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Læknaneminn - 01.04.2016, Qupperneq 38

Læknaneminn - 01.04.2016, Qupperneq 38
Ri trý nt e fn i 38 Heimildaskrá 1. Doudna J. Genome-editing revolution: My whirlwind year with CRISPR. Nature 2015;528:469-71. 2. Fisher T. Centre 0246 (The Francis Crick Institute at Mill Hill) – application for research licence renewal for research project R0162. In: authority Hfe, ed. 14. January 20162016. 3. Ishino Y, Shinagawa H, Makino K, Amemura M, Nakata A. Nucleotide sequence of the iap gene, responsible for alkaline phosphatase isozyme conversion in Escherichia coli, and identification of the gene product. Journal of Bacteriology 1987;169:5429-33. 4. Mojica FJ, Ferrer C, Juez G, Rodriguez- Valera F. Long stretches of short tandem repeats are present in the largest replicons of the Archaea Haloferax mediterranei and Haloferax volcanii and could be involved in replicon partitioning. Molecular microbiology 1995;17:85-93. 5. Mojica FJ, Diez-Villasenor C, Soria E, Juez G. Biological significance of a family of regularly spaced repeats in the genomes of Archaea, Bacteria and mitochondria. Molecular microbiology 2000;36:244-6. 6. Jansen R, Embden JD, Gaastra W, Schouls LM. Identification of genes that are associated with DNA repeats in prokaryotes. Molecular microbiology 2002;43:1565-75. 7. Tang TH, Bachellerie JP, Rozhdestvensky T, et al. Identification of 86 candidates for small non-messenger RNAs from the archaeon Archaeoglobus fulgidus. Proceedings of the National Academy of Sciences of the United States of America 2002;99:7536-41. 8. Bolotin A, Quinquis B, Sorokin A, Ehrlich SD. Clustered regularly interspaced short palindrome repeats (CRISPRs) have spacers of extrachromosomal origin. Microbiology (Reading, England) 2005;151:2551-61. 9. Mojica FJ, Diez-Villasenor C, Garcia- Martinez J, Soria E. Intervening sequences of regularly spaced prokaryotic repeats derive from foreign genetic elements. Journal of molecular evolution 2005;60:174-82. 10. Barrangou R, Fremaux C, Deveau H, et al. CRISPR provides acquired resistance against viruses in prokaryotes. Science (New York, NY) 2007;315:1709-12. 11. Deltcheva E, Chylinski K, Sharma CM, et al. CRISPR RNA maturation by trans-encoded small RNA and host factor RNase III. Nature 2011;471:602-7. 12. Nunez JK, Lee AS, Engelman A, Doudna JA. Integrase-mediated spacer acquisition during CRISPR-Cas adaptive immunity. Nature 2015;519:193-8. 13. Jinek M, Chylinski K, Fonfara I, Hauer M, Doudna JA, Charpentier E. A programmable dual-RNA-guided DNA endonuclease in adaptive bacterial immunity. Science (New York, NY) 2012;337:816-21. 14. Jinek M, East A, Cheng A, Lin S, Ma E, Doudna J. RNA-programmed genome editing in human cells. eLife 2013;2:e00471. 15. Shen B, Zhang W, Zhang J, et al. Efficient genome modification by CRISPR-Cas9 nickase with minimal off-target effects. Nature methods 2014;11:399-402. 16. Cong L, Ran FA, Cox D, et al. Multiplex Genome Engineering Using CRISPR/ Cas Systems. Science (New York, NY) 2013;339:819-23. 17. Guirouilh-Barbat J, Huck S, Bertrand P, et al. Impact of the KU80 pathway on NHEJ-induced genome rearrangements in mammalian cells. Molecular cell 2004;14:611-23. 18. Weterings E, Chen DJ. The endless tale of non-homologous end-joining. Cell research 2008;18:114-24. 19. Fu Y, Foden JA, Khayter C, et al. High- frequency off-target mutagenesis induced by CRISPR-Cas nucleases in human cells. Nature biotechnology 2013;31:822-6. 20. Veres A, Gosis BS, Ding Q, et al. 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 2014;15:27-30. 21. Kleinstiver BP, Pattanayak V, Prew MS, et al. High-fidelity CRISPR–Cas9 nucleases with no detectable genome-wide off-target effects. Nature 2016;529:490-5. 22. Baltimore D, Berg P, Botchan M, et al. Biotechnology. A prudent path forward for genomic engineering and germline gene modification. Science (New York, NY) 2015;348:36-8. 23. Niu Y, Shen B, Cui Y, et al. Generation of gene-modified cynomolgus monkey via Cas9/ RNA-mediated gene targeting in one-cell embryos. Cell 2014;156:836-43. 24. Lög um tæknifrjóvgun og notkun kynfrumna og fósturvísa manna til stofnfrumurannsókna. In: Alþingi, ed.: Skrifstofa Alþingis; 2008. 25. Liang P, Xu Y, Zhang X, et al. CRISPR/ Cas9-mediated gene editing in human tripronuclear zygotes. Protein & Cell 2015;6:363-72. 26. Dahdouh EM, Balayla J, Audibert F, et al. Technical Update: Preimplantation Genetic Diagnosis and Screening. Journal of obstetrics and gynaecology Canada : JOGC = Journal d’obstetrique et gynecologie du Canada : JOGC 2015;37:451-63. 27. Brian R. Walker NRC, Stuart H. Ralston, Ian D. Penman. Davidson’s Principles and Practice of Medicine: Elsevier; 2014. 28. Kaiser J. CRISPR helps heal mice with muscular dystrophy. Science (New York, NY) 2015. 29. Kennedy EM, Kornepati AV, Cullen BR. Targeting hepatitis B virus cccDNA using CRISPR/Cas9. Antiviral research 2015;123:188-92. 30. Han AP. UMass Scientists Lead Effort to Excise Latent HIV With CRISPR/Cas9. Genomeweb 2015. 31. Jing W, Zhang X, Sun W, Hou X, Yao Z, Zhu Y. CRISPR/CAS9-Mediated Genome Editing of miRNA-155 Inhibits Proinflammatory Cytokine Production by RAW264.7 Cells. BioMed research international 2015;2015:326042. 32. Nafissi N, Foldvari M. Neuroprotective therapies in glaucoma: II. Genetic nanotechnology tools. Frontiers in neuroscience 2015;9:355. 33. Wold WSM, Toth K. Adenovirus Vectors for Gene Therapy, Vaccination and Cancer Gene Therapy. Current gene therapy 2013;13:421- 33. Glæsibæ | Álfheimum 74 | 104 Reykjavík | Þjónusta á landsbyggðinni | Sími 568 6880 Heyrnarmælingar Fagleg ráðgjöf - Vönduð heyrnartæki
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