US 7078387B1
· Leiden et al.
· 2006
[cited by applicant]
US 20220333172A1
· Cheng et al.
· 2022
[cited by applicant]
WO 1993003769A1
· 1993
[cited by applicant]
WO 1993009239A1
· 1993
[cited by applicant]
WO 1993019191A1
· 1993
[cited by applicant]
WO 1994012649A2
· 1994
[cited by applicant]
WO 1994028938A1
· 1995
[cited by applicant]
WO 1995000655A1
· 1995
[cited by applicant]
WO 1995011984A2
· 1995
[cited by applicant]
WO 2011160052A2
· 2011
[cited by applicant]
WO 2013176772A1
· 2013
[cited by applicant]
WO 2016148994A1
· 2016
[cited by applicant]
Cheng et al., Casilio: a versatile CRISPR-Cas9-Pumilio hybrid for gene regulation and genomic labeling. Cell Research (2016), 26: 254-257 (Year: 2016).
[cited by examiner]
Yi and Verhaak, Abstract 2564: Tracing extrachromosomal DNA inheritance patterns in glioblastoma using CRISPR. Cancer Res (2019) 79 (13_Supplement): 2564 (Year: 2019).
[cited by examiner]
DeCarvalho et al., Discordant inheritance of chromosomal and extrachromosomal DNA elements contributes to dynamic disease evolution in glioblastoma. Nat Genet. (2018) 50(5): 708-717 (Year: 2018).
[cited by examiner]
Chen et al., Dynamic Imaging of Genomic Loci in Living Human Cells by an Optimized CRISPR/Cas System. Cell (2013), 155: 1479-1491 (Year: 2013).
[cited by examiner]
Qin et al., Live cell imaging of low- and non-repetitive chromosome loci using CRISPR-Cas9. Nature Communications (2017), 8: 14725 (Year: 2017).
[cited by examiner]
Ma et al., CRISPR-Sirius: RNA scaffolds for signal amplification in genome imaging. Nature Methods (2018), 15: 928-931 (Year: 2018).
[cited by examiner]
Mao et al., CRISPR/dual-FRET molecular beacon for sensitive live-cell imaging of non-repetitive genomic loci. Nucleic Acids Research (2019), 47(20), e131 (Year: 2019).
[cited by examiner]
Verhaak et al., Extrachromosomal oncogene amplification in tumour pathogenesis and evolution. Nature Reviews (2019), 19: 283-288 (Year: 2019).
[cited by examiner]
Kanda et al., Histone-GFP fusion protein enables sensitive analysis of chromosome dynamics in living mammalian cells. Current Biology (1998), 8: 377-385 (Year: 1998).
[cited by examiner]
Kanda et al., Mitotic segregation of viral and cellular acentric extrachromosomal molecules by chromosome tethering. Journal of Cell Science (2000), 114: 49-58 (Year: 2000).
[cited by examiner]
Maass et al., Spatiotemporal allele organization by allele-specific CRISPR live-cell imaging (SNP-CLING). Nature Structural and Molecular Biology (2018), 25: 176-184 (Year: 2018).
[cited by examiner]
Cheong and Hall, Engineering RNA sequence specificityof Pumilio repeats. PNAS (2006), 103: 13635-13639 (Year: 2006).
[cited by examiner]
Wu et al., Progress and challenges for live-cell imaging of genomic loci using CRISPR-based platforms. Genomics Proteomics Bioinformatics (2019), 17: 119-128 (Year: 2019).
[cited by examiner]
Chaudhary et al., Visualizing live chromatin dynamics through CRISPR-based imaging techniques. Molecules and Cells (2021), 44: 627-636 (Year: 2021).
[cited by examiner]
Cheng et al., Casilio: a versatile CRISPR-Cas9-Pumilio hybrid for gene regulation and genomic labeling. Cell Res. Feb. 2016;26(2):254-7. doi: 10.1038/cr.2016.3. Epub Jan. 15, 2016.
[cited by applicant]
Filipovska et al., A universal code for RNA recognition by PUF proteins. Nat Chem Biol. May 15, 2011;7(7):425-7. doi: 10.1038/nchembio.577.
[cited by applicant]
National Human Genome Research Institute, “Telomere”, updated Jun. 7, 2023, https://www.genome.gov/genetics-glossary/Telomere#:˜:text=A%20telomere%20is%20a%20region,successfully%2C%20and%20the%20cell%20dies, accessed Ju…
[cited by applicant]
National Human Genome Research Institute, “Centromere”, updated Jun. 7, 2023, https://www.genome.gov/genetics-glossary/Centromere, accessed Jun. 12, 2023.
[cited by applicant]
Abil et al. “Modular assembly of designer PUF proteins for specific post-transcriptional regulation of endogenous RNA”. Journal of Biological Engineering 8:7, (2014).
[cited by applicant]
Ali et al. “Gene transfer into the mouse retina mediated by an adeno-associated viral vector”. Hum Mol Genet. May 1996;5(5):591-4.
[cited by applicant]
Ali et al. “Adeno-associated virus gene transfer to mouse retina”. Hum Gene Ther. 1998;9:81-86.
[cited by applicant]
Bennett et al. “Real-time, noninvasive in vivo assessment of Adeno-asoociated virus-mediated retinal transduction”. Invest Ophthalmol Vis Sci. 1997;38:2857-2863.
[cited by applicant]
Bitter et al. “Expression and secretion vectors for yeast”. Methods Enzymol. 1987;153:516-44.
[cited by applicant]
Boch et al. “Xanthomonas AvrBs3 Family-Type III Effectors: Discovery and Function”. Annual Review of Phytopathology 48: 419-36, (2010).
[cited by applicant]
Boch. “TALEs of genome targeting”. Nat Biotechnol. 29(2): 135-136, (Feb. 2011).
[cited by applicant]
Borras et al. “Adenoviral reporter gene transfer to the human trabecular meshwork does not alter aqueous humor butflow. Relevance for potential gene therapy of glaucoma”. Gene Ther. 6(4):515-24, (Apr. 1999).
[cited by applicant]
Cermak et al. “Efficient design and assembly of custom TALEN and other TAL effector-based constructs for DNA targeting”. Nucleic Acids Res. 39(12): e82, (Apr. 2011).
[cited by applicant]
Cheng et al. “CRISPR-mediated multiplexed live cell imaging of non-repetitive genomic loci with one guide RNA per locus”. Nature 13(1):1871, (2022).
[cited by applicant]
Christian et al. “Targeting DNA double-strand breaks with TAL effector nucleases”. Genetics 186(2): 757-761, (Jul. 2010).
[cited by applicant]
Flannery et al. “Efficient photoreceptor-targeted gene expression in vivo by recombinant adeno-associated virus”. Proc Natl Acad Sci U S A. Jun. 24, 1997;94(13):6916-21.
[cited by applicant]
Flotte et al. “Stable in vivo expression of the cystic fibrosis transmembrane conductance regulator with an adeno-associated virus vector”. Proc Natl Acad Sci U S A. Nov. 15, 1993;90(22):10613-7.
[cited by applicant]
Gabsalilow et al. “Site- and strand-specific nicking of DNA by fusion proteins derived from MutH and I-Scel or TALE repeats”. Nucleic Acids Res. 41(7): e83, (Feb. 2013).
[cited by applicant]
Harrington et al. “Programmed DNA destruction by miniature CRISPR-Cas14 enzymes”. Science 362(6416): 839-842, (Oct. 2018).
[cited by applicant]
Jomary et al. “Rescue of photoreceptor function by AAV-mediated gene transfer in a mouse model of inherited retinal degeneration”. Gene Ther. Jul. 1997;4(7):683-90.
[cited by applicant]
Juillerat et al. “Optimized tuning of TALEN specificity using non-conventional RVDs”. Sci Rep. 5: 8150, (Jan. 2015).
[cited by applicant]
Kim et al. “Hybrid restriction enzymes: zinc finger fusions to Fok I cleavage domain”. Proc Natl Acad Sci U S A. Feb. 6, 1996; 93(3): 1156-1160.
[cited by applicant]
Li et al. “In vivo transfer of a reporter gene to the retina mediated by an adenoviral vector”. Invest Ophthalmol Vis Sci. 35(5): 2543-9, (Apr. 1994).
[cited by applicant]
Li et al. “Phenotype correction in retinal pigment epithelium in murine mucopolysaccharidosis VII by adenovirus-mediated gene transfer”. Proc Natl Acad Sci U S A. Aug. 15, 1995; 92(17): 7700-7704.
[cited by applicant]
Mendelson et al. “Expression and rescue of a nonselected marker from an integrated AAV vector”. Virology. Sep. 1988;166(1):154-65.
[cited by applicant]
Miyoshi et al. “Stable and efficient gene transfer into the retina using an HIV-based lentiviral vector”. Proc Natl Acad Sci U S A. Sep. 16, 1997;94(19):10319-23.
[cited by applicant]
Moscou et al. “A simple cipher governs DNA recognition by TAL effectors”. Science 326 (5959): 1501, (Dec. 2009).
[cited by applicant]
Panyam et al. “Biodegradable nanoparticles for drug and gene delivery to cells and tissue”. Adv Drug Deliv Rev. 55(3): 329-347, (Feb. 2003).
[cited by applicant]
Ramirez et al. “Engineered zinc finger nickases induce homology-directed repair with reduced mutagenic effects”. Nucleic Acids Research 40(12): 5560-5568, (Feb. 2012).
[cited by applicant]
Rolling et al. “Evaluation of adeno-associated virus-mediated gene transfer into the rat retina by clinical fluorescence photography”. Hum. Gene Ther. 1999, 10: 641-648.
[cited by applicant]
Sakamoto et al. “A vitrectomy improves the transfection efficiency of adenoviral vector-mediated gene transfer to Müller cells”. Gene Ther. Aug. 1998;5(8):1088-97.
[cited by applicant]
Samulski et al. “Helper-free stocks of recombinant adeno-associated viruses: normal integration does not require viral gene expression”. J Virol. Sep. 1989;63(9):3822-8.
[cited by applicant]
Takahashi et al. “Rescue from Photoreceptor Degeneration in therd Mouse by Human Immunodeficiency Virus Vector-Mediated Gene Transfer”. J Virol. Sep. 1999;73(9):7812-6.
[cited by applicant]
Tam et al. “The Puf family of RNA-binding proteins in plants: phylogeny, structural modeling, activity and subcellular localization”. BMC Plant Biology 10: 44, (2010).
[cited by applicant]
Turner et al. “Extrachromosomal oncogene amplification drives tumour evolution and genetic heterogeneity”. Nature 543(7643): 122-135, (Mar. 2017).
[cited by applicant]
Lower et al. “Special Issue: Repetitive DNA Sequences”. Genes (Basel) 10(11):896, (2019).
[cited by applicant]
Qin et al. “Live cell imaging of low- and non-repetitive chromosome loci using CRISPR-Cas9”, Nature Communications 8: 14725, (2017).
[cited by applicant]
Pedelacq et al., “Engineering and characterization of a superfolder green fluorescent protein”, Nat. Biotechnol. 24: 79-88, 2005.
[cited by applicant]