-
1
-
-
33750600143
-
Circumstances of death in adult sickle cell disease patients
-
DOI 10.1002/ajh.20685
-
Darbari DS, Kple-Faget P, Kwagyan J, Rana S, Gordeuk VR, Castro O. Circumstances of death in adult sickle cell disease patients. Am J Hematol. 2006;81(11):858-863. (Pubitemid 44682188)
-
(2006)
American Journal of Hematology
, vol.81
, Issue.11
, pp. 858-863
-
-
Darbari, D.S.1
Kple-Faget, P.2
Kwagyan, J.3
Rana, S.4
Gordeuk, V.R.5
Castro, O.6
-
2
-
-
0028291736
-
Mortality in sickle cell disease. Life expectancy and risk factors for early death
-
Platt OS, Brambilla DJ, Rosse WF, et al. Mortality in sickle cell disease: life expectancy and risk factors for early death. N Engl J Med. 1994;330(23):1639-1644. (Pubitemid 124005049)
-
(1994)
New England Journal of Medicine
, vol.330
, Issue.23
, pp. 1639-1644
-
-
Platt, O.S.1
Brambilla, D.J.2
Rosse, W.F.3
Milner, P.F.4
Castro, O.5
Steinberg, M.H.6
Klug, P.P.7
-
3
-
-
0030745927
-
National trends in the mortality of children with sickle cell disease, 1968 through 1992
-
Davis H, Schoendorf KC, Gergen PJ, Moore RM Jr. National trends in the mortality of children with sickle cell disease, 1968 through 1992. Am J Public Health. 1997;87(8):1317-1322.
-
(1997)
Am J Public Health
, vol.87
, Issue.8
, pp. 1317-1322
-
-
Davis, H.1
Schoendorf, K.C.2
Gergen, P.J.3
Moore Jr., R.M.4
-
5
-
-
0030133622
-
Barriers to bone marrow transplantation for sickle cell anemia
-
Walters MC, Patience M, Leisenring W, et al. Barriers to bone marrow transplantation for sickle cell anemia. Biol Blood Marrow Transplant. 1996;2(2):100-104. (Pubitemid 126488201)
-
(1996)
Biology of Blood and Marrow Transplantation
, vol.2
, Issue.2
, pp. 100-104
-
-
Walters, M.C.1
Patience, M.2
Leisenring, W.3
Eckman, J.R.4
Buchanan, G.R.5
Rogers, Z.R.6
Olivieri, N.F.7
Vichinsky, E.8
Davies, S.C.9
Mentzer, W.C.10
Powars, D.11
Scott, J.P.12
Bernadin, F.13
Ohene-Frempong, K.14
Darbyshire, P.J.15
Wayne, A.16
Roberts, I.A.G.17
Dinndorf, P.18
Brandalise, S.19
Sanders, J.E.20
Matthews, D.C.21
Appelbaum, F.R.22
Storb, R.23
Sullivan, K.M.24
more..
-
6
-
-
38949124765
-
Late effects of myeloablative bone marrow transplantation (BMT) in sickle cell disease (SCD) [6]
-
DOI 10.1182/blood-2007-10-118257
-
Fitzhugh CD, Perl S, Hsieh MM. Late effects of myeloablative bone marrow transplantation (BMT) in sickle cell disease (SCD) [letter]. Blood. 2008;111(3):1742-1743; author reply 1744. (Pubitemid 351213472)
-
(2008)
Blood
, vol.111
, Issue.3
, pp. 1742-1743
-
-
Fitzhugh, C.D.1
Perl, S.2
Hsieh, M.M.3
-
7
-
-
34948830175
-
Long-term results of related myeloablative stem-cell transplantation to cure sickle cell disease
-
DOI 10.1182/blood-2007-03-079665
-
Bernaudin F, Socie G, Kuentz M, et al. Long-term results of related myeloablative stem-cell transplantation to cure sickle cell disease. Blood. 2007;110(7):2749-2756. (Pubitemid 47523201)
-
(2007)
Blood
, vol.110
, Issue.7
, pp. 2749-2756
-
-
Bernaudin, F.1
Socie, G.2
Kuentz, M.3
Chevret, S.4
Duval, M.5
Bertrand, Y.6
Vannier, J.-P.7
Yakouben, K.8
Thuret, I.9
Bordigoni, P.10
Fischer, A.11
Lutz, P.12
Stephan, J.-L.13
Dhedin, N.14
Plouvier, E.15
Margueritte, G.16
Bories, D.17
Verlhac, S.18
Esperou, H.19
Coic, L.20
Vernant, J.-P.21
Gluckman, E.22
more..
-
8
-
-
0035861452
-
Correction of sickle cell disease in transgenic mouse models by gene therapy
-
DOI 10.1126/science.1065806
-
Pawliuk R, Westerman KA, Fabry ME, et al. Correction of sickle cell disease in transgenic mouse models by gene therapy. Science. 2001;294(5550):2368-2371. (Pubitemid 33140563)
-
(2001)
Science
, vol.294
, Issue.5550
, pp. 2368-2371
-
-
Pawliuk, R.1
Westerman, K.A.2
Fabry, M.E.3
Payen, E.4
Tighe, R.5
Bouhassira, E.E.6
Acharya, S.A.7
Ellis, J.8
London, I.M.9
Eaves, C.J.10
Humphries, R.K.11
Beuzard, Y.12
Nagel, R.L.13
Leboulch, P.14
-
9
-
-
0344305491
-
Correction of a mouse model of sickle cell disease: Lentiviral/ antisickling beta-globin gene transduction of unmobilized, purified hematopoietic stem cells
-
Levasseur DN, Ryan TM, Pawlik KM, Townes TM. Correction of a mouse model of sickle cell disease: lentiviral/antisickling beta-globin gene transduction of unmobilized, purified hematopoietic stem cells. Blood. 2003;102(13):4312-4319.
-
(2003)
Blood
, vol.102
, Issue.13
, pp. 4312-4319
-
-
Levasseur, D.N.1
Ryan, T.M.2
Pawlik, K.M.3
Townes, T.M.4
-
10
-
-
9444281434
-
Successful correction of the human β-thalassemia major phenotype using a lentiviral vector
-
DOI 10.1182/blood-2004-04-1427
-
Puthenveetil G, Scholes J, Carbonell D, et al. Successful correction of the human beta-thalassemia major phenotype using a lentiviral vector. Blood. 2004;104(12):3445-3453. (Pubitemid 39564412)
-
(2004)
Blood
, vol.104
, Issue.12
, pp. 3445-3453
-
-
Puthenveetil, G.1
Scholes, J.2
Carbonell, D.3
Qureshi, N.4
Xia, P.5
Zeng, L.6
Li, S.7
Yu, Y.8
Hiti, A.L.9
Yee, J.-K.10
Malik, P.11
-
11
-
-
0035525735
-
High-level erythroid-specific gene expression in primary human and murine hematopoietic cells with self-inactivating lentiviral vectors
-
Moreau-Gaudry F, Xia P, Jiang G, et al. High-level erythroid-specific gene expression in primary human and murine hematopoietic cells with self-inactivating lentiviral vectors. Blood. 2001;98(9):2664-2672.
-
(2001)
Blood
, vol.98
, Issue.9
, pp. 2664-2672
-
-
Moreau-Gaudry, F.1
Xia, P.2
Jiang, G.3
-
12
-
-
0034657848
-
Locus control region activity by 5'HS3 requires a functional interaction with β-globin gene regulatory elements: Expression of novel β/γ-globin hybrid transgenes
-
Rubin JE, Pasceri P, Wu X, Leboulch P, Ellis J. Locus control region activity by 5′HS3 requires a functional interaction with beta-globin gene regulatory elements: expression of novel beta/gamma-globin hybrid transgenes. Blood. 2000;95(10):3242-3249. (Pubitemid 30321180)
-
(2000)
Blood
, vol.95
, Issue.10
, pp. 3242-3249
-
-
Rubin, J.E.1
Pasceri, P.2
Wu, X.3
Leboulch, P.4
Ellis, J.5
-
13
-
-
34548791721
-
Improved Human β-globin expression from self-inactivating lentiviral vectors carrying the chicken hypersensitive site-4 (cHS4) insulator element
-
DOI 10.1038/sj.mt.6300259, PII 6300259
-
Arumugam PI, Scholes J, Perelman N, Xia P, Yee JK, Malik P. Improved human beta-globin expression from self-inactivating lentiviral vectors carrying the chicken hypersensitive site-4 (cHS4) insulator element. Mol Ther. 2007;15(10):1863-1871. (Pubitemid 47434195)
-
(2007)
Molecular Therapy
, vol.15
, Issue.10
, pp. 1863-1871
-
-
Arumugam, P.I.1
Scholes, J.2
Perelman, N.3
Xia, P.4
Yee, J.-K.5
Malik, P.6
-
14
-
-
1842408336
-
Transgenic knockout mice with exclusively human sickle hemoglobin and sickle cell disease
-
DOI 10.1126/science.278.5339.876
-
Pászty C, Brion CM, Manci E, et al. Transgenic knockout mice with exclusively human sickle hemoglobin and sickle cell disease. Science. 1997;278(5339):876-878. (Pubitemid 27467927)
-
(1997)
Science
, vol.278
, Issue.5339
, pp. 876-878
-
-
Paszty, C.1
Brion, C.M.2
Manci, E.3
Witkowska, H.E.4
Stevens, M.E.5
Mohandas, N.6
Rubin, E.M.7
-
15
-
-
32644437616
-
Pathology of Berkeley sickle cell mice: Similarities and differences with human sickle cell disease
-
Manci EA, Hillery CA, Bodian CA, Zhang ZG, Lutty GA, Coller BS. Pathology of Berkeley sickle cell mice: similarities and differences with human sickle cell disease. Blood. 2006;107(4):1651-1658.
-
(2006)
Blood
, vol.107
, Issue.4
, pp. 1651-1658
-
-
Manci, E.A.1
Hillery, C.A.2
Bodian, C.A.3
Zhang, Z.G.4
Lutty, G.A.5
Coller, B.S.6
-
17
-
-
0035877966
-
Effects of mixed hematopoietic chimerism in a mouse model of bone marrow transplantation for sickle cell anemia
-
Iannone R, Luznik L, Engstrom LW, et al. Effects of mixed hematopoietic chimerism in a mouse model of bone marrow transplantation for sickle cell anemia. Blood. 2001;97(12):3960-3965.
-
(2001)
Blood
, vol.97
, Issue.12
, pp. 3960-3965
-
-
Iannone, R.1
Luznik, L.2
Engstrom, L.W.3
-
18
-
-
12144289379
-
Results of minimally toxic nonmyeloablative transplantation in patients with sickle cell anemia and β-thalassemia
-
DOI 10.1016/S1083-8791(03)00192-7, PII S1083879103001927
-
Iannone R, Casella JF, Fuchs EJ, et al. Results of minimally toxic nonmyeloablative transplantation in patients with sickle cell anemia and beta-thalassemia. Biol Blood Marrow Transplant. 2003;9(8):519-528. (Pubitemid 38351796)
-
(2003)
Biology of Blood and Marrow Transplantation
, vol.9
, Issue.8
, pp. 519-528
-
-
Iannone, R.1
Casella, J.F.2
Fuchs, E.J.3
Chen, A.R.4
Jones, R.J.5
Woolfrey, A.6
Amylon, M.7
Sullivan, K.M.8
Storb, R.F.9
Walters, M.C.10
-
19
-
-
0033508588
-
Clinical potential of in vitro measured red cell deformability, a myth?
-
Hardeman MR, Ince C. Clinical potential of in vitro measured red cell deformability, a myth? Clin Hemorheol Microcirc. 1999;21(3-4):277-284. (Pubitemid 30130904)
-
(1999)
Clinical Hemorheology and Microcirculation
, vol.21
, Issue.3-4
, pp. 277-284
-
-
Hardeman, M.R.1
Ince, C.2
-
20
-
-
0032525818
-
Time-dependent changes in the density and hemoglobin F content of biotin-labeled sickle cells
-
Franco RS, Lohmann J, Silberstein EB, et al. Time-dependent changes in the density and hemoglobin F content of biotin-labeled sickle cells. J Clin Invest. 1998;101(12):2730-2740. (Pubitemid 28294582)
-
(1998)
Journal of Clinical Investigation
, vol.101
, Issue.12
, pp. 2730-2740
-
-
Franco, R.S.1
Lohmann, J.2
Silberstein, E.B.3
Mayfield-Pratt, G.4
Palascak, M.5
Nemeth, T.A.6
Joiner, C.H.7
Weiner, M.8
Rucknagel, D.L.9
-
21
-
-
63649132974
-
Correction of murine sickle cell disease using gamma-globin lentiviral vectors to mediate high-level expression of fetal hemoglobin
-
Pestina TI, Hargrove PW, Jay D, Gray JT, Boyd KM, Persons DA. Correction of murine sickle cell disease using gamma-globin lentiviral vectors to mediate high-level expression of fetal hemoglobin. Mol Ther. 2009;17(2):245-252.
-
(2009)
Mol Ther
, vol.17
, Issue.2
, pp. 245-252
-
-
Pestina, T.I.1
Hargrove, P.W.2
Jay, D.3
Gray, J.T.4
Boyd, K.M.5
Persons, D.A.6
-
22
-
-
0031593688
-
+ cells in ADA-deficient SCID neonates
-
DOI 10.1038/nm0798-775
-
Kohn DB, Hershfield MS, Carbonaro D, et al. T lymphocytes with a normal ADA gene accumulate after transplantation of transduced autologous umbilical cord blood CD34+ cells in ADA-deficient SCID neonates. Nat Med. 1998;4(7):775-780. (Pubitemid 28331017)
-
(1998)
Nature Medicine
, vol.4
, Issue.7
, pp. 775-780
-
-
Kohn, D.B.1
Hershfield, M.S.2
Carbonaro, D.3
Shigeoka, A.4
Brooks, J.5
Smogorzewska, E.M.6
Barsky, L.W.7
Chan, R.8
Burotto, F.9
Annett, G.10
Nolta, J.A.11
Crooks, G.12
Kapoor, N.13
Elder, M.14
Wara, D.15
Bowen, T.16
Madsen, E.17
Snyder, F.F.18
Bastian, J.19
Muul, L.20
Blaese, R.M.21
Weinberg, K.22
Parkman, R.23
more..
-
23
-
-
0037189401
-
Correction of ADA-SCID by stem cell gene therapy combined with nonmyeloablative conditioning
-
DOI 10.1126/science.1070104
-
Aiuti A, Slavin S, Aker M, et al. Correction of ADA-SCID by stem cell gene therapy combined with nonmyeloablative conditioning. Science. 2002;296(5577):2410-2413. (Pubitemid 34734219)
-
(2002)
Science
, vol.296
, Issue.5577
, pp. 2410-2413
-
-
Aiuti, A.1
Slavin, S.2
Aker, M.3
Ficara, F.4
Deola, S.5
Mortellaro, A.6
Morecki, S.7
Andolfi, G.8
Tabucchi, A.9
Carlucci, F.10
Marinello, E.11
Cattaneo, F.12
Vai, S.13
Servida, P.14
Miniero, R.15
Roncarolo, M.G.16
Bordignon, C.17
-
24
-
-
59449098985
-
Gene therapy for immunodeficiency due to adenosine deaminase deficiency
-
Aiuti A, Cattaneo F, Galimberti S, et al. Gene therapy for immunodeficiency due to adenosine deaminase deficiency. N Engl J Med. 2009;360(5):447-458.
-
(2009)
N Engl J Med
, vol.360
, Issue.5
, pp. 447-458
-
-
Aiuti, A.1
Cattaneo, F.2
Galimberti, S.3
-
25
-
-
0030999757
-
Hemoglobin-specific antibody in a multiply transfused patient with sickle cell disease
-
Noronha PA, Vida LN, Park CL, Honig GR. Hemoglobin-specific antibody in a multiply transfused patient with sickle cell disease. Blood. 1997;89(6):2155-2158. (Pubitemid 27132133)
-
(1997)
Blood
, vol.89
, Issue.6
, pp. 2155-2158
-
-
Noronha, P.A.1
Vida, L.N.2
Park, C.L.3
Honig, G.R.4
-
26
-
-
30544436003
-
A genetic strategy to treat sickle cell anemia by coregulating globin transgene expression and RNA interference
-
DOI 10.1038/nbt1176, PII NBT1176
-
Samakoglu S, Lisowski L, Budak-Alpdogan T, et al. A genetic strategy to treat sickle cell anemia by coregulating globin transgene expression and RNA interference. Nat Biotechnol. 2006;24(1):89-94. (Pubitemid 43083171)
-
(2006)
Nature Biotechnology
, vol.24
, Issue.1
, pp. 89-94
-
-
Samakoglu, S.1
Lisowski, L.2
Budak-Alpdogan, T.3
Usachenko, Y.4
Acuto, S.5
Di Marzo, R.6
Maggio, A.7
Zhu, P.8
Tisdale, J.F.9
Riviere, I.10
Sadelain, M.11
-
27
-
-
0028032847
-
Sickle cell disease of transgenic SAD mice
-
Trudel M, De Paepe ME, Chretien N, et al. Sickle cell disease of transgenic SAD mice. Blood. 1994;84(9):3189-3197. (Pubitemid 24328114)
-
(1994)
Blood
, vol.84
, Issue.9
, pp. 3189-3197
-
-
Trudel, M.1
De Paepe, M.E.2
Chretien, N.3
Saadane, N.4
Jacmain, J.5
Sorette, M.6
Hoang, T.7
Beuzard, Y.8
-
28
-
-
17644441354
-
Genetic correction of sickle cell disease: Insights using transgenic mouse models
-
DOI 10.1038/72279
-
Blouin MJ, Beauchemin H, Wright A, et al. Genetic correction of sickle cell disease: insights using transgenic mouse models. Nat Med. 2000;6(2):177-182. (Pubitemid 30082362)
-
(2000)
Nature Medicine
, vol.6
, Issue.2
, pp. 177-182
-
-
Blouin, M.-J.1
Beauchemin, H.2
Wright, A.3
De Paepe, M.4
Soretie, M.5
Bleau, A.-M.6
Nakamoto, B.7
Ou, C.-N.8
Stamatoyannopoulos, G.9
Trudel, M.10
-
29
-
-
0035863541
-
Second generation knockout sickle mice: The effect of HbF
-
Fabry ME, Suzuka SM, Weinberg RS, et al. Second generation knockout sickle mice: the effect of HbF. Blood. 2001;97(2):410-418.
-
(2001)
Blood
, vol.97
, Issue.2
, pp. 410-418
-
-
Fabry, M.E.1
Suzuka, S.M.2
Weinberg, R.S.3
-
30
-
-
0037443467
-
The degree of phenotypic correction of murine β-thalassemia intermedia following lentiviral-mediated transfer of a human γ-globin gene is influenced by chromosomal position effects and vector copy number
-
DOI 10.1182/blood-2002-07-2211
-
Persons DA, Hargrove PW, Allay ER, Hanawa H, Nienhuis AW. The degree of phenotypic correction of murine beta-thalassemia intermedia following lentiviral-mediated transfer of a human gamma-globin gene is influenced by chromosomal position effects and vector copy number. Blood. 2003;101(6):2175- 2183. (Pubitemid 36302055)
-
(2003)
Blood
, vol.101
, Issue.6
, pp. 2175-2183
-
-
Persons, D.A.1
Hargrove, P.W.2
Allay, E.R.3
Hanawa, H.4
Nienhuis, A.W.5
-
31
-
-
0034307656
-
2-Deoxy 5-azacytidine and fetal hemoglobin induction in sickle cell anemia
-
Koshy M, Dorn L, Bressler L, et al. 2-deoxy 5-azacytidine and fetal hemoglobin induction in sickle cell anemia. Blood. 2000;96(7):2379-2384. (Pubitemid 30745258)
-
(2000)
Blood
, vol.96
, Issue.7
, pp. 2379-2384
-
-
Koshy, M.1
Dorn, L.2
Bressler, L.3
Molokie, R.4
Lavelle, D.5
Talischy, N.6
Hoffman, R.7
Van Overveld, W.8
Desimone, J.9
-
32
-
-
0023130331
-
Hydroxyurea-induced augmentation of fetal hemoglobin production in patients with sickle cell anemia
-
Charache S, Dover GJ, Moyer MA, Moore JW. Hydroxyurea-induced augmentation of fetal hemoglobin production in patients with sickle cell anemia. Blood. 1987;69(1):109-116. (Pubitemid 17007083)
-
(1987)
Blood
, vol.69
, Issue.1
, pp. 109-116
-
-
Charache, S.1
Dover, G.J.2
Moyer, M.A.3
Moore, J.W.4
-
33
-
-
0031809842
-
Fetal hemoglobin and F-cell responses to long-term hydroxyurea treatment in young sickle cell patients: The French Study Group on Sickle Cell Disease
-
Maier-Redelsperger M, de Montalembert M, Flahault A, et al. Fetal hemoglobin and F-cell responses to long-term hydroxyurea treatment in young sickle cell patients: The French Study Group on Sickle Cell Disease. Blood. 1998;91(12):4472-4479.
-
(1998)
Blood
, vol.91
, Issue.12
, pp. 4472-4479
-
-
Maier-Redelsperger, M.1
De Montalembert, M.2
Flahault, A.3
-
34
-
-
0033505007
-
Physiologic decline in fetal hemoglobin parameters in infants with sickle cell disease: Implications for pharmacological intervention
-
Marcus SJ, Ware RE. Physiologic decline in fetal hemoglobin parameters in infants with sickle cell disease: implications for pharmacological intervention. J Pediatr Hematol Oncol. 1999;21(5):407-411.
-
(1999)
J Pediatr Hematol Oncol
, vol.21
, Issue.5
, pp. 407-411
-
-
Marcus, S.J.1
Ware, R.E.2
-
35
-
-
0028113849
-
Variation in fetal hemoglobin parameters and predicted hemoglobin S polymerization in sickle cell children in the first two years of life: Parisian prospective study on sickle cell disease
-
Maier-Redelsperger M, Noguchi CT, de Montalembert M, et al. Variation in fetal hemoglobin parameters and predicted hemoglobin S polymerization in sickle cell children in the first two years of life: Parisian Prospective Study on Sickle Cell Disease. Blood. 1994;84(9):3182-3188. (Pubitemid 24328113)
-
(1994)
Blood
, vol.84
, Issue.9
, pp. 3182-3188
-
-
Maier-Redelsperger, M.1
Noguchi, C.T.2
De Montalembert, M.3
Rodgers, G.P.4
Schechter, A.N.5
Gourbil, A.6
Blanchard, D.7
Jais, J.P.8
Ducrocq, R.9
Peltier, J.-Y.10
Cottat, M.-C.11
Lacaille, F.12
Belloy, M.13
Elion, J.14
Labie, D.15
Girot, R.16
-
36
-
-
0037414164
-
Effect of Hydroxyurea on Mortality and Morbidity in Adult Sickle Cell Anemia: Risks and Benefits Up to 9 Years of Treatment
-
DOI 10.1001/jama.289.13.1645
-
Steinberg MH, Barton F, Castro O, et al. Effect of hydroxyurea on mortality and morbidity in adult sickle cell anemia: risks and benefits up to 9 years of treatment. JAMA. 2003;289(13):1645-1651. (Pubitemid 37430269)
-
(2003)
Journal of the American Medical Association
, vol.289
, Issue.13
, pp. 1645-1651
-
-
Steinberg, M.H.1
Barton, F.2
Castro, O.3
Pegelow, C.H.4
Ballas, S.K.5
Kutlar, A.6
Orringer, E.7
Bellevue, R.8
Olivieri, N.9
Eckman, J.10
Varma, M.11
Ramirez, G.12
Adler, B.13
Smith, W.14
Carlos, T.15
Ataga, K.16
Decastro, L.17
Bigelow, C.18
Saunthararajah, Y.19
Telfer, M.20
Vichinsky, E.21
Claster, S.22
Shurin, S.23
Bridges, K.24
Waclawiw, M.25
Bonds, D.26
Terrin, M.27
more..
-
37
-
-
10744229369
-
Chimerism and cure: Hematologic and pathologic correction of murine sickle cell disease
-
DOI 10.1182/blood-2003-03-0712
-
Kean LS, Manci EA, Perry J, et al. Chimerism and cure: hematologic and pathologic correction of murine sickle cell disease. Blood. 2003;102(13):4582- 4593. (Pubitemid 37494128)
-
(2003)
Blood
, vol.102
, Issue.13
, pp. 4582-4593
-
-
Kean, L.S.1
Manci, E.A.2
Perry, J.3
Balkan, C.4
Coley, S.5
Holtzclaw, D.6
Adams, A.B.7
Larsen, C.P.8
Hsu, L.L.9
Archer, D.R.10
-
38
-
-
0035544031
-
Stable mixed hematopoietic chimerism after bone marrow transplantation for sickle cell anemia
-
Walters MC, Patience M, Leisenring W, et al. Stable mixed hematopoietic chimerism after bone marrow transplantation for sickle cell anemia. Biol Blood Marrow Transplant. 2001;7(12):665-673. (Pubitemid 34055819)
-
(2001)
Biology of Blood and Marrow Transplantation
, vol.7
, Issue.12
, pp. 665-673
-
-
Walters, M.C.1
Patience, M.2
Leisenring, W.3
Rogers, Z.R.4
Aquino, V.M.5
Buchanan, G.R.6
Roberts, I.A.G.7
Yeager, A.M.8
Hsu, L.9
Adamkiewicz, T.10
Kurtzberg, J.11
Vichinsky, E.12
Storer, B.13
Storb, R.14
Sullivan, K.M.15
-
39
-
-
84900578474
-
Hematopoietic stem cell gene therapy trial with lentiviral vector in X-linked adrenoleukodystrophy
-
Abstract 821
-
Cavazzana-Calvo M, Cartier N, Abina SH-B, et al. Hematopoietic stem cell gene therapy trial with lentiviral vector in X-linked adrenoleukodystrophy. Blood (ASH Annual Meeting Abstracts). 2008;(suppl)112. Abstract 821.
-
(2008)
Blood (ASH Annual Meeting Abstracts)
, Issue.SUPPL.
, pp. 112
-
-
Cavazzana-Calvo, M.1
Cartier, N.2
Abina, S.H.-B.3
-
40
-
-
0242515921
-
+ cells from adrenoleukodystrophy patients with HIV- Derived vector mediated long-term engraftment of NOD/SCID mice
-
DOI 10.1016/S1525-0016(03)00002-9
-
Benhamida S, Pflumio F, Dubart-Kupperschmitt A, et al. Transduced CD34+ cells from adreno-leukodystrophy patients with HIV-derived vector mediate long-term engraftment of NOD/SCID mice. Mol Ther. 2003;7(3):317-324. (Pubitemid 36503855)
-
(2003)
Molecular Therapy
, vol.7
, Issue.3
, pp. 317-324
-
-
Benhamida, S.1
Pflumio, F.2
Dubart-Kupperschmitt, A.3
Zhao-Emonet, J.-C.4
Cavazzana-Calvo, M.5
Rocchiccioli, F.6
Fichelson, S.7
Aubourg, P.8
Charneau, P.9
Cartier, N.10
-
41
-
-
13244269889
-
Hematopoietic stem cell transplantation for multiply transfused patients with sickle cell disease and thalassemia after low-dose total body irradiation, fludarabine, and rabbit anti-thymocyte globulin
-
DOI 10.1038/sj.bmt.1704745
-
Horan JT, Liesveld JL, Fenton P, Blumberg N, Walters MC. Hematopoietic stem cell transplantation for multiply transfused patients with sickle cell disease and thalassemia after low-dose total body irradiation, fludarabine, and rabbit antithymocyte globulin. Bone Marrow Transplant. 2005;35(2):171-177. (Pubitemid 40185933)
-
(2005)
Bone Marrow Transplantation
, vol.35
, Issue.2
, pp. 171-177
-
-
Horan, J.T.1
Liesveld, J.L.2
Fenton, P.3
Blumberg, N.4
Walters, M.C.5
-
42
-
-
0035804287
-
Bone marrow transplantation without myeloablation for sickle cell disease
-
DOI 10.1056/NEJM200101043440119
-
Krishnamurti L, Blazar BR, Wagner JE. Bone marrow transplantation without myeloablation for sickle cell disease. N Engl J Med. 2001;344(1):68. (Pubitemid 32064856)
-
(2001)
New England Journal of Medicine
, vol.344
, Issue.1
, pp. 68
-
-
Krishnamurti, L.1
Blazar, B.R.2
Wagner, J.E.3
-
43
-
-
0036493491
-
A cure for murine sickle cell disease through stable mixed chimerism and tolerance induction after nonmyeloablative conditioning and major histocompatibility complex-mismatched bone marrow transplantation
-
Kean LS, Durham MM, Adams AB, et al. A cure for murine sickle cell disease through stable mixed chimerism and tolerance induction after nonmyeloablative conditioning and major histocompatibility complex-mismatched bone marrow transplantation. Blood. 2002;99(5):1840-1849.
-
(2002)
Blood
, vol.99
, Issue.5
, pp. 1840-1849
-
-
Kean, L.S.1
Durham, M.M.2
Adams, A.B.3
-
44
-
-
53749086728
-
Stable long-term donor engraftment following reduced-intensity hematopoietic cell transplantation for sickle cell disease
-
Krishnamurti L, Kharbanda S, Biernacki MA, et al. Stable long-term donor engraftment following reduced-intensity hematopoietic cell transplantation for sickle cell disease. Biol Blood Marrow Transplant. 2008;14(11):1270-1278.
-
(2008)
Biol Blood Marrow Transplant
, vol.14
, Issue.11
, pp. 1270-1278
-
-
Krishnamurti, L.1
Kharbanda, S.2
Biernacki, M.A.3
-
45
-
-
39549110741
-
An experimental system for the evaluation of retroviral vector design to diminish the risk for proto-oncogene activation
-
Ryu BY, Evans-Galea MV, Gray JT, Bodine DM, Persons DA, Nienhuis AW. An experimental system for the evaluation of retroviral vector design to diminish the risk for proto-oncogene activation. Blood. 2008;111(4):1866-1875.
-
(2008)
Blood
, vol.111
, Issue.4
, pp. 1866-1875
-
-
Ryu, B.Y.1
Evans-Galea, M.V.2
Gray, J.T.3
Bodine, D.M.4
Persons, D.A.5
Nienhuis, A.W.6
-
46
-
-
34748902850
-
A chromatin insulator blocks interactions between globin regulatory elements and cellular promoters in erythroid cells
-
Ryu BY, Persons DA, Evans-Galea MV, Gray JT, Nienhuis AW. A chromatin insulator blocks interactions between globin regulatory elements and cellular promoters in erythroid cells. Blood Cells Mol Dis. 2007;39(3):221-228.
-
(2007)
Blood Cells Mol Dis
, vol.39
, Issue.3
, pp. 221-228
-
-
Ryu, B.Y.1
Persons, D.A.2
Evans-Galea, M.V.3
Gray, J.T.4
Nienhuis, A.W.5
-
47
-
-
33745108790
-
Hematopoietic stem cell gene transfer in a tumor-prone mouse model uncovers low genotoxicity of lentiviral vector integration
-
DOI 10.1038/nbt1216, PII N1216
-
Montini E, Cesana D, Schmidt M, et al. Hematopoietic stem cell gene transfer in a tumor-prone mouse model uncovers low genotoxicity of lentiviral vector integration. Nat Biotechnol. 2006;24(6):687-696. (Pubitemid 43882120)
-
(2006)
Nature Biotechnology
, vol.24
, Issue.6
, pp. 687-696
-
-
Montini, E.1
Cesana, D.2
Schmidt, M.3
Sanvito, F.4
Ponzoni, M.5
Bartholomae, C.6
Sergi, L.S.7
Benedicenti, F.8
Ambrosi, A.9
Di Serio, C.10
Doglioni, C.11
Von Kalle, C.12
Naldini, L.13
-
48
-
-
9644262537
-
Lenti in red: Progress in gene therapy for human hemoglobinopathies
-
DOI 10.1172/JCI200423132
-
von Kalle C, Baum C, Williams DA. Lenti in red: progress in gene therapy for human hemoglobinopathies. J Clin Invest. 2004;114(7):889-891. (Pubitemid 39578714)
-
(2004)
Journal of Clinical Investigation
, vol.114
, Issue.7
, pp. 889-891
-
-
Von Kalle, C.1
Baum, C.2
Williams, D.A.3
|