-
1
-
-
0028884057
-
The molecular basis of paroxysmal nocturnal hemoglobinuria
-
Rosse WF, Ware RE. The molecular basis of paroxysmal nocturnal hemoglobinuria. Blood. 1995;86:3277-3286.
-
(1995)
Blood
, vol.86
, pp. 3277-3286
-
-
Rosse, W.F.1
Ware, R.E.2
-
2
-
-
0037800971
-
Affected erythrocytes of patients with paroxysmal nocturnal hemoglobinuria are deficient in the complement regulatory protein, decay accelerating factor
-
Nicholson-Weller A, March JP, Rosenfeld SI, Austen KF. Affected erythrocytes of patients with paroxysmal nocturnal hemoglobinuria are deficient in the complement regulatory protein, decay accelerating factor. Proc Natl Acad Sci U S A. 1983;80:5066-5070.
-
(1983)
Proc Natl Acad Sci U S A
, vol.80
, pp. 5066-5070
-
-
Nicholson-Weller, A.1
March, J.P.2
Rosenfeld, S.I.3
Austen, K.F.4
-
3
-
-
0025774079
-
Heterogeneous expression of decay accelerating factor and CD59/membrane attack complex inhibition factor on paroxysmal nocturnal haemoglobinuria (PNH) erythrocytes
-
Shichishima T, Terasawa T, Hashimoto C, Ohto H, Uchida T, Maruyama Y. Heterogeneous expression of decay accelerating factor and CD59/membrane attack complex inhibition factor on paroxysmal nocturnal haemoglobinuria (PNH) erythrocytes. Br J Haematol. 1991;78:545-550.
-
(1991)
Br J Haematol
, vol.78
, pp. 545-550
-
-
Shichishima, T.1
Terasawa, T.2
Hashimoto, C.3
Ohto, H.4
Uchida, T.5
Maruyama, Y.6
-
4
-
-
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. 1992;79:1385-1392.
-
(1992)
Blood
, vol.79
, pp. 1385-1392
-
-
Young, N.S.1
-
5
-
-
0029873584
-
Glycosylphosphatidylinositol-anchor-deficient mice: Implications for clonal dominance of mutant cells in paroxysmal nocturnal hemoglobinuria
-
Kawagoe K, Kitamura D, Okabe M, et al. Glycosylphosphatidylinositol-anchor-deficient mice: implications for clonal dominance of mutant cells in paroxysmal nocturnal hemoglobinuria. Blood. 1996;87:3600-3606.
-
(1996)
Blood
, vol.87
, pp. 3600-3606
-
-
Kawagoe, K.1
Kitamura, D.2
Okabe, M.3
-
6
-
-
0030739941
-
Resistance to apoptosis caused by PIG-A gene mutations in paroxysmal nocturnal hemoglobinuria
-
Brodsky RA, Vala MS, Barber JP, Medof ME, Jones RJ. Resistance to apoptosis caused by PIG-A gene mutations in paroxysmal nocturnal hemoglobinuria. Proc Natl Acad Sci U S A. 1997;94:8756-8760.
-
(1997)
Proc Natl Acad Sci U S A
, vol.94
, pp. 8756-8760
-
-
Brodsky, R.A.1
Vala, M.S.2
Barber, J.P.3
Medof, M.E.4
Jones, R.J.5
-
7
-
-
0033377512
-
Cytotoxicity against lymphoblastoid cells mediated by a T-cell clone from an aplastic anaemia patient: Role of CD59 on target cells
-
Takami A, Zang W, Wang H, Matsuda T, Nakao S. Cytotoxicity against lymphoblastoid cells mediated by a T-cell clone from an aplastic anaemia patient: role of CD59 on target cells. Br J Haematol. 1999;107:791-796.
-
(1999)
Br J Haematol
, vol.107
, pp. 791-796
-
-
Takami, A.1
Zang, W.2
Wang, H.3
Matsuda, T.4
Nakao, S.5
-
8
-
-
0034113617
-
HSP 70 stimulates cytokine production through a CD14-dependent pathway, demonstrating its dual role as a chaperone and cytokine
-
Asea A, Kraeft S-K, Kurt-Jones EA, et al. HSP 70 stimulates cytokine production through a CD14-dependent pathway, demonstrating its dual role as a chaperone and cytokine. Nat Med. 2000;6:435-442.
-
(2000)
Nat Med
, vol.6
, pp. 435-442
-
-
Asea, A.1
Kraeft, S.-K.2
Kurt-Jones, E.A.3
-
9
-
-
0034307521
-
Abnormal T-cell repertoire is consistent with immune process underlying the pathogenesis of paroxysmal nocturnal hemoglobinuria
-
Karadimitris A, Manavalan JS, Thaler HT, et al. Abnormal T-cell repertoire is consistent with immune process underlying the pathogenesis of paroxysmal nocturnal hemoglobinuria. Blood. 2000;96:2613-2620.
-
(2000)
Blood
, vol.96
, pp. 2613-2620
-
-
Karadimitris, A.1
Manavalan, J.S.2
Thaler, H.T.3
-
10
-
-
0032836138
-
Defective TCR signaling events in glycosylphosphatidylinositol-deficient T cells derived from paroxysmal nocturnal hemoglobinuria patients
-
Romagnoli P, Bron C. Defective TCR signaling events in glycosylphosphatidylinositol-deficient T cells derived from paroxysmal nocturnal hemoglobinuria patients. Int Immunol. 1999;11:1411-1422.
-
(1999)
Int Immunol
, vol.11
, pp. 1411-1422
-
-
Romagnoli, P.1
Bron, C.2
-
11
-
-
0033819055
-
Genetic and environmental effects in paroxysmal nocturnal hemoglobinuria: This little PIG-A goes "Why? Why? Why?"
-
Young NS, Maciejewski JP. Genetic and environmental effects in paroxysmal nocturnal hemoglobinuria: this little PIG-A goes "Why? Why? Why?" J Clin Invest. 2000;106:637-641.
-
(2000)
J Clin Invest
, vol.106
, pp. 637-641
-
-
Young, N.S.1
Maciejewski, J.P.2
-
12
-
-
0030822192
-
Apoptosis resistance of blood cells from patients with paroxysmal nocturnal hemoglobinuria, aplastic anemia, and myelodysplastic syndrome
-
Horikawa K, Nakakuma H, Kawaguchi T, et al. Apoptosis resistance of blood cells from patients with paroxysmal nocturnal hemoglobinuria, aplastic anemia, and myelodysplastic syndrome. Blood. 1997;90:2716-2722.
-
(1997)
Blood
, vol.90
, pp. 2716-2722
-
-
Horikawa, K.1
Nakakuma, H.2
Kawaguchi, T.3
-
13
-
-
0032189025
-
The PIG-A mutation and absence of glycosylphosphatidylinositol-linked proteins do not confer resistance to apoptosis in paroxysmal nocturnal hemoglobinuria
-
Ware RE, Nishimura J, Moody MA, Smith C, Rosse WF, Howard TA. The PIG-A mutation and absence of glycosylphosphatidylinositol-linked proteins do not confer resistance to apoptosis in paroxysmal nocturnal hemoglobinuria. Blood. 1998;92:2541-2550.
-
(1998)
Blood
, vol.92
, pp. 2541-2550
-
-
Ware, R.E.1
Nishimura, J.2
Moody, M.A.3
Smith, C.4
Rosse, W.F.5
Howard, T.A.6
-
14
-
-
0030921456
-
Relationship between the phenotypes of circulating erythrocytes and cultured erythroblasts in paroxysmal nocturnal hemoglobinuria
-
Shichishima T, Saitoh Y, Terasawa T, Ogawa K, Maruyama Y. Relationship between the phenotypes of circulating erythrocytes and cultured erythroblasts in paroxysmal nocturnal hemoglobinuria. Blood. 1997;90:435-443.
-
(1997)
Blood
, vol.90
, pp. 435-443
-
-
Shichishima, T.1
Saitoh, Y.2
Terasawa, T.3
Ogawa, K.4
Maruyama, Y.5
-
15
-
-
0029824262
-
- hematopoiesis is reconstituted following intercellular transfer of GPI-anchored proteins
-
- hematopoiesis is reconstituted following intercellular transfer of GPI-anchored proteins. Proc Natl Acad Sci U S A. 1996;93:7938-7943.
-
(1996)
Proc Natl Acad Sci U S A
, vol.93
, pp. 7938-7943
-
-
Dunn, D.E.1
Yu, J.2
Nagarajan, S.3
-
16
-
-
0014060844
-
The aplastic anaemia-paroxysmal nocturnal haemoglobinuria syndrome
-
Lewis SM, Dacie JV. The aplastic anaemia-paroxysmal nocturnal haemoglobinuria syndrome. Br J Haematol. 1967;13:236-251.
-
(1967)
Br J Haematol
, vol.13
, pp. 236-251
-
-
Lewis, S.M.1
Dacie, J.V.2
-
17
-
-
0028802443
-
Natural history of paroxysmal nocturnal hemoglobinuria
-
Hillmen P, Lewis SM, Bessler M, Luzzatto L, Dacie JV. Natural history of paroxysmal nocturnal hemoglobinuria. N Engl J Med. 1995;333:1253-1258.
-
(1995)
N Engl J Med
, vol.333
, pp. 1253-1258
-
-
Hillmen, P.1
Lewis, S.M.2
Bessler, M.3
Luzzatto, L.4
Dacie, J.V.5
-
18
-
-
16044365965
-
Paroxysmal nocturnal hemoglobinuria: Long-term follow-up and prognostic factors
-
Socié G, Mary J-Y, de Gramont A, et al. Paroxysmal nocturnal hemoglobinuria: long-term follow-up and prognostic factors. Lancet. 1996;348:573-577.
-
(1996)
Lancet
, vol.348
, pp. 573-577
-
-
Socié, G.1
Mary, J.-Y.2
De Gramont, A.3
-
19
-
-
0024804936
-
Prognostic features of paroxysmal nocturnal hemoglobinuria in Japan
-
Fujioka S, Asai T. Prognostic features of paroxysmal nocturnal hemoglobinuria in Japan. Nippon Ketsueki Gakkai Zasshi. 1989;52:1386-1394.
-
(1989)
Nippon Ketsueki Gakkai Zasshi
, vol.52
, pp. 1386-1394
-
-
Fujioka, S.1
Asai, T.2
-
20
-
-
0023789856
-
Late haematological complications in severe aplastic anaemia
-
Tichelli A, Gratwohl A, Wursch A, Nissen C, Speck B. Late haematological complications in severe aplastic anaemia. Br J Haematol. 1988;69:413-418.
-
(1988)
Br J Haematol
, vol.69
, pp. 413-418
-
-
Tichelli, A.1
Gratwohl, A.2
Wursch, A.3
Nissen, C.4
Speck, B.5
-
21
-
-
0024269782
-
A multicenter trial of antithymocyte globulin in aplastic anemia and related diseases
-
Young N, Griffith P, Brittain E, et al. A multicenter trial of antithymocyte globulin in aplastic anemia and related diseases. Blood. 1988;72:1861-1869.
-
(1988)
Blood
, vol.72
, pp. 1861-1869
-
-
Young, N.1
Griffith, P.2
Brittain, E.3
-
22
-
-
0025999919
-
Paroxysmal nocturnal hemoglobinuria with onset in childhood and adolescence
-
Ware RE, Hall SE, Rosse WF. Paroxysmal nocturnal hemoglobinuria with onset in childhood and adolescence. N Engl J Med. 1991;325:991-996.
-
(1991)
N Engl J Med
, vol.325
, pp. 991-996
-
-
Ware, R.E.1
Hall, S.E.2
Rosse, W.F.3
-
23
-
-
0025269632
-
Does HLA-DR predict response to specific immunosuppressive therapy in aplastic anaemia?
-
letter
-
Rugman FP, Ashby D, Davies JM, Does HLA-DR predict response to specific immunosuppressive therapy in aplastic anaemia? [letter]. Br J Haematol. 1990;74:545-546.
-
(1990)
Br J Haematol
, vol.74
, pp. 545-546
-
-
Rugman, F.P.1
Ashby, D.2
Davies, J.M.3
-
24
-
-
0026691343
-
HLA-DR2 predicts a favorable response to cyclosporin therapy in patients with bone marrow failure
-
Nakao S, Yamaguchi M, Saito M, et al. HLA-DR2 predicts a favorable response to cyclosporin therapy in patients with bone marrow failure [letter]. Am J Hematol. 1992;40:239-240.
-
(1992)
Am J Hematol
, vol.40
, pp. 239-240
-
-
Nakao, S.1
Yamaguchi, M.2
Saito, M.3
-
25
-
-
0022624147
-
Increased frequency of DR2 in patients with aplastic anaemia and increased DR sharing in their parents
-
Chapuis B, von Fliedner M, Merica JH, et al. Increased frequency of DR2 in patients with aplastic anaemia and increased DR sharing in their parents. Br J Haematol. 1986;63:51-57.
-
(1986)
Br J Haematol
, vol.63
, pp. 51-57
-
-
Chapuis, B.1
Von Fliedner, M.2
Merica, J.H.3
-
26
-
-
0028335812
-
An increased HLA DR2 frequency is seen in aplastic anemia patients
-
Nimer SD, Ireland P, Meshkinpour A, Frane M. An increased HLA DR2 frequency is seen in aplastic anemia patients. Blood. 1994;84:923-927.
-
(1994)
Blood
, vol.84
, pp. 923-927
-
-
Nimer, S.D.1
Ireland, P.2
Meshkinpour, A.3
Frane, M.4
-
27
-
-
0034199513
-
Aplastic anemia is associated with HLA-DRB1*1501 in northern Han Chinese
-
Shao W, Tian D, Liu C, Sun X, Zhang X. Aplastic anemia is associated with HLA-DRB1*1501 in northern Han Chinese. Int J Hematol. 2000;71:350-352.
-
(2000)
Int J Hematol
, vol.71
, pp. 350-352
-
-
Shao, W.1
Tian, D.2
Liu, C.3
Sun, X.4
Zhang, X.5
-
29
-
-
0018899359
-
HLA antigens in paroxysmal nocturnal hemoglobinuria
-
Ustariz CR, Aree S, Hernández P, Almaguer M, Perez S, Ballester JM. HLA antigens in paroxysmal nocturnal hemoglobinuria. Acta Haematol. 1980;63:52-54.
-
(1980)
Acta Haematol
, vol.63
, pp. 52-54
-
-
Ustariz, C.R.1
Aree, S.2
Hernández, P.3
Almaguer, M.4
Perez, S.5
Ballester, J.M.6
-
30
-
-
0034793917
-
Limited heterogeneity of T cell receptor BV usage in aplastic anemia
-
Zeng W, Maciejewski JP, Chen G, Young NS. Limited heterogeneity of T cell receptor BV usage in aplastic anemia. J Clin Invest. 2001;108:765-773.
-
(2001)
J Clin Invest
, vol.108
, pp. 765-773
-
-
Zeng, W.1
Maciejewski, J.P.2
Chen, G.3
Young, N.S.4
-
32
-
-
0025099787
-
Isolation and characterization of a zinc finger polypeptide gene at the human chromosome 11 Wilms' tumor locus
-
Call KM, Glaser T, Ito CY, et al. Isolation and characterization of a zinc finger polypeptide gene at the human chromosome 11 Wilms' tumor locus. Cell. 1990;60:509-520.
-
(1990)
Cell
, vol.60
, pp. 509-520
-
-
Call, K.M.1
Glaser, T.2
Ito, C.Y.3
-
33
-
-
0030035437
-
Expression pattern of WT1 and GATA-1 in AML with chromosome 16q22 abnormalities
-
Patmasiriwat P, Faizer GC, Claxton D, Kantarjian H, Saunders GF. Expression pattern of WT1 and GATA-1 in AML with chromosome 16q22 abnormalities. Leukemia. 1996;10:1127-1133.
-
(1996)
Leukemia
, vol.10
, pp. 1127-1133
-
-
Patmasiriwat, P.1
Faizer, G.C.2
Claxton, D.3
Kantarjian, H.4
Saunders, G.F.5
-
34
-
-
0031010990
-
Expression of the Wilms' tumor gene (WT1) in normal hematopoiesis
-
Baird PN, Simmonds PJ. Expression of the Wilms' tumor gene (WT1) in normal hematopoiesis. Exp Hematol. 1997;25:312-320.
-
(1997)
Exp Hematol
, vol.25
, pp. 312-320
-
-
Baird, P.N.1
Simmonds, P.J.2
-
35
-
-
0031135108
-
+ hematopoietic progenitors during fetal development and early clonogenic growth
-
+ hematopoietic progenitors during fetal development and early clonogenic growth [letter]. Blood. 1997;89:3486-3487.
-
(1997)
Blood
, vol.89
, pp. 3486-3487
-
-
Menssen, H.D.1
Renkl, H.-J.2
Entezami, M.3
Thiel, E.4
-
36
-
-
0027054125
-
The expression of the Wilms' tumor gene, WT1, in the developing mammalian embryo
-
Armstrong JF, Pritchard-Jones K, Bickmore WA, Hastie ND, Bard JB. The expression of the Wilms' tumor gene, WT1, in the developing mammalian embryo. Mech Dev. 1993;40:85-97.
-
(1993)
Mech Dev
, vol.40
, pp. 85-97
-
-
Armstrong, J.F.1
Pritchard-Jones, K.2
Bickmore, W.A.3
Hastie, N.D.4
Bard, J.B.5
-
37
-
-
0027161785
-
Physical and functional interaction between WT1 and p53 proteins
-
Maheswaran S, Park S, Bernard A, et al. Physical and functional interaction between WT1 and p53 proteins. Proc Natl Acad Sci U S A. 1993;90:5100-5104.
-
(1993)
Proc Natl Acad Sci U S A
, vol.90
, pp. 5100-5104
-
-
Maheswaran, S.1
Park, S.2
Bernard, A.3
-
38
-
-
10544225383
-
A novel repressor, par-4, modulates transcription and growth suppression functions of the Wilms' tumor suppressor WT1
-
Johnstone RW, See RH, Sells SF, et al. A novel repressor, par-4, modulates transcription and growth suppression functions of the Wilms' tumor suppressor WT1. Mol Cell Biol. 1996;16:6945-6956.
-
(1996)
Mol Cell Biol
, vol.16
, pp. 6945-6956
-
-
Johnstone, R.W.1
See, R.H.2
Sells, S.F.3
-
39
-
-
0032080221
-
Ciao 1 is a novel WD40 protein that interacts with the tumor suppressor protein WT1
-
Johnstone RW, Wang J, Tommerup N, Vissing H, Roberts T, Shi Y. Ciao 1 is a novel WD40 protein that interacts with the tumor suppressor protein WT1. J Biol Chem. 1998;273:10880-10887.
-
(1998)
J Biol Chem
, vol.273
, pp. 10880-10887
-
-
Johnstone, R.W.1
Wang, J.2
Tommerup, N.3
Vissing, H.4
Roberts, T.5
Shi, Y.6
-
40
-
-
0034112824
-
Human cytotoxic T-lymphocyte responses specific for peptides of wild-type Wilms' tumor gene WT1 product
-
Oka Y, Elisseeva OA, Tsuboi A, et al. Human cytotoxic T-lymphocyte responses specific for peptides of wild-type Wilms' tumor gene WT1 product. Immunogenetics. 2000;51:99-107.
-
(2000)
Immunogenetics
, vol.51
, pp. 99-107
-
-
Oka, Y.1
Elisseeva, O.A.2
Tsuboi, A.3
-
41
-
-
0034176750
-
Selective elimination of leukemic CD34 (+) progenitor cells by cytotoxic T lymphocytes specific for WT1
-
Gao L, Bellantuono I, Elsasser A, et al. Selective elimination of leukemic CD34 (+) progenitor cells by cytotoxic T lymphocytes specific for WT1. Blood. 2000;95:2198-2203.
-
(2000)
Blood
, vol.95
, pp. 2198-2203
-
-
Gao, L.1
Bellantuono, I.2
Elsasser, A.3
-
42
-
-
0033966369
-
HLA class I-restricted lysis of leukemia cells by a CD8 (+) cytotoxic T-lymphocyte clone specific for WT1 peptide
-
Ohminami H, Yasukawa M, Fujita S, et al. HLA class I-restricted lysis of leukemia cells by a CD8 (+) cytotoxic T-lymphocyte clone specific for WT1 peptide. Blood. 2000;95:286-293.
-
(2000)
Blood
, vol.95
, pp. 286-293
-
-
Ohminami, H.1
Yasukawa, M.2
Fujita, S.3
-
43
-
-
0034663331
-
Immunity to WT1 in the animal model and in patients with acute myeloid leukemia
-
Gaiger A, Reese V, Disis ML, Cheever MA. Immunity to WT1 in the animal model and in patients with acute myeloid leukemia. Blood. 2000;96:1480-1489.
-
(2000)
Blood
, vol.96
, pp. 1480-1489
-
-
Gaiger, A.1
Reese, V.2
Disis, M.L.3
Cheever, M.A.4
-
44
-
-
0028130136
-
WT1 as a new prognostic factor and a new marker for the detection of minimal residual disease in acute leukemia
-
Inoue K, Sugiyama H, Ogawa H, et al. WT1 as a new prognostic factor and a new marker for the detection of minimal residual disease in acute leukemia. Blood. 1994;84:3071-3079.
-
(1994)
Blood
, vol.84
, pp. 3071-3079
-
-
Inoue, K.1
Sugiyama, H.2
Ogawa, H.3
-
45
-
-
0030997045
-
Detection by monoclonal antibodies of the Wilms' tumor (WT1) nuclear protein in patients with acute leukemia
-
Messen HD, Renkl HJ, Rodeck U, Kari C, Schwartz S, Thiel E. Detection by monoclonal antibodies of the Wilms' tumor (WT1) nuclear protein in patients with acute leukemia. Int J Cancer. 1997;70:518-523.
-
(1997)
Int J Cancer
, vol.70
, pp. 518-523
-
-
Messen, H.D.1
Renkl, H.J.2
Rodeck, U.3
Kari, C.4
Schwartz, S.5
Thiel, E.6
-
46
-
-
0033049268
-
The Wilms' tumor gene WT1 is a good marker for diagnosis of disease progression of myelodysplastic syndromes
-
Tamaki H, Ogawa H, Ohyashiki K, et al. The Wilms' tumor gene WT1 is a good marker for diagnosis of disease progression of myelodysplastic syndromes. Leukemia. 1999;13:393-399.
-
(1999)
Leukemia
, vol.13
, pp. 393-399
-
-
Tamaki, H.1
Ogawa, H.2
Ohyashiki, K.3
-
47
-
-
0027380002
-
Diagnosis of paroxysmal nocturnal haemoglobinuria by phenotypic analysis of erythrocytes using two-colour flow cytometry with monoclonal antibodies to DAF and CD59/MACIF
-
Shichishima T, Terasawa T, Saitoh Y, Hashimoto C, Ohto H, Maruyama Y. Diagnosis of paroxysmal nocturnal haemoglobinuria by phenotypic analysis of erythrocytes using two-colour flow cytometry with monoclonal antibodies to DAF and CD59/MACIF. Br J Haematol. 1993;85:378-386.
-
(1993)
Br J Haematol
, vol.85
, pp. 378-386
-
-
Shichishima, T.1
Terasawa, T.2
Saitoh, Y.3
Hashimoto, C.4
Ohto, H.5
Maruyama, Y.6
-
48
-
-
0029981029
-
The use of monoclonal antibodies and flow cytometry in the diagnosis of paroxysmal nocturnal hemoglobinuria
-
Hall SE, Rosse WF. The use of monoclonal antibodies and flow cytometry in the diagnosis of paroxysmal nocturnal hemoglobinuria. Blood. 1996; 87:5332-5340.
-
(1996)
Blood
, vol.87
, pp. 5332-5340
-
-
Hall, S.E.1
Rosse, W.F.2
-
49
-
-
0017162163
-
Proposal for the classification of the acute leukaemias
-
Bennett JM, Catovsky D, Daniel M-T, et al. Proposal for the classification of the acute leukaemias. Br J Haematol. 1976;33:451-458.
-
(1976)
Br J Haematol
, vol.33
, pp. 451-458
-
-
Bennett, J.M.1
Catovsky, D.2
Daniel, M.-T.3
-
50
-
-
0024942585
-
Aplastic anemia: Immunosuppressive therapy in multi center trial in Japan
-
Kitamura K, Urabe A. Aplastic anemia: immunosuppressive therapy in multi center trial in Japan. Nippon Ketsueki Gakkai Zasshi. 1989;52:1361-1369.
-
(1989)
Nippon Ketsueki Gakkai Zasshi
, vol.52
, pp. 1361-1369
-
-
Kitamura, K.1
Urabe, A.2
-
51
-
-
0035053036
-
The distribution of PIG-A gene abnormalities in paroxysmal nocturnal hemoglobinuria granulocytes and cultured erythroblasts
-
Noji H, Shichishima T, Saitoh Y, et al. The distribution of PIG-A gene abnormalities in paroxysmal nocturnal hemoglobinuria granulocytes and cultured erythroblasts. Exp Hematol. 2001;29:391-400.
-
(2001)
Exp Hematol
, vol.29
, pp. 391-400
-
-
Noji, H.1
Shichishima, T.2
Saitoh, Y.3
-
52
-
-
0024424989
-
Amino-terminal amino acid sequence and chemical and functional properties of a membrane attack complexinhibitory factor from human erythrocyte membranes
-
Sugita Y, Mazda T, Tomita M. Amino-terminal amino acid sequence and chemical and functional properties of a membrane attack complexinhibitory factor from human erythrocyte membranes. J Biochem. 1989;106:589-592.
-
(1989)
J Biochem
, vol.106
, pp. 589-592
-
-
Sugita, Y.1
Mazda, T.2
Tomita, M.3
-
53
-
-
0000163138
-
Analysis and cloning of eukaryotic genomic DNA
-
Nolan C, ed. Cold Spring Harbor Laboratory Press. Cold Spring Harbor, NY
-
Sambrook J, Fritsch EF, Maniatis T. Analysis and cloning of eukaryotic genomic DNA. In: Nolan C, ed. Molecular Cloning, A Laboratory Manual. 2nd ed. Vol 2. Cold Spring Harbor Laboratory Press. Cold Spring Harbor, NY: 1989:9.1-9.59.
-
(1989)
Molecular Cloning, A Laboratory Manual. 2nd ed.
, vol.2
, pp. 91-959
-
-
Sambrook, J.1
Fritsch, E.F.2
Maniatis, T.3
-
54
-
-
0027938006
-
Serologic and nucleotide sequencing analyses of a novel DR52-associated DRB1 allele with the DR 'NJ25' specificity, designated DRB1*1307
-
Kaneshige T, Hashimoto M, Matsumoto Y, et al. Serologic and nucleotide sequencing analyses of a novel DR52-associated DRB1 allele with the DR 'NJ25' specificity, designated DRB1*1307. Hum Immunol. 1991;41:151-159.
-
(1991)
Hum Immunol
, vol.41
, pp. 151-159
-
-
Kaneshige, T.1
Hashimoto, M.2
Matsumoto, Y.3
-
55
-
-
0028304848
-
Comprehensive typing of DQB1 alleles by PCR-RFLP
-
Sengar DPS, Goldstein R. Comprehensive typing of DQB1 alleles by PCR-RFLP. Tissue Antigens. 1994;43:242-248.
-
(1994)
Tissue Antigens
, vol.43
, pp. 242-248
-
-
Sengar, D.P.S.1
Goldstein, R.2
-
56
-
-
0027195760
-
HLA-DQB1 and -DQA1 typing by PCR amplification with sequence-specific primers (PCR-SSP) in 2 hours
-
Olerup O, Aldener A, Fogdell A. HLA-DQB1 and -DQA1 typing by PCR amplification with sequence-specific primers (PCR-SSP) in 2 hours. Tissue Antigens. 1993;41:119-134.
-
(1993)
Tissue Antigens
, vol.41
, pp. 119-134
-
-
Olerup, O.1
Aldener, A.2
Fogdell, A.3
-
57
-
-
0028129769
-
Gene frequencies and haplotype associations within the HLA region in 916 unrelated Japanese individuals
-
Hashimoto M, Kinoshita T, Yamasaki M, et al. Gene frequencies and haplotype associations within the HLA region in 916 unrelated Japanese individuals. Tissue Antigens. 1994;44:166-173.
-
(1994)
Tissue Antigens
, vol.44
, pp. 166-173
-
-
Hashimoto, M.1
Kinoshita, T.2
Yamasaki, M.3
-
58
-
-
0034519493
-
Allele frequencies and haplotypic associations defined by allelic DNA typing at HLA class I and class loci in the Japanese population
-
Saito S, Ota S, Yamada E, Inoko H, Ota M. Allele frequencies and haplotypic associations defined by allelic DNA typing at HLA class I and class loci in the Japanese population. Tissue Antigens. 2000;56:522-529.
-
(2000)
Tissue Antigens
, vol.56
, pp. 522-529
-
-
Saito, S.1
Ota, S.2
Yamada, E.3
Inoko, H.4
Ota, M.5
-
60
-
-
0025861818
-
Detection of specific polymerase chain reaction product by utilizing the 5′-3′ exonuclease activity of Thermus aquaticus DNA polymerase
-
Holland PM, Abramson RD, Watson R, Gelfand DH. Detection of specific polymerase chain reaction product by utilizing the 5′-3′ exonuclease activity of Thermus aquaticus DNA polymerase. Proc Natl Acad Sci U S A. 1991;88:7276-7280.
-
(1991)
Proc Natl Acad Sci U S A
, vol.88
, pp. 7276-7280
-
-
Holland, P.M.1
Abramson, R.D.2
Watson, R.3
Gelfand, D.H.4
-
61
-
-
0032708065
-
Real-time RT-PCR for the detection and quantitation of AML/MTG8 fusion transcripts in t(8; 21)-positive AML patients
-
Krauter J, Watties MP, Nagel S, et al. Real-time RT-PCR for the detection and quantitation of AML/MTG8 fusion transcripts in t(8; 21)-positive AML patients. Br J Haematol. 1999;107:80-85.
-
(1999)
Br J Haematol
, vol.107
, pp. 80-85
-
-
Krauter, J.1
Watties, M.P.2
Nagel, S.3
-
62
-
-
0028033610
-
Identification of a specific HLA class II haplotype strongly associated with susceptibility to cyclosporindependent aplastic anemia
-
Nakao S, Takamatsu H, Chuhjo T, et al. Identification of a specific HLA class II haplotype strongly associated with susceptibility to cyclosporindependent aplastic anemia. Blood. 1994;84:4257-4261.
-
(1994)
Blood
, vol.84
, pp. 4257-4261
-
-
Nakao, S.1
Takamatsu, H.2
Chuhjo, T.3
-
63
-
-
0028897137
-
A pathogenetic link between aplastic anemia and paroxysmal nocturnal hemoglobinuria is suggested by a high frequency of aplastic anemia patients with a deficiency of phosphatidylinositol glycan anchored proteins
-
Schrezenmeier H, Hertenstein B, Wagner B, Raghavachar A, Heimpel H. A pathogenetic link between aplastic anemia and paroxysmal nocturnal hemoglobinuria is suggested by a high frequency of aplastic anemia patients with a deficiency of phosphatidylinositol glycan anchored proteins. Exp Hematol. 1995;23:81-87.
-
(1995)
Exp Hematol
, vol.23
, pp. 81-87
-
-
Schrezenmeier, H.1
Hertenstein, B.2
Wagner, B.3
Raghavachar, A.4
Heimpel, H.5
-
64
-
-
0033031417
-
Genetic instability and the etiology of somatic PIG-A mutations in paroxysmal nocturnal hemoglobinuria
-
Purow DB, Howard TA, Marcus SJ, Rosse WF, Ware RE. Genetic instability and the etiology of somatic PIG-A mutations in paroxysmal nocturnal hemoglobinuria. Blood Cells Mol Dis. 1999;15:81-91.
-
(1999)
Blood Cells Mol Dis
, vol.15
, pp. 81-91
-
-
Purow, D.B.1
Howard, T.A.2
Marcus, S.J.3
Rosse, W.F.4
Ware, R.E.5
-
65
-
-
0030797846
-
Increased frequency of somatic mutations at glycophorin A loci in patients with aplastic anaemia, myelodysplastic syndrome and paroxysmal nocturnal haemoglobinuria
-
Hattori H, Machii T, Ueda E, Shibano M, Kageyama T. Increased frequency of somatic mutations at glycophorin A loci in patients with aplastic anaemia, myelodysplastic syndrome and paroxysmal nocturnal haemoglobinuria. Br J Haematol. 1997;98:384-391.
-
(1997)
Br J Haematol
, vol.98
, pp. 384-391
-
-
Hattori, H.1
Machii, T.2
Ueda, E.3
Shibano, M.4
Kageyama, T.5
-
66
-
-
0035901533
-
The Wilms tumor suppressor WT1 directs stage-specific quiescence and differentiation of human hematopoietic progenitor cells
-
Ellisen LW, Carlesso N, Cheng T, Scadden DT, Haber DA. The Wilms tumor suppressor WT1 directs stage-specific quiescence and differentiation of human hematopoietic progenitor cells. EMBO J. 2001;20:1897-1909.
-
(2001)
EMBO J
, vol.20
, pp. 1897-1909
-
-
Ellisen, L.W.1
Carlesso, N.2
Cheng, T.3
Scadden, D.T.4
Haber, D.A.5
-
67
-
-
9544233528
-
Long-term follow-up of minimal residual disease in leukemia patients by monitoring WT1 (Wilms tumor gene) expression levels
-
Inoue K, Ogawa H, Yamagami T, et al. Long-term follow-up of minimal residual disease in leukemia patients by monitoring WT1 (Wilms tumor gene) expression levels. Blood. 1996;88:2267-2278.
-
(1996)
Blood
, vol.88
, pp. 2267-2278
-
-
Inoue, K.1
Ogawa, H.2
Yamagami, T.3
|