-
1
-
-
84923106217
-
Therapeutic genome editing: Prospects and challenges
-
Cox DBT, Platt RJ, Zhang F. Therapeutic genome editing: prospects and challenges. Nat Med 2015; 21: 121-131.
-
(2015)
Nat Med
, vol.21
, pp. 121-131
-
-
Cox, D.B.T.1
Platt, R.J.2
Zhang, F.3
-
2
-
-
84902185906
-
Genome engineering with targetable nucleases
-
Carroll D. Genome engineering with targetable nucleases. Annu Rev Biochem 2014; 83: 409-439.
-
(2014)
Annu Rev Biochem
, vol.83
, pp. 409-439
-
-
Carroll, D.1
-
3
-
-
84921710429
-
Genome engineering: The next genomic revolution
-
Gersbach CA. Genome engineering: the next genomic revolution. Nat Meth 2014; 11: 1009-1011.
-
(2014)
Nat Meth
, vol.11
, pp. 1009-1011
-
-
Gersbach, C.A.1
-
4
-
-
84928054835
-
Genome editing at the crossroads of delivery, specificity, and fidelity
-
Maggio I, Gonçalves MAFV. Genome editing at the crossroads of delivery, specificity, and fidelity. Trends Biotech 2015; 33: 280-291.
-
(2015)
Trends Biotech
, vol.33
, pp. 280-291
-
-
Maggio, I.1
Gonçalves, M.A.F.V.2
-
5
-
-
84879264708
-
ZFN TALEN and CRISPR/Cas-based methods for genome engineering
-
Gaj T, Gersbach CA, Barbas CF 3rd. ZFN, TALEN, and CRISPR/Cas-based methods for genome engineering. Trends Biotech 2013; 31: 397-405.
-
(2013)
Trends Biotech
, vol.31
, pp. 397-405
-
-
Gaj, T.1
Gersbach, C.A.2
Barbas, C.F.3
-
6
-
-
84895487305
-
Gene editing of CCR5 in autologous CD4 T cells of persons infected with HIV
-
Tebas P, Stein D, Tang WW, Frank I, Wang SQ, Lee G et al. Gene editing of CCR5 in autologous CD4 T cells of persons infected with HIV. N Engl J Med 2014; 370: 901-910.
-
(2014)
N Engl J Med
, vol.370
, pp. 901-910
-
-
Tebas, P.1
Stein, D.2
Tang, W.W.3
Frank, I.4
Wang, S.Q.5
Lee, G.6
-
7
-
-
84942903938
-
Multiplex genome-edited T-cell manufacturing platform for 'Off-the-Shelf' adoptive T-cell immunotherapies
-
Poirot L, Philip B, Schiffer-Mannioui C, Le Clerre D, Chion-Sotinel I, Derniame S et al. Multiplex genome-edited T-cell manufacturing platform for 'Off-the-Shelf' adoptive T-cell immunotherapies. Cancer Res 2015; 75: 3853-3864.
-
(2015)
Cancer Res
, vol.75
, pp. 3853-3864
-
-
Poirot, L.1
Philip, B.2
Schiffer-Mannioui, C.3
Le Clerre, D.4
Chion-Sotinel, I.5
Derniame, S.6
-
8
-
-
84946500152
-
CRISPR-Cas: From the bacterial adaptive immune system to a versatile tool for genome engineering
-
Kirchner M, Schneider S. CRISPR-Cas: from the bacterial adaptive immune system to a versatile tool for genome engineering. Angew Chem Int Ed 2015; 54: 13508-13514.
-
(2015)
Angew Chem Int Ed
, vol.54
, pp. 13508-13514
-
-
Kirchner, M.1
Schneider, S.2
-
9
-
-
84926612621
-
The new frontier of genome engineering with CRISPR-Cas9
-
Doudna JA, Charpentier E. The new frontier of genome engineering with CRISPR-Cas9. Science 2014; 346: 6213.
-
(2014)
Science
, vol.346
, pp. 6213
-
-
Doudna, J.A.1
Charpentier, E.2
-
10
-
-
84892765883
-
Genome-scale CRISPR-Cas9 knockout screening in human cells
-
Shalem O, Sanjana NE, Hartenian E, Shi X, Scott DA, Mikkelsen TS et al. Genome-scale CRISPR-Cas9 knockout screening in human cells. Science 2014; 343: 84-87.
-
(2014)
Science
, vol.343
, pp. 84-87
-
-
Shalem, O.1
Sanjana, N.E.2
Hartenian, E.3
Shi, X.4
Scott, D.A.5
Mikkelsen, T.S.6
-
11
-
-
84873729095
-
Multiplex genome engineering using CRISPR/Cas systems
-
Cong L, Ran FA, Cox D, Lin S, Barretto R, Habib N et al. Multiplex genome engineering using CRISPR/Cas systems. Science 2013; 339: 819-823.
-
(2013)
Science
, vol.339
, pp. 819-823
-
-
Cong, L.1
Ran, F.A.2
Cox, D.3
Lin, S.4
Barretto, R.5
Habib, N.6
-
12
-
-
84865070369
-
A programmable dual-RNA-guided DNA endonuclease in adaptive bacterial immunity
-
Jinek M, Chylinski K, Fonfara I, Hauer M, Doudna JA, Charpentier E. A programmable dual-RNA-guided DNA endonuclease in adaptive bacterial immunity. Science 2012; 337: 816-821.
-
(2012)
Science
, vol.337
, pp. 816-821
-
-
Jinek, M.1
Chylinski, K.2
Fonfara, I.3
Hauer, M.4
Doudna, J.A.5
Charpentier, E.6
-
13
-
-
84873734105
-
RNA-guided human genome engineering via Cas9
-
Mali P, Yang L, Esvelt KM, Aach J, Guell M, DiCarlo JE et al. RNA-guided human genome engineering via Cas9. Science 2013; 339: 823-826.
-
(2013)
Science
, vol.339
, pp. 823-826
-
-
Mali, P.1
Yang, L.2
Esvelt, K.M.3
Aach, J.4
Guell, M.5
DiCarlo, J.E.6
-
14
-
-
84902096048
-
Development and applications of CRISPR-Cas9 for genome engineering
-
Hsu PD, Lander ES, Zhang F. Development and applications of CRISPR-Cas9 for genome engineering. Cell 2014; 15: 1262-1278.
-
(2014)
Cell
, vol.15
, pp. 1262-1278
-
-
Hsu, P.D.1
Lander, E.S.2
Zhang, F.3
-
15
-
-
84884856342
-
Cas9 as a versatile tool for engineering biology
-
Mali P, Esvelt KM, Church GM. Cas9 as a versatile tool for engineering biology. Nat Meth 2013; 10: 957-963.
-
(2013)
Nat Meth
, vol.10
, pp. 957-963
-
-
Mali, P.1
Esvelt, K.M.2
Church, G.M.3
-
16
-
-
84900314611
-
CRISPR-Cas systems for editing, regulating and targeting genomes
-
Sander JD, Joung JK. CRISPR-Cas systems for editing, regulating and targeting genomes. Nat Biotech 2014; 32: 347-355.
-
(2014)
Nat Biotech
, vol.32
, pp. 347-355
-
-
Sander, J.D.1
Joung, J.K.2
-
17
-
-
84973861610
-
The democratization of gene editing: Insights from site-specific cleavage and double-strand break repair
-
Jasin M, Haber JE. The democratization of gene editing: insights from site-specific cleavage and double-strand break repair. DNA Repair 2016; 44: 6-16.
-
(2016)
DNA Repair
, vol.44
, pp. 6-16
-
-
Jasin, M.1
Haber, J.E.2
-
18
-
-
84946571462
-
Delivering the goods: Scientists seek a way to make CRISPR-Cas gene editing more targeted
-
Keener AB. Delivering the goods: scientists seek a way to make CRISPR-Cas gene editing more targeted. Nat Med 2015; 21: 1239-1241.
-
(2015)
Nat Med
, vol.21
, pp. 1239-1241
-
-
Keener, A.B.1
-
19
-
-
84973595431
-
Engineering delivery vehicles for genome editing
-
Nelson CE, Gersbach CA. Engineering delivery vehicles for genome editing. Annu Rev Chem Biomol Eng 2016; 7: 637-662.
-
(2016)
Annu Rev Chem Biomol Eng
, vol.7
, pp. 637-662
-
-
Nelson, C.E.1
Gersbach, C.A.2
-
20
-
-
84937569497
-
Delivery and specificity of CRISPR/Cas9 genome editing technologies for human gene therapy
-
Gori JL, Hsu PD, Maeder ML, Shen S, Welstead GG, Bumcrot D. Delivery and specificity of CRISPR/Cas9 genome editing technologies for human gene therapy. Hum Gene Ther 2015; 26: 443-451.
-
(2015)
Hum Gene Ther
, vol.26
, pp. 443-451
-
-
Gori, J.L.1
Hsu, P.D.2
Maeder, M.L.3
Shen, S.4
Welstead, G.G.5
Bumcrot, D.6
-
21
-
-
84937569734
-
Challenges in CRISPR/Cas9 delivery: Potential roles of nonviral vectors
-
Li L, He Z-Y, Wei X-W, Gao G-P, Wei Y-Q. Challenges in CRISPR/Cas9 delivery: potential roles of nonviral vectors. Hum Gene Ther 2015; 26: 452-462.
-
(2015)
Hum Gene Ther
, vol.26
, pp. 452-462
-
-
Li, L.1
He, Z.-Y.2
Wei, X.-W.3
Gao, G.-P.4
Wei, Y.-Q.5
-
22
-
-
84939857195
-
Delivery and therapeutic applications of gene editing technologies ZFNs, TALENs, and CRISPR/Cas9
-
LaFountaine JS, Fathe K, Smyth HDC. Delivery and therapeutic applications of gene editing technologies ZFNs, TALENs, and CRISPR/Cas9. Int J Pharm 2015; 494(1): 180-194.
-
(2015)
Int J Pharm
, vol.494
, Issue.1
, pp. 180-194
-
-
LaFountaine, J.S.1
Fathe, K.2
Smyth, H.D.C.3
-
23
-
-
84929672850
-
Current and future delivery systems for engineered nucleases: ZFN, TALEN and RGEN
-
Ain QU, Chung JY, Kim Y-H. Current and future delivery systems for engineered nucleases: ZFN, TALEN and RGEN. J Control Release 2015; 205: 120-127.
-
(2015)
J Control Release
, vol.205
, pp. 120-127
-
-
Ain, Q.U.1
Chung, J.Y.2
Kim, Y.-H.3
-
24
-
-
84926418276
-
Construction and characterization of adenoviral vectors for the delivery of TALENs into human cells
-
Holkers M, Cathomen T, Gonçalves MAFV. Construction and characterization of adenoviral vectors for the delivery of TALENs into human cells. Methods 2014; 69: 179-187.
-
(2014)
Methods
, vol.69
, pp. 179-187
-
-
Holkers, M.1
Cathomen, T.2
Gonçalves, M.A.F.V.3
-
25
-
-
79960424171
-
In vivo genome editing restores haemostasis in a mouse model of haemophilia
-
Li H, Haurigot V, Doyon Y, Li T, Wong SY, Bhagwat AS et al. In vivo genome editing restores haemostasis in a mouse model of haemophilia. Nature 2011; 475: 217-221.
-
(2011)
Nature
, vol.475
, pp. 217-221
-
-
Li, H.1
Haurigot, V.2
Doyon, Y.3
Li, T.4
Wong, S.Y.5
Bhagwat, A.S.6
-
26
-
-
84964018483
-
Lentivirus pre-packed with Cas9 protein for safer gene editing
-
Choi JG, Dang Y, Abraham S, Ma H, Zhang J, Guo H et al. Lentivirus pre-packed with Cas9 protein for safer gene editing. Gene Ther 2016; 23: 627-633.
-
(2016)
Gene Ther
, vol.23
, pp. 627-633
-
-
Choi, J.G.1
Dang, Y.2
Abraham, S.3
Ma, H.4
Zhang, J.5
Guo, H.6
-
27
-
-
85044694762
-
Targeted genome editing by lentiviral protein transduction of zinc-finger and TAL-effector nucleases
-
Cai Y, Bak RO, Mikkelsen JG. Targeted genome editing by lentiviral protein transduction of zinc-finger and TAL-effector nucleases. eLife 2014; 3: e01911.
-
(2014)
ELife
, vol.3
, pp. e01911
-
-
Cai, Y.1
Bak, R.O.2
Mikkelsen, J.G.3
-
28
-
-
84960389900
-
Engineered viruses as genome editing devices
-
Chen X, Goncalves MAFV. Engineered viruses as genome editing devices. Mol Ther 2016; 44: 447-457.
-
(2016)
Mol Ther
, vol.44
, pp. 447-457
-
-
Chen, X.1
Goncalves, M.A.F.V.2
-
29
-
-
84927514894
-
In vivo genome editing using Staphylococcus aureus Cas9
-
Ran FA, Cong L, Yan WX, Scott DA, Gootenberg JS, Kriz AJ et al. In vivo genome editing using Staphylococcus aureus Cas9. Nature 2015; 520: 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
-
30
-
-
84930943161
-
Rapid and highly efficient mammalian cell engineering via Cas9 protein transfection
-
Liang X, Potter J, Kumar S, Zou Y, Quintanilla R, Sridharan M et al. Rapid and highly efficient mammalian cell engineering via Cas9 protein transfection. J Biotech 2015; 208: 44-53.
-
(2015)
J Biotech
, vol.208
, pp. 44-53
-
-
Liang, X.1
Potter, J.2
Kumar, S.3
Zou, Y.4
Quintanilla, R.5
Sridharan, M.6
-
31
-
-
84961288301
-
Cationic lipid-mediated delivery of proteins enables efficient protein-based genome editing in vitro and in vivo
-
Zuris JA, Thompson DB, Shu Y, Guilinger JP, Bessen JL, Hu JH et al. Cationic lipid-mediated delivery of proteins enables efficient protein-based genome editing in vitro and in vivo. Nat Biotech 2015; 33: 73-80.
-
(2015)
Nat Biotech
, 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
-
32
-
-
84901834420
-
Highly efficient RNA-guided genome editing in human cells via delivery of purified Cas9 ribonucleoproteins
-
Kim S, Kim D, Cho SW, Kim J, Kim J-S. Highly efficient RNA-guided genome editing in human cells via delivery of purified Cas9 ribonucleoproteins. Genome Res 2014; 24: 1012-1019.
-
(2014)
Genome Res
, vol.24
, pp. 1012-1019
-
-
Kim, S.1
Kim, D.2
Cho, S.W.3
Kim, J.4
Kim, J.-S.5
-
33
-
-
84940184252
-
Generation of knock-in primary human T cells using Cas9 ribonucleoproteins
-
Schumann K, Lin S, Boyer E, Simeonov DR, Subramaniam M, Gate RE et al. Generation of knock-in primary human T cells using Cas9 ribonucleoproteins. Proc Natl Acad Sci USA 2015; 112: 10437-10442.
-
(2015)
Proc Natl Acad Sci USA
, vol.112
, pp. 10437-10442
-
-
Schumann, K.1
Lin, S.2
Boyer, E.3
Simeonov, D.R.4
Subramaniam, M.5
Gate, R.E.6
-
34
-
-
36349003379
-
Hydrodynamic gene delivery: Its principles and applications
-
Suda T, Liu D. Hydrodynamic gene delivery: its principles and applications. Mol Ther 2007; 15: 2063-2069.
-
(2007)
Mol Ther
, vol.15
, pp. 2063-2069
-
-
Suda, T.1
Liu, D.2
-
35
-
-
84902095353
-
Genome editing with Cas9 in adult mice corrects a disease mutation and phenotype
-
Yin H, Xue W, Chen S, Bogorad RL, Benedetti E, Grompe M et al. Genome editing with Cas9 in adult mice corrects a disease mutation and phenotype. Nat Biotech 2014; 32(6): 551-553.
-
(2014)
Nat Biotech
, vol.32
, Issue.6
, pp. 551-553
-
-
Yin, H.1
Xue, W.2
Chen, S.3
Bogorad, R.L.4
Benedetti, E.5
Grompe, M.6
-
36
-
-
33746087320
-
Tyrosinemia type I-diagnostic issues and prenatal diagnosis
-
Bijarnia S, Puri RD, Ruel J, Gray GF, Jenkinson L, Verma IC. Tyrosinemia type I-diagnostic issues and prenatal diagnosis. Indian J Pediatr 2006; 73(2): 163-165.
-
(2006)
Indian J Pediatr
, vol.73
, Issue.2
, pp. 163-165
-
-
Bijarnia, S.1
Puri, R.D.2
Ruel, J.3
Gray, G.F.4
Jenkinson, L.5
Verma, I.C.6
-
37
-
-
84863954601
-
Efficient intracellular delivery of nucleic acid pharmaceuticals using cell-penetrating pep-tides
-
Nakase I, Akita H, Kogure K, Gräslund A, Langel Ü, Harashima H et al. Efficient intracellular delivery of nucleic acid pharmaceuticals using cell-penetrating pep-tides. Acc Chem Res 2012; 45: 1132-1139.
-
(2012)
Acc Chem Res
, vol.45
, pp. 1132-1139
-
-
Nakase, I.1
Akita, H.2
Kogure, K.3
Gräslund, A.4
Langel, Ü.5
Harashima, H.6
-
38
-
-
85005982592
-
Targeted genome engineering in human induced pluripotent stem cells by penetrating TALENs
-
Ru R, Yao Y, Yu S, Yin B, Xu W, Zhao S et al. Targeted genome engineering in human induced pluripotent stem cells by penetrating TALENs. Cell Regen 2013; 2: 5.
-
(2013)
Cell Regen
, vol.2
, pp. 5
-
-
Ru, R.1
Yao, Y.2
Yu, S.3
Yin, B.4
Xu, W.5
Zhao, S.6
-
39
-
-
84901838361
-
Cell-penetrating peptide-mediated delivery of TALEN proteins via bioconjugation for genome engineering
-
Liu J, Gaj T, Patterson JT, Sirk SJ, Barbas Iii CF. Cell-penetrating peptide-mediated delivery of TALEN proteins via bioconjugation for genome engineering. PLoS One 2014; 9: e85755.
-
(2014)
PLoS One
, vol.9
, pp. e85755
-
-
Liu, J.1
Gaj, T.2
Patterson, J.T.3
Sirk, S.J.4
Barbas, C.F.5
-
40
-
-
84901843996
-
Gene disruption by cell-penetrating peptide-mediated delivery of Cas9 protein and guide RNA
-
Ramakrishna S, Kwaku Dad A-B, Beloor J, Gopalappa R, Lee S-K, Kim H. Gene disruption by cell-penetrating peptide-mediated delivery of Cas9 protein and guide RNA. Genome Res 2014; 24: 1020-1027.
-
(2014)
Genome Res
, vol.24
, pp. 1020-1027
-
-
Ramakrishna, S.1
Kwaku Dad, A.-B.2
Beloor, J.3
Gopalappa, R.4
Lee, S.-K.5
Kim, H.6
-
41
-
-
84922469442
-
Therapeutic applications of the cell-penetrating HIV-1 Tat peptide
-
Rizzuti M, Nizzardo M, Zanetta C, Ramirez A, Corti S. Therapeutic applications of the cell-penetrating HIV-1 Tat peptide. Drug Discov Today 2015; 20: 76-85.
-
(2015)
Drug Discov Today
, vol.20
, pp. 76-85
-
-
Rizzuti, M.1
Nizzardo, M.2
Zanetta, C.3
Ramirez, A.4
Corti, S.5
-
42
-
-
84904544984
-
Non-viral vectors for gene-based therapy
-
Yin H, Kanasty RL, Eltoukhy AA, Vegas AJ, Dorkin JR, Anderson DG. Non-viral vectors for gene-based therapy. Nat Rev Genet 2014; 15: 541-555.
-
(2014)
Nat Rev Genet
, vol.15
, pp. 541-555
-
-
Yin, H.1
Kanasty, R.L.2
Eltoukhy, A.A.3
Vegas, A.J.4
Dorkin, J.R.5
Anderson, D.G.6
-
43
-
-
79959487372
-
Tailoring nanocarriers for intracellular protein delivery
-
Gu Z, Biswas A, Zhao M, Tang Y. Tailoring nanocarriers for intracellular protein delivery. Chem Soc Rev 2011; 40: 3638-3655.
-
(2011)
Chem Soc Rev
, vol.40
, pp. 3638-3655
-
-
Gu, Z.1
Biswas, A.2
Zhao, M.3
Tang, Y.4
-
44
-
-
36849067019
-
Nanocarriers as an emerging platform for cancer therapy
-
Peer D, Karp JM, Hong S, FaroKHzad OC, Margalit R, Langer R. Nanocarriers as an emerging platform for cancer therapy. Nat Nanotech 2007; 2: 751-760.
-
(2007)
Nat Nanotech
, vol.2
, pp. 751-760
-
-
Peer, D.1
Karp, J.M.2
Hong, S.3
Farokhzad, O.C.4
Margalit, R.5
Langer, R.6
-
45
-
-
0022858683
-
A new concept for macromolecular therapeutics in cancer-chemotherapy-mechanism of tumoritropic accumulation of proteins and the antitumor agent smancs
-
Matsumura Y, Maeda H. A new concept for macromolecular therapeutics in cancer-chemotherapy-mechanism of tumoritropic accumulation of proteins and the antitumor agent smancs. Cancer Res 1986; 46: 6387-6392.
-
(1986)
Cancer Res
, vol.46
, pp. 6387-6392
-
-
Matsumura, Y.1
Maeda, H.2
-
46
-
-
18244365849
-
Protein drug stability: A formulation challenge
-
Frokjaer S, Otzen DE. Protein drug stability: a formulation challenge. Nat Rev Drug Discov 2005; 4: 298-306.
-
(2005)
Nat Rev Drug Discov
, vol.4
, pp. 298-306
-
-
Frokjaer, S.1
Otzen, D.E.2
-
47
-
-
18944373328
-
Highly efficient endogenous human gene correction using designed zinc-finger nucleases
-
Urnov FD, Miller JC, Lee Y-L, Beausejour CM, Rock JM, Augustus S et al. Highly efficient endogenous human gene correction using designed zinc-finger nucleases. Nature 2005; 435: 646-651.
-
(2005)
Nature
, vol.435
, pp. 646-651
-
-
Urnov, F.D.1
Miller, J.C.2
Lee, Y.-L.3
Beausejour, C.M.4
Rock, J.M.5
Augustus, S.6
-
48
-
-
77952011493
-
Zinc-finger nucleases as a novel therapeutic strategy for targeting hepatitis B virus DNAs
-
Cradick TJ, Keck K, Bradshaw S, Jamieson AC, McCaffrey AP. Zinc-finger nucleases as a novel therapeutic strategy for targeting hepatitis B virus DNAs. Mol Ther 2010; 18: 947-954.
-
(2010)
Mol Ther
, vol.18
, pp. 947-954
-
-
Cradick, T.J.1
Keck, K.2
Bradshaw, S.3
Jamieson, A.C.4
McCaffrey, A.P.5
-
49
-
-
84920484581
-
TALEN-mediated targeting of HPV oncogenes ameliorates HPV-related cervical malignancy
-
Hu Z, Ding W, Zhu D, Yu L, Jiang X, Wang X et al. TALEN-mediated targeting of HPV oncogenes ameliorates HPV-related cervical malignancy. J Clin Invest 2015; 125: 425-436.
-
(2015)
J Clin Invest
, vol.125
, pp. 425-436
-
-
Hu, Z.1
Ding, W.2
Zhu, D.3
Yu, L.4
Jiang, X.5
Wang, X.6
-
50
-
-
84930947142
-
In vivo genome editing using nuclease-encoding mRNA corrects SP-B deficiency
-
Mahiny AJ, Dewerth A, Mays LE, Alkhaled M, Mothes B, Malaeksefat E et al. In vivo genome editing using nuclease-encoding mRNA corrects SP-B deficiency. Nat Biotech 2015; 33: 584-586.
-
(2015)
Nat Biotech
, vol.33
, pp. 584-586
-
-
Mahiny, A.J.1
Dewerth, A.2
Mays, L.E.3
Alkhaled, M.4
Mothes, B.5
Malaeksefat, E.6
-
51
-
-
84962593365
-
Efficient delivery of genome-editing proteins using bioreducible lipid nanoparticles
-
Wang M, Zuris JA, Meng F, Rees H, Sun S, Deng P et al. Efficient delivery of genome-editing proteins using bioreducible lipid nanoparticles. Proc Natl Acad Sci USA 2016; 113: 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
-
52
-
-
84908051604
-
Enhanced intracellular siRNA delivery using bioreducible lipid-like nanoparticles
-
Wang M, Alberti K, Varone A, Pouli D, Georgakoudi I, Xu Q. Enhanced intracellular siRNA delivery using bioreducible lipid-like nanoparticles. Adv Health Mater 2014; 3: 1398-1403.
-
(2014)
Adv Health Mater
, vol.3
, pp. 1398-1403
-
-
Wang, M.1
Alberti, K.2
Varone, A.3
Pouli, D.4
Georgakoudi, I.5
Xu, Q.6
-
53
-
-
84924190196
-
Combinatorial library strategies for synthesis of cationic lipid-like nanoparticles and their potential medical applications
-
Altinoglu S, Wang M, Xu Q. Combinatorial library strategies for synthesis of cationic lipid-like nanoparticles and their potential medical applications. Nano-medicine 2015; 10: 643-657.
-
(2015)
Nano-medicine
, vol.10
, pp. 643-657
-
-
Altinoglu, S.1
Wang, M.2
Xu, Q.3
-
54
-
-
84915746589
-
Reactive oxygen species-responsive protein modification and its intracellular delivery for targeted cancer therapy
-
Wang M, Sun S, Neufeld CI, Perez-Ramirez B, Xu Q. Reactive oxygen species-responsive protein modification and its intracellular delivery for targeted cancer therapy. Angew Chem Int Ed 2014; 53: 13444-13448.
-
(2014)
Angew Chem Int Ed
, vol.53
, pp. 13444-13448
-
-
Wang, M.1
Sun, S.2
Neufeld, C.I.3
Perez-Ramirez, B.4
Xu, Q.5
-
55
-
-
84896754899
-
Combinatorially designed lipid-like nanoparticles for intracellular delivery of cytotoxic protein for cancer therapy
-
Wang M, Alberti K, Sun S, Arellano C, Xu Q. Combinatorially designed lipid-like nanoparticles for intracellular delivery of cytotoxic protein for cancer therapy. Angew Chem Int Ed 2014; 53: 2893-2898.
-
(2014)
Angew Chem Int Ed
, vol.53
, pp. 2893-2898
-
-
Wang, M.1
Alberti, K.2
Sun, S.3
Arellano, C.4
Xu, Q.5
-
56
-
-
84868238441
-
A combinatorial library of unsaturated lipidoids for efficient intracellular gene delivery
-
Wang M, Sun S, Alberti K, Xu Q. A combinatorial library of unsaturated lipidoids for efficient intracellular gene delivery. ACS Synth Biol 2012; 1: 403-407.
-
(2012)
ACS Synth Biol
, vol.1
, pp. 403-407
-
-
Wang, M.1
Sun, S.2
Alberti, K.3
Xu, Q.4
-
57
-
-
84862947496
-
Combinatorial library of lipidoids for in vitro DNA delivery
-
Sun S, Wang M, Knupp S, Soto-Feliciano Y, Hu X, Kaplan D et al. Combinatorial library of lipidoids for in vitro DNA delivery. Bioconjugate Chem 2012; 23: 135-140.
-
(2012)
Bioconjugate Chem
, vol.23
, pp. 135-140
-
-
Sun, S.1
Wang, M.2
Knupp, S.3
Soto-Feliciano, Y.4
Hu, X.5
Kaplan, D.6
-
58
-
-
84884289987
-
DOPE facilitates quaternized lipidoids (QLDs) for in vitro DNA delivery
-
Sun S, Wang M, Alberti K, Choy A, Xu Q. DOPE facilitates quaternized lipidoids (QLDs) for in vitro DNA delivery. Nanomedicine 2013; 9: 849-854.
-
(2013)
Nanomedicine
, vol.9
, pp. 849-854
-
-
Sun, S.1
Wang, M.2
Alberti, K.3
Choy, A.4
Xu, Q.5
-
59
-
-
84942821644
-
Self-assembled DNA nanoclews for the efficient delivery of CRISPR-Cas9 for genome editing
-
Sun W, Ji W, Hall JM, Hu Q, Wang C, Beisel CL et al. Self-assembled DNA nanoclews for the efficient delivery of CRISPR-Cas9 for genome editing. Angew Chem Int Ed 2015; 54: 12029-12033.
-
(2015)
Angew Chem Int Ed
, 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
-
60
-
-
84928393912
-
Efficient intracellular delivery of native proteins
-
D'Astolfo Diego S, Pagliero Romina J, Pras A, Karthaus Wouter R, Clevers H, Prasad V et al. Efficient intracellular delivery of native proteins. Cell 2015; 161: 674-690.
-
(2015)
Cell
, vol.161
, pp. 674-690
-
-
D'Astolfo Diego, S.1
Pagliero Romina, J.2
Pras, A.3
Karthaus Wouter, R.4
Clevers, H.5
Prasad, V.6
-
61
-
-
84960882884
-
Therapeutic genome editing by combined viral and non-viral delivery of CRISPR system components in vivo
-
Yin H, Song C-Q, Dorkin JR, Zhu LJ, Li Y, Wu Q et al. Therapeutic genome editing by combined viral and non-viral delivery of CRISPR system components in vivo. Nat Biotech 2016; 34: 328-333.
-
(2016)
Nat Biotech
, 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
|