MA47239A - Stratégie optimisée pour des modifications par saut d'exon à l'aide de crispr/cas9 avec des séquences de guidage triple - Google Patents

Stratégie optimisée pour des modifications par saut d'exon à l'aide de crispr/cas9 avec des séquences de guidage triple

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Publication number
MA47239A
MA47239A MA047239A MA47239A MA47239A MA 47239 A MA47239 A MA 47239A MA 047239 A MA047239 A MA 047239A MA 47239 A MA47239 A MA 47239A MA 47239 A MA47239 A MA 47239A
Authority
MA
Morocco
Prior art keywords
cas9
crispr
exon skip
optimized strategy
triple
Prior art date
Application number
MA047239A
Other languages
English (en)
French (fr)
Inventor
Leonela Amoasii
Eric Olson
Original Assignee
Univ Texas
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by Univ Texas filed Critical Univ Texas
Publication of MA47239A publication Critical patent/MA47239A/fr

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    • C12N9/14Hydrolases (3)
    • C12N9/16Hydrolases (3) acting on ester bonds (3.1)
    • C12N9/22Ribonucleases [RNase]; Deoxyribonucleases [DNase]
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    • A61P21/00Drugs for disorders of the muscular or neuromuscular system
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    • A61P21/04Drugs for disorders of the muscular or neuromuscular system for myasthenia gravis
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    • C12N2310/00Structure or type of the nucleic acid
    • C12N2310/10Type of nucleic acid
    • C12N2310/20Type of nucleic acid involving clustered regularly interspaced short palindromic repeats [CRISPR]
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    • C12N2320/33Alteration of splicing
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    • C12N2750/14111Dependovirus, e.g. adenoassociated viruses
    • C12N2750/14141Use of virus, viral particle or viral elements as a vector
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  • Pharmacology & Pharmacy (AREA)
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MA047239A 2017-01-05 2018-01-05 Stratégie optimisée pour des modifications par saut d'exon à l'aide de crispr/cas9 avec des séquences de guidage triple MA47239A (fr)

Applications Claiming Priority (3)

Application Number Priority Date Filing Date Title
US201762442606P 2017-01-05 2017-01-05
US201762544449P 2017-08-11 2017-08-11
US201762596298P 2017-12-08 2017-12-08

Publications (1)

Publication Number Publication Date
MA47239A true MA47239A (fr) 2019-11-13

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MA047239A MA47239A (fr) 2017-01-05 2018-01-05 Stratégie optimisée pour des modifications par saut d'exon à l'aide de crispr/cas9 avec des séquences de guidage triple

Country Status (22)

Country Link
US (1) US20190338311A1 (OSRAM)
EP (1) EP3565897B1 (OSRAM)
JP (1) JP2020503869A (OSRAM)
KR (1) KR102606174B1 (OSRAM)
CN (1) CN110506115A (OSRAM)
AU (1) AU2018205521A1 (OSRAM)
BR (1) BR112019013962A2 (OSRAM)
CA (1) CA3048635A1 (OSRAM)
CL (1) CL2019001882A1 (OSRAM)
CO (1) CO2019008181A2 (OSRAM)
CR (1) CR20190326A (OSRAM)
DK (1) DK3565897T3 (OSRAM)
DO (1) DOP2019000179A (OSRAM)
EC (1) ECSP19056408A (OSRAM)
IL (1) IL267786A (OSRAM)
JO (1) JOP20190166A1 (OSRAM)
MA (1) MA47239A (OSRAM)
MX (1) MX2019008064A (OSRAM)
PE (1) PE20191357A1 (OSRAM)
PH (1) PH12019501561A1 (OSRAM)
SG (1) SG11201906147VA (OSRAM)
WO (1) WO2018129296A1 (OSRAM)

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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
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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
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WO2020210776A1 (en) * 2019-04-12 2020-10-15 Duke University Crispr/cas-based base editing composition for restoring dystrophin function
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EP3966327A1 (en) 2019-05-08 2022-03-16 Vertex Pharmaceuticals Incorporated 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
WO2021072276A1 (en) * 2019-10-11 2021-04-15 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
MX2022009883A (es) * 2020-02-13 2022-10-03 Tenaya Therapeutics Inc Vectores de genoterapia para tratar enfermedades cardíacas.
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
US20230348870A1 (en) * 2020-04-27 2023-11-02 Duke University Gene editing of satellite cells in vivo using aav vectors encoding muscle-specific promoters
CN115011598A (zh) * 2020-09-02 2022-09-06 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
EP4211242A1 (en) * 2020-09-09 2023-07-19 Vertex Pharmaceuticals Incorporated Compositions and methods for treatment of duchenne muscular dystrophy
US11638761B2 (en) 2021-07-09 2023-05-02 Dyne Therapeutics, Inc. Muscle targeting complexes and uses thereof for treating Facioscapulohumeral muscular dystrophy
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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
WO2023172115A1 (ko) * 2022-03-10 2023-09-14 주식회사 진코어 Nhej 복구 경로 조절을 통해 핵산 세그먼트의 결실 효율을 증가시키기 위한 조성물 및 방법
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

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