-
2
-
-
0031721137
-
Use of the green fluorescent protein as a marker to identify and track genetically modified hematopoietic cells
-
(1998)
Nat Med
, vol.4
, pp. 1201-1205
-
-
Persons, D.A.1
-
3
-
-
0032402140
-
Highly efficient transduction of the green fluorescent protein gene in human umbilical cord blood stem cells capable of cobblestone formation in long-term cultures and multilineage engraftment of immunodeficient mice
-
(1998)
Blood
, vol.92
, pp. 4013-4022
-
-
van Hennik, P.B.1
-
4
-
-
0033571561
-
Improved expression in hematopoietic and lymphoid cells in mice after transplantation of bone marrow transduced with a modified retroviral vector
-
(1999)
Blood
, vol.94
, pp. 3337-3349
-
-
Halene, S.1
-
6
-
-
0025724075
-
Treatment of genetic defects in hematopoietic cell function by gene transfer
-
(1991)
Blood
, vol.78
, pp. 2481-2492
-
-
Karlsson, S.1
-
7
-
-
85134284401
-
Gene transfer and transgene expression in hematopoietic cells
-
Strauss M, Barranger JA (eds). Concepts in Gene Therapy. DeGruyter: Berlin
-
(1997)
, pp. 233-266
-
-
Baum, C.1
-
10
-
-
0032188998
-
Transduction of murine bone marrow cells with an MDR1 vector enables ex vivo stem cell expansion, but these expanded grafts cause a myeloproliferative syndrome in transplanted mice
-
(1998)
Blood
, vol.92
, pp. 2269-2279
-
-
Bunting, K.D.1
-
11
-
-
0034141489
-
Long-term multilineage expression in peripheral blood from a Moloney murine leukemia virus vector after serial transplantation of transduced bone marrow cells
-
(2000)
Blood
, vol.95
, pp. 829-836
-
-
Austin, T.W.1
-
12
-
-
0033587635
-
Dose-dependent transduction of vesicular stomatitis virus G protein-pseudotyped retrovirus vector into human solid tumour cell lines and murine fibroblasts
-
(1999)
Virology
, vol.260
, pp. 109-115
-
-
Arai, T.1
Takada, M.2
Ui, M.3
Iba, H.4
-
13
-
-
0032567339
-
Generation of destabilized green fluorescent protein as a transcription reporter
-
(1998)
J Biol Chem
, vol.273
, pp. 34970-34975
-
-
Li, X.1
-
14
-
-
0034182866
-
CD34 splice variant: An attractive marker for selection of gene-modified cells
-
(2000)
Mol Ther
, vol.1
, pp. 448-456
-
-
Fehse, B.1
-
16
-
-
0031932432
-
Entry of amphotropic and 10A1 pseudotyped murine retroviruses is restricted in hematopoietic stem cell lines
-
(1998)
J Virol
, vol.72
, pp. 1424-1430
-
-
von Laer, D.1
-
17
-
-
0034171107
-
Superior transduction of mouse hematopoietic stem cells with 10A1 and VSV-G pseudotyped retrovirus vectors
-
(2000)
Mol Ther
, vol.1
, pp. 330-338
-
-
Barrette, S.1
-
19
-
-
0034131481
-
Efficient retrovirus-mediated transfer of the multidrug resistance 1 gene into autologous human long-term repopulating hematopoietic stem cells
-
(2000)
Nat Med
, vol.6
, pp. 652-658
-
-
Abonour, R.1
-
24
-
-
0032531012
-
Improved gene transfer into baboon marrow repopulating cells using recombinant human fibronectin fragment CH-296 in combination with interleukin-6, stem cell factor, FLT-3 ligand, and megakaryocyte growth and development factor
-
(1998)
Blood
, vol.92
, pp. 1878-1886
-
-
Kiem, H.P.1
-
26
-
-
0032213335
-
High efficiency gene transfer to human hematopoietic SCID-repopulating cells under serum-free conditions
-
(1998)
Blood
, vol.92
, pp. 3163-3171
-
-
Schilz, A.J.1
-
27
-
-
0342470476
-
Quantitative assessment of retroviral transfer of the human multidrug resistance 1 gene to human mobilized peripheral blood progenitor cells engrafted in nonobese diabetic/severe combined immunodeficient mice
-
(2000)
Blood
, vol.95
, pp. 1237-1248
-
-
Schiedlmeier, B.1
-
28
-
-
0033981566
-
A defined window for efficient gene marking of severe combined immunodeficient-repopulating cells using a gibbon ape leukemia virus-pseudotyped retroviral vector
-
(2000)
Hum Gene Ther
, vol.11
, pp. 91-100
-
-
Demaison, C.1
-
29
-
-
16044366110
-
Colocalization of retrovirus and target cells on specific fibronectin fragments increases genetic transduction of mammalian cells
-
(1996)
Nat Med
, vol.2
, pp. 876-882
-
-
Hanenberg, H.1
-
30
-
-
0033182903
-
Activation conditions determine susceptibility of murine primary T-lymphocytes to retroviral infection
-
(1999)
J Gene Med
, vol.1
, pp. 341-351
-
-
Hagani, A.B.1
-
31
-
-
0034633678
-
Stimulation of mouse bone marrow cells with kit ligand, FLT3 ligand, and thrombopoietin leads to efficient retrovirus-mediated gene transfer to stem cells, whereas interleukin 3 and interleukin 11 reduce transduction long-term repopulating cells
-
(2000)
Hum Gene Ther
, vol.11
, pp. 2129-2141
-
-
Wognum, A.W.1
-
32
-
-
0033613827
-
Transduction of human CD34+ cells that mediate long-term engraftment of NOD/SCID mice by HIV vectors
-
(1999)
Science
, vol.283
, pp. 682-686
-
-
Miyoshi, H.1
-
33
-
-
13044309472
-
Stable transduction of quiescent CD34(+)CD38(-) human hematopoietic cells by HIV-1-based lentiviral vectors
-
(1999)
Proc Natl Acad Sci USA
, vol.96
, pp. 2988-2993
-
-
Case, S.S.1
-
35
-
-
0028883813
-
Novel retroviral vectors for efficient expression of the multidrug-resistance (mdr-1) gene in early hemopoietic cells
-
(1995)
J Virol
, vol.69
, pp. 7541-7547
-
-
Baum, C.1
-
37
-
-
0031958593
-
Scaffold attachment region-mediated enhancement of retroviral vector expression in primary T cells
-
(1998)
J Virol
, vol.72
, pp. 3720-3728
-
-
Agarwal, M.1
-
38
-
-
0030808926
-
The potent enhancer activity of the polycythemic strain of spleen focus-forming virus in hematopoietic cells is governed by a binding site for Sp1 in the upstream control region and by a unique enhancer core exclusive target for PEBP/CBF
-
(1994)
J Virol
, vol.71
, pp. 6323-6331
-
-
Baum, C.1
-
40
-
-
0033562853
-
Transcriptional targeting of retroviral vectors to the erythroblastic progeny of transduced hematopoietic stem cells
-
(1999)
Blood
, vol.93
, pp. 3276-3285
-
-
Grande, A.1
|