JPH09505728A - フラボバクテリウム・オケアノコイテス(foki)制限エンドヌクレアーゼにおける機能ドメイン - Google Patents
フラボバクテリウム・オケアノコイテス(foki)制限エンドヌクレアーゼにおける機能ドメインInfo
- Publication number
- JPH09505728A JPH09505728A JP7510290A JP51029095A JPH09505728A JP H09505728 A JPH09505728 A JP H09505728A JP 7510290 A JP7510290 A JP 7510290A JP 51029095 A JP51029095 A JP 51029095A JP H09505728 A JPH09505728 A JP H09505728A
- Authority
- JP
- Japan
- Prior art keywords
- endonuclease
- dna
- dna segment
- foki
- domain
- 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.)
- Withdrawn
Links
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Abstract
Description
Claims (1)
- 【特許請求の範囲】 1.IIS型エンドヌクレアーゼの認識ドメインをコードする単離されたDN Aセグメントであって、前記IIS型エンドヌクレアーゼの配列特異的認識活性 を含むDNAセグメント。 2.請求項1に記載のDNAセグメントであって、前記IIS型エンドヌクレ アーゼがFokI制限エンドヌクレアーゼであるDNAセグメント。 3.請求項2に記載のDNAセグメントであって、前記コードされるタンパク が、SDSポリアクリルアミドゲル電気泳動により測定したときに約41キロド ルトンの分子量を有するDNAセグメント。 4.請求項3に記載のDNAセグメントであって、FokI制限エンドヌクレ アーゼのアミノ酸1〜382をコードするDNAセグメント。 5.IIS型エンドヌクレアーゼの触媒ドメインをコードする単離されたDN Aセグメントであって、前記IIS型エンドヌクレアーゼの開裂活性を含むDN Aセグメント。 6.請求項5に記載のDNAセグメントであって、前記IIS型エンドヌクレ アーゼがFokI制限エンドヌクレアーゼであるDNAセグメント。 7.請求項6に記載のDNAセグメントであって、前記コードされるタンパク が、SDSポリアクリルアミドゲル電気泳動により測定したときに約25キロド ルトンの分子量を有するDNAセグメント。 8.請求項7に記載のDNAセグメントであって、FokIエンドヌクレアー ゼのアミノ酸383〜578をコードするDNAセグメント。 9.実質的にFokI制限エンドヌクレアーゼのN末端からなる単離されたタ ンパクであって、前記エンドヌクレアーゼの配列特異的認識活性を有するタンパ ク。 10.請求項9に記載のタンパクであって、FokI制限エンドヌクレアーゼ のアミノ酸1〜382であるタンパク。 11.実質的にFokI制限エンドヌクレアーゼのC末端からなる単離された タンパクであって、前記エンドヌクレアーゼの開裂活性を有するタンパク。 12.請求項11に記載のタンパクであって、FokI制限エンドヌクレアー ゼのアミノ酸383〜578であるタンパク。 13.DNA構築物であって: (i)IIS型エンドヌクレアーゼの開裂活性を含むIIS型エンドヌクレ アーゼの触媒ドメインをコードする第一のDNAセグメントと; (ii)前記IIS型エンドヌクレアーゼの認識ドメイン以外の配列特異的認 識ドメインをコードする第二のDNAセグメントと; (iii)ベクターとを具備し、 前記第一のDNAセグメントおよび前記第二のDNAセグメントは、単一のタ ンパクが産生されるように、前記ベクターに対して動作可能に連結されているD NA構築物。 14.請求項13に記載のDNA構築物であって、前記IIS型エンドヌクレ アーゼがFokI制限エンドヌクレアーゼであるDNA構築物。 15.請求項14に記載のDNA構築物であって、前記認識ドメインが、ジン クフィンガーモチーフ;ホメオドメインモチーフ;リプレッサのDNA結合性ド メイン;POUドメインモチーフ(真核転写レギュレータ);発癌遺伝子のDN A結合性ドメイン;および>6塩基対を認識する他の天然に存在する配列特異的 なDNA結合性タンパクからなる群から選択されるDNA構築物。 16.請求項15に記載のDNA構築物であって、前記認識ドメインがUbx のホメオドメインであるDNA構築物。 17.原核細胞であって: (i)IIS型エンドヌクレアーゼの開裂活性を含むIIS型エンドヌクレ アーゼの触媒ドメインをコードする第一のDNAセグメントと; (ii)前記IIS型エンドヌクレアーゼの認識ドメイン以外の配列特異的認 識ドメインをコードする第二のDNAセグメントと; (iii)ベクターとを含んでおり、 前記第一のDNAセグメントおよび前記第二のDNAセグメントは、単一のタ ンパクが産生されるように、前記ベクターに対して動作可能に連結されているD NA構築物。 18.請求項17に記載の原核細胞であって、前記第一のDNAセグメントが FokIの触媒ドメイン(FN)をコー ドし、前記第二のDNAセグメントがUbxのホメオドメインをコードする原核 細胞。 19.IIS型エンドヌクレアーゼの触媒ドメインを含むハイブリッド制限酵 素であって、前記IIS型エンドヌクレアーゼ以外の酵素の認識ドメインに対し て共有結合的に結合された前記IIS型エンドヌクレアーゼの開裂活性を含んだ ハイブリッド制限酵素。 20.請求項19に記載のハイブリッド制限酵素であって、前記認識ドメイン (前記ハイブリッド制限酵素の一部なす)が、ジンクフィンガーモチーフ;ホメ オドメインモチーフ;POUドメインモチーフ;リプレッサのDNA結合性ドメ イン;発癌遺伝子のDNA結合性ドメイン;および>6塩基対を認識する他の天 然に存在する配列特異的なDNA結合性タンパクからなる群から選択されるハイ ブリッド制限酵素。 21.請求項20に記載のハイブリッド制限酵素であって、前記認識ドメイン がUbxのホメオドメインであるハイブリッド制限酵素。 22.請求項21に記載のハイブリッド制限酵素であって、前記II型エンド ヌクレアーゼがFokI制限エンドヌクレアーゼであり、前記ハイブリッド酵素 がUbx−FNであるハイブリッド制限酵素。 23. DNA構築物であって: (i)IIS型エンドヌクレアーゼの開裂活性を含んだIIS型エンドヌク レアーゼの触媒ドメインをコードする第一のDNAセグメントと; (ii)前記IIS型エンドヌクレアーゼの認識ドメイン以外の配列特異的認 識ドメインをコードする第二のDNAセグメントと; (iii)前記第一のDNAセグメントおよび前記第二のDNAセグメントの 間に挿入された、1以上のコドンを含む第三のDNAセグメントと; (iv)ベクターとを含み、 前記第一のDNAセグメント、前記第二のDNAセグメントおよび前記第三の DNAセグメントは、単一のタンパクが産生されるように、前記ベクターに対し て動作可能に連結されているDNA構築物。 24.請求項23に記載のDNA構築物であって、前記IIS型エンドヌクレ アーゼがFokI制限エンドヌクレアーゼであるDNA構築物。 25.請求項24に記載のDNA構築物であって、前記第三のDNAセグメン トが実質的に4コドンからなるDNA構築物。 26.請求項25に記載のDNA構築物であって、前記第三のDNAセグメン トの前記4コドンが、前記エンドヌクレアーゼをコードする遺伝子のヌクレオチ ド1152に挿入されているDNA構築物。 27.請求項24に記載のDNA構築物であって、前記第三のDNAセグメン トが実質的に7コドンからなるDNAセグメント。 28.請求項24に記載のDNA構築物であって、前記認 識ドメインが、ジンクフィンガーモチーフ;ホメオドメインモチーフ;POUド メインモチーフ;リプレッサのDNA結合性ドメイン;発癌遺伝子のDNA結合 性ドメイン;および>6塩基対を認識する他の天然に存在する配列特異的なDN A結合性タンパクからなる群から選択されるDNA構築物。 30.原核細胞であって: (i)IIS型エンドヌクレアーゼの開裂活性を含んだIIS型エンドヌク レアーゼの触媒ドメインをコードする第一のDNAセグメントと; (ii)前記IIS型エンドヌクレアーゼの認識ドメイン以外の配列特異的認 識ドメインをコードする第二のDNAセグメントと; (iii)前記第一のDNAセグメントおよび前記第二のDNAセグメントの 間に挿入された、1以上のコドンを含む第三のDNAセグメントと; (iv)ベクターとを含み、 前記第一のDNAセグメント、前記第二のDNAセグメントおよび前記第三の DNAセグメントは、単一のタンパクが産生されるように、前記ベクターに対し て動作可能に連結されているDNA構築物。 31.請求項30に記載の原核細胞であって、前記第三のDNAセグメントが 実質的に4コドンからなる細胞。 32.請求項30に記載の原核細胞であって、前記第三のDNAセグメントが 実質的に7コドンからなる細胞。 33.請求項30の原核細胞によって産生された、単離さ れたIIS型ハイブリッドエンドヌクレアーゼ。 34.IIS型エンドヌクレアーゼのN末端(該II型エンドヌクレアーゼの 配列特異的認識活性を含む)をコードする単離されたDNAセグメントであって 、前記II型エンドヌクレアーゼはFokI制限エンドヌクレアーゼであり、且 つ前記N末端はSDS−ポリアクリルアミドゲル電気泳動で測定したときに約4 1キロドルトンの分子量を有するDNAセグメント。 35.IIS型エンドヌクレアーゼのC末端(該II型エンドヌクレアーゼの 開裂活性を含む)をコードする単離されたDNAセグメントであって、前記II 型エンドヌクレアーゼはFokI制限エンドヌクレアーゼであり、且つ前記C末 端はSDS−ポリアクリルアミドゲル電気泳動で測定したときに約25キロドル トンの分子量を有するDNAセグメント。 36.実質的にFokI制限エンドヌクレアーゼのN末端からなる単離された タンパクであって、該タンパクは前記エンドヌクレアーゼの配列特異的認識活性 を有し、且つ該タンパクはFokI制限エンドヌクレアーゼのアミノ酸1〜38 2であるタンパク。 37.実質的にFokI制限エンドヌクレアーゼのC末端からなる単離された タンパクであって、該タンパクは前記エンドヌクレアーゼのヌクレアーゼ活性を 有し、且つ該タンパクはFokI制限エンドヌクレアーゼのアミノ酸383〜5 87であるタンパク。
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US08/126,564 US5436150A (en) | 1992-04-03 | 1993-09-27 | Functional domains in flavobacterium okeanokoities (foki) restriction endonuclease |
PCT/US1994/009143 WO1995009233A1 (en) | 1993-09-27 | 1994-08-23 | Functional domains in flavobacterium okeanokoites (foki) restriction endonuclease |
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JP2007230093A Withdrawn JP2008005851A (ja) | 1993-09-27 | 2007-09-05 | フラボバクテリウム・オケアノコイテス(foki)制限エンドヌクレアーゼにおける機能ドメイン |
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AU (1) | AU687435B2 (ja) |
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Families Citing this family (367)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US5436150A (en) * | 1992-04-03 | 1995-07-25 | The Johns Hopkins University | Functional domains in flavobacterium okeanokoities (foki) restriction endonuclease |
US5916794A (en) * | 1992-04-03 | 1999-06-29 | Johns Hopkins University | Methods for inactivating target DNA and for detecting conformational change in a nucleic acid |
US6140466A (en) | 1994-01-18 | 2000-10-31 | The Scripps Research Institute | Zinc finger protein derivatives and methods therefor |
US20050084885A1 (en) * | 1994-01-18 | 2005-04-21 | The Scripps Research Institute | Zinc finger protein derivatives and methods therefor |
GB9824544D0 (en) | 1998-11-09 | 1999-01-06 | Medical Res Council | Screening system |
JP4118327B2 (ja) | 1994-08-20 | 2008-07-16 | ゲンダック・リミテッド | Dna認識のための結合タンパク質におけるまたはそれに関連する改良 |
AU719001B2 (en) * | 1994-12-29 | 2000-05-04 | Massachusetts Institute Of Technology | Chimeric DNA-binding proteins |
WO1996040882A1 (en) * | 1995-06-07 | 1996-12-19 | The Ohio State University | Artificial restriction endonuclease |
US6261797B1 (en) | 1996-01-29 | 2001-07-17 | Stratagene | Primer-mediated polynucleotide synthesis and manipulation techniques |
GB9710809D0 (en) | 1997-05-23 | 1997-07-23 | Medical Res Council | Nucleic acid binding proteins |
US6444421B1 (en) | 1997-11-19 | 2002-09-03 | The United States Of America As Represented By The Department Of Health And Human Services | Methods for detecting intermolecular interactions in vivo and in vitro |
US6410248B1 (en) | 1998-01-30 | 2002-06-25 | Massachusetts Institute Of Technology | General strategy for selecting high-affinity zinc finger proteins for diverse DNA target sites |
ATE466952T1 (de) * | 1998-03-02 | 2010-05-15 | Massachusetts Inst Technology | Poly-zinkfinger-proteine mit verbesserten linkern |
DE69932813D1 (de) | 1998-03-17 | 2006-09-28 | Gendaq Ltd | Nukleinsäurebindungsproteine |
US6453242B1 (en) | 1999-01-12 | 2002-09-17 | Sangamo Biosciences, Inc. | Selection of sites for targeting by zinc finger proteins and methods of designing zinc finger proteins to bind to preselected sites |
US7070934B2 (en) | 1999-01-12 | 2006-07-04 | Sangamo Biosciences, Inc. | Ligand-controlled regulation of endogenous gene expression |
US6534261B1 (en) | 1999-01-12 | 2003-03-18 | Sangamo Biosciences, Inc. | Regulation of endogenous gene expression in cells using zinc finger proteins |
US7013219B2 (en) | 1999-01-12 | 2006-03-14 | Sangamo Biosciences, Inc. | Regulation of endogenous gene expression in cells using zinc finger proteins |
US6599692B1 (en) | 1999-09-14 | 2003-07-29 | Sangamo Bioscience, Inc. | Functional genomics using zinc finger proteins |
WO2000046386A2 (en) | 1999-02-03 | 2000-08-10 | The Children's Medical Center Corporation | Gene repair involving the induction of double-stranded dna cleavage at a chromosomal target site |
JP2002535994A (ja) * | 1999-02-03 | 2002-10-29 | ザ チルドレンズ メディカル センター コーポレイション | 標的dnaのインビボ除去による遺伝子修復 |
US6794136B1 (en) | 2000-11-20 | 2004-09-21 | Sangamo Biosciences, Inc. | Iterative optimization in the design of binding proteins |
US20030104526A1 (en) * | 1999-03-24 | 2003-06-05 | Qiang Liu | Position dependent recognition of GNN nucleotide triplets by zinc fingers |
US7030215B2 (en) * | 1999-03-24 | 2006-04-18 | Sangamo Biosciences, Inc. | Position dependent recognition of GNN nucleotide triplets by zinc fingers |
JP5180417B2 (ja) * | 1999-04-28 | 2013-04-10 | ジェネンコー・インターナショナル・インク | 特異的に標的化された触媒性アンタゴニストおよびその使用 |
CA2387035A1 (en) | 1999-10-13 | 2001-04-19 | Sequenom, Inc. | Methods for generating databases and databases for identifying polymorphic genetic markers |
US20030207297A1 (en) * | 1999-10-13 | 2003-11-06 | Hubert Koster | Methods for generating databases and databases for identifying polymorphic genetic markers |
US20030190644A1 (en) | 1999-10-13 | 2003-10-09 | Andreas Braun | Methods for generating databases and databases for identifying polymorphic genetic markers |
DE60023936T2 (de) * | 1999-12-06 | 2006-05-24 | Sangamo Biosciences Inc., Richmond | Methoden zur verwendung von randomisierten zinkfingerprotein-bibliotheken zur identifizierung von genfunktionen |
AU2001226935B2 (en) * | 2000-01-24 | 2006-06-22 | Gendaq Limited | Nucleic acid binding polypeptides characterized by flexible linkers connected nucleic acid binding modules |
AU5077401A (en) | 2000-02-08 | 2001-08-20 | Sangamo Biosciences Inc | Cells for drug discovery |
AU5391401A (en) | 2000-04-28 | 2001-11-12 | Sangamo Biosciences Inc | Targeted modification of chromatin structure |
US6958214B2 (en) * | 2000-07-10 | 2005-10-25 | Sequenom, Inc. | Polymorphic kinase anchor proteins and nucleic acids encoding the same |
EP1303608A2 (en) * | 2000-07-21 | 2003-04-23 | Syngenta Participations AG | Zinc finger domain recognition code and uses thereof |
US20030082561A1 (en) * | 2000-07-21 | 2003-05-01 | Takashi Sera | Zinc finger domain recognition code and uses thereof |
US7067317B2 (en) * | 2000-12-07 | 2006-06-27 | Sangamo Biosciences, Inc. | Regulation of angiogenesis with zinc finger proteins |
CA2431308C (en) * | 2000-12-07 | 2010-04-13 | Sangamo Biosciences, Inc. | Regulation of angiogenesis with zinc finger proteins |
AU2002241946B2 (en) | 2001-01-22 | 2007-04-26 | Sangamo Therapeutics, Inc. | Modified zinc finger binding proteins |
EP2266396A3 (en) | 2001-09-24 | 2011-06-15 | Sangamo BioSciences, Inc. | Modulation of stem cells using zinc finger proteins |
US7262054B2 (en) * | 2002-01-22 | 2007-08-28 | Sangamo Biosciences, Inc. | Zinc finger proteins for DNA binding and gene regulation in plants |
CN100575485C (zh) | 2002-01-23 | 2009-12-30 | 犹他大学研究基金会 | 使用锌指核酸酶的定向染色体诱变 |
WO2009095742A1 (en) * | 2008-01-31 | 2009-08-06 | Cellectis | New i-crei derived single-chain meganuclease and uses thereof |
US20100151556A1 (en) * | 2002-03-15 | 2010-06-17 | Cellectis | Hybrid and single chain meganucleases and use thereof |
DK1485475T3 (da) * | 2002-03-15 | 2008-01-21 | Cellectis | Hybrid meganuklease og enkeltkædet maganuklease og brug deraf |
EP2368982A3 (en) * | 2002-03-21 | 2011-10-12 | Sangamo BioSciences, Inc. | Methods and compositions for using zinc finger endonucleases to enhance homologous recombination |
US7101697B2 (en) * | 2002-04-30 | 2006-09-05 | Charité—Universitätsmedizin Berlin | Restriction endonucleases, method of synthesis and use thereof |
AU2003228809A1 (en) | 2002-05-03 | 2003-11-17 | Sequenom, Inc. | Kinase anchor protein muteins, peptides thereof, and related methods |
CA2396345C (en) * | 2002-07-31 | 2007-04-10 | Rousseau Metal Inc. | Frontal latch handle assembly |
US7361635B2 (en) * | 2002-08-29 | 2008-04-22 | Sangamo Biosciences, Inc. | Simultaneous modulation of multiple genes |
US9447434B2 (en) * | 2002-09-05 | 2016-09-20 | California Institute Of Technology | Use of chimeric nucleases to stimulate gene targeting |
US7563600B2 (en) | 2002-09-12 | 2009-07-21 | Combimatrix Corporation | Microarray synthesis and assembly of gene-length polynucleotides |
US7820378B2 (en) * | 2002-11-27 | 2010-10-26 | Sequenom, Inc. | Fragmentation-based methods and systems for sequence variation detection and discovery |
EP3202899B1 (en) | 2003-01-28 | 2020-10-21 | Cellectis | Custom-made meganuclease and use thereof |
EP1618216A2 (en) * | 2003-04-25 | 2006-01-25 | Sequenom, Inc. | Fragmentation-based methods and systems for de novo sequencing |
US20120196370A1 (en) | 2010-12-03 | 2012-08-02 | Fyodor Urnov | Methods and compositions for targeted genomic deletion |
US7888121B2 (en) | 2003-08-08 | 2011-02-15 | Sangamo Biosciences, Inc. | Methods and compositions for targeted cleavage and recombination |
ES2808687T3 (es) | 2003-08-08 | 2021-03-01 | Sangamo Therapeutics Inc | Métodos y composiciones para escisión dirigida y recombinación |
US11311574B2 (en) | 2003-08-08 | 2022-04-26 | Sangamo Therapeutics, Inc. | Methods and compositions for targeted cleavage and recombination |
US8409861B2 (en) | 2003-08-08 | 2013-04-02 | Sangamo Biosciences, Inc. | Targeted deletion of cellular DNA sequences |
US9394565B2 (en) * | 2003-09-05 | 2016-07-19 | Agena Bioscience, Inc. | Allele-specific sequence variation analysis |
CA2539439C (en) | 2003-09-19 | 2012-10-23 | Sangamo Biosciences, Inc. | Engineered zinc finger proteins for regulation of gene expression |
PT2025756E (pt) | 2003-11-18 | 2011-09-28 | Bayer Bioscience Nv | Inserção direccionada de adn em plantas |
US7972854B2 (en) | 2004-02-05 | 2011-07-05 | Sangamo Biosciences, Inc. | Methods and compositions for targeted cleavage and recombination |
US7608394B2 (en) | 2004-03-26 | 2009-10-27 | Sequenom, Inc. | Methods and compositions for phenotype identification based on nucleic acid methylation |
WO2005098050A2 (en) * | 2004-03-26 | 2005-10-20 | Sequenom, Inc. | Base specific cleavage of methylation-specific amplification products in combination with mass analysis |
EP1802772A4 (en) * | 2004-09-10 | 2008-12-31 | Sequenom Inc | METHOD FOR NUCLEIC ACID SEQUENCE ANALYSIS WITH GREAT RANGE |
KR20070060115A (ko) | 2004-09-16 | 2007-06-12 | 상가모 바이오사이언스 인코포레이티드 | 단백질 생산을 위한 조성물 및 방법 |
JP2008523786A (ja) * | 2004-10-18 | 2008-07-10 | コドン デバイシズ インコーポレイテッド | 高忠実度合成ポリヌクレオチドのアセンブリ方法 |
US20070122817A1 (en) * | 2005-02-28 | 2007-05-31 | George Church | Methods for assembly of high fidelity synthetic polynucleotides |
JP5639336B2 (ja) | 2005-04-04 | 2014-12-10 | バイエル・クロップサイエンス・エヌ・ヴェーBayer Cropscience N.V. | 選ばれたdna配列を除去するための方法および手段 |
EP1913149A4 (en) | 2005-07-26 | 2009-08-05 | Sangamo Biosciences Inc | TARGETED INTEGRATION AND EXPRESSION OF EXOGENOUS NUCLEIC ACID SEQUENCES |
WO2009134714A2 (en) * | 2008-04-28 | 2009-11-05 | Precision Biosciences, Inc. | Fusion molecules of rationally-designed dna-binding proteins and effector domains |
WO2007047859A2 (en) | 2005-10-18 | 2007-04-26 | Precision Biosciences | Rationally-designed meganucleases with altered sequence specificity and dna-binding affinity |
WO2007060495A1 (en) * | 2005-10-25 | 2007-05-31 | Cellectis | I-crei homing endonuclease variants having novel cleavage specificity and use thereof |
US7627401B2 (en) | 2006-02-07 | 2009-12-01 | Glenbrook Associates, Inc. | System and method for remotely regulating the power consumption of an electric appliance |
WO2007136685A2 (en) * | 2006-05-19 | 2007-11-29 | Sangamo Biosciences, Inc. | Methods and compositions for inactivation of dihydrofolate reductase |
EP2206782A1 (en) | 2006-05-25 | 2010-07-14 | Sangamo BioSciences, Inc. | Methods and compositions for gene inactivation |
SI2049663T1 (sl) | 2006-08-11 | 2015-12-31 | Dow Agrosciences Llc | Homologna rekombinacija, posredovana z nukleazo s cinkovim prstom |
WO2008027558A2 (en) | 2006-08-31 | 2008-03-06 | Codon Devices, Inc. | Iterative nucleic acid assembly using activation of vector-encoded traits |
CA2664414C (en) | 2006-09-28 | 2016-07-12 | Bayer Bioscience N.V. | Methods and means for removal of a selected dna sequence |
EP2089427B1 (en) * | 2006-11-13 | 2014-07-30 | Sangamo BioSciences, Inc. | Zinc finger nuclease for targeting the human glucocorticoid receptor locus |
WO2008076290A2 (en) | 2006-12-14 | 2008-06-26 | Dow Agrosciences Llc | Optimized non-canonical zinc finger proteins |
WO2008130629A2 (en) * | 2007-04-19 | 2008-10-30 | Codon Devices, Inc. | Engineered nucleases and their uses for nucleic acid assembly |
US8110379B2 (en) | 2007-04-26 | 2012-02-07 | Sangamo Biosciences, Inc. | Targeted integration into the PPP1R12C locus |
EP2160467B1 (en) | 2007-06-05 | 2015-10-28 | Bayer CropScience NV | Methods and means for exact replacement of target dna in eukaryotic organisms |
EP2171052B1 (en) | 2007-07-12 | 2014-08-27 | Sangamo BioSciences, Inc. | Methods and compositions for inactivating alpha 1,6 fucosyltransferase (fut 8) gene expression |
CA2700231C (en) * | 2007-09-27 | 2018-09-18 | Sangamo Biosciences, Inc. | Rapid in vivo identification of biologically active nucleases |
DK2205749T3 (en) | 2007-09-27 | 2016-08-22 | Dow Agrosciences Llc | MODIFIED PROTEINS zinc finger, which target the 5-enolpyruvylshikimate-3-phosphate synthase genes |
US8563314B2 (en) | 2007-09-27 | 2013-10-22 | Sangamo Biosciences, Inc. | Methods and compositions for modulating PD1 |
US11235026B2 (en) | 2007-09-27 | 2022-02-01 | Sangamo Therapeutics, Inc. | Methods and compositions for modulating PD1 |
WO2009054985A1 (en) | 2007-10-25 | 2009-04-30 | Sangamo Biosciences, Inc. | Methods and compositions for targeted integration |
EP2215252A4 (en) * | 2007-12-07 | 2011-01-26 | Prec Biosciences Inc | MEGANUCLEASES DESIGNED RATIONALLY WITH IDENTIFICATION SEQUENCES FOUND IN HUMAN GENOME DNAASE HYPERSENSIVE REGIONS |
WO2009114321A2 (en) * | 2008-03-11 | 2009-09-17 | Precision Biosciencs, Inc. | Rationally-designed meganucleases for maize genome engineering |
US20100071083A1 (en) * | 2008-03-12 | 2010-03-18 | Smith James J | Temperature-dependent meganuclease activity |
AU2009238629C1 (en) | 2008-04-14 | 2015-04-30 | Sangamo Therapeutics, Inc. | Linear donor constructs for targeted integration |
WO2009146179A1 (en) | 2008-04-15 | 2009-12-03 | University Of Iowa Research Foundation | Zinc finger nuclease for the cftr gene and methods of use thereof |
AU2009258117B2 (en) | 2008-06-10 | 2014-10-09 | Sangamo Therapeutics, Inc. | Methods and compositions for generation of Bax- and Bak-deficient cell lines |
EP3211075B1 (en) * | 2008-07-14 | 2018-10-24 | Precision Biosciences, Inc. | Recognition sequences for i-crei-derived meganucleases and uses thereof |
WO2010019526A1 (en) * | 2008-08-14 | 2010-02-18 | Brent Lee | Dynamic filtration device using centrifugal force |
EP2313515B1 (en) | 2008-08-22 | 2015-03-04 | Sangamo BioSciences, Inc. | Methods and compositions for targeted single-stranded cleavage and targeted integration |
WO2010053518A2 (en) | 2008-10-29 | 2010-05-14 | Sangamo Biosciences, Inc. | Methods and compositions for inactivating glutamine synthetase gene expression |
US20110023159A1 (en) * | 2008-12-04 | 2011-01-27 | Sigma-Aldrich Co. | Ovine genome editing with zinc finger nucleases |
US20110023149A1 (en) * | 2008-12-04 | 2011-01-27 | Sigma-Aldrich Co. | Genomic editing of genes involved in tumor suppression in animals |
US20110023153A1 (en) * | 2008-12-04 | 2011-01-27 | Sigma-Aldrich Co. | Genomic editing of genes involved in alzheimer's disease |
US20110030072A1 (en) * | 2008-12-04 | 2011-02-03 | Sigma-Aldrich Co. | Genome editing of immunodeficiency genes in animals |
US20110023147A1 (en) * | 2008-12-04 | 2011-01-27 | Sigma-Aldrich Co. | Genomic editing of prion disorder-related genes in animals |
US20110023141A1 (en) * | 2008-12-04 | 2011-01-27 | Sigma-Aldrich Co. | Genomic editing of genes involved with parkinson's disease |
US20110023140A1 (en) * | 2008-12-04 | 2011-01-27 | Sigma-Aldrich Co. | Rabbit genome editing with zinc finger nucleases |
US20110023150A1 (en) * | 2008-12-04 | 2011-01-27 | Sigma-Aldrich Co. | Genome editing of genes associated with schizophrenia in animals |
US20110023156A1 (en) * | 2008-12-04 | 2011-01-27 | Sigma-Aldrich Co. | Feline genome editing with zinc finger nucleases |
US20110016539A1 (en) * | 2008-12-04 | 2011-01-20 | Sigma-Aldrich Co. | Genome editing of neurotransmission-related genes in animals |
US20110023146A1 (en) * | 2008-12-04 | 2011-01-27 | Sigma-Aldrich Co. | Genomic editing of genes involved in secretase-associated disorders |
US20110016540A1 (en) * | 2008-12-04 | 2011-01-20 | Sigma-Aldrich Co. | Genome editing of genes associated with trinucleotide repeat expansion disorders in animals |
US20110016546A1 (en) * | 2008-12-04 | 2011-01-20 | Sigma-Aldrich Co. | Porcine genome editing with zinc finger nucleases |
US20110023158A1 (en) * | 2008-12-04 | 2011-01-27 | Sigma-Aldrich Co. | Bovine genome editing with zinc finger nucleases |
US20110023139A1 (en) * | 2008-12-04 | 2011-01-27 | Sigma-Aldrich Co. | Genomic editing of genes involved in cardiovascular disease |
US20110016543A1 (en) * | 2008-12-04 | 2011-01-20 | Sigma-Aldrich Co. | Genomic editing of genes involved in inflammation |
US20110023154A1 (en) * | 2008-12-04 | 2011-01-27 | Sigma-Aldrich Co. | Silkworm genome editing with zinc finger nucleases |
US20110023152A1 (en) * | 2008-12-04 | 2011-01-27 | Sigma-Aldrich Co. | Genome editing of cognition related genes in animals |
US20110023145A1 (en) * | 2008-12-04 | 2011-01-27 | Sigma-Aldrich Co. | Genomic editing of genes involved in autism spectrum disorders |
US20110016541A1 (en) * | 2008-12-04 | 2011-01-20 | Sigma-Aldrich Co. | Genome editing of sensory-related genes in animals |
US20110023148A1 (en) * | 2008-12-04 | 2011-01-27 | Sigma-Aldrich Co. | Genome editing of addiction-related genes in animals |
US20110016542A1 (en) * | 2008-12-04 | 2011-01-20 | Sigma-Aldrich Co. | Canine genome editing with zinc finger nucleases |
US20110023143A1 (en) * | 2008-12-04 | 2011-01-27 | Sigma-Aldrich Co. | Genomic editing of neurodevelopmental genes in animals |
WO2010065123A1 (en) | 2008-12-04 | 2010-06-10 | Sangamo Biosciences, Inc. | Genome editing in rats using zinc-finger nucleases |
US20110023157A1 (en) * | 2008-12-04 | 2011-01-27 | Sigma-Aldrich Co. | Equine genome editing with zinc finger nucleases |
US20110023144A1 (en) * | 2008-12-04 | 2011-01-27 | Sigma-Aldrich Co. | Genomic editing of genes involved in amyotrophyic lateral sclerosis disease |
US20110023151A1 (en) * | 2008-12-04 | 2011-01-27 | Sigma-Aldrich Co. | Genome editing of abc transporters |
AR074783A1 (es) | 2008-12-17 | 2011-02-09 | Dow Agrosciences Llc | Metodos y composiciones para expresar uno o mas productos de un acido nucleico exogeno integrado al locus zp15 de una celula vegetal |
EP2206723A1 (en) | 2009-01-12 | 2010-07-14 | Bonas, Ulla | Modular DNA-binding domains |
US20110239315A1 (en) | 2009-01-12 | 2011-09-29 | Ulla Bonas | Modular dna-binding domains and methods of use |
EP2419511B1 (en) | 2009-04-09 | 2018-01-17 | Sangamo Therapeutics, Inc. | Targeted integration into stem cells |
US8772008B2 (en) * | 2009-05-18 | 2014-07-08 | Sangamo Biosciences, Inc. | Methods and compositions for increasing nuclease activity |
JP5798116B2 (ja) | 2009-06-30 | 2015-10-21 | サンガモ バイオサイエンシーズ, インコーポレイテッド | 生物活性のあるヌクレアーゼの迅速なスクリーニングおよびヌクレアーゼ修飾細胞の単離 |
US20120171771A1 (en) | 2009-07-08 | 2012-07-05 | Cellular Dynamics International, Inc. | Modified ips cells having a mutant form of a human immunodeficiency virus (hiv) cellular entry gene |
EP2461819A4 (en) * | 2009-07-28 | 2013-07-31 | Sangamo Biosciences Inc | METHODS AND COMPOSITIONS FOR TREATING TRI-NUCLEOTIDE REPEAT DISORDERS |
CA2770312A1 (en) | 2009-08-11 | 2011-02-17 | Sangamo Biosciences, Inc. | Organisms homozygous for targeted modification |
EP2722392B1 (en) * | 2009-10-22 | 2017-11-22 | Dow AgroSciences LLC | Engineered zinc finger proteins targeting plant genes involved in fatty acid biosynthesis |
WO2011056872A2 (en) | 2009-11-03 | 2011-05-12 | Gen9, Inc. | Methods and microfluidic devices for the manipulation of droplets in high fidelity polynucleotide assembly |
US8956828B2 (en) | 2009-11-10 | 2015-02-17 | Sangamo Biosciences, Inc. | Targeted disruption of T cell receptor genes using engineered zinc finger protein nucleases |
WO2011066185A1 (en) | 2009-11-25 | 2011-06-03 | Gen9, Inc. | Microfluidic devices and methods for gene synthesis |
EP2510096B2 (en) | 2009-12-10 | 2018-02-07 | Regents of the University of Minnesota | Tal effector-mediated dna modification |
US9217144B2 (en) | 2010-01-07 | 2015-12-22 | Gen9, Inc. | Assembly of high fidelity polynucleotides |
CN102812034B (zh) * | 2010-01-22 | 2016-08-03 | 陶氏益农公司 | 靶向基因组改造 |
WO2011100058A1 (en) * | 2010-02-09 | 2011-08-18 | Sangamo Biosciences, Inc. | Targeted genomic modification with partially single-stranded donor molecules |
JP5922095B2 (ja) | 2010-03-29 | 2016-05-24 | ザ・トラステイーズ・オブ・ザ・ユニバーシテイ・オブ・ペンシルベニア | 薬理学的に誘導される導入遺伝子アブレーション系 |
US9315825B2 (en) | 2010-03-29 | 2016-04-19 | The Trustees Of The University Of Pennsylvania | Pharmacologically induced transgene ablation system |
SG185367A1 (en) | 2010-04-26 | 2012-12-28 | Sangamo Biosciences Inc | Genome editing of a rosa locus using zinc-finger nucleases |
JP5898179B2 (ja) | 2010-05-03 | 2016-04-06 | サンガモ バイオサイエンシーズ, インコーポレイテッド | ジンクフィンガーモジュールを連結するための組成物 |
CA2798988C (en) | 2010-05-17 | 2020-03-10 | Sangamo Biosciences, Inc. | Tal-effector (tale) dna-binding polypeptides and uses thereof |
US9593317B2 (en) | 2010-06-09 | 2017-03-14 | Bayer Cropscience Nv | Methods and means to modify a plant genome at a nucleotide sequence commonly used in plant genome engineering |
WO2011154159A1 (en) | 2010-06-09 | 2011-12-15 | Bayer Bioscience N.V. | Methods and means to modify a plant genome at a nucleotide sequence commonly used in plant genome engineering |
JP6050230B2 (ja) | 2010-07-21 | 2016-12-21 | サンガモ バイオサイエンシーズ, インコーポレイテッド | Hla遺伝子座の修飾のための方法及び組成物 |
EP3489359A1 (en) | 2010-07-23 | 2019-05-29 | Sigma Aldrich Co. LLC | Genome editing using targeting endonucleases and single-stranded nucleic acids |
EP3511420B1 (en) | 2010-09-27 | 2021-04-07 | Sangamo Therapeutics, Inc. | Compositions for inhibiting viral entry into cells |
CA2814143C (en) | 2010-10-12 | 2020-09-08 | The Children's Hospital Of Philadelphia | Methods and compositions for treating hemophilia b |
WO2012064975A1 (en) | 2010-11-12 | 2012-05-18 | Gen9, Inc. | Protein arrays and methods of using and making the same |
JP6118725B2 (ja) | 2010-11-12 | 2017-04-19 | ジェン9・インコーポレイテッドGen9,INC. | 核酸合成のための方法およびデバイス |
WO2012092379A2 (en) | 2010-12-29 | 2012-07-05 | Sigma-Aldrich Co. Llc | Cells having disrupted expression of proteins involved in adme and toxicology processes |
WO2012094132A1 (en) | 2011-01-05 | 2012-07-12 | Sangamo Biosciences, Inc. | Methods and compositions for gene correction |
WO2012168124A1 (en) | 2011-06-06 | 2012-12-13 | Bayer Cropscience Nv | Methods and means to modify a plant genome at a preselected site |
ES2671733T3 (es) | 2011-06-30 | 2018-06-08 | Sigma Aldrich Co. Llc | Células deficientes en ácido CMP-N-acetilneuramínico hidroxilasa y/o glucoproteína alfa-1,3-galactosil transferasa |
US9161995B2 (en) | 2011-07-25 | 2015-10-20 | Sangamo Biosciences, Inc. | Methods and compositions for alteration of a cystic fibrosis transmembrane conductance regulator (CFTR) gene |
AU2012299691B2 (en) | 2011-08-22 | 2015-01-29 | BASF Agricultural Solutions Seed US LLC | Methods and means to modify a plant genome |
LT3594340T (lt) | 2011-08-26 | 2021-10-25 | Gen9, Inc. | Kompozicijos ir būdai, skirti nukleorūgščių didelio tikslumo sąrankai |
EP3498833B1 (en) | 2011-09-21 | 2023-08-16 | Sangamo Therapeutics, Inc. | Methods and compositions for regulation of transgene expression |
US20140283819A1 (en) | 2011-10-12 | 2014-09-25 | Bayer Cropscience Ag | Plants with decreased activity of a starch dephosphorylating enzyme |
AU2012323042B2 (en) | 2011-10-12 | 2015-01-15 | Bayer Cropscience Ag | Plants with decreased activity of a starch dephosphorylating enzyme |
US9222105B2 (en) | 2011-10-27 | 2015-12-29 | Sangamo Biosciences, Inc. | Methods and compositions for modification of the HPRT locus |
JP6144691B2 (ja) | 2011-11-16 | 2017-06-07 | サンガモ セラピューティクス, インコーポレイテッド | 修飾されたdna結合タンパク質およびその使用 |
ES2733248T3 (es) | 2012-01-11 | 2019-11-28 | Sigma Aldrich Co Llc | Producción de proteínas recombinantes con glicoformas simples |
MX359327B (es) | 2012-02-29 | 2018-09-25 | Sangamo Biosciences Inc | Composiciones y sus usos para tratar y prevenir la enfermedad de huntington. |
US9150853B2 (en) | 2012-03-21 | 2015-10-06 | Gen9, Inc. | Methods for screening proteins using DNA encoded chemical libraries as templates for enzyme catalysis |
CA2871008C (en) | 2012-04-23 | 2022-11-22 | Bayer Cropscience Nv | Targeted genome engineering in plants |
CA2871505C (en) | 2012-04-24 | 2021-10-12 | Gen9, Inc. | Methods for sorting nucleic acids and multiplexed preparative in vitro cloning |
US9523098B2 (en) | 2012-05-02 | 2016-12-20 | Dow Agrosciences Llc | Targeted modification of malate dehydrogenase |
WO2013169802A1 (en) | 2012-05-07 | 2013-11-14 | Sangamo Biosciences, Inc. | Methods and compositions for nuclease-mediated targeted integration of transgenes |
US11120889B2 (en) | 2012-05-09 | 2021-09-14 | Georgia Tech Research Corporation | Method for synthesizing a nuclease with reduced off-site cleavage |
KR20150023670A (ko) | 2012-06-12 | 2015-03-05 | 제넨테크, 인크. | 조건적 녹아웃 대립유전자의 생성 방법 및 이를 위한 조성물 |
US20150225734A1 (en) | 2012-06-19 | 2015-08-13 | Regents Of The University Of Minnesota | Gene targeting in plants using dna viruses |
AU2013280661A1 (en) | 2012-06-25 | 2015-01-22 | Gen9, Inc. | Methods for nucleic acid assembly and high throughput sequencing |
WO2014011901A2 (en) | 2012-07-11 | 2014-01-16 | Sangamo Biosciences, Inc. | Methods and compositions for delivery of biologics |
US10648001B2 (en) | 2012-07-11 | 2020-05-12 | Sangamo Therapeutics, Inc. | Method of treating mucopolysaccharidosis type I or II |
AU2013289206B2 (en) | 2012-07-11 | 2018-08-09 | Sangamo Therapeutics, Inc. | Methods and compositions for the treatment of lysosomal storage diseases |
MX367081B (es) | 2012-08-29 | 2019-08-05 | Sangamo Biosciences Inc | Modificación genética mediada por nucleasas para usarse en el tratamiento de una condición genética. |
US9937205B2 (en) | 2012-09-04 | 2018-04-10 | The Trustees Of The University Of Pennsylvania | Inhibition of diacylglycerol kinase to augment adoptive T cell transfer |
CN105264067B (zh) | 2012-09-07 | 2020-11-10 | 美国陶氏益农公司 | Fad3性能基因座及相应的能够诱导靶向断裂的靶位点特异性结合蛋白 |
UA118090C2 (uk) | 2012-09-07 | 2018-11-26 | ДАУ АГРОСАЙЄНСІЗ ЕлЕлСі | Спосіб інтегрування послідовності нуклеїнової кислоти, що представляє інтерес, у ген fad2 у клітині сої та специфічний для локусу fad2 білок, що зв'язується, здатний індукувати спрямований розрив |
HUE050797T2 (hu) | 2012-10-10 | 2021-01-28 | Sangamo Therapeutics Inc | T-sejt módosító vegyületek és alkalmazásaik |
CN104968193B (zh) | 2012-11-01 | 2021-02-09 | 塞尔克蒂斯股份有限公司 | 用于生成治疗性蛋白质的植物 |
AR093980A1 (es) | 2012-12-13 | 2015-07-01 | Dow Agrosciences Llc | Genes de precision que tienen como objetivo un locus particular en el maiz |
WO2014096972A2 (en) | 2012-12-21 | 2014-06-26 | Cellectis | Potatoes with reduced cold-induced sweetening |
AU2014207618A1 (en) | 2013-01-16 | 2015-08-06 | Emory University | Cas9-nucleic acid complexes and uses related thereto |
US10113162B2 (en) | 2013-03-15 | 2018-10-30 | Cellectis | Modifying soybean oil composition through targeted knockout of the FAD2-1A/1B genes |
CN113563476A (zh) | 2013-03-15 | 2021-10-29 | 通用医疗公司 | 遗传和表观遗传调节蛋白至特定基因组基因座的rna引导的靶向 |
US10760064B2 (en) | 2013-03-15 | 2020-09-01 | The General Hospital Corporation | RNA-guided targeting of genetic and epigenomic regulatory proteins to specific genomic loci |
JP6346266B2 (ja) | 2013-03-21 | 2018-06-20 | サンガモ セラピューティクス, インコーポレイテッド | 操作されたジンクフィンガータンパク質ヌクレアーゼを使用するt細胞受容体遺伝子の標的化された破壊 |
CN105121650A (zh) | 2013-04-02 | 2015-12-02 | 拜尔作物科学公司 | 真核生物中的靶向基因组工程 |
KR102192599B1 (ko) | 2013-04-05 | 2020-12-18 | 다우 아그로사이언시즈 엘엘씨 | 식물의 게놈 내의 외인성 서열의 통합을 위한 방법 및 조성물 |
WO2014186435A2 (en) | 2013-05-14 | 2014-11-20 | University Of Georgia Research Foundation, Inc. | Compositions and methods for reducing neointima formation |
CN116083487A (zh) | 2013-05-15 | 2023-05-09 | 桑格摩生物治疗股份有限公司 | 用于治疗遗传病状的方法和组合物 |
US10011850B2 (en) | 2013-06-21 | 2018-07-03 | The General Hospital Corporation | Using RNA-guided FokI Nucleases (RFNs) to increase specificity for RNA-Guided Genome Editing |
EP3039136B8 (en) | 2013-08-28 | 2020-12-16 | Sangamo Therapeutics, Inc. | Compositions for linking dna-binding domains and cleavage domains |
RU2675824C2 (ru) | 2013-09-11 | 2018-12-25 | Игл Байолоджикс, Инк. | Жидкие белковые составы, содержащие ионные жидкости |
AU2014337248B2 (en) | 2013-10-17 | 2020-09-24 | Sangamo Therapeutics, Inc. | Delivery methods and compositions for nuclease-mediated genome engineering |
BR102014027466B1 (pt) | 2013-11-04 | 2022-09-27 | Dow Agrosciences Llc | Molécula de ácido nucleico recombinante, método para produzir uma célula vegetal transgênica e usos de uma planta de soja, parte de planta de soja ou célula de planta de soja transgênica |
AU2014341927B2 (en) | 2013-11-04 | 2017-12-14 | Corteva Agriscience Llc | Optimal maize loci |
MX364662B (es) | 2013-11-04 | 2019-05-03 | Dow Agrosciences Llc | Óptimos loci de maíz. |
CN105934524A (zh) | 2013-11-11 | 2016-09-07 | 桑格摩生物科学股份有限公司 | 用于治疗亨廷顿氏病的方法和组合物 |
PT3068881T (pt) | 2013-11-13 | 2019-05-31 | Childrens Medical Center | Regulação da expressão de genes mediada por nucleases |
EP2878667A1 (en) | 2013-11-29 | 2015-06-03 | Institut Pasteur | TAL effector means useful for partial or full deletion of DNA tandem repeats |
JP6535684B2 (ja) | 2013-12-09 | 2019-06-26 | サンガモ セラピューティクス, インコーポレイテッド | ゲノム操作のための方法および組成物 |
RS60514B1 (sr) | 2014-02-03 | 2020-08-31 | Sangamo Therapeutics Inc | Postupci i sastavi za tretman beta talasemije |
DK3102702T3 (da) | 2014-02-05 | 2019-06-17 | Fraunhofer Ges Forschung | Fejlfri sekvensering af DNA |
SG10201807208RA (en) | 2014-03-04 | 2018-09-27 | Sigma Aldrich Co Llc | Viral resistant cells and uses thereof |
CN106459894B (zh) | 2014-03-18 | 2020-02-18 | 桑格摩生物科学股份有限公司 | 用于调控锌指蛋白表达的方法和组合物 |
EP3134729A1 (en) | 2014-04-22 | 2017-03-01 | Q-State Biosciences, Inc. | Analysis of compounds for pain and sensory disorders |
WO2015164748A1 (en) | 2014-04-24 | 2015-10-29 | Sangamo Biosciences, Inc. | Engineered transcription activator like effector (tale) proteins |
US11918695B2 (en) | 2014-05-09 | 2024-03-05 | Yale University | Topical formulation of hyperbranched polymer-coated particles |
WO2015172153A1 (en) | 2014-05-09 | 2015-11-12 | Yale University | Topical formulation of hyperbranched polyglycerol-coated particles thereof |
WO2015175642A2 (en) | 2014-05-13 | 2015-11-19 | Sangamo Biosciences, Inc. | Methods and compositions for prevention or treatment of a disease |
WO2015184262A1 (en) | 2014-05-30 | 2015-12-03 | The Board Of Trustees Of The Leland Stanford Junior University | Compositions and methods of delivering treatments for latent viral infections |
US9970001B2 (en) | 2014-06-05 | 2018-05-15 | Sangamo Therapeutics, Inc. | Methods and compositions for nuclease design |
CA2952906A1 (en) | 2014-06-20 | 2015-12-23 | Cellectis | Potatoes with reduced granule-bound starch synthase |
WO2016011029A2 (en) | 2014-07-14 | 2016-01-21 | Washington State University | Nanos knock-out that ablates germline cells |
JP7113618B2 (ja) | 2014-07-15 | 2022-08-05 | ジュノー セラピューティクス インコーポレイテッド | 養子細胞療法用の操作された細胞 |
WO2016025759A1 (en) | 2014-08-14 | 2016-02-18 | Shen Yuelei | Dna knock-in system |
SG11201702134RA (en) | 2014-09-16 | 2017-04-27 | Sangamo Therapeutics Inc | Methods and compositions for nuclease-mediated genome engineering and correction in hematopoietic stem cells |
KR102630014B1 (ko) | 2014-10-01 | 2024-01-25 | 더 제너럴 하스피탈 코포레이션 | 뉴클레아제-유도 상동성-지정 복구의 효율 증가 방법 |
SG11201702614SA (en) | 2014-10-01 | 2017-04-27 | Eagle Biolog Inc | Polysaccharide and nucleic acid formulations containing viscosity-lowering agents |
US10889834B2 (en) | 2014-12-15 | 2021-01-12 | Sangamo Therapeutics, Inc. | Methods and compositions for enhancing targeted transgene integration |
EP3247366A4 (en) | 2015-01-21 | 2018-10-31 | Sangamo Therapeutics, Inc. | Methods and compositions for identification of highly specific nucleases |
US10048275B2 (en) | 2015-03-13 | 2018-08-14 | Q-State Biosciences, Inc. | Cardiotoxicity screening methods |
EP4335918A3 (en) | 2015-04-03 | 2024-04-17 | Dana-Farber Cancer Institute, Inc. | Composition and methods of genome editing of b-cells |
EP3286322A1 (en) | 2015-04-21 | 2018-02-28 | Novartis AG | Rna-guided gene editing system and uses thereof |
DK3289080T3 (da) | 2015-04-30 | 2021-11-08 | Univ Columbia | Genterapi til autosomalt dominante sygdomme |
CA2986583A1 (en) | 2015-05-21 | 2016-11-24 | Q-State Biosciences, Inc. | Optogenetics microscope |
WO2016196282A1 (en) | 2015-05-29 | 2016-12-08 | Agenovir Corporation | Compositions and methods for cell targeted hpv treatment |
MA43344A (fr) | 2015-05-29 | 2018-04-11 | Juno Therapeutics Inc | Composition et procédés de régulation des interactions inhibitrices dans les cellules génétiquement modifiées |
US10117911B2 (en) | 2015-05-29 | 2018-11-06 | Agenovir Corporation | Compositions and methods to treat herpes simplex virus infections |
US9957501B2 (en) | 2015-06-18 | 2018-05-01 | Sangamo Therapeutics, Inc. | Nuclease-mediated regulation of gene expression |
US10450585B2 (en) | 2015-07-13 | 2019-10-22 | Sangamo Therapeutics, Inc. | Delivery methods and compositions for nuclease-mediated genome engineering |
MA42895A (fr) | 2015-07-15 | 2018-05-23 | Juno Therapeutics Inc | Cellules modifiées pour thérapie cellulaire adoptive |
US10091975B2 (en) | 2015-08-06 | 2018-10-09 | The Curators Of The University Of Missouri | Pathogen-resistant animals having modified CD163 genes |
US9512446B1 (en) | 2015-08-28 | 2016-12-06 | The General Hospital Corporation | Engineered CRISPR-Cas9 nucleases |
US9926546B2 (en) | 2015-08-28 | 2018-03-27 | The General Hospital Corporation | Engineered CRISPR-Cas9 nucleases |
US10837024B2 (en) | 2015-09-17 | 2020-11-17 | Cellectis | Modifying messenger RNA stability in plant transformations |
WO2017106528A2 (en) | 2015-12-18 | 2017-06-22 | Sangamo Biosciences, Inc. | Targeted disruption of the t cell receptor |
IL297018A (en) | 2015-12-18 | 2022-12-01 | Sangamo Therapeutics Inc | Directed cleavage of cell mhc receptor |
ES2895430T3 (es) | 2016-01-15 | 2022-02-21 | Univ Minnesota | Métodos y composiciones para el tratamiento de enfermedad neurológica |
KR20180101442A (ko) | 2016-02-02 | 2018-09-12 | 상가모 테라퓨틱스, 인코포레이티드 | Dna-결합 도메인 및 절단 도메인을 연결시키기 위한 조성물 |
EP3410843A1 (en) | 2016-02-02 | 2018-12-12 | Cellectis | Modifying soybean oil composition through targeted knockout of the fad3a/b/c genes |
WO2017143061A1 (en) | 2016-02-16 | 2017-08-24 | Yale University | Compositions and methods for treatment of cystic fibrosis |
JP2019508037A (ja) | 2016-02-16 | 2019-03-28 | イェール ユニバーシティーYale Universit | 標的化遺伝子編集を増強するための組成物およびその使用方法 |
WO2017147536A1 (en) | 2016-02-24 | 2017-08-31 | The Rockefeller University | Embryonic cell-based therapeutic candidate screening systems, models for huntington's disease and uses thereof |
WO2017165167A1 (en) | 2016-03-23 | 2017-09-28 | The Regents Of The University Of California | Methods of treating mitochondrial disorders |
US20190117799A1 (en) | 2016-04-01 | 2019-04-25 | The Brigham And Women's Hospital, Inc. | Stimuli-responsive nanoparticles for biomedical applications |
WO2017189914A1 (en) | 2016-04-27 | 2017-11-02 | Massachusetts Institute Of Technology | Sequence-controlled polymer random access memory storage |
US11410746B2 (en) | 2016-04-27 | 2022-08-09 | Massachusetts Institute Of Technology | Stable nanoscale nucleic acid assemblies and methods thereof |
US11021713B2 (en) | 2016-05-25 | 2021-06-01 | Cargill, Incorporated | Engineered nucleases to generate deletion mutants in plants |
MA44031B1 (fr) | 2016-05-26 | 2021-06-30 | Nunhemes B V | Plantes produisant des fruits sans graines |
WO2017205846A1 (en) | 2016-05-27 | 2017-11-30 | Aadigen, Llc | Peptides and nanoparticles for intracellular delivery of genome-editing molecules |
CN110291402B (zh) | 2016-06-27 | 2023-09-01 | 朱诺治疗学股份有限公司 | 鉴定肽表位的方法、结合此类表位的分子和相关用途 |
MA45491A (fr) | 2016-06-27 | 2019-05-01 | Juno Therapeutics Inc | Épitopes à restriction cmh-e, molécules de liaison et procédés et utilisations associés |
EP4219462A1 (en) | 2016-07-13 | 2023-08-02 | Vertex Pharmaceuticals Incorporated | Methods, compositions and kits for increasing genome editing efficiency |
JP2019520844A (ja) | 2016-07-21 | 2019-07-25 | マックスサイト インコーポレーティッド | ゲノムdnaを改変するための方法および組成物 |
WO2018031920A1 (en) | 2016-08-11 | 2018-02-15 | The Jackson Laboratory | Methods and compositions relating to improved human red blood cell survival in genetically modified immunodeficient non-human animals |
SG10201913315SA (en) | 2016-08-24 | 2020-02-27 | Sangamo Therapeutics Inc | Regulation of gene expression using engineered nucleases |
SG11201901364VA (en) | 2016-08-24 | 2019-03-28 | Sangamo Therapeutics Inc | Engineered target specific nucleases |
WO2018044920A1 (en) | 2016-08-29 | 2018-03-08 | The Regents Of The University Of California | Topical formulations based on ionic species for skin treatment |
US20190225974A1 (en) | 2016-09-23 | 2019-07-25 | BASF Agricultural Solutions Seed US LLC | Targeted genome optimization in plants |
US10961505B2 (en) | 2016-10-05 | 2021-03-30 | FUJIFILM Cellular Dynamics, Inc. | Generating mature lineages from induced pluripotent stem cells with MECP2 disruption |
ES2939646T3 (es) | 2016-10-13 | 2023-04-25 | Juno Therapeutics Inc | Métodos y composiciones de inmunoterapia que comprenden moduladores de la vía metabólica del triptófano |
EP3528852A4 (en) | 2016-10-20 | 2020-06-03 | Sangamo Therapeutics, Inc. | METHODS AND COMPOSITIONS FOR THE TREATMENT OF FABRY'S DISEASE |
WO2018081138A1 (en) | 2016-10-24 | 2018-05-03 | Yale University | Biodegradable contraceptive implants |
WO2018081775A1 (en) | 2016-10-31 | 2018-05-03 | Sangamo Therapeutics, Inc. | Gene correction of scid-related genes in hematopoietic stem and progenitor cells |
WO2018144097A1 (en) | 2016-11-04 | 2018-08-09 | Akeagen Llc | Genetically modified non-human animals and methods for producing heavy chain-only antibodies |
US11332713B2 (en) | 2016-11-16 | 2022-05-17 | KSQ Therapeutics, Inc. | Gene-regulating compositions and methods for improved immunotherapy |
CA3042857A1 (en) | 2016-11-16 | 2018-05-24 | Cellectis | Methods for altering amino acid content in plants through frameshift mutations |
WO2018102612A1 (en) | 2016-12-02 | 2018-06-07 | Juno Therapeutics, Inc. | Engineered b cells and related compositions and methods |
CN110249051A (zh) | 2016-12-08 | 2019-09-17 | 凯斯西储大学 | 增强功能性髓鞘产生的方法和组合物 |
WO2018112470A1 (en) | 2016-12-16 | 2018-06-21 | The Brigham And Women's Hospital, Inc. | Co-delivery of nucleic acids for simultaneous suppression and expression of target genes |
WO2018140478A1 (en) | 2017-01-24 | 2018-08-02 | Sigma-Aldrich Co. Llc | Viral resistant cells and culture systems |
CN110891417B (zh) | 2017-03-21 | 2023-05-23 | 杰克逊实验室 | 表达人APOE4和小鼠Trem2 p.R47H的遗传修饰小鼠及其使用方法 |
WO2018187493A1 (en) | 2017-04-04 | 2018-10-11 | Yale University | Compositions and methods for in utero delivery |
KR20190140950A (ko) | 2017-04-20 | 2019-12-20 | 오레곤 헬스 앤드 사이언스 유니버시티 | 인간 유전자 교정 |
WO2018198049A1 (en) | 2017-04-25 | 2018-11-01 | Cellectis | Alfalfa with reduced lignin composition |
SG10202112528QA (en) | 2017-05-12 | 2021-12-30 | Jackson Lab | Nsg mice lacking mhc class i and class ii |
DK3538645T3 (da) | 2017-06-20 | 2021-04-19 | Inst Curie | Immunceller der mangler suv39h1 |
US11851679B2 (en) | 2017-11-01 | 2023-12-26 | Juno Therapeutics, Inc. | Method of assessing activity of recombinant antigen receptors |
US10940171B2 (en) | 2017-11-10 | 2021-03-09 | Massachusetts Institute Of Technology | Microbial production of pure single stranded nucleic acids |
WO2019100053A1 (en) | 2017-11-20 | 2019-05-23 | University Of Georgia Research Foundation, Inc. | Compositions and methods for modulating hif-2α to improve muscle generation and repair |
EP3501268B1 (en) | 2017-12-22 | 2021-09-15 | KWS SAAT SE & Co. KGaA | Regeneration of plants in the presence of histone deacetylase inhibitors |
EP3508581A1 (en) | 2018-01-03 | 2019-07-10 | Kws Saat Se | Regeneration of genetically modified plants |
CN111566121A (zh) | 2018-01-12 | 2020-08-21 | 巴斯夫欧洲公司 | 小麦7a染色体上决定每穗小穗数QTL的基因 |
AU2019209292B2 (en) | 2018-01-17 | 2023-10-05 | Vertex Pharmaceuticals Incorporated | Quinoxalinone compounds, compositions, methods, and kits for increasing genome editing efficiency |
CN111757876B (zh) | 2018-01-17 | 2024-03-22 | 沃泰克斯药物股份有限公司 | Dna-pk抑制剂 |
CA3088788A1 (en) | 2018-01-17 | 2019-07-25 | Vertex Pharmaceuticals Incorporated | Dna-pk inhibitors |
JP7275152B2 (ja) | 2018-02-08 | 2023-05-17 | サンガモ セラピューティクス, インコーポレイテッド | 操作された標的特異的なヌクレアーゼ |
EP3765092A4 (en) | 2018-03-15 | 2022-01-12 | KSQ Therapeutics, Inc. | GENE REGULATORY COMPOSITIONS AND METHODS FOR IMPROVED IMMUNOTHERAPY |
US20190284553A1 (en) | 2018-03-15 | 2019-09-19 | KSQ Therapeutics, Inc. | Gene-regulating compositions and methods for improved immunotherapy |
EP3768327A4 (en) | 2018-03-23 | 2022-04-13 | The Trustees of Columbia University in the City of New York | GENE EDIT FOR AUTOSOMAL DOMINANT DISEASES |
EP3545756A1 (en) | 2018-03-28 | 2019-10-02 | KWS SAAT SE & Co. KGaA | Regeneration of plants in the presence of inhibitors of the histone methyltransferase ezh2 |
JP2021520211A (ja) | 2018-04-05 | 2021-08-19 | ジュノー セラピューティクス インコーポレイテッド | 組換え受容体を発現するt細胞、関連ポリヌクレオチド、および方法 |
CA3094468A1 (en) | 2018-04-05 | 2019-10-10 | Juno Therapeutics, Inc. | Methods of producing cells expressing a recombinant receptor and related compositions |
EP3567111A1 (en) | 2018-05-09 | 2019-11-13 | KWS SAAT SE & Co. KGaA | Gene for resistance to a pathogen of the genus heterodera |
US20210254087A1 (en) | 2018-06-15 | 2021-08-19 | KWS SAAT SE & Co. KGaA | Methods for enhancing genome engineering efficiency |
AU2019285085B2 (en) | 2018-06-15 | 2024-04-18 | KWS SAAT SE & Co. KGaA | Methods for improving genome engineering and regeneration in plant II |
US20220025388A1 (en) | 2018-06-15 | 2022-01-27 | KWS SAAT SE & Co. KGaA | Methods for improving genome engineering and regeneration in plant |
US11291176B2 (en) | 2018-06-15 | 2022-04-05 | Nunhems B.V. | Seedless watermelon plants comprising modifications in an ABC transporter gene |
WO2019246483A1 (en) | 2018-06-21 | 2019-12-26 | The Jackson Laboratory | Genetically modified mouse models of alzheimer's disease |
WO2020028617A1 (en) | 2018-08-01 | 2020-02-06 | University Of Georgia Research Foundation, Inc. | Compositions and methods for improving embryo development |
IL280951B1 (en) | 2018-08-23 | 2024-04-01 | Sangamo Therapeutics Inc | Engineered target-specific base editors |
MX2021002266A (es) | 2018-08-31 | 2021-05-27 | Univ Yale | Composiciones y metodos para aumentar la edicion de genes basados en nucleasa y triplex. |
WO2020051283A1 (en) | 2018-09-05 | 2020-03-12 | The Regents Of The University Of California | Generation of heritably gene-edited plants without tissue culture |
EP3623379A1 (en) | 2018-09-11 | 2020-03-18 | KWS SAAT SE & Co. KGaA | Beet necrotic yellow vein virus (bnyvv)-resistance modifying gene |
WO2020061161A1 (en) | 2018-09-18 | 2020-03-26 | Sangamo Therapeutics, Inc. | Programmed cell death 1 (pd1) specific nucleases |
SG11202104561YA (en) | 2018-11-08 | 2021-05-28 | Triton Algae Innovations Inc | Compositions and methods for incorporating heme from algae in edible products |
KR20200071198A (ko) | 2018-12-10 | 2020-06-19 | 네오이뮨텍, 인코퍼레이티드 | Nrf2 발현 조절 기반 T 세포 항암면역치료법 |
CA3123890A1 (en) | 2019-01-04 | 2020-07-09 | Cargill Incorporated | Engineered nucleases to generate mutations in plants |
US11419932B2 (en) | 2019-01-24 | 2022-08-23 | Massachusetts Institute Of Technology | Nucleic acid nanostructure platform for antigen presentation and vaccine formulations formed therefrom |
US20220112511A1 (en) | 2019-01-29 | 2022-04-14 | The University Of Warwick | Methods for enhancing genome engineering efficiency |
EP3708651A1 (en) | 2019-03-12 | 2020-09-16 | KWS SAAT SE & Co. KGaA | Improving plant regeneration |
KR20210146986A (ko) | 2019-04-02 | 2021-12-06 | 상가모 테라퓨틱스, 인코포레이티드 | 베타-지중해빈혈의 치료 방법 |
JP2022526429A (ja) | 2019-04-10 | 2022-05-24 | ザ ユニバーシティ オブ ユタ リサーチ ファウンデイション | Amdの処置のためのhtra1調節 |
KR20220016475A (ko) | 2019-05-01 | 2022-02-09 | 주노 쎄러퓨티크스 인코퍼레이티드 | 변형된 tgfbr2 유전자 좌에서 재조합 수용체를 발현하는 세포, 관련 폴리뉴클레오티드 및 방법 |
WO2020223571A1 (en) | 2019-05-01 | 2020-11-05 | Juno Therapeutics, Inc. | Cells expressing a chimeric receptor from a modified cd247 locus, related polynucleotides and methods |
US11905532B2 (en) | 2019-06-25 | 2024-02-20 | Massachusetts Institute Of Technology | Compositions and methods for molecular memory storage and retrieval |
EP3757219A1 (en) | 2019-06-28 | 2020-12-30 | KWS SAAT SE & Co. KGaA | Enhanced plant regeneration and transformation by using grf1 booster gene |
CA3146895A1 (en) | 2019-07-23 | 2021-01-28 | Mnemo Therapeutics | Immune cells defective for suv39h1 |
CN115151275A (zh) | 2019-08-30 | 2022-10-04 | 耶鲁大学 | 用于向细胞递送核酸的组合物和方法 |
BR112022009067A2 (pt) | 2019-11-12 | 2022-08-09 | Kws Saat Se & Co Kgaa | Gene para resistência a um patógeno do gênero heterodera |
JP2023525513A (ja) | 2020-05-06 | 2023-06-16 | セレクティス ソシエテ アノニム | 細胞ゲノムにおける外因性配列の標的化挿入のための方法 |
US20230279440A1 (en) | 2020-05-06 | 2023-09-07 | Cellectis S.A. | Methods to genetically modify cells for delivery of therapeutic proteins |
WO2021231661A2 (en) | 2020-05-13 | 2021-11-18 | Juno Therapeutics, Inc. | Process for producing donor-batched cells expressing a recombinant receptor |
JP2023531531A (ja) | 2020-06-26 | 2023-07-24 | ジュノ セラピューティクス ゲーエムベーハー | 組換え受容体を条件付きで発現する操作されたt細胞、関連ポリヌクレオチド、および方法 |
CN116096864A (zh) | 2020-07-30 | 2023-05-09 | 居里研究所 | Socs1缺陷的免疫细胞 |
WO2022046760A2 (en) | 2020-08-25 | 2022-03-03 | Kite Pharma, Inc. | T cells with improved functionality |
CN116802203A (zh) | 2020-11-04 | 2023-09-22 | 朱诺治疗学股份有限公司 | 从经修饰的恒定cd3免疫球蛋白超家族链基因座表达嵌合受体的细胞、相关多核苷酸和方法 |
CA3200855A1 (en) | 2020-11-16 | 2022-05-19 | Pig Improvement Company Uk Limited | Influenza a-resistant animals having edited anp32 genes |
EP4019638A1 (en) | 2020-12-22 | 2022-06-29 | KWS SAAT SE & Co. KGaA | Promoting regeneration and transformation in beta vulgaris |
EP4019639A1 (en) | 2020-12-22 | 2022-06-29 | KWS SAAT SE & Co. KGaA | Promoting regeneration and transformation in beta vulgaris |
CA3208944A1 (en) | 2021-03-22 | 2022-09-29 | Edith NALBANDIAN | Method to assess potency of viral vector particles |
CA3218511A1 (en) | 2021-05-10 | 2022-11-17 | Sqz Biotechnologies Company | Methods for delivering genome editing molecules to the nucleus or cytosol of a cell and uses thereof |
WO2022251644A1 (en) | 2021-05-28 | 2022-12-01 | Lyell Immunopharma, Inc. | Nr4a3-deficient immune cells and uses thereof |
EP4347826A1 (en) | 2021-06-02 | 2024-04-10 | Lyell Immunopharma, Inc. | Nr4a3-deficient immune cells and uses thereof |
WO2022271548A2 (en) | 2021-06-23 | 2022-12-29 | Massachusetts Institute Of Technology | Compositions, methods and systems for the delivery of gene editing material to cells |
WO2023064924A1 (en) | 2021-10-14 | 2023-04-20 | Codiak Biosciences, Inc. | Modified producer cells for extracellular vesicle production |
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WO2024100604A1 (en) | 2022-11-09 | 2024-05-16 | Juno Therapeutics Gmbh | Methods for manufacturing engineered immune cells |
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EP0589958A4 (en) * | 1991-06-11 | 1995-04-26 | Gen Hospital Corp | UNIVERSAL NUCLEASES ACTING ON A SPECIFIED SITE. |
US5436150A (en) * | 1992-04-03 | 1995-07-25 | The Johns Hopkins University | Functional domains in flavobacterium okeanokoities (foki) restriction endonuclease |
JPH08510375A (ja) * | 1993-02-12 | 1996-11-05 | ザ・ジョンズ−ホプキンス・ユニバーシティー | フラボバクテリウム・オケアノコイテス(foki)制限エンドヌクレアーゼの機能ドメイン |
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- 1994-08-23 EP EP94925854A patent/EP0721502A4/en not_active Withdrawn
- 1994-08-23 JP JP7510290A patent/JPH09505728A/ja not_active Withdrawn
- 1994-08-23 CA CA002170986A patent/CA2170986A1/en not_active Abandoned
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2006
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- 2012-02-23 JP JP2012037730A patent/JP2012135316A/ja not_active Withdrawn
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JP4081119B2 (ja) | 2008-04-23 |
JP2012135316A (ja) | 2012-07-19 |
JP2008005851A (ja) | 2008-01-17 |
EP0721502A1 (en) | 1996-07-17 |
AU7563694A (en) | 1995-04-18 |
WO1995009233A1 (en) | 1995-04-06 |
EP0721502A4 (en) | 1997-02-12 |
US5436150A (en) | 1995-07-25 |
JP2009072201A (ja) | 2009-04-09 |
AU687435B2 (en) | 1998-02-26 |
JP2006254921A (ja) | 2006-09-28 |
JP2013081471A (ja) | 2013-05-09 |
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