JP2012516686A - Cftrを発現する細胞株およびそれらを使用する方法 - Google Patents
Cftrを発現する細胞株およびそれらを使用する方法 Download PDFInfo
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| JP2016505254A (ja) * | 2012-12-12 | 2016-02-25 | ルサッフル・エ・コンパニーLesaffre Et Compagnie | 下痢を治療および/または予防するプロバイオティクス株 |
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|---|---|---|---|---|
| EP2245046B1 (en) * | 2008-01-22 | 2019-09-04 | Chromocell Corporation | Novel cell lines expressing nav and methods using them |
| CA2713885A1 (en) * | 2008-02-01 | 2009-08-20 | Chromocell Corporation | Novel cell lines and methods |
| WO2011014740A2 (en) | 2009-07-31 | 2011-02-03 | Chromocell Corporation | Methods and composition for identifying and validating modulators of cell fate |
| WO2012162468A1 (en) * | 2011-05-25 | 2012-11-29 | Janssen Pharmaceutica Nv | Thiazol derivatives as pro -matrix metalloproteinase inhibitors |
| US20130014288A1 (en) * | 2011-06-06 | 2013-01-10 | Carnegie Mellon University | Novel reporter-tagged recombinant membrane proteins with transmembrane linkers |
| WO2017196843A1 (en) * | 2016-05-09 | 2017-11-16 | Proteostasis Therapeutics, Inc. | Methods of identifying cftr modulators |
| US11723579B2 (en) | 2017-09-19 | 2023-08-15 | Neuroenhancement Lab, LLC | Method and apparatus for neuroenhancement |
| US11717686B2 (en) | 2017-12-04 | 2023-08-08 | Neuroenhancement Lab, LLC | Method and apparatus for neuroenhancement to facilitate learning and performance |
| US12280219B2 (en) | 2017-12-31 | 2025-04-22 | NeuroLight, Inc. | Method and apparatus for neuroenhancement to enhance emotional response |
| US11478603B2 (en) | 2017-12-31 | 2022-10-25 | Neuroenhancement Lab, LLC | Method and apparatus for neuroenhancement to enhance emotional response |
| US11364361B2 (en) | 2018-04-20 | 2022-06-21 | Neuroenhancement Lab, LLC | System and method for inducing sleep by transplanting mental states |
| WO2020056418A1 (en) | 2018-09-14 | 2020-03-19 | Neuroenhancement Lab, LLC | System and method of improving sleep |
| US11786694B2 (en) | 2019-05-24 | 2023-10-17 | NeuroLight, Inc. | Device, method, and app for facilitating sleep |
| CN111910008B (zh) * | 2020-08-21 | 2022-05-31 | 云南农业大学 | 一种鸡生长发育相关的分子标记及其应用 |
Citations (1)
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| WO2001003722A1 (en) * | 1999-07-09 | 2001-01-18 | Mayo Foundation For Medical Education And Research | Cftr polypeptides, fragments thereof and methods of use to overcome biosynthetic misprocessing |
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| US20020164782A1 (en) * | 1999-02-10 | 2002-11-07 | Gregory Richard J. | Adenovirus vectors for gene therapy |
| WO2004020596A2 (en) * | 2002-08-30 | 2004-03-11 | University Of Pittsburgh Of The Commonwealth System Of Higher Education | Polypeptides for increasing mutant cftr channel activity |
| AU2005251745A1 (en) * | 2004-06-04 | 2005-12-22 | The Regents Of The University Of California | Compounds having activity in increasing ion transport by mutant-CFTR and uses thereof |
| WO2006101740A2 (en) * | 2005-03-18 | 2006-09-28 | The Regents Of The University Of California | Compounds having activity in correcting mutant-cftr processing and uses thereof |
| CA2602793C (en) * | 2005-04-13 | 2016-11-22 | Astrazeneca Ab | A host cell comprising a vector for production of proteins requiring gamma-carboxylation |
| MX2008014437A (es) * | 2006-05-19 | 2008-11-27 | Scripps Research Inst | Tratamiento de desplegamiento de proteinas. |
| WO2008121199A2 (en) * | 2007-03-28 | 2008-10-09 | University Of Iowa Research Foundation | Transgenic animal models of disease |
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2010
- 2010-02-01 US US13/147,327 patent/US20120058918A1/en not_active Abandoned
- 2010-02-01 MX MX2011008131A patent/MX2011008131A/es not_active Application Discontinuation
- 2010-02-01 JP JP2011548377A patent/JP2012516686A/ja active Pending
- 2010-02-01 CA CA2751215A patent/CA2751215A1/en not_active Abandoned
- 2010-02-01 EP EP10736545A patent/EP2393930A4/en not_active Withdrawn
- 2010-02-01 WO PCT/US2010/022778 patent/WO2010088630A2/en not_active Ceased
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2014
- 2014-11-24 US US14/552,192 patent/US20150315554A1/en not_active Abandoned
Patent Citations (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| WO2001003722A1 (en) * | 1999-07-09 | 2001-01-18 | Mayo Foundation For Medical Education And Research | Cftr polypeptides, fragments thereof and methods of use to overcome biosynthetic misprocessing |
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JP2016505254A (ja) * | 2012-12-12 | 2016-02-25 | ルサッフル・エ・コンパニーLesaffre Et Compagnie | 下痢を治療および/または予防するプロバイオティクス株 |
Also Published As
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|---|---|
| EP2393930A4 (en) | 2012-08-15 |
| MX2011008131A (es) | 2012-01-20 |
| CA2751215A1 (en) | 2010-08-05 |
| EP2393930A2 (en) | 2011-12-14 |
| US20120058918A1 (en) | 2012-03-08 |
| WO2010088630A3 (en) | 2010-11-25 |
| US20150315554A1 (en) | 2015-11-05 |
| WO2010088630A2 (en) | 2010-08-05 |
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