|
JPH10501686A
(ja)
|
1994-04-13 |
1998-02-17 |
ザ ロックフェラー ユニヴァーシティ |
神経系の細胞へのdnaのaav仲介送達
|
|
US20020159979A1
(en)
|
1994-06-06 |
2002-10-31 |
Children's Hospital, Inc. |
Adeno-associated virus materials and methods
|
|
US5658785A
(en)
*
|
1994-06-06 |
1997-08-19 |
Children's Hospital, Inc. |
Adeno-associated virus materials and methods
|
|
EP0785991A1
(de)
*
|
1994-10-13 |
1997-07-30 |
Deutsches Krebsforschungszentrum Stiftung des öffentlichen Rechts |
Bereitstellung von rep-negativen aav-mutanten und hierfür verwendbare zellen
|
|
US5856152A
(en)
*
|
1994-10-28 |
1999-01-05 |
The Trustees Of The University Of Pennsylvania |
Hybrid adenovirus-AAV vector and methods of use therefor
|
|
US6342390B1
(en)
|
1994-11-23 |
2002-01-29 |
The United States Of America As Represented By The Secretary Of Health And Human Services |
Lipid vesicles containing adeno-associated virus rep protein for transgene integration and gene therapy
|
|
US6326356B1
(en)
|
1996-10-18 |
2001-12-04 |
Board Of Regents, The University Of Texas System |
Suppression of neu overexpression using a mini-E1A gene
|
|
WO1996017947A1
(en)
*
|
1994-12-06 |
1996-06-13 |
Targeted Genetics Corporation |
Packaging cell lines for generation of high titers of recombinant aav vectors
|
|
US6924128B2
(en)
|
1994-12-06 |
2005-08-02 |
Targeted Genetics Corporation |
Packaging cell lines for generation of high titers of recombinant AAV vectors
|
|
US5843742A
(en)
*
|
1994-12-16 |
1998-12-01 |
Avigen Incorporated |
Adeno-associated derived vector systems for gene delivery and integration into target cells
|
|
US5795587A
(en)
*
|
1995-01-23 |
1998-08-18 |
University Of Pittsburgh |
Stable lipid-comprising drug delivery complexes and methods for their production
|
|
US20020103147A1
(en)
|
1997-09-05 |
2002-08-01 |
Hammond H. Kirk |
Gene therapy for congestive heart failure
|
|
US6752987B1
(en)
|
1995-02-28 |
2004-06-22 |
The Regents Of The University Of California |
Adenovirus encoding human adenylylcyclase (AC) VI
|
|
US6100242A
(en)
|
1995-02-28 |
2000-08-08 |
The Regents Of The University Of California |
Gene therapies for enhancing cardiac function
|
|
US20030069173A1
(en)
*
|
1998-03-16 |
2003-04-10 |
Life Technologies, Inc. |
Peptide-enhanced transfections
|
|
US6051429A
(en)
*
|
1995-06-07 |
2000-04-18 |
Life Technologies, Inc. |
Peptide-enhanced cationic lipid transfections
|
|
US6093570A
(en)
|
1995-06-07 |
2000-07-25 |
The University Of North Carolina At Chapel Hill |
Helper virus-free AAV production
|
|
US6506379B1
(en)
|
1995-06-07 |
2003-01-14 |
Ariad Gene Therapeutics, Inc. |
Intramuscular delivery of recombinant AAV
|
|
US6187757B1
(en)
|
1995-06-07 |
2001-02-13 |
Ariad Pharmaceuticals, Inc. |
Regulation of biological events using novel compounds
|
|
US5622856A
(en)
*
|
1995-08-03 |
1997-04-22 |
Avigen |
High efficiency helper system for AAV vector production
|
|
US6001650A
(en)
|
1995-08-03 |
1999-12-14 |
Avigen, Inc. |
High-efficiency wild-type-free AAV helper functions
|
|
US6027931A
(en)
*
|
1995-08-03 |
2000-02-22 |
Avigen, Inc. |
High-efficiency AA V helper functions
|
|
DE69631480T2
(de)
*
|
1995-08-03 |
2004-11-25 |
Avigen Inc., Alameda |
Helfersystem zur wirkungssteigerung der aav-vektorproduktion
|
|
US6086913A
(en)
*
|
1995-11-01 |
2000-07-11 |
University Of British Columbia |
Liposomal delivery of AAV vectors
|
|
JP3881382B2
(ja)
*
|
1995-12-01 |
2007-02-14 |
イントロヘーネ ベスローテン フェンノートシャップ |
安定にトランスフェクションされた哺乳類細胞における調節されたタンパク質発現
|
|
EP0906440A1
(de)
*
|
1996-03-04 |
1999-04-07 |
Targeted Genetics Corporation |
Verfahren zur transduktion von zellen in blutgefässen unter verwendung von rekombinanten aav vektoren
|
|
US6245735B1
(en)
|
1996-07-29 |
2001-06-12 |
The Brigham And Women's Hospital, Inc. |
Methods and products for treating pseudomonas infection
|
|
CA2264482A1
(en)
*
|
1996-09-06 |
1998-03-12 |
The Trustees Of The University Of Pennsylvania |
An inducible method for production of recombinant adeno-associated viruses utilizing t7 polymerase
|
|
WO1998010086A1
(en)
*
|
1996-09-06 |
1998-03-12 |
Trustees Of The University Of Pennsylvania |
Methods using cre-lox for production of recombinant adeno-associated viruses
|
|
AU744873B2
(en)
|
1996-11-06 |
2002-03-07 |
Regents Of The University Of California, The |
Isolated tumor necrosis factor receptor releasing enzyme, compositions comprising the enzyme and methods of the use thereof
|
|
CA2270285A1
(en)
|
1996-12-18 |
1998-06-25 |
Targeted Genetics Corporation |
Aav split-packaging genes and cell lines comprising such genes for use in the production of recombinant aav vectors
|
|
EP0856585A1
(de)
*
|
1997-01-29 |
1998-08-05 |
Introgene B.V. |
Ein induzierbares Replications- und Expressionssystem
|
|
US6403370B1
(en)
|
1997-02-10 |
2002-06-11 |
Genstar Therapeutics Corporation |
Oncolytic/immunogenic complementary-adenoviral vector system
|
|
US8703480B1
(en)
|
1997-03-21 |
2014-04-22 |
Enzo Therapeutics, Inc. |
Biological function effecting viral vectors and chimeric cells useful as packaging cell lines and target cells
|
|
IL131979A0
(en)
*
|
1997-03-21 |
2001-03-19 |
Enzo Therapeutics Inc |
Vectors and viral vectors and packaging cell lines for propagating the same
|
|
WO1998048005A1
(en)
*
|
1997-04-24 |
1998-10-29 |
University Of Washington |
Targeted gene modification by parvoviral vectors
|
|
US6689605B1
(en)
*
|
1997-05-22 |
2004-02-10 |
Uab Research Foundation |
Controlling immune response to specific antigens
|
|
WO1998052615A1
(en)
*
|
1997-05-22 |
1998-11-26 |
Uab Research Foundation |
Controlling immune response to specific antigens
|
|
US6251677B1
(en)
|
1997-08-25 |
2001-06-26 |
The Trustees Of The University Of Pennsylvania |
Hybrid adenovirus-AAV virus and methods of use thereof
|
|
CA2995542A1
(en)
|
1997-09-05 |
1999-03-11 |
Genzyme Corporation |
Methods for generating high titer helper-free preparations of recombinant aav vectors
|
|
US6566118B1
(en)
|
1997-09-05 |
2003-05-20 |
Targeted Genetics Corporation |
Methods for generating high titer helper-free preparations of released recombinant AAV vectors
|
|
US6995006B2
(en)
|
1997-09-05 |
2006-02-07 |
Targeted Genetics Corporation |
Methods for generating high titer helper-free preparations of released recombinant AAV vectors
|
|
WO1999014354A1
(en)
|
1997-09-19 |
1999-03-25 |
The Trustees Of The University Of The Pennsylvania |
Methods and vector constructs useful for production of recombinant aav
|
|
JP2001520051A
(ja)
*
|
1997-10-21 |
2001-10-30 |
ターゲテッド ジェネティックス コーポレイション |
組換えaavベクターの産生のための増幅可能アデノ随伴ウイルス(aav)パッケージングカセット
|
|
JP2001520047A
(ja)
*
|
1997-10-21 |
2001-10-30 |
ターゲテッド ジェネティックス コーポレイション |
組換えaavベクターと共に使用するための転写活性化された逆方向末端反復(itr)
|
|
US6346415B1
(en)
*
|
1997-10-21 |
2002-02-12 |
Targeted Genetics Corporation |
Transcriptionally-activated AAV inverted terminal repeats (ITRS) for use with recombinant AAV vectors
|
|
US6642051B1
(en)
*
|
1997-10-21 |
2003-11-04 |
Targeted Genetics Corporation |
Amplifiable adeno-associated virus(AAV) packaging cassettes for the production of recombinant AAV vectors
|
|
US6984635B1
(en)
|
1998-02-13 |
2006-01-10 |
Board Of Trustees Of The Leland Stanford Jr. University |
Dimerizing agents, their production and use
|
|
US6294379B1
(en)
|
1998-02-25 |
2001-09-25 |
The Regents Of The University Of California |
Efficient AAV vectors
|
|
US6953690B1
(en)
|
1998-03-20 |
2005-10-11 |
The Trustees Of The University Of Pennsylvania |
Compositions and methods for helper-free production of recombinant adeno-associated viruses
|
|
US20060183228A1
(en)
*
|
1998-03-24 |
2006-08-17 |
Enzo Therapeutics, Inc. |
Viral vectors with surface or envelope components
|
|
DE69918090T2
(de)
|
1998-04-24 |
2005-06-16 |
University Of Florida, Gainesville |
Rekombinanter adeno-assoziierter viraler vektor, der alpha-1 antitrypsin kodiert, zur gentherapie
|
|
US6436392B1
(en)
|
1998-05-20 |
2002-08-20 |
University Of Iowa Research Foundation |
Adeno-associated virus vectors
|
|
US6146874A
(en)
*
|
1998-05-27 |
2000-11-14 |
University Of Florida |
Method of preparing recombinant adeno-associated virus compositions
|
|
EP1097244A4
(de)
*
|
1998-07-22 |
2002-08-07 |
Immusol Inc |
Substantiell vollständige ribozymbibliotheken
|
|
EP2942393A1
(de)
|
1998-09-04 |
2015-11-11 |
Genzyme Corporation |
Verfahren zur erzeugung helferfreier präparate mit hohem titer aus freigesetzten rekombinanten aav-vektoren
|
|
US6200560B1
(en)
*
|
1998-10-20 |
2001-03-13 |
Avigen, Inc. |
Adeno-associated virus vectors for expression of factor VIII by target cells
|
|
US6221349B1
(en)
|
1998-10-20 |
2001-04-24 |
Avigen, Inc. |
Adeno-associated vectors for expression of factor VIII by target cells
|
|
US7129043B1
(en)
*
|
1998-10-22 |
2006-10-31 |
Duke University |
Methods of screening for risk of proliferative disease and methods for the treatment of proliferative disease
|
|
CA2350882C
(en)
|
1998-11-12 |
2011-02-22 |
Life Technologies Corporation |
Transfection reagents
|
|
ES2639020T3
(es)
|
1998-11-27 |
2017-10-25 |
Ucb Pharma S.A. |
Composiciones y métodos para incrementar la mineralización de la substancia ósea
|
|
US20040009535A1
(en)
|
1998-11-27 |
2004-01-15 |
Celltech R&D, Inc. |
Compositions and methods for increasing bone mineralization
|
|
US6387368B1
(en)
|
1999-02-08 |
2002-05-14 |
The Trustees Of The University Of Pennsylvania |
Hybrid adenovirus-AAV virus and methods of use thereof
|
|
US6258595B1
(en)
|
1999-03-18 |
2001-07-10 |
The Trustees Of The University Of Pennsylvania |
Compositions and methods for helper-free production of recombinant adeno-associated viruses
|
|
JP4693244B2
(ja)
|
1999-03-18 |
2011-06-01 |
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 |
組換えアデノ随伴ウイルスのヘルパー無しの生産のための組成物および方法
|
|
US6893865B1
(en)
*
|
1999-04-28 |
2005-05-17 |
Targeted Genetics Corporation |
Methods, compositions, and cells for encapsidating recombinant vectors in AAV particles
|
|
EP1939300A1
(de)
|
1999-05-28 |
2008-07-02 |
Targeted Genetics Corporation |
Verfahren und Zusammensetzung zur Senkung des Spiegels des Tumornekrosefaktors (TNF) bei TNF-assoziierten Leiden
|
|
US6537540B1
(en)
*
|
1999-05-28 |
2003-03-25 |
Targeted Genetics Corporation |
Methods and composition for lowering the level of tumor necrosis factor (TNF) in TNF-associated disorders
|
|
EP1916258B1
(de)
|
1999-08-09 |
2014-04-23 |
Targeted Genetics Corporation |
Erweiterte Expression einer einstämmigen, heterologen Nukleotidsequenz von rekombinanten viralen Vektoren durch Modellierung der Sequenz mit stammübergreifenden Basispaaren
|
|
US6596535B1
(en)
|
1999-08-09 |
2003-07-22 |
Targeted Genetics Corporation |
Metabolically activated recombinant viral vectors and methods for the preparation and use
|
|
US7115391B1
(en)
|
1999-10-01 |
2006-10-03 |
Genovo, Inc. |
Production of recombinant AAV using adenovirus comprising AAV rep/cap genes
|
|
JP2003511082A
(ja)
*
|
1999-10-12 |
2003-03-25 |
ザ・ユニヴァーシティ・オヴ・ノース・キャロライナ・アト・チャペル・ヒル |
第viii因子をコードするアデノ随伴ウィルスベクターとその使用法
|
|
AU3988401A
(en)
*
|
2000-02-25 |
2001-09-03 |
Ludwig Inst Cancer Res |
Materials and methods involving hybrid vascular endothelial growth factor dnas and proteins
|
|
CA2416156A1
(en)
*
|
2000-07-28 |
2002-02-07 |
University Of Maryland, Baltimore |
Accessory cholera enterotoxin and analogs thereof as activators of calcium dependent chloride channel
|
|
US7507542B2
(en)
|
2001-05-08 |
2009-03-24 |
Ucb Sa |
Method for regulating immune function using the FOXP3 protein
|
|
WO2002094854A2
(en)
|
2001-05-21 |
2002-11-28 |
The Brigham And Women's Hospital, Inc. |
P.aeruginosa mucoid exopolysaccharide specific binding peptides
|
|
US7119172B2
(en)
|
2001-05-21 |
2006-10-10 |
The Brigham And Women's Hospital, Inc. |
P. aeruginosa mucoid exopolysaccharide specific binding peptides
|
|
US6844192B2
(en)
|
2001-06-29 |
2005-01-18 |
Wake Forest University |
Adenovirus E4 protein variants for virus production
|
|
WO2003073991A2
(en)
*
|
2002-03-01 |
2003-09-12 |
Celltech R & D, Inc. |
Methods to increase or decrease bone density
|
|
US7510872B2
(en)
*
|
2003-02-26 |
2009-03-31 |
Nationwide Children's Hospital |
Recombinant adeno-associated virus production
|
|
JP4979067B2
(ja)
|
2003-05-01 |
2012-07-18 |
ジェンザイム・コーポレーション |
神経代謝性疾患についての遺伝子治療
|
|
US20070037284A1
(en)
*
|
2003-06-04 |
2007-02-15 |
Enzo Therapeutics, Inc. |
Vectors for expressing exogenous gene or exogenous nucleic acid sequences
|
|
US9532994B2
(en)
|
2003-08-29 |
2017-01-03 |
The Regents Of The University Of California |
Agents and methods for enhancing bone formation by oxysterols in combination with bone morphogenic proteins
|
|
CA2538843A1
(en)
*
|
2003-09-12 |
2005-03-24 |
Vertex Pharmaceuticals Incorporated |
Animal model for protease activity and liver damage
|
|
US7422741B2
(en)
|
2004-03-05 |
2008-09-09 |
Vegenics Limited |
VEGFR-3 fusion proteins
|
|
US7582442B2
(en)
|
2004-03-16 |
2009-09-01 |
The Regents Of The University Of Michigan |
Methods and compositions for using aleveolar macrophage phospholipase A2
|
|
US7319015B2
(en)
*
|
2004-03-16 |
2008-01-15 |
The Regents Of The University Of Michigan |
Methods and compositions for using alveolar macrophage phospholipase A2
|
|
US20090233986A1
(en)
*
|
2004-07-27 |
2009-09-17 |
Mount Sinai School Of Medicine |
Methods and compositions for using sax2
|
|
FI20050753A7
(fi)
|
2004-09-03 |
2006-03-04 |
Licentia Oy |
Uudet peptidit
|
|
WO2006101629A2
(en)
*
|
2005-02-17 |
2006-09-28 |
Vertex Pharmaceuticals Incorporated |
SODIUM CHANNEL PROTEIN TYPE III α-SUBUNIT SPLICE VARIANT
|
|
AU2006242129A1
(en)
*
|
2005-05-02 |
2006-11-09 |
Genzyme Corporation |
Gene therapy for spinal cord disorders
|
|
AU2006243776A1
(en)
|
2005-05-02 |
2006-11-09 |
Genzyme Corporation |
Gene therapy for neurometabolic disorders
|
|
ES2363758T3
(es)
|
2005-08-15 |
2011-08-16 |
Vegenics Pty Ltd |
Vegf y pdgf modificados con propiedades angiogénicas mejoradas.
|
|
US7972813B2
(en)
*
|
2005-09-30 |
2011-07-05 |
Vertex Pharmaceuticals Incorporated |
Tetrodotoxin-resistant sodium channel alpha subunit
|
|
US20080200408A1
(en)
*
|
2005-09-30 |
2008-08-21 |
Mccormack Kenneth |
Deletion mutants of tetrodotoxin-resistant sodium channel alpha subunit
|
|
PL1969003T3
(pl)
|
2005-12-14 |
2011-05-31 |
Herantis Pharma Plc |
Zastosowanie białka czynnika neurotroficznego
|
|
US20090214496A1
(en)
*
|
2006-01-30 |
2009-08-27 |
Licentia Ltd. |
Bmx/etk tyrosine kinase gene therapy materials and methods
|
|
SI1986661T1
(sl)
|
2006-02-08 |
2018-12-31 |
Genzyme Corporation |
Genska terapija za Niemann-Pickovo bolezen tipa A
|
|
AU2007217366A1
(en)
|
2006-02-27 |
2007-08-30 |
The Regents Of The University Of California |
Oxysterol compounds and the hedgehog pathway
|
|
ES2429225T3
(es)
|
2006-05-17 |
2013-11-13 |
The Ludwig Institute For Cancer Research |
Anticuerpos anti VEGF-B para tratamiento o profilaxis de diabetes de tipo II o síndrome metabólico
|
|
HUE044182T2
(hu)
|
2006-06-07 |
2019-10-28 |
Genzyme Corp |
Génterápia amiotrófiás laterális szklerózis és más gerincvelõ-rendellenességek kezelésére
|
|
WO2008011344A2
(en)
*
|
2006-07-17 |
2008-01-24 |
Nationwide Children's Hospital Inc. |
Disruption of programmed death-1 (pd-1) ligands to adjuvant adeno-associated virus vector vaccines
|
|
EP3146982B1
(de)
|
2006-10-03 |
2019-08-21 |
Genzyme Corporation |
Gentherapie für amyotrophe lateralsklerose und andere rückenmarkserkrankungen
|
|
WO2008067480A2
(en)
|
2006-11-29 |
2008-06-05 |
Nationwide Children's Hospital |
Myostatin inhibition for enhancing muscle and/or improving muscle function
|
|
CN104383556B
(zh)
|
2007-05-16 |
2018-06-05 |
布里格姆妇女医院 |
突触核蛋白病的治疗
|
|
PL2158322T3
(pl)
|
2007-06-06 |
2017-10-31 |
Genzyme Corp |
Terapia genowa dla lizosomalnych chorób spichrzeniowych
|
|
FI20070808A0
(fi)
|
2007-10-25 |
2007-10-25 |
Mart Saarma |
GDNF:n silmukointivariantit ja niiden käytöt
|
|
US9526737B2
(en)
|
2007-12-03 |
2016-12-27 |
The Regents Of The University Of California |
Oxysterols for activation of hedgehog signaling, osteoinduction, antiadipogenesis, and Wnt signaling
|
|
US20090196854A1
(en)
*
|
2008-02-04 |
2009-08-06 |
Kytos Biosystems S.A. |
Methods and compositions for use of crl 5803 cells for expression of biotherapeutics and encapsulated cell-based delivery
|
|
FI20080326A0
(fi)
|
2008-04-30 |
2008-04-30 |
Licentia Oy |
Neurotroofinen tekijä MANF ja sen käytöt
|
|
WO2010002895A2
(en)
|
2008-06-30 |
2010-01-07 |
The Regents Of The University Of Michigan |
Lysosomal phospholipase a2 (lpla2) activity as a diagnostic and therapeutic target for identifying and treating systemic lupus erythematosis
|
|
US11219696B2
(en)
|
2008-12-19 |
2022-01-11 |
Nationwide Children's Hospital |
Delivery of polynucleotides using recombinant AAV9
|
|
US9415121B2
(en)
|
2008-12-19 |
2016-08-16 |
Nationwide Children's Hospital |
Delivery of MECP2 polynucleotide using recombinant AAV9
|
|
SI3988660T1
(sl)
|
2009-05-02 |
2025-09-30 |
Genzyme Corporation |
Genska terapija za nevrodegenerativne motnje
|
|
CA2816883A1
(en)
|
2010-11-23 |
2012-05-31 |
Presage Biosciences, Inc. |
Therapeutic methods and compositions for solid delivery
|
|
US20140155469A1
(en)
|
2011-04-19 |
2014-06-05 |
The Research Foundation Of State University Of New York |
Adeno-associated-virus rep sequences, vectors and viruses
|
|
EP3495472B1
(de)
|
2011-04-21 |
2023-11-15 |
Nationwide Children's Hospital, Inc. |
Rekombinante virusprodukte und verfahren zur expressionshemmung von myotilin
|
|
US10196636B2
(en)
|
2011-04-21 |
2019-02-05 |
Nationwide Children's Hospital, Inc. |
Recombinant virus products and methods for inhibition of expression of myotilin
|
|
ES2748577T3
(es)
|
2011-05-19 |
2020-03-17 |
Univ Michigan Regents |
Agentes de fijación de la integrina alfa-2 y uso de los mismos para inhibir la proliferación de las células de cáncer
|
|
US20130039888A1
(en)
|
2011-06-08 |
2013-02-14 |
Nationwide Children's Hospital Inc. |
Products and methods for delivery of polynucleotides by adeno-associated virus for lysosomal storage disorders
|
|
CA2842798C
(en)
|
2011-07-25 |
2021-02-23 |
Nationwide Children's Hospital, Inc. |
Recombinant virus products and methods for inhibition of expression of dux4
|
|
CN110777124A
(zh)
|
2011-10-27 |
2020-02-11 |
威尔斯达眼科制剂公司 |
编码视杆细胞来源的视锥细胞活力因子的载体
|
|
US9434928B2
(en)
|
2011-11-23 |
2016-09-06 |
Nationwide Children's Hospital, Inc. |
Recombinant adeno-associated virus delivery of alpha-sarcoglycan polynucleotides
|
|
EP2785683B1
(de)
|
2011-11-30 |
2020-02-05 |
Ludwig Institute for Cancer Research Ltd. |
Inkt-zellmodulatoren und verwendungsverfahren dafür
|
|
GB201120860D0
(en)
|
2011-12-05 |
2012-01-18 |
Cambridge Entpr Ltd |
Cancer immunotherapy
|
|
JP6468843B2
(ja)
|
2012-02-17 |
2019-02-13 |
ザ スキーペンズ アイ リサーチ インスティチュート |
ヒト網膜前駆細胞の表現型プロファイル
|
|
CA2872751A1
(en)
|
2012-05-07 |
2013-11-14 |
The Regents Of The University Of California |
Oxysterol analogue oxy133 induces osteogenesis and hedgehog signaling and inhibits adipogenesis
|
|
WO2013184209A1
(en)
|
2012-06-04 |
2013-12-12 |
Ludwig Institute For Cancer Research Ltd. |
Mif for use in methods of treating subjects with a neurodegenerative disorder
|
|
CA2880653C
(en)
|
2012-08-01 |
2022-05-17 |
Nationwide Children's Hospital |
Intrathecal delivery of recombinant adeno-associated virus 9
|
|
WO2014039916A1
(en)
|
2012-09-06 |
2014-03-13 |
The University Of Chicago |
Antisense polynucleotides to induce exon skipping and methods of treating dystrophies
|
|
CA2885216A1
(en)
|
2012-09-17 |
2014-03-20 |
The Research Institute At Nationwide Children's Hospital |
Compositions and methods for treating amyotrophic lateral sclerosis
|
|
MY170528A
(en)
|
2013-02-18 |
2019-08-09 |
Vegenics Pty Ltd |
Vegfr-3 ligand binding molecules and uses thereof
|
|
AU2014251099B2
(en)
|
2013-04-08 |
2019-01-17 |
The University Of Kansas |
Chimeric adeno-associated virus/ bocavirus parvovirus vector
|
|
US9862945B2
(en)
|
2013-04-20 |
2018-01-09 |
Research Institute At Nationwide Children's Hospital |
Recombinant adeno-associated virus delivery of exon 2-targeted U7SNRNA polynucleotide constructs
|
|
JP2016517888A
(ja)
|
2013-05-02 |
2016-06-20 |
ザ リージェンツ オブ ザ ユニバーシティ オブ カリフォルニア |
骨選択的骨形成のオキシステロール骨標的薬剤
|
|
JP2016523835A
(ja)
|
2013-05-15 |
2016-08-12 |
リージェンツ オブ ザ ユニバーシティ オブ ミネソタ |
中枢神経系へのアデノ随伴ウイルスを介した遺伝子導入
|
|
WO2014191630A2
(en)
|
2013-05-28 |
2014-12-04 |
Helsingin Yliopisto |
Non-human animal model encoding a non-functional manf gene
|
|
RS63942B1
(sr)
|
2013-08-27 |
2023-02-28 |
Res Inst Nationwide Childrens Hospital |
Proizvodi i postupci za lečenje amiotrofične lateralne skleroze
|
|
US11078464B2
(en)
*
|
2013-08-30 |
2021-08-03 |
Amgen Inc. |
High titer recombinant AAV vector production in adherent and suspension cells
|
|
US9725719B2
(en)
|
2013-11-05 |
2017-08-08 |
The Research Institute At Nationwide Children's Hospital |
Compositions and methods for inhibiting NF-κB and SOD-1 to treat amyotrophic lateral sclerosis
|
|
US10047130B2
(en)
|
2014-03-18 |
2018-08-14 |
Washington University |
Methods and compositions for red-shifted chromophore substitution for optogenetic applications
|
|
US10195280B2
(en)
|
2014-07-15 |
2019-02-05 |
Life Technologies Corporation |
Compositions and methods for efficient delivery of molecules to cells
|
|
CA2957661A1
(en)
|
2014-08-09 |
2016-02-18 |
Kevin FLANIGAN |
Methods and materials for activating an internal ribosome entry site in exon 5 of the dmd gene
|
|
US10842886B2
(en)
|
2014-10-10 |
2020-11-24 |
Research Institute At Nationwide Children's Hospital |
Guided injections for AAV gene transfer to muscle
|
|
EP3690024A1
(de)
|
2014-11-05 |
2020-08-05 |
The Research Institute at Nationwide Children's Hospital |
Verfahren und materialien zur herstellung rekombinanter viren in eukaryotischen mikroalgen
|
|
CN107427666B
(zh)
|
2015-01-30 |
2022-11-04 |
加利福尼亚大学校董 |
脊髓软膜下基因递送系统
|
|
MA41451A
(fr)
|
2015-02-04 |
2017-12-12 |
Univ Washington |
Constructions anti-tau
|
|
WO2016135558A2
(en)
|
2015-02-23 |
2016-09-01 |
Crispr Therapeutics Ag |
Materials and methods for treatment of hemoglobinopathies
|
|
EP3280451B8
(de)
|
2015-04-08 |
2019-09-25 |
The United States of America, as represented by the Secretary, Department of Health and Human Services |
Virale gentherapie zur behandlung von cholesterinspeicherungserkrankung oder -störung
|
|
US10273483B2
(en)
|
2015-04-08 |
2019-04-30 |
The University Of Chicago |
Compositions and methods for correcting limb girdle muscular dystrophy type 2C using exon skipping
|
|
CA2985235A1
(en)
|
2015-05-07 |
2016-11-10 |
Shire Human Genetic Therapies, Inc. |
Glucocerebrosidase gene therapy for parkinson's disease
|
|
KR20220082100A
(ko)
|
2015-05-15 |
2022-06-16 |
리젠츠 오브 더 유니버시티 오브 미네소타 |
중추 신경계로의 아데노-연관 치료적 전달
|
|
US10017832B2
(en)
|
2015-08-25 |
2018-07-10 |
Washington University |
Compositions and methods for site specific recombination at asymmetric sites
|
|
KR102799163B1
(ko)
|
2015-09-17 |
2025-04-21 |
더 리서치 인스티튜트 앳 네이션와이드 칠드런스 하스피탈 |
Galgt2 유전자 치료 방법 및 물질
|
|
WO2017064546A1
(en)
|
2015-09-24 |
2017-04-20 |
Crispr Therapeutics Ag |
Novel family of rna-programmable endonucleases and their uses in genome editing and other applications
|
|
EP4279084B1
(de)
|
2015-10-28 |
2025-06-11 |
Vertex Pharmaceuticals Inc. |
Materialien und verfahren zur behandlung von duchenne-muskeldystrophie
|
|
US11866727B2
(en)
|
2015-11-06 |
2024-01-09 |
Crispr Therapeutics Ag |
Materials and methods for treatment of glycogen storage disease type 1A
|
|
CN108463211B
(zh)
|
2015-11-16 |
2022-09-27 |
全国儿童医院研究所 |
用于治疗肌联蛋白类肌病和其它肌联蛋白病变的材料和方法
|
|
WO2017093804A2
(en)
|
2015-12-01 |
2017-06-08 |
Crispr Therapeutics Ag |
Materials and methods for treatment of alpha-1 antitrypsin deficiency
|
|
CA3009308A1
(en)
|
2015-12-23 |
2017-06-29 |
Chad Albert COWAN |
Materials and methods for treatment of amyotrophic lateral sclerosis and/or frontal temporal lobular degeneration
|
|
US11938193B2
(en)
|
2016-01-08 |
2024-03-26 |
Washington University |
Compositions comprising chemerin and methods of use thereof
|
|
EP3411078A1
(de)
|
2016-02-02 |
2018-12-12 |
Crispr Therapeutics AG |
Materialien und verfahren zur behandlung von schwerer kombinierter immundefizienz (scid) oder omenn-syndrom
|
|
WO2017139381A1
(en)
|
2016-02-08 |
2017-08-17 |
University Of Iowa Research Foundation |
Methods to produce chimeric adeno-associated virus/bocavirus parvovirus
|
|
WO2017141109A1
(en)
|
2016-02-18 |
2017-08-24 |
Crispr Therapeutics Ag |
Materials and methods for treatment of severe combined immunodeficiency (scid) or omenn syndrome
|
|
WO2017147509A1
(en)
|
2016-02-25 |
2017-08-31 |
Marco Colonna |
Compositions comprising trem2 and methods of use thereof
|
|
JP6966463B2
(ja)
|
2016-02-26 |
2021-11-17 |
リサーチ インスティチュート アット ネイションワイド チルドレンズ ホスピタル |
組換えウイルス産物及びdux4エクソンスキッピングを誘導するための方法
|
|
WO2017155973A1
(en)
|
2016-03-07 |
2017-09-14 |
University Of Iowa Research Foundation |
Aav-mediated expression using a synthetic promoter and enhancer
|
|
US11083799B2
(en)
|
2016-03-16 |
2021-08-10 |
Crispr Therapeutics Ag |
Materials and methods for treatment of hereditary haemochromatosis
|
|
AU2017241534A1
(en)
|
2016-03-28 |
2018-10-04 |
The Regents Of The University Of California |
Method and composition for treating neuronal hyper-excitability
|
|
BR112018070249A2
(pt)
|
2016-04-02 |
2019-01-29 |
Research Institute At Nationwide Children's Hospital |
sistema promotor de u6 modificada para expressão específica de tecido
|
|
CN109121395B
(zh)
|
2016-04-15 |
2022-08-09 |
全国儿童医院研究所 |
腺相关病毒载体递送β-肌聚糖和微RNA-29以及肌营养不良症的治疗
|
|
WO2017181011A1
(en)
|
2016-04-15 |
2017-10-19 |
Research Institute At Nationwide Children's Hospital |
Adeno-associated virus vector delivery of microrna-29 to treat muscular dystrophy
|
|
JP6974349B2
(ja)
|
2016-04-18 |
2021-12-01 |
クリスパー セラピューティクス アクチェンゲゼルシャフト |
ヘモグロビン異常症の処置のための材料及び方法
|
|
WO2017191503A1
(en)
|
2016-05-05 |
2017-11-09 |
Crispr Therapeutics Ag |
Materials and methods for treatment of hemoglobinopathies
|
|
US12173305B2
(en)
|
2016-05-26 |
2024-12-24 |
University Of Iowa Research Foundation |
cis and trans requirements for terminal resolution of human bocavirus 1
|
|
CA3029119A1
(en)
|
2016-06-29 |
2018-01-04 |
Crispr Therapeutics Ag |
Materials and methods for treatment of friedreich ataxia and other related disorders
|
|
WO2018002762A1
(en)
|
2016-06-29 |
2018-01-04 |
Crispr Therapeutics Ag |
Materials and methods for treatment of amyotrophic lateral sclerosis (als) and other related disorders
|
|
US11427838B2
(en)
|
2016-06-29 |
2022-08-30 |
Vertex Pharmaceuticals Incorporated |
Materials and methods for treatment of myotonic dystrophy type 1 (DM1) and other related disorders
|
|
EP4650364A3
(de)
|
2016-07-06 |
2026-01-21 |
Vertex Pharmaceuticals Incorporated |
Materialien und verfahren zur behandlung von schmerzbedingten erkrankungen
|
|
EP3481857B1
(de)
|
2016-07-06 |
2026-02-11 |
Vertex Pharmaceuticals Incorporated |
Materialien und verfahren zur behandlung von schmerzbedingten erkrankungen
|
|
WO2018007871A1
(en)
|
2016-07-08 |
2018-01-11 |
Crispr Therapeutics Ag |
Materials and methods for treatment of transthyretin amyloidosis
|
|
WO2018020323A2
(en)
|
2016-07-25 |
2018-02-01 |
Crispr Therapeutics Ag |
Materials and methods for treatment of fatty acid disorders
|
|
IL309808B2
(en)
|
2016-11-15 |
2025-04-01 |
Univ Minnesota |
Method for improving neurological function in MPSI and MPSII and other neurological disorders
|
|
IL322146A
(en)
|
2016-11-17 |
2025-09-01 |
Nationwide Childrens Hospital Inc |
Intrathecal administration of adenovirus encoding methyl-CpG-binding protein 2
|
|
CA3045667A1
(en)
|
2016-12-13 |
2018-06-21 |
Seattle Children's Hospital (dba Seattle Children's Research Institute) |
Methods of exogenous drug activation of chemical-induced signaling complexes expressed in engineered cells in vitro and in vivo
|
|
US11142775B2
(en)
|
2017-01-13 |
2021-10-12 |
University Of Iowa Research Foundation |
Bocaparvovirus small noncoding RNA and uses thereof
|
|
WO2018150271A1
(en)
|
2017-02-17 |
2018-08-23 |
Lonza Ltd. |
Mammalian cells for producing adeno-associated viruses
|
|
AU2018224387B2
(en)
|
2017-02-22 |
2024-08-08 |
Crispr Therapeutics Ag |
Compositions and methods for gene editing
|
|
WO2018154462A2
(en)
|
2017-02-22 |
2018-08-30 |
Crispr Therapeutics Ag |
Materials and methods for treatment of spinocerebellar ataxia type 2 (sca2) and other spinocerebellar ataxia type 2 protein (atxn2) gene related conditions or disorders
|
|
EP3585899A1
(de)
|
2017-02-22 |
2020-01-01 |
CRISPR Therapeutics AG |
Materialien und verfahren zur behandlung von primärer hyperoxalurie typ 1 (ph1) und anderen mit dem alanin-glyoxylataminotransferase (agxt)-gen assoziierten erkrankungen oder störungen
|
|
WO2018154439A1
(en)
|
2017-02-22 |
2018-08-30 |
Crispr Therapeutics Ag |
Materials and methods for treatment of spinocerebellar ataxia type 1 (sca1) and other spinocerebellar ataxia type 1 protein (atxn1) gene related conditions or disorders
|
|
WO2018154418A1
(en)
|
2017-02-22 |
2018-08-30 |
Crispr Therapeutics Ag |
Materials and methods for treatment of early onset parkinson's disease (park1) and other synuclein, alpha (snca) gene related conditions or disorders
|
|
US11338045B2
(en)
|
2017-03-17 |
2022-05-24 |
Newcastle University |
Adeno-associated virus vector delivery of a fragment of micro-dystrophin to treat muscular dystrophy
|
|
CN110997923B
(zh)
|
2017-03-17 |
2024-01-02 |
全国儿童医院研究所 |
腺相关病毒载体递送肌肉特异性微肌营养不良蛋白以治疗肌营养不良症
|
|
RU2019133002A
(ru)
|
2017-03-24 |
2021-04-26 |
Зе Юнивёрсити Корт Оф Зе Юнивёрсити Оф Эдинбург |
ЭКСПРЕССИОННЫЕ КАССЕТЫ MeCP2
|
|
BR112019023608A2
(pt)
|
2017-05-12 |
2020-05-26 |
Crispr Therapeutics Ag |
Materiais e métodos para células manipuladas e seus usos em imuno-oncologia
|
|
CA3068010A1
(en)
|
2017-06-20 |
2018-12-27 |
The United States Of America, As Represented By The Secretary, Department Of Health And Human Services |
Codon-optimized human npc1 genes for the treatment of niemann-pick type c1 deficiency and related conditions
|
|
WO2019011817A1
(en)
|
2017-07-08 |
2019-01-17 |
Genethon |
TREATMENT OF SPINAL AMYOTROPHY
|
|
CN110892064A
(zh)
|
2017-07-25 |
2020-03-17 |
牛津遗传学有限公司 |
腺病毒载体
|
|
MA49923A
(fr)
|
2017-10-02 |
2020-06-24 |
Res Inst Nationwide Childrens Hospital |
Système de déciblage de miarn pour interférence spécifique d'un tissu
|
|
US20220080055A9
(en)
|
2017-10-17 |
2022-03-17 |
Crispr Therapeutics Ag |
Compositions and methods for gene editing for hemophilia a
|
|
WO2019078916A1
(en)
|
2017-10-18 |
2019-04-25 |
Research Institute At Nationwide Children's Hospital |
ADENO-ASSOCIATED VIRUS VECTOR ADMINISTRATION OF MUSCLE-SPECIFIC MICRO-DYSTROPHINE TO TREAT MUSCLE DYSTROPHY
|
|
MX2020004035A
(es)
|
2017-10-20 |
2020-11-09 |
Res Inst Nationwide Childrens Hospital |
Métodos y materiales para terapia génica con nt-3.
|
|
MA50849A
(fr)
|
2017-10-26 |
2020-09-02 |
Vertex Pharma |
Substances et procédés pour le traitement d'hémoglobinopathies
|
|
EP4585229A3
(de)
|
2017-11-08 |
2026-01-14 |
Novartis AG |
Mittel und verfahren zur herstellung von viralen vektoren und deren verwendung
|
|
MA50579A
(fr)
|
2017-11-09 |
2020-09-16 |
Crispr Therapeutics Ag |
Systèmes crispr/cas ou crispr/cpf1 à auto-inactivation (sin) et leurs utilisations
|
|
EP3714055A1
(de)
|
2017-11-21 |
2020-09-30 |
CRISPR Therapeutics AG |
Materialien und verfahren zur behandlung von autosomal-dominanter retinitis pigmentosa
|
|
IL274702B2
(en)
|
2017-11-27 |
2026-04-01 |
Coda Biotherapeutics Inc |
Compounds and methods for neurological diseases
|
|
CA3084825A1
(en)
|
2017-12-14 |
2019-06-20 |
Crispr Therapeutics Ag |
Novel rna-programmable endonuclease systems and their use in genome editing and other applications
|
|
CA3084633A1
(en)
|
2017-12-21 |
2019-06-27 |
Crispr Therapeutics Ag |
Materials and methods for treatment of usher syndrome type 2a and/or non-syndromic autosomal recessive retinitis pigmentosa (arrp)
|
|
AU2018393050A1
(en)
|
2017-12-21 |
2020-06-18 |
Bayer Healthcare Llc |
Materials and methods for treatment of Usher Syndrome Type 2A
|
|
EP3737762A1
(de)
|
2018-01-12 |
2020-11-18 |
CRISPR Therapeutics AG |
Zusammensetzungen und verfahren zur geneditierung von genen durch transferrin-targeting
|
|
AU2019216257B2
(en)
|
2018-01-31 |
2025-11-20 |
Research Institute At Nationwide Children's Hospital |
Gene therapy for limb-girdle muscular dystrophy type 2C
|
|
MA51787A
(fr)
|
2018-02-05 |
2020-12-16 |
Vertex Pharma |
Substances et méthodes de traitement d'hémoglobinopathies
|
|
EP3749768A1
(de)
|
2018-02-05 |
2020-12-16 |
Vertex Pharmaceuticals Incorporated |
Materialien und verfahren zur behandlung von hämoglobinopathien
|
|
EP3752616A1
(de)
|
2018-02-16 |
2020-12-23 |
CRISPR Therapeutics AG |
Zusammensetzungen und verfahren zur geneditierung durch targeting von fibrinogen-alpha
|
|
JP7550648B2
(ja)
|
2018-03-19 |
2024-09-13 |
クリスパー セラピューティクス アーゲー |
新規rnaプログラム可能エンドヌクレアーゼ系およびその使用
|
|
MX2020010465A
(es)
|
2018-04-03 |
2021-01-08 |
|
Vectores de virus para direccionamiento a tejidos oftalmicos.
|
|
CA3095179A1
(en)
|
2018-04-03 |
2019-10-10 |
Stridebio, Inc. |
Antibody-evading virus vectors
|
|
BR112020020266A2
(pt)
|
2018-04-03 |
2021-01-19 |
Stridebio, Inc. |
Vetores de vírus com evasão de anticorpos
|
|
WO2019204668A1
(en)
|
2018-04-18 |
2019-10-24 |
Casebia Therapeutics Limited Liability Partnership |
Compositions and methods for knockdown of apo(a) by gene editing for treatment of cardiovascular disease
|
|
CA3091490A1
(en)
|
2018-04-27 |
2019-10-31 |
Seattle Children's Hospital (dba Seattle Children's Research Institute) |
Rapamycin resistant cells
|
|
AU2019272848A1
(en)
|
2018-05-22 |
2020-12-03 |
The Brigham And Women's Hospital, Inc. |
Gene therapy for alzheimer's disease
|
|
JP7478675B2
(ja)
|
2018-06-08 |
2024-05-07 |
ノバルティス アーゲー |
薬物製品の効力を測定するための細胞ベースアッセイ
|
|
US12258395B2
(en)
|
2018-06-11 |
2025-03-25 |
University Of Florida Research Foundation, Incorporated |
Materials and methods for treating stress-related disorders and cancer
|
|
GB201809588D0
(en)
|
2018-06-12 |
2018-07-25 |
Univ Bristol |
Materials and methods for modulating intraocular and intracranial pressure
|
|
JP7534961B2
(ja)
|
2018-06-18 |
2024-08-15 |
リサーチ インスティチュート アット ネイションワイド チルドレンズ ホスピタル |
ジストログリカノパチーおよびラミニン欠損筋ジストロフィーを治療するための組換えアデノ随伴ウイルス生成物および方法
|
|
IL324506A
(en)
|
2018-06-18 |
2026-01-01 |
Res Inst Nationwide Childrens Hospital |
Adeno-associated virus vector for delivery of muscle-specific microdystrophin for the treatment of muscular dystrophy
|
|
IL279789B2
(en)
|
2018-06-29 |
2026-04-01 |
Res Inst Nationwide Childrens Hospital |
Recombinant adeno-associated virus products and methods for treating limb girdle muscular dystrophy 2A
|
|
AU2019326551A1
(en)
|
2018-08-22 |
2021-03-18 |
Research Institute At Nationwide Children's Hospital |
Recombinant virus products and methods for inhibiting expression of dystrophia myotonica protein kinase and/or interfering with a trinucleotide repeat expansion in the 3' untranslated region of the DMPK gene
|
|
AU2019328270B2
(en)
|
2018-08-29 |
2026-02-26 |
Research Institute At Nationwide Children's Hospital |
Products and methods for inhibition of expression of mutant GARS protein
|
|
US12239699B2
(en)
|
2018-09-11 |
2025-03-04 |
Shanghai Public Health Clinical Center |
Immunogen for broad-spectrum influenza vaccine and application thereof
|
|
JP7520826B2
(ja)
|
2018-10-17 |
2024-07-23 |
クリスパー・セラピューティクス・アクチェンゲゼルシャフト |
導入遺伝子を送達するための組成物および方法
|
|
CA3121191A1
(en)
|
2018-11-28 |
2020-06-04 |
Crispr Therapeutics Ag |
Optimized mrna encoding cas9 for use in lnps
|
|
EP3886919A1
(de)
|
2018-11-30 |
2021-10-06 |
Novartis AG |
Aav-virusvektoren und verwendungen davon
|
|
US20220042045A1
(en)
|
2018-12-21 |
2022-02-10 |
Genethon |
Expression cassettes for gene therapy vectors
|
|
JP2022516515A
(ja)
|
2018-12-31 |
2022-02-28 |
リサーチ インスティチュート アット ネイションワイド チルドレンズ ホスピタル |
Rna標的化crispr-cas13bを使用するdux4 rna発現停止
|
|
AU2020218501B2
(en)
|
2019-02-04 |
2026-01-29 |
Research Institute At Nationwide Children's Hospital |
Adeno-associated virus delivery of CLN6 polynucleotide
|
|
AR118005A1
(es)
|
2019-02-04 |
2021-09-08 |
Res Institute At Nationwide ChildrenS Hospital |
Administración del virus adenoasociado de polinucleótido de cln3
|
|
SG11202108357PA
(en)
|
2019-02-15 |
2021-08-30 |
Crispr Therapeutics Ag |
Gene editing for hemophilia a with improved factor viii expression
|
|
KR20210133242A
(ko)
|
2019-02-26 |
2021-11-05 |
더 리서치 인스티튜트 앳 네이션와이드 칠드런스 하스피탈 |
B-사르코글리칸의 아데노 관련 바이러스 벡터 전달 및 근이영양증의 치료
|
|
US20220145274A1
(en)
|
2019-03-12 |
2022-05-12 |
Crispr Therapeutics Ag |
Novel high fidelity rna-programmable endonuclease systems and uses thereof
|
|
CN113727992A
(zh)
|
2019-03-21 |
2021-11-30 |
斯特里迪比奥公司 |
重组腺相关病毒载体
|
|
US20220193259A1
(en)
|
2019-04-15 |
2022-06-23 |
Sanford Research |
Gene therapy for treating or preventing visual effects in batten disease
|
|
MX2021012681A
(es)
|
2019-04-15 |
2022-03-25 |
Spirovant Sciences Inc |
Composiciones y metodos para el tratamiento de la fibrosis quistica.
|
|
SG11202111353QA
(en)
|
2019-04-15 |
2021-11-29 |
Univ Iowa Res Found |
Methods and compositions for transgene expression
|
|
EP3966327A1
(de)
|
2019-05-08 |
2022-03-16 |
Vertex Pharmaceuticals Incorporated |
Crispr/cas all-in-two-vektorsystemen zur behandlung von dmd
|
|
JP7707081B2
(ja)
|
2019-05-17 |
2025-07-14 |
リサーチ インスティチュート アット ネイションワイド チルドレンズ ホスピタル |
網膜細胞を標的とした最適化された遺伝子治療
|
|
CA3141712A1
(en)
|
2019-05-24 |
2020-12-03 |
The Brigham And Women's Hospital, Inc. |
Gene therapy for alzheimer's disease
|
|
US12173290B2
(en)
|
2019-06-28 |
2024-12-24 |
Crispr Therapeutics Ag |
Materials and methods for controlling gene editing
|
|
CN114174514A
(zh)
|
2019-07-25 |
2022-03-11 |
诺华股份有限公司 |
可调节的表达系统
|
|
CA3150964A1
(en)
|
2019-08-21 |
2021-02-25 |
Research Institute At Nationwide Children's Hospital |
Adeno-associated virus vector delivery of alpha-sarcoglycan and the treatment of muscular dystrophy
|
|
JP7781052B2
(ja)
|
2019-08-21 |
2025-12-05 |
トレイムス バイオ, インコーポレイテッド |
神経学的疾患のための組成物および方法
|
|
US20230416776A1
(en)
|
2019-10-08 |
2023-12-28 |
Regents Of The University Of Minnesota |
Crispr-mediated human genome editing with vectors
|
|
MX2022004353A
(es)
|
2019-10-17 |
2022-07-19 |
|
Casete de transferencia de aav.
|
|
CN114787180A
(zh)
|
2019-10-17 |
2022-07-22 |
斯特里迪比奥公司 |
用于治疗c型尼曼-匹克病的腺相关病毒载体
|
|
AU2020366531A1
(en)
|
2019-10-18 |
2022-05-26 |
Research Institute At Nationwide Children's Hospital |
Gene therapy targeting cochlear cells
|
|
JP7781057B2
(ja)
|
2019-10-18 |
2025-12-05 |
リサーチ インスティチュート アット ネイションワイド チルドレンズ ホスピタル |
Irf2bpl遺伝子の変異に関連する障害の治療のための材料および方法
|
|
US20230211018A1
(en)
|
2019-11-22 |
2023-07-06 |
Research Institute At Nationwide Children's Hospital |
Materials and methods for treatment of disorders associated with the ighmbp2 gene
|
|
AU2020393917A1
(en)
|
2019-11-29 |
2022-06-23 |
Paros Bio, Inc. |
Gene therapy for neurodegenerative disorders
|
|
EP4077687A1
(de)
|
2019-12-20 |
2022-10-26 |
Research Institute at Nationwide Children's Hospital |
Optimierte gentherapie zum targeting von muskeln bei muskelerkrankungen
|
|
US12665049B2
(en)
|
2020-01-17 |
2026-06-23 |
AskBio, Inc. |
Systems and methods for synthetic regulatory sequence design or production
|
|
WO2021168124A1
(en)
|
2020-02-18 |
2021-08-26 |
Research Institute At Nationwide Children's Hospital |
Aav-mediated targeting of mirna in the treatment of x-linked disorders
|
|
CN115379863A
(zh)
|
2020-04-14 |
2022-11-22 |
吉尼松公司 |
用于治疗酸性神经酰胺酶缺乏症的载体
|
|
EP4164668A1
(de)
|
2020-06-15 |
2023-04-19 |
Research Institute at Nationwide Children's Hospital |
Adeno-assoziierte virusvektorverabreichung für muskeldystrophien
|
|
US20230242941A1
(en)
|
2020-06-30 |
2023-08-03 |
Eric Yuen |
Methods and compositions for administering recombinant viral vectors
|
|
WO2022011099A1
(en)
|
2020-07-08 |
2022-01-13 |
Regents Of The University Of Minnesota |
Modified hexosaminidase and uses thereof
|
|
WO2022018638A1
(en)
|
2020-07-21 |
2022-01-27 |
Crispr Therapeutics Ag |
Genome-editing compositions and methods to modulate faah for treatment of neurological disorders
|
|
JP2023542614A
(ja)
|
2020-08-19 |
2023-10-11 |
サレプタ セラピューティクス, インコーポレイテッド |
レット症候群の治療のためのアデノ随伴ウイルスベクター
|
|
US20230414787A1
(en)
|
2020-08-27 |
2023-12-28 |
University Of Iowa Research Foundation |
Gene knock-out for treatment of glaucoma
|
|
GB202013940D0
(en)
|
2020-09-04 |
2020-10-21 |
Synpromics Ltd |
Regulatory nucleic acid sequences
|
|
TWI887479B
(zh)
|
2020-09-08 |
2025-06-21 |
美商薩羅塔治療公司 |
表現γ-肌聚醣之腺相關病毒載體之全身性遞送及肌肉失養症之治療
|
|
JP2023541444A
(ja)
|
2020-09-15 |
2023-10-02 |
リサーチ インスティチュート アット ネイションワイド チルドレンズ ホスピタル |
筋ジストロフィー患者における多様なdmd変異の補正のためのaav媒介性の相同性非依存的標的化組み込み遺伝子編集
|
|
US20240261434A1
(en)
|
2020-09-28 |
2024-08-08 |
Research Institute At Nationwide Children's Hospital |
Products and methods for treating muscular dystrophy
|
|
WO2022070107A1
(en)
|
2020-09-30 |
2022-04-07 |
Crispr Therapeutics Ag |
Materials and methods for treatment of amyotrophic lateral sclerosis
|
|
US20230374542A1
(en)
|
2020-10-07 |
2023-11-23 |
Asklepios Biopharmaceutical, Inc. |
Therapeutic adeno-associated virus delivery of fukutin related protein (fkrp) for treating dystroglycanopathy. disorders including limb girdle 21 (lgmd21)
|
|
CA3203585A1
(en)
|
2020-11-30 |
2022-06-02 |
Research Institute At Nationwide Children's Hospital |
Compositions and methods for treating facioscapulohumeral muscular dystrophy (fshd)
|
|
EP4263829A1
(de)
|
2020-12-17 |
2023-10-25 |
Vertex Pharmaceuticals Incorporated |
Zusammensetzungen und verfahren zur bearbeitung von beta-globin zur behandlung von hämglobinopathien
|
|
WO2022164860A1
(en)
|
2021-01-27 |
2022-08-04 |
Research Institute At Nationwide Children's Hospital |
Materials and methods for the treatment of lysosomal acid lipase deficiency (lal-d)
|
|
US20240093191A1
(en)
|
2021-02-03 |
2024-03-21 |
Research Institute At Nationwide Children's Hospital |
Compositions and methods for treating disease associated with dux4 overexpression
|
|
WO2022170038A1
(en)
|
2021-02-05 |
2022-08-11 |
Amicus Therapeutics, Inc. |
Adeno-associated virus delivery of cln3 polynucleotide
|
|
US20240316217A1
(en)
|
2021-02-05 |
2024-09-26 |
Regents Of The University Of Minnesota |
Methods for preventing cardiac or skeletal defects in diseases including mucopolysaccharidoses
|
|
EP4301462A1
(de)
|
2021-03-04 |
2024-01-10 |
Research Institute at Nationwide Children's Hospital |
Produkte und verfahren zur behandlung von dystrophinbasierten myopathien mit crispr-cas9 zur korrektur von dmd-exon-duplikationen
|
|
CN115427561B
(zh)
|
2021-03-09 |
2024-06-04 |
辉大(上海)生物科技有限公司 |
工程化CRISPR/Cas13系统及其用途
|
|
WO2022221424A1
(en)
|
2021-04-13 |
2022-10-20 |
Research Institute At Nationwide Children's Hospital |
Recombinant adeno-associated virus encoding methyl-cpg binding protein 2 for treating pitt hopkins syndrome via intrathecal delivery
|
|
US12275941B2
(en)
|
2021-04-15 |
2025-04-15 |
Research Institute At Nationwide Children's Hospital |
Products and methods for inhibition of expression of dynamin-1 variants
|
|
EP4323011A1
(de)
|
2021-04-15 |
2024-02-21 |
Spirovant Sciences, Inc. |
Verfahren und zusammensetzungen zur behandlung von zystischer fibrose
|
|
AU2022262420A1
(en)
|
2021-04-23 |
2023-11-16 |
Research Institute At Nationwide Children's Hospital |
Products and methods for treating muscular dystrophy
|
|
US20240425877A1
(en)
|
2021-05-07 |
2024-12-26 |
Ucl Business Ltd |
Abca4 genome editing
|
|
BR112023024078A2
(pt)
|
2021-05-17 |
2024-01-30 |
Sarepta Therapeutics Inc |
Produção de vetores de aav recombinantes para o tratamento de distrofia muscular
|
|
EP4108263A3
(de)
|
2021-06-02 |
2023-03-22 |
Research Institute at Nationwide Children's Hospital |
Rekombinante adeno-assoziierte virusprodukte und verfahren zur behandlung von gliedergürtel-muskeldystrophie 2a
|
|
EP4101928A1
(de)
|
2021-06-11 |
2022-12-14 |
Bayer AG |
Programmierbare typ-v-rna-endonukleasesysteme
|
|
MX2023014774A
(es)
|
2021-06-11 |
2024-01-15 |
Bayer Ag |
Nuevos sistemas de endonucleasas programables de arn tipo v.
|
|
WO2023283962A1
(en)
|
2021-07-16 |
2023-01-19 |
Huigene Therapeutics Co., Ltd. |
Modified aav capsid for gene therapy and methods thereof
|
|
CA3228365A1
(en)
|
2021-08-11 |
2023-02-16 |
Solid Biosciences Inc. |
Treatment of muscular dystrophy
|
|
EP4144841A1
(de)
|
2021-09-07 |
2023-03-08 |
Bayer AG |
Neue programmierbare rna-endonuklease-systeme mit verbesserter pam-spezifität und deren verwendung
|
|
JP2024534410A
(ja)
|
2021-09-16 |
2024-09-20 |
ノバルティス アーゲー |
新規転写因子
|
|
US20240401046A1
(en)
|
2021-10-07 |
2024-12-05 |
Research Institute At Nationwide Children' S Hospital |
Products and methods for myelin protein zero silencing and treating cmt1b disease
|
|
WO2023060233A1
(en)
|
2021-10-08 |
2023-04-13 |
Amicus Therapeutics, Inc. |
Biomarkers for lysosomal storage diseases
|
|
US12285497B2
(en)
|
2021-10-15 |
2025-04-29 |
Research Institute At Nationwide Children's Hospital |
Self-complementary adeno-associated virus vector and its use in treatment of muscular dystrophy
|
|
AU2022386664A1
(en)
|
2021-11-12 |
2024-06-13 |
Research Institute At Nationwide Children's Hospital |
Materials and methods for slc6a1 gene therapy
|
|
US20230279431A1
(en)
|
2021-11-30 |
2023-09-07 |
Research Institute At Nationwide Children's Hospital |
Self-Complementary Adeno-Associated Virus Vector and its Use in Treatment of Muscular Dystrophy
|
|
EP4198047A1
(de)
|
2021-12-16 |
2023-06-21 |
Genethon |
Erhöhung des gentransfers von fukutin-verwandtem protein unter verwendung modifizierter itr-sequenzen
|
|
EP4198048A1
(de)
|
2021-12-16 |
2023-06-21 |
Genethon |
Calpain-3-gentransfersteigerung unter verwendung von modifizierten itr-sequenzen
|
|
EP4198046A1
(de)
|
2021-12-16 |
2023-06-21 |
Genethon |
Erhöhung des gentransfers von alpha-sarcoglykan unter verwendung von modifizierten itr-sequenzen
|
|
EP4198134A1
(de)
|
2021-12-16 |
2023-06-21 |
Genethon |
Transfererhöhung des gamma-sarcoglycan-gens unter verwendung von modifizierten itr-sequenzen
|
|
EP4453013A1
(de)
|
2021-12-21 |
2024-10-30 |
Research Institute at Nationwide Children's Hospital |
Materialien und verfahren zur behandlung von muskeldystrophie bei gliedmassengürteln
|
|
EP4453191A1
(de)
|
2021-12-23 |
2024-10-30 |
Bayer Aktiengesellschaft |
Neuartige programmierbare endonukleasesysteme für kleine v-rna
|
|
WO2023166425A1
(en)
|
2022-03-01 |
2023-09-07 |
Crispr Therapeutics Ag |
Methods and compositions for treating angiopoietin-like 3 (angptl3) related conditions
|
|
WO2023168400A2
(en)
|
2022-03-03 |
2023-09-07 |
Research Institute At Nationwide Children's Hospital |
Materials and methods for the treatment of eif2b5 mutations and diseases resulting therefrom
|
|
AU2023250649A1
(en)
|
2022-04-04 |
2024-11-14 |
The Regents Of The University Of California |
Genetic complementation compositions and methods
|
|
CA3255627A1
(en)
|
2022-05-06 |
2023-11-09 |
Novartis Ag |
NEW VP2 FUSION POLYPEPTIDES OF RECOMBINANT AAV
|
|
JP2025523399A
(ja)
|
2022-06-08 |
2025-07-23 |
リサーチ インスティチュート アット ネイションワイド チルドレンズ ホスピタル |
変異型又は病原性kcnq3発現に関連する疾患又は状態を治療するための生成物及び方法
|
|
WO2023237587A1
(en)
|
2022-06-10 |
2023-12-14 |
Bayer Aktiengesellschaft |
Novel small type v rna programmable endonuclease systems
|
|
AU2023303015A1
(en)
|
2022-07-06 |
2025-01-23 |
Research Institute At Nationwide Children's Hospital |
Adeno-associated virus delivery of cln1 polynucleotide
|
|
WO2024035782A1
(en)
|
2022-08-10 |
2024-02-15 |
Aav Gene Therapeutics, Inc. |
Aav-mediated intramuscular delivery of insulin
|
|
EP4590838A1
(de)
|
2022-09-23 |
2025-07-30 |
Sarepta Therapeutics, Inc. |
Rekombinante aav-vektoren zur behandlung von muskeldystrophie
|
|
WO2024081706A1
(en)
|
2022-10-11 |
2024-04-18 |
Research Institute At Nationwide Children's Hospital |
Adeno-associated virus delivery to treat spinal muscular atrophy with respiratory distress type 1 (smard1) and charcot-marie-tooth type 2s (cmt2s)
|
|
AU2023364350A1
(en)
|
2022-10-19 |
2025-06-05 |
Affinia Therapeutics Inc. |
Recombinant aavs with improved tropism and specificity
|
|
WO2024092171A1
(en)
|
2022-10-26 |
2024-05-02 |
University Of Iowa Research Foundation |
Method to deliver large genes using virus and a dna recombination system
|
|
EP4608856A1
(de)
|
2022-10-27 |
2025-09-03 |
CARGO Therapeutics, Inc. |
Zusammensetzungen und verfahren für verbesserte immuntherapien
|
|
CN120569476A
(zh)
|
2022-11-30 |
2025-08-29 |
安铂生物公司 |
用于靶向反式剪接的方法和组合物
|
|
US20260209732A1
(en)
|
2022-12-13 |
2026-07-23 |
Bayer Aktiengesellschaft |
Engineered type v rna programmable endonucleases and their uses
|
|
US20260216373A1
(en)
|
2023-01-13 |
2026-07-30 |
Amicus Therapeutics, Inc. |
Gene Therapy Constructs for the Treatment of Pompe Disease
|
|
KR20250138783A
(ko)
|
2023-02-01 |
2025-09-22 |
사렙타 쎄러퓨틱스 인코퍼레이티드 |
rAAV 생산 방법
|
|
WO2024168276A2
(en)
|
2023-02-09 |
2024-08-15 |
Cargo Therapeutics, Inc. |
Compositions and methods for immunotherapies
|
|
CN121285568A
(zh)
|
2023-03-30 |
2026-01-06 |
制药五有限责任公司 |
编码视杆细胞源性视锥细胞活力因子和人IgK信号序列的载体
|
|
JP2026516715A
(ja)
|
2023-04-18 |
2026-05-26 |
リサーチ インスティチュート アット ネイションワイド チルドレンズ ホスピタル |
肢帯型筋ジストロフィーr9及び先天性筋ジストロフィー1cを治療するための遺伝子療法
|
|
AU2024265705A1
(en)
|
2023-05-02 |
2025-11-20 |
Research Institute At Nationwide Children's Hospital |
Gene therapy for treatment of protein misfolding diseases
|
|
AU2024265701A1
(en)
|
2023-05-02 |
2025-12-04 |
Research Institute At Nationwide Children's Hospital |
A modular system to convert therapeutic microrna expression cassettes from polymerase iii-based to polymerase ii-based promoters
|
|
WO2024229115A1
(en)
|
2023-05-02 |
2024-11-07 |
Research Institute At Nationwide Children's Hospital |
Treatment of multiple sclerosis using nt-3 gene therapy
|
|
JP2026517843A
(ja)
|
2023-05-03 |
2026-06-02 |
アイオーエックス セラピューティクス リミテッド |
Inkt細胞調節剤リポソーム組成物及び使用方法
|
|
AU2024271851A1
(en)
|
2023-05-16 |
2025-12-18 |
Affinia Therapeutics Inc. |
Recombinant aavs with improved tropism and specificity
|
|
WO2024254319A1
(en)
|
2023-06-07 |
2024-12-12 |
Research Institute At Nationwide Children's Hospital |
Gene therapy for lysosomal acid lipase deficiency (lal-d)
|
|
EP4727966A1
(de)
|
2023-06-13 |
2026-04-22 |
Research Institute at Nationwide Children's Hospital |
Materialien und verfahren zur behandlung von neurofibromin-1-mutationen und daraus resultierende erkrankungen
|
|
WO2025022290A1
(en)
|
2023-07-21 |
2025-01-30 |
Crispr Therapeutics Ag |
Modulating expression of alas1 (5'-aminolevulinate synthase 1) gene
|
|
EP4512403A1
(de)
|
2023-08-22 |
2025-02-26 |
Friedrich-Schiller-Universität Jena |
Neuropeptid b und w-rezeptor als ziel zur behandlung von stimmungsstörungen und/oder chronischem stress
|
|
TW202521691A
(zh)
|
2023-10-06 |
2025-06-01 |
美商藍岩醫療公司 |
經工程化之v型rna可程式核酸內切酶及其用途
|
|
WO2025096498A1
(en)
|
2023-10-30 |
2025-05-08 |
Research Institute At Nationwide Children's Hospital |
Compositions and methods for treating diseases or conditions associated with progerin expression
|
|
TW202540200A
(zh)
|
2023-12-01 |
2025-10-16 |
美商基利科學股份有限公司 |
抗fap-light融合蛋白及其用途
|
|
US12655424B2
(en)
|
2024-02-05 |
2026-06-16 |
Amber Bio Inc. |
Methods and compositions for trans-splicing utilizing small nuclear RNAs and small nucleolar RNAs
|
|
WO2025179121A1
(en)
|
2024-02-21 |
2025-08-28 |
Research Institute At Nationwide Children's Hospital |
Exon 17-targeted nucleic acids, compositions, and methods for treatment of dystrophin-based myopathies
|
|
WO2025186726A1
(en)
|
2024-03-05 |
2025-09-12 |
Crispr Therapeutics Ag |
Modulating expression of agt (angiotensinogen) gene
|
|
WO2025188993A2
(en)
|
2024-03-07 |
2025-09-12 |
Research Institute At Nationwide Children's Hospital |
Gene therapy for treating gne-related disorders
|
|
TW202548023A
(zh)
|
2024-03-14 |
2025-12-16 |
美商雅菲納治療公司 |
用於生產重組腺相關病毒的質體系統
|
|
WO2025212838A1
(en)
|
2024-04-03 |
2025-10-09 |
Research Institute At Nationwide Children's Hospital |
Products and methods for treating diseases or disorders associated with dux4 overexpression
|
|
WO2025227063A1
(en)
|
2024-04-26 |
2025-10-30 |
Affinia Therapeutics Inc. |
Recombinant aavs with improved tropism and specificity
|
|
WO2025226343A1
(en)
|
2024-04-26 |
2025-10-30 |
Research Institute At Nationwide Children's Hospital |
Products and methods to inhibit expression of dynamin-1 variants and replace dynamin-1
|
|
WO2025235425A1
(en)
|
2024-05-06 |
2025-11-13 |
Research Institute At Nationwide Children's Hospital |
Improved proviral plasmids
|
|
WO2025235491A1
(en)
|
2024-05-07 |
2025-11-13 |
Affinia Therapeutics Inc. |
Recombinant aav for treatment of cardiac diseases
|
|
WO2025240690A2
(en)
|
2024-05-15 |
2025-11-20 |
Research Institute At Nationwide Children's Hospital |
Products and methods for treating diseases or conditions associated with progerin expression from an aberrant lmna gene
|
|
TW202613313A
(zh)
|
2024-05-31 |
2026-04-01 |
美商薩羅塔治療公司 |
肌向性raav
|
|
WO2025259871A1
(en)
|
2024-06-14 |
2025-12-18 |
Gilead Sciences, Inc. |
Anti-ccr8 antibodies and uses thereof
|
|
WO2026028089A1
(en)
|
2024-07-29 |
2026-02-05 |
Novartis Ag |
Compositions and methods for the treatment of lysosomal acid lipase deficiency (lal-d)
|
|
WO2026072752A1
(en)
|
2024-09-27 |
2026-04-02 |
Pharma Cinq, Llc |
Rod-derived cone viability factor fusion protein
|
|
WO2026094009A1
(en)
|
2024-11-04 |
2026-05-07 |
Insmed Incorporated |
Compositions and methods for treating duchenne muscular dystrophy
|
|
WO2026107323A1
(en)
|
2024-11-15 |
2026-05-21 |
Research Institute At Nationwide Children's Hospital |
Products and methods for full-length smchd1 expression using split inteins
|
|
WO2026150302A1
(en)
|
2025-01-09 |
2026-07-16 |
Novartis Ag |
Novel aav rep/cap encoding constructs
|
|
WO2026150324A1
(en)
|
2025-01-10 |
2026-07-16 |
Sarepta Therapeutics, Inc. |
Compositions and methods for treating dysferlinopathies
|
|
US12686869B1
(en)
|
2026-01-23 |
2026-07-21 |
Amber Bio Inc. |
Methods and compositions for trans-splicing utilizing trifunctional elements
|