JP2020500541A5 - - Google Patents

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Publication number
JP2020500541A5
JP2020500541A5 JP2019530778A JP2019530778A JP2020500541A5 JP 2020500541 A5 JP2020500541 A5 JP 2020500541A5 JP 2019530778 A JP2019530778 A JP 2019530778A JP 2019530778 A JP2019530778 A JP 2019530778A JP 2020500541 A5 JP2020500541 A5 JP 2020500541A5
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JP
Japan
Prior art keywords
sequence encoding
promoter
composition
grna
sequence
Prior art date
Legal status (The legal status 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 status listed.)
Pending
Application number
JP2019530778A
Other languages
English (en)
Japanese (ja)
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JP2020500541A (ja
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Publication date
Application filed filed Critical
Priority claimed from PCT/US2017/065268 external-priority patent/WO2018107003A1/en
Publication of JP2020500541A publication Critical patent/JP2020500541A/ja
Publication of JP2020500541A5 publication Critical patent/JP2020500541A5/ja
Pending legal-status Critical Current

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JP2019530778A 2016-12-08 2017-12-08 ヒト化デュシェンヌ型筋ジストロフィー変異を有するdmdレポーターモデル Pending JP2020500541A (ja)

Applications Claiming Priority (3)

Application Number Priority Date Filing Date Title
US201662431699P 2016-12-08 2016-12-08
US62/431,699 2016-12-08
PCT/US2017/065268 WO2018107003A1 (en) 2016-12-08 2017-12-08 Dmd reporter models containing humanized duschene muscular dystrophy mutations

Publications (2)

Publication Number Publication Date
JP2020500541A JP2020500541A (ja) 2020-01-16
JP2020500541A5 true JP2020500541A5 (https=) 2021-01-21

Family

ID=60888655

Family Applications (1)

Application Number Title Priority Date Filing Date
JP2019530778A Pending JP2020500541A (ja) 2016-12-08 2017-12-08 ヒト化デュシェンヌ型筋ジストロフィー変異を有するdmdレポーターモデル

Country Status (6)

Country Link
US (1) US20190364862A1 (https=)
EP (1) EP3551752A1 (https=)
JP (1) JP2020500541A (https=)
AU (1) AU2017370730A1 (https=)
CA (1) CA3046220A1 (https=)
WO (1) WO2018107003A1 (https=)

Families Citing this family (20)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US9828582B2 (en) 2013-03-19 2017-11-28 Duke University Compositions and methods for the induction and tuning of gene expression
WO2016130600A2 (en) 2015-02-09 2016-08-18 Duke University Compositions and methods for epigenome editing
KR102787119B1 (ko) 2015-11-30 2025-03-27 듀크 유니버시티 유전자 편집에 의한 인간 디스트로핀 유전자의 교정을 위한 치료용 표적 및 사용 방법
US20190127713A1 (en) 2016-04-13 2019-05-02 Duke University Crispr/cas9-based repressors for silencing gene targets in vivo and methods of use
JP7490211B2 (ja) 2016-07-19 2024-05-27 デューク ユニバーシティ Cpf1に基づくゲノム編集の治療適用
EP3617311B1 (en) * 2017-03-30 2024-11-20 Kyoto University Method for inducing exon skipping by genome editing
US20200260698A1 (en) * 2017-08-18 2020-08-20 The Board Of Regents Of The University Of Texas System Exon deletion correction of duchenne muscular dystrophy mutations in the dystrophin actin binding domain 1 using crispr genome editing
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
EP3740580A4 (en) 2018-01-19 2021-10-20 Duke University GENOME ENGINEERING WITH CRISPR-CAS SYSTEMS IN EUKARYONTS
EP3810775A1 (en) * 2018-06-21 2021-04-28 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
US11168141B2 (en) 2018-08-02 2021-11-09 Dyne Therapeutics, Inc. Muscle targeting complexes and uses thereof for treating dystrophinopathies
CA3108282A1 (en) 2018-08-02 2020-02-06 Dyne Therapeutics, Inc. Muscle targeting complexes and uses thereof for treating dystrophinopathies
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
SG11202100928QA (en) 2018-08-02 2021-02-25 Dyne Therapeutics Inc Muscle targeting complexes and uses thereof for treating facioscapulohumeral muscular dystrophy
US20210047649A1 (en) 2019-05-08 2021-02-18 Vertex Pharmaceuticals Incorporated Crispr/cas all-in-two vector systems for treatment of dmd
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
US11969475B2 (en) 2021-07-09 2024-04-30 Dyne Therapeutics, Inc. Muscle targeting complexes and uses thereof for treating facioscapulohumeral muscular dystrophy
US11771776B2 (en) 2021-07-09 2023-10-03 Dyne Therapeutics, Inc. Muscle targeting complexes and uses thereof for treating dystrophinopathies
US11638761B2 (en) 2021-07-09 2023-05-02 Dyne Therapeutics, Inc. Muscle targeting complexes and uses thereof for treating Facioscapulohumeral muscular dystrophy
WO2023178338A2 (en) * 2022-03-18 2023-09-21 University Of Florida Research Foundation, Incorporated Methods and compositions for treating tmem43 related cardiomyopathy with a viral vector

Family Cites Families (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4873191A (en) 1981-06-12 1989-10-10 Ohio University Genetic transformation of zygotes
EP0273085A1 (en) 1986-12-29 1988-07-06 IntraCel Corporation A method for internalizing nucleic acids into eukaryotic cells
CA2861247C (en) * 2011-12-28 2021-11-16 Nippon Shinyaku Co., Ltd. Antisense nucleic acids
AU2013266968B2 (en) 2012-05-25 2017-06-29 Emmanuelle CHARPENTIER Methods and compositions for RNA-directed target DNA modification and for RNA-directed modulation of transcription

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