-
1
-
-
0024334289
-
Decay-accelerating factor: Biochemistry, molecular biology and function
-
Lublin DM, Atkinson JP: Decay-accelerating factor: Biochemistry, molecular biology and function. Ann Rev Immunol 7:35, 1989
-
(1989)
Ann Rev Immunol
, vol.7
, pp. 35
-
-
Lublin, D.M.1
Atkinson, J.P.2
-
2
-
-
0023196218
-
The gene encoding decay-accelerating factor (DAF) is located in the complement-regulatory locus on the long arm of chromosome 1
-
Lublin DM, Lemons RS, LeBeau MM, Holers VM, Tykocinski ML, Medof ME, Atkinson JP: The gene encoding decay-accelerating factor (DAF) is located in the complement-regulatory locus on the long arm of chromosome 1. J Exp Med 165:1731, 1987
-
(1987)
J Exp Med
, vol.165
, pp. 1731
-
-
Lublin, D.M.1
Lemons, R.S.2
LeBeau, M.M.3
Holers, V.M.4
Tykocinski, M.L.5
Medof, M.E.6
Atkinson, J.P.7
-
3
-
-
0023214843
-
Decay-acceleratinng factor. Genetic polymorphism and linkage to the RCA (regulator of complement activation) gene cluster in humans
-
Rey-Campos J, Rubinstein P, Rodriguez de Cordoba S: Decay-acceleratinng factor. Genetic polymorphism and linkage to the RCA (regulator of complement activation) gene cluster in humans. J Exp Med 166:246, 1987
-
(1987)
J Exp Med
, vol.166
, pp. 246
-
-
Rey-Campos, J.1
Rubinstein, P.2
Rodriguez De Cordoba, S.3
-
4
-
-
0019964513
-
Isolation of a human erythrocyte membrane glycoprotein with decay-accelerating activity for C3-convertases of the complement system
-
Nicholson-Weller A, Burge J, Fearon DT, Weller PF, Austen KF: Isolation of a human erythrocyte membrane glycoprotein with decay-accelerating activity for C3-convertases of the complement system. J Immunol 129:184, 1982
-
(1982)
J Immunol
, vol.129
, pp. 184
-
-
Nicholson-Weller, A.1
Burge, J.2
Fearon, D.T.3
Weller, P.F.4
Austen, K.F.5
-
5
-
-
0020579753
-
Paroxysmal nocturnal haemoglobinurea: Deficiency in factor H-like functions of the abnormal erythrocytes
-
Pangburn MK, Schreiber RD, Trombold JS, Muller-Eberhard HJ: Paroxysmal nocturnal haemoglobinurea: Deficiency in factor H-like functions of the abnormal erythrocytes. J Exp Med 157:1971, 1983
-
(1983)
J Exp Med
, vol.157
, pp. 1971
-
-
Pangburn, M.K.1
Schreiber, R.D.2
Trombold, J.S.3
Muller-Eberhard, H.J.4
-
6
-
-
0021910555
-
Amelioration of lytic abnormalities of paroxysmal nocturnal hemoglobinuria with decay-accelerating factor
-
Medof ME, Kinoshita T, Silber R, Nussenzweig V: Amelioration of lytic abnormalities of paroxysmal nocturnal hemoglobinuria with decay-accelerating factor. Proc Natl Acad Sci USA 82:2980, 1985
-
(1985)
Proc Natl Acad Sci USA
, vol.82
, pp. 2980
-
-
Medof, M.E.1
Kinoshita, T.2
Silber, R.3
Nussenzweig, V.4
-
7
-
-
0022649422
-
The control of complement activation by the blood cells in paroxysmal nocturnal hemoglobinuria
-
Rosse WF: The control of complement activation by the blood cells in paroxysmal nocturnal hemoglobinuria. Blood 67:268, 1986
-
(1986)
Blood
, vol.67
, pp. 268
-
-
Rosse, W.F.1
-
8
-
-
2642667758
-
Host cell protection from complement by glycosylphosphatidylinositol-anchored complement inhibitors and their deficiencies in paroxysmal nocturnal haemoglobinuria
-
Melchers F, Albert ED, Nichlin L (eds). New York, NY, Springer-Verlag
-
Kinoshita T: Host cell protection from complement by glycosylphosphatidylinositol-anchored complement inhibitors and their deficiencies in paroxysmal nocturnal haemoglobinuria, in Melchers F, Albert ED, Nichlin L (eds): Progress in Immunology (vol 7). New York, NY, Springer-Verlag, 1989. p 178
-
(1989)
Progress in Immunology
, vol.7
, pp. 178
-
-
Kinoshita, T.1
-
9
-
-
0026726694
-
Mapping of epitopes, glycosylation sites, and complement regulatory domains in human decay accelerating factor
-
Coyne K, Hall S, Thompson E, Arce MA, Kinoshita T, Fujita T, Anstee DA, Rosse WF, Lublin DM: Mapping of epitopes, glycosylation sites, and complement regulatory domains in human decay accelerating factor. J Immunol 149:2906, 1992
-
(1992)
J Immunol
, vol.149
, pp. 2906
-
-
Coyne, K.1
Hall, S.2
Thompson, E.3
Arce, M.A.4
Kinoshita, T.5
Fujita, T.6
Anstee, D.A.7
Rosse, W.F.8
Lublin, D.M.9
-
10
-
-
0022540116
-
Biosynthesis and glycosylation of the human complement regulatory protein decay-accelerating factor
-
Lublin DM, Krsek-Staples J, Pangburn MK, Atkinson JP: Biosynthesis and glycosylation of the human complement regulatory protein decay-accelerating factor. J Immunol 137:1629, 1986
-
(1986)
J Immunol
, vol.137
, pp. 1629
-
-
Lublin, D.M.1
Krsek-Staples, J.2
Pangburn, M.K.3
Atkinson, J.P.4
-
11
-
-
0028406273
-
Structure and function of decay accelerating factor CDSS
-
Nicholson-Weller A, Wang CE: Structure and function of decay accelerating factor CDSS. J Lab Clin Med 123:485, 1994
-
(1994)
J Lab Clin Med
, vol.123
, pp. 485
-
-
Nicholson-Weller, A.1
Wang, C.E.2
-
12
-
-
0023677213
-
Identification of human erythrocyte blood group antigens on decay accelerating factor (DAF) and an-erythrocyte pheuotype negative for DAF
-
Telen MJ, Hall SE, Green AM, Moulds JJ, Rosse WF: Identification of human erythrocyte blood group antigens on decay accelerating factor (DAF) and an-erythrocyte pheuotype negative for DAF. J Exp Med 167:93, 1988
-
(1988)
J Exp Med
, vol.167
, pp. 93
-
-
Telen, M.J.1
Hall, S.E.2
Green, A.M.3
Moulds, J.J.4
Rosse, W.F.5
-
13
-
-
0001858779
-
Evidence that Cromer-related blood group antigens are carried on decay accelerating factor (DAF) suggests that the Inab. phenotype is a novel form of DAF deficiency
-
abstr
-
Parsons SF, Spring FA, Meny AH, Uchikawa M, Mallinoson G, Anstee DJ, Rawiison V, Daha M: Evidence that Cromer-related blood group antigens are carried on decay accelerating factor (DAF) suggests that the Inab. phenotype is a novel form of DAF deficiency. 20th Congr Int Soc Blood Transfus 116, 1988 (abstr)
-
(1988)
20th Congr Int Soc Blood Transfus
, vol.116
-
-
Parsons, S.F.1
Spring, F.A.2
Meny, A.H.3
Uchikawa, M.4
Mallinoson, G.5
Anstee, D.J.6
Rawiison, V.7
Daha, M.8
-
14
-
-
0024384090
-
Cromer-related antigens-blood group determinants on decay-accelerating factor
-
Daniels GL: Cromer-related antigens-blood group determinants on decay-accelerating factor. Vox Sang 56:205, 1988
-
(1988)
Vox Sang
, vol.56
, pp. 205
-
-
Daniels, G.L.1
-
15
-
-
0020403769
-
A possible null phenotype in the Cromer blood group complex
-
Daniels GL, Tohyama H, Uchikawa M: A possible null phenotype in the Cromer blood group complex. Transfusion 22:362, 1982
-
(1982)
Transfusion
, vol.22
, pp. 362
-
-
Daniels, G.L.1
Tohyama, H.2
Uchikawa, M.3
-
16
-
-
0000887653
-
The Inab phenotype: Another example found
-
abstr
-
Walthers L, Salem M, Tessel J, Laird-Fryer B, Moulds JJ: The Inab phenotype: Another example found. Transfusion 23:423, 1983 (abstr)
-
(1983)
Transfusion
, vol.23
, pp. 423
-
-
Walthers, L.1
Salem, M.2
Tessel, J.3
Laird-Fryer, B.4
Moulds, J.J.5
-
17
-
-
0023812006
-
A family showing inheritance of the Inab phenotype
-
Lin RC, Herman J, Henry L, Daniels GL: A family showing inheritance of the Inab phenotype. Transfusion 28:427, 1988
-
(1988)
Transfusion
, vol.28
, pp. 427
-
-
Lin, R.C.1
Herman, J.2
Henry, L.3
Daniels, G.L.4
-
18
-
-
0024371622
-
Studies on the defect which causes absence of decay accelerating factor (DAF) from the peripheral blood cells of an individual with the Inab phenotype
-
Tate CG, Uchikawa M, Tanner MJA, Judson PA, Parsons SF, Mallinson G, Anstee DJ: Studies on the defect which causes absence of decay accelerating factor (DAF) from the peripheral blood cells of an individual with the Inab phenotype. Biochem J 261:489, 1989
-
(1989)
Biochem J
, vol.261
, pp. 489
-
-
Tate, C.G.1
Uchikawa, M.2
Tanner, M.J.A.3
Judson, P.A.4
Parsons, S.F.5
Mallinson, G.6
Anstee, D.J.7
-
19
-
-
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 MJA: Molecular basis of reduced or absent expression of decay-accelerating factor in Cromer blood group phenotypes. Blood 84:1276, 1994
-
(1994)
Blood
, vol.84
, pp. 1276
-
-
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.A.9
-
20
-
-
0023277545
-
Single-step method of RNA isolation by acid guanidinium thiocyanate-phenol-chloroform extraction
-
Chomczynski P, Sacchi N: Single-step method of RNA isolation by acid guanidinium thiocyanate-phenol-chloroform extraction. Anal Biochem 162:156, 1987
-
(1987)
Anal Biochem
, vol.162
, pp. 156
-
-
Chomczynski, P.1
Sacchi, N.2
-
21
-
-
0010991242
-
Cloning and characterization of cDNAs encoding the complete sequence of decay-accelerating factor of human complement
-
Medof ME, Lublin DM, Holers MH, Ayers DJ, Getty RR, Leykam JF, Atkinson JP, Tykocinski ML: Cloning and characterization of cDNAs encoding the complete sequence of decay-accelerating factor of human complement. Proc Natl Acad Sci USA 84:2007, 1987
-
(1987)
Proc Natl Acad Sci USA
, vol.84
, pp. 2007
-
-
Medof, M.E.1
Lublin, D.M.2
Holers, M.H.3
Ayers, D.J.4
Getty, R.R.5
Leykam, J.F.6
Atkinson, J.P.7
Tykocinski, M.L.8
-
22
-
-
0025728266
-
Characterization of the decay-accelerating factor gene promoter region
-
Ewulonu UK, Ravi L, Medof ME: Characterization of the decay-accelerating factor gene promoter region. Proc Natl Acad Sci USA 88:4675, 1991
-
(1991)
Proc Natl Acad Sci USA
, vol.88
, pp. 4675
-
-
Ewulonu, U.K.1
Ravi, L.2
Medof, M.E.3
-
23
-
-
0023878704
-
A hemagglutinin of uropathogenic Escherichia coli recognizes the Dr blood group antigen
-
Nowicki B, Moulds J, Hull R, Hull S: A hemagglutinin of uropathogenic Escherichia coli recognizes the Dr blood group antigen. Infect Immun 56:1057, 1988
-
(1988)
Infect Immun
, vol.56
, pp. 1057
-
-
Nowicki, B.1
Moulds, J.2
Hull, R.3
Hull, S.4
-
24
-
-
0025053264
-
Inherited complete deficiency of 20-kilodalton homologous restriction factor (CD59) as a cause of paroxysmal nocturnal hemoglobinuria
-
Yamashina M, Ueda E, Kinoshita T, Takami T, Ojima A, Ono H, Tanaka H, Kondo N, Orii T, Okada N, Okada H, Inoue K, Kitani T: Inherited complete deficiency of 20-kilodalton homologous restriction factor (CD59) as a cause of paroxysmal nocturnal hemoglobinuria. N Engl J Med 323: 1184, 1990
-
(1990)
N Engl J Med
, vol.323
, pp. 1184
-
-
Yamashina, M.1
Ueda, E.2
Kinoshita, T.3
Takami, T.4
Ojima, A.5
Ono, H.6
Tanaka, H.7
Kondo, N.8
Orii, T.9
Okada, N.10
Okada, H.11
Inoue, K.12
Kitani, T.13
-
25
-
-
0028107348
-
Discrimination of human HLA-DRB1 alleles by PCR-SSCP method
-
Bannai M, Tokunaga K, Lin L, Kuwata S, Mazda T, Amaki I, Fujisawa K, Juji T: Discrimination of human HLA-DRB1 alleles by PCR-SSCP method. Eur J Immunogenet 21:1, 1994
-
(1994)
Eur J Immunogenet
, vol.21
, pp. 1
-
-
Bannai, M.1
Tokunaga, K.2
Lin, L.3
Kuwata, S.4
Mazda, T.5
Amaki, I.6
Fujisawa, K.7
Juji, T.8
-
26
-
-
0023651307
-
RNA splice junctions of different classes of eukaryotes: Sequence statistics and functional implications in gene expression
-
Shapiro MB, Senapathy P: RNA splice junctions of different classes of eukaryotes: Sequence statistics and functional implications in gene expression. Nucleic Acids Res 15:7155, 1987
-
(1987)
Nucleic Acids Res
, vol.15
, pp. 7155
-
-
Shapiro, M.B.1
Senapathy, P.2
-
27
-
-
0026794668
-
The mutational spectrum of single base-pair substitutions in mRNA splice junctions of human genes: Causes and consequences
-
Krawczak M, Reiss J, Cooper DN: The mutational spectrum of single base-pair substitutions in mRNA splice junctions of human genes: Causes and consequences. Hum Genet 90:41, 1992
-
(1992)
Hum Genet
, vol.90
, pp. 41
-
-
Krawczak, M.1
Reiss, J.2
Cooper, D.N.3
-
28
-
-
0026337156
-
Biochemical studies on the red blood cells from a patient with the Inab phenotype (decay-accelerating factor deficiency)
-
Reid ME, Mallinson G, Sim RB, Poole J, Pausch V, Merry AH, Liew YW, Tanner MJA: Biochemical studies on the red blood cells from a patient with the Inab phenotype (decay-accelerating factor deficiency). Blood 78:3291, 1991
-
(1991)
Blood
, vol.78
, pp. 3291
-
-
Reid, M.E.1
Mallinson, G.2
Sim, R.B.3
Poole, J.4
Pausch, V.5
Merry, A.H.6
Liew, Y.W.7
Tanner, M.J.A.8
|