PT3066201T - Métodos e composições relacionadas com crispr com arng reguladores - Google Patents

Métodos e composições relacionadas com crispr com arng reguladores

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Publication number
PT3066201T
PT3066201T PT148027725T PT14802772T PT3066201T PT 3066201 T PT3066201 T PT 3066201T PT 148027725 T PT148027725 T PT 148027725T PT 14802772 T PT14802772 T PT 14802772T PT 3066201 T PT3066201 T PT 3066201T
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PT
Portugal
Prior art keywords
crispr
methods
compositions related
regulatory ranges
regulatory
Prior art date
Application number
PT148027725T
Other languages
English (en)
Inventor
Palestrant Deborah
Mata-Fink Jordi
Borisy Alexis
Zhang Feng
Davidson Beverly
Rodriguez Edgardo
Original Assignee
Massachusetts Inst Technology
Broad Inst Inc
Editas Medicine Inc
The Univ Of Iowa Research Foundation
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Family has litigation
First worldwide family litigation filed litigation Critical https://patents.darts-ip.com/?family=51952032&utm_source=google_patent&utm_medium=platform_link&utm_campaign=public_patent_search&patent=PT3066201(T) "Global patent litigation dataset” by Darts-ip is licensed under a Creative Commons Attribution 4.0 International License.
Application filed by Massachusetts Inst Technology, Broad Inst Inc, Editas Medicine Inc, The Univ Of Iowa Research Foundation filed Critical Massachusetts Inst Technology
Publication of PT3066201T publication Critical patent/PT3066201T/pt

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    • C12N15/00Mutation or genetic engineering; DNA or RNA concerning genetic engineering, vectors, e.g. plasmids, or their isolation, preparation or purification; Use of hosts therefor
    • C12N15/09Recombinant DNA-technology
    • C12N15/87Introduction of foreign genetic material using processes not otherwise provided for, e.g. co-transformation
    • C12N15/90Stable introduction of foreign DNA into chromosome
    • C12N15/902Stable introduction of foreign DNA into chromosome using homologous recombination
    • AHUMAN NECESSITIES
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    • C12N15/00Mutation or genetic engineering; DNA or RNA concerning genetic engineering, vectors, e.g. plasmids, or their isolation, preparation or purification; Use of hosts therefor
    • C12N15/09Recombinant DNA-technology
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    • C12N15/00Mutation or genetic engineering; DNA or RNA concerning genetic engineering, vectors, e.g. plasmids, or their isolation, preparation or purification; Use of hosts therefor
    • C12N15/09Recombinant DNA-technology
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    • C12N15/00Mutation or genetic engineering; DNA or RNA concerning genetic engineering, vectors, e.g. plasmids, or their isolation, preparation or purification; Use of hosts therefor
    • C12N15/09Recombinant DNA-technology
    • C12N15/11DNA or RNA fragments; Modified forms thereof; Non-coding nucleic acids having a biological activity
    • C12N15/113Non-coding nucleic acids modulating the expression of genes, e.g. antisense oligonucleotides; Antisense DNA or RNA; Triplex- forming oligonucleotides; Catalytic nucleic acids, e.g. ribozymes; Nucleic acids used in co-suppression or gene silencing
    • C12N15/1137Non-coding nucleic acids modulating the expression of genes, e.g. antisense oligonucleotides; Antisense DNA or RNA; Triplex- forming oligonucleotides; Catalytic nucleic acids, e.g. ribozymes; Nucleic acids used in co-suppression or gene silencing against enzymes
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    • C12N15/00Mutation or genetic engineering; DNA or RNA concerning genetic engineering, vectors, e.g. plasmids, or their isolation, preparation or purification; Use of hosts therefor
    • C12N15/09Recombinant DNA-technology
    • C12N15/63Introduction of foreign genetic material using vectors; Vectors; Use of hosts therefor; Regulation of expression
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    • C12N9/00Enzymes; Proenzymes; Compositions thereof; Processes for preparing, activating, inhibiting, separating or purifying enzymes
    • C12N9/14Hydrolases (3)
    • C12N9/16Hydrolases (3) acting on ester bonds (3.1)
    • C12N9/22Ribonucleases [RNase]; Deoxyribonucleases [DNase]
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    • C12N2310/00Structure or type of the nucleic acid
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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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    • C12N2800/00Nucleic acids vectors
    • C12N2800/80Vectors containing sites for inducing double-stranded breaks, e.g. meganuclease restriction sites

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  • Bioinformatics & Cheminformatics (AREA)
  • Wood Science & Technology (AREA)
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  • Biotechnology (AREA)
  • General Engineering & Computer Science (AREA)
  • General Health & Medical Sciences (AREA)
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  • Physics & Mathematics (AREA)
  • Medicinal Chemistry (AREA)
  • Virology (AREA)
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  • Epidemiology (AREA)
  • Animal Behavior & Ethology (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Veterinary Medicine (AREA)
  • Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)
  • Micro-Organisms Or Cultivation Processes Thereof (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Medicines Containing Material From Animals Or Micro-Organisms (AREA)
  • Breeding Of Plants And Reproduction By Means Of Culturing (AREA)
  • General Preparation And Processing Of Foods (AREA)
PT148027725T 2013-11-07 2014-11-07 Métodos e composições relacionadas com crispr com arng reguladores PT3066201T (pt)

Applications Claiming Priority (1)

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US201361901215P 2013-11-07 2013-11-07

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PT3066201T true PT3066201T (pt) 2018-06-04

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US (5) US9834791B2 (pt)
EP (3) EP4372090A3 (pt)
JP (4) JP2016536021A (pt)
KR (3) KR102380245B1 (pt)
CN (2) CN106459995B (pt)
AU (3) AU2014346559B2 (pt)
CA (2) CA3255265A1 (pt)
DK (1) DK3066201T3 (pt)
ES (1) ES2670983T3 (pt)
LT (1) LT3066201T (pt)
NO (1) NO3123224T3 (pt)
PT (1) PT3066201T (pt)
WO (1) WO2015070083A1 (pt)

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* Cited by examiner, † Cited by third party
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