US 5399363A
· Liversidge et al.
· 1995
[cited by applicant]
US 5543158A
· Gref et al.
· 1996
[cited by applicant]
US 5552157A
· Yagi et al.
· 1996
[cited by applicant]
US 5565213A
· Nakamori et al.
· 1996
[cited by applicant]
US 5567434A
· Szoka
· 1996
[cited by applicant]
US 5641515A
· Ramtoola et al.
· 1997
[cited by applicant]
US 5656016A
· Ogden
· 1997
[cited by applicant]
US 5697899A
· Hillman et al.
· 1997
[cited by applicant]
US 5738868A
· Shinkarenko
· 1998
[cited by applicant]
US 5741516A
· Webb et al.
· 1998
[cited by applicant]
US 5770219A
· Chiang et al.
· 1998
[cited by applicant]
US 5779708A
· Wu
· 1998
[cited by applicant]
US 5783208A
· Venkateshwaran et al.
· 1998
[cited by applicant]
US 5795587A
· Gao et al.
· 1998
[cited by applicant]
US 5797898A
· Santini et al.
· 1998
[cited by applicant]
US 6177403B1
· Stedman et al.
· 2001
[cited by applicant]
US 20180066279A9
· Gao et al.
· 2018
[cited by applicant]
Xu, Lingfei, et al. “CMV-β-Actin Promoter Directs Higher Expression from an Adeno-Associated Viral Vector in the Liver than the Cytomegalovirus or Elongation Factor 1α Promoter and Results in Therapeutic Levels of Human…
[cited by examiner]
Shen, Xuan, et al. “Characterization of the Relationship of AAV Capsid Domain Swapping to Liver Transduction Efficiency.” Molecular Therapy, vol. 15, No. 11, Nov. 2007, pp. 1955-1962. DOI.org (Crossref), https://doi.org…
[cited by examiner]
McCarty, Douglas M. “Self-Complementary AAV Vectors; Advances and Applications.” Molecular Therapy, vol. 16, No. 10, Oct. 2008, pp. 1648-1656. DOI.org (Crossref), https://doi.org/10.1038/mt.2008.171. (Year: 2008).
[cited by examiner]
Senís, Elena, et al. “CRISPR/Cas9-mediated Genome Engineering: An Adeno-associated Viral (AAV) Vector Toolbox.” Biotechnology Journal, vol. 9, No. 11, Nov. 2014, pp. 1402-1412. DOI.org (Crossref), https://doi.org/10.100…
[cited by examiner]
Abudayyeh, Omar O., et al. “RNA Targeting with CRISPR-Cas13.” Nature, vol. 550, No. 7675, Oct. 2017, pp. 280-284. DOI.org (Crossref), https://doi.org/10.1038/nature24049. (Year: 2017).
[cited by examiner]
Jarrett, Kelsey E., et al. “Somatic Genome Editing with CRISPR/Cas9 Generates and Corrects a Metabolic Disease.” Scientific Reports, vol. 7, No. 1, Mar. 2017, p. 44624. DOI.org (Crossref), https://doi.org/10.1038/srep44…
[cited by examiner]
Petit, Lolita, et al. “Rod Outer Segment Development Influences AAV-Mediated Photoreceptor Transduction After Subretinal Injection.” Human Gene Therapy, vol. 28, No. 6, Jun. 2017, pp. 464-481. DOI.org (Crossref), https:…
[cited by examiner]
Mendell, Jerry R., et al. “Single-Dose Gene-Replacement Therapy for Spinal Muscular Atrophy.” New England Journal of Medicine, vol. 377, No. 18, Nov. 2017, pp. 1713-1722. DOI.org (Crossref), https://doi.org/10.1056/NEJM…
[cited by examiner]
Cao, Jian, et al. “The Multiplexed CRISPR Targeting Platforms.” Drug Discovery Today: Technologies, vol. 28, Aug. 2018, pp. 53-61. DOI.org (Crossref), https://doi.org/10.1016/j.ddtec.2018.01.001. (Year: 2018).
[cited by examiner]
Schindele, Patrick, et al. “Transforming Plant Biology and Breeding with CRISPR /Cas9, Cas12 and Cas13.” FEBS Letters, vol. 592 , No. 12, Jun. 2018, pp. 1954-1967. DOI.org (Crossref), https://doi.org/10.1002/1873-3468.1…
[cited by examiner]
Liu, Wenyi, et al. “Applications and Challenges of CRISPR-Cas Gene-Editing to Disease Treatment in Clinics.” Precision Clinical Medicine, vol. 4, No. 3, Sep. 2021, pp. 179-191. DOI.org (Crossref), https://doi.org/10.109…
[cited by examiner]
International Search Report and Written Opinion for Application No. PCT/US2020/027774, mailed Jul. 21, 2020.
[cited by applicant]
International Preliminary Report on Patentability for Application No. PCT/US2020/027774, mailed Oct. 21, 2021.
[cited by applicant]
Bourlais et al., Ophthalmic drug delivery systems—recent advances. Prog Retin Eye Res. Jan. 1998;17(1):33-58. doi: 10.1016/s1350-9462(97)00002-5.
[cited by applicant]
Gossen et al., Tight control of gene expression in mammalian cells by tetracycline-responsive promoters. Proc Natl Acad Sci U S A. Jun. 15, 1992;89(12):5547-51. doi: 10.1073/pnas.89.12.5547.
[cited by applicant]
Hansal et al.,. Cutting Edge: Induction of antigen-specific hyporesponsiveness by transplantation of hemopoietic cells containing an MHC class I transgene regulated by a lymphocyte-specific promoter. J Immunol. Aug. 1, …
[cited by applicant]
Harvey et al., Inducible control of gene expression: prospects for gene therapy. Curr Opin Chem Biol. Aug. 1998;2(4):512-8. doi: 10.1016/s1367-5931(98)80128-2.
[cited by applicant]
Konermann et al., Transcriptome Engineering with RNA-Targeting Type VI-D CRISPR Effectors. Cell. Apr. 19, 2018;173(3):665-676.e14. Suppl. Info. 7pages. doi: 10.1016/j.cell.2018.02.033. Epub Mar. 15, 2018.
[cited by applicant]
Magari et al., Pharmacologic control of a humanized gene therapy system implanted into nude mice. J Clin Invest. Dec. 1, 1997;100(11):2865-72. doi: 10.1172/JCI119835.
[cited by applicant]
No et al., Ecdysone-inducible gene expression in mammalian cells and transgenic mice. Proc Natl Acad Sci U S A. Apr. 16, 1996;93(8):3346-51. doi: 10.1073/pnas.93.8.3346.
[cited by applicant]
Piccioli et al., Neuroantibodies: ectopic expression of a recombinant anti-substance P antibody in the central nervous system of transgenic mice. Neuron. Aug. 1995;15(2):373-84. doi: 10.1016/0896-6273(95)90041-1.
[cited by applicant]
Piccioli et al., Neuroantibodies: molecular cloning of a monoclonal antibody against substance P for expression in the central nervous system. Proc Natl Acad Sci U S A. Jul. 1, 1991;88(13):5611-5. doi: 10.1073/pnas.88.1…
[cited by applicant]
Wang et al., Ligand-inducible and liver-specific target gene expression in transgenic mice. Nat Biotechnol. Mar. 1997;15(3):239-43. doi: 10.1038/nbt0397-239.
[cited by applicant]
Wang et al., Positive and negative regulation of gene expression in eukaryotic cells with an inducible transcriptional regulator. Gene Ther. May 1997;4(5):432-41. doi: 10.1038/sj.gt.3300402.
[cited by applicant]
Yoon et al., Streamlined ex vivo and in vivo genome editing in mouse embryos using recombinant adeno-associated viruses. Nat Commun. Jan. 29, 2018;9(1):412. Suppl. Info. 20 pages. doi: 10.1038/s41467-017-02706-7.
[cited by applicant]
Extended European Search Report for Application No. 20788338.0, mailed Jun. 1, 2023.
[cited by applicant]
Chadwick et al., Reduced Blood Lipid Levels With In Vivo CRISPR-Cas9 Base Editing of ANGPTL3. Circulation. Feb. 27, 2018;137(9):975-977. doi: 10.1161/CIRCULATIONAHA.117.031335.
[cited by applicant]
Fitzgerald et al., A Highly Durable RNAi Therapeutic Inhibitor of PCSK9. N Engl J Med. May 4, 2017;376(18):e38. doi: 10.1056/NEJMc1703361.
[cited by applicant]
Granados-Riveron et al., CRISPR-Cas13 Precision Transcriptome Engineering in Cancer. Cancer Res. Aug. 1, 2018;78(15):4107-4113. doi: 10.1158/0008-5472.CAN-18-0785. Epub Jul. 18, 2018.
[cited by applicant]
Jarrett et al., Somatic genome editing with CRISPR/Cas9 generates and corrects a metabolic disease. Sci Rep. Mar. 16, 2017:7:44624. doi: 10.1038/srep44624.
[cited by applicant]
Koornneef et al., Apolipoprotein B knockdown by AAV-delivered shRNA lowers plasma cholesterol in mice. Mol Ther. Apr. 2011;19(4):731-40. doi: 10.1038/mt.2011.6. Epub Feb. 8, 2011.
[cited by applicant]
Thakore et al., RNA-guided transcriptional silencing in vivo with S. aureus CRISPR-Cas9 repressors. Nat Commun. Apr. 26, 2018;9(1):1674. doi: 10.1038/s41467-018-04048-4.
[cited by applicant]
Wang et al., Meganuclease targeting of PCSK9 in macaque liver leads to stable reduction in serum cholesterol. Nat Biotechnol. Sep. 2018;36(8):717-725. doi: 10.1038/nbt.4182. Epub Jul. 9, 2018.
[cited by applicant]
Zhou et al., Deletion of the B-B' and C-C' regions of inverted terminal repeats reduces rAAV productivity but increases transgene expression. Sci Rep. Jul. 14, 2017;7(1):5432. doi: 10.1038/s41598-017-04054-4.
[cited by applicant]