US20020173643A1
(en)
*
|
1995-04-14 |
2002-11-21 |
Kappes John C. |
Fusion protein delivery system and uses thereof
|
EP1760151B1
(de)
*
|
1996-11-20 |
2012-03-21 |
Crucell Holland B.V. |
Adenovirus-Zusammensetzungen erhältlich durch ein verbessertes Produktions- und Reinigungsverfahren
|
US6566118B1
(en)
|
1997-09-05 |
2003-05-20 |
Targeted Genetics Corporation |
Methods for generating high titer helper-free preparations of released recombinant AAV vectors
|
US6989264B2
(en)
|
1997-09-05 |
2006-01-24 |
Targeted Genetics Corporation |
Methods for generating high titer helper-free preparations of released recombinant AAV vectors
|
CA2830694C
(en)
*
|
1997-09-05 |
2018-02-27 |
Genzyme Corporation |
Methods for generating high titer helper-free preparations of recombinant aav vectors
|
US7033595B1
(en)
|
1998-08-04 |
2006-04-25 |
Purdue Research Foundation |
Pseudotyped retroviruses and stable cell lines for their production
|
JP4472182B2
(ja)
*
|
1998-09-04 |
2010-06-02 |
ターゲティッド ジェネティクス コーポレイション |
放出された組換えaavベクターの高力価のヘルパーを含まない調製物を生成するための方法
|
EP2942393A1
(de)
|
1998-09-04 |
2015-11-11 |
Genzyme Corporation |
Verfahren zur erzeugung helferfreier präparate mit hohem titer aus freigesetzten rekombinanten aav-vektoren
|
JP2003510024A
(ja)
*
|
1999-08-09 |
2003-03-18 |
インサイト・ゲノミックス・インコーポレイテッド |
プロテアーゼ及びプロテアーゼインヒビター
|
AU7353500A
(en)
*
|
1999-09-10 |
2001-04-10 |
Incyte Genomics, Inc. |
Apoptosis proteins
|
US6790614B1
(en)
|
1999-11-19 |
2004-09-14 |
Novartis Ag |
Selectable cell surface marker genes
|
AU2001238534A1
(en)
|
2000-02-25 |
2001-09-03 |
Cambridge Drug Discovery, Ltd. |
Methods for identifying candidate polynucleotide molecules encoding a protease
|
JP2004507212A
(ja)
*
|
2000-03-03 |
2004-03-11 |
インサイト・ゲノミックス・インコーポレイテッド |
Gタンパク質共役受容体
|
US6849454B2
(en)
|
2000-03-07 |
2005-02-01 |
St. Jude Children's Research Hospital |
Highly efficient gene transfer into human repopulating stem cells by RD114 pseudotyped retroviral vector particles
|
WO2001098323A2
(en)
|
2000-06-16 |
2001-12-27 |
Incyte Genomics, Inc. |
G-protein coupled receptors
|
US7608704B2
(en)
*
|
2000-11-08 |
2009-10-27 |
Incyte Corporation |
Secreted proteins
|
HUP0400882A3
(en)
*
|
2001-05-11 |
2011-01-28 |
Wellstat Biologics Corp |
Oncolytic virus therapy
|
WO2003070902A2
(en)
*
|
2002-02-20 |
2003-08-28 |
Incyte Corporation |
Receptors and membrane-associated proteins
|
AU2003237374A1
(en)
*
|
2002-06-04 |
2003-12-19 |
Centers For Disease Control And Prevention |
Improved pseudotyped retroviruses
|
US20040009158A1
(en)
*
|
2002-07-11 |
2004-01-15 |
Washington University |
Promotion of neovascularization using bone marrow-derived endothelial-progenitor cells
|
AU2003265431A1
(en)
*
|
2002-08-13 |
2004-02-25 |
Incyte Corporation |
Cell adhesion and extracellular matrix proteins
|
US20070219353A1
(en)
*
|
2002-09-03 |
2007-09-20 |
Incyte Corporation |
Immune Response Associated Proteins
|
WO2004033636A2
(en)
*
|
2002-10-04 |
2004-04-22 |
Incyte Corporation |
Protein modification and maintenance molecules
|
US20050164275A1
(en)
*
|
2002-10-18 |
2005-07-28 |
Incyte Corporation |
Phosphodiesterases
|
WO2004044166A2
(en)
*
|
2002-11-12 |
2004-05-27 |
Incyte Corporation |
Carbohydrate-associated proteins
|
US20070065820A1
(en)
*
|
2002-11-13 |
2007-03-22 |
Xin Jiang |
Lipid-associated molecules
|
US20070009516A1
(en)
*
|
2002-11-26 |
2007-01-11 |
Tran Uyen K |
Immune response-associated proteins
|
US7829682B1
(en)
|
2003-04-30 |
2010-11-09 |
Incyte Corporation |
Human β-adrenergic receptor kinase nucleic acid molecule
|
CA2545938A1
(en)
*
|
2003-11-12 |
2005-05-26 |
Universite Laval |
High-titer retroviral packaging cells
|
ES2710099T3
(es)
|
2004-09-24 |
2019-04-23 |
Mesoblast Inc |
Progenie de células precursoras mesenquimales expandidas multipotenciales (MEMP) y sus usos
|
EP2361970A1
(de)
|
2004-09-24 |
2011-08-31 |
Angioblast Systems Incorporated |
Verfahren zur Verbesserung der Vermehrung und/oder des Überlebens von Mesenchymalvorläuferzellen (MPC)
|
US8325826B2
(en)
*
|
2005-03-09 |
2012-12-04 |
Qualcomm Incorporated |
Methods and apparatus for transmitting signals facilitating antenna control
|
US7826807B2
(en)
*
|
2005-03-09 |
2010-11-02 |
Qualcomm Incorporated |
Methods and apparatus for antenna control in a wireless terminal
|
EP2399991B1
(de)
|
2005-04-12 |
2017-09-27 |
Mesoblast, Inc. |
Isolierung von erwachsenen Stammzellen durch nicht gewebespezifische Alkali-Phosphatase
|
US20070020238A1
(en)
*
|
2005-06-01 |
2007-01-25 |
David Baltimore |
Method of targeted gene delivery using viral vectors
|
EP3418297B1
(de)
*
|
2005-12-13 |
2023-04-05 |
Kyoto University |
Nuklearumprogrammierungsfaktor
|
US20090227032A1
(en)
*
|
2005-12-13 |
2009-09-10 |
Kyoto University |
Nuclear reprogramming factor and induced pluripotent stem cells
|
US8129187B2
(en)
*
|
2005-12-13 |
2012-03-06 |
Kyoto University |
Somatic cell reprogramming by retroviral vectors encoding Oct3/4. Klf4, c-Myc and Sox2
|
US8278104B2
(en)
*
|
2005-12-13 |
2012-10-02 |
Kyoto University |
Induced pluripotent stem cells produced with Oct3/4, Klf4 and Sox2
|
CA2650270C
(en)
*
|
2006-04-28 |
2015-06-23 |
Universite Laval |
High-titer retroviral packaging cells
|
US7720485B2
(en)
*
|
2006-07-14 |
2010-05-18 |
Qualcomm Incorporated |
Methods and apparatus related to assignment in a wireless communications system
|
US7724853B2
(en)
*
|
2006-07-14 |
2010-05-25 |
Qualcomm Incorporated |
Enabling mobile switched antennas
|
US8225186B2
(en)
|
2006-07-14 |
2012-07-17 |
Qualcomm Incorporated |
Ecoding and decoding methods and apparatus for use in a wireless communication system
|
EP2520168B1
(de)
|
2006-07-21 |
2014-03-19 |
California Institute of Technology |
Zielgesteuerte Genabgabe für die Immunisierung mit Dendritenzellen
|
ES2569365T3
(es)
|
2006-11-29 |
2016-05-10 |
Nationwide Children's Hospital |
Inhibición de miostatina para la potenciación de músculo y/o la mejora de la función muscular
|
US8609411B2
(en)
|
2007-05-04 |
2013-12-17 |
Whitehead Institute For Biomedical Research |
Ex vivo expansion of human hematopoietic stem cells
|
US9213999B2
(en)
*
|
2007-06-15 |
2015-12-15 |
Kyoto University |
Providing iPSCs to a customer
|
JP2008307007A
(ja)
*
|
2007-06-15 |
2008-12-25 |
Bayer Schering Pharma Ag |
出生後のヒト組織由来未分化幹細胞から誘導したヒト多能性幹細胞
|
CA2694107C
(en)
|
2007-08-06 |
2018-03-27 |
Angioblast Systems, Inc. |
Method for generating, repairing and/or maintaining connective tissue in vivo
|
TWI325401B
(en)
*
|
2007-12-17 |
2010-06-01 |
Duen Gang Mou |
Vessel structure
|
SG10201400329YA
(en)
|
2008-05-02 |
2014-05-29 |
Univ Kyoto |
Method of nuclear reprogramming
|
WO2010019997A1
(en)
|
2008-08-18 |
2010-02-25 |
Angioblast Systems, Inc. |
Monoclonal antibody stro-4
|
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
|
NZ597804A
(en)
|
2009-07-24 |
2013-10-25 |
Immune Design Corp |
Lentiviral vectors pseudotyped with a sindbis virus envelope glycoprotein
|
CN108744262A
(zh)
|
2010-11-23 |
2018-11-06 |
普莱萨格生命科学公司 |
用于实体递送的治疗方法和组合物
|
US10196636B2
(en)
|
2011-04-21 |
2019-02-05 |
Nationwide Children's Hospital, Inc. |
Recombinant virus products and methods for inhibition of expression of myotilin
|
ES2702496T3
(es)
|
2011-04-21 |
2019-03-01 |
Nationwide Childrens Hospital Inc |
Productos de virus recombinante y procedimientos para la inhibición de la expresión de la miotilina
|
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
|
WO2013016352A1
(en)
|
2011-07-25 |
2013-01-31 |
Nationwide Children's Hospital, Inc. |
Recombinant virus products and methods for inhibition of expression of dux4
|
US9434928B2
(en)
|
2011-11-23 |
2016-09-06 |
Nationwide Children's Hospital, Inc. |
Recombinant adeno-associated virus delivery of alpha-sarcoglycan polynucleotides
|
US9713635B2
(en)
|
2012-03-30 |
2017-07-25 |
Immune Design Corp. |
Materials and methods for producing improved lentiviral vector particles
|
AU2013237900B2
(en)
|
2012-03-30 |
2017-07-27 |
Immune Design Corp. |
Lentiviral vector particles having improved transduction efficiency for cells expressing DC- SIGN
|
US8323662B1
(en)
|
2012-03-30 |
2012-12-04 |
Immune Design Corp. |
Methods useful for generating highly mannosylated pseudotyped lentiviral vector particles comprising a Vpx protein
|
US20150252384A1
(en)
|
2012-08-01 |
2015-09-10 |
National Children's Hospital |
Intrathecal delivery of recombinant adeno-associated virus 9
|
EP2879682B1
(de)
|
2012-08-01 |
2018-03-21 |
United Therapeutics Corporation |
Behandlung von pulmonal-arteriellem hochdruck mit mesenchymalen stammzellen
|
WO2014022376A2
(en)
|
2012-08-01 |
2014-02-06 |
United Therapeutics Corporation |
Treatment of pulmonary arterial hypertension with prostacyclin-treated endothelial progenitor cells
|
EP2895606A4
(de)
|
2012-09-17 |
2016-07-06 |
Res Inst Nationwide Childrens Hospital |
Zusammensetzungen und verfahren zur behandlung von amyotropher lateralsklerose (als)
|
AU2014205557B2
(en)
|
2013-01-09 |
2017-08-10 |
United Therapeutics Corporation |
Treatment of vasculopathy with prostacyclin and mesenchymal stem cells
|
JP6461917B2
(ja)
|
2013-04-20 |
2019-01-30 |
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 |
エクソン2標的U7snRNAポリヌクレオチド構築物の組換えアデノ随伴ウイルスによる送達
|
WO2014183071A2
(en)
|
2013-05-10 |
2014-11-13 |
Whitehead Institute For Biomedical Research |
In vitro production of red blood cells with sortaggable proteins
|
RS63942B1
(sr)
|
2013-08-27 |
2023-02-28 |
Res Inst Nationwide Childrens Hospital |
Proizvodi i postupci za lečenje amiotrofične lateralne skleroze
|
EP3065784A4
(de)
|
2013-11-05 |
2017-05-10 |
The Research Institute at Nationwide Children's Hospital |
Zusammensetzungen und verfahren zur hemmung von nf-kb und sod-1 zur behandlung von amyotropher lateralsklerose
|
US10047130B2
(en)
|
2014-03-18 |
2018-08-14 |
Washington University |
Methods and compositions for red-shifted chromophore substitution for optogenetic applications
|
CA3205555A1
(en)
*
|
2014-04-25 |
2015-10-29 |
Genethon |
Treatment of hyperbilirubinemia
|
EP3572516A1
(de)
|
2014-08-09 |
2019-11-27 |
The Research Institute at Nationwide Children's Hospital |
Verfahren und materialien zur aktivierung einer internen ribosomeintrittsstelle in exon 5 des dmd-gens
|
WO2016057975A2
(en)
|
2014-10-10 |
2016-04-14 |
Research Institute At Nationwide Children's Hospital |
Guided injections for aav gene transfer to muscle
|
EP3215602B1
(de)
|
2014-11-05 |
2019-12-25 |
The Research Institute at Nationwide Children's Hospital |
Verfahren und materialien zur herstellung rekombinanter viren in eukaryotischen mikroalgen
|
MA41451A
(fr)
|
2015-02-04 |
2017-12-12 |
Univ Washington |
Constructions anti-tau
|
BR112017017810A2
(pt)
|
2015-02-23 |
2018-04-10 |
Crispr Therapeutics Ag |
materiais e métodos para tratamento de hemoglobinopatias
|
JP7187151B2
(ja)
*
|
2015-04-10 |
2022-12-12 |
プレジデント アンド フェローズ オブ ハーバード カレッジ |
生存細胞の画像解析のための方法及び装置
|
US10017832B2
(en)
|
2015-08-25 |
2018-07-10 |
Washington University |
Compositions and methods for site specific recombination at asymmetric sites
|
CA2998636A1
(en)
|
2015-09-17 |
2017-03-23 |
Research Institute At Nationwide Children's Hospital |
Methods and materials for galgt2 gene therapy
|
AU2016339053A1
(en)
|
2015-09-24 |
2018-04-12 |
Crispr Therapeutics Ag |
Novel family of RNA-programmable endonucleases and their uses in genome editing and other applications
|
CN108513546A
(zh)
|
2015-10-28 |
2018-09-07 |
克里斯珀医疗股份公司 |
用于治疗杜氏肌营养不良症的材料和方法
|
CN109328231A
(zh)
|
2015-11-06 |
2019-02-12 |
克里斯普治疗股份公司 |
用于治疗1a型糖原贮积病的材料和方法
|
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
|
JP7061067B2
(ja)
|
2015-12-14 |
2022-04-27 |
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 |
クリグラー・ナジャー症候群の処置のための組成物
|
BR112018012894A2
(pt)
|
2015-12-23 |
2018-12-04 |
Crispr Therapeutics Ag |
materiais e métodos para tratamento de esclerose lateral amiotrófica e/ou degeneração lobular frontotemporal
|
WO2017120589A1
(en)
|
2016-01-08 |
2017-07-13 |
Washington University |
Compositions comprising chemerin and methods of use thereof
|
WO2017134529A1
(en)
|
2016-02-02 |
2017-08-10 |
Crispr Therapeutics Ag |
Materials and methods for treatment of severe combined immunodeficiency (scid) or omenn syndrome
|
EP3416689B1
(de)
|
2016-02-18 |
2023-01-18 |
CRISPR Therapeutics AG |
Materialien und verfahren zur behandlung von schwerer kombinierter immundefizienz (scid) oder omenn syndrome
|
US11066456B2
(en)
|
2016-02-25 |
2021-07-20 |
Washington University |
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
|
EP3429632B1
(de)
|
2016-03-16 |
2023-01-04 |
CRISPR Therapeutics AG |
Materialien und verfahren zur behandlung von erblicher haemochromatose
|
WO2017173411A1
(en)
|
2016-04-02 |
2017-10-05 |
Research Institute At Nation Wide Children's Hospital |
Modified u6 promoter system for tissue specific expression
|
MY195439A
(en)
|
2016-04-15 |
2023-01-21 |
Res Inst Nationwide Childrens Hospital |
Adeno-Associated Virus Vector Delivery of B-Sarcoglycan and Microrna-29 and the Treatment of Muscular Dystrophy
|
MA45477A
(fr)
|
2016-04-15 |
2019-02-20 |
Res Inst Nationwide Childrens Hospital |
Administration à vecteurs de virus adéno-associé de microarn-29 et micro-dystrophine pour traiter la dystrophie musculaire
|
KR102351329B1
(ko)
|
2016-04-18 |
2022-01-18 |
크리스퍼 테라퓨틱스 아게 |
혈색소병증의 치료를 위한 물질 및 방법
|
WO2017191503A1
(en)
|
2016-05-05 |
2017-11-09 |
Crispr Therapeutics Ag |
Materials and methods for treatment of hemoglobinopathies
|
EP3478829A1
(de)
|
2016-06-29 |
2019-05-08 |
Crispr Therapeutics AG |
Materialien und verfahren zur behandlung von myotoner dystrophie typ 1 (dm1) und anderen erkrankungen
|
CA3029119A1
(en)
|
2016-06-29 |
2018-01-04 |
Crispr Therapeutics Ag |
Materials and methods for treatment of friedreich ataxia and other related disorders
|
US11174469B2
(en)
|
2016-06-29 |
2021-11-16 |
Crispr Therapeutics Ag |
Materials and methods for treatment of Amyotrophic Lateral Sclerosis (ALS) and other related disorders
|
CA3029141A1
(en)
|
2016-07-06 |
2018-01-11 |
Crispr Therapeutics Ag |
Materials and methods for treatment of pain related disorders
|
AU2017292169B2
(en)
|
2016-07-06 |
2021-12-23 |
Vertex Pharmaceuticals Incorporated |
Materials and methods for treatment of pain related disorders
|
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
|
CA3041514A1
(en)
|
2016-10-24 |
2018-05-03 |
United Therapeutics Corporation |
Enhancement of msc immunomodulatory properties by treprostinil
|
WO2018094251A1
(en)
|
2016-11-17 |
2018-05-24 |
Kaspar Brian K |
Intrathecal delivery of recombinant adeno-associated virus encoding methyl-cpg binding protein 2
|
WO2018111834A1
(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
|
US11559588B2
(en)
|
2017-02-22 |
2023-01-24 |
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
|
EP3585807A1
(de)
|
2017-02-22 |
2020-01-01 |
CRISPR Therapeutics AG |
Materialien und verfahren zur behandlung der parkinson-krankheit im frühstadium (park1) und anderer zustände oder störungen im zusammenhang mit dem synuclein-alpha (snca)-gen
|
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
|
US20200216857A1
(en)
|
2017-02-22 |
2020-07-09 |
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
|
AU2018224387B2
(en)
|
2017-02-22 |
2024-08-08 |
Crispr Therapeutics Ag |
Compositions and methods for gene editing
|
MA47800A
(fr)
|
2017-03-17 |
2020-01-22 |
Univ Newcastle |
Délivrance par vecteur viral adéno-associé d'un fragment de micro-dystrophine pour traiter la dystrophie musculaire
|
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
|
BR112019023608A2
(pt)
|
2017-05-12 |
2020-05-26 |
Crispr Therapeutics Ag |
Materiais e métodos para células manipuladas e seus usos em imuno-oncologia
|
EP3652324A1
(de)
|
2017-07-08 |
2020-05-20 |
Genethon |
Behandlung von spinaler muskelatrophie
|
KR20200067190A
(ko)
|
2017-10-17 |
2020-06-11 |
크리스퍼 테라퓨틱스 아게 |
A형 혈우병을 위한 유전자 편집용 조성물 및 방법
|
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
|
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(ko)
|
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2020-07-08 |
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|
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(fr)
|
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|
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|
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|
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(de)
|
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|
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(en)
|
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|
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(en)
|
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|
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(en)
|
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|
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(zh)
|
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|
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|
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|
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(fr)
|
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|
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|
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|
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|
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|
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(ja)
|
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|
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|
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|
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|
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|
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|
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|
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(en)
|
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|
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|
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|
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(en)
|
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|
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|
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|
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|
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|
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|
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|
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|
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|
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|
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|
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|
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|
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|
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|
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|
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|
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(en)
|
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|
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|
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|
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|
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|
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|
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|
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|
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|
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|
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|
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|
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|
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|
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|
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(ko)
|
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|
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|
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|
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|
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|
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(ja)
|
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|
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|
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|
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(en)
|
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|
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(en)
|
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|
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|
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|
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|
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|
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(zh)
|
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|
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|
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|
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|
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|
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(de)
|
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|
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(ja)
|
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|
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(en)
|
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|
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|
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|
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|
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|
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(en)
|
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|
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|
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|
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|
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Huigene Therapeutics Co., Ltd. |
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|
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|
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|
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(en)
|
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|
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|
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|
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(ja)
|
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|
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|
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|
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|
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|
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|
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|
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|
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|
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|
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|
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|
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|
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(zh)
|
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|
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|
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|
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|
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|
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|
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|
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|
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|
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|
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(en)
|
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|
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|
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|
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|
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(en)
|
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|
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(en)
|
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The Regents Of The University Of California |
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|
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(en)
|
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Novartis Ag |
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|
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(en)
|
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|
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|
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|
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(en)
|
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|
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(en)
|
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Aav Gene Therapeutics, Inc. |
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|
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(en)
|
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Research Institute At Nationwide Children's Hospital |
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|
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(en)
|
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Cargo Therapeutics, Inc. |
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|
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(en)
|
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|
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(en)
|
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|
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(en)
|
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Raav production methods
|
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(en)
|
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2024-08-15 |
Cargo Therapeutics, Inc. |
Compositions and methods for immunotherapies
|