-
1
-
-
0027396618
-
Evolution of clinical understanding: Paroxysmal nocturnal hemoglobinuria as a paradigm
-
Rosse WF: Evolution of clinical understanding: Paroxysmal nocturnal hemoglobinuria as a paradigm. Am J Hematol 42:122, 1993.
-
(1993)
Am J Hematol
, vol.42
, pp. 122
-
-
Rosse, W.F.1
-
2
-
-
0011812238
-
Paroxysmal nocturnal hemoglobinuria
-
Lee GR, Bithell TC, Foerster J, Athens JW, Lukens JN (eds): Philadelphia: Lea & Febiger
-
Lee GR: Paroxysmal nocturnal hemoglobinuria. In Lee GR, Bithell TC, Foerster J, Athens JW, Lukens JN (eds): "Wintrobe's Clinical Hematology" Ed 9. Vol 1. Philadelphia: Lea & Febiger, 1993, p 1232.
-
(1993)
"Wintrobe's Clinical Hematology" Ed 9
, vol.1
, pp. 1232
-
-
Lee, G.R.1
-
3
-
-
0026588963
-
Marrow transplantation for paroxysmal nocturnal hemoglobinuria
-
Kawahara K, Witherspoon RP, Storb R: Marrow transplantation for paroxysmal nocturnal hemoglobinuria. Am J Hematol 39:283, 1992.
-
(1992)
Am J Hematol
, vol.39
, pp. 283
-
-
Kawahara, K.1
Witherspoon, R.P.2
Storb, R.3
-
4
-
-
0013911413
-
Immune lysis of normal human and paroxysmal nocturnal hemoglobinuria (PNH) red blood cells. I. the sensitivity of PNH red cells to lysis by complement and specific antibody
-
Rosse WF, Dacie JV: Immune lysis of normal human and paroxysmal nocturnal hemoglobinuria (PNH) red blood cells. I. The sensitivity of PNH red cells to lysis by complement and specific antibody. J Clin Invest 45:736, 1966.
-
(1966)
J Clin Invest
, vol.45
, pp. 736
-
-
Rosse, W.F.1
Dacie, J.V.2
-
5
-
-
0020072940
-
Increased enzymatic activity of the alternative pathway convertase when bound to the erythrocytes of paroxysmal nocturnal hemoglobinuria
-
Parker CJ, Baker PJ, Rosse WF: Increased enzymatic activity of the alternative pathway convertase when bound to the erythrocytes of paroxysmal nocturnal hemoglobinuria. J Clin Invest 69:337, 1982.
-
(1982)
J Clin Invest
, vol.69
, pp. 337
-
-
Parker, C.J.1
Baker, P.J.2
Rosse, W.F.3
-
6
-
-
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
-
7
-
-
0021922659
-
Deficiency of the complement regulatory protein, "decay-accelerating factor," on membranes of granulocytes, monocytes, and platelets in paroxysmal nocturnal hemoglobinuria
-
Nicholson-Weller A, Spicer DB, Austen KF: Deficiency of the complement regulatory protein, "decay-accelerating factor," on membranes of granulocytes, monocytes, and platelets in paroxysmal nocturnal hemoglobinuria. N Engl J Med 312:1091, 1985.
-
(1985)
N Engl J Med
, vol.312
, pp. 1091
-
-
Nicholson-Weller, A.1
Spicer, D.B.2
Austen, K.F.3
-
8
-
-
0021910555
-
Amelioration of lytic abnormalities of paroxysmal nocturnal hemoglobinuria with decayaccelerating factor
-
Medof ME, Kinoshita T, Silber R, Nussetizweig V: Amelioration of lytic abnormalities of paroxysmal nocturnal hemoglobinuria with decayaccelerating 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
Nussetizweig, V.4
-
9
-
-
0021836875
-
Enhanced complement-mediated lysis of type III paroxysmal nocturnal hemoglobinuria erythrocytes involves increased C9 binding and polymerization
-
Hu VW, Nicholson-Weller A: Enhanced complement-mediated lysis of type III paroxysmal nocturnal hemoglobinuria erythrocytes involves increased C9 binding and polymerization. Proc Natl Acad Sci USA 82:5520, 1985.
-
(1985)
Proc Natl Acad Sci USA
, vol.82
, pp. 5520
-
-
Hu, V.W.1
Nicholson-Weller, A.2
-
10
-
-
0023763076
-
Isolation from human erythrocytes of a new membrane protein which inhibits the formation of complement transmembrane channels
-
Sugita Y, Nakano Y, Tomita M: Isolation from human erythrocytes of a new membrane protein which inhibits the formation of complement transmembrane channels. J Biochem 104:633, 1988.
-
(1988)
J Biochem
, vol.104
, pp. 633
-
-
Sugita, Y.1
Nakano, Y.2
Tomita, M.3
-
11
-
-
0024419650
-
A novel membrane glycoprotein capable of inhibiting membrane attack by homologous complement
-
Okada N, Harada R, Fujita T, Okada H: A novel membrane glycoprotein capable of inhibiting membrane attack by homologous complement. Int Immunol 1:205, 1989.
-
(1989)
Int Immunol
, vol.1
, pp. 205
-
-
Okada, N.1
Harada, R.2
Fujita, T.3
Okada, H.4
-
12
-
-
0024411828
-
Isolation and characterization of a membrane protein from normal human erythrocytes that inhibits reactive lysis of the erythrocytes of paroxysmal nocturnal hemoglobinuria
-
Holguin MH, Fredrick LR, Bernshaw NJ, Wilcox LA, Parker CJ: Isolation and characterization of a membrane protein from normal human erythrocytes that inhibits reactive lysis of the erythrocytes of paroxysmal nocturnal hemoglobinuria. J Clin Invest 84:7, 1989.
-
(1989)
J Clin Invest
, vol.84
, pp. 7
-
-
Holguin, M.H.1
Fredrick, L.R.2
Bernshaw, N.J.3
Wilcox, L.A.4
Parker, C.J.5
-
13
-
-
0027251555
-
Expression of decay-accelerating factor and CD59 in lymphocyte subsets of healthy individuals and paroxysmal nocturnal hemoglobinuria patients
-
Nagakura S, Nakakuma H, Horikawa K, et al.: Expression of decay-accelerating factor and CD59 in lymphocyte subsets of healthy individuals and paroxysmal nocturnal hemoglobinuria patients. Am J Hematol 43:14, 1993.
-
(1993)
Am J Hematol
, vol.43
, pp. 14
-
-
Nagakura, S.1
Nakakuma, H.2
Horikawa, K.3
-
14
-
-
0027181250
-
Complement-induced vesiculation and exposure of membrane prothrombinase sites in platelets of paroxysmal nocturnal hemoglobinuria
-
Wiedmer T, Hall SE, Ortel TL, Kane WH, Rosse WF, Sims PJ: Complement-induced vesiculation and exposure of membrane prothrombinase sites in platelets of paroxysmal nocturnal hemoglobinuria. Blood 82:1192, 1993.
-
(1993)
Blood
, vol.82
, pp. 1192
-
-
Wiedmer, T.1
Hall, S.E.2
Ortel, T.L.3
Kane, W.H.4
Rosse, W.F.5
Sims, P.J.6
-
15
-
-
0025053264
-
Inherited complete deficiency of 20-kilodalton homologous restriction factor (CD59) as a cause of paroxysmal nocturnal hemoglobinuria
-
Yamashina M, Ueda E, Kinoshita T, et al.: 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
-
16
-
-
0023677213
-
Identification of human erythrocyte blood group antigens on decay accelerating factor (DAF) and an erythrocyte phenotype 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 phenotype negative for DAF. J Exp Med 167:1993, 1988.
-
(1988)
J Exp Med
, vol.167
, pp. 1993
-
-
Telen, M.J.1
Hall, S.E.2
Green, A.M.3
Moulds, J.J.4
Rosse, W.F.5
-
17
-
-
0023261906
-
Paroxysmal nocturnal hemoglobinuria type III. Lack of an erythrocyte membrane protein restricting the lysis of C5b-9
-
Hänsch GM, Schönermark S, Roelcke D: Paroxysmal nocturnal hemoglobinuria type III. Lack of an erythrocyte membrane protein restricting the lysis of C5b-9. J Clin Invest 80:7, 1987.
-
(1987)
J Clin Invest
, vol.80
, pp. 7
-
-
Hänsch, G.M.1
Schönermark, S.2
Roelcke, D.3
-
18
-
-
0023107563
-
Deficiency of the homologous restriction factor in paroxysmal nocturnal hemoglobinuria
-
Zalman LS, Wood LM, Frank MM, Müller-Eberhard HJ: Deficiency of the homologous restriction factor in paroxysmal nocturnal hemoglobinuria. J Exp Med 165:572, 1987.
-
(1987)
J Exp Med
, vol.165
, pp. 572
-
-
Zalman, L.S.1
Wood, L.M.2
Frank, M.M.3
Müller-Eberhard, H.J.4
-
19
-
-
0019328958
-
Role of phosphatidylinositol in attachment of alkaline phosphatase to membranes
-
Low MG, Zilversmit DB: Role of phosphatidylinositol in attachment of alkaline phosphatase to membranes. Biochemistry 19:3913, 1980.
-
(1980)
Biochemistry
, vol.19
, pp. 3913
-
-
Low, M.G.1
Zilversmit, D.B.2
-
20
-
-
0024230917
-
Structural characterization of the glycoinositol phospholipid membrane anchor of human erythrocyte acetylcholinesterase by fast atom bombardment mass spectrometry
-
Roberts WL, Santikarn S, Reinhold VN, Rosenberry TL: Structural characterization of the glycoinositol phospholipid membrane anchor of human erythrocyte acetylcholinesterase by fast atom bombardment mass spectrometry. J Biol Chem 263:18776, 1988.
-
(1988)
J Biol Chem
, vol.263
, pp. 18776
-
-
Roberts, W.L.1
Santikarn, S.2
Reinhold, V.N.3
Rosenberry, T.L.4
-
21
-
-
0023944337
-
Cell-surface anchoring of proteins via glycosyl-phosphatidylinositol structures
-
Ferguson MAJ, Williams AF: Cell-surface anchoring of proteins via glycosyl-phosphatidylinositol structures. Annu Rev Biochem 57:285, 1988.
-
(1988)
Annu Rev Biochem
, vol.57
, pp. 285
-
-
Ferguson, M.A.J.1
Williams, A.F.2
-
22
-
-
0027294030
-
The structure and biosynthesis of glycosyl phosphatidyl-inositol protein anchors
-
Englund PT: The structure and biosynthesis of glycosyl phosphatidyl-inositol protein anchors. Annu Rev Biochem 62:121, 1993.
-
(1993)
Annu Rev Biochem
, vol.62
, pp. 121
-
-
Englund, P.T.1
-
23
-
-
0022970401
-
Decay-accelerating factor of complement is anchored to cells by a C-terminal glycolipid
-
Medof ME, Walter EI, Roberts WL, Haas R, Rosenberry TL: Decay-accelerating factor of complement is anchored to cells by a C-terminal glycolipid. Biochemistry 25:6740, 1986.
-
(1986)
Biochemistry
, vol.25
, pp. 6740
-
-
Medof, M.E.1
Walter, E.I.2
Roberts, W.L.3
Haas, R.4
Rosenberry, T.L.5
-
24
-
-
0025202564
-
Deficiency of glycosyl-phosphatidylinositol-linked membrane glycoproteins of leukocytes in paroxysmal nocturnal hemoglobinuria, description of a new diagnostic cytofluorometric assay
-
van der School CE, Huizinga TWJ, van't Veer-Korthof ET, Wijmans R, Pinkster J, von dem Borne AEGKr: Deficiency of glycosyl-phosphatidylinositol-linked membrane glycoproteins of leukocytes in paroxysmal nocturnal hemoglobinuria, description of a new diagnostic cytofluorometric assay. Blood 76:1853, 1990.
-
(1990)
Blood
, vol.76
, pp. 1853
-
-
Van Der School, C.E.1
Huizinga, T.W.J.2
Van't Veer-Korthof, E.T.3
Wijmans, R.4
Pinkster, J.5
Von Dem Borne, A.E.G.Kr.6
-
25
-
-
0028918097
-
Markedly high population of affected reticulocytes negative for decay-accelerating factor and CD59 in paroxysmal nocturnal hemoglobinuria
-
Iwamoto N, Kawaguchi T, Nagakura S, et al.: Markedly high population of affected reticulocytes negative for decay-accelerating factor and CD59 in paroxysmal nocturnal hemoglobinuria. Blood 85:2228, 1995.
-
(1995)
Blood
, vol.85
, pp. 2228
-
-
Iwamoto, N.1
Kawaguchi, T.2
Nagakura, S.3
-
26
-
-
0028944403
-
Paroxysmal nocturnal hemoglobinuria clone in bone marrow of patients with pancytopenia
-
Nakakuma H, Nagakura S, Iwamolo N, et al.: Paroxysmal nocturnal hemoglobinuria clone in bone marrow of patients with pancytopenia. Blood 85:1371, 1995.
-
(1995)
Blood
, vol.85
, pp. 1371
-
-
Nakakuma, H.1
Nagakura, S.2
Iwamolo, N.3
-
27
-
-
0029130529
-
Proposal for a classification of the clinical stages of paroxysmal nocturnal hemoglobinuria
-
Nakakuma H, Kawaguchi T, Horikawa K, et al.: Proposal for a classification of the clinical stages of paroxysmal nocturnal hemoglobinuria. Blood 86:2051, 1995.
-
(1995)
Blood
, vol.86
, pp. 2051
-
-
Nakakuma, H.1
Kawaguchi, T.2
Horikawa, K.3
-
28
-
-
0023871975
-
Normal polymorphic variations and transcription of the decay accelerating factor gene in paroxysmal nocturnal hemoglobinuria cells
-
Stafford HA, Tykocinski ML, Lublin DM, et al.: Normal polymorphic variations and transcription of the decay accelerating factor gene in paroxysmal nocturnal hemoglobinuria cells. Proc Natl Acad Sci USA 85:880, 1988.
-
(1988)
Proc Natl Acad Sci USA
, vol.85
, pp. 880
-
-
Stafford, H.A.1
Tykocinski, M.L.2
Lublin, D.M.3
-
29
-
-
0024539163
-
Differences in the expression of alkaline phosphatase mRNA in chronic myelogenous leukemia and paroxysmal nocturnal hemoglobinuria polymorphonuclear leukocytes
-
Rambaldi A, Terao M, Bettoni S, et al.: Differences in the expression of alkaline phosphatase mRNA in chronic myelogenous leukemia and paroxysmal nocturnal hemoglobinuria polymorphonuclear leukocytes. Blood 73:1113, 1989.
-
(1989)
Blood
, vol.73
, pp. 1113
-
-
Rambaldi, A.1
Terao, M.2
Bettoni, S.3
-
30
-
-
0025064231
-
Synthesis of aberrant decay-accelerating factor proteins by affected paroxysmal nocturnal hemoglobinuria leukocytes
-
Carothers DJ, Hazra SV, Andreson SW, Medof ME: Synthesis of aberrant decay-accelerating factor proteins by affected paroxysmal nocturnal hemoglobinuria leukocytes. J Clin Invest 85:47, 1990.
-
(1990)
J Clin Invest
, vol.85
, pp. 47
-
-
Carothers, D.J.1
Hazra, S.V.2
Andreson, S.W.3
Medof, M.E.4
-
31
-
-
0026600639
-
Defective glycosylphosphatidyl-inositol anchor synthesis in paroxysmal nocturnal hemoglobinuria granulocytes
-
Mahoney JF, Urakaze M, Hall S, et al.: Defective glycosylphosphatidyl-inositol anchor synthesis in paroxysmal nocturnal hemoglobinuria granulocytes. Blood 79:1400, 1992.
-
(1992)
Blood
, vol.79
, pp. 1400
-
-
Mahoney, J.F.1
Urakaze, M.2
Hall, S.3
-
32
-
-
0021999569
-
Cell-surface-antigen mutants of haematopoietic cells. Tools to study differentiation, biosynthesis and function
-
Hyman R: Cell-surface-antigen mutants of haematopoietic cells. Tools to study differentiation, biosynthesis and function. Biochem J 225:27, 1985.
-
(1985)
Biochem J
, vol.225
, pp. 27
-
-
Hyman, R.1
-
33
-
-
0025823110
-
Defective glycosyl phosphatidylinositol biosynthesis in extracts of three Thy-1 negative lymphoma cell mutants
-
Stevens VL, Raetz CRH: Defective glycosyl phosphatidylinositol biosynthesis in extracts of three Thy-1 negative lymphoma cell mutants. J Biol Chem 266:10039, 1991.
-
(1991)
J Biol Chem
, vol.266
, pp. 10039
-
-
Stevens, V.L.1
Raetz, C.R.H.2
-
34
-
-
0027295959
-
Impaired glycosylation of glycosylphosphatidylinositol-anchor synthesis in paroxysmal nocturnal hemoglobinuria leukocytes
-
Hidaka M, Nagakura S, Horikawa K, et al.: Impaired glycosylation of glycosylphosphatidylinositol-anchor synthesis in paroxysmal nocturnal hemoglobinuria leukocytes. Biochem Biophys Res Commun 191:571, 1993.
-
(1993)
Biochem Biophys Res Commun
, vol.191
, pp. 571
-
-
Hidaka, M.1
Nagakura, S.2
Horikawa, K.3
-
35
-
-
0024515848
-
A novel pathway for glycan assembly: Biosynthesis of the glycosylphosphatidylinositol anchor of the trypanosome variant surface glycoprotein
-
Masterson WJ, Doering TL, Hart GW, Englund PT: A novel pathway for glycan assembly: Biosynthesis of the glycosylphosphatidylinositol anchor of the trypanosome variant surface glycoprotein. Cell 56: 793, 1989.
-
(1989)
Cell
, vol.56
, pp. 793
-
-
Masterson, W.J.1
Doering, T.L.2
Hart, G.W.3
Englund, P.T.4
-
36
-
-
0026780907
-
Synthesis of mannosylglucosami-nylinositol phospholipids in normal but not paroxysmal nocturnal hemoglobinuria cells
-
Hirose S, Ravi L, Prince GM, et al.: Synthesis of mannosylglucosami-nylinositol phospholipids in normal but not paroxysmal nocturnal hemoglobinuria cells. Proc Natl Acad Sci USA 89:6025, 1992.
-
(1992)
Proc Natl Acad Sci USA
, vol.89
, pp. 6025
-
-
Hirose, S.1
Ravi, L.2
Prince, G.M.3
-
37
-
-
0027198876
-
Specific defect in N-acetylglucosamine incorporation in the biosynthesis of the glycosylphosphatidylinositol anchor in cloned cell lines from patients with paroxysmal nocturnal hemoglobinuria
-
Hillmen P, Bessler M, Mason PJ, Watkins WM, Luzzatto L: Specific defect in N-acetylglucosamine incorporation in the biosynthesis of the glycosylphosphatidylinositol anchor in cloned cell lines from patients with paroxysmal nocturnal hemoglobinuria. Proc Natl Acad Sci USA 90:5272, 1993.
-
(1993)
Proc Natl Acad Sci USA
, vol.90
, pp. 5272
-
-
Hillmen, P.1
Bessler, M.2
Mason, P.J.3
Watkins, W.M.4
Luzzatto, L.5
-
39
-
-
0027412005
-
Deficient biosynthesis of N-acetylglucosaminyl-phosphatidylinositol, the first intermediate of glycosyl phosphatidylinositol anchor biosynthesis, in cell lines established from patients with paroxysmal nocturnal hemoglobinuria
-
Takahashi M, Takeda J, Hirose S, et al.: Deficient biosynthesis of N-acetylglucosaminyl-phosphatidylinositol, the first intermediate of glycosyl phosphatidylinositol anchor biosynthesis, in cell lines established from patients with paroxysmal nocturnal hemoglobinuria. J Exp Med 177:517, 1993.
-
(1993)
J Exp Med
, vol.177
, pp. 517
-
-
Takahashi, M.1
Takeda, J.2
Hirose, S.3
-
40
-
-
0028123686
-
Glycosyl-phosphatidylinositol anchor synthesis in paroxysmal nocturnal hemoglobinuria: Partial or complete defect in an early step
-
Norris J, Sharon H, Ware RE, et al.: Glycosyl-phosphatidylinositol anchor synthesis in paroxysmal nocturnal hemoglobinuria: Partial or complete defect in an early step. Blood 83:816, 1994.
-
(1994)
Blood
, vol.83
, pp. 816
-
-
Norris, J.1
Sharon, H.2
Ware, R.E.3
-
41
-
-
0027412627
-
The cloning of PIG-A, a component in the early step of GPI-anchor biosynthesis
-
Miyata T, Takeda J, Iida Y, et al.: The cloning of PIG-A, a component in the early step of GPI-anchor biosynthesis. Science 259:1318, 1993.
-
(1993)
Science
, vol.259
, pp. 1318
-
-
Miyata, T.1
Takeda, J.2
Iida, Y.3
-
42
-
-
0027310539
-
Deficiency of the GPI anchor caused by a somatic mutation of the PIG-A gene in paroxysmal nocturnal hemoglobinuria
-
Takeda J, Miyata T, Kawagoe K, et al.: Deficiency of the GPI anchor caused by a somatic mutation of the PIG-A gene in paroxysmal nocturnal hemoglobinuria. Cell 73:703, 1993.
-
(1993)
Cell
, vol.73
, pp. 703
-
-
Takeda, J.1
Miyata, T.2
Kawagoe, K.3
-
43
-
-
0028057618
-
Abnormalities of PIG-A transcripts in granulocytes from patients with paroxysmal nocturnal hemoglobinuria
-
Miyata T, Yamada N, Iida Y, et al.: Abnormalities of PIG-A transcripts in granulocytes from patients with paroxysmal nocturnal hemoglobinuria. N Engl J Med 330:249, 1994.
-
(1994)
N Engl J Med
, vol.330
, pp. 249
-
-
Miyata, T.1
Yamada, N.2
Iida, Y.3
-
44
-
-
0027309010
-
Paroxysmal nocturnal hemoglobinuria: Correction of abnormal phenotype by somatic cell hybridization
-
Hillmen P, Bessler M, Bungey J, Luzzatto L: Paroxysmal nocturnal hemoglobinuria: Correction of abnormal phenotype by somatic cell hybridization. Somat Cell Mol Genet 19:123, 1993.
-
(1993)
Somat Cell Mol Genet
, vol.19
, pp. 123
-
-
Hillmen, P.1
Bessler, M.2
Bungey, J.3
Luzzatto, L.4
-
45
-
-
0028057807
-
Paroxysmal nocturnal haemoglobinuria (PNH) is caused by somatic mutations in the PIG-A gene
-
Bessler M, Mason PJ, Hillmen P, et al.: Paroxysmal nocturnal haemoglobinuria (PNH) is caused by somatic mutations in the PIG-A gene. EMBO J 13:110, 1994.
-
(1994)
EMBO J
, vol.13
, pp. 110
-
-
Bessler, M.1
Mason, P.J.2
Hillmen, P.3
-
46
-
-
0028353422
-
Mutations within the Piga gene in patients with paroxysmal nocturnal hemoglobinuria
-
Ware RE, Rosse WF, Howard TA: Mutations within the Piga gene in patients with paroxysmal nocturnal hemoglobinuria. Blood 83:2418, 1994.
-
(1994)
Blood
, vol.83
, pp. 2418
-
-
Ware, R.E.1
Rosse, W.F.2
Howard, T.A.3
-
47
-
-
0029163277
-
Somatic mutations of PIG-A in Thai patients with paroxysmal nocturnal hemoglobinuria
-
Pramoonjago P, Wanachiwanawin W, Chinprasertsak S, Pattanapanayasat K, Takeda J, Kinoshita T: Somatic mutations of PIG-A in Thai patients with paroxysmal nocturnal hemoglobinuria. Blood 86:1736, 1995.
-
(1995)
Blood
, vol.86
, pp. 1736
-
-
Pramoonjago, P.1
Wanachiwanawin, W.2
Chinprasertsak, S.3
Pattanapanayasat, K.4
Takeda, J.5
Kinoshita, T.6
-
48
-
-
0028885951
-
Mutations in the PIG-A gene causing paroxysmal nocturnal hemoglobinuria are mainly of the frameshift type
-
Nafa K, Mason PJ, Hillmen P, Luzzatto L, Bessler M: Mutations in the PIG-A gene causing paroxysmal nocturnal hemoglobinuria are mainly of the frameshift type. Blood 86:4650, 1995.
-
(1995)
Blood
, vol.86
, pp. 4650
-
-
Nafa, K.1
Mason, P.J.2
Hillmen, P.3
Luzzatto, L.4
Bessler, M.5
-
49
-
-
0028299834
-
Somatic mutations and cellular selection in paroxysmal nocturnal haemoglobinuria
-
Bessler M, Mason P, Hillmen P, Luzzatto L: Somatic mutations and cellular selection in paroxysmal nocturnal haemoglobinuria. Lancet 343:951, 1994.
-
(1994)
Lancet
, vol.343
, pp. 951
-
-
Bessler, M.1
Mason, P.2
Hillmen, P.3
Luzzatto, L.4
-
50
-
-
0025326911
-
Altered expression of gangliosides in erythrocytes of paroxysmal nocturnal hemoglobinuria
-
Nakakuma H, Kawaguchi T, Horikawa K, et al.: Altered expression of gangliosides in erythrocytes of paroxysmal nocturnal hemoglobinuria. J Clin Invest 85:1456, 1990.
-
(1990)
J Clin Invest
, vol.85
, pp. 1456
-
-
Nakakuma, H.1
Kawaguchi, T.2
Horikawa, K.3
-
51
-
-
0021271683
-
Abnormality of glycophorin-α on paroxysmal nocturnal hemoglobinuria erythrocytes
-
Parker CJ, Soldato CM, Rosse WF: Abnormality of glycophorin-α on paroxysmal nocturnal hemoglobinuria erythrocytes. J Clin Invest 73:1130, 1984.
-
(1984)
J Clin Invest
, vol.73
, pp. 1130
-
-
Parker, C.J.1
Soldato, C.M.2
Rosse, W.F.3
-
52
-
-
0026785442
-
Review: Polyagglutination
-
Judd WJ, Review: Polyagglutination. Immunohematology 8:58, 1992.
-
(1992)
Immunohematology
, vol.8
, pp. 58
-
-
Judd, W.J.1
-
53
-
-
0025720753
-
Hemolysis of human erythrocytes is a new bioactivity of gangliosides
-
Horikawa K, Nakakuma H, Nagakura S, et al.: Hemolysis of human erythrocytes is a new bioactivity of gangliosides. J Exp Med 174:1385, 1991.
-
(1991)
J Exp Med
, vol.174
, pp. 1385
-
-
Horikawa, K.1
Nakakuma, H.2
Nagakura, S.3
-
54
-
-
0029092765
-
Expression of cryptantigen Th on paroxysmal nocturnal hemoglobinuria erythrocytes in association with a hemolytic exacerbation
-
Nakakuma H, Hidaka M, Nagakura S, et al.: Expression of cryptantigen Th on paroxysmal nocturnal hemoglobinuria erythrocytes in association with a hemolytic exacerbation. J Clin Invest 96:201, 1995.
-
(1995)
J Clin Invest
, vol.96
, pp. 201
-
-
Nakakuma, H.1
Hidaka, M.2
Nagakura, S.3
-
55
-
-
0002676667
-
The auto-immune haemolytic anaemias
-
Dacie J (ed): Edinburgh: Churchill Livingstone
-
Dacie J: The auto-immune haemolytic anaemias. In Dacie J (ed): "The Haemolytic Anaemias." Ed 3. Vol 3. Edinburgh: Churchill Livingstone, 1992, pp 1-528.
-
(1992)
"The Haemolytic Anaemias." Ed 3
, vol.3
, pp. 1-528
-
-
Dacie, J.1
-
56
-
-
23444456730
-
Haemolysis induced by ascorbic acid in paroxysmal nocturnal hemoglobinuria
-
Iwamoto N, Kawaguchi T, Horikawa K, et al.: Haemolysis induced by ascorbic acid in paroxysmal nocturnal hemoglobinuria. Lancet 343:357, 1994.
-
(1994)
Lancet
, vol.343
, pp. 357
-
-
Iwamoto, N.1
Kawaguchi, T.2
Horikawa, K.3
-
57
-
-
0028295447
-
Development of the glycosylphosphatidylinositol-anchoring defect characteristic for paroxysmal nocturnal hemoglobinuria in patients with aplastic anemia
-
Schubert J, Vogt HG, Zielinska-Skowronek M, et al.: Development of the glycosylphosphatidylinositol-anchoring defect characteristic for paroxysmal nocturnal hemoglobinuria in patients with aplastic anemia. Blood 83:2323, 1994.
-
(1994)
Blood
, vol.83
, pp. 2323
-
-
Schubert, J.1
Vogt, H.G.2
Zielinska-Skowronek, M.3
-
58
-
-
0026596863
-
The problem of clonality in aplastic anemia: Dr. Dameshek's riddle, restated
-
Young NS: The problem of clonality in aplastic anemia: Dr. Dameshek's riddle, restated. Blood 79:1385, 1992.
-
(1992)
Blood
, vol.79
, pp. 1385
-
-
Young, N.S.1
-
59
-
-
0028911097
-
PIG-A, DAF and proto-oncogene expression in paroxysmal nocturnal haemoglobinuria-associated acute myelogeneous leukaemia blasts
-
Stafford HA, Nagarajan S, Weinberg JB, Medof ME: PIG-A, DAF and proto-oncogene expression in paroxysmal nocturnal haemoglobinuria-associated acute myelogeneous leukaemia blasts. Br J Haematol 89:72, 1995.
-
(1995)
Br J Haematol
, vol.89
, pp. 72
-
-
Stafford, H.A.1
Nagarajan, S.2
Weinberg, J.B.3
Medof, M.E.4
-
60
-
-
0026557778
-
The receptor for urokinase-type plasminogen activator is deficient on peripheral blood leukocytes in patients with paroxysmal nocturnal hemoglobinuria
-
Ploug M, Plesner T, Rønne E, et al.: The receptor for urokinase-type plasminogen activator is deficient on peripheral blood leukocytes in patients with paroxysmal nocturnal hemoglobinuria. Blood 79:1447, 1992.
-
(1992)
Blood
, vol.79
, pp. 1447
-
-
Ploug, M.1
Plesner, T.2
Rønne, E.3
-
61
-
-
0023687039
-
The monocyte differentiation antigen, CD 14, is anchored to the cell membrane by a phosphatidylinositol linkage
-
Haziot A, Chen S, Ferrero E, Low MG, Silber R, Goyert SM: The monocyte differentiation antigen, CD 14, is anchored to the cell membrane by a phosphatidylinositol linkage. J Immunol 141:547, 1988.
-
(1988)
J Immunol
, vol.141
, pp. 547
-
-
Haziot, A.1
Chen, S.2
Ferrero, E.3
Low, M.G.4
Silber, R.5
Goyert, S.M.6
-
62
-
-
0024282583
-
The major Fc receptor in blood has a phosphatidylinositol anchor and is deficient in paroxysmal nocturnal hemoglobinuria
-
Selvaraj P, Rosse WF, Silber R, Springer TA: The major Fc receptor in blood has a phosphatidylinositol anchor and is deficient in paroxysmal nocturnal hemoglobinuria. Nature 333:565, 1988.
-
(1988)
Nature
, vol.333
, pp. 565
-
-
Selvaraj, P.1
Rosse, W.F.2
Silber, R.3
Springer, T.A.4
-
63
-
-
0001245835
-
Paroxysmal nocturnal hemoglobinuria. II. Erythrocyte acetylcholinesterase defect
-
Auditore JV, Hartmann RC: Paroxysmal nocturnal hemoglobinuria. II. Erythrocyte acetylcholinesterase defect. Am J Med 27:401, 1959.
-
(1959)
Am J Med
, vol.27
, pp. 401
-
-
Auditore, J.V.1
Hartmann, R.C.2
-
64
-
-
0000982629
-
Biochemical studies on leucocytes. II. Phosphatase activity in chronic lymphatic leucemia, acute leucemia, and miscellaneous hematologic conditions
-
Beck WS, Valentine WN: Biochemical studies on leucocytes. II. Phosphatase activity in chronic lymphatic leucemia, acute leucemia, and miscellaneous hematologic conditions. J Lab Clin Med 38:245, 1951.
-
(1951)
J Lab Clin Med
, vol.38
, pp. 245
-
-
Beck, W.S.1
Valentine, W.N.2
-
65
-
-
0025945826
-
Diagnosis of paroxysmal nocturnal hemoglobinuria using immunophenotyping of peripheral blood cells
-
Schubert J, Alvarado M, Uciechowski P, et al.: Diagnosis of paroxysmal nocturnal hemoglobinuria using immunophenotyping of peripheral blood cells. Br J Haematol 79:487, 1991.
-
(1991)
Br J Haematol
, vol.79
, pp. 487
-
-
Schubert, J.1
Alvarado, M.2
Uciechowski, P.3
-
66
-
-
0027138872
-
A deficiency in CDw52 (Campath-1 antigen) of paroxysmal nocturnal hemoglobinuria lymphocytes
-
Nagakura S, Kawaguchi T, Horikawa K, et al.: A deficiency in CDw52 (Campath-1 antigen) of paroxysmal nocturnal hemoglobinuria lymphocytes. Blood 82:3790, 1993.
-
(1993)
Blood
, vol.82
, pp. 3790
-
-
Nagakura, S.1
Kawaguchi, T.2
Horikawa, K.3
-
67
-
-
0023578991
-
Deficiency of lymphocyte function-associated antigen 3 (LFA-3) in paroxysmal nocturnal hemoglobinuria. Functional correlates and evidence for a phosphatidylinositol membrane anchor
-
Selvaraj P, Dustin ML, Silber R, Low MG, Springer TA: Deficiency of lymphocyte function-associated antigen 3 (LFA-3) in paroxysmal nocturnal hemoglobinuria. Functional correlates and evidence for a phosphatidylinositol membrane anchor. J Exp Med 166:1011, 1987.
-
(1987)
J Exp Med
, vol.166
, pp. 1011
-
-
Selvaraj, P.1
Dustin, M.L.2
Silber, R.3
Low, M.G.4
Springer, T.A.5
-
68
-
-
0027458428
-
Antibody By114 is selective for the 90 kD PI-linked component of the CD66 antigen: A new reagent for the study of paroxysmal nocturnal haemoglobinuria
-
Mayne KM, Pulford K, Jones M, et al.: Antibody By114 is selective for the 90 kD PI-linked component of the CD66 antigen: A new reagent for the study of paroxysmal nocturnal haemoglobinuria. Br J Haematol 83:30, 1993.
-
(1993)
Br J Haematol
, vol.83
, pp. 30
-
-
Mayne, K.M.1
Pulford, K.2
Jones, M.3
-
69
-
-
0026513379
-
Isolation of the JMH antigen on a novel phosphatidylinositol-linked human membrane protein
-
Bobolis KA, Moulds JJ, Telen MJ: Isolation of the JMH antigen on a novel phosphatidylinositol-linked human membrane protein. Blood 79:1574, 1992.
-
(1992)
Blood
, vol.79
, pp. 1574
-
-
Bobolis, K.A.1
Moulds, J.J.2
Telen, M.J.3
-
70
-
-
0026652116
-
The biological chemistry of folate receptors
-
Antony A: The biological chemistry of folate receptors. Blood 79: 2807, 1992.
-
(1992)
Blood
, vol.79
, pp. 2807
-
-
Antony, A.1
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