JP2019515914A5 - - Google Patents

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Publication number
JP2019515914A5
JP2019515914A5 JP2018555262A JP2018555262A JP2019515914A5 JP 2019515914 A5 JP2019515914 A5 JP 2019515914A5 JP 2018555262 A JP2018555262 A JP 2018555262A JP 2018555262 A JP2018555262 A JP 2018555262A JP 2019515914 A5 JP2019515914 A5 JP 2019515914A5
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JP
Japan
Prior art keywords
seq
nuclease
guide rna
guide
guides
Prior art date
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Pending
Application number
JP2018555262A
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English (en)
Japanese (ja)
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JP2019515914A (ja
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Publication date
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Priority claimed from PCT/US2017/028981 external-priority patent/WO2017185054A1/en
Publication of JP2019515914A publication Critical patent/JP2019515914A/ja
Publication of JP2019515914A5 publication Critical patent/JP2019515914A5/ja
Pending legal-status Critical Current

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JP2018555262A 2016-04-22 2017-04-21 転写因子4内のトリヌクレオチドリピートと関連する疾患の治療のための組成物および方法 Pending JP2019515914A (ja)

Applications Claiming Priority (3)

Application Number Priority Date Filing Date Title
US201662326700P 2016-04-22 2016-04-22
US62/326,700 2016-04-22
PCT/US2017/028981 WO2017185054A1 (en) 2016-04-22 2017-04-21 Compositions and methods for treatment of diseases associated with trinucleotide repeats in transcription factor four

Publications (2)

Publication Number Publication Date
JP2019515914A JP2019515914A (ja) 2019-06-13
JP2019515914A5 true JP2019515914A5 (enExample) 2020-06-11

Family

ID=58692575

Family Applications (1)

Application Number Title Priority Date Filing Date
JP2018555262A Pending JP2019515914A (ja) 2016-04-22 2017-04-21 転写因子4内のトリヌクレオチドリピートと関連する疾患の治療のための組成物および方法

Country Status (11)

Country Link
US (2) US20190142972A1 (enExample)
EP (1) EP3445375A1 (enExample)
JP (1) JP2019515914A (enExample)
KR (1) KR20180134412A (enExample)
CN (1) CN109414450A (enExample)
AU (1) AU2017254718A1 (enExample)
BR (1) BR112018071439A2 (enExample)
CA (1) CA3021647A1 (enExample)
CO (1) CO2018012433A2 (enExample)
MX (1) MX2018012873A (enExample)
WO (1) WO2017185054A1 (enExample)

Families Citing this family (19)

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MX2017016921A (es) * 2015-07-02 2018-04-10 Univ Johns Hopkins Tratamientos basados en crispr / cas9.
WO2022072458A1 (en) * 2020-09-29 2022-04-07 Avellino Lab Usa, Inc. Crispr/cas9 targeted excision of the intronic ctg18.1 trinucleotide repeat expansion of tcf4 as a therapy in fuchs' endothelial corneal dystrophy
AU2017379073B2 (en) 2016-12-22 2023-12-14 Intellia Therapeutics, Inc. Compositions and methods for treating alpha-1 antitrypsin deficiency
WO2018165541A1 (en) 2017-03-10 2018-09-13 The Board Of Regents Of The University Of Texas System Treatment of fuchs' endothelial corneal dystrophy
US20230201373A1 (en) * 2017-12-15 2023-06-29 Regents Of The University Of Minnesota Crispr-mediated genome editing with vectors
CN109929872A (zh) * 2017-12-18 2019-06-25 中国科学院遗传与发育生物学研究所 一种通过基因编辑技术创制番茄白果材料的方法
US11891635B2 (en) 2017-12-21 2024-02-06 Max-Delbrück-Centrum Für Molekulare Medizin In Der Helmholtz-Gemeinschaft Nucleic acid sequence replacement by NHEJ
US20190151470A1 (en) * 2018-01-21 2019-05-23 RoverMed BioSciences, LLC Nanoparticles comprising protein-polynucleotide complexes and for delivering protein based complexes
TW202045186A (zh) * 2019-02-28 2020-12-16 弗里德里希 E 克魯斯 細胞外基質調節劑
CA3131919A1 (en) * 2019-02-28 2020-09-03 Regeneron Pharmaceuticals, Inc. Adeno-associated virus vectors for the delivery of therapeutics
US20230349888A1 (en) * 2020-04-27 2023-11-02 Duke University A high-throughput screening method to discover optimal grna pairs for crispr-mediated exon deletion
CN111944814B (zh) * 2020-08-24 2022-07-15 武汉纽福斯生物科技有限公司 寡核苷酸、病毒载体及其应用和RNAi药物制剂
CN111944813B (zh) * 2020-08-24 2022-07-15 武汉纽福斯生物科技有限公司 核苷酸、病毒载体及其应用和RNAi药物制剂
IL303506A (en) 2020-12-11 2023-08-01 Intellia Therapeutics Inc Polynucleotides, compositions, and methods for genome editing involving deamination
AU2022216614A1 (en) 2021-02-05 2023-02-23 Christiana Care Gene Editing Institute, Inc. Methods of and compositions for reducing gene expression and/or activity
EP4430185A1 (en) * 2021-11-09 2024-09-18 Prime Medicine, Inc. Genome editing compositions and methods for treatment of fuchs endothelial corneal dystrophy
US12297285B2 (en) 2022-06-24 2025-05-13 Orna Therapeutics, Inc. Circular RNA encoding chimeric antigen receptors targeting BCMA
WO2024226536A1 (en) * 2023-04-24 2024-10-31 The General Hospital Corporation Methods and compositions for modifying genetic repeats
WO2025128871A2 (en) 2023-12-13 2025-06-19 Renagade Therapeutics Management Inc. Lipid nanoparticles comprising coding rna molecules for use in gene editing and as vaccines and therapeutic agents

Family Cites Families (10)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2006007712A1 (en) 2004-07-19 2006-01-26 Protiva Biotherapeutics, Inc. Methods comprising polyethylene glycol-lipid conjugates for delivery of therapeutic agents
WO2013101711A1 (en) * 2011-12-30 2013-07-04 Mayo Foundation For Medical Education And Research Assessing likelihood of developing fuchs' corneal dystrophy
LT3401400T (lt) * 2012-05-25 2019-06-10 The Regents Of The University Of California Būdai ir kompozicijos, skirtos rnr molekulės nukreipiamai tikslinės dnr modifikacijai ir rnr molekulės nukreipiamam transkripcijos moduliavimui
WO2014093701A1 (en) * 2012-12-12 2014-06-19 The Broad Institute, Inc. Functional genomics using crispr-cas systems, compositions, methods, knock out libraries and applications thereof
JP6352950B2 (ja) 2013-03-08 2018-07-04 ノバルティス アーゲー 活性薬物の送達のための脂質と脂質組成物
KR102523466B1 (ko) * 2013-11-07 2023-04-20 에디타스 메디신, 인코포레이티드 지배적인 gRNA를 이용하는 CRISPR-관련 방법 및 조성물
BR112016013213A2 (pt) * 2013-12-12 2017-12-05 Massachusetts Inst Technology administração, uso e aplicações terapêuticas dos sistemas crispr-cas e composições para visar distúrbios e doenças usando componentes de administração de partículas
EP3872066A1 (en) 2013-12-19 2021-09-01 Novartis AG Lipids and lipid compositions for the delivery of active agents
SG10201912171PA (en) * 2014-04-18 2020-02-27 Editas Medicine Inc Crispr-cas-related methods, compositions and components for cancer immunotherapy
MX2017016921A (es) * 2015-07-02 2018-04-10 Univ Johns Hopkins Tratamientos basados en crispr / cas9.

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