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US Patent 8936910 Method for selective oligonucleotide modification

Patent 8936910 was granted and assigned to Antisense Pharma on January, 2015 by the United States Patent and Trademark Office.

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Patent abstractTimelineTable: Further ResourcesReferences
Is a
Patent
Patent
1

Patent attributes

Current Assignee
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Antisense Pharma
1
Patent Jurisdiction
United States Patent and Trademark Office
United States Patent and Trademark Office
1
Patent Number
89369101
Patent Inventor Names
Bernd Betzler1
Andreas Mitsch1
Anneliese Schneider1
Frank Jaschinski1
Karl-Hermann Schlingensiepen1
Date of Patent
January 20, 2015
1
Patent Application Number
137032601
Date Filed
June 10, 2011
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Patent Citations Received
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US Patent 12104156 Compositions and methods of treating facioscapulohumeral muscular dystrophy
2
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US Patent 12071621 Anti-transferrin receptor antibody-PMO conjugates for inducing DMD exon 44 skipping
3
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US Patent 11707532 Compositions and methods of treating muscle dystrophy
4
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US Patent 11712478 Compositions and methods of treating muscle atrophy and myotonic dystrophy
5
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US Patent 12071485 Compositions and methods of treating facioscapulohumeral muscular dystrophy
6
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US Patent 11834510 Anti-transferrin receptor antibodies and uses thereof
7
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US Patent 11912779 Compositions and methods of treating facioscapulohumeral muscular dystrophy
8
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US Patent 11872287 Compositions and methods of treating muscle atrophy and myotonic dystrophy
9
...
Patent Primary Examiner
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Jezia Riley
1
Patent abstract

Method for producing a modified oligonucleotide, wherein at least one polymer, preferably polyalkylene oxide, and/or a compound is covalently bound to the 5′-end or the 3′-end of the oligonucleotide via native ligation forming a native ligation site, with the proviso that the polymer and/or the compound is not a protein or peptide, if only the 5′-end of the oligonucleotide is modified by binding of the polymer or compound via native ligation. The invention is further directed to a modified oligonucleotide obtainable by the inventive method as well as the use of such modified oligonucleotide for the preparation of a medicament for preventing and/or treating a tumor, formation of metastasis, an immune disease or disorder, a cardiovascular disease or disorder, and/or a viral disease or disorder.

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