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US Patent 9598468 Polypeptides and vectors for targeting HER2/

Patent 9598468 was granted and assigned to University of Florida on March, 2017 by the United States Patent and Trademark Office.

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Patent

Patent attributes

Current Assignee
University of Florida
University of Florida
Patent Jurisdiction
United States Patent and Trademark Office
United States Patent and Trademark Office
Patent Number
9598468
Date of Patent
March 21, 2017
Patent Application Number
14117871
Date Filed
May 18, 2012
Patent Citations Received
‌
US Patent 12123002 Compositions and methods of treating amyotrophic lateral sclerosis (ALS)
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US Patent 12104163 Adeno-associated virus vectors for treatment of Rett syndrome
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US Patent 12116384 Virus vectors for targeting ophthalmic tissues
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US Patent 12116589 Treatment of amyotrophic lateral sclerosis (ALS)
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US Patent 11697825 Compositions and methods for the production of scAAV
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US Patent 11752181 Compositions and methods of treating Huntington's disease
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US Patent 11759506 AADC polynucleotides for the treatment of Parkinson's disease
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US Patent 11905523 Adeno-associated viral vectors for treatment of Niemann-Pick Disease type-C
0
...
Patent Primary Examiner
‌
Nicole Kinsey White
Patent abstract

Various aspects of the invention provide for capsids, parvovirus capsids, hybrid parvovirus capsids, parvovirus vectors, hybrid parvovirus vectors, hybrid parvovirus particles and parvovirus particles containing polypeptides in which the sequence YCDGFYACYMDV (SEQ ID NO: 3) has been substituted into the VP2 loop of the B19 capsid protein. Polypeptides in which the sequence YCDGFYACYMDV (SEQ ID NO: 3) has been substituted into the VP2 loop of the B19 capsid protein are also provided (e.g., SEQ ID NO: 2). Other aspects of the invention provides capsids, parvovirus capsids, hybrid parvovirus capsids, parvovirus vectors, hybrid parvovirus vectors, hybrid parvovirus particles and parvovirus particles containing a polypeptide comprising SEQ ID NO: 2. Also provided in various aspects of the invention a pharmaceutical compositions and methods of delivering therapeutic agents and/or reporter peptides/proteins to target cells. Finally, methods of treating diseases characterized by cells expressing HER2/neu receptors are also provided.

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