SG10201804974RA - Compositions and Methods of Use of Crispr-Cas Systems in Nucleotide Repeat Disorders - Google Patents
Compositions and Methods of Use of Crispr-Cas Systems in Nucleotide Repeat DisordersInfo
- Publication number
- SG10201804974RA SG10201804974RA SG10201804974RA SG10201804974RA SG10201804974RA SG 10201804974R A SG10201804974R A SG 10201804974RA SG 10201804974R A SG10201804974R A SG 10201804974RA SG 10201804974R A SG10201804974R A SG 10201804974RA SG 10201804974R A SG10201804974R A SG 10201804974RA
- Authority
- SG
- Singapore
- Prior art keywords
- methods
- compositions
- systems
- nucleotide repeat
- crispr
- Prior art date
Links
- 238000000034 method Methods 0.000 title abstract 5
- 239000000203 mixture Substances 0.000 title abstract 3
- 239000002773 nucleotide Substances 0.000 title abstract 2
- 125000003729 nucleotide group Chemical group 0.000 title 1
- 239000013598 vector Substances 0.000 abstract 3
- 108091033409 CRISPR Proteins 0.000 abstract 2
- 238000010354 CRISPR gene editing Methods 0.000 abstract 2
- 230000009918 complex formation Effects 0.000 abstract 1
- 201000010099 disease Diseases 0.000 abstract 1
- 208000037265 diseases, disorders, signs and symptoms Diseases 0.000 abstract 1
- 210000003527 eukaryotic cell Anatomy 0.000 abstract 1
- 238000005457 optimization Methods 0.000 abstract 1
- 210000000056 organ Anatomy 0.000 abstract 1
- 230000001988 toxicity Effects 0.000 abstract 1
- 231100000419 toxicity Toxicity 0.000 abstract 1
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- C12N9/22—Ribonucleases RNAses, DNAses
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Abstract
COMPOSITIONS AND MET HODS OF USE OF CRISP R - CAS SYSTEMS IN NUCLEOTIDE REPEAT DI SORDERS The invention provides for delivery, engineering and optimization of systems, methods, and compositions for manipulation of sequences and/or activities of target 5 sequences. Provided are delivery systems and tissues or organ which are targeted as sites for deliver y . Also provided are vectors and vector systems some of which encode one or more co mponents of a SIN CRISPR complex, as well as methods for the design and use of such vectors. Also provided are methods of directing SIN CRISPR complex formation in eukaryotic cells to ensure enhanced specificity for target recognition and avoidance of toxi city 10 and to edit or modify a target site in a genomic locus of interest to alter or improve the status of a disease or a condition. Figure 1 15
Applications Claiming Priority (3)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US201361915150P | 2013-12-12 | 2013-12-12 | |
US201462010888P | 2014-06-11 | 2014-06-11 | |
US201462010879P | 2014-06-11 | 2014-06-11 |
Publications (1)
Publication Number | Publication Date |
---|---|
SG10201804974RA true SG10201804974RA (en) | 2018-07-30 |
Family
ID=52273577
Family Applications (2)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
SG10201804974RA SG10201804974RA (en) | 2013-12-12 | 2014-12-12 | Compositions and Methods of Use of Crispr-Cas Systems in Nucleotide Repeat Disorders |
SG10201804973TA SG10201804973TA (en) | 2013-12-12 | 2014-12-12 | Compositions and Methods of Use of Crispr-Cas Systems in Nucleotide Repeat Disorders |
Family Applications After (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
SG10201804973TA SG10201804973TA (en) | 2013-12-12 | 2014-12-12 | Compositions and Methods of Use of Crispr-Cas Systems in Nucleotide Repeat Disorders |
Country Status (12)
Country | Link |
---|---|
US (5) | US20160354487A1 (en) |
EP (4) | EP3080257A1 (en) |
JP (2) | JP6625055B2 (en) |
KR (2) | KR20160097331A (en) |
CN (2) | CN106029880A (en) |
AU (2) | AU2014362245A1 (en) |
BR (2) | BR112016013520A2 (en) |
CA (2) | CA2932436A1 (en) |
IL (2) | IL246116B (en) |
MX (2) | MX2016007325A (en) |
SG (2) | SG10201804974RA (en) |
WO (2) | WO2015089354A1 (en) |
Families Citing this family (308)
Publication number | Priority date | Publication date | Assignee | Title |
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WO2013066438A2 (en) | 2011-07-22 | 2013-05-10 | President And Fellows Of Harvard College | Evaluation and improvement of nuclease cleavage specificity |
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EP3434776A1 (en) | 2012-12-12 | 2019-01-30 | The Broad Institute, Inc. | Methods, models, systems, and apparatus for identifying target sequences for cas enzymes or crispr-cas systems for target sequences and conveying results thereof |
JP2016501531A (en) | 2012-12-12 | 2016-01-21 | ザ・ブロード・インスティテュート・インコーポレイテッド | Delivery, engineering and optimization of systems, methods and compositions for sequence manipulation and therapeutic applications |
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CA2915842C (en) | 2013-06-17 | 2022-11-29 | The Broad Institute, Inc. | Delivery and use of the crispr-cas systems, vectors and compositions for hepatic targeting and therapy |
EP4245853A3 (en) | 2013-06-17 | 2023-10-18 | The Broad Institute, Inc. | Optimized crispr-cas double nickase systems, methods and compositions for sequence manipulation |
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US9163284B2 (en) | 2013-08-09 | 2015-10-20 | President And Fellows Of Harvard College | Methods for identifying a target site of a Cas9 nuclease |
US9359599B2 (en) | 2013-08-22 | 2016-06-07 | President And Fellows Of Harvard College | Engineered transcription activator-like effector (TALE) domains and uses thereof |
US9340800B2 (en) | 2013-09-06 | 2016-05-17 | President And Fellows Of Harvard College | Extended DNA-sensing GRNAS |
US9322037B2 (en) | 2013-09-06 | 2016-04-26 | President And Fellows Of Harvard College | Cas9-FokI fusion proteins and uses thereof |
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SG10201804974RA (en) * | 2013-12-12 | 2018-07-30 | Broad Inst Inc | Compositions and Methods of Use of Crispr-Cas Systems in Nucleotide Repeat Disorders |
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CN118813621A (en) | 2013-12-12 | 2024-10-22 | 布罗德研究所有限公司 | Delivery, use and therapeutic applications of CRISPR-CAS systems and compositions for genome editing |
CA3161903A1 (en) | 2014-02-11 | 2015-08-20 | The Regents Of The University Of Colorado | Crispr enabled multiplexed genome engineering |
AU2015231353B2 (en) * | 2014-03-18 | 2020-11-05 | Sangamo Therapeutics, Inc. | Methods and compositions for regulation of zinc finger protein expression |
EP4410805A3 (en) | 2014-03-18 | 2024-11-27 | University of Massachusetts | Raav-based compositions and methods for treating amyotrophic lateral sclerosis |
WO2015173436A1 (en) * | 2014-05-16 | 2015-11-19 | Vrije Universiteit Brussel | Genetic correction of myotonic dystrophy type 1 |
EP3177718B1 (en) | 2014-07-30 | 2022-03-16 | President and Fellows of Harvard College | Cas9 proteins including ligand-dependent inteins |
US10435685B2 (en) * | 2014-08-19 | 2019-10-08 | Pacific Biosciences Of California, Inc. | Compositions and methods for enrichment of nucleic acids |
CA2963693A1 (en) | 2014-10-10 | 2016-04-14 | Editas Medicine, Inc. | Compositions and methods for promoting homology directed repair |
SG11201703148TA (en) | 2014-11-05 | 2017-05-30 | Voyager Therapeutics Inc | Aadc polynucleotides for the treatment of parkinson's disease |
CA2963820A1 (en) | 2014-11-07 | 2016-05-12 | Editas Medicine, Inc. | Methods for improving crispr/cas-mediated genome-editing |
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WO2016077687A1 (en) | 2014-11-14 | 2016-05-19 | Voyager Therapeutics, Inc. | Compositions and methods of treating amyotrophic lateral sclerosis (als) |
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