MXPA04011134A - Metodo para identificar compuestos que interactuan con las proteinas de transmembrana. - Google Patents
Metodo para identificar compuestos que interactuan con las proteinas de transmembrana.Info
- Publication number
- MXPA04011134A MXPA04011134A MXPA04011134A MXPA04011134A MXPA04011134A MX PA04011134 A MXPA04011134 A MX PA04011134A MX PA04011134 A MXPA04011134 A MX PA04011134A MX PA04011134 A MXPA04011134 A MX PA04011134A MX PA04011134 A MXPA04011134 A MX PA04011134A
- Authority
- MX
- Mexico
- Prior art keywords
- cells
- receptor
- nls
- protein
- gfp
- Prior art date
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| US37170402P | 2002-04-12 | 2002-04-12 | |
| US37941902P | 2002-05-13 | 2002-05-13 | |
| US38757002P | 2002-06-12 | 2002-06-12 | |
| US42289102P | 2002-11-01 | 2002-11-01 | |
| US44255603P | 2003-01-27 | 2003-01-27 | |
| PCT/CA2003/000542 WO2003087836A1 (en) | 2002-04-12 | 2003-04-11 | Method of identifying transmembrane protein-interacting compounds |
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| MXPA04011134A true MXPA04011134A (es) | 2005-08-15 |
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| MXPA04011134A MXPA04011134A (es) | 2002-04-12 | 2003-04-11 | Metodo para identificar compuestos que interactuan con las proteinas de transmembrana. |
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| DK1495330T3 (da) * | 2002-04-12 | 2009-05-18 | Brian F O'dowd | Fremgangsmåde til at identificere forbindelser, som påvirker transmembran-proteiner |
| DE602005020320D1 (de) * | 2004-06-16 | 2010-05-12 | Affinergy Inc | Grenzflächenbiomaterialien zur förderung der anhaftung von zielanalyten |
| CN1944647B (zh) * | 2006-08-23 | 2010-05-12 | 华东师范大学 | 多巴胺受体新亚型d5b基因及编码的蛋白与应用 |
| JP4929462B2 (ja) | 2007-01-29 | 2012-05-09 | 国立大学法人高知大学 | 細胞膜上分子と相互作用する化合物の検出方法 |
| JP5213075B2 (ja) * | 2007-06-15 | 2013-06-19 | ジェネラックス・コーポレイション | 腫瘍の画像化および/または処置のための微生物 |
| JP5230397B2 (ja) * | 2008-12-18 | 2013-07-10 | 独立行政法人科学技術振興機構 | 抗膜貫通型タンパク質抗体の抗原結合部位を決定する方法 |
| CN102580091B (zh) * | 2011-01-12 | 2014-12-10 | 中国科学院上海生命科学研究院 | 增强阿片镇痛剂的镇痛作用的方法及试剂 |
| US8643360B1 (en) * | 2012-09-02 | 2014-02-04 | George S. Cargill, III | In-water voltage gradient detector |
| TWI472617B (zh) * | 2012-09-17 | 2015-02-11 | Nat Univ Chung Hsing | 調控大分子進入細胞內之蛋白質及其調控大分子進入細胞內之方法 |
| US10513711B2 (en) | 2014-08-13 | 2019-12-24 | Dupont Us Holding, Llc | Genetic targeting in non-conventional yeast using an RNA-guided endonuclease |
| KR102424721B1 (ko) | 2014-11-06 | 2022-07-25 | 이 아이 듀폰 디 네모아 앤드 캄파니 | Rna-유도 엔도뉴클레아제의 세포 내로의 펩티드 매개성 전달 |
| EP3294877A1 (en) | 2015-05-15 | 2018-03-21 | Pioneer Hi-Bred International, Inc. | Rapid characterization of cas endonuclease systems, pam sequences and guide rna elements |
| FI4144844T3 (fi) | 2015-10-12 | 2025-11-24 | Dupont Us Holding Llc | Suojatut dna-templaatit geenimuokkaukseen ja homologisen rekombinaation lisäämiseen soluissa ja niiden käyttömenetelmät |
| WO2018071362A1 (en) | 2016-10-13 | 2018-04-19 | Pioneer Hi-Bred International, Inc. | Generating northern leaf blight resistant maize |
| KR20180069832A (ko) | 2015-10-20 | 2018-06-25 | 파이어니어 하이 부렛드 인터내쇼날 인코포레이팃드 | 유도 cas 시스템을 통한 비기능성 유전자 산물에 대한 기능 회복 및 이용 방법 |
| BR112018007796A2 (pt) | 2015-11-06 | 2018-10-30 | Du Pont | plantas de soja, partes de plantas de soja ou sementes de soja, método para selecionar uma célula de soja, métodos de seleção de uma célula de soja e de produção de um locus e molécula de ácido nucleico |
| EP3387134B1 (en) | 2015-12-11 | 2020-10-14 | Danisco US Inc. | Methods and compositions for enhanced nuclease-mediated genome modification and reduced off-target site effects |
| EP3390631B1 (en) | 2015-12-18 | 2020-04-08 | Danisco US Inc. | Methods and compositions for t-rna based guide rna expression |
| US11136589B2 (en) | 2016-01-26 | 2021-10-05 | Pioneer Hi-Bred International, Inc. | Waxy corn |
| EP3699280A3 (en) | 2016-03-11 | 2020-11-18 | Pioneer Hi-Bred International, Inc. | Novel cas9 systems and methods of use |
| US20190161742A1 (en) | 2016-03-11 | 2019-05-30 | Pioneer Hi-Bred International, Inc. | Novel cas9 systems and methods of use |
| WO2017155715A1 (en) | 2016-03-11 | 2017-09-14 | Pioneer Hi-Bred International, Inc. | Novel cas9 systems and methods of use |
| AU2017286122A1 (en) | 2016-06-14 | 2018-11-22 | Pioneer Hi-Bred International, Inc. | Use of Cpf1 endonuclease for plant genome modifications |
| CA3018430A1 (en) | 2016-06-20 | 2017-12-28 | Pioneer Hi-Bred International, Inc. | Novel cas systems and methods of use |
| JP7356351B2 (ja) | 2016-12-12 | 2023-10-04 | エクセラ・バイオサイエンシーズ・インコーポレイテッド | マイクロキャピラリーアレイを使用したスクリーニングのための方法およびシステム |
| WO2018125832A1 (en) | 2016-12-30 | 2018-07-05 | xCella Biosciences, Inc. | Multi-stage sample recovery system |
| US11519009B2 (en) | 2017-01-09 | 2022-12-06 | University Of Massachusetts | Complexes for gene deletion and editing |
| MX2020005726A (es) | 2017-12-15 | 2020-08-13 | Danisco Us Inc | Variantes de cas9 y metodos de uso. |
| CN108178790B (zh) * | 2018-01-18 | 2021-09-07 | 上海药明康德新药开发有限公司 | 一种将细胞膜分离以便对跨膜蛋白进行dna编码化合物库筛选的方法 |
| US12084676B2 (en) | 2018-02-23 | 2024-09-10 | Pioneer Hi-Bred International, Inc. | Cas9 orthologs |
| US20220030788A1 (en) | 2018-10-16 | 2022-02-03 | Pioneer Hi-Bred International, Inc. | Genome edited fine mapping and causal gene identification |
| ES3039910T3 (en) | 2018-12-06 | 2025-10-27 | Xcella Biosciences Inc | Lateral loading of microcapillary arrays |
| AU2019398351A1 (en) | 2018-12-14 | 2021-06-03 | Pioneer Hi-Bred International, Inc. | Novel CRISPR-Cas systems for genome editing |
| CA3126735A1 (en) | 2019-01-11 | 2020-07-16 | Omeros Corporation | Methods and compositions for treating cancer |
| MX2021012157A (es) | 2019-04-05 | 2022-01-06 | Danisco Us Inc | Métodos para la integración de polinucleótidos en el genoma de bacillus usando constructos de adn recombinante circular dual y composiciones de los mismos. |
| MX2021012158A (es) | 2019-04-05 | 2022-01-06 | Danisco Us Inc | Métodos para la integración de una secuencia de adn donante en el genoma de bacillus usando constructos de adn recombinante lineal y composiciones de los mismos. |
| KR102329302B1 (ko) * | 2019-09-30 | 2021-11-22 | 한국과학기술연구원 | 도파민 d1형 수용체의 활성 측정용 적색 형광 단백질 기반 바이오센서 |
| WO2023105244A1 (en) | 2021-12-10 | 2023-06-15 | Pig Improvement Company Uk Limited | Editing tmprss2/4 for disease resistance in livestock |
| KR102833970B1 (ko) * | 2022-02-23 | 2025-07-17 | 충남대학교산학협력단 | 핵수송 신호 펩타이드가 접합된 핵산 전달용 2세대 폴리아미도아민 덴드리머 고분자 유도체 |
| WO2024013514A2 (en) | 2022-07-15 | 2024-01-18 | Pig Improvement Company Uk Limited | Gene edited livestock animals having coronavirus resistance |
| WO2024118882A1 (en) | 2022-12-01 | 2024-06-06 | Genencor International Bv | Iterative multiplex genome engineering in microbial cells using a selection marker swapping system |
| WO2024118881A1 (en) | 2022-12-01 | 2024-06-06 | Genencor International Bv | Iterative muliplex genome engineering in microbial cells using a bidirectional selection marker system |
| WO2024118876A1 (en) | 2022-12-01 | 2024-06-06 | Genencor International Bv | Iterative multiplex genome engineering in microbial cells using a recombinant self-excisable selection marker system |
| WO2024196921A1 (en) | 2023-03-20 | 2024-09-26 | Pioneer Hi-Bred International, Inc. | Cas polypeptides with altered pam recognition |
Family Cites Families (7)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US20030022277A1 (en) * | 1995-05-05 | 2003-01-30 | Daniel R. Soppet | Human neuropeptide receptor |
| US6004808A (en) * | 1996-06-21 | 1999-12-21 | Aurora Biosciences Corporation | Promiscuous G-protein compositions and their use |
| US5891646A (en) | 1997-06-05 | 1999-04-06 | Duke University | Methods of assaying receptor activity and constructs useful in such methods |
| US6383761B2 (en) | 1997-07-28 | 2002-05-07 | The Regents Of The University Of California | Methods and compositions for identifying modulators of G-protein-coupled receptors |
| AU2001243145A1 (en) * | 2000-02-09 | 2001-08-20 | Human Genome Sciences, Inc. | Human g-protein chemokine receptor (ccr5) hdgnr10 |
| AU2001284974A1 (en) | 2000-08-16 | 2002-02-25 | The Trustees Of Columbia University In The City Of New York | Quantitative assessment of erbb/her receptors in biological fluids |
| DK1495330T3 (da) | 2002-04-12 | 2009-05-18 | Brian F O'dowd | Fremgangsmåde til at identificere forbindelser, som påvirker transmembran-proteiner |
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