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Volumn 11, Issue 3, 2016, Pages

Homology directed knockin of point mutations in the zebrafish tardbp and fus genes in ALS using the CRISPR/Cas9 system

Author keywords

[No Author keywords available]

Indexed keywords

CASPASE 9; CRISPR ASSOCIATED PROTEIN; FUSED IN SARCOMA PROTEIN; DNA BINDING PROTEIN; OLIGODEOXYRIBONUCLEOTIDE; RNA BINDING PROTEIN FUS; SINGLE STRANDED DNA; TARDBP PROTEIN, ZEBRAFISH; ZEBRAFISH PROTEIN;

EID: 84960908143     PISSN: None     EISSN: 19326203     Source Type: Journal    
DOI: 10.1371/journal.pone.0150188     Document Type: Article
Times cited : (105)

References (16)
  • 1
    • 42649120983 scopus 로고    scopus 로고
    • TARDBP mutations in individuals with sporadic and familial amyotrophic lateral sclerosis
    • 18372902
    • Kabashi E, Valdmanis PN, Dion P, Spiegelman D, McConkey BJ, et al. (2008) TARDBP mutations in individuals with sporadic and familial amyotrophic lateral sclerosis. Nat Genet 40: 572-574. doi: 10.1038/ng.132 PMID: 18372902
    • (2008) Nat Genet , vol.40 , pp. 572-574
    • Kabashi, E.1    Valdmanis, P.N.2    Dion, P.3    Spiegelman, D.4    McConkey, B.J.5
  • 2
    • 41149180753 scopus 로고    scopus 로고
    • TDP-43 mutations in familial and sporadic amyotrophic lateral sclerosis
    • 18309045
    • Sreedharan J, Blair IP, Tripathi VB, Hu X, Vance C, et al. (2008) TDP-43 Mutations in Familial and Sporadic Amyotrophic Lateral Sclerosis. Science 319: 1668-1672. doi: 10.1126/science.1154584 PMID: 18309045
    • (2008) Science , vol.319 , pp. 1668-1672
    • Sreedharan, J.1    Blair, I.P.2    Tripathi, V.B.3    Hu, X.4    Vance, C.5
  • 3
    • 61349162349 scopus 로고    scopus 로고
    • Mutations in FUS, an RNA Processing Protein, Cause Familial Amyotrophic Lateral Sclerosis Type 6
    • 19251628
    • Vance C, Rogelj B, Hortobágyi T, De Vos KJ, Nishimura AL, et al. (2009) Mutations in FUS, an RNA Processing Protein, Cause Familial Amyotrophic Lateral Sclerosis Type 6. Science 323: 1208-1211. doi: 10.1126/science.1165942 PMID: 19251628
    • (2009) Science , vol.323 , pp. 1208-1211
    • Vance, C.1    Rogelj, B.2    Hortobágyi, T.3    De Vos, K.J.4    Nishimura, A.L.5
  • 4
    • 61349156118 scopus 로고    scopus 로고
    • Mutations in the FUS/TLS gene on chromosome 16 cause familial amyotrophic lateral sclerosis
    • 19251627
    • Kwiatkowski TJ, Bosco DA, LeClerc AL, Tamrazian E, Vanderburg CR, et al. (2009) Mutations in the FUS/TLS Gene on Chromosome 16 Cause Familial Amyotrophic Lateral Sclerosis. Science 323: 1205-1208. doi: 10.1126/science.1166066 PMID: 19251627
    • (2009) Science , vol.323 , pp. 1205-1208
    • Kwiatkowski, T.J.1    Bosco, D.A.2    LeClerc, A.L.3    Tamrazian, E.4    Vanderburg, C.R.5
  • 5
    • 84155171976 scopus 로고    scopus 로고
    • Understanding the role of TDP-43 and FUS/TLS in ALS and beyond
    • 21813273
    • Da Cruz S, Cleveland DW (2011) Understanding the role of TDP-43 and FUS/TLS in ALS and beyond. Current Opinion in Neurobiology 21: 904-919. doi: 10.1016/j.conb.2011.05.029 PMID: 21813273
    • (2011) Current Opinion in Neurobiology , vol.21 , pp. 904-919
    • Da Cruz, S.1    Cleveland, D.W.2
  • 6
    • 77950360176 scopus 로고    scopus 로고
    • Gain and loss of function of ALSrelated mutations of TARDBP (TDP-43) cause motor deficits in vivo
    • 19959528
    • Kabashi E, Lin L, Tradewell ML, Dion PA, Bercier V, et al. (2010) Gain and loss of function of ALSrelated mutations of TARDBP (TDP-43) cause motor deficits in vivo. Human Molecular Genetics 19: 671-683. doi: 10.1093/hmg/ddp534 PMID: 19959528
    • (2010) Human Molecular Genetics , vol.19 , pp. 671-683
    • Kabashi, E.1    Lin, L.2    Tradewell, M.L.3    Dion, P.A.4    Bercier, V.5
  • 7
    • 80052374038 scopus 로고    scopus 로고
    • FUS and TARDBP but not SOD1 interact in genetic models of amyotrophic lateral sclerosis
    • 21829392
    • Kabashi E, Bercier V, Lissouba A, Liao M, Brustein E, et al. (2011) FUS and TARDBP but not SOD1 interact in genetic models of amyotrophic lateral sclerosis. PLoS Genet 7: e1002214. doi: 10.1371/ journal.pgen.1002214 PMID: 21829392
    • (2011) PLoS Genet , vol.7
    • Kabashi, E.1    Bercier, V.2    Lissouba, A.3    Liao, M.4    Brustein, E.5
  • 8
    • 84875508368 scopus 로고    scopus 로고
    • Loss of ALS-associated TDP-43 in zebrafish causes muscle degeneration, vascular dysfunction, and reduced motor neuron axon outgrowth
    • Schmid B, Hruscha A, Hogl S, Banzhaf-Strathmann J, Strecker K, et al. (2013) Loss of ALS-associated TDP-43 in zebrafish causes muscle degeneration, vascular dysfunction, and reduced motor neuron axon outgrowth. Proceedings of the National Academy of Sciences 110: 4986-4991.
    • (2013) Proceedings of the National Academy of Sciences , vol.110 , pp. 4986-4991
    • Schmid, B.1    Hruscha, A.2    Hogl, S.3    Banzhaf-Strathmann, J.4    Strecker, K.5
  • 9
    • 84878511239 scopus 로고    scopus 로고
    • Tardbpl splicing rescues motor neuron and axonal development in a mutant tardbp zebrafish
    • 23427147
    • Hewamadduma CAA, Grierson AJ, Ma TP, Pan L, Moens CB, et al. (2013) Tardbpl splicing rescues motor neuron and axonal development in a mutant tardbp zebrafish. Human Molecular Genetics 22: 2376-2386. doi: 10.1093/hmg/ddt082 PMID: 23427147
    • (2013) Human Molecular Genetics , vol.22 , pp. 2376-2386
    • Hewamadduma, C.A.A.1    Grierson, A.J.2    Ma, T.P.3    Pan, L.4    Moens, C.B.5
  • 10
    • 84868342049 scopus 로고    scopus 로고
    • In vivo genome editing using a high-efficiency TALEN system
    • 23000899
    • Bedell VM, Wang Y, Campbell JM, Poshusta TL, Starker CG, et al. (2012) In vivo genome editing using a high-efficiency TALEN system. Nature 491: 114-118. doi: 10.1038/nature11537 PMID: 23000899
    • (2012) Nature , vol.491 , pp. 114-118
    • Bedell, V.M.1    Wang, Y.2    Campbell, J.M.3    Poshusta, T.L.4    Starker, C.G.5
  • 12
    • 84893762088 scopus 로고    scopus 로고
    • Oligonucleotide-based targeted gene editing in C. Elegans via the CRISPR/Cas9 system
    • 24418757
    • Zhao P, Zhang Z, Ke H, Yue Y, Xue D (2014) Oligonucleotide-based targeted gene editing in C. elegans via the CRISPR/Cas9 system. Cell Res 24: 247-250. doi: 10.1038/cr.2014.9 PMID: 24418757
    • (2014) Cell Res , vol.24 , pp. 247-250
    • Zhao, P.1    Zhang, Z.2    Ke, H.3    Yue, Y.4    Xue, D.5
  • 13
    • 84904654756 scopus 로고    scopus 로고
    • Optimized CRISPR/Cas tools for efficient germline and somatic genome engineering in Drosophila
    • Port F, Chen H-M, Lee T, Bullock SL (2014) Optimized CRISPR/Cas tools for efficient germline and somatic genome engineering in Drosophila. Proceedings of the National Academy of Sciences 111: E2967-E2976.
    • (2014) Proceedings of the National Academy of Sciences , vol.111 , pp. E2967-E2976
    • Port, F.1    Chen, H.-M.2    Lee, T.3    Bullock, S.L.4
  • 14
    • 84903185106 scopus 로고    scopus 로고
    • Rapid generation of mouse models with defined point mutations by the CRISPR/Cas9 system
    • Inui M, Miyado M, Igarashi M, Tamano M, Kubo A, et al. (2014) Rapid generation of mouse models with defined point mutations by the CRISPR/Cas9 system. Sci Rep 4.
    • (2014) Sci Rep , pp. 4
    • Inui, M.1    Miyado, M.2    Igarashi, M.3    Tamano, M.4    Kubo, A.5
  • 15
    • 84882788354 scopus 로고    scopus 로고
    • Efficient multiplex biallelic zebrafish genome editing using a CRISPR nuclease system
    • Jao L-E, Wente SR, ChenW(2013) Efficient multiplex biallelic zebrafish genome editing using a CRISPR nuclease system. Proceedings of the National Academy of Sciences 110: 13904-13909.
    • (2013) Proceedings of the National Academy of Sciences , vol.110 , pp. 13904-13909
    • Jao, L.-E.1    Wente, S.R.2    Chen, W.3


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.