-
1
-
-
0034614637
-
The hallmarks of cancer
-
Hanahan D, Weinberg RA. The hallmarks of cancer. Cell. 2000;100:57-70.
-
(2000)
Cell
, vol.100
, pp. 57-70
-
-
Hanahan, D.1
Weinberg, R.A.2
-
2
-
-
79952284127
-
Hallmarks of cancer: the next generation
-
Hanahan D, Weinberg RA. Hallmarks of cancer: the next generation. Cell. 2011;144:646-74.
-
(2011)
Cell
, vol.144
, pp. 646-674
-
-
Hanahan, D.1
Weinberg, R.A.2
-
3
-
-
84892833777
-
Discovery and saturation analysis of cancer genes across 21 tumour types
-
Lawrence MS, Stojanov P, Mermel CH, Robinson JT, Garraway LA, Golub TR, et al. Discovery and saturation analysis of cancer genes across 21 tumour types. Nature. 2014;505:495-501.
-
(2014)
Nature
, vol.505
, pp. 495-501
-
-
Lawrence, M.S.1
Stojanov, P.2
Mermel, C.H.3
Robinson, J.T.4
Garraway, L.A.5
Golub, T.R.6
-
4
-
-
84913594397
-
Genome editing. The new frontier of genome engineering with CRISPR-Cas9
-
Doudna JA, Charpentier E. Genome editing. The new frontier of genome engineering with CRISPR-Cas9. Science. 2014;346:1258096.
-
(2014)
Science
, vol.346
-
-
Doudna, J.A.1
Charpentier, E.2
-
5
-
-
0037169361
-
Cancer modeling in the modern era: progress and challenges
-
Van Dyke T, Jacks T. Cancer modeling in the modern era: progress and challenges. Cell. 2002;108:135-44.
-
(2002)
Cell
, vol.108
, pp. 135-144
-
-
Dyke, T.1
Jacks, T.2
-
6
-
-
84858397489
-
Life in the fast lane: mammalian disease models in the genomics era
-
Dow LE, Lowe SW. Life in the fast lane: mammalian disease models in the genomics era. Cell. 2012;148:1099-109.
-
(2012)
Cell
, vol.148
, pp. 1099-1109
-
-
Dow, L.E.1
Lowe, S.W.2
-
7
-
-
84898778301
-
A guide to genome engineering with programmable nucleases
-
Kim H, Kim J-S. A guide to genome engineering with programmable nucleases. Nat Rev Genet. 2014;15:321-34.
-
(2014)
Nat Rev Genet
, vol.15
, pp. 321-334
-
-
Kim, H.1
Kim, J.-S.2
-
8
-
-
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;157:1262-78.
-
(2014)
Cell
, vol.157
, pp. 1262-1278
-
-
Hsu, P.D.1
Lander, E.S.2
Zhang, F.3
-
9
-
-
84884856342
-
Cas9 as a versatile tool for engineering biology
-
Mali P, Esvelt KM, Church GM. Cas9 as a versatile tool for engineering biology. Nat Methods. 2013;10:957-63.
-
(2013)
Nat Methods
, vol.10
, pp. 957-963
-
-
Mali, P.1
Esvelt, K.M.2
Church, G.M.3
-
10
-
-
84900314611
-
CRISPR-Cas systems for editing, regulating and targeting genomes
-
Sander JD, Joung JK. CRISPR-Cas systems for editing, regulating and targeting genomes. Nat Biotechnol. 2014;32:347-55.
-
(2014)
Nat Biotechnol
, vol.32
, pp. 347-355
-
-
Sander, J.D.1
Joung, J.K.2
-
11
-
-
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;337:816-21.
-
(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
-
12
-
-
84876567971
-
RNA-programmed genome editing in human cells
-
Jinek M, East A, Cheng A, Lin S, Ma E, Doudna J. RNA-programmed genome editing in human cells. Elife. 2013;2, e00471.
-
(2013)
Elife
, vol.2
-
-
Jinek, M.1
East, A.2
Cheng, A.3
Lin, S.4
Ma, E.5
Doudna, J.6
-
13
-
-
84874624936
-
Targeted genome engineering in human cells with the Cas9 RNA-guided endonuclease
-
Cho SW, Kim S, Kim JM, Kim JS. Targeted genome engineering in human cells with the Cas9 RNA-guided endonuclease. Nat Biotechnol. 2013;31:230-2.
-
(2013)
Nat Biotechnol
, vol.31
, pp. 230-232
-
-
Cho, S.W.1
Kim, S.2
Kim, J.M.3
Kim, J.S.4
-
14
-
-
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;339:819-23.
-
(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
-
15
-
-
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;339:823-6.
-
(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
-
16
-
-
84884165315
-
DNA targeting specificity of RNA-guided Cas9 nucleases
-
Hsu PD, Scott DA, Weinstein JA, Ran FA, Konermann S, Agarwala V, et al. DNA targeting specificity of RNA-guided Cas9 nucleases. Nat Biotechnol. 2013;31:827-32.
-
(2013)
Nat Biotechnol
, vol.31
, pp. 827-832
-
-
Hsu, P.D.1
Scott, D.A.2
Weinstein, J.A.3
Ran, F.A.4
Konermann, S.5
Agarwala, V.6
-
17
-
-
84877707375
-
One-step generation of mice carrying mutations in multiple genes by CRISPR/Cas-mediated genome engineering
-
Wang H, Yang H, Shivalila CS, Dawlaty MM, Cheng AW, Zhang F, et al. One-step generation of mice carrying mutations in multiple genes by CRISPR/Cas-mediated genome engineering. Cell. 2013;153:910-8.
-
(2013)
Cell
, vol.153
, pp. 910-918
-
-
Wang, H.1
Yang, H.2
Shivalila, C.S.3
Dawlaty, M.M.4
Cheng, A.W.5
Zhang, F.6
-
18
-
-
84884289608
-
One-step generation of mice carrying reporter and conditional alleles by CRISPR/Cas-mediated genome engineering
-
Yang H, Wang H, Shivalila CS, Cheng AW, Shi L, Jaenisch R. One-step generation of mice carrying reporter and conditional alleles by CRISPR/Cas-mediated genome engineering. Cell. 2013;154:1370-9.
-
(2013)
Cell
, vol.154
, pp. 1370-1379
-
-
Yang, H.1
Wang, H.2
Shivalila, C.S.3
Cheng, A.W.4
Shi, L.5
Jaenisch, R.6
-
19
-
-
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 Biotechnol. 2014;32:551-3.
-
(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
-
20
-
-
84899490344
-
Targeted genomic rearrangements using CRISPR/Cas technology
-
Choi PS, Meyerson M. Targeted genomic rearrangements using CRISPR/Cas technology. Nat Commun. 2014;5:3728.
-
(2014)
Nat Commun
, vol.5
, pp. 3728
-
-
Choi, P.S.1
Meyerson, M.2
-
21
-
-
84923384373
-
Deletions, inversions, duplications: engineering of structural variants using CRISPR/Cas in mice
-
Kraft K, Geuer S, Will AJ, Chan WL, Paliou C, Borschiwer M, et al. Deletions, inversions, duplications: engineering of structural variants using CRISPR/Cas in mice. Cell Rep. 2015;10:833-9.
-
(2015)
Cell Rep
, vol.10
, pp. 833-839
-
-
Kraft, K.1
Geuer, S.2
Will, A.J.3
Chan, W.L.4
Paliou, C.5
Borschiwer, M.6
-
22
-
-
84922735816
-
In vivo engineering of oncogenic chromosomal rearrangements with the CRISPR/Cas9 system
-
Maddalo D, Manchado E, Concepcion CP, Bonetti C, Vidigal JA, Han Y-C, et al. In vivo engineering of oncogenic chromosomal rearrangements with the CRISPR/Cas9 system. Nature. 2014;516:423-7.
-
(2014)
Nature
, vol.516
, pp. 423-427
-
-
Maddalo, D.1
Manchado, E.2
Concepcion, C.P.3
Bonetti, C.4
Vidigal, J.A.5
Han, Y.-C.6
-
23
-
-
84901951241
-
Engineering human tumour-associated chromosomal translocations with the RNA-guided CRISPR-Cas9 system
-
Torres R, Martin MC, Garcia A, Cigudosa JC, Ramirez JC, Rodriguez-Perales S. Engineering human tumour-associated chromosomal translocations with the RNA-guided CRISPR-Cas9 system. Nat Commun. 2014;5:3964.
-
(2014)
Nat Commun
, vol.5
, pp. 3964
-
-
Torres, R.1
Martin, M.C.2
Garcia, A.3
Cigudosa, J.C.4
Ramirez, J.C.5
Rodriguez-Perales, S.6
-
24
-
-
84923118778
-
Rapid modelling of cooperating genetic events in cancer through somatic genome editing
-
Sanchez-Rivera FJ, Papagiannakopoulos T, Romero R, Tammela T, Bauer MR, Bhutkar A, et al. Rapid modelling of cooperating genetic events in cancer through somatic genome editing. Nature. 2014;516:428-31.
-
(2014)
Nature
, vol.516
, pp. 428-431
-
-
Sanchez-Rivera, F.J.1
Papagiannakopoulos, T.2
Romero, R.3
Tammela, T.4
Bauer, M.R.5
Bhutkar, A.6
-
25
-
-
84908190503
-
CRISPR-mediated direct mutation of cancer genes in the mouse liver
-
Xue W, Chen S, Yin H, Tammela T, Papagiannakopoulos T, Joshi NS, et al. CRISPR-mediated direct mutation of cancer genes in the mouse liver. Nature. 2014;514:380-5.
-
(2014)
Nature
, vol.514
, pp. 380-385
-
-
Xue, W.1
Chen, S.2
Yin, H.3
Tammela, T.4
Papagiannakopoulos, T.5
Joshi, N.S.6
-
26
-
-
84905029498
-
Generating genetically modified mice using CRISPR/Cas-mediated genome engineering
-
Yang H, Wang H, Jaenisch R. Generating genetically modified mice using CRISPR/Cas-mediated genome engineering. Nat Protoc. 2014;9:1956-68.
-
(2014)
Nat Protoc
, vol.9
, pp. 1956-1968
-
-
Yang, H.1
Wang, H.2
Jaenisch, R.3
-
27
-
-
84929135130
-
Epigenome editing by a CRISPR-Cas9-based acetyltransferase activates genes from promoters and enhancers
-
Hilton IB, D'Ippolito AM, Vockley CM, Thakore PI, Crawford GE, Reddy TE, et al. Epigenome editing by a CRISPR-Cas9-based acetyltransferase activates genes from promoters and enhancers. Nat Biotechnol. 2015;33:510-7.
-
(2015)
Nat Biotechnol
, vol.33
, pp. 510-517
-
-
Hilton, I.B.1
D'Ippolito, A.M.2
Vockley, C.M.3
Thakore, P.I.4
Crawford, G.E.5
Reddy, T.E.6
-
28
-
-
84938945636
-
Cloning-free CRISPR/Cas system facilitates functional cassette knock-in in mice
-
Aida T, Chiyo K, Usami T, Ishikubo H, Imahashi R, Wada Y, et al. Cloning-free CRISPR/Cas system facilitates functional cassette knock-in in mice. Genome Biol. 2015;16:87.
-
(2015)
Genome Biol
, vol.16
, pp. 87
-
-
Aida, T.1
Chiyo, K.2
Usami, T.3
Ishikubo, H.4
Imahashi, R.5
Wada, Y.6
-
29
-
-
84923779856
-
CRISPR/Cas-mediated genome editing in the rat via direct injection of one-cell embryos
-
Shao Y, Guan Y, Wang L, Qiu Z, Liu M, Chen Y, et al. CRISPR/Cas-mediated genome editing in the rat via direct injection of one-cell embryos. Nat Protoc. 2014;9:2493-512.
-
(2014)
Nat Protoc
, vol.9
, pp. 2493-2512
-
-
Shao, Y.1
Guan, Y.2
Wang, L.3
Qiu, Z.4
Liu, M.5
Chen, Y.6
-
30
-
-
84894081986
-
Generation of gene-modified cynomolgus monkey via Cas9/RNA-mediated gene targeting in one-cell embryos
-
Niu Y, Shen B, Cui Y, Chen Y, Wang J, Wang L, et al. Generation of gene-modified cynomolgus monkey via Cas9/RNA-mediated gene targeting in one-cell embryos. Cell. 2014;156:836-43.
-
(2014)
Cell
, vol.156
, pp. 836-843
-
-
Niu, Y.1
Shen, B.2
Cui, Y.3
Chen, Y.4
Wang, J.5
Wang, L.6
-
31
-
-
84907486054
-
TALEN-mediated somatic mutagenesis in murine models of cancer
-
Zhang S, Li L, Kendrick SL, Gerard RD, Zhu H. TALEN-mediated somatic mutagenesis in murine models of cancer. Cancer Res. 2014;74:5311-21.
-
(2014)
Cancer Res
, vol.74
, pp. 5311-5321
-
-
Zhang, S.1
Li, L.2
Kendrick, S.L.3
Gerard, R.D.4
Zhu, H.5
-
32
-
-
84906079358
-
Permanent alteration of PCSK9 with in vivo CRISPR-Cas9 genome editing
-
Ding Q, Strong A, Patel KM, Ng SL, Gosis BS, Regan SN, et al. Permanent alteration of PCSK9 with in vivo CRISPR-Cas9 genome editing. Circ Res. 2014;115:488-92.
-
(2014)
Circ Res
, vol.115
, pp. 488-492
-
-
Ding, Q.1
Strong, A.2
Patel, K.M.3
Ng, S.L.4
Gosis, B.S.5
Regan, S.N.6
-
33
-
-
84908245956
-
Efficient gene editing in adult mouse livers via adenoviral delivery of CRISPR/Cas9
-
Cheng R, Peng J, Yan Y, Cao P, Wang J, Qiu C, et al. Efficient gene editing in adult mouse livers via adenoviral delivery of CRISPR/Cas9. FEBS Lett. 2014;588:3954-8.
-
(2014)
FEBS Lett
, vol.588
, pp. 3954-3958
-
-
Cheng, R.1
Peng, J.2
Yan, Y.3
Cao, P.4
Wang, J.5
Qiu, C.6
-
34
-
-
84926061715
-
In vivo interrogation of gene function in the mammalian brain using CRISPR-Cas9
-
Swiech L, Heidenreich M, Banerjee A, Habib N, Li Y, Trombetta J, et al. In vivo interrogation of gene function in the mammalian brain using CRISPR-Cas9. Nat Biotechnol. 2014;33:102-6.
-
(2014)
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
-
35
-
-
84912101598
-
CRISPR-Cas9 knockin mice for genome editing and cancer modeling
-
Platt RJ, Chen S, Zhou Y, Yim MJ, Swiech L, Kempton HR, et al. CRISPR-Cas9 knockin mice for genome editing and cancer modeling. Cell. 2014;159:440-55.
-
(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
-
36
-
-
84926652112
-
Inducible in vivo genome editing with CRISPR-Cas9
-
Dow LE, Fisher J, O'Rourke KP, Muley A, Kastenhuber ER, Livshits G, et al. Inducible in vivo genome editing with CRISPR-Cas9. Nat Biotechnol. 2015;33:390-4.
-
(2015)
Nat Biotechnol
, vol.33
, pp. 390-394
-
-
Dow, L.E.1
Fisher, J.2
O'Rourke, K.P.3
Muley, A.4
Kastenhuber, E.R.5
Livshits, G.6
-
37
-
-
84905388288
-
Characterization of genomic deletion efficiency mediated by clustered regularly interspaced palindromic repeats (CRISPR)/Cas9 nuclease system in mammalian cells
-
Canver MC, Bauer DE, Dass A, Yien YY, Chung J, Masuda T, et al. Characterization of genomic deletion efficiency mediated by clustered regularly interspaced palindromic repeats (CRISPR)/Cas9 nuclease system in mammalian cells. J Biol Chem. 2014;289:21312-24.
-
(2014)
J Biol Chem
, vol.289
, pp. 21312-21324
-
-
Canver, M.C.1
Bauer, D.E.2
Dass, A.3
Yien, Y.Y.4
Chung, J.5
Masuda, T.6
-
38
-
-
84907976219
-
Chromosomal translocations in human cells are generated by canonical nonhomologous end-joining
-
Ghezraoui H, Piganeau M, Renouf B, Renaud JB, Sallmyr A, Ruis B, et al. Chromosomal translocations in human cells are generated by canonical nonhomologous end-joining. Mol Cell. 2014;55:829-42.
-
(2014)
Mol Cell
, vol.55
, pp. 829-842
-
-
Ghezraoui, H.1
Piganeau, M.2
Renouf, B.3
Renaud, J.B.4
Sallmyr, A.5
Ruis, B.6
-
39
-
-
84912078930
-
Simple and rapid in vivo generation of chromosomal rearrangements using CRISPR/Cas9 technology
-
Blasco RB, Karaca E, Ambrogio C, Cheong TC, Karayol E, Minero VG, et al. Simple and rapid in vivo generation of chromosomal rearrangements using CRISPR/Cas9 technology. Cell Rep. 2014;9:1219-27.
-
(2014)
Cell Rep
, vol.9
, pp. 1219-1227
-
-
Blasco, R.B.1
Karaca, E.2
Ambrogio, C.3
Cheong, T.C.4
Karayol, E.5
Minero, V.G.6
-
40
-
-
84937545421
-
A versatile reporter system for CRISPR-mediated chromosomal rearrangements
-
Li Y, Park A, Mou H, Anderson DG, Jacks T, Weng ZP, et al. A versatile reporter system for CRISPR-mediated chromosomal rearrangements. Genome Biol. 2015;16:111.
-
(2015)
Genome Biol
, vol.16
, pp. 111
-
-
Li, Y.1
Park, A.2
Mou, H.3
Anderson, D.G.4
Jacks, T.5
Weng, Z.P.6
-
41
-
-
84911422892
-
Generation of mouse models of myeloid malignancy with combinatorial genetic lesions using CRISPR-Cas9 genome editing
-
Heckl D, Kowalczyk MS, Yudovich D, Belizaire R, Puram RV, McConkey ME, et al. Generation of mouse models of myeloid malignancy with combinatorial genetic lesions using CRISPR-Cas9 genome editing. Nat Biotechnol. 2014;32:941-6.
-
(2014)
Nat Biotechnol
, vol.32
, pp. 941-946
-
-
Heckl, D.1
Kowalczyk, M.S.2
Yudovich, D.3
Belizaire, R.4
Puram, R.V.5
McConkey, M.E.6
-
42
-
-
84888781186
-
Repurposing CRISPR/Cas9 for in situ functional assays
-
Malina A, Mills JR, Cencic R, Yan Y, Fraser J, Schippers LM, et al. Repurposing CRISPR/Cas9 for in situ functional assays. Genes Dev. 2013;27:2602-14.
-
(2013)
Genes Dev
, vol.27
, pp. 2602-2614
-
-
Malina, A.1
Mills, J.R.2
Cencic, R.3
Yan, Y.4
Fraser, J.5
Schippers, L.M.6
-
43
-
-
84900420439
-
MLL3 is a haploinsufficient 7q tumor suppressor in acute myeloid leukemia
-
Chen C, Liu Y, Rappaport AR, Kitzing T, Schultz N, Zhao Z, et al. MLL3 is a haploinsufficient 7q tumor suppressor in acute myeloid leukemia. Cancer Cell. 2014;25:652-65.
-
(2014)
Cancer Cell
, vol.25
, pp. 652-665
-
-
Chen, C.1
Liu, Y.2
Rappaport, A.R.3
Kitzing, T.4
Schultz, N.5
Zhao, Z.6
-
44
-
-
84924621296
-
An inducible lentiviral guide RNA platform enables the identification of tumor-essential genes and tumor-promoting mutations in vivo
-
Aubrey BJ, Kelly GL, Kueh AJ, Brennan MS, O'Connor L, Milla L, et al. An inducible lentiviral guide RNA platform enables the identification of tumor-essential genes and tumor-promoting mutations in vivo. Cell Rep. 2015;10:1422-32.
-
(2015)
Cell Rep
, vol.10
, pp. 1422-1432
-
-
Aubrey, B.J.1
Kelly, G.L.2
Kueh, A.J.3
Brennan, M.S.4
O'Connor, L.5
Milla, L.6
-
45
-
-
0035893252
-
Analysis of lung tumor initiation and progression using conditional expression of oncogenic K-ras
-
Jackson EL, Willis N, Mercer K, Bronson RT, Crowley D, Montoya R, et al. Analysis of lung tumor initiation and progression using conditional expression of oncogenic K-ras. Genes Dev. 2001;15:3243-8.
-
(2001)
Genes Dev
, vol.15
, pp. 3243-3248
-
-
Jackson, E.L.1
Willis, N.2
Mercer, K.3
Bronson, R.T.4
Crowley, D.5
Montoya, R.6
-
46
-
-
11144356354
-
Endogenous oncogenic K-ras G12D stimulates proliferation and widespread neoplastic and developmental defects
-
Tuveson DA, Shaw AT, Willis NA, Silver DP, Jackson EL, Chang S, et al. Endogenous oncogenic K-ras G12D stimulates proliferation and widespread neoplastic and developmental defects. Cancer Cell. 2001;5:375-87.
-
(2001)
Cancer Cell
, vol.5
, pp. 375-387
-
-
Tuveson, D.A.1
Shaw, A.T.2
Willis, N.A.3
Silver, D.P.4
Jackson, E.L.5
Chang, S.6
-
47
-
-
68149157175
-
Conditional mouse lung cancer models using adenoviral or lentiviral delivery of Cre recombinase
-
DuPage M, Dooley AL, Jacks T. Conditional mouse lung cancer models using adenoviral or lentiviral delivery of Cre recombinase. Nat Protoc. 2009;4:1064-72.
-
(2009)
Nat Protoc
, vol.4
, pp. 1064-1072
-
-
DuPage, M.1
Dooley, A.L.2
Jacks, T.3
-
48
-
-
84876835924
-
Nkx2-1 represses a latent gastric differentiation program in lung adenocarcinoma
-
Snyder EL, Watanabe H, Magendantz M, Hoersch S, Chen TA, Wang DG, et al. Nkx2-1 represses a latent gastric differentiation program in lung adenocarcinoma. Mol Cell. 2013;50:185-99.
-
(2013)
Mol Cell
, vol.50
, pp. 185-199
-
-
Snyder, E.L.1
Watanabe, H.2
Magendantz, M.3
Hoersch, S.4
Chen, T.A.5
Wang, D.G.6
-
50
-
-
84892765883
-
Genome-scale CRISPR-Cas9 knockout screening in human cells
-
Shalem O, Sanjana NE, Hartenian E, Shi X, Scott DA, Mikkelson T, et al. Genome-scale CRISPR-Cas9 knockout screening in human cells. Science. 2014;343:84-7.
-
(2014)
Science
, vol.343
, pp. 84-87
-
-
Shalem, O.1
Sanjana, N.E.2
Hartenian, E.3
Shi, X.4
Scott, D.A.5
Mikkelson, T.6
-
51
-
-
84892749369
-
Genetic screens in human cells using the CRISPR/Cas9 system
-
Wang T, Wei JJ, Sabatini DM, Lander ES. Genetic screens in human cells using the CRISPR/Cas9 system. Science. 2014;343:80-4.
-
(2014)
Science
, vol.343
, pp. 80-84
-
-
Wang, T.1
Wei, J.J.2
Sabatini, D.M.3
Lander, E.S.4
-
52
-
-
84904739968
-
DNA sequencing and CRISPR-Cas9 gene editing for target validation in mammalian cells
-
Smurnyy Y, Cai M, Wu H, McWhinnie E, Tallarico JA, Yang Y, et al. DNA sequencing and CRISPR-Cas9 gene editing for target validation in mammalian cells. Nat Chem Biol. 2014;10:623-5.
-
(2014)
Nat Chem Biol
, vol.10
, pp. 623-625
-
-
Smurnyy, Y.1
Cai, M.2
Wu, H.3
McWhinnie, E.4
Tallarico, J.A.5
Yang, Y.6
Feng, Y.7
-
53
-
-
84923106217
-
Therapeutic genome editing: prospects and challenges
-
Cox DB, Platt RJ, Zhang F. Therapeutic genome editing: prospects and challenges. Nat Med. 2015;21:121-31.
-
(2015)
Nat Med
, vol.21
, pp. 121-131
-
-
Cox, D.B.1
Platt, R.J.2
Zhang, F.3
-
54
-
-
84890033064
-
Functional repair of CFTR by CRISPR/Cas9 in intestinal stem cell organoids of cystic fibrosis patients
-
Schwank G, Koo BK, Sasselli V, Dekkers J, Heo I, Demircan T, et al. Functional repair of CFTR by CRISPR/Cas9 in intestinal stem cell organoids of cystic fibrosis patients. Cell Stem Cell. 2013;13:653-8.
-
(2013)
Cell Stem Cell
, vol.13
, pp. 653-658
-
-
Schwank, G.1
Koo, B.K.2
Sasselli, V.3
Dekkers, J.4
Heo, I.5
Demircan, T.6
-
55
-
-
84890050551
-
Correction of a genetic disease in mouse via use of CRISPR-Cas9
-
Wu Y, Liang D, Wang Y, Bai M, Tang W, Bao S, et al. Correction of a genetic disease in mouse via use of CRISPR-Cas9. Cell Stem Cell. 2013;13:659-62.
-
(2013)
Cell Stem Cell
, vol.13
, pp. 659-662
-
-
Wu, Y.1
Liang, D.2
Wang, Y.3
Bai, M.4
Tang, W.5
Bao, S.6
-
56
-
-
84907200149
-
Prevention of muscular dystrophy in mice by CRISPR/Cas9-mediated editing of germline DNA
-
Long C, McAnally JR, Shelton JM, Mireault AA, Bassel-Duby R, Olson EN. Prevention of muscular dystrophy in mice by CRISPR/Cas9-mediated editing of germline DNA. Science. 2014;345:1184-8.
-
(2014)
Science
, vol.345
, pp. 1184-1188
-
-
Long, C.1
McAnally, J.R.2
Shelton, J.M.3
Mireault, A.A.4
Bassel-Duby, R.5
Olson, E.N.6
-
57
-
-
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 Biotechnol. 2014;33:73-80.
-
(2014)
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
-
58
-
-
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 JS. Highly efficient RNA-guided genome editing in human cells via delivery of purified Cas9 ribonucleoproteins. Genome Res. 2014;24:1012-9.
-
(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
-
59
-
-
84923297110
-
A split-Cas9 architecture for inducible genome editing and transcription modulation
-
Zetsche B, Volz SE, Zhang F. A split-Cas9 architecture for inducible genome editing and transcription modulation. Nat Biotechnol. 2015;33:139-42.
-
(2015)
Nat Biotechnol
, vol.33
, pp. 139-142
-
-
Zetsche, B.1
Volz, S.E.2
Zhang, F.3
-
60
-
-
84924322574
-
Rational design of a split-Cas9 enzyme complex
-
Wright AV, Sternberg SH, Taylor DW, Staahl BT, Bardales JA, Kornfeld JE, et al. Rational design of a split-Cas9 enzyme complex. Proc Natl Acad Sci U S A. 2015;112:2984-9.
-
(2015)
Proc Natl Acad Sci U S A
, 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
-
61
-
-
84887104139
-
Orthogonal Cas9 proteins for RNA-guided gene regulation and editing
-
Esvelt KM, Mali P, BraffJL, Moosburner M, Yaung SJ, Church GM. Orthogonal Cas9 proteins for RNA-guided gene regulation and editing. Nat Methods. 2013;10:1116-21.
-
(2013)
Nat Methods
, vol.10
, pp. 1116-1121
-
-
Esvelt, K.M.1
Mali, P.2
Braff, J.L.3
Moosburner, M.4
Yaung, S.J.5
Church, G.M.6
-
62
-
-
84884663630
-
Efficient genome engineering in human pluripotent stem cells using Cas9 from Neisseria meningitidis
-
Hou Z, Zhang Y, Propson NE, Howden SE, Chu LF, Sontheimer EJ, et al. Efficient genome engineering in human pluripotent stem cells using Cas9 from Neisseria meningitidis. Proc Natl Acad Sci U S A. 2013;110:15644-9.
-
(2013)
Proc Natl Acad Sci U S A
, vol.110
, pp. 15644-15649
-
-
Hou, Z.1
Zhang, Y.2
Propson, N.E.3
Howden, S.E.4
Chu, L.F.5
Sontheimer, E.J.6
-
63
-
-
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;520:186-91.
-
(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
-
64
-
-
84928775846
-
A prudent path forward for genomic engineering and germline gene modification
-
Baltimore BD, Berg P, Botchan M, Carroll D, Charo RA, Church G, et al. A prudent path forward for genomic engineering and germline gene modification. Science. 2015;348:36-8.
-
(2015)
Science
, vol.348
, pp. 36-38
-
-
Baltimore, B.D.1
Berg, P.2
Botchan, M.3
Carroll, D.4
Charo, R.A.5
Church, G.6
-
65
-
-
84884160273
-
CAS9 transcriptional activators for target specificity screening and paired nickases for cooperative genome engineering
-
Mali P, Aach J, Stranges PB, Esvelt KM, Moosburner M, Kosuri S, et al. CAS9 transcriptional activators for target specificity screening and paired nickases for cooperative genome engineering. Nat Biotechnol. 2013;31:833-8.
-
(2013)
Nat Biotechnol
, vol.31
, pp. 833-838
-
-
Mali, P.1
Aach, J.2
Stranges, P.B.3
Esvelt, K.M.4
Moosburner, M.5
Kosuri, S.6
-
66
-
-
84884288934
-
Double nicking by RNA-guided CRISPR Cas9 for enhanced genome editing specificity
-
Ran FA, Hsu PD, Lin CY, Gootenberg JS, Konermann S, Trevino AE, et al. Double nicking by RNA-guided CRISPR Cas9 for enhanced genome editing specificity. Cell. 2013;154:1380-9.
-
(2013)
Cell
, vol.154
, pp. 1380-1389
-
-
Ran, F.A.1
Hsu, P.D.2
Lin, C.Y.3
Gootenberg, J.S.4
Konermann, S.5
Trevino, A.E.6
-
67
-
-
84896929630
-
Improving CRISPR-Cas nuclease specificity using truncated guide RNAs
-
Fu Y, Sander JD, Reyon D, Cascio VM, Joung JK. Improving CRISPR-Cas nuclease specificity using truncated guide RNAs. Nat Biotechnol. 2013;32:279-84.
-
(2013)
Nat Biotechnol
, vol.32
, pp. 279-284
-
-
Fu, Y.1
Sander, J.D.2
Reyon, D.3
Cascio, V.M.4
Joung, J.K.5
-
68
-
-
84902210542
-
Fusion of catalytically inactive Cas9 to FokI nuclease improves the specificity of genome modification
-
Guilinger JP, Thompson DB, Liu DR. Fusion of catalytically inactive Cas9 to FokI nuclease improves the specificity of genome modification. Nat Biotechnol. 2014;32:577-82.
-
(2014)
Nat Biotechnol
, vol.32
, pp. 577-582
-
-
Guilinger, J.P.1
Thompson, D.B.2
Liu, D.R.3
-
69
-
-
84902204289
-
Dimeric CRISPR RNA-guided FokI nucleases for highly specific genome editing
-
Tsai SQ, Wyvekens N, Khayter C, Foden JA, Thapar V, Reyon D, et al. Dimeric CRISPR RNA-guided FokI nucleases for highly specific genome editing. Nat Biotechnol. 2014;32:569-76.
-
(2014)
Nat Biotechnol
, vol.32
, pp. 569-576
-
-
Tsai, S.Q.1
Wyvekens, N.2
Khayter, C.3
Foden, J.A.4
Thapar, V.5
Reyon, D.6
-
70
-
-
84923266604
-
GUIDE-seq enables genome-wide profiling of off-target cleavage by CRISPR-Cas nucleases
-
Tsai SQ, Zheng Z, Nguyen NT, Liebers M, Topkar VV, Thapar V, et al. GUIDE-seq enables genome-wide profiling of off-target cleavage by CRISPR-Cas nucleases. Nat Biotechnol. 2015;33:187-97.
-
(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
-
71
-
-
84880570576
-
High-frequency off-target mutagenesis induced by CRISPR-Cas nucleases in human cells
-
Fu Y, Foden JA, Khayter C, Maeder ML, Reyon D, Joung JK, et al. High-frequency off-target mutagenesis induced by CRISPR-Cas nucleases in human cells. Nat Biotechnol. 2013;31:822-6.
-
(2013)
Nat Biotechnol
, vol.31
, pp. 822-826
-
-
Fu, Y.1
Foden, J.A.2
Khayter, C.3
Maeder, M.L.4
Reyon, D.5
Joung, J.K.6
-
72
-
-
84902095352
-
Genome-wide binding of the CRISPR endonuclease Cas9 in mammalian cells
-
Wu X, Scott DA, Kriz AJ, Chiu AC, Hsu PD, Dadon DB, et al. Genome-wide binding of the CRISPR endonuclease Cas9 in mammalian cells. Nat Biotechnol. 2014;32:670-6.
-
(2014)
Nat Biotechnol
, vol.32
, pp. 670-676
-
-
Wu, X.1
Scott, D.A.2
Kriz, A.J.3
Chiu, A.C.4
Hsu, P.D.5
Dadon, D.B.6
-
73
-
-
84939289057
-
Applications of the CRISPR-Cas9 system in cancer biology
-
In press.
-
Sanchez-Rivera FJ, Jacks T. Applications of the CRISPR-Cas9 system in cancer biology. Nat Rev Cancer. In press.
-
Nat Rev Cancer.
-
-
Sanchez-Rivera, F.J.1
Jacks, T.2
-
74
-
-
84930939029
-
Discovery of cancer drug targets by CRISPR-Cas9 screening of protein domains
-
Shi J, Wang E, Milazzo JP, Wang Z, Kinney JB, Vakoc CR. Discovery of cancer drug targets by CRISPR-Cas9 screening of protein domains. Nat Biotechnol. 2015. doi: 10.1038/nbt.3235.
-
(2015)
Nat Biotechnol
-
-
Shi, J.1
Wang, E.2
Milazzo, J.P.3
Wang, Z.4
Kinney, J.B.5
Vakoc, C.R.6
-
75
-
-
84923141668
-
CRISPR-Cas9-based photoactivatable transcription system
-
Nihongaki Y, Yamamoto S, Kawano F, Suzuki H, Sato M. CRISPR-Cas9-based photoactivatable transcription system. Chem Biol. 2015;22:169-74.
-
(2015)
Chem Biol
, vol.22
, pp. 169-174
-
-
Nihongaki, Y.1
Yamamoto, S.2
Kawano, F.3
Suzuki, H.4
Sato, M.5
-
76
-
-
84925534357
-
A light-inducible CRISPR-Cas9 system for control of endogenous gene activation
-
Polstein LR, Gersbach CA. A light-inducible CRISPR-Cas9 system for control of endogenous gene activation. Nat Chem Biol. 2015;11:198-200.
-
(2015)
Nat Chem Biol
, vol.11
, pp. 198-200
-
-
Polstein, L.R.1
Gersbach, C.A.2
-
77
-
-
84925008880
-
Genome-wide CRISPR screen in a mouse model of tumor growth and metastasis
-
Chen S, Sanjana NE, Zheng K, Shalem O, Lee K, Shi X, et al. Genome-wide CRISPR screen in a mouse model of tumor growth and metastasis. Cell. 2014;160:1246-60.
-
(2014)
Cell
, vol.160
, pp. 1246-1260
-
-
Chen, S.1
Sanjana, N.E.2
Zheng, K.3
Shalem, O.4
Lee, K.5
Shi, X.6
-
78
-
-
56349121125
-
An oncogenomics-based in vivo RNAi screen identifies tumor suppressors in liver cancer
-
Zender L, Xue W, Zuber J, Semighini CP, Krasnitz A, Ma B, et al. An oncogenomics-based in vivo RNAi screen identifies tumor suppressors in liver cancer. Cell. 2008;135:852-64.
-
(2008)
Cell
, vol.135
, pp. 852-864
-
-
Zender, L.1
Xue, W.2
Zuber, J.3
Semighini, C.P.4
Krasnitz, A.5
Ma, B.6
-
79
-
-
84921540377
-
Rational design of highly active sgRNAs for CRISPR-Cas9-mediated gene inactivation
-
Doench JG, Hartenian E, Graham DB, Tothova Z, Hegde M, Smith I, et al. Rational design of highly active sgRNAs for CRISPR-Cas9-mediated gene inactivation. Nat Biotechnol. 2014;32:1262-7.
-
(2014)
Nat Biotechnol
, vol.32
, pp. 1262-1267
-
-
Doench, J.G.1
Hartenian, E.2
Graham, D.B.3
Tothova, Z.4
Hegde, M.5
Smith, I.6
-
80
-
-
84893287073
-
E-CRISP: fast CRISPR target site identification
-
Heigwer F, Kerr G, Boutros M. E-CRISP: fast CRISPR target site identification. Nat Methods. 2014;11:122-3.
-
(2014)
Nat Methods
, vol.11
, pp. 122-123
-
-
Heigwer, F.1
Kerr, G.2
Boutros, M.3
-
81
-
-
84896308706
-
Cas-OFFinder: a fast and versatile algorithm that searches for potential off-target sites of Cas9 RNA-guided endonucleases
-
Bae S, Park J, Kim JS. Cas-OFFinder: a fast and versatile algorithm that searches for potential off-target sites of Cas9 RNA-guided endonucleases. Bioinformatics. 2014;30:1473-5.
-
(2014)
Bioinformatics
, vol.30
, pp. 1473-1475
-
-
Bae, S.1
Park, J.2
Kim, J.S.3
-
82
-
-
84907573408
-
CRISPRseek: a bioconductor package to identify target-specific guide RNAs for CRISPR-Cas9 genome-editing systems
-
Zhu LJ, Holmes BR, Aronin N, Brodsky MH. CRISPRseek: a bioconductor package to identify target-specific guide RNAs for CRISPR-Cas9 genome-editing systems. PLoS One. 2014;9, e108424.
-
(2014)
PLoS One
, vol.9
-
-
Zhu, L.J.1
Holmes, B.R.2
Aronin, N.3
Brodsky, M.H.4
-
83
-
-
84905262730
-
Improved vectors and genome-wide libraries for CRISPR screening
-
Sanjana NE, Shalem O, Zhang F. Improved vectors and genome-wide libraries for CRISPR screening. Nat Methods. 2014;11:783-4.
-
(2014)
Nat Methods
, vol.11
, pp. 783-784
-
-
Sanjana, N.E.1
Shalem, O.2
Zhang, F.3
-
84
-
-
84923105032
-
Microhomology-mediated end-joining-dependent integration of donor DNA in cells and animals using TALENs and CRISPR/Cas9
-
Nakade S, Tsubota T, Sakane Y, Kume S, Sakamoto N, Obara M, et al. Microhomology-mediated end-joining-dependent integration of donor DNA in cells and animals using TALENs and CRISPR/Cas9. Nat Commun. 2014;5:1-8.
-
(2014)
Nat Commun
, vol.5
, pp. 1-8
-
-
Nakade, S.1
Tsubota, T.2
Sakane, Y.3
Kume, S.4
Sakamoto, N.5
Obara, M.6
-
85
-
-
84903516238
-
Microhomology-based choice of Cas9 nuclease target sites
-
Bae S, Kweon J, Kim HS, Kim JS. Microhomology-based choice of Cas9 nuclease target sites. Nat Methods. 2014;11:705-6.
-
(2014)
Nat Methods
, vol.11
, pp. 705-706
-
-
Bae, S.1
Kweon, J.2
Kim, H.S.3
Kim, J.S.4
-
86
-
-
84930923547
-
Multi-kilobase homozygous targeted gene replacement in human induced pluripotent stem cells
-
Byrne SM, Ortiz L, Mali P, Aach J, Church GM. Multi-kilobase homozygous targeted gene replacement in human induced pluripotent stem cells. Nucleic Acids Res. 2015;43, e21.
-
(2015)
Nucleic Acids Res
, vol.43
-
-
Byrne, S.M.1
Ortiz, L.2
Mali, P.3
Aach, J.4
Church, G.M.5
-
87
-
-
84983792922
-
Enhanced homology-directed human genome engineering by controlled timing of CRISPR/Cas9 delivery
-
Lin S, Staahl BT, Alla RK, Doudna JA. Enhanced homology-directed human genome engineering by controlled timing of CRISPR/Cas9 delivery. Elife. 2015;3, e04766.
-
(2015)
Elife
, vol.3
-
-
Lin, S.1
Staahl, B.T.2
Alla, R.K.3
Doudna, J.A.4
-
88
-
-
84924911665
-
Small molecules enhance CRISPR genome editing in pluripotent stem cells
-
Yu C, Liu Y, Ma T, Liu K, Xu S, Zhang Y, et al. Small molecules enhance CRISPR genome editing in pluripotent stem cells. Cell Stem Cell. 2015;16:142-7.
-
(2015)
Cell Stem Cell
, vol.16
, pp. 142-147
-
-
Yu, C.1
Liu, Y.2
Ma, T.3
Liu, K.4
Xu, S.5
Zhang, Y.6
-
89
-
-
84908352138
-
Genome-scale CRISPR-mediated control of gene repression and activation
-
Gilbert LA, Horlbeck MA, Adamson B, Villalta JE, Chen Y, Whitehead EH, et al. Genome-scale CRISPR-mediated control of gene repression and activation. Cell. 2014;159:647-61.
-
(2014)
Cell
, vol.159
, pp. 647-661
-
-
Gilbert, L.A.1
Horlbeck, M.A.2
Adamson, B.3
Villalta, J.E.4
Chen, Y.5
Whitehead, E.H.6
-
90
-
-
84880571335
-
CRISPR-mediated modular RNA-guided regulation of transcription in eukaryotes
-
Gilbert LA, Larson MH, Morsut L, Liu Z, Brar GA, Torres SE, et al. CRISPR-mediated modular RNA-guided regulation of transcription in eukaryotes. Cell. 2013;154:442-51.
-
(2013)
Cell
, vol.154
, pp. 442-451
-
-
Gilbert, L.A.1
Larson, M.H.2
Morsut, L.3
Liu, Z.4
Brar, G.A.5
Torres, S.E.6
-
91
-
-
84874687019
-
Repurposing CRISPR as an RNA-guided platform for sequence-specific control of gene expression
-
Qi LS, Larson MH, Gilbert LA, Doudna JA, Weissman JS, Arkin AP, et al. Repurposing CRISPR as an RNA-guided platform for sequence-specific control of gene expression. Cell. 2013;152:1173-83.
-
(2013)
Cell
, vol.152
, pp. 1173-1183
-
-
Qi, L.S.1
Larson, M.H.2
Gilbert, L.A.3
Doudna, J.A.4
Weissman, J.S.5
Arkin, A.P.6
-
92
-
-
84886993480
-
CRISPR interference (CRISPRi) for sequence-specific control of gene expression
-
Larson MH, Gilbert LA, Wang X, Lim WA, Weissman JS, Qi LS. CRISPR interference (CRISPRi) for sequence-specific control of gene expression. Nat Protoc. 2013;8:2180-96.
-
(2013)
Nat Protoc
, vol.8
, pp. 2180-2196
-
-
Larson, M.H.1
Gilbert, L.A.2
Wang, X.3
Lim, W.A.4
Weissman, J.S.5
Qi, L.S.6
-
93
-
-
84885180675
-
Multiplexed activation of endogenous genes by CRISPR-on, an RNA-guided transcriptional activator system
-
Cheng AW, Wang H, Yang H, Shi L, Katz Y, Theunissen TW, et al. Multiplexed activation of endogenous genes by CRISPR-on, an RNA-guided transcriptional activator system. Cell Res. 2013;23:1163-71.
-
(2013)
Cell Res
, vol.23
, pp. 1163-1171
-
-
Cheng, A.W.1
Wang, H.2
Yang, H.3
Shi, L.4
Katz, Y.5
Theunissen, T.W.6
-
94
-
-
84890460786
-
Cas9 effector-mediated regulation of transcription and differentiation in human pluripotent stem cells
-
Kearns NA, Genga RM, Enuameh MS, Garber M, Wolfe SA, Maehr R. Cas9 effector-mediated regulation of transcription and differentiation in human pluripotent stem cells. Development. 2013;141:219-23.
-
(2013)
Development
, vol.141
, pp. 219-223
-
-
Kearns, N.A.1
Genga, R.M.2
Enuameh, M.S.3
Garber, M.4
Wolfe, S.A.5
Maehr, R.6
-
95
-
-
84920992414
-
Engineering complex synthetic transcriptional programs with CRISPR RNA scaffolds
-
Zalatan JG, Lee ME, Almeida R, Gilbert LA, Whitehead EH, La Russa M, et al. Engineering complex synthetic transcriptional programs with CRISPR RNA scaffolds. Cell. 2015;160:339-50.
-
(2015)
Cell
, vol.160
, pp. 339-350
-
-
Zalatan, J.G.1
Lee, M.E.2
Almeida, R.3
Gilbert, L.A.4
Whitehead, E.H.5
Russa, M.6
-
96
-
-
84923096541
-
Genome-scale transcriptional activation by an engineered CRISPR-Cas9 complex
-
Konermann S, Brigham MD, Trevino AE, Joung J, Abudayyeh OO, Barcena C, et al. Genome-scale transcriptional activation by an engineered CRISPR-Cas9 complex. Nature. 2015;517:583-8.
-
(2015)
Nature
, vol.517
, pp. 583-588
-
-
Konermann, S.1
Brigham, M.D.2
Trevino, A.E.3
Joung, J.4
Abudayyeh, O.O.5
Barcena, C.6
|