-
1
-
-
0035160706
-
Tolerance to solid organ transplants through transfer of MHC class II genes
-
Sonntag KC, Emery DW, Yasumoto A, et al. Tolerance to solid organ transplants through transfer of MHC class II genes. J Clin Invest 2000; 107: 65.
-
(2000)
J Clin Invest
, vol.107
, pp. 65
-
-
Sonntag, K.C.1
Emery, D.W.2
Yasumoto, A.3
-
2
-
-
0032544673
-
Inhibition of xenoreactive natural antibody production by retroviral gene therapy
-
Bracy JL, Sachs DH, Iacomini J. Inhibition of xenoreactive natural antibody production by retroviral gene therapy. Science 1998; 281: 1845.
-
(1998)
Science
, vol.281
, pp. 1845
-
-
Bracy, J.L.1
Sachs, D.H.2
Iacomini, J.3
-
3
-
-
0028797986
-
Specific unresponsiveness to a retrovirally-transferred class I antigen is controlled through the helper pathway
-
Fraser CC, Sykes M, Lee RS, et al. Specific unresponsiveness to a retrovirally-transferred class I antigen is controlled through the helper pathway. J Immunol 1995; 154: 1587.
-
(1995)
J Immunol
, vol.154
, pp. 1587
-
-
Fraser, C.C.1
Sykes, M.2
Lee, R.S.3
-
4
-
-
0036190812
-
Adenoviral transfer of a single donor-specific MHC class I gene to recipient bone marrow cells can induce specific immunological unresponsiveness in vivo
-
Fry JW, Morris PJ, Wood KJ. Adenoviral transfer of a single donor-specific MHC class I gene to recipient bone marrow cells can induce specific immunological unresponsiveness in vivo. Gene Ther 2002; 9: 220.
-
(2002)
Gene Ther
, vol.9
, pp. 220
-
-
Fry, J.W.1
Morris, P.J.2
Wood, K.J.3
-
5
-
-
0344888981
-
Haematopoietic stem cells transduced with a single donor class I major histocompatibility complex gene can induce operational tolerance to fully allogeneic cardiac allografts
-
Wong W, Fry J, Hyde K, et al. Haematopoietic stem cells transduced with a single donor class I major histocompatibility complex gene can induce operational tolerance to fully allogeneic cardiac allografts. Transplant Proc 1999; 31: 886.
-
(1999)
Transplant Proc
, vol.31
, pp. 886
-
-
Wong, W.1
Fry, J.2
Hyde, K.3
-
6
-
-
0029785313
-
Use of gene therapy to suppress the antigen-specific immune responses in mice to an HLA antigen
-
Schumacher IK, Newberg MH, Jackson JD, et al. Use of gene therapy to suppress the antigen-specific immune responses in mice to an HLA antigen. Transplantation 1996; 62: 831.
-
(1996)
Transplantation
, vol.62
, pp. 831
-
-
Schumacher, I.K.1
Newberg, M.H.2
Jackson, J.D.3
-
7
-
-
0141856330
-
Engraftment of retroviral EGFP-transduced bone marrow in mice prevents rejection of EGFP-transgenic skin grafts
-
Andersson G, Denaro M, Johnson K, et al. Engraftment of retroviral EGFP-transduced bone marrow in mice prevents rejection of EGFP-transgenic skin grafts. Mol Ther 2003; 8: 385.
-
(2003)
Mol Ther
, vol.8
, pp. 385
-
-
Andersson, G.1
Denaro, M.2
Johnson, K.3
-
8
-
-
0029958876
-
Isolation and functional properties of murine hematopoietic stem cells that are replicating in vivo
-
Goodell MA, Brose K, Paradis G, et al. Isolation and functional properties of murine hematopoietic stem cells that are replicating in vivo. J Exp Med 1996; 183: 1797.
-
(1996)
J Exp Med
, vol.183
, pp. 1797
-
-
Goodell, M.A.1
Brose, K.2
Paradis, G.3
-
9
-
-
0031435428
-
Dye efflux studies suggest that hematopoietic stem cells expressing low or undetectable levels of CD34 antigen exist in multiple species
-
Goodell MA, Rosenzweig M, Kim H, et al. Dye efflux studies suggest that hematopoietic stem cells expressing low or undetectable levels of CD34 antigen exist in multiple species. Nat Med 1997; 3: 1337.
-
(1997)
Nat Med
, vol.3
, pp. 1337
-
-
Goodell, M.A.1
Rosenzweig, M.2
Kim, H.3
-
10
-
-
0142150968
-
Phenotype correction of Fanconi anemia groupA hematopoietic stem cells using lentiviral vector
-
Yamada K, Ramezani A, Hawley RG, et al. Phenotype correction of Fanconi anemia groupA hematopoietic stem cells using lentiviral vector. Molec Ther 2003; 8: 600.
-
(2003)
Molec Ther
, vol.8
, pp. 600
-
-
Yamada, K.1
Ramezani, A.2
Hawley, R.G.3
-
12
-
-
0027595949
-
The basic science of gene therapy
-
Mulligan RC. The basic science of gene therapy. Science 1993; 260: 926.
-
(1993)
Science
, vol.260
, pp. 926
-
-
Mulligan, R.C.1
-
13
-
-
0025279872
-
Gene transfer by retrovirus vectors occurs only in cells that are actively replicating at the time of infection
-
Miller DG, Adam MA, Miller AD. Gene transfer by retrovirus vectors occurs only in cells that are actively replicating at the time of infection. Mol Cell Biol 1990; 10: 4239.
-
(1990)
Mol Cell Biol
, vol.10
, pp. 4239
-
-
Miller, D.G.1
Adam, M.A.2
Miller, A.D.3
-
14
-
-
0028055281
-
Passage through mitosis is required for oncoretroviruses but not for the human immunodeficiency virus
-
Lewis PF, Emerman M. Passage through mitosis is required for oncoretroviruses but not for the human immunodeficiency virus. J Virol 1994; 68: 510.
-
(1994)
J Virol
, vol.68
, pp. 510
-
-
Lewis, P.F.1
Emerman, M.2
-
15
-
-
0027376309
-
A nuclear localization signal within HIV-1 matrix protein that governs infection of non-dividing cells
-
Bukrinsky MI, Haggerty S, Dempsey MP, et al. A nuclear localization signal within HIV-1 matrix protein that governs infection of non-dividing cells. Nature 1993; 365: 666.
-
(1993)
Nature
, vol.365
, pp. 666
-
-
Bukrinsky, M.I.1
Haggerty, S.2
Dempsey, M.P.3
-
16
-
-
0030987672
-
HIV-1 infection of nondividing cells through the recognition of integrase by the importin/karyopherin pathway
-
Gallay P, Hope T, Chin D, et al. HIV-1 infection of nondividing cells through the recognition of integrase by the importin/karyopherin pathway. Proc Natl Acad Sci USA 1997; 94: 9825.
-
(1997)
Proc Natl Acad Sci USA
, vol.94
, pp. 9825
-
-
Gallay, P.1
Hope, T.2
Chin, D.3
-
17
-
-
0028821383
-
HIV-1 infection of nondividing cells: C-terminal tyrosine phosphorylation of the viral matrix protein is a key regulator
-
Gallay P, Swingler S, Aiken C, et al. HIV-1 infection of nondividing cells: C-terminal tyrosine phosphorylation of the viral matrix protein is a key regulator. Cell 1995; 80: 379.
-
(1995)
Cell
, vol.80
, pp. 379
-
-
Gallay, P.1
Swingler, S.2
Aiken, C.3
-
18
-
-
0030928619
-
Gene therapy-promises, problems and prospects [news]
-
Verma IM, Somia N. Gene therapy-promises, problems and prospects [news]. Nature 1997; 389: 239.
-
(1997)
Nature
, vol.389
, pp. 239
-
-
Verma, I.M.1
Somia, N.2
-
19
-
-
0033613827
-
Transduction of human CD34+ cells that mediate long-term engraftment of NOD/SCID mice by HIV vectors
-
Miyoshi H, Smith KA, Mosier DE, et al. Transduction of human CD34+ cells that mediate long-term engraftment of NOD/SCID mice by HIV vectors. Science 1999; 283: 682.
-
(1999)
Science
, vol.283
, pp. 682
-
-
Miyoshi, H.1
Smith, K.A.2
Mosier, D.E.3
-
20
-
-
0033831002
-
Lentiviral vector transduction of hematopoietic stem cells that mediate long-term reconstitution of lethally irradiated mice
-
Chen W, Wu X, Levasseur DN, et al. Lentiviral vector transduction of hematopoietic stem cells that mediate long-term reconstitution of lethally irradiated mice. Stem Cells 2000; 18: 352.
-
(2000)
Stem Cells
, vol.18
, pp. 352
-
-
Chen, W.1
Wu, X.2
Levasseur, D.N.3
-
21
-
-
0036981203
-
Induction of chimerism in mice using human MHC class I-mismatched Hoechst 33342 side population donor stem cells
-
Jackson JD, Zhou G, Kuszynski CA, et al. Induction of chimerism in mice using human MHC class I-mismatched Hoechst 33342 side population donor stem cells. Cell Transpl 2002; 11: 779.
-
(2002)
Cell Transpl
, vol.11
, pp. 779
-
-
Jackson, J.D.1
Zhou, G.2
Kuszynski, C.A.3
-
22
-
-
0029862497
-
A stable human-derived packaging cell line for production of high titer retrovirus/vesicular stomatitis virus G pseudotypes
-
Ory DS, Neugeboren BA, Mulligan RC. A stable human-derived packaging cell line for production of high titer retrovirus/vesicular stomatitis virus G pseudotypes. Proc Natl Acad Sci USA 1996; 93: 11400.
-
(1996)
Proc Natl Acad Sci USA
, vol.93
, pp. 11400
-
-
Ory, D.S.1
Neugeboren, B.A.2
Mulligan, R.C.3
-
23
-
-
0030467991
-
Transduction of nondividing cells using pseudotyped defective high-titer HIV type 1 particles
-
Reiser J, Harmison G, Kluepfel-Stahl S, et al. Transduction of nondividing cells using pseudotyped defective high-titer HIV type 1 particles. Proc Natl Acad Sci USA 1996; 93: 15266.
-
(1996)
Proc Natl Acad Sci USA
, vol.93
, pp. 15266
-
-
Reiser, J.1
Harmison, G.2
Kluepfel-Stahl, S.3
-
25
-
-
0029785313
-
Use of gene therapy to suppress the antigen-specific immune responses in mice to an HLA antigen
-
Schumacher IK, Newberg MH, Jackson JD, et al. Use of gene therapy to suppress the antigen-specific immune responses in mice to an HLA antigen. Transplantation 1996; 62: 831.
-
(1996)
Transplantation
, vol.62
, pp. 831
-
-
Schumacher, I.K.1
Newberg, M.H.2
Jackson, J.D.3
-
26
-
-
0023832325
-
Fine specificity and idiotype diversity of the murine anti-HLA-A2, A28 monoclonal antibodies CR11-351 and KS1
-
Tsujisaki M, Sakaguchi K, Igarashi M, et al. Fine specificity and idiotype diversity of the murine anti-HLA-A2, A28 monoclonal antibodies CR11-351 and KS1. Transplantation 1988; 45: 632.
-
(1988)
Transplantation
, vol.45
, pp. 632
-
-
Tsujisaki, M.1
Sakaguchi, K.2
Igarashi, M.3
-
27
-
-
0034663167
-
Homing and engraftment potential of Sca-1(+)lin(-) cells fractionated on the basis of adhesion molecule expression and position in cell cycle
-
Orschell-Traycoff CM, Hiatt K, Dagher RN, et al. Homing and engraftment potential of Sca-1(+)lin(-) cells fractionated on the basis of adhesion molecule expression and position in cell cycle. Blood 2000; 96: 1380.
-
(2000)
Blood
, vol.96
, pp. 1380
-
-
Orschell-Traycoff, C.M.1
Hiatt, K.2
Dagher, R.N.3
-
28
-
-
0031838419
-
Collection, tumor contamination, and engraftment kinetics of highly purified hematopoietic progenitor cells to support high dose therapy in multiple myeloma
-
Tricot G, Gazitt Y, Leemhuis T, et al. Collection, tumor contamination, and engraftment kinetics of highly purified hematopoietic progenitor cells to support high dose therapy in multiple myeloma. Blood 1998; 91: 4489.
-
(1998)
Blood
, vol.91
, pp. 4489
-
-
Tricot, G.1
Gazitt, Y.2
Leemhuis, T.3
-
29
-
-
0034129270
-
Transplantation of CD34+ peripheral blood cells selected using a fully automated immunomagnetic system in patienls with high-risk breast cancer: Results of a prospective randomized multicenler clinical trial
-
Yanovich S, Mitsky P, Cornelia K, et al. Transplantation of CD34+ peripheral blood cells selected using a fully automated immunomagnetic system in patienls with high-risk breast cancer: results of a prospective randomized multicenler clinical trial. Bone Marrow Transplant 2000; 25: 1165.
-
(2000)
Bone Marrow Transplant
, vol.25
, pp. 1165
-
-
Yanovich, S.1
Mitsky, P.2
Cornelia, K.3
-
30
-
-
0032956732
-
Transduction of human progenitor hematopoietic stem cells by human immunodeficiency virus type 1-based vectors is cell cycle dependent
-
Sutton RE, Reitsma MJ, Uchida N, et al. Transduction of human progenitor hematopoietic stem cells by human immunodeficiency virus type 1-based vectors is cell cycle dependent. J Virol 1999; 73: 3649.
-
(1999)
J Virol
, vol.73
, pp. 3649
-
-
Sutton, R.E.1
Reitsma, M.J.2
Uchida, N.3
-
31
-
-
0037366196
-
Cytokines, including stem cell factor alone, enhance lentiviral transduction in nondividing human LTCIC and NOD/ SCID repopulating cells
-
Zielski SP, Gerson SL. Cytokines, including stem cell factor alone, enhance lentiviral transduction in nondividing human LTCIC and NOD/ SCID repopulating cells. Mol Ther 2003; 7: 325.
-
(2003)
Mol Ther
, vol.7
, pp. 325
-
-
Zielski, S.P.1
Gerson, S.L.2
-
32
-
-
0036252492
-
High-level transduction and gene expression in hematopoietic repopulating cells using a human immunodeficiency virus type-1 based lentiviral vector containing an internal spleen focus forming virus promoter
-
Demaison C, Parsley K, Brouns G, et al. High-level transduction and gene expression in hematopoietic repopulating cells using a human immunodeficiency virus type-1 based lentiviral vector containing an internal spleen focus forming virus promoter. Hum Gene Ther 2002; 13: 803.
-
(2002)
Hum Gene Ther
, vol.13
, pp. 803
-
-
Demaison, C.1
Parsley, K.2
Brouns, G.3
-
33
-
-
0037114698
-
Lentiviral gene transfer and ex vivo expansion of human primitive stem cells capable of primary, secondary, and tertiary multilineage repopulation in NOD/SCID mice
-
Piacibello W, Bruno S, Sanavio F, et al. Lentiviral gene transfer and ex vivo expansion of human primitive stem cells capable of primary, secondary, and tertiary multilineage repopulation in NOD/SCID mice. Blood 2002; 100: 4391.
-
(2002)
Blood
, vol.100
, pp. 4391
-
-
Piacibello, W.1
Bruno, S.2
Sanavio, F.3
-
34
-
-
0036846846
-
Lentivirus-mediated gene transfer into hematopoietic repopulating cells in baboons
-
Horn PA, Morris JC, Bukovsky AA, et al. Lentivirus-mediated gene transfer into hematopoietic repopulating cells in baboons. Gene Ther 2002; 9: 1464.
-
(2002)
Gene Ther
, vol.9
, pp. 1464
-
-
Horn, P.A.1
Morris, J.C.2
Bukovsky, A.A.3
-
35
-
-
0029796633
-
Long-term lymphohematopoietic reconstitution by a single CD34- low/negative hematopoietic stem cell
-
Osawa M, Hanada K, Hamada H, et al. Long-term lymphohematopoietic reconstitution by a single CD34- low/negative hematopoietic stem cell. Science 1996; 273: 242.
-
(1996)
Science
, vol.273
, pp. 242
-
-
Osawa, M.1
Hanada, K.2
Hamada, H.3
-
36
-
-
0031979170
-
Human bone marrow CD34- cells engraft in vivo and undergo multilineage expression that includes giving rise to CD34+ cells
-
Zanjani ED, Almeida-Porada G, Livingston AG, et al. Human bone marrow CD34- cells engraft in vivo and undergo multilineage expression that includes giving rise to CD34+ cells. Exp Hematology 1998; 26: 353.
-
(1998)
Exp Hematology
, vol.26
, pp. 353
-
-
Zanjani, E.D.1
Almeida-Porada, G.2
Livingston, A.G.3
-
37
-
-
0032857031
-
Reversible expression of CD34 by murine hematopoietic stem cells
-
Sato T, Laver JH, Ogawa M. Reversible expression of CD34 by murine hematopoietic stem cells. Blood 1999; 94: 2548.
-
(1999)
Blood
, vol.94
, pp. 2548
-
-
Sato, T.1
Laver, J.H.2
Ogawa, M.3
-
38
-
-
0029996147
-
In vivo gene delivery and stable transduction of nondividing cells by a lentiviral vector
-
Naldini L, Blomer U, Gallay P, et al. In vivo gene delivery and stable transduction of nondividing cells by a lentiviral vector. Science 1996; 272: 263.
-
(1996)
Science
, vol.272
, pp. 263
-
-
Naldini, L.1
Blomer, U.2
Gallay, P.3
-
39
-
-
0033986340
-
Efficient lentiviral transduction of liver requires cell cycling in vivo
-
Park F, Ohashi K, Chiu W, et al. Efficient lentiviral transduction of liver requires cell cycling in vivo. Nat Genet 2000; 24: 49.
-
(2000)
Nat Genet
, vol.24
, pp. 49
-
-
Park, F.1
Ohashi, K.2
Chiu, W.3
-
40
-
-
0034670033
-
Lentivirus-based vectors transduce mouse hematopoietic stem cells with similar efficiency to Moloney murine leukemia virus-based vectors
-
Barrette S, Douglas JL, Seidel NE, et al. Lentivirus-based vectors transduce mouse hematopoietic stem cells with similar efficiency to Moloney murine leukemia virus-based vectors. Blood 2000; 96: 3385.
-
(2000)
Blood
, vol.96
, pp. 3385
-
-
Barrette, S.1
Douglas, J.L.2
Seidel, N.E.3
-
41
-
-
0034469216
-
Lentivirus gene transfer in murine hematopoietic progenitor cells is compromised by a delay in proviral integration and results in transduction mosaicism and heterogeneous gene expression in progeny cells
-
Mikkola H, Woods NB, Sjogren M, et al. Lentivirus gene transfer in murine hematopoietic progenitor cells is compromised by a delay in proviral integration and results in transduction mosaicism and heterogeneous gene expression in progeny cells. J Virol 2000; 74: 11911.
-
(2000)
J Virol
, vol.74
, pp. 11911
-
-
Mikkola, H.1
Woods, N.B.2
Sjogren, M.3
-
42
-
-
0032978712
-
Woodchuck hepatitis virus post-transcriptional regulatory element enhances expression of transgenes delivered by retroviral vectors
-
Zufferey R, Donello JE, Trono D, et al. Woodchuck hepatitis virus post-transcriptional regulatory element enhances expression of transgenes delivered by retroviral vectors. J Virol 1999; 73: 2886.
-
(1999)
J Virol
, vol.73
, pp. 2886
-
-
Zufferey, R.1
Donello, J.E.2
Trono, D.3
-
43
-
-
0031950572
-
Woodchuck hepatitis virus contains a tripartite post-transcriptional regulatory element
-
Donello JE, Loeb JE, Hope TJ. Woodchuck hepatitis virus contains a tripartite post-transcriptional regulatory element. J Virol 1998; 72: 5085.
-
(1998)
J Virol
, vol.72
, pp. 5085
-
-
Donello, J.E.1
Loeb, J.E.2
Hope, T.J.3
-
44
-
-
0036143801
-
Lentiviral vector-mediated transduction of murine CD34- hematopoietic stem cells
-
Tahara-Hanaoka S, Sudo K, Ema H, et al. Lentiviral vector-mediated transduction of murine CD34- hematopoietic stem cells. Exp Hematology 2002; 30: 11.
-
(2002)
Exp Hematology
, vol.30
, pp. 11
-
-
Tahara-Hanaoka, S.1
Sudo, K.2
Ema, H.3
-
45
-
-
0032548403
-
Efficient transduction of hemopoietic CD34+ progenitors of human origin using an original retroviral vector derived from Fr-MuLV-FB29: In vitro assessment
-
Cohen-Haguenauer O, Restrepo LM, Masset M, et al. Efficient transduction of hemopoietic CD34+ progenitors of human origin using an original retroviral vector derived from Fr-MuLV-FB29: in vitro assessment. Hum Gene Ther 1998; 9: 207.
-
(1998)
Hum Gene Ther
, vol.9
, pp. 207
-
-
Cohen-Haguenauer, O.1
Restrepo, L.M.2
Masset, M.3
-
46
-
-
0035173080
-
Simplified retroviral vector gcsap with murine stem cell virus long terminal repeat allows high and continued expression of enhanced green fluorescent protein by human hematopoietic progenitors engrafted in nonobese diabetic/severe combined immunodeficient mice
-
Kaneko S, Onodera M, Fujiki Y, et al. Simplified retroviral vector gcsap with murine stem cell virus long terminal repeat allows high and continued expression of enhanced green fluorescent protein by human hematopoietic progenitors engrafted in nonobese diabetic/severe combined immunodeficient mice. Hum Gene Ther 2001; 12: 35.
-
(2001)
Hum Gene Ther
, vol.12
, pp. 35
-
-
Kaneko, S.1
Onodera, M.2
Fujiki, Y.3
-
47
-
-
0030051967
-
Ex vivo expansion of murine marrow cells with IL3, IL-6, IL-11, and stem cell factor leads to impaired engraftment in irradiated hosts
-
Peters SO, Kittler EL, Ramshaw HS, et al. Ex vivo expansion of murine marrow cells with IL3, IL-6, IL-11, and stem cell factor leads to impaired engraftment in irradiated hosts. Blood 1996; 87: 30.
-
(1996)
Blood
, vol.87
, pp. 30
-
-
Peters, S.O.1
Kittler, E.L.2
Ramshaw, H.S.3
-
48
-
-
0032708005
-
Competitive repopulation of retrovirally transduced hematopietic stem cells
-
Qin S, Ward M, Raftopoulos H, et al. Competitive repopulation of retrovirally transduced hematopietic stem cells. Br J Hematol 1999; 107: 162-168.
-
(1999)
Br J Hematol
, vol.107
, pp. 162-168
-
-
Qin, S.1
Ward, M.2
Raftopoulos, H.3
|