-
1
-
-
84937908208
-
Engineered CRISPR-Cas9 nucleases with altered PAM specificities
-
1 Kleinstiver, B.P., Prew, M.S., Tsai, S.Q., Topkar, V.V., Nguyen, N.T., Zheng, Z., Gonzales, A.P., Li, Z., Peterson, R.T., Yeh, J.R., et al. Engineered CRISPR-Cas9 nucleases with altered PAM specificities. Nature 523 (2015), 481–485.
-
(2015)
Nature
, vol.523
, pp. 481-485
-
-
Kleinstiver, B.P.1
Prew, M.S.2
Tsai, S.Q.3
Topkar, V.V.4
Nguyen, N.T.5
Zheng, Z.6
Gonzales, A.P.7
Li, Z.8
Peterson, R.T.9
Yeh, J.R.10
-
2
-
-
84927514894
-
In vivo genome editing using Staphylococcus aureus Cas9
-
2 Ran, F.A., Cong, L., Yan, W.X., Scott, D.A., Gootenberg, J.S., Kriz, A.J., Zetsche, B., Shalem, O., Wu, X., Makarova, K.S., et al. In vivo genome editing using Staphylococcus aureus Cas9. Nature 520 (2015), 186–191.
-
(2015)
Nature
, vol.520
, pp. 186-191
-
-
Ran, F.A.1
Cong, L.2
Yan, W.X.3
Scott, D.A.4
Gootenberg, J.S.5
Kriz, A.J.6
Zetsche, B.7
Shalem, O.8
Wu, X.9
Makarova, K.S.10
-
3
-
-
84929761323
-
Adeno-associated virus at 50: a golden anniversary of discovery, research, and gene therapy success–a personal perspective
-
3 Hastie, E., Samulski, R.J., Adeno-associated virus at 50: a golden anniversary of discovery, research, and gene therapy success–a personal perspective. Hum. Gene Ther. 26 (2015), 257–265.
-
(2015)
Hum. Gene Ther.
, vol.26
, pp. 257-265
-
-
Hastie, E.1
Samulski, R.J.2
-
4
-
-
84926061715
-
In vivo interrogation of gene function in the mammalian brain using CRISPR-Cas9
-
4 Swiech, L., Heidenreich, M., Banerjee, A., Habib, N., Li, Y., Trombetta, J., Sur, M., Zhang, F., In vivo interrogation of gene function in the mammalian brain using CRISPR-Cas9. Nat. Biotechnol. 33 (2015), 102–106.
-
(2015)
Nat. Biotechnol.
, vol.33
, pp. 102-106
-
-
Swiech, L.1
Heidenreich, M.2
Banerjee, A.3
Habib, N.4
Li, Y.5
Trombetta, J.6
Sur, M.7
Zhang, F.8
-
5
-
-
84961288301
-
Cationic lipid-mediated delivery of proteins enables efficient protein-based genome editing in vitro and in vivo
-
5 Zuris, J.A., Thompson, D.B., Shu, Y., Guilinger, J.P., Bessen, J.L., Hu, J.H., Maeder, M.L., Joung, J.K., Chen, Z.Y., Liu, D.R., Cationic lipid-mediated delivery of proteins enables efficient protein-based genome editing in vitro and in vivo. Nat. Biotechnol. 33 (2015), 73–80.
-
(2015)
Nat. Biotechnol.
, vol.33
, pp. 73-80
-
-
Zuris, J.A.1
Thompson, D.B.2
Shu, Y.3
Guilinger, J.P.4
Bessen, J.L.5
Hu, J.H.6
Maeder, M.L.7
Joung, J.K.8
Chen, Z.Y.9
Liu, D.R.10
-
6
-
-
84902095353
-
Genome editing with Cas9 in adult mice corrects a disease mutation and phenotype
-
6 Yin, H., Xue, W., Chen, S., Bogorad, R.L., Benedetti, E., Grompe, M., Koteliansky, V., Sharp, P.A., Jacks, T., Anderson, D.G., Genome editing with Cas9 in adult mice corrects a disease mutation and phenotype. Nat. Biotechnol. 32 (2014), 551–553.
-
(2014)
Nat. Biotechnol.
, vol.32
, pp. 551-553
-
-
Yin, H.1
Xue, W.2
Chen, S.3
Bogorad, R.L.4
Benedetti, E.5
Grompe, M.6
Koteliansky, V.7
Sharp, P.A.8
Jacks, T.9
Anderson, D.G.10
-
7
-
-
84960882884
-
Therapeutic genome editing by combined viral and non-viral delivery of CRISPR system components in vivo
-
7 Yin, H., Song, C.Q., Dorkin, J.R., Zhu, L.J., Li, Y., Wu, Q., Park, A., Yang, J., Suresh, S., Bizhanova, A., et al. Therapeutic genome editing by combined viral and non-viral delivery of CRISPR system components in vivo. Nat. Biotechnol. 34 (2016), 328–333.
-
(2016)
Nat. Biotechnol.
, vol.34
, pp. 328-333
-
-
Yin, H.1
Song, C.Q.2
Dorkin, J.R.3
Zhu, L.J.4
Li, Y.5
Wu, Q.6
Park, A.7
Yang, J.8
Suresh, S.9
Bizhanova, A.10
-
8
-
-
84887772816
-
Newer gene editing technologies toward HIV gene therapy
-
8 Manjunath, N., Yi, G., Dang, Y., Shankar, P., Newer gene editing technologies toward HIV gene therapy. Viruses 5 (2013), 2748–2766.
-
(2013)
Viruses
, vol.5
, pp. 2748-2766
-
-
Manjunath, N.1
Yi, G.2
Dang, Y.3
Shankar, P.4
-
9
-
-
84876407799
-
Targeted gene disruption to cure HIV
-
9 Stone, D., Kiem, H.P., Jerome, K.R., Targeted gene disruption to cure HIV. Curr. Opin. HIV AIDS 8 (2013), 217–223.
-
(2013)
Curr. Opin. HIV AIDS
, vol.8
, pp. 217-223
-
-
Stone, D.1
Kiem, H.P.2
Jerome, K.R.3
-
10
-
-
84919904581
-
CCR5 gene disruption via lentiviral vectors expressing Cas9 and single guided RNA renders cells resistant to HIV-1 infection
-
10 Wang, W., Ye, C., Liu, J., Zhang, D., Kimata, J.T., Zhou, P., CCR5 gene disruption via lentiviral vectors expressing Cas9 and single guided RNA renders cells resistant to HIV-1 infection. PLoS ONE, 9, 2014, e115987.
-
(2014)
PLoS ONE
, vol.9
, pp. e115987
-
-
Wang, W.1
Ye, C.2
Liu, J.3
Zhang, D.4
Kimata, J.T.5
Zhou, P.6
-
11
-
-
84905643812
-
RNA-directed gene editing specifically eradicates latent and prevents new HIV-1 infection
-
11 Hu, W., Kaminski, R., Yang, F., Zhang, Y., Cosentino, L., Li, F., Luo, B., Alvarez-Carbonell, D., Garcia-Mesa, Y., Karn, J., et al. RNA-directed gene editing specifically eradicates latent and prevents new HIV-1 infection. Proc. Natl. Acad. Sci. USA 111 (2014), 11461–11466.
-
(2014)
Proc. Natl. Acad. Sci. USA
, vol.111
, pp. 11461-11466
-
-
Hu, W.1
Kaminski, R.2
Yang, F.3
Zhang, Y.4
Cosentino, L.5
Li, F.6
Luo, B.7
Alvarez-Carbonell, D.8
Garcia-Mesa, Y.9
Karn, J.10
-
12
-
-
84883305437
-
Harnessing the CRISPR/Cas9 system to disrupt latent HIV-1 provirus
-
12 Ebina, H., Misawa, N., Kanemura, Y., Koyanagi, Y., Harnessing the CRISPR/Cas9 system to disrupt latent HIV-1 provirus. Sci. Rep., 3, 2013, 2510.
-
(2013)
Sci. Rep.
, vol.3
, pp. 2510
-
-
Ebina, H.1
Misawa, N.2
Kanemura, Y.3
Koyanagi, Y.4
-
13
-
-
84924365668
-
Use of the CRISPR/Cas9 system as an intracellular defense against HIV-1 infection in human cells
-
13 Liao, H.K., Gu, Y., Diaz, A., Marlett, J., Takahashi, Y., Li, M., Suzuki, K., Xu, R., Hishida, T., Chang, C.J., et al. Use of the CRISPR/Cas9 system as an intracellular defense against HIV-1 infection in human cells. Nat. Commun., 6, 2015, 6413.
-
(2015)
Nat. Commun.
, vol.6
, pp. 6413
-
-
Liao, H.K.1
Gu, Y.2
Diaz, A.3
Marlett, J.4
Takahashi, Y.5
Li, M.6
Suzuki, K.7
Xu, R.8
Hishida, T.9
Chang, C.J.10
-
14
-
-
84928739868
-
The CRISPR/Cas9 system inactivates latent HIV-1 proviral DNA
-
14 Zhu, W., Lei, R., Le Duff, Y., Li, J., Guo, F., Wainberg, M.A., Liang, C., The CRISPR/Cas9 system inactivates latent HIV-1 proviral DNA. Retrovirology, 12, 2015, 22.
-
(2015)
Retrovirology
, vol.12
, pp. 22
-
-
Zhu, W.1
Lei, R.2
Le Duff, Y.3
Li, J.4
Guo, F.5
Wainberg, M.A.6
Liang, C.7
-
15
-
-
84960482311
-
Elimination of HIV-1 genomes from human T-lymphoid cells by CRISPR/Cas9 gene editing
-
15 Kaminski, R., Chen, Y., Fischer, T., Tedaldi, E., Napoli, A., Zhang, Y., Karn, J., Hu, W., Khalili, K., Elimination of HIV-1 genomes from human T-lymphoid cells by CRISPR/Cas9 gene editing. Sci. Rep., 6, 2016, 22555.
-
(2016)
Sci. Rep.
, vol.6
, pp. 22555
-
-
Kaminski, R.1
Chen, Y.2
Fischer, T.3
Tedaldi, E.4
Napoli, A.5
Zhang, Y.6
Karn, J.7
Hu, W.8
Khalili, K.9
-
16
-
-
84961226661
-
Functional screening of guide RNAs targeting the regulatory and structural HIV-1 viral genome for a cure of AIDS
-
16 Yin, C., Zhang, T., Li, F., Yang, F., Putatunda, R., Young, W.B., Khalili, K., Hu, W., Zhang, Y., Functional screening of guide RNAs targeting the regulatory and structural HIV-1 viral genome for a cure of AIDS. AIDS 30 (2016), 1163–1174.
-
(2016)
AIDS
, vol.30
, pp. 1163-1174
-
-
Yin, C.1
Zhang, T.2
Li, F.3
Yang, F.4
Putatunda, R.5
Young, W.B.6
Khalili, K.7
Hu, W.8
Zhang, Y.9
-
17
-
-
84969706258
-
Excision of HIV-1 DNA by gene editing: a proof-of-concept in vivo study
-
17 Kaminski, R., Bella, R., Yin, C., Otte, J., Ferrante, P., Gendelman, H.E., Li, H., Booze, R., Gordon, J., Hu, W., Khalili, K., Excision of HIV-1 DNA by gene editing: a proof-of-concept in vivo study. Gene Ther. 23 (2016), 690–695.
-
(2016)
Gene Ther.
, vol.23
, pp. 690-695
-
-
Kaminski, R.1
Bella, R.2
Yin, C.3
Otte, J.4
Ferrante, P.5
Gendelman, H.E.6
Li, H.7
Booze, R.8
Gordon, J.9
Hu, W.10
Khalili, K.11
-
18
-
-
55749089404
-
Visualizing fewer than 10 mouse T cells with an enhanced firefly luciferase in immunocompetent mouse models of cancer
-
18 Rabinovich, B.A., Ye, Y., Etto, T., Chen, J.Q., Levitsky, H.I., Overwijk, W.W., Cooper, L.J., Gelovani, J., Hwu, P., Visualizing fewer than 10 mouse T cells with an enhanced firefly luciferase in immunocompetent mouse models of cancer. Proc. Natl. Acad. Sci. USA 105 (2008), 14342–14346.
-
(2008)
Proc. Natl. Acad. Sci. USA
, vol.105
, pp. 14342-14346
-
-
Rabinovich, B.A.1
Ye, Y.2
Etto, T.3
Chen, J.Q.4
Levitsky, H.I.5
Overwijk, W.W.6
Cooper, L.J.7
Gelovani, J.8
Hwu, P.9
-
19
-
-
20144362235
-
A mouse model for study of systemic HIV-1 infection, antiviral immune responses, and neuroinvasiveness
-
19 Potash, M.J., Chao, W., Bentsman, G., Paris, N., Saini, M., Nitkiewicz, J., Belem, P., Sharer, L., Brooks, A.I., Volsky, D.J., A mouse model for study of systemic HIV-1 infection, antiviral immune responses, and neuroinvasiveness. Proc. Natl. Acad. Sci. USA 102 (2005), 3760–3765.
-
(2005)
Proc. Natl. Acad. Sci. USA
, vol.102
, pp. 3760-3765
-
-
Potash, M.J.1
Chao, W.2
Bentsman, G.3
Paris, N.4
Saini, M.5
Nitkiewicz, J.6
Belem, P.7
Sharer, L.8
Brooks, A.I.9
Volsky, D.J.10
-
20
-
-
84939961087
-
Genome editing strategies: potential tools for eradicating HIV-1/AIDS
-
20 Khalili, K., Kaminski, R., Gordon, J., Cosentino, L., Hu, W., Genome editing strategies: potential tools for eradicating HIV-1/AIDS. J. Neurovirol. 21 (2015), 310–321.
-
(2015)
J. Neurovirol.
, vol.21
, pp. 310-321
-
-
Khalili, K.1
Kaminski, R.2
Gordon, J.3
Cosentino, L.4
Hu, W.5
-
21
-
-
84940368054
-
Crystal structure of Staphylococcus aureus Cas9
-
21 Nishimasu, H., Cong, L., Yan, W.X., Ran, F.A., Zetsche, B., Li, Y., Kurabayashi, A., Ishitani, R., Zhang, F., Nureki, O., Crystal structure of Staphylococcus aureus Cas9. Cell 162 (2015), 1113–1126.
-
(2015)
Cell
, vol.162
, pp. 1113-1126
-
-
Nishimasu, H.1
Cong, L.2
Yan, W.X.3
Ran, F.A.4
Zetsche, B.5
Li, Y.6
Kurabayashi, A.7
Ishitani, R.8
Zhang, F.9
Nureki, O.10
-
22
-
-
84947714470
-
Characterization of Staphylococcus aureus Cas9: a smaller Cas9 for all-in-one adeno-associated virus delivery and paired nickase applications
-
22 Friedland, A.E., Baral, R., Singhal, P., Loveluck, K., Shen, S., Sanchez, M., Marco, E., Gotta, G.M., Maeder, M.L., Kennedy, E.M., et al. Characterization of Staphylococcus aureus Cas9: a smaller Cas9 for all-in-one adeno-associated virus delivery and paired nickase applications. Genome Biol., 16, 2015, 257.
-
(2015)
Genome Biol.
, vol.16
, pp. 257
-
-
Friedland, A.E.1
Baral, R.2
Singhal, P.3
Loveluck, K.4
Shen, S.5
Sanchez, M.6
Marco, E.7
Gotta, G.M.8
Maeder, M.L.9
Kennedy, E.M.10
-
23
-
-
74049085498
-
Effect of genome size on AAV vector packaging
-
23 Wu, Z., Yang, H., Colosi, P., Effect of genome size on AAV vector packaging. Mol. Ther. 18 (2010), 80–86.
-
(2010)
Mol. Ther.
, vol.18
, pp. 80-86
-
-
Wu, Z.1
Yang, H.2
Colosi, P.3
-
24
-
-
43049119982
-
Serotype-dependent packaging of large genes in adeno-associated viral vectors results in effective gene delivery in mice
-
24 Allocca, M., Doria, M., Petrillo, M., Colella, P., Garcia-Hoyos, M., Gibbs, D., Kim, S.R., Maguire, A., Rex, T.S., Di Vicino, U., et al. Serotype-dependent packaging of large genes in adeno-associated viral vectors results in effective gene delivery in mice. J. Clin. Invest. 118 (2008), 1955–1964.
-
(2008)
J. Clin. Invest.
, vol.118
, pp. 1955-1964
-
-
Allocca, M.1
Doria, M.2
Petrillo, M.3
Colella, P.4
Garcia-Hoyos, M.5
Gibbs, D.6
Kim, S.R.7
Maguire, A.8
Rex, T.S.9
Di Vicino, U.10
-
25
-
-
22544462537
-
Packaging capacity of adeno-associated virus serotypes: impact of larger genomes on infectivity and postentry steps
-
25 Grieger, J.C., Samulski, R.J., Packaging capacity of adeno-associated virus serotypes: impact of larger genomes on infectivity and postentry steps. J. Virol. 79 (2005), 9933–9944.
-
(2005)
J. Virol.
, vol.79
, pp. 9933-9944
-
-
Grieger, J.C.1
Samulski, R.J.2
-
26
-
-
33947410764
-
Self-complementary recombinant adeno-associated viral vectors: packaging capacity and the role of rep proteins in vector purity
-
26 Wu, J., Zhao, W., Zhong, L., Han, Z., Li, B., Ma, W., Weigel-Kelley, K.A., Warrington, K.H., Srivastava, A., Self-complementary recombinant adeno-associated viral vectors: packaging capacity and the role of rep proteins in vector purity. Hum. Gene Ther. 18 (2007), 171–182.
-
(2007)
Hum. Gene Ther.
, vol.18
, pp. 171-182
-
-
Wu, J.1
Zhao, W.2
Zhong, L.3
Han, Z.4
Li, B.5
Ma, W.6
Weigel-Kelley, K.A.7
Warrington, K.H.8
Srivastava, A.9
-
27
-
-
44949131860
-
In vitro and in vivo gene therapy vector evolution via multispecies interbreeding and retargeting of adeno-associated viruses
-
27 Grimm, D., Lee, J.S., Wang, L., Desai, T., Akache, B., Storm, T.A., Kay, M.A., In vitro and in vivo gene therapy vector evolution via multispecies interbreeding and retargeting of adeno-associated viruses. J. Virol. 82 (2008), 5887–5911.
-
(2008)
J. Virol.
, vol.82
, pp. 5887-5911
-
-
Grimm, D.1
Lee, J.S.2
Wang, L.3
Desai, T.4
Akache, B.5
Storm, T.A.6
Kay, M.A.7
-
28
-
-
84862599159
-
Enhancing the clinical potential of AAV vectors by capsid engineering to evade pre-existing immunity
-
28 Bartel, M., Schaffer, D., Büning, H., Enhancing the clinical potential of AAV vectors by capsid engineering to evade pre-existing immunity. Front. Microbiol., 2, 2011, 204.
-
(2011)
Front. Microbiol.
, vol.2
, pp. 204
-
-
Bartel, M.1
Schaffer, D.2
Büning, H.3
-
29
-
-
0026007043
-
HIV-associated nephropathy in transgenic mice expressing HIV-1 genes
-
29 Dickie, P., Felser, J., Eckhaus, M., Bryant, J., Silver, J., Marinos, N., Notkins, A.L., HIV-associated nephropathy in transgenic mice expressing HIV-1 genes. Virology 185 (1991), 109–119.
-
(1991)
Virology
, vol.185
, pp. 109-119
-
-
Dickie, P.1
Felser, J.2
Eckhaus, M.3
Bryant, J.4
Silver, J.5
Marinos, N.6
Notkins, A.L.7
-
30
-
-
0026584860
-
Progressive glomerulosclerosis and enhanced renal accumulation of basement membrane components in mice transgenic for human immunodeficiency virus type 1 genes
-
30 Kopp, J.B., Klotman, M.E., Adler, S.H., Bruggeman, L.A., Dickie, P., Marinos, N.J., Eckhaus, M., Bryant, J.L., Notkins, A.L., Klotman, P.E., Progressive glomerulosclerosis and enhanced renal accumulation of basement membrane components in mice transgenic for human immunodeficiency virus type 1 genes. Proc. Natl. Acad. Sci. USA 89 (1992), 1577–1581.
-
(1992)
Proc. Natl. Acad. Sci. USA
, vol.89
, pp. 1577-1581
-
-
Kopp, J.B.1
Klotman, M.E.2
Adler, S.H.3
Bruggeman, L.A.4
Dickie, P.5
Marinos, N.J.6
Eckhaus, M.7
Bryant, J.L.8
Notkins, A.L.9
Klotman, P.E.10
-
31
-
-
84955278331
-
HIV promotes NLRP3 inflammasome complex activation in murine HIV-associated nephropathy
-
31 Haque, S., Lan, X., Wen, H., Lederman, R., Chawla, A., Attia, M., Bongu, R.P., Husain, M., Mikulak, J., Saleem, M.A., et al. HIV promotes NLRP3 inflammasome complex activation in murine HIV-associated nephropathy. Am. J. Pathol. 186 (2016), 347–358.
-
(2016)
Am. J. Pathol.
, vol.186
, pp. 347-358
-
-
Haque, S.1
Lan, X.2
Wen, H.3
Lederman, R.4
Chawla, A.5
Attia, M.6
Bongu, R.P.7
Husain, M.8
Mikulak, J.9
Saleem, M.A.10
-
32
-
-
84940048188
-
Cardiac dysfunction in HIV-1 transgenic mouse: role of stress and BAG3
-
32 Cheung, J.Y., Gordon, J., Wang, J., Song, J., Zhang, X.Q., Tilley, D.G., Gao, E., Koch, W.J., Rabinowitz, J., Klotman, P.E., et al. Cardiac dysfunction in HIV-1 transgenic mouse: role of stress and BAG3. Clin. Transl. Sci. 8 (2015), 305–310.
-
(2015)
Clin. Transl. Sci.
, vol.8
, pp. 305-310
-
-
Cheung, J.Y.1
Gordon, J.2
Wang, J.3
Song, J.4
Zhang, X.Q.5
Tilley, D.G.6
Gao, E.7
Koch, W.J.8
Rabinowitz, J.9
Klotman, P.E.10
-
33
-
-
84867638233
-
HIV-1 alters neural and glial progenitor cell dynamics in the central nervous system: coordinated response to opiates during maturation
-
33 Hahn, Y.K., Podhaizer, E.M., Hauser, K.F., Knapp, P.E., HIV-1 alters neural and glial progenitor cell dynamics in the central nervous system: coordinated response to opiates during maturation. Glia 60 (2012), 1871–1887.
-
(2012)
Glia
, vol.60
, pp. 1871-1887
-
-
Hahn, Y.K.1
Podhaizer, E.M.2
Hauser, K.F.3
Knapp, P.E.4
-
34
-
-
80051546230
-
Viral infection and neural stem/progenitor cell's fate: implications in brain development and neurological disorders
-
34 Das, S., Basu, A., Viral infection and neural stem/progenitor cell's fate: implications in brain development and neurological disorders. Neurochem. Int. 59 (2011), 357–366.
-
(2011)
Neurochem. Int.
, vol.59
, pp. 357-366
-
-
Das, S.1
Basu, A.2
-
35
-
-
77957241751
-
Human immunodeficiency virus type 1 Tat modulates proliferation and differentiation of human neural precursor cells: implication in NeuroAIDS
-
35 Mishra, M., Taneja, M., Malik, S., Khalique, H., Seth, P., Human immunodeficiency virus type 1 Tat modulates proliferation and differentiation of human neural precursor cells: implication in NeuroAIDS. J. Neurovirol. 16 (2010), 355–367.
-
(2010)
J. Neurovirol.
, vol.16
, pp. 355-367
-
-
Mishra, M.1
Taneja, M.2
Malik, S.3
Khalique, H.4
Seth, P.5
-
36
-
-
37349007643
-
Long-term HIV-1 infection of neural progenitor populations
-
36 Rothenaigner, I., Kramer, S., Ziegler, M., Wolff, H., Kleinschmidt, A., Brack-Werner, R., Long-term HIV-1 infection of neural progenitor populations. AIDS 21 (2007), 2271–2281.
-
(2007)
AIDS
, vol.21
, pp. 2271-2281
-
-
Rothenaigner, I.1
Kramer, S.2
Ziegler, M.3
Wolff, H.4
Kleinschmidt, A.5
Brack-Werner, R.6
-
37
-
-
34447299925
-
Evidence of human immunodeficiency virus type 1 infection of nestin-positive neural progenitors in archival pediatric brain tissue
-
37 Schwartz, L., Civitello, L., Dunn-Pirio, A., Ryschkewitsch, S., Berry, E., Cavert, W., Kinzel, N., Lawrence, D.M., Hazra, R., Major, E.O., Evidence of human immunodeficiency virus type 1 infection of nestin-positive neural progenitors in archival pediatric brain tissue. J. Neurovirol. 13 (2007), 274–283.
-
(2007)
J. Neurovirol.
, vol.13
, pp. 274-283
-
-
Schwartz, L.1
Civitello, L.2
Dunn-Pirio, A.3
Ryschkewitsch, S.4
Berry, E.5
Cavert, W.6
Kinzel, N.7
Lawrence, D.M.8
Hazra, R.9
Major, E.O.10
-
38
-
-
84964402753
-
Tripartite containing motif 32 modulates proliferation of human neural precursor cells in HIV-1 neurodegeneration
-
38 Fatima, M., Kumari, R., Schwamborn, J.C., Mahadevan, A., Shankar, S.K., Raja, R., Seth, P., Tripartite containing motif 32 modulates proliferation of human neural precursor cells in HIV-1 neurodegeneration. Cell Death Differ. 23 (2016), 776–786.
-
(2016)
Cell Death Differ.
, vol.23
, pp. 776-786
-
-
Fatima, M.1
Kumari, R.2
Schwamborn, J.C.3
Mahadevan, A.4
Shankar, S.K.5
Raja, R.6
Seth, P.7
-
39
-
-
84942889079
-
A new model for post-integration latency in macroglial cells to study HIV-1 reservoirs of the brain
-
39 Schneider, M., Tigges, B., Meggendorfer, M., Helfer, M., Ziegenhain, C., Brack-Werner, R., A new model for post-integration latency in macroglial cells to study HIV-1 reservoirs of the brain. AIDS 29 (2015), 1147–1159.
-
(2015)
AIDS
, vol.29
, pp. 1147-1159
-
-
Schneider, M.1
Tigges, B.2
Meggendorfer, M.3
Helfer, M.4
Ziegenhain, C.5
Brack-Werner, R.6
-
40
-
-
85009820178
-
Productive infection of human neural progenitor cells by R5 tropic HIV-1: opiate co-exposure heightens infectivity and functional vulnerability
-
40 Balinang, J.M., Masvekar, R.R., Hauser, K.F., Knapp, P.E., Productive infection of human neural progenitor cells by R5 tropic HIV-1: opiate co-exposure heightens infectivity and functional vulnerability. AIDS 31 (2017), 753–764.
-
(2017)
AIDS
, vol.31
, pp. 753-764
-
-
Balinang, J.M.1
Masvekar, R.R.2
Hauser, K.F.3
Knapp, P.E.4
-
41
-
-
84959152780
-
Single point mutation in adeno-associated viral vectors -DJ capsid leads to improvement for gene delivery in vivo
-
41 Mao, Y., Wang, X., Yan, R., Hu, W., Li, A., Wang, S., Li, H., Single point mutation in adeno-associated viral vectors -DJ capsid leads to improvement for gene delivery in vivo. BMC Biotechnol., 16, 2016, 1.
-
(2016)
BMC Biotechnol.
, vol.16
, pp. 1
-
-
Mao, Y.1
Wang, X.2
Yan, R.3
Hu, W.4
Li, A.5
Wang, S.6
Li, H.7
-
42
-
-
84960863986
-
A dual AAV system enables the Cas9-mediated correction of a metabolic liver disease in newborn mice
-
42 Yang, Y., Wang, L., Bell, P., McMenamin, D., He, Z., White, J., Yu, H., Xu, C., Morizono, H., Musunuru, K., et al. A dual AAV system enables the Cas9-mediated correction of a metabolic liver disease in newborn mice. Nat. Biotechnol. 34 (2016), 334–338.
-
(2016)
Nat. Biotechnol.
, vol.34
, pp. 334-338
-
-
Yang, Y.1
Wang, L.2
Bell, P.3
McMenamin, D.4
He, Z.5
White, J.6
Yu, H.7
Xu, C.8
Morizono, H.9
Musunuru, K.10
-
43
-
-
84896315121
-
Adeno-associated viral serotypes produce differing titers and differentially transduce neurons within the rat basal and lateral amygdala
-
43 Holehonnur, R., Luong, J.A., Chaturvedi, D., Ho, A., Lella, S.K., Hosek, M.P., Ploski, J.E., Adeno-associated viral serotypes produce differing titers and differentially transduce neurons within the rat basal and lateral amygdala. BMC Neurosci., 15, 2014, 28.
-
(2014)
BMC Neurosci.
, vol.15
, pp. 28
-
-
Holehonnur, R.1
Luong, J.A.2
Chaturvedi, D.3
Ho, A.4
Lella, S.K.5
Hosek, M.P.6
Ploski, J.E.7
-
44
-
-
84923266604
-
GUIDE-seq enables genome-wide profiling of off-target cleavage by CRISPR-Cas nucleases
-
44 Tsai, S.Q., Zheng, Z., Nguyen, N.T., Liebers, M., Topkar, V.V., Thapar, V., Wyvekens, N., Khayter, C., Iafrate, A.J., Le, L.P., et al. GUIDE-seq enables genome-wide profiling of off-target cleavage by CRISPR-Cas nucleases. Nat. Biotechnol. 33 (2015), 187–197.
-
(2015)
Nat. Biotechnol.
, vol.33
, pp. 187-197
-
-
Tsai, S.Q.1
Zheng, Z.2
Nguyen, N.T.3
Liebers, M.4
Topkar, V.V.5
Thapar, V.6
Wyvekens, N.7
Khayter, C.8
Iafrate, A.J.9
Le, L.P.10
-
45
-
-
84923275611
-
Genome-wide detection of DNA double-stranded breaks induced by engineered nucleases
-
45 Frock, R.L., Hu, J., Meyers, R.M., Ho, Y.J., Kii, E., Alt, F.W., Genome-wide detection of DNA double-stranded breaks induced by engineered nucleases. Nat. Biotechnol. 33 (2015), 179–186.
-
(2015)
Nat. Biotechnol.
, vol.33
, pp. 179-186
-
-
Frock, R.L.1
Hu, J.2
Meyers, R.M.3
Ho, Y.J.4
Kii, E.5
Alt, F.W.6
-
46
-
-
84903943282
-
Whole-genome sequencing analysis reveals high specificity of CRISPR/Cas9 and TALEN-based genome editing in human iPSCs
-
46 Smith, C., Gore, A., Yan, W., Abalde-Atristain, L., Li, Z., He, C., Wang, Y., Brodsky, R.A., Zhang, K., Cheng, L., Ye, Z., Whole-genome sequencing analysis reveals high specificity of CRISPR/Cas9 and TALEN-based genome editing in human iPSCs. Cell Stem Cell 15 (2014), 12–13.
-
(2014)
Cell Stem Cell
, vol.15
, pp. 12-13
-
-
Smith, C.1
Gore, A.2
Yan, W.3
Abalde-Atristain, L.4
Li, Z.5
He, C.6
Wang, Y.7
Brodsky, R.A.8
Zhang, K.9
Cheng, L.10
Ye, Z.11
-
47
-
-
84904010334
-
Low incidence of off-target mutations in individual CRISPR-Cas9 and TALEN targeted human stem cell clones detected by whole-genome sequencing
-
47 Veres, A., Gosis, B.S., Ding, Q., Collins, R., Ragavendran, A., Brand, H., Erdin, S., Cowan, C.A., Talkowski, M.E., Musunuru, K., Low incidence of off-target mutations in individual CRISPR-Cas9 and TALEN targeted human stem cell clones detected by whole-genome sequencing. Cell Stem Cell 15 (2014), 27–30.
-
(2014)
Cell Stem Cell
, vol.15
, pp. 27-30
-
-
Veres, A.1
Gosis, B.S.2
Ding, Q.3
Collins, R.4
Ragavendran, A.5
Brand, H.6
Erdin, S.7
Cowan, C.A.8
Talkowski, M.E.9
Musunuru, K.10
-
48
-
-
84947078456
-
CRISPR/gRNA-directed synergistic activation mediator (SAM) induces specific, persistent and robust reactivation of the HIV-1 latent reservoirs
-
48 Zhang, Y., Yin, C., Zhang, T., Li, F., Yang, W., Kaminski, R., Fagan, P.R., Putatunda, R., Young, W.B., Khalili, K., Hu, W., CRISPR/gRNA-directed synergistic activation mediator (SAM) induces specific, persistent and robust reactivation of the HIV-1 latent reservoirs. Sci. Rep., 5, 2015, 16277.
-
(2015)
Sci. Rep.
, vol.5
, pp. 16277
-
-
Zhang, Y.1
Yin, C.2
Zhang, T.3
Li, F.4
Yang, W.5
Kaminski, R.6
Fagan, P.R.7
Putatunda, R.8
Young, W.B.9
Khalili, K.10
Hu, W.11
-
49
-
-
84866519161
-
Mice chronically infected with chimeric HIV resist peripheral and brain superinfection: a model of protective immunity to HIV. J
-
49 Kelschenbach, J.L., Saini, M., Hadas, E., Gu, C.J., Chao, W., Bentsman, G., Hong, J.P., Hanke, T., Sharer, L.R., Potash, M.J., et al. Mice chronically infected with chimeric HIV resist peripheral and brain superinfection: a model of protective immunity to HIV. J. Neuroimmune Pharmacol 7 (2012), 380–387.
-
(2012)
Neuroimmune Pharmacol
, vol.7
, pp. 380-387
-
-
Kelschenbach, J.L.1
Saini, M.2
Hadas, E.3
Gu, C.J.4
Chao, W.5
Bentsman, G.6
Hong, J.P.7
Hanke, T.8
Sharer, L.R.9
Potash, M.J.10
-
50
-
-
84944768937
-
Visualization and quantification of simian immunodeficiency virus-infected cells using non-invasive molecular imaging
-
50 Song, J., Cai, Z., White, A.G., Jin, T., Wang, X., Kadayakkara, D., Anderson, C.J., Ambrose, Z., Young, W.B., Visualization and quantification of simian immunodeficiency virus-infected cells using non-invasive molecular imaging. J. Gen. Virol. 96 (2015), 3131–3142.
-
(2015)
J. Gen. Virol.
, vol.96
, pp. 3131-3142
-
-
Song, J.1
Cai, Z.2
White, A.G.3
Jin, T.4
Wang, X.5
Kadayakkara, D.6
Anderson, C.J.7
Ambrose, Z.8
Young, W.B.9
-
51
-
-
85015257690
-
Promise and problems associated with the use of recombinant AAV for the delivery of anti-HIV antibodies
-
51 Fuchs, S.P., Desrosiers, R.C., Promise and problems associated with the use of recombinant AAV for the delivery of anti-HIV antibodies. Mol. Ther. Methods Clin. Dev., 3, 2016, 16068.
-
(2016)
Mol. Ther. Methods Clin. Dev.
, vol.3
, pp. 16068
-
-
Fuchs, S.P.1
Desrosiers, R.C.2
-
52
-
-
85010868233
-
Antibody gene transfer with adeno-associated viral vectors as a method for HIV prevention
-
52 Brady, J.M., Baltimore, D., Balazs, A.B., Antibody gene transfer with adeno-associated viral vectors as a method for HIV prevention. Immunol. Rev. 275 (2017), 324–333.
-
(2017)
Immunol. Rev.
, vol.275
, pp. 324-333
-
-
Brady, J.M.1
Baltimore, D.2
Balazs, A.B.3
-
53
-
-
84962726170
-
CRISPR/Cas9-derived mutations both inhibit HIV-1 replication and accelerate viral escape
-
53 Wang, Z., Pan, Q., Gendron, P., Zhu, W., Guo, F., Cen, S., Wainberg, M.A., Liang, C., CRISPR/Cas9-derived mutations both inhibit HIV-1 replication and accelerate viral escape. Cell Rep. 15 (2016), 481–489.
-
(2016)
Cell Rep.
, vol.15
, pp. 481-489
-
-
Wang, Z.1
Pan, Q.2
Gendron, P.3
Zhu, W.4
Guo, F.5
Cen, S.6
Wainberg, M.A.7
Liang, C.8
-
54
-
-
84960380460
-
CRISPR-Cas9 can inhibit HIV-1 replication but NHEJ repair facilitates virus escape
-
54 Wang, G., Zhao, N., Berkhout, B., Das, A.T., CRISPR-Cas9 can inhibit HIV-1 replication but NHEJ repair facilitates virus escape. Mol. Ther. 24 (2016), 522–526.
-
(2016)
Mol. Ther.
, vol.24
, pp. 522-526
-
-
Wang, G.1
Zhao, N.2
Berkhout, B.3
Das, A.T.4
-
55
-
-
84921697027
-
Generation of genomic deletions in mammalian cell lines via CRISPR/Cas9
-
55 Bauer, D.E., Canver, M.C., Orkin, S.H., Generation of genomic deletions in mammalian cell lines via CRISPR/Cas9. J. Vis. Exp., 95, 2015, e52118.
-
(2015)
J. Vis. Exp.
, vol.95
, pp. e52118
-
-
Bauer, D.E.1
Canver, M.C.2
Orkin, S.H.3
-
56
-
-
84930628716
-
High-throughput screens in mammalian cells using the CRISPR-Cas9 system
-
56 Peng, J., Zhou, Y., Zhu, S., Wei, W., High-throughput screens in mammalian cells using the CRISPR-Cas9 system. FEBS J. 282 (2015), 2089–2096.
-
(2015)
FEBS J.
, vol.282
, pp. 2089-2096
-
-
Peng, J.1
Zhou, Y.2
Zhu, S.3
Wei, W.4
-
57
-
-
84922535144
-
Multiplex CRISPR/Cas9-based genome engineering from a single lentiviral vector
-
57 Kabadi, A.M., Ousterout, D.G., Hilton, I.B., Gersbach, C.A., Multiplex CRISPR/Cas9-based genome engineering from a single lentiviral vector. Nucleic Acids Res., 42, 2014, e147.
-
(2014)
Nucleic Acids Res.
, vol.42
, pp. e147
-
-
Kabadi, A.M.1
Ousterout, D.G.2
Hilton, I.B.3
Gersbach, C.A.4
-
58
-
-
84924764258
-
Safety of gene therapy: new insights to a puzzling case
-
58 Rothe, M., Schambach, A., Biasco, L., Safety of gene therapy: new insights to a puzzling case. Curr. Gene Ther. 14 (2014), 429–436.
-
(2014)
Curr. Gene Ther.
, vol.14
, pp. 429-436
-
-
Rothe, M.1
Schambach, A.2
Biasco, L.3
-
59
-
-
84883268937
-
Immune responses to AAV vectors: overcoming barriers to successful gene therapy
-
59 Mingozzi, F., High, K.A., Immune responses to AAV vectors: overcoming barriers to successful gene therapy. Blood 122 (2013), 23–36.
-
(2013)
Blood
, vol.122
, pp. 23-36
-
-
Mingozzi, F.1
High, K.A.2
-
60
-
-
84978196200
-
AAV vectorization of DSB-mediated gene editing technologies
-
60 Moser, R.J., Hirsch, M.L., AAV vectorization of DSB-mediated gene editing technologies. Curr. Gene Ther. 16 (2016), 207–219.
-
(2016)
Curr. Gene Ther.
, vol.16
, pp. 207-219
-
-
Moser, R.J.1
Hirsch, M.L.2
-
61
-
-
84912101598
-
CRISPR-Cas9 knockin mice for genome editing and cancer modeling
-
61 Platt, R.J., Chen, S., Zhou, Y., Yim, M.J., Swiech, L., Kempton, H.R., Dahlman, J.E., Parnas, O., Eisenhaure, T.M., Jovanovic, M., et al. CRISPR-Cas9 knockin mice for genome editing and cancer modeling. Cell 159 (2014), 440–455.
-
(2014)
Cell
, vol.159
, pp. 440-455
-
-
Platt, R.J.1
Chen, S.2
Zhou, Y.3
Yim, M.J.4
Swiech, L.5
Kempton, H.R.6
Dahlman, J.E.7
Parnas, O.8
Eisenhaure, T.M.9
Jovanovic, M.10
-
62
-
-
84908382195
-
CRISPR/Cas9-mediated genome engineering: an adeno-associated viral (AAV) vector toolbox
-
62 Senís, E., Fatouros, C., Große, S., Wiedtke, E., Niopek, D., Mueller, A.K., Börner, K., Grimm, D., CRISPR/Cas9-mediated genome engineering: an adeno-associated viral (AAV) vector toolbox. Biotechnol. J. 9 (2014), 1402–1412.
-
(2014)
Biotechnol. J.
, vol.9
, pp. 1402-1412
-
-
Senís, E.1
Fatouros, C.2
Große, S.3
Wiedtke, E.4
Niopek, D.5
Mueller, A.K.6
Börner, K.7
Grimm, D.8
-
63
-
-
84955101517
-
Genome engineering using adeno-associated virus (AAV)
-
63 Howes, R., Schofield, C., Genome engineering using adeno-associated virus (AAV). Methods Mol. Biol. 1239 (2015), 75–103.
-
(2015)
Methods Mol. Biol.
, vol.1239
, pp. 75-103
-
-
Howes, R.1
Schofield, C.2
-
64
-
-
84976561853
-
AAV-mediated CRISPR/Cas gene editing of retinal cells in vivo
-
64 Hung, S.S., Chrysostomou, V., Li, F., Lim, J.K., Wang, J.H., Powell, J.E., Tu, L., Daniszewski, M., Lo, C., Wong, R.C., et al. AAV-mediated CRISPR/Cas gene editing of retinal cells in vivo. Invest. Ophthalmol. Vis. Sci. 57 (2016), 3470–3476.
-
(2016)
Invest. Ophthalmol. Vis. Sci.
, vol.57
, pp. 3470-3476
-
-
Hung, S.S.1
Chrysostomou, V.2
Li, F.3
Lim, J.K.4
Wang, J.H.5
Powell, J.E.6
Tu, L.7
Daniszewski, M.8
Lo, C.9
Wong, R.C.10
-
65
-
-
84924322574
-
Rational design of a split-Cas9 enzyme complex
-
65 Wright, A.V., Sternberg, S.H., Taylor, D.W., Staahl, B.T., Bardales, J.A., Kornfeld, J.E., Doudna, J.A., Rational design of a split-Cas9 enzyme complex. Proc. Natl. Acad. Sci. USA 112 (2015), 2984–2989.
-
(2015)
Proc. Natl. Acad. Sci. USA
, vol.112
, pp. 2984-2989
-
-
Wright, A.V.1
Sternberg, S.H.2
Taylor, D.W.3
Staahl, B.T.4
Bardales, J.A.5
Kornfeld, J.E.6
Doudna, J.A.7
-
66
-
-
84923297110
-
A split-Cas9 architecture for inducible genome editing and transcription modulation
-
66 Zetsche, B., Volz, S.E., Zhang, F., A split-Cas9 architecture for inducible genome editing and transcription modulation. Nat. Biotechnol. 33 (2015), 139–142.
-
(2015)
Nat. Biotechnol.
, vol.33
, pp. 139-142
-
-
Zetsche, B.1
Volz, S.E.2
Zhang, F.3
-
67
-
-
84977106633
-
Ligand-binding domains of nuclear receptors facilitate tight control of split CRISPR activity
-
67 Nguyen, D.P., Miyaoka, Y., Gilbert, L.A., Mayerl, S.J., Lee, B.H., Weissman, J.S., Conklin, B.R., Wells, J.A., Ligand-binding domains of nuclear receptors facilitate tight control of split CRISPR activity. Nat. Commun., 7, 2016, 12009.
-
(2016)
Nat. Commun.
, vol.7
, pp. 12009
-
-
Nguyen, D.P.1
Miyaoka, Y.2
Gilbert, L.A.3
Mayerl, S.J.4
Lee, B.H.5
Weissman, J.S.6
Conklin, B.R.7
Wells, J.A.8
-
68
-
-
84961782000
-
Chemical and biophysical modulation of Cas9 for tunable genome engineering
-
68 Nuñez, J.K., Harrington, L.B., Doudna, J.A., Chemical and biophysical modulation of Cas9 for tunable genome engineering. ACS Chem. Biol. 11 (2016), 681–688.
-
(2016)
ACS Chem. Biol.
, vol.11
, pp. 681-688
-
-
Nuñez, J.K.1
Harrington, L.B.2
Doudna, J.A.3
-
69
-
-
84934784068
-
Trans-spliced Cas9 allows cleavage of HBB and CCR5 genes in human cells using compact expression cassettes
-
69 Fine, E.J., Appleton, C.M., White, D.E., Brown, M.T., Deshmukh, H., Kemp, M.L., Bao, G., Trans-spliced Cas9 allows cleavage of HBB and CCR5 genes in human cells using compact expression cassettes. Sci. Rep., 5, 2015, 10777.
-
(2015)
Sci. Rep.
, vol.5
, pp. 10777
-
-
Fine, E.J.1
Appleton, C.M.2
White, D.E.3
Brown, M.T.4
Deshmukh, H.5
Kemp, M.L.6
Bao, G.7
-
70
-
-
84901195977
-
Multiplexed and programmable regulation of gene networks with an integrated RNA and CRISPR/Cas toolkit in human cells
-
70 Nissim, L., Perli, S.D., Fridkin, A., Perez-Pinera, P., Lu, T.K., Multiplexed and programmable regulation of gene networks with an integrated RNA and CRISPR/Cas toolkit in human cells. Mol. Cell 54 (2014), 698–710.
-
(2014)
Mol. Cell
, vol.54
, pp. 698-710
-
-
Nissim, L.1
Perli, S.D.2
Fridkin, A.3
Perez-Pinera, P.4
Lu, T.K.5
-
71
-
-
84897546295
-
Self-processing of ribozyme-flanked RNAs into guide RNAs in vitro and in vivo for CRISPR-mediated genome editing
-
71 Gao, Y., Zhao, Y., Self-processing of ribozyme-flanked RNAs into guide RNAs in vitro and in vivo for CRISPR-mediated genome editing. J. Integr. Plant Biol. 56 (2014), 343–349.
-
(2014)
J. Integr. Plant Biol.
, vol.56
, pp. 343-349
-
-
Gao, Y.1
Zhao, Y.2
-
72
-
-
84903217296
-
Multiplex genome engineering in human cells using all-in-one CRISPR/Cas9 vector system
-
72 Sakuma, T., Nishikawa, A., Kume, S., Chayama, K., Yamamoto, T., Multiplex genome engineering in human cells using all-in-one CRISPR/Cas9 vector system. Sci. Rep., 4, 2014, 5400.
-
(2014)
Sci. Rep.
, vol.4
, pp. 5400
-
-
Sakuma, T.1
Nishikawa, A.2
Kume, S.3
Chayama, K.4
Yamamoto, T.5
-
73
-
-
84855927237
-
Generation of HIV latency in humanized BLT mice
-
73 Denton, P.W., Olesen, R., Choudhary, S.K., Archin, N.M., Wahl, A., Swanson, M.D., Chateau, M., Nochi, T., Krisko, J.F., Spagnuolo, R.A., et al. Generation of HIV latency in humanized BLT mice. J. Virol. 86 (2012), 630–634.
-
(2012)
J. Virol.
, vol.86
, pp. 630-634
-
-
Denton, P.W.1
Olesen, R.2
Choudhary, S.K.3
Archin, N.M.4
Wahl, A.5
Swanson, M.D.6
Chateau, M.7
Nochi, T.8
Krisko, J.F.9
Spagnuolo, R.A.10
-
74
-
-
84962593365
-
Efficient delivery of genome-editing proteins using bioreducible lipid nanoparticles
-
74 Wang, M., Zuris, J.A., Meng, F., Rees, H., Sun, S., Deng, P., Han, Y., Gao, X., Pouli, D., Wu, Q., et al. Efficient delivery of genome-editing proteins using bioreducible lipid nanoparticles. Proc. Natl. Acad. Sci. USA 113 (2016), 2868–2873.
-
(2016)
Proc. Natl. Acad. Sci. USA
, vol.113
, pp. 2868-2873
-
-
Wang, M.1
Zuris, J.A.2
Meng, F.3
Rees, H.4
Sun, S.5
Deng, P.6
Han, Y.7
Gao, X.8
Pouli, D.9
Wu, Q.10
-
75
-
-
84942821644
-
Self-assembled DNA nanoclews for the efficient delivery of CRISPR-Cas9 for genome editing
-
75 Sun, W., Ji, W., Hall, J.M., Hu, Q., Wang, C., Beisel, C.L., Gu, Z., Self-assembled DNA nanoclews for the efficient delivery of CRISPR-Cas9 for genome editing. Angew. Chem. Int. Ed. Engl. 54 (2015), 12029–12033.
-
(2015)
Angew. Chem. Int. Ed. Engl.
, vol.54
, pp. 12029-12033
-
-
Sun, W.1
Ji, W.2
Hall, J.M.3
Hu, Q.4
Wang, C.5
Beisel, C.L.6
Gu, Z.7
-
76
-
-
84966588701
-
Generation of a stable packaging cell line producing high-titer PPT-deleted integration-deficient lentiviral vectors
-
76 Hu, P., Li, Y., Sands, M.S., McCown, T., Kafri, T., Generation of a stable packaging cell line producing high-titer PPT-deleted integration-deficient lentiviral vectors. Mol. Ther. Methods Clin. Dev., 2, 2015, 15025.
-
(2015)
Mol. Ther. Methods Clin. Dev.
, vol.2
, pp. 15025
-
-
Hu, P.1
Li, Y.2
Sands, M.S.3
McCown, T.4
Kafri, T.5
-
77
-
-
84964981058
-
Improved delivery of Cas9 protein/gRNA complexes using lipofectamine CRISPRMAX
-
77 Yu, X., Liang, X., Xie, H., Kumar, S., Ravinder, N., Potter, J., de Mollerat du Jeu, X., Chesnut, J.D., Improved delivery of Cas9 protein/gRNA complexes using lipofectamine CRISPRMAX. Biotechnol. Lett. 38 (2016), 919–929.
-
(2016)
Biotechnol. Lett.
, vol.38
, pp. 919-929
-
-
Yu, X.1
Liang, X.2
Xie, H.3
Kumar, S.4
Ravinder, N.5
Potter, J.6
de Mollerat du Jeu, X.7
Chesnut, J.D.8
-
78
-
-
84992743464
-
Methods for optimizing CRISPR-Cas9 genome editing specificity
-
78 Tycko, J., Myer, V.E., Hsu, P.D., Methods for optimizing CRISPR-Cas9 genome editing specificity. Mol. Cell 63 (2016), 355–370.
-
(2016)
Mol. Cell
, vol.63
, pp. 355-370
-
-
Tycko, J.1
Myer, V.E.2
Hsu, P.D.3
-
79
-
-
84949791988
-
Broadening the targeting range of Staphylococcus aureus CRISPR-Cas9 by modifying PAM recognition
-
79 Kleinstiver, B.P., Prew, M.S., Tsai, S.Q., Nguyen, N.T., Topkar, V.V., Zheng, Z., Joung, J.K., Broadening the targeting range of Staphylococcus aureus CRISPR-Cas9 by modifying PAM recognition. Nat. Biotechnol. 33 (2015), 1293–1298.
-
(2015)
Nat. Biotechnol.
, vol.33
, pp. 1293-1298
-
-
Kleinstiver, B.P.1
Prew, M.S.2
Tsai, S.Q.3
Nguyen, N.T.4
Topkar, V.V.5
Zheng, Z.6
Joung, J.K.7
-
80
-
-
84960392032
-
Genome-wide target specificities of CRISPR-Cas9 nucleases revealed by multiplex Digenome-seq
-
80 Kim, D., Kim, S., Kim, S., Park, J., Kim, J.S., Genome-wide target specificities of CRISPR-Cas9 nucleases revealed by multiplex Digenome-seq. Genome Res. 26 (2016), 406–415.
-
(2016)
Genome Res.
, vol.26
, pp. 406-415
-
-
Kim, D.1
Kim, S.2
Kim, S.3
Park, J.4
Kim, J.S.5
-
81
-
-
84923846574
-
Digenome-seq: genome-wide profiling of CRISPR-Cas9 off-target effects in human cells
-
81 Kim, D., Bae, S., Park, J., Kim, E., Kim, S., Yu, H.R., Hwang, J., Kim, J.I., Kim, J.S., Digenome-seq: genome-wide profiling of CRISPR-Cas9 off-target effects in human cells. Nat. Methods 12 (2015), 237–243.
-
(2015)
Nat. Methods
, vol.12
, pp. 237-243
-
-
Kim, D.1
Bae, S.2
Park, J.3
Kim, E.4
Kim, S.5
Yu, H.R.6
Hwang, J.7
Kim, J.I.8
Kim, J.S.9
-
82
-
-
84931291649
-
Somatic CRISPR/Cas9-mediated tumour suppressor disruption enables versatile brain tumour modelling
-
82 Zuckermann, M., Hovestadt, V., Knobbe-Thomsen, C.B., Zapatka, M., Northcott, P.A., Schramm, K., Belic, J., Jones, D.T., Tschida, B., Moriarity, B., et al. Somatic CRISPR/Cas9-mediated tumour suppressor disruption enables versatile brain tumour modelling. Nat. Commun., 6, 2015, 7391.
-
(2015)
Nat. Commun.
, vol.6
, pp. 7391
-
-
Zuckermann, M.1
Hovestadt, V.2
Knobbe-Thomsen, C.B.3
Zapatka, M.4
Northcott, P.A.5
Schramm, K.6
Belic, J.7
Jones, D.T.8
Tschida, B.9
Moriarity, B.10
-
83
-
-
84923086605
-
Targeted and genome-wide sequencing reveal single nucleotide variations impacting specificity of Cas9 in human stem cells
-
83 Yang, L., Grishin, D., Wang, G., Aach, J., Zhang, C.Z., Chari, R., Homsy, J., Cai, X., Zhao, Y., Fan, J.B., et al. Targeted and genome-wide sequencing reveal single nucleotide variations impacting specificity of Cas9 in human stem cells. Nat. Commun., 5, 2014, 5507.
-
(2014)
Nat. Commun.
, vol.5
, pp. 5507
-
-
Yang, L.1
Grishin, D.2
Wang, G.3
Aach, J.4
Zhang, C.Z.5
Chari, R.6
Homsy, J.7
Cai, X.8
Zhao, Y.9
Fan, J.B.10
-
84
-
-
0033022953
-
Recombinant adeno-associated virus purification using novel methods improves infectious titer and yield
-
84 Zolotukhin, S., Byrne, B.J., Mason, E., Zolotukhin, I., Potter, M., Chesnut, K., Summerford, C., Samulski, R.J., Muzyczka, N., Recombinant adeno-associated virus purification using novel methods improves infectious titer and yield. Gene Ther. 6 (1999), 973–985.
-
(1999)
Gene Ther.
, vol.6
, pp. 973-985
-
-
Zolotukhin, S.1
Byrne, B.J.2
Mason, E.3
Zolotukhin, I.4
Potter, M.5
Chesnut, K.6
Summerford, C.7
Samulski, R.J.8
Muzyczka, N.9
-
85
-
-
34447581119
-
Optimized production and concentration of lentiviral vectors containing large inserts
-
85 al Yacoub, N., Romanowska, M., Haritonova, N., Foerster, J., Optimized production and concentration of lentiviral vectors containing large inserts. J. Gene Med. 9 (2007), 579–584.
-
(2007)
J. Gene Med.
, vol.9
, pp. 579-584
-
-
al Yacoub, N.1
Romanowska, M.2
Haritonova, N.3
Foerster, J.4
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