A.5
Gauthier, P.6
-
20
-
-
42949094614
-
Non-invasive fetal RHD genotyping from maternal plasma. Use of a new developed Free DNA Fetal Kit RhD
-
Rouillac-Le Sciellour C., Serazin V., Brossard Y., Cudin O., Le Van Kim C., Colin Y., et al. Non-invasive fetal RHD genotyping from maternal plasma. Use of a new developed Free DNA Fetal Kit RhD. Transfus Clin Biol 2007, 14:572-577.
-
(2007)
Transfus Clin Biol
, vol.14
, pp. 572-577
-
-
Rouillac-Le Sciellour, C.1
Serazin, V.2
Brossard, Y.3
Cudin, O.4
Le Van Kim, C.5
Colin, Y.6
-
21
-
-
1242288240
-
Luminex technology for HLA typing by PCR-SSO and identification of HLA antibody specificities
-
Cesbron-Gautier A., Simon P., Achard L., Cury S., Follea G., Bignon J.D. Luminex technology for HLA typing by PCR-SSO and identification of HLA antibody specificities. Ann Biol Clin (Paris) 2004, 62:93-98.
-
(2004)
Ann Biol Clin (Paris)
, vol.62
, pp. 93-98
-
-
Cesbron-Gautier, A.1
Simon, P.2
Achard, L.3
Cury, S.4
Follea, G.5
Bignon, J.D.6
-
22
-
-
79954633959
-
HLA and transfusion: new approaches with Luminex technology
-
Giannoli C., Nguyen T.K., Dubois V. HLA and transfusion: new approaches with Luminex technology. Transfus Clin Biol 2011, 18:218-223.
-
(2011)
Transfus Clin Biol
, vol.18
, pp. 218-223
-
-
Giannoli, C.1
Nguyen, T.K.2
Dubois, V.3
-
23
-
-
28544446736
-
Applications of Luminex xMAP technology for rapid, high-throughput multiplexed nucleic acid detection
-
Dunbar S.A. Applications of Luminex xMAP technology for rapid, high-throughput multiplexed nucleic acid detection. Clin Chim Acta 2006, 363:71-82.
-
(2006)
Clin Chim Acta
, vol.363
, pp. 71-82
-
-
Dunbar, S.A.1
-
24
-
-
39749179829
-
Blood group genotyping for Jk(a)/Jk(b), Fy(a)/Fy(b), S/s, K/k, Kp(a)/Kp(b), Js(a)/Js(b), Co(a)/Co(b), and Lu(a)/Lu(b) with microarray beads
-
Karpasitou K., Drago F., Crespiatico L., Paccapelo C., Truglio F., Frison S., et al. Blood group genotyping for Jk(a)/Jk(b), Fy(a)/Fy(b), S/s, K/k, Kp(a)/Kp(b), Js(a)/Js(b), Co(a)/Co(b), and Lu(a)/Lu(b) with microarray beads. Transfusion 2008, 48:505-512.
-
(2008)
Transfusion
, vol.48
, pp. 505-512
-
-
Karpasitou, K.1
Drago, F.2
Crespiatico, L.3
Paccapelo, C.4
Truglio, F.5
Frison, S.6
-
25
-
-
67650260793
-
Microarray beads for identifying blood group single nucleotide polymorphisms
-
Drago F., Karpasitou K., Poli F. Microarray beads for identifying blood group single nucleotide polymorphisms. Transfus Med Hemother 2009, 36:157-160.
-
(2009)
Transfus Med Hemother
, vol.36
, pp. 157-160
-
-
Drago, F.1
Karpasitou, K.2
Poli, F.3
-
26
-
-
69549113042
-
HLA genotyping and antibody characterization using the luminex multiplex technology
-
Heinemann F.M. HLA genotyping and antibody characterization using the luminex multiplex technology. Transfus Med Hemother 2009, 36:273-278.
-
(2009)
Transfus Med Hemother
, vol.36
, pp. 273-278
-
-
Heinemann, F.M.1
-
27
-
-
84878109955
-
-
ISBT. Terminology for blood group alleles.
-
ISBT. Terminology for blood group alleles. 2012. http://ibgrlbloodcouk/ISBTPAges/AlleleTerminology/Allele-Terminologyhtm.
-
(2012)
-
-
-
28
-
-
0019467583
-
Determination of nucleotide sequences in DNA
-
Sanger F. Determination of nucleotide sequences in DNA. Biosci Rep 1981, 1:3-18.
-
(1981)
Biosci Rep
, vol.1
, pp. 3-18
-
-
Sanger, F.1
-
30
-
-
0023047540
-
Fluorescence detection in automated DNA sequence analysis
-
Smith L.M., Sanders J.Z., Kaiser R.J., Hughes P., Dodd C., Connell C.R., et al. Fluorescence detection in automated DNA sequence analysis. Nature 1986, 321:674-679.
-
(1986)
Nature
, vol.321
, pp. 674-679
-
-
Smith, L.M.1
Sanders, J.Z.2
Kaiser, R.J.3
Hughes, P.4
Dodd, C.5
Connell, C.R.6
-
31
-
-
18544388692
-
Rapid genotyping of blood group antigens by multiplex polymerase chain reaction and DNA microarray hybridization
-
Beiboer S.H., Wieringa-Jelsma T., Maaskant-Van Wijk P.A., van der Schoot C.E., van Zwieten R., Roos D., et al. Rapid genotyping of blood group antigens by multiplex polymerase chain reaction and DNA microarray hybridization. Transfusion 2005, 45:667-679.
-
(2005)
Transfusion
, vol.45
, pp. 667-679
-
-
Beiboer, S.H.1
Wieringa-Jelsma, T.2
Maaskant-Van Wijk, P.A.3
van der Schoot, C.E.4
van Zwieten, R.5
Roos, D.6
-
32
-
-
18544388550
-
A flexible array format for large-scale, rapid blood group DNA typing
-
Hashmi G., Shariff T., Seul M., Vissavajjhala P., Hue-Roye K., Charles-Pierre D., et al. A flexible array format for large-scale, rapid blood group DNA typing. Transfusion 2005, 45:680-688.
-
(2005)
Transfusion
, vol.45
, pp. 680-688
-
-
Hashmi, G.1
Shariff, T.2
Seul, M.3
Vissavajjhala, P.4
Hue-Roye, K.5
Charles-Pierre, D.6
-
33
-
-
18544375772
-
High-throughput multiplex single-nucleotide polymorphism analysis for red cell and platelet antigen genotypes
-
Denomme G.A., Van Oene M. High-throughput multiplex single-nucleotide polymorphism analysis for red cell and platelet antigen genotypes. Transfusion 2005, 45:660-666.
-
(2005)
Transfusion
, vol.45
, pp. 660-666
-
-
Denomme, G.A.1
Van Oene, M.2
-
34
-
-
73649090025
-
High-throughput red blood cell antigen genotyping using a nanofluidic real-time polymerase chain reaction platform
-
Hopp K., Weber K., Bellissimo D., Johnson S.T., Pietz B. High-throughput red blood cell antigen genotyping using a nanofluidic real-time polymerase chain reaction platform. Transfusion 2010, 50:40-46.
-
(2010)
Transfusion
, vol.50
, pp. 40-46
-
-
Hopp, K.1
Weber, K.2
Bellissimo, D.3
Johnson, S.T.4
Pietz, B.5
-
35
-
-
73449136406
-
SNP genotyping by the 5'-nuclease reaction: advances in high-throughput genotyping with nonmodel organisms
-
Seeb J.E., Pascal C.E., Ramakrishnan R., Seeb L.W. SNP genotyping by the 5'-nuclease reaction: advances in high-throughput genotyping with nonmodel organisms. Methods Mol Biol 2009, 578:277-292.
-
(2009)
Methods Mol Biol
, vol.578
, pp. 277-292
-
-
Seeb, J.E.1
Pascal, C.E.2
Ramakrishnan, R.3
Seeb, L.W.4
-
36
-
-
71649090975
-
High-throughput single nucleotide polymorphism genotyping using nanofluidic Dynamic Arrays
-
Wang J., Lin M., Crenshaw A., Hutchinson A., Hicks B., Yeager M., et al. High-throughput single nucleotide polymorphism genotyping using nanofluidic Dynamic Arrays. BMC Genomics 2009, 10:561.
-
(2009)
BMC Genomics
, vol.10
, pp. 561
-
-
Wang, J.1
Lin, M.2
Crenshaw, A.3
Hutchinson, A.4
Hicks, B.5
Yeager, M.6
-
37
-
-
28544451371
-
Typing of single nucleotide polymorphisms by MALDI mass spectrometry: principles and diagnostic applications
-
Sauer S. Typing of single nucleotide polymorphisms by MALDI mass spectrometry: principles and diagnostic applications. Clin Chim Acta 2006, 363:95-105.
-
(2006)
Clin Chim Acta
, vol.363
, pp. 95-105
-
-
Sauer, S.1
-
38
-
-
41149159604
-
Non-invasive genotyping fetal Kell blood group (KEL1) using cell-free fetal DNA in maternal plasma by MALDI-TOF mass spectrometry
-
Li Y., Finning K., Daniels G., Hahn S., Zhong X., Holzgreve W. Non-invasive genotyping fetal Kell blood group (KEL1) using cell-free fetal DNA in maternal plasma by MALDI-TOF mass spectrometry. Prenat Diagn 2008, 28:203-208.
-
(2008)
Prenat Diagn
, vol.28
, pp. 203-208
-
-
Li, Y.1
Finning, K.2
Daniels, G.3
Hahn, S.4
Zhong, X.5
Holzgreve, W.6
-
39
-
-
58849136375
-
Matrix-assisted laser desorption/ionization time-of-flight mass spectrometry for genotyping of human platelet-specific antigens
-
Garritsen H.S., Fan A.X., Bosse N., Hannig H., Kelsch R., Kroll H., et al. Matrix-assisted laser desorption/ionization time-of-flight mass spectrometry for genotyping of human platelet-specific antigens. Transfusion 2009, 49:252-258.
-
(2009)
Transfusion
, vol.49
, pp. 252-258
-
-
Garritsen, H.S.1
Fan, A.X.2
Bosse, N.3
Hannig, H.4
Kelsch, R.5
Kroll, H.6
-
40
-
-
84872232876
-
Matrix-assisted laser desorption/ionisation, time-of-flight mass spectrometry-based blood group genotyping-the alternative approach
-
Gassner C., Meyer S., Frey B.M., Vollmert C. Matrix-assisted laser desorption/ionisation, time-of-flight mass spectrometry-based blood group genotyping-the alternative approach. Transfus Med Rev 2013, 27:2-9.
-
(2013)
Transfus Med Rev
, vol.27
, pp. 2-9
-
-
Gassner, C.1
Meyer, S.2
Frey, B.M.3
Vollmert, C.4
-
41
-
-
72849144434
-
Sequencing technologies - the next generation
-
Metzker M.L. Sequencing technologies - the next generation. Nat Rev Genet 2010, 11:31-46.
-
(2010)
Nat Rev Genet
, vol.11
, pp. 31-46
-
-
Metzker, M.L.1
-
42
-
-
0027478270
-
Solid phase DNA minisequencing by an enzymatic luminometric inorganic pyrophosphate detection assay
-
Nyren P., Pettersson B., Uhlen M. Solid phase DNA minisequencing by an enzymatic luminometric inorganic pyrophosphate detection assay. Anal Biochem 1993, 208:171-175.
-
(1993)
Anal Biochem
, vol.208
, pp. 171-175
-
-
Nyren, P.1
Pettersson, B.2
Uhlen, M.3
-
43
-
-
79551676183
-
A multi-site study using high-resolution HLA genotyping by next generation sequencing
-
Holcomb C.L., Hoglund B., Anderson M.W., Blake L.A., Bohme I., Egholm M., et al. A multi-site study using high-resolution HLA genotyping by next generation sequencing. Tissue Antigens 2011, 77:206-217.
-
(2011)
Tissue Antigens
, vol.77
, pp. 206-217
-
-
Holcomb, C.L.1
Hoglund, B.2
Anderson, M.W.3
Blake, L.A.4
Bohme, I.5
Egholm, M.6
-
44
-
-
0346096786
-
Allelic genes of blood group antigens: a source of human mutations and cSNPs documented in the Blood Group Antigen Gene Mutation Database
-
Blumenfeld O.O., Patnaik S.K. 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
-
45
-
-
0029984078
-
Molecular basis of the altered antigenic expression of RhD in weak D(Du) and RhC/e in RN phenotypes
-
Rouillac C., Gane P., Cartron J., Le Pennec P.Y., Cartron J.P., Colin Y. Molecular basis of the altered antigenic expression of RhD in weak D(Du) and RhC/e in RN phenotypes. Blood 1996, 87:4853-4861.
-
(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
-
46
-
-
0028177918
-
Glycophorin He(Sta) of the human red blood cell membrane is encoded by a complex hybrid gene resulting from two recombinational events
-
Huang C.H., Lomas C., Daniels G., Blumenfeld O.O. Glycophorin He(Sta) of the human red blood cell membrane is encoded by a complex hybrid gene resulting from two recombinational events. Blood 1994, 83:3369-3376.
-
(1994)
Blood
, vol.83
, pp. 3369-3376
-
-
Huang, C.H.1
Lomas, C.2
Daniels, G.3
Blumenfeld, O.O.4
-
47
-
-
33746136983
-
The RHCE allele ceCF: the molecular basis of Crawford (RH43)
-
Flegel W.A., Wagner F.F., Chen Q., Schlanser G., Frame T., Westhoff C.M., et al. The RHCE allele ceCF: the molecular basis of Crawford (RH43). Transfusion 2006, 46:1334-1342.
-
(2006)
Transfusion
, vol.46
, pp. 1334-1342
-
-
Flegel, W.A.1
Wagner, F.F.2
Chen, Q.3
Schlanser, G.4
Frame, T.5
Westhoff, C.M.6
-
48
-
-
38349140072
-
The 262T>C silent mutation of the platelet beta 3-integrin gene is not restricted to a single family
-
Bertrand G., Kaplan C. The 262T>C silent mutation of the platelet beta 3-integrin gene is not restricted to a single family. Transfusion 2008, 48:402.
-
(2008)
Transfusion
, vol.48
, pp. 402
-
-
Bertrand, G.1
Kaplan, C.2
|