-
1
-
-
0037222389
-
Selective depletion or blockade of Kupffer cells leads to enhanced and prolonged hepatic transgene expression using high-capacity adenoviral vectors
-
Schiedner, G, Hertel, S, Johnston, M, Dries, V, Van Rooijen, N and Kochanek, S (2003). Selective depletion or blockade of Kupffer cells leads to enhanced and prolonged hepatic transgene expression using high-capacity adenoviral vectors. Mol Ther 7: 35-43.
-
(2003)
Mol Ther
, vol.7
, pp. 35-43
-
-
Schiedner, G.1
Hertel, S.2
Johnston, M.3
Dries, V.4
Van Rooijen, N.5
Kochanek, S.6
-
2
-
-
56449103203
-
Clearance of adenovirus by Kupffer cells is mediated by scavenger receptors, natural antibodies, and complement
-
Xu, Z, Tian, J, Smith, JS and Byrnes, AP (2008). Clearance of adenovirus by Kupffer cells is mediated by scavenger receptors, natural antibodies, and complement. J Virol 82: 11705-11713.
-
(2008)
J Virol
, vol.82
, pp. 11705-11713
-
-
Xu, Z.1
Tian, J.2
Smith, J.S.3
Byrnes, A.P.4
-
3
-
-
44349168239
-
Interaction of systemically delivered adenovirus vectors with Kupffer cells in mouse liver
-
Smith, JS, Xu, Z, Tian, J, Stevenson, SC and Byrnes, AP (2008). Interaction of systemically delivered adenovirus vectors with Kupffer cells in mouse liver. Hum Gene Ther 19: 547-554.
-
(2008)
Hum Gene Ther
, vol.19
, pp. 547-554
-
-
Smith, J.S.1
Xu, Z.2
Tian, J.3
Stevenson, S.C.4
Byrnes, A.P.5
-
4
-
-
48349083683
-
Substitution of hexon hypervariable region 5 of adenovirus serotype 5 abrogates blood factor binding and limits gene transfer to liver
-
Vigant, F, Descamps, D, Jullienne, B, Esselin, S, Connault, E, Opolon, P et al. (2008). Substitution of hexon hypervariable region 5 of adenovirus serotype 5 abrogates blood factor binding and limits gene transfer to liver. Mol Ther 16: 1474-1480.
-
(2008)
Mol Ther
, vol.16
, pp. 1474-1480
-
-
Vigant, F.1
Descamps, D.2
Jullienne, B.3
Esselin, S.4
Connault, E.5
Opolon, P.6
-
5
-
-
38849134279
-
Adenovirus serotype 5 hexon mediates liver gene transfer
-
Waddington, SN, McVey, JH, Bhella, D, Parker, AL, Barker, K, Atoda, H et al. (2008). Adenovirus serotype 5 hexon mediates liver gene transfer. Cell 132: 397-409.
-
(2008)
Cell
, vol.132
, pp. 397-409
-
-
Waddington, S.N.1
McVey, J.H.2
Bhella, D.3
Parker, A.L.4
Barker, K.5
Atoda, H.6
-
6
-
-
44349193581
-
Adenovirus serotype 5 hexon is critical for virus infection of hepatocytes in vivo
-
Kalyuzhniy, O, Di Paolo, NC, Silvestry, M, Hofherr, SE, Barry, MA, Stewart, PL et al. (2008). Adenovirus serotype 5 hexon is critical for virus infection of hepatocytes in vivo. Proc Natl Acad Sci USA 105: 5483-5488.
-
(2008)
Proc Natl Acad Sci USA
, vol.105
, pp. 5483-5488
-
-
Kalyuzhniy, O.1
Di Paolo, N.C.2
Silvestry, M.3
Hofherr, S.E.4
Barry, M.A.5
Stewart, P.L.6
-
7
-
-
77953475685
-
An ex vivo loop system models the toxicity and effcacy of PEGylated and unmodifed adenovirus serotype 5 in whole human blood
-
Danielsson, A, Elgue, G, Nilsson, BM, Nilsson, B, Lambris, JD, Tötterman, TH et al. (2010). An ex vivo loop system models the toxicity and effcacy of PEGylated and unmodifed adenovirus serotype 5 in whole human blood. Gene Ther 17: 752-762.
-
(2010)
Gene Ther
, vol.17
, pp. 752-762
-
-
Danielsson, A.1
Elgue, G.2
Nilsson, B.M.3
Nilsson, B.4
Lambris, J.D.5
Tötterman, T.H.6
-
8
-
-
37549043879
-
Fully detargeted polyethylene glycol-coated adenovirus vectors are potent genetic vaccines and escape from pre-existing anti-adenovirus antibodies
-
Wortmann, A, Vöhringer, S, Engler, T, Corjon, S, Schirmbeck, R, Reimann, J et al. (2008). Fully detargeted polyethylene glycol-coated adenovirus vectors are potent genetic vaccines and escape from pre-existing anti-adenovirus antibodies. Mol Ther 16: 154-162.
-
(2008)
Mol Ther
, vol.16
, pp. 154-162
-
-
Wortmann, A.1
Vöhringer, S.2
Engler, T.3
Corjon, S.4
Schirmbeck, R.5
Reimann, J.6
-
9
-
-
34548020561
-
Effective tumor targeted gene transfer using PEGylated adenovirus vector via systemic administration
-
Gao, JQ, Eto, Y, Yoshioka, Y, Sekiguchi, F, Kurachi, S, Morishige, T et al. (2007). Effective tumor targeted gene transfer using PEGylated adenovirus vector via systemic administration. J Control Release 122: 102-110.
-
(2007)
J Control Release
, vol.122
, pp. 102-110
-
-
Gao, J.Q.1
Eto, Y.2
Yoshioka, Y.3
Sekiguchi, F.4
Kurachi, S.5
Morishige, T.6
-
10
-
-
54949092481
-
Targeting of adenovirus vectors to the LRP receptor family with the high-affnity ligand RAP via combined genetic and chemical modifcation of the pIX capsomere
-
Corjon, S, Wortmann, A, Engler, T, Van Rooijen, N, Kochanek, S and Kreppel, F (2008). Targeting of adenovirus vectors to the LRP receptor family with the high-affnity ligand RAP via combined genetic and chemical modifcation of the pIX capsomere. Mol Ther 16: 1813-1824.
-
(2008)
Mol Ther
, vol.16
, pp. 1813-1824
-
-
Corjon, S.1
Wortmann, A.2
Engler, T.3
Van Rooijen, N.4
Kochanek, S.5
Kreppel, F.6
-
11
-
-
33846529157
-
Fiber-modifed adenovirus vectors decrease liver toxicity through reduced IL-6 production
-
Koizumi, N, Yamaguchi, T, Kawabata, K, Sakurai, F, Sasaki, T, Watanabe, Y et al. (2007). Fiber-modifed adenovirus vectors decrease liver toxicity through reduced IL-6 production. J Immunol 178: 1767-1773.
-
(2007)
J Immunol
, vol.178
, pp. 1767-1773
-
-
Koizumi, N.1
Yamaguchi, T.2
Kawabata, K.3
Sakurai, F.4
Sasaki, T.5
Watanabe, Y.6
-
12
-
-
33645912596
-
Improved hepatic transduction, reduced systemic vector dissemination, and long-term transgene expression by delivering helper-dependent adenoviral vectors into the surgically isolated liver of nonhuman primates
-
Brunetti-Pierri, N, Ng, T, Iannitti, DA, Palmer, DJ, Beaudet, AL, Finegold, MJ et al. (2006). Improved hepatic transduction, reduced systemic vector dissemination, and long-term transgene expression by delivering helper-dependent adenoviral vectors into the surgically isolated liver of nonhuman primates. Hum Gene Ther 17: 391-404.
-
(2006)
Hum Gene Ther
, vol.17
, pp. 391-404
-
-
Brunetti-Pierri, N.1
Ng, T.2
Iannitti, D.A.3
Palmer, D.J.4
Beaudet, A.L.5
Finegold, M.J.6
-
13
-
-
33947244363
-
Pseudo-hydrodynamic delivery of helper-dependent adenoviral vectors into non-human primates for liver-directed gene therapy
-
Brunetti-Pierri, N, Stapleton, GE, Palmer, DJ, Zuo, Y, Mane, VP, Finegold, MJ et al. (2007). Pseudo-hydrodynamic delivery of helper-dependent adenoviral vectors into non-human primates for liver-directed gene therapy. Mol Ther 15: 732-740.
-
(2007)
Mol Ther
, vol.15
, pp. 732-740
-
-
Brunetti-Pierri, N.1
Stapleton, G.E.2
Palmer, D.J.3
Zuo, Y.4
Mane, V.P.5
Finegold, M.J.6
-
14
-
-
0034633740
-
Effcient transformation of primary human amniocytes by E1 functions of Ad5: Generation of new cell lines for adenoviral vector production
-
Schiedner, G, Hertel, S and Kochanek, S (2000). Effcient transformation of primary human amniocytes by E1 functions of Ad5: generation of new cell lines for adenoviral vector production. Hum Gene Ther 11: 2105-2116.
-
(2000)
Hum Gene Ther
, vol.11
, pp. 2105-2116
-
-
Schiedner, G.1
Hertel, S.2
Kochanek, S.3
-
15
-
-
77957832543
-
Capsomere-specifc fuorescent labeling of adenovirus vector particles allows for detailed analysis of intracellular particle traffcking and of the performance of bioresponsive bonds for vector capsid modifcations
-
Espenlaub, S, Corjon, S, Engler, T, Fella, C, Ogris, M, Wagner, E et al. (2010). Capsomere-specifc fuorescent labeling of adenovirus vector particles allows for detailed analysis of intracellular particle traffcking and of the performance of bioresponsive bonds for vector capsid modifcations. Hum Gene Ther 21: 1155-1167.
-
(2010)
Hum Gene Ther
, vol.21
, pp. 1155-1167
-
-
Espenlaub, S.1
Corjon, S.2
Engler, T.3
Fella, C.4
Ogris, M.5
Wagner, E.6
-
16
-
-
20844445679
-
Combined genetic and chemical capsid modifcations enable fexible and effcient de- and retargeting of adenovirus vectors
-
Kreppel, F, Gackowski, J, Schmidt, E and Kochanek, S (2005). Combined genetic and chemical capsid modifcations enable fexible and effcient de- and retargeting of adenovirus vectors. Mol Ther 12: 107-117.
-
(2005)
Mol Ther
, vol.12
, pp. 107-117
-
-
Kreppel, F.1
Gackowski, J.2
Schmidt, E.3
Kochanek, S.4
-
17
-
-
9244221679
-
Prediction of the viscosity radius and the size exclusion chromatography behavior of PEGylated proteins
-
Fee, CJ and Van Alstine, JM (2004). Prediction of the viscosity radius and the size exclusion chromatography behavior of PEGylated proteins. Bioconjug Chem 15: 1304-1313.
-
(2004)
Bioconjug Chem
, vol.15
, pp. 1304-1313
-
-
Fee, C.J.1
Van Alstine, J.M.2
-
18
-
-
38849134279
-
Adenovirus serotype 5 hexon mediates liver gene transfer
-
Waddington, SN, McVey, JH, Bhella, D, Parker, AL, Barker, K, Atoda, H et al. (2008). Adenovirus serotype 5 hexon mediates liver gene transfer. Cell 132: 397-409.
-
(2008)
Cell
, vol.132
, pp. 397-409
-
-
Waddington, S.N.1
McVey, J.H.2
Bhella, D.3
Parker, A.L.4
Barker, K.5
Atoda, H.6
-
19
-
-
44349193581
-
Adenovirus serotype 5 hexon is critical for virus infection of hepatocytes in vivo
-
Kalyuzhniy, O, McVey, JH, Bhella, D, Parker, AL, Barker, K, Atoda, H et al. (2008) Adenovirus serotype 5 hexon is critical for virus infection of hepatocytes in vivo. Proc Natl Acad Sci U.S.A 105: 5483-5488.
-
(2008)
Proc Natl Acad Sci U.S.A
, vol.105
, pp. 5483-5488
-
-
Kalyuzhniy, O.1
McVey, J.H.2
Bhella, D.3
Parker, A.L.4
Barker, K.5
Atoda, H.6
-
20
-
-
16844382964
-
CAR: A virus receptor within the tight junction
-
Coyne, CB and Bergelson, JM (2005). CAR: a virus receptor within the tight junction. Adv Drug Deliv Rev 57: 869-882.
-
(2005)
Adv Drug Deliv Rev
, vol.57
, pp. 869-882
-
-
Coyne, C.B.1
Bergelson, J.M.2
-
21
-
-
0036000329
-
Correction of the nonlinear dose response improves the viability of adenoviral vectors for gene therapy of Fabry disease
-
Ziegler, RJ, Li, C, Cherry, M, Zhu, Y, Hempel, D, Van Rooijen, N et al. (2002). Correction of the nonlinear dose response improves the viability of adenoviral vectors for gene therapy of Fabry disease. Hum Gene Ther 13: 935-945.
-
(2002)
Hum Gene Ther
, vol.13
, pp. 935-945
-
-
Ziegler, R.J.1
Li, C.2
Cherry, M.3
Zhu, Y.4
Hempel, D.5
Van Rooijen, N.6
-
22
-
-
0030943732
-
Macrophage depletion increases the safety, effcacy and persistence of adenovirus-mediated gene transfer in vivo
-
Kuzmin, AI, Finegold, MJ and Eisensmith, RC (1997). Macrophage depletion increases the safety, effcacy and persistence of adenovirus-mediated gene transfer in vivo. Gene Ther 4: 309-316.
-
(1997)
Gene Ther
, vol.4
, pp. 309-316
-
-
Kuzmin, A.I.1
Finegold, M.J.2
Eisensmith, R.C.3
-
23
-
-
0037372398
-
Therapeutic factor VIII levels and negligible toxicity in mouse and dog models of hemophilia A following gene therapy with high-capacity adenoviral vectors
-
Chuah, MK, Schiedner, G, Thorrez, L, Brown, B, Johnston, M, Gillijns, V et al. (2003). Therapeutic factor VIII levels and negligible toxicity in mouse and dog models of hemophilia A following gene therapy with high-capacity adenoviral vectors. Blood 101: 1734-1743.
-
(2003)
Blood
, vol.101
, pp. 1734-1743
-
-
Chuah, M.K.1
Schiedner, G.2
Thorrez, L.3
Brown, B.4
Johnston, M.5
Gillijns, V.6
-
24
-
-
0034266550
-
In vivo dose threshold effect of adenovirus-mediated factor VIII gene therapy in hemophiliac mice
-
Bristol, JA, Shirley, P, Idamakanti, N, Kaleko, M and Connelly, S (2000). In vivo dose threshold effect of adenovirus-mediated factor VIII gene therapy in hemophiliac mice. Mol Ther 2: 223-232.
-
(2000)
Mol Ther
, vol.2
, pp. 223-232
-
-
Bristol, J.A.1
Shirley, P.2
Idamakanti, N.3
Kaleko, M.4
Connelly, S.5
-
25
-
-
0034632396
-
Development of a rapid method for the PEGylation of adenoviruses with enhanced transduction and improved stability under harsh storage conditions
-
Croyle, MA, Yu, QC and Wilson, JM (2000). Development of a rapid method for the PEGylation of adenoviruses with enhanced transduction and improved stability under harsh storage conditions. Hum Gene Ther 11: 1713-1722.
-
(2000)
Hum Gene Ther
, vol.11
, pp. 1713-1722
-
-
Croyle, M.A.1
Yu, Q.C.2
Wilson, J.M.3
-
26
-
-
34848845849
-
Polyethylene glycol modifcation of adenovirus reduces platelet activation, endothelial cell activation, and thrombocytopenia
-
Hofherr, SE, Mok, H, Gushiken, FC, Lopez, JA and Barry, MA (2007). Polyethylene glycol modifcation of adenovirus reduces platelet activation, endothelial cell activation, and thrombocytopenia. Hum Gene Ther 18: 837-848.
-
(2007)
Hum Gene Ther
, vol.18
, pp. 837-848
-
-
Hofherr, S.E.1
Mok, H.2
Gushiken, F.C.3
Lopez, J.A.4
Barry, M.A.5
-
27
-
-
0033587174
-
PEGylation of adenovirus with retention of infectivity and protection from neutralizing antibody in vitro and in vivo
-
O'Riordan, CR, Lachapelle, A, Delgado, C, Parkes, V, Wadsworth, SC, Smith, AE et al. (1999). PEGylation of adenovirus with retention of infectivity and protection from neutralizing antibody in vitro and in vivo. Hum Gene Ther 10: 1349-1358.
-
(1999)
Hum Gene Ther
, vol.10
, pp. 1349-1358
-
-
O'Riordan, C.R.1
Lachapelle, A.2
Delgado, C.3
Parkes, V.4
Wadsworth, S.C.5
Smith, A.E.6
-
28
-
-
37549008707
-
Modifcation of adenovirus gene transfer vectors with synthetic polymers: A scientifc review and technical guide
-
Kreppel, F and Kochanek, S (2008). Modifcation of adenovirus gene transfer vectors with synthetic polymers: a scientifc review and technical guide. Mol Ther 16: 16-29.
-
(2008)
Mol Ther
, vol.16
, pp. 16-29
-
-
Kreppel, F.1
Kochanek, S.2
-
29
-
-
68649104639
-
Chemical modifcation with high molecular weight polyethylene glycol reduces transduction of hepatocytes and increases effcacy of intravenously delivered oncolytic adenovirus
-
Doronin, K, Shashkova, EV, May, SM, Hofherr, SE and Barry, MA (2009). Chemical modifcation with high molecular weight polyethylene glycol reduces transduction of hepatocytes and increases effcacy of intravenously delivered oncolytic adenovirus. Hum Gene Ther 20: 975-988.
-
(2009)
Hum Gene Ther
, vol.20
, pp. 975-988
-
-
Doronin, K.1
Shashkova, E.V.2
May, S.M.3
Hofherr, S.E.4
Barry, M.A.5
-
30
-
-
37549043879
-
Fully detargeted polyethylene glycol-coated adenovirus vectors are potent genetic vaccines and escape from pre-existing anti-adenovirus antibodies
-
Wortmann, A, Vöhringer, S, Engler, T, Corjon, S, Schirmbeck, R, Reimann, J et al. (2008). Fully detargeted polyethylene glycol-coated adenovirus vectors are potent genetic vaccines and escape from pre-existing anti-adenovirus antibodies. Mol Ther 16: 154-162.
-
(2008)
Mol Ther
, vol.16
, pp. 154-162
-
-
Wortmann, A.1
Vöhringer, S.2
Engler, T.3
Corjon, S.4
Schirmbeck, R.5
Reimann, J.6
-
31
-
-
10944247251
-
Evaluation of polyethylene glycol modifcation of frst-generation and helper-dependent adenoviral vectors to reduce innate immune responses
-
Mok, H, Palmer, DJ, Ng, P and Barry, MA (2005). Evaluation of polyethylene glycol modifcation of frst-generation and helper-dependent adenoviral vectors to reduce innate immune responses. Mol Ther 11: 66-79.
-
(2005)
Mol Ther
, vol.11
, pp. 66-79
-
-
Mok, H.1
Palmer, D.J.2
Ng, P.3
Barry, M.A.4
-
32
-
-
0036412085
-
PEGylation of E1-deleted adenovirus vectors allows signifcant gene expression on readministration to liver
-
Croyle, MA, Chirmule, N, Zhang, Y and Wilson, JM (2002). PEGylation of E1-deleted adenovirus vectors allows signifcant gene expression on readministration to liver. Hum Gene Ther 13: 1887-1900.
-
(2002)
Hum Gene Ther
, vol.13
, pp. 1887-1900
-
-
Croyle, M.A.1
Chirmule, N.2
Zhang, Y.3
Wilson, J.M.4
-
33
-
-
33646861014
-
Comparison of adenovirus fber, protein IX, and hexon capsomeres as scaffolds for vector purifcation and cell targeting
-
Campos, SK and Barry, MA (2006). Comparison of adenovirus fber, protein IX, and hexon capsomeres as scaffolds for vector purifcation and cell targeting. Virology 349: 453-462.
-
(2006)
Virology
, vol.349
, pp. 453-462
-
-
Campos, S.K.1
Barry, M.A.2
-
34
-
-
0035077806
-
Polymer-coated adenovirus permits effcient retargeting and evades neutralising antibodies
-
Fisher, KD, Stallwood, Y, Green, NK, Ulbrich, K, Mautner, V and Seymour, LW (2001). Polymer-coated adenovirus permits effcient retargeting and evades neutralising antibodies. Gene Ther 8: 341-348.
-
(2001)
Gene Ther
, vol.8
, pp. 341-348
-
-
Fisher, K.D.1
Stallwood, Y.2
Green, N.K.3
Ulbrich, K.4
Mautner, V.5
Seymour, L.W.6
-
35
-
-
62549159111
-
Cetuximab retargeting of adenovirus via the epidermal growth factor receptor for treatment of intraperitoneal ovarian cancer
-
Morrison, J, Briggs, SS, Green, NK, Thoma, C, Fisher, KD, Kehoe, S et al. (2009). Cetuximab retargeting of adenovirus via the epidermal growth factor receptor for treatment of intraperitoneal ovarian cancer. Hum Gene Ther 20: 239-251.
-
(2009)
Hum Gene Ther
, vol.20
, pp. 239-251
-
-
Morrison, J.1
Briggs, S.S.2
Green, N.K.3
Thoma, C.4
Fisher, K.D.5
Kehoe, S.6
-
36
-
-
0042199037
-
Targeting adenoviral vectors using heterofunctional polyethylene glycol FGF2 conjugates
-
Lanciotti, J, Song, A, Doukas, J, Sosnowski, B, Pierce, G, Gregory, R et al. (2003). Targeting adenoviral vectors using heterofunctional polyethylene glycol FGF2 conjugates. Mol Ther 8: 99-107.
-
(2003)
Mol Ther
, vol.8
, pp. 99-107
-
-
Lanciotti, J.1
Song, A.2
Doukas, J.3
Sosnowski, B.4
Pierce, G.5
Gregory, R.6
-
37
-
-
48349083683
-
Substitution of hexon hypervariable region 5 of adenovirus serotype 5 abrogates blood factor binding and limits gene transfer to liver
-
Vigant, F, Descamps, D, Jullienne, B, Esselin, S, Connault, E, Opolon, P et al. (2008). Substitution of hexon hypervariable region 5 of adenovirus serotype 5 abrogates blood factor binding and limits gene transfer to liver. Mol Ther 16: 1474-1480.
-
(2008)
Mol Ther
, vol.16
, pp. 1474-1480
-
-
Vigant, F.1
Descamps, D.2
Jullienne, B.3
Esselin, S.4
Connault, E.5
Opolon, P.6
-
38
-
-
0346872991
-
Improved system for helper-dependent adenoviral vector production
-
Palmer, D and Ng, P (2003). Improved system for helper-dependent adenoviral vector production. Mol Ther 8: 846-852.
-
(2003)
Mol Ther
, vol.8
, pp. 846-852
-
-
Palmer, D.1
Ng, P.2
-
39
-
-
84934443073
-
Methods for the production of helper-dependent adenoviral vectors
-
Palmer, DJ and Ng, P (2008). Methods for the production of helper-dependent adenoviral vectors. Methods Mol Biol 433: 33-53.
-
(2008)
Methods Mol Biol
, vol.433
, pp. 33-53
-
-
Palmer, D.J.1
Ng, P.2
-
40
-
-
0036019186
-
A DNA-based method to assay total and infectious particle contents and helper virus contamination in high-capacity adenoviral vector preparations
-
Kreppel, F, Biermann, V, Kochanek, S and Schiedner, G (2002). A DNA-based method to assay total and infectious particle contents and helper virus contamination in high-capacity adenoviral vector preparations. Hum Gene Ther 13: 1151-1156.
-
(2002)
Hum Gene Ther
, vol.13
, pp. 1151-1156
-
-
Kreppel, F.1
Biermann, V.2
Kochanek, S.3
Schiedner, G.4
-
41
-
-
0028111256
-
Liposome mediated depletion of macrophages: Mechanism of action, preparation of liposomes and applications
-
Van Rooijen, N and Sanders, A (1994). Liposome mediated depletion of macrophages: mechanism of action, preparation of liposomes and applications. J Immunol Methods 174: 83-93.
-
(1994)
J Immunol Methods
, vol.174
, pp. 83-93
-
-
Van Rooijen, N.1
Sanders, A.2
|