CA3048635A1 - Optimized strategy for exon skipping modifications using crispr/cas9 with triple guide sequences - Google Patents
Optimized strategy for exon skipping modifications using crispr/cas9 with triple guide sequences Download PDFInfo
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- CA3048635A1 CA3048635A1 CA3048635A CA3048635A CA3048635A1 CA 3048635 A1 CA3048635 A1 CA 3048635A1 CA 3048635 A CA3048635 A CA 3048635A CA 3048635 A CA3048635 A CA 3048635A CA 3048635 A1 CA3048635 A1 CA 3048635A1
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- C12N15/79—Vectors or expression systems specially adapted for eukaryotic hosts
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Applications Claiming Priority (7)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US201762442606P | 2017-01-05 | 2017-01-05 | |
| US62/442,606 | 2017-01-05 | ||
| US201762544449P | 2017-08-11 | 2017-08-11 | |
| US62/544,449 | 2017-08-11 | ||
| US201762596298P | 2017-12-08 | 2017-12-08 | |
| US62/596,298 | 2017-12-08 | ||
| PCT/US2018/012558 WO2018129296A1 (en) | 2017-01-05 | 2018-01-05 | Optimized strategy for exon skipping modifications using crispr/cas9 with triple guide sequences |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| CA3048635A1 true CA3048635A1 (en) | 2018-07-12 |
Family
ID=61193018
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| CA3048635A Pending CA3048635A1 (en) | 2017-01-05 | 2018-01-05 | Optimized strategy for exon skipping modifications using crispr/cas9 with triple guide sequences |
Country Status (22)
Families Citing this family (36)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| EP2841572B1 (en) | 2012-04-27 | 2019-06-19 | Duke University | Genetic correction of mutated genes |
| US9828582B2 (en) | 2013-03-19 | 2017-11-28 | Duke University | Compositions and methods for the induction and tuning of gene expression |
| US10676726B2 (en) | 2015-02-09 | 2020-06-09 | Duke University | Compositions and methods for epigenome editing |
| US11970710B2 (en) | 2015-10-13 | 2024-04-30 | Duke University | Genome engineering with Type I CRISPR systems in eukaryotic cells |
| EP3384055B1 (en) | 2015-11-30 | 2025-07-16 | Duke University | Therapeutic targets for the correction of the human dystrophin gene by gene editing and methods of use |
| US20190127713A1 (en) | 2016-04-13 | 2019-05-02 | Duke University | Crispr/cas9-based repressors for silencing gene targets in vivo and methods of use |
| US12214056B2 (en) | 2016-07-19 | 2025-02-04 | Duke University | Therapeutic applications of CPF1-based genome editing |
| CN110892069B (zh) * | 2017-03-30 | 2024-02-09 | 国立大学法人京都大学 | 基于基因组编辑的外显子跳跃诱导方法 |
| EP3735462A1 (en) * | 2018-01-05 | 2020-11-11 | The Board of Regents of The University of Texas System | Therapeutic crispr/cas9 compositions and methods of use |
| US20210261962A1 (en) * | 2018-06-21 | 2021-08-26 | The Board Of Regents Of The University Of Texas System | Correction of dystrophin exon 43, exon 45, or exon 52 deletions in duchenne muscular dystrophy |
| EA202190416A1 (ru) | 2018-08-02 | 2021-06-23 | Дайн Терапьютикс, Инк. | Мышечно-специфические комлексы и их применение для лечения плече-лопаточно-лицевой мышечной дистрофии |
| MX2021001281A (es) | 2018-08-02 | 2021-07-15 | Dyne Therapeutics Inc | Complejos dirigidos a músculos y sus usos para el tratamiento de distrofinopatías. |
| US12018087B2 (en) | 2018-08-02 | 2024-06-25 | Dyne Therapeutics, Inc. | Muscle-targeting complexes comprising an anti-transferrin receptor antibody linked to an oligonucleotide and methods of delivering oligonucleotide to a subject |
| US11168141B2 (en) | 2018-08-02 | 2021-11-09 | Dyne Therapeutics, Inc. | Muscle targeting complexes and uses thereof for treating dystrophinopathies |
| JP7395159B2 (ja) * | 2018-12-11 | 2023-12-11 | 国立大学法人京都大学 | ゲノムdnaに欠失を誘導する方法 |
| WO2020142714A1 (en) * | 2019-01-04 | 2020-07-09 | Exonics Therapeutics, Inc. | Aav expression cassette and aav vectors comprising the same |
| WO2020181264A1 (en) | 2019-03-07 | 2020-09-10 | The Trustees Of Columbia University In The City Of New York | Rna-guided dna integration using tn7-like transposons |
| EP3952884A4 (en) * | 2019-04-12 | 2023-03-22 | Duke University | Crispr/cas-based base editing composition for restoring dystrophin function |
| EP3952925A4 (en) * | 2019-04-12 | 2024-01-24 | The Regents of the University of California | COMPOSITIONS AND METHODS FOR MODIFYING DYSTROPHIN GENES |
| WO2020225606A1 (en) | 2019-05-08 | 2020-11-12 | Crispr Therapeutics Ag | Crispr/cas all-in-two vector systems for treatment of dmd |
| KR102264115B1 (ko) * | 2019-05-10 | 2021-06-14 | 한국과학기술연구원 | 무-운반체 다중 CRISPR/Cas 9 유전자 편집 복합체 및 그의 용도 |
| CN110499333A (zh) * | 2019-08-01 | 2019-11-26 | 广州德赫生物科技有限公司 | 用于修复dmd基因突变的核酸序列及系统 |
| US20240091379A1 (en) * | 2019-10-11 | 2024-03-21 | Yale University | Compositions and methods for upregulating isoforms of dystrophin as therapy for duchenne muscular dystrophy (dmd) |
| KR102455623B1 (ko) * | 2019-10-29 | 2022-10-18 | 주식회사 진코어 | CRISPR/Cas12f1 시스템 효율화를 위한 엔지니어링 된 가이드 RNA 및 그 용도 |
| IL295529A (en) | 2020-02-13 | 2022-10-01 | Tenaya Therapeutics Inc | Gene therapy vectors for treating heart disease |
| CN111172191B (zh) * | 2020-02-21 | 2020-12-22 | 浙江大学 | 一种高效基因敲除载体及其应用 |
| JP2023515709A (ja) * | 2020-04-27 | 2023-04-13 | デューク ユニバーシティ | 筋肉特異的プロモーターをコードするaavベクターを使用するインビボでの衛星細胞の遺伝子編集 |
| CN112063621B (zh) * | 2020-09-02 | 2022-06-28 | 西湖大学 | 杜氏肌营养不良症相关的外显子剪接增强子、sgRNA、基因编辑工具及应用 |
| JP2023540783A (ja) * | 2020-09-09 | 2023-09-26 | バーテックス ファーマシューティカルズ インコーポレイテッド | デュシェンヌ型筋ジストロフィーの治療のための組成物及び方法 |
| US11771776B2 (en) | 2021-07-09 | 2023-10-03 | Dyne Therapeutics, Inc. | Muscle targeting complexes and uses thereof for treating dystrophinopathies |
| US11969475B2 (en) | 2021-07-09 | 2024-04-30 | Dyne Therapeutics, Inc. | Muscle targeting complexes and uses thereof for treating facioscapulohumeral muscular dystrophy |
| JP2024525608A (ja) | 2021-07-09 | 2024-07-12 | ダイン セラピューティクス,インコーポレーテッド | ジストロフィン異常症を処置するための筋標的化複合体および製剤 |
| US11638761B2 (en) | 2021-07-09 | 2023-05-02 | Dyne Therapeutics, Inc. | Muscle targeting complexes and uses thereof for treating Facioscapulohumeral muscular dystrophy |
| WO2023159103A1 (en) * | 2022-02-17 | 2023-08-24 | The Board Of Regents Of The University Of Texas System | CRISPR/SpCas9 VARIANT AND METHODS FOR ENHANCED CORRECTON OF DUCHENNE MUSCULAR DYSTROPHY MUTATIONS |
| US20250361529A1 (en) * | 2022-03-10 | 2025-11-27 | Genkore Inc. | Gene editing system for treating duchenne muscular dystrophy, and method of treating disease using same |
| CN115820642B (zh) * | 2022-11-11 | 2023-10-10 | 昆明理工大学 | 一种用于治疗杜氏肌营养不良症的CRISPR-Cas9系统 |
Family Cites Families (12)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| EP1737966B1 (en) * | 2004-04-02 | 2012-05-09 | Board of Regents, The University of Texas System | Cancer specific promoters |
| WO2013176772A1 (en) | 2012-05-25 | 2013-11-28 | The Regents Of The University Of California | Methods and compositions for rna-directed target dna modification and for rna-directed modulation of transcription |
| ES2987399T3 (es) * | 2013-06-05 | 2024-11-14 | Univ Duke | Edición génica guiada por ARN y regulación génica |
| ES2821149T3 (es) * | 2014-03-12 | 2021-04-23 | Prec Biosciences Inc | Eliminación del exón del gen de la distrofina mediante nucleasas modificadas genéticamente |
| CA2959130A1 (en) * | 2014-08-11 | 2016-02-18 | The Board Of Regents Of The University Of Texas System | Prevention of muscular dystrophy by crispr/cas9-mediated gene editing |
| WO2016089866A1 (en) * | 2014-12-01 | 2016-06-09 | President And Fellows Of Harvard College | Rna-guided systems for in vivo gene editing |
| JP6832280B2 (ja) * | 2015-01-16 | 2021-02-24 | ユニバーシティ オブ ワシントンUniversity of Washington | 新規のマイクロジストロフィンおよび使用の関連する方法 |
| CA2981715A1 (en) * | 2015-04-06 | 2016-10-13 | The Board Of Trustees Of The Leland Stanford Junior University | Chemically modified guide rnas for crispr/cas-mediated gene regulation |
| CA2983364A1 (en) * | 2015-04-27 | 2016-11-03 | Genethon | Compositions and methods for the treatment of nucleotide repeat expansion disorders |
| CN108513546A (zh) * | 2015-10-28 | 2018-09-07 | 克里斯珀医疗股份公司 | 用于治疗杜氏肌营养不良症的材料和方法 |
| EP3384055B1 (en) * | 2015-11-30 | 2025-07-16 | Duke University | Therapeutic targets for the correction of the human dystrophin gene by gene editing and methods of use |
| US20170362635A1 (en) * | 2016-06-20 | 2017-12-21 | University Of Washington | Muscle-specific crispr/cas9 editing of genes |
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2017
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2018
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2019
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| AU2018205521A1 (en) | 2019-07-18 |
| JP2020503869A (ja) | 2020-02-06 |
| PH12019501561A1 (en) | 2019-09-09 |
| ECSP19056408A (es) | 2019-09-30 |
| BR112019013962A2 (pt) | 2020-02-11 |
| DOP2019000179A (es) | 2019-11-15 |
| WO2018129296A1 (en) | 2018-07-12 |
| KR20190100967A (ko) | 2019-08-29 |
| SG11201906147VA (en) | 2019-08-27 |
| US20190338311A1 (en) | 2019-11-07 |
| MX2019008064A (es) | 2020-07-20 |
| CL2019001882A1 (es) | 2019-10-04 |
| DK3565897T3 (da) | 2025-02-10 |
| CR20190326A (es) | 2019-10-02 |
| CN110506115A (zh) | 2019-11-26 |
| EP3565897A1 (en) | 2019-11-13 |
| EP3565897B1 (en) | 2024-12-11 |
| CO2019008181A2 (es) | 2019-10-31 |
| MA47239A (fr) | 2019-11-13 |
| IL267786A (en) | 2019-09-26 |
| PE20191357A1 (es) | 2019-10-01 |
| KR102606174B1 (ko) | 2023-11-27 |
| JOP20190166A1 (ar) | 2019-07-02 |
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