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US Patent 11542496 Cytosine to guanine base editor

Patent 11542496 was granted and assigned to President and Fellows of Harvard College on January, 2023 by the United States Patent and Trademark Office.

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Is a
Patent
Patent

Patent attributes

Patent Applicant
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President and Fellows of Harvard College
Current Assignee
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President and Fellows of Harvard College
Patent Jurisdiction
United States Patent and Trademark Office
United States Patent and Trademark Office
Patent Number
11542496
Date of Patent
January 3, 2023
Patent Application Number
16492553
Date Filed
March 9, 2018
Patent Citations
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US Patent 10150955 Stabilized reverse transcriptase fusion proteins
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US Patent 10011868 Reactivity-dependent and interaction-dependent PCR
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US Patent 10053725 In situ interaction determination
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US Patent 10059940 Chemically ligated RNAs for CRISPR/Cas9-lgRNA complexes as antiviral therapeutic agents
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US Patent 10077453 CAS9 proteins including ligand-dependent inteins
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US Patent 10113163 Adenosine nucleobase editors and uses thereof
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US Patent 10682410 Delivery system for functional nucleases
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US Patent 10704062 CAS9 proteins including ligand-dependent inteins
...
Patent Citations Received
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US Patent 12133884 Methods of substituting pathogenic amino acids using programmable base editor systems
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US Patent 11912985 Methods and compositions for simultaneous editing of both strands of a target double-stranded nucleotide sequence
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US Patent 11920181 Nuclease profiling system
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US Patent 11932884 High efficiency base editors comprising Gam
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US Patent 11999947 Adenosine nucleobase editors and uses thereof
0
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US Patent 12006520 Evaluation and improvement of nuclease cleavage specificity
0
0
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US Patent 12084663 Incorporation of unnatural amino acids into proteins using base editing
0
Patent Primary Examiner
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Anand U Desai

Some aspects of this disclosure provide compositions, strategies, systems, reagents, methods, and kits that are useful for the targeted editing of nucleic acids, including editing a single site within the genome of a cell or subject, e.g., within the human genome. In some embodiments, fusion proteins capable of inducing a cytosine (C) to guanine (G) change in a nucleic acid (e.g., genomic DNA) are provided. In some embodiments, fusion proteins of a nucleic acid programmable DNA binding protein (e.g., Cas9) and nucleic acid editing proteins or protein domains, e.g., deaminase domains, polymerase domains, and/or base excision enzymes are provided. In some embodiments, methods for targeted nucleic acid editing are provided. In some embodiments, reagents and kits for the generation of targeted nucleic acid editing proteins, e.g., fusion proteins of a nucleic acid programmable DNA binding protein (e.g., Cas9), and nucleic acid editing proteins or domains, are provided.

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