-
1
-
-
1242293622
-
Universal red blood cells-enzymatic conversion of blood group a and B antigens
-
M.L. Olsson, C.A. Hill, and H. de la Vega Universal red blood cells-enzymatic conversion of blood group A and B antigens Transfus. Clin. Biol. 11 2004 33 39
-
(2004)
Transfus. Clin. Biol.
, vol.11
, pp. 33-39
-
-
Olsson, M.L.1
Hill, C.A.2
De La Vega, H.3
-
2
-
-
0038267253
-
Using haemovigilance data to set blood safety priorities
-
L.M. Williamson Using haemovigilance data to set blood safety priorities Vox Sang. 83 2002 65 69 (Suppl 1)
-
(2002)
Vox Sang.
, vol.83
, pp. 65-69
-
-
Williamson, L.M.1
-
3
-
-
0013906002
-
Immunochemical studies on blood groups. XXXIV. Structures of some oligosaccharides produced by alkaline degradation of blood group A, B, and H substances
-
K.O. Lloyd, E.A. Kabat, and E.J. Layug Immunochemical studies on blood groups. XXXIV. Structures of some oligosaccharides produced by alkaline degradation of blood group A, B, and H substances Biochemistry 5 1966 1489 1501
-
(1966)
Biochemistry
, vol.5
, pp. 1489-1501
-
-
Lloyd, K.O.1
Kabat, E.A.2
Layug, E.J.3
-
4
-
-
0013774527
-
Some products of the degradation of blood group substances by alkaline borohydride
-
K.O. Lloyd, and E.A. Kabat Some products of the degradation of blood group substances by alkaline borohydride Biochem. Biophys. Res. Commun. 16 1964 385 390
-
(1964)
Biochem. Biophys. Res. Commun.
, vol.16
, pp. 385-390
-
-
Lloyd, K.O.1
Kabat, E.A.2
-
5
-
-
0021988466
-
Repetitive a epitope (type 3 chain A) defined by blood group A1-specific monoclonal antibody TH-1: Chemical basis of qualitative A1 and A2 distinction
-
H. Clausen, S.B. Levery, and E. Nudelman Repetitive A epitope (type 3 chain A) defined by blood group A1-specific monoclonal antibody TH-1: Chemical basis of qualitative A1 and A2 distinction Proc. Natl. Acad. Sci. U. S. A. 82 1985 1199 1203
-
(1985)
Proc. Natl. Acad. Sci. U. S. A.
, vol.82
, pp. 1199-1203
-
-
Clausen, H.1
Levery, S.B.2
Nudelman, E.3
-
6
-
-
0025270738
-
Molecular genetic basis of the histo-blood group ABO system
-
F. Yamamoto, H. Clausen, and T. White Molecular genetic basis of the histo-blood group ABO system Nature 345 1990 229 233
-
(1990)
Nature
, vol.345
, pp. 229-233
-
-
Yamamoto, F.1
Clausen, H.2
White, T.3
-
7
-
-
0026673851
-
Human histo-blood group A2 transferase coded by A2 allele, one of the a subtypes, is characterized by a single base deletion in the coding sequence, which results in an additional domain at the carboxyl terminal
-
F. Yamamoto, P.D. McNeill, and S. Hakomori Human histo-blood group A2 transferase coded by A2 allele, one of the A subtypes, is characterized by a single base deletion in the coding sequence, which results in an additional domain at the carboxyl terminal Biochem. Biophys. Res. Commun. 187 1992 366 374
-
(1992)
Biochem. Biophys. Res. Commun.
, vol.187
, pp. 366-374
-
-
Yamamoto, F.1
McNeill, P.D.2
Hakomori, S.3
-
8
-
-
0034888001
-
The ABO blood group gene: A locus of considerable genetic diversity
-
M.A. Chester, and M.L. Olsson The ABO blood group gene: A locus of considerable genetic diversity Transfus. Med. Rev. 15 2001 177 200
-
(2001)
Transfus. Med. Rev.
, vol.15
, pp. 177-200
-
-
Chester, M.A.1
Olsson, M.L.2
-
9
-
-
4644325805
-
Genetic basis of blood group diversity
-
J.R. Storry, and M.L. Olsson Genetic basis of blood group diversity Br. J. Haematol. 126 2004 759 771
-
(2004)
Br. J. Haematol.
, vol.126
, pp. 759-771
-
-
Storry, J.R.1
Olsson, M.L.2
-
10
-
-
0027477218
-
Molecular genetic analysis of the ABO blood group system: 2. cis-AB alleles
-
F. Yamamoto, P.D. McNeill, and Y. Kominato Molecular genetic analysis of the ABO blood group system: 2. cis-AB alleles Vox Sang. 64 1993 120 123
-
(1993)
Vox Sang.
, vol.64
, pp. 120-123
-
-
Yamamoto, F.1
McNeill, P.D.2
Kominato, Y.3
-
11
-
-
0027503637
-
Molecular genetic analysis of the ABO blood group system: 3. A(X) and B(A) alleles
-
F. Yamamoto, P.D. McNeill, and M. Yamamoto Molecular genetic analysis of the ABO blood group system: 3. A(X) and B(A) alleles Vox Sang. 64 1993 171 174
-
(1993)
Vox Sang.
, vol.64
, pp. 171-174
-
-
Yamamoto, F.1
McNeill, P.D.2
Yamamoto, M.3
-
13
-
-
0032170084
-
Heterogeneity of the blood group Ax allele: Genetic recombination of common alleles can result in the Ax phenotype
-
M.L. Olsson, and M.A. Chester Heterogeneity of the blood group Ax allele: Genetic recombination of common alleles can result in the Ax phenotype Transfus. Med. 8 1998 231 238
-
(1998)
Transfus. Med.
, vol.8
, pp. 231-238
-
-
Olsson, M.L.1
Chester, M.A.2
-
14
-
-
0036725060
-
The structural basis for specificity in human ABO(H) blood group biosynthesis
-
S.I. Patenaude, N.O. Seto, and S.N. Borisova The structural basis for specificity in human ABO(H) blood group biosynthesis Nat. Struct. Biol. 9 2002 685 690
-
(2002)
Nat. Struct. Biol.
, vol.9
, pp. 685-690
-
-
Patenaude, S.I.1
Seto, N.O.2
Borisova, S.N.3
-
16
-
-
6344225078
-
In vivo survival of poly(ethylene-glycol)-coated red blood cells in the rabbit
-
J. Armstrong, R. Wenby, and H. Meiselman In vivo survival of poly(ethylene-glycol)-coated red blood cells in the rabbit Blood 102 2003 320a (abstr)
-
(2003)
Blood
, vol.102
-
-
Armstrong, J.1
Wenby, R.2
Meiselman, H.3
-
17
-
-
0029555428
-
Multiple-unit and second transfusions of red cells enzymatically converted from group B to group O: Report on the end of phase 1 trials
-
L.L. Lenny, R. Hurst, and A. Zhu Multiple-unit and second transfusions of red cells enzymatically converted from group B to group O: Report on the end of phase 1 trials Transfusion 35 1995 899 902
-
(1995)
Transfusion
, vol.35
, pp. 899-902
-
-
Lenny, L.L.1
Hurst, R.2
Zhu, A.3
-
18
-
-
0028213906
-
Transfusions to group O subjects of 2 units of red cells enzymatically converted from group B to group O
-
L.L. Lenny, R. Hurst, and J. Goldstein Transfusions to group O subjects of 2 units of red cells enzymatically converted from group B to group O Transfusion 34 1994 209 214
-
(1994)
Transfusion
, vol.34
, pp. 209-214
-
-
Lenny, L.L.1
Hurst, R.2
Goldstein, J.3
-
19
-
-
0033725180
-
Transfusion to blood group a and O patients of group B RBCs that have been enzymatically converted to group O
-
M.S. Kruskall, J.P. AuBuchon, and K.Y. Anthony Transfusion to blood group A and O patients of group B RBCs that have been enzymatically converted to group O Transfusion 40 2000 1290 1298
-
(2000)
Transfusion
, vol.40
, pp. 1290-1298
-
-
Kruskall, M.S.1
Aubuchon, J.P.2
Anthony, K.Y.3
-
20
-
-
0020041868
-
Group B erythrocytes enzymatically converted to group O survive normally in A, B, and O individuals
-
J. Goldstein, G. Siviglia, and R. Hurst Group B erythrocytes enzymatically converted to group O survive normally in A, B, and O individuals Science 215 1982 168 170
-
(1982)
Science
, vol.215
, pp. 168-170
-
-
Goldstein, J.1
Siviglia, G.2
Hurst, R.3
-
21
-
-
4444223819
-
New developments in immunohaematology
-
M.L. Olsson New developments in immunohaematology Vox Sang. 87 2004 66 71 (Suppl 2)
-
(2004)
Vox Sang.
, vol.87
, pp. 66-71
-
-
Olsson, M.L.1
-
22
-
-
0028176046
-
Glycoproteins with Gal alpha 4Gal are absent from human erythrocyte membranes, indicating that glycolipids are the sole carriers of blood group P activities
-
Z. Yang, J. Bergstrom, and K.A. Karlsson Glycoproteins with Gal alpha 4Gal are absent from human erythrocyte membranes, indicating that glycolipids are the sole carriers of blood group P activities J. Biol. Chem. 269 1994 14620 14624
-
(1994)
J. Biol. Chem.
, vol.269
, pp. 14620-14624
-
-
Yang, Z.1
Bergstrom, J.2
Karlsson, K.A.3
-
23
-
-
0028917379
-
The P blood group system: Biochemical, serological, and clinical aspects
-
P.F. Spitalnik, and S.L. Spitalnik The P blood group system: Biochemical, serological, and clinical aspects Transfus. Med. Rev. 9 1995 110 122
-
(1995)
Transfus. Med. Rev.
, vol.9
, pp. 110-122
-
-
Spitalnik, P.F.1
Spitalnik, S.L.2
-
24
-
-
84956384309
-
Further observations on individual differences in human blood
-
K.L.P. Landsteiner Further observations on individual differences in human blood Proc. Soc. Exp. Biol. Med. 24 1927 941 942
-
(1927)
Proc. Soc. Exp. Biol. Med.
, vol.24
, pp. 941-942
-
-
Landsteiner, K.L.P.1
-
26
-
-
0021673440
-
Biosynthesis of the sphingoid bases: A provocation
-
N.S. Radin Biosynthesis of the sphingoid bases: A provocation J. Lipid Res. 25 1984 1536 1540
-
(1984)
J. Lipid Res.
, vol.25
, pp. 1536-1540
-
-
Radin, N.S.1
-
27
-
-
0024869543
-
The Ii and P blood group systems
-
D.M. Marcus The Ii and P blood group systems Immunol. Ser. 43 1989 701 712
-
(1989)
Immunol. Ser.
, vol.43
, pp. 701-712
-
-
Marcus, D.M.1
-
29
-
-
0037466315
-
An evolving hierarchical family classification for glycosyltransferases
-
P.M. Coutinho, E. Deleury, and G.J. Davies An evolving hierarchical family classification for glycosyltransferases J. Mol. Biol. 328 2003 307 317
-
(2003)
J. Mol. Biol.
, vol.328
, pp. 307-317
-
-
Coutinho, P.M.1
Deleury, E.2
Davies, G.J.3
-
30
-
-
0034595848
-
k UDP-galactose: Galbeta-4G1cbeta1-cer alpha1, 4-galactosyltransferase. Molecular genetic basis of the P phenotype
-
k UDP-galactose: Galbeta-4G1cbeta1-cer alpha1, 4-galactosyltransferase. Molecular genetic basis of the P phenotype J. Biol. Chem. 275 2000 16723 16729
-
(2000)
J. Biol. Chem.
, vol.275
, pp. 16723-16729
-
-
Steffensen, R.1
Carlier, K.2
Wiels, J.3
-
31
-
-
0034704073
-
Expression cloning of human globoside synthase cDNAs. Identification of beta 3Gal-T3 as UDP-N-acetylgalactosamine: Globotriaosylceramide beta 1,3-N-acetylgalactosaminyltransferase
-
T. Okajima, Y. Nakamura, and M. Uchikawa Expression cloning of human globoside synthase cDNAs. Identification of beta 3Gal-T3 as UDP-N- acetylgalactosamine: Globotriaosylceramide beta 1,3-N- acetylgalactosaminyltransferase J. Biol. Chem. 275 2000 40498 40503
-
(2000)
J. Biol. Chem.
, vol.275
, pp. 40498-40503
-
-
Okajima, T.1
Nakamura, Y.2
Uchikawa, M.3
-
32
-
-
0037119419
-
Molecular basis of the globoside-deficient P(k) blood group phenotype. Identification of four inactivating mutations in the UDP-N-acetylgalactosamine: Globotriaosylceramide 3-beta-N-acetylgalactosaminyltransferase gene
-
A. Hellberg, J. Poole, and M.L. Olsson Molecular basis of the globoside-deficient P(k) blood group phenotype. Identification of four inactivating mutations in the UDP-N-acetylgalactosamine: Globotriaosylceramide 3-beta-N-acetylgalactosaminyltransferase gene J. Biol. Chem. 277 2002 29455 29459
-
(2002)
J. Biol. Chem.
, vol.277
, pp. 29455-29459
-
-
Hellberg, A.1
Poole, J.2
Olsson, M.L.3
-
33
-
-
0014264388
-
Studies on human antibodies. VI. Selective variations in subgroup composition and genetic markers
-
W.J. Yount, M.M. Dorner, and H.G. Kunkel Studies on human antibodies. VI. Selective variations in subgroup composition and genetic markers J. Exp. Med. 127 1968 633 646
-
(1968)
J. Exp. Med.
, vol.127
, pp. 633-646
-
-
Yount, W.J.1
Dorner, M.M.2
Kunkel, H.G.3
-
34
-
-
0017729566
-
Pigeon breeder's disease and P blood groups
-
M.F. Radermecker, and M.W. Bruwier Pigeon breeder's disease and P blood groups Chest 72 1977 546 547
-
(1977)
Chest
, vol.72
, pp. 546-547
-
-
Radermecker, M.F.1
Bruwier, M.W.2
-
36
-
-
0023219515
-
The association of anti-P and early abortion
-
R.S. Shirey, P.M. Ness, and T.S. Kickler The association of anti-P and early abortion Transfusion 27 1987 189 191
-
(1987)
Transfusion
, vol.27
, pp. 189-191
-
-
Shirey, R.S.1
Ness, P.M.2
Kickler, T.S.3
-
37
-
-
0023618568
-
Early treatment by plasmapheresis in a woman with multiple abortions and the rare blood group P
-
Y. Shechter, I.E. Timor-Tritsch, and N. Lewit Early treatment by plasmapheresis in a woman with multiple abortions and the rare blood group P Vox Sang. 53 1987 135 138
-
(1987)
Vox Sang.
, vol.53
, pp. 135-138
-
-
Shechter, Y.1
Timor-Tritsch, I.E.2
Lewit, N.3
-
38
-
-
0018771017
-
Reaction of antibodies that cause paroxysmal cold hemoglobinuria (PCH) with globoside and Forssman glycosphingolipids
-
G.A. Schwarting, S.K. Kundu, and D.M. Marcus Reaction of antibodies that cause paroxysmal cold hemoglobinuria (PCH) with globoside and Forssman glycosphingolipids Blood 53 1979 186 192
-
(1979)
Blood
, vol.53
, pp. 186-192
-
-
Schwarting, G.A.1
Kundu, S.K.2
Marcus, D.M.3
-
40
-
-
0026324207
-
Inhibition of entry of HIV-1 in neural cell lines by antibodies against galactosyl ceramide
-
J.M. Harouse, S. Bhat, and S.L. Spitalnik Inhibition of entry of HIV-1 in neural cell lines by antibodies against galactosyl ceramide Science 253 1991 320 323
-
(1991)
Science
, vol.253
, pp. 320-323
-
-
Harouse, J.M.1
Bhat, S.2
Spitalnik, S.L.3
-
41
-
-
0025738161
-
Galactosyl ceramide or a derivative is an essential component of the neural receptor for human immunodeficiency virus type 1 envelope glycoprotein gp120
-
S. Bhat, S.L. Spitalnik, and F. Gonzalez-Scarano Galactosyl ceramide or a derivative is an essential component of the neural receptor for human immunodeficiency virus type 1 envelope glycoprotein gp120 Proc. Natl. Acad. Sci. U. S. A. 88 1991 7131 7134
-
(1991)
Proc. Natl. Acad. Sci. U. S. A.
, vol.88
, pp. 7131-7134
-
-
Bhat, S.1
Spitalnik, S.L.2
Gonzalez-Scarano, F.3
-
42
-
-
0037192816
-
Identification of a common sphingolipid-binding domain in Alzheimer, prion, and HIV-1 proteins
-
R. Mahfoud, N. Garmy, and M. Maresca Identification of a common sphingolipid-binding domain in Alzheimer, prion, and HIV-1 proteins J. Biol. Chem. 277 2002 11292 11296
-
(2002)
J. Biol. Chem.
, vol.277
, pp. 11292-11296
-
-
Mahfoud, R.1
Garmy, N.2
Maresca, M.3
-
43
-
-
0036794561
-
A novel soluble analog of the HIV-1 fusion cofactor, globotriaosylceramide (Gb(3)), eliminates the cholesterol requirement for high affinity gp120/Gb(3) interaction
-
R. Mahfoud, M. Mylvaganam, and C.A. Lingwood A novel soluble analog of the HIV-1 fusion cofactor, globotriaosylceramide (Gb(3)), eliminates the cholesterol requirement for high affinity gp120/Gb(3) interaction J. Lipid Res. 43 2002 1670 1679
-
(2002)
J. Lipid Res.
, vol.43
, pp. 1670-1679
-
-
Mahfoud, R.1
Mylvaganam, M.2
Lingwood, C.A.3
-
44
-
-
0028024550
-
Human parvoviruses: Implications for transfusion medicine
-
N.L. Luban Human parvoviruses: Implications for transfusion medicine Transfusion 34 1994 821 827
-
(1994)
Transfusion
, vol.34
, pp. 821-827
-
-
Luban, N.L.1
-
45
-
-
0345257726
-
Alpha5beta1 integrin as a cellular coreceptor for human parvovirus B19: Requirement of functional activation of beta1 integrin for viral entry
-
K.A. Weigel-Kelley, M.C. Yoder, and A. Srivastava Alpha5beta1 integrin as a cellular coreceptor for human parvovirus B19: Requirement of functional activation of beta1 integrin for viral entry Blood 102 2003 3927 3933
-
(2003)
Blood
, vol.102
, pp. 3927-3933
-
-
Weigel-Kelley, K.A.1
Yoder, M.C.2
Srivastava, A.3
-
46
-
-
4043181370
-
Hemolytic uremic syndrome revisited: Shiga toxin, factor H, and fibrin generation
-
D.P. Blackall, and M.B. Marques Hemolytic uremic syndrome revisited: Shiga toxin, factor H, and fibrin generation Am. J. Clin. Pathol. 121 2004 S81 S88 (Suppl)
-
(2004)
Am. J. Clin. Pathol.
, vol.121
-
-
Blackall, D.P.1
Marques, M.B.2
-
47
-
-
0024564286
-
Endocytosis from coated pits of Shiga toxin: A glycolipid-binding protein from Shigella dysenteriae 1
-
K. Sandvig, S. Olsnes, and J.E. Brown Endocytosis from coated pits of Shiga toxin: A glycolipid-binding protein from Shigella dysenteriae 1 J. Cell Biol. 108 1989 1331 1343
-
(1989)
J. Cell Biol.
, vol.108
, pp. 1331-1343
-
-
Sandvig, K.1
Olsnes, S.2
Brown, J.E.3
-
48
-
-
0027257477
-
Susceptibility to hemolytic-uremic syndrome relates to erythrocyte glycosphingolipid patterns
-
D.S. Newburg, P. Chaturvedi, and E.L. Lopez Susceptibility to hemolytic-uremic syndrome relates to erythrocyte glycosphingolipid patterns J. Infect. Dis. 168 1993 476 479
-
(1993)
J. Infect. Dis.
, vol.168
, pp. 476-479
-
-
Newburg, D.S.1
Chaturvedi, P.2
Lopez, E.L.3
-
49
-
-
0036087654
-
The epithelial cell cytoskeleton and intracellular trafficking. I. Shiga toxin B-subunit system: Retrograde transport, intracellular vectorization, and more
-
L. Johannes The epithelial cell cytoskeleton and intracellular trafficking. I. Shiga toxin B-subunit system: Retrograde transport, intracellular vectorization, and more Am. J. Physiol. Gastrointest. Liver Physiol. 283 2002 G1 G7
-
(2002)
Am. J. Physiol. Gastrointest. Liver Physiol.
, vol.283
-
-
Johannes, L.1
-
50
-
-
0037373313
-
Shiga toxin 1 triggers a ribotoxic stress response leading to p38 and JNK activation and induction of apoptosis in intestinal epithelial cells
-
W.E. Smith, A.V. Kane, and S.T. Campbell Shiga toxin 1 triggers a ribotoxic stress response leading to p38 and JNK activation and induction of apoptosis in intestinal epithelial cells Infect. Immun. 71 2003 1497 1504
-
(2003)
Infect. Immun.
, vol.71
, pp. 1497-1504
-
-
Smith, W.E.1
Kane, A.V.2
Campbell, S.T.3
-
51
-
-
0035203097
-
Role of lipid rafts in Shiga toxin 1 interaction with the apical surface of Caco-2 cells
-
O. Kovbasnjuk, M. Edidin, and M. Donowitz Role of lipid rafts in Shiga toxin 1 interaction with the apical surface of Caco-2 cells J. Cell Sci. 114 2001 4025 4031
-
(2001)
J. Cell Sci.
, vol.114
, pp. 4025-4031
-
-
Kovbasnjuk, O.1
Edidin, M.2
Donowitz, M.3
-
52
-
-
0034031642
-
Functional and structural aspects of the Kell blood group system
-
S. Lee, D. Russo, and C. Redman Functional and structural aspects of the Kell blood group system Transfus. Med. Rev. 14 2000 93 103
-
(2000)
Transfus. Med. Rev.
, vol.14
, pp. 93-103
-
-
Lee, S.1
Russo, D.2
Redman, C.3
-
53
-
-
0034081001
-
The Kell blood group system: Kell and XK membrane proteins
-
S. Lee, D. Russo, and C.M. Redman The Kell blood group system: Kell and XK membrane proteins Semin. Hematol. 37 2000 113 121
-
(2000)
Semin. Hematol.
, vol.37
, pp. 113-121
-
-
Lee, S.1
Russo, D.2
Redman, C.M.3
-
54
-
-
1442349704
-
Review: The Kell, Duffy, and Kidd blood group systems
-
C.M. Westhoff, and M.E. Reid Review: The Kell, Duffy, and Kidd blood group systems Immunohematology 20 2004 37 49
-
(2004)
Immunohematology
, vol.20
, pp. 37-49
-
-
Westhoff, C.M.1
Reid, M.E.2
-
55
-
-
0025779323
-
Molecular cloning and primary structure of Kell blood group protein
-
S. Lee, E.D. Zambas, and W.L. Marsh Molecular cloning and primary structure of Kell blood group protein Proc. Natl. Acad. Sci. U. S. A. 88 1991 6353 6357
-
(1991)
Proc. Natl. Acad. Sci. U. S. A.
, vol.88
, pp. 6353-6357
-
-
Lee, S.1
Zambas, E.D.2
Marsh, W.L.3
-
56
-
-
0141958299
-
Active amino acids of the Kell blood group protein and model of the ectodomain based on the structure of neutral endopeptidase 24.11
-
S. Lee, A.K. Debnath, and C.M. Redman Active amino acids of the Kell blood group protein and model of the ectodomain based on the structure of neutral endopeptidase 24.11 Blood 102 2003 3028 3034
-
(2003)
Blood
, vol.102
, pp. 3028-3034
-
-
Lee, S.1
Debnath, A.K.2
Redman, C.M.3
-
57
-
-
0033566651
-
Proteolytic processing of big endothelin-3 by the Kell blood group protein
-
S. Lee, M. Lin, and A. Mele Proteolytic processing of big endothelin-3 by the Kell blood group protein Blood 94 1999 1440 1450
-
(1999)
Blood
, vol.94
, pp. 1440-1450
-
-
Lee, S.1
Lin, M.2
Mele, A.3
-
58
-
-
0030820550
-
Molecular basis of Kell blood group phenotypes
-
S. Lee Molecular basis of Kell blood group phenotypes Vox Sang. 73 1997 1 11
-
(1997)
Vox Sang.
, vol.73
, pp. 1-11
-
-
Lee, S.1
-
59
-
-
0028998230
-
A novel common Kell antigen, TOU, and its spatial relationship to other Kell antigens
-
J. Jones, M.E. Reid, and R. Oyen A novel common Kell antigen, TOU, and its spatial relationship to other Kell antigens Vox Sang. 69 1995 53 60
-
(1995)
Vox Sang.
, vol.69
, pp. 53-60
-
-
Jones, J.1
Reid, M.E.2
Oyen, R.3
-
60
-
-
0034681296
-
Structure of human neutral endopeptidase (neprilysin) complexed with phosphoramidon
-
C. Oefner, A. D'Arcy, and M. Hennig Structure of human neutral endopeptidase (neprilysin) complexed with phosphoramidon J. Mol. Biol. 296 2000 341 349
-
(2000)
J. Mol. Biol.
, vol.296
, pp. 341-349
-
-
Oefner, C.1
D'Arcy, A.2
Hennig, M.3
-
61
-
-
0033168805
-
Identification of a defect in the intracellular trafficking of a Kell blood group variant
-
K. Yazdanbakhsh, S. Lee, and Q. Yu Identification of a defect in the intracellular trafficking of a Kell blood group variant Blood 94 1999 310 318
-
(1999)
Blood
, vol.94
, pp. 310-318
-
-
Yazdanbakhsh, K.1
Lee, S.2
Yu, Q.3
-
62
-
-
0035920205
-
Molecular defects underlying the Kell null phenotype
-
S. Lee, D.C. Russo, and A.P. Reiner Molecular defects underlying the Kell null phenotype J. Biol. Chem. 276 2001 27281 27289
-
(2001)
J. Biol. Chem.
, vol.276
, pp. 27281-27289
-
-
Lee, S.1
Russo, D.C.2
Reiner, A.P.3
-
63
-
-
0033999555
-
High-level, stable expression of blood group antigens in a heterologous system
-
K. Yazdanbakhsh, R. Oyen, and Q. Yu High-level, stable expression of blood group antigens in a heterologous system Am. J. Hematol. 63 2000 114 124
-
(2000)
Am. J. Hematol.
, vol.63
, pp. 114-124
-
-
Yazdanbakhsh, K.1
Oyen, R.2
Yu, Q.3
-
64
-
-
0347634501
-
Pancytopenia due to suppressed hematopoiesis in a case of fatal hemolytic disease of the newborn associated with anti-K supported by molecular K1 typing
-
T. Wagner, B. Resch, and F. Reiterer Pancytopenia due to suppressed hematopoiesis in a case of fatal hemolytic disease of the newborn associated with anti-K supported by molecular K1 typing J. Pediatr. Hematol. Oncol. 26 2004 13 15
-
(2004)
J. Pediatr. Hematol. Oncol.
, vol.26
, pp. 13-15
-
-
Wagner, T.1
Resch, B.2
Reiterer, F.3
-
65
-
-
0032546227
-
Inhibition of erythroid progenitor cells by anti-Kell antibodies in fetal alloimmune anemia
-
J.I. Vaughan, M. Manning, and R.M. Warwick Inhibition of erythroid progenitor cells by anti-Kell antibodies in fetal alloimmune anemia N. Engl. J. Med. 338 1998 798 803
-
(1998)
N. Engl. J. Med.
, vol.338
, pp. 798-803
-
-
Vaughan, J.I.1
Manning, M.2
Warwick, R.M.3
-
67
-
-
0036125344
-
Kell expression on myeloid progenitor cells
-
T. Wagner, G. Lanzer, and K. Geissler Kell expression on myeloid progenitor cells Leuk. Lymphoma 43 2002 479 485
-
(2002)
Leuk. Lymphoma
, vol.43
, pp. 479-485
-
-
Wagner, T.1
Lanzer, G.2
Geissler, K.3
-
68
-
-
0037227032
-
Causes of fetal anemia in hemolytic disease due to anti-K
-
G. Daniels, A. Hadley, and C.A. Green Causes of fetal anemia in hemolytic disease due to anti-K Transfusion 43 2003 115 116
-
(2003)
Transfusion
, vol.43
, pp. 115-116
-
-
Daniels, G.1
Hadley, A.2
Green, C.A.3
-
69
-
-
0037225919
-
Prenatal typing of Rh and Kell blood group system antigens: The edge of a watershed
-
C.E. van der Schoot, G.H. Tax, and R.J. Rijnders Prenatal typing of Rh and Kell blood group system antigens: The edge of a watershed Transfus. Med. Rev. 17 2003 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
-
70
-
-
0036375099
-
Blood group antigen profile predicted by molecular biology-use of real-time polymerase chain reaction to genotype important KEL, JK, RHD, and RHCE alleles
-
F. Araujo, C. Pereira, and F. Monteiro Blood group antigen profile predicted by molecular biology-use of real-time polymerase chain reaction to genotype important KEL, JK, RHD, and RHCE alleles Immunohematology 18 2002 59 64
-
(2002)
Immunohematology
, vol.18
, pp. 59-64
-
-
Araujo, F.1
Pereira, C.2
Monteiro, F.3
-
71
-
-
0035202829
-
McLeod neuroacanthocytosis: Genotype and phenotype
-
A. Danek, J.P. Rubio, and L. Rampoldi McLeod neuroacanthocytosis: Genotype and phenotype Ann. Neurol. 50 2001 755 764
-
(2001)
Ann. Neurol.
, vol.50
, pp. 755-764
-
-
Danek, A.1
Rubio, J.P.2
Rampoldi, L.3
-
72
-
-
0028263898
-
Isolation of the gene for McLeod syndrome that encodes a novel membrane transport protein
-
M. Ho, J. Chelly, and N. Carter Isolation of the gene for McLeod syndrome that encodes a novel membrane transport protein Cell 77 1994 869 880
-
(1994)
Cell
, vol.77
, pp. 869-880
-
-
Ho, M.1
Chelly, J.2
Carter, N.3
-
73
-
-
0346121321
-
An unusual phenotype of McLeod syndrome with late onset axonal neuropathy
-
M. Wada, M. Kimura, and M. Daimon An unusual phenotype of McLeod syndrome with late onset axonal neuropathy J. Neurol. Neurosurg. Psychiatry 74 2003 1697 1698
-
(2003)
J. Neurol. Neurosurg. Psychiatry
, vol.74
, pp. 1697-1698
-
-
Wada, M.1
Kimura, M.2
Daimon, M.3
-
74
-
-
0042662876
-
McLeod syndrome resulting from a novel XK mutation
-
B.K. Singleton, C.A. Green, and S. Renaud McLeod syndrome resulting from a novel XK mutation Br. J. Haematol. 122 2003 682 685
-
(2003)
Br. J. Haematol.
, vol.122
, pp. 682-685
-
-
Singleton, B.K.1
Green, C.A.2
Renaud, S.3
-
75
-
-
0038307154
-
McLeod phenotype associated with a XK missense mutation without hematologic, neuromuscular, or cerebral involvement
-
H.H. Jung, M. Hergerberg, and M. Vogt McLeod phenotype associated with a XK missense mutation without hematologic, neuromuscular, or cerebral involvement Transfusion 43 2003 928 938
-
(2003)
Transfusion
, vol.43
, pp. 928-938
-
-
Jung, H.H.1
Hergerberg, M.2
Vogt, M.3
-
76
-
-
0036519357
-
Point mutations causing the McLeod phenotype
-
D.C. Russo, S. Lee, and M.E. Reid Point mutations causing the McLeod phenotype Transfusion 42 2002 287 293
-
(2002)
Transfusion
, vol.42
, pp. 287-293
-
-
Russo, D.C.1
Lee, S.2
Reid, M.E.3
-
77
-
-
7244256221
-
A McLeod phenotype detected by random screening for K:-4 [Kp(b-)] blood donors in Brazil
-
S. Wendel, R. Fontao-Wendel, and J.E. Levi A McLeod phenotype detected by random screening for K:-4 [Kp(b-)] blood donors in Brazil Transfusion 44 2004 1579 1587
-
(2004)
Transfusion
, vol.44
, pp. 1579-1587
-
-
Wendel, S.1
Fontao-Wendel, R.2
Levi, J.E.3
-
78
-
-
0007611121
-
The first non-CGD McLeod phenotype male to make anti-Kx: Definition of the molecular basis
-
R. Oyen, B.L. Powell, and M.E. Reid The first non-CGD McLeod phenotype male to make anti-Kx: Definition of the molecular basis Transfusion 39 1999 90S (abstr)
-
(1999)
Transfusion
, vol.39
-
-
Oyen, R.1
Powell, B.L.2
Reid, M.E.3
-
79
-
-
0034659823
-
RHD gene deletion occurred in the Rhesus box
-
F.F. Wagner, and W.A. Flegel RHD gene deletion occurred in the Rhesus box Blood 95 2000 3662 3668
-
(2000)
Blood
, vol.95
, pp. 3662-3668
-
-
Wagner, F.F.1
Flegel, W.A.2
-
80
-
-
0034114775
-
Gene organization and rearrangements at the human Rhesus blood group locus revealed by fiber-FISH analysis
-
Y. Suto, Y. Ishikawa, and H. Hyodo Gene organization and rearrangements at the human Rhesus blood group locus revealed by fiber-FISH analysis Hum. Genet. 106 2000 164 171
-
(2000)
Hum. Genet.
, vol.106
, pp. 164-171
-
-
Suto, Y.1
Ishikawa, Y.2
Hyodo, H.3
-
81
-
-
0036659930
-
The DAU allele cluster of the RHD gene
-
F.F. Wagner, B. Ladewig, and K.S. Angert The DAU allele cluster of the RHD gene Blood 100 2002 306 311
-
(2002)
Blood
, vol.100
, pp. 306-311
-
-
Wagner, F.F.1
Ladewig, B.2
Angert, K.S.3
-
82
-
-
1442275829
-
Review: The molecular basis of the Rh blood group phenotypes
-
F.F. Wagner, and W.A. Flegel Review: The molecular basis of the Rh blood group phenotypes Immunohematology 20 2004 23 36
-
(2004)
Immunohematology
, vol.20
, pp. 23-36
-
-
Wagner, F.F.1
Flegel, W.A.2
|