CN1067722C - 腺病毒载体 - Google Patents
腺病毒载体 Download PDFInfo
- Publication number
- CN1067722C CN1067722C CN94192150A CN94192150A CN1067722C CN 1067722 C CN1067722 C CN 1067722C CN 94192150 A CN94192150 A CN 94192150A CN 94192150 A CN94192150 A CN 94192150A CN 1067722 C CN1067722 C CN 1067722C
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- adenovirus
- cell
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- dna
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Images
Classifications
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- C—CHEMISTRY; METALLURGY
- C12—BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
- C12N—MICROORGANISMS OR ENZYMES; COMPOSITIONS THEREOF; PROPAGATING, PRESERVING, OR MAINTAINING MICROORGANISMS; MUTATION OR GENETIC ENGINEERING; CULTURE MEDIA
- C12N15/00—Mutation or genetic engineering; DNA or RNA concerning genetic engineering, vectors, e.g. plasmids, or their isolation, preparation or purification; Use of hosts therefor
- C12N15/09—Recombinant DNA-technology
- C12N15/63—Introduction of foreign genetic material using vectors; Vectors; Use of hosts therefor; Regulation of expression
- C12N15/79—Vectors or expression systems specially adapted for eukaryotic hosts
- C12N15/85—Vectors or expression systems specially adapted for eukaryotic hosts for animal cells
- C12N15/86—Viral vectors
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P25/00—Drugs for disorders of the nervous system
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P35/00—Antineoplastic agents
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P7/00—Drugs for disorders of the blood or the extracellular fluid
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07K—PEPTIDES
- C07K14/00—Peptides having more than 20 amino acids; Gastrins; Somatostatins; Melanotropins; Derivatives thereof
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07K—PEPTIDES
- C07K14/00—Peptides having more than 20 amino acids; Gastrins; Somatostatins; Melanotropins; Derivatives thereof
- C07K14/435—Peptides having more than 20 amino acids; Gastrins; Somatostatins; Melanotropins; Derivatives thereof from animals; from humans
- C07K14/52—Cytokines; Lymphokines; Interferons
- C07K14/54—Interleukins [IL]
- C07K14/55—IL-2
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K38/00—Medicinal preparations containing peptides
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K39/00—Medicinal preparations containing antigens or antibodies
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K48/00—Medicinal preparations containing genetic material which is inserted into cells of the living body to treat genetic diseases; Gene therapy
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- C—CHEMISTRY; METALLURGY
- C12—BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
- C12N—MICROORGANISMS OR ENZYMES; COMPOSITIONS THEREOF; PROPAGATING, PRESERVING, OR MAINTAINING MICROORGANISMS; MUTATION OR GENETIC ENGINEERING; CULTURE MEDIA
- C12N2710/00—MICROORGANISMS OR ENZYMES; COMPOSITIONS THEREOF; PROPAGATING, PRESERVING, OR MAINTAINING MICROORGANISMS; MUTATION OR GENETIC ENGINEERING; CULTURE MEDIA dsDNA viruses
- C12N2710/00011—Details
- C12N2710/10011—Adenoviridae
- C12N2710/10311—Mastadenovirus, e.g. human or simian adenoviruses
- C12N2710/10341—Use of virus, viral particle or viral elements as a vector
- C12N2710/10343—Use of virus, viral particle or viral elements as a vector viral genome or elements thereof as genetic vector
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- Life Sciences & Earth Sciences (AREA)
- Chemical & Material Sciences (AREA)
- Genetics & Genomics (AREA)
- Organic Chemistry (AREA)
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- Diabetes (AREA)
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- Medicines Containing Material From Animals Or Micro-Organisms (AREA)
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Abstract
Description
Claims (11)
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
FR9305954A FR2705361B1 (fr) | 1993-05-18 | 1993-05-18 | Vecteurs viraux et utilisation en thérapie génique. |
FR93/05954 | 1993-05-18 |
Publications (2)
Publication Number | Publication Date |
---|---|
CN1124040A CN1124040A (zh) | 1996-06-05 |
CN1067722C true CN1067722C (zh) | 2001-06-27 |
Family
ID=9447235
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
CN94192150A Expired - Lifetime CN1067722C (zh) | 1993-05-18 | 1994-05-06 | 腺病毒载体 |
Country Status (26)
Country | Link |
---|---|
US (1) | US6294377B1 (zh) |
EP (1) | EP0698108B2 (zh) |
JP (2) | JP3995259B2 (zh) |
KR (1) | KR100379569B1 (zh) |
CN (1) | CN1067722C (zh) |
AT (1) | ATE209686T1 (zh) |
AU (1) | AU696495B2 (zh) |
BR (1) | BR9406720A (zh) |
CA (1) | CA2163256C (zh) |
CZ (1) | CZ284903B6 (zh) |
DE (1) | DE69429260T3 (zh) |
DK (1) | DK0698108T4 (zh) |
ES (1) | ES2167365T5 (zh) |
FI (1) | FI118538B (zh) |
FR (1) | FR2705361B1 (zh) |
HU (1) | HU221340B1 (zh) |
IL (1) | IL109644A (zh) |
NO (1) | NO320818B1 (zh) |
NZ (1) | NZ266475A (zh) |
PL (1) | PL182814B1 (zh) |
PT (1) | PT698108E (zh) |
RU (1) | RU2233333C2 (zh) |
SK (1) | SK282354B6 (zh) |
UA (1) | UA66417C2 (zh) |
WO (1) | WO1994026914A1 (zh) |
ZA (1) | ZA943358B (zh) |
Families Citing this family (120)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US6410010B1 (en) | 1992-10-13 | 2002-06-25 | Board Of Regents, The University Of Texas System | Recombinant P53 adenovirus compositions |
CA2108144A1 (en) | 1991-03-06 | 1992-09-07 | Jack A. Roth | Methods and compositions for the selective inhibition of gene expression |
US5747469A (en) | 1991-03-06 | 1998-05-05 | Board Of Regents, The University Of Texas System | Methods and compositions comprising DNA damaging agents and p53 |
IL113052A0 (en) | 1994-03-23 | 1995-06-29 | Rhone Poulenc Rorer Sa | Recombinant viruses, their preparation and their use in gene therapy |
JP3816518B2 (ja) * | 1994-06-10 | 2006-08-30 | ジェンベク、インコーポレイティッド | 相補的なアデノウイルスベクター系と細胞系 |
FR2722507B1 (fr) * | 1994-07-12 | 1996-08-14 | Rhone Poulenc Rorer Sa | Adenovirus comportant un gene codant pour une no synthase |
FR2724320B1 (fr) * | 1994-09-13 | 1996-12-20 | Transgene Sa | Nouvel implant pour le traitement des maladies acquises |
FR2725213B1 (fr) * | 1994-10-04 | 1996-11-08 | Rhone Poulenc Rorer Sa | Vecteurs viraux et utilisation en therapie genique |
FR2726285B1 (fr) | 1994-10-28 | 1996-11-29 | Centre Nat Rech Scient | Adenovirus depourvus de particules contaminantes viables, preparation et utilisation |
FR2727689A1 (fr) | 1994-12-01 | 1996-06-07 | Transgene Sa | Nouveau procede de preparation d'un vecteur viral |
US6752987B1 (en) | 1995-02-28 | 2004-06-22 | The Regents Of The University Of California | Adenovirus encoding human adenylylcyclase (AC) VI |
JP3961019B2 (ja) | 1995-02-28 | 2007-08-15 | 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 | 遺伝子転移媒介の血管形成療法 |
FR2731710B1 (fr) * | 1995-03-14 | 1997-04-30 | Rhone Poulenc Rorer Sa | Virus recombinants exprimant la lecithine cholesterol acyltransferase et utilisations en therapie genique |
FR2732357B1 (fr) | 1995-03-31 | 1997-04-30 | Rhone Poulenc Rorer Sa | Vecteurs viraux et utilisation pour le traitement des desordres hyperproliferatifs, notamment de la restenose |
US5698202A (en) * | 1995-06-05 | 1997-12-16 | The Wistar Institute Of Anatomy & Biology | Replication-defective adenovirus human type 5 recombinant as a rabies vaccine carrier |
US6281010B1 (en) | 1995-06-05 | 2001-08-28 | The Trustees Of The University Of Pennsylvania | Adenovirus gene therapy vehicle and cell line |
US5756283A (en) * | 1995-06-05 | 1998-05-26 | The Trustees Of The University Of Pennsylvania | Method for improved production of recombinant adeno-associated viruses for gene therapy |
US6019978A (en) * | 1995-06-05 | 2000-02-01 | The Wistar Institute Of Anatomy And Biology | Replication-defective adenovirus human type 5 recombinant as a vaccine carrier |
CA2222140C (en) * | 1995-06-15 | 2010-11-23 | Introgene B.V. | Packaging systems for human recombinant adenovirus to be used in gene therapy |
US6265212B1 (en) | 1995-06-15 | 2001-07-24 | Introgene B.V. | Packaging systems for human recombinant adenovirus to be used in gene therapy |
US6783980B2 (en) | 1995-06-15 | 2004-08-31 | Crucell Holland B.V. | Packaging systems for human recombinant adenovirus to be used in gene therapy |
AUPN477695A0 (en) * | 1995-08-14 | 1995-09-07 | Commonwealth Scientific And Industrial Research Organisation | Gene therapy |
FR2740344B1 (fr) * | 1995-10-31 | 1997-11-21 | Rhone Poulenc Rorer Sa | Application de la proteine gax au traitement de cancers |
DE69740033D1 (de) * | 1996-07-03 | 2010-12-09 | Merial Inc | Rekombinanter hunde-adenovirus 2 (cav2), welcher exogene dna enthält |
AU4255397A (en) * | 1996-09-06 | 1998-03-26 | Trustees Of The University Of Pennsylvania, The | Chimpanzee adenovirus vectors |
IL132323A0 (en) | 1997-04-28 | 2001-03-19 | Rhone Poulenc Rorer Sa | Adenovirus-mediated intratumoral delivery of an angiogenesis antagonist for the treatment of tumors |
ATE374247T1 (de) | 1997-10-14 | 2007-10-15 | Darwin Molecular Corp | Thymidinkinase mutanten und fusionproteine mit thymidinkinase und guanylatekinase aktivitäten |
US6875606B1 (en) | 1997-10-23 | 2005-04-05 | The United States Of America As Represented By The Department Of Veterans Affairs | Human α-7 nicotinic receptor promoter |
US6653088B1 (en) | 1997-10-24 | 2003-11-25 | Aventis Pharma S.A. | Interaction test for the investigation of inhibitory molecules of the interaction between a presenilin and the β-amyloid peptide |
ATE302267T1 (de) | 1998-01-08 | 2005-09-15 | Aventis Pharma Inc | Transgenes kaninchen, dass ein funktionelles menschliches lipoprotein(a) exprimiert |
US6670188B1 (en) | 1998-04-24 | 2003-12-30 | Crucell Holland B.V. | Packaging systems for human recombinant adenovirus to be used in gene therapy |
US6225456B1 (en) | 1998-05-07 | 2001-05-01 | University Technololy Corporation | Ras suppressor SUR-5 |
US6506889B1 (en) | 1998-05-19 | 2003-01-14 | University Technology Corporation | Ras suppressor SUR-8 and related compositions and methods |
EP1105479B1 (en) | 1998-08-11 | 2011-01-12 | Darwin Discovery Limited | Identification of the gene causing the mouse scurfy phenotype and its human ortholog |
ES2350454T3 (es) | 1998-11-27 | 2011-01-24 | Ucb Pharma S.A. | Composiciones y métodos para incrementar la mineralización de la sustancia ósea. |
US20040009535A1 (en) | 1998-11-27 | 2004-01-15 | Celltech R&D, Inc. | Compositions and methods for increasing bone mineralization |
US7063850B1 (en) | 1998-12-22 | 2006-06-20 | University Of Tennessee Research Foundation | Protective antigen of group A Streptococci |
US6441156B1 (en) * | 1998-12-30 | 2002-08-27 | The United States Of America As Represented By The Department Of Health And Human Services | Calcium channel compositions and methods of use thereof |
FR2794771B1 (fr) | 1999-06-11 | 2001-08-10 | Aventis Pharma Sa | Adenovirus recombinants codant pour le transporteur specifique de l'iode (nis) |
FR2799472B1 (fr) | 1999-10-07 | 2004-07-16 | Aventis Pharma Sa | Preparation d'adenovirus recombinants et de banques adenovirales |
AU2460001A (en) | 1999-12-27 | 2001-07-09 | Regents Of The University Of California, The | Gene therapy for congestive heart failure |
EA008480B1 (ru) | 2000-01-12 | 2007-06-29 | Йейл Юниверсити | Выделенный полинуклеотид (варианты), содержащий его вектор и клетка-хозяин, кодируемый им полипептид рецептора nogo, уменьшающий опосредованное этим рецептором ингибирование роста аксонов (варианты), выделенное антитело и фармацевтическая композиция на их основе |
KR20080046750A (ko) | 2000-03-24 | 2008-05-27 | 바이오스피어 메디칼 인코포레이티드 | 능동 색전화용 미소구 |
GB0018307D0 (en) | 2000-07-26 | 2000-09-13 | Aventis Pharm Prod Inc | Polypeptides |
US7060442B2 (en) | 2000-10-30 | 2006-06-13 | Regents Of The University Of Michigan | Modulators on Nod2 signaling |
EP2402359A1 (en) | 2000-12-28 | 2012-01-04 | Wyeth LLC | Recombinant protective protein from streptococcus pneumoniae |
EP1967525B1 (en) | 2001-05-08 | 2012-11-14 | Darwin Molecular Corporation | A method for regulating immune function in primates using the foxp3 protein |
AUPR518501A0 (en) | 2001-05-22 | 2001-06-14 | Unisearch Limited | Yin yang-1 |
WO2003004088A2 (en) | 2001-07-05 | 2003-01-16 | Aventis Pharma S.A. | Method of administration of a gene of interest to the heart and vasculature |
US7108975B2 (en) | 2001-09-21 | 2006-09-19 | Regents Of The University Of Michigan | Atlastin |
US7582425B2 (en) | 2001-09-21 | 2009-09-01 | The Regents Of The University Of Michigan | Atlastin |
US20040023910A1 (en) * | 2001-09-28 | 2004-02-05 | Zhiming Zhang | Use of cyr61 in the treatment and diagnosis of human uterine leiomyomas |
MX339524B (es) | 2001-10-11 | 2016-05-30 | Wyeth Corp | Composiciones inmunogenicas novedosas para la prevencion y tratamiento de enfermedad meningococica. |
CA2463008A1 (en) | 2001-10-26 | 2003-07-24 | Id Biomedical Corporation Of Washington | Efficient protein expression system |
WO2003049763A1 (en) | 2001-12-12 | 2003-06-19 | Fh Faulding & Co Limited | Composition for the preservation of viruses |
US20030158112A1 (en) | 2002-02-15 | 2003-08-21 | Johns Hopkins University School Of Medicine | Selective induction of apoptosis to treat ocular disease |
NZ554740A (en) | 2002-05-24 | 2009-01-31 | Schering Corp | Neutralizing human anti-IGFR antibody |
US7785608B2 (en) | 2002-08-30 | 2010-08-31 | Wyeth Holdings Corporation | Immunogenic compositions for the prevention and treatment of meningococcal disease |
FR2845395B1 (fr) * | 2002-10-08 | 2008-05-30 | Agronomique Inst Nat Rech | Vecteurs adenoviraux recombinants et leurs applications |
WO2005020928A2 (en) | 2003-08-29 | 2005-03-10 | The Regents Of The University Of California | Agents and methods for enhancing bone formation by oxysterols in combination with bone morphogenic proteins |
US7432057B2 (en) | 2004-01-30 | 2008-10-07 | Michigan State University | Genetic test for PSE-susceptible turkeys |
CN102816742B (zh) | 2004-05-26 | 2014-04-09 | 普西奥克瑟斯医疗有限公司 | 用于治疗癌症的嵌合腺病毒 |
US7604798B2 (en) | 2004-07-15 | 2009-10-20 | Northwestern University | Methods and compositions for importing nucleic acids into cell nuclei |
AU2005274948B2 (en) | 2004-07-16 | 2011-09-22 | Genvec, Inc. | Vaccines against aids comprising CMV/R-nucleic acid constructs |
EP2002003B1 (en) | 2005-05-27 | 2015-12-30 | Ospedale San Raffaele S.r.l. | Gene vector comprising mi-rna |
EP1993558B1 (en) | 2006-02-27 | 2014-07-30 | The Regents of The University of California | Oxysterol compounds and the hedgehog pathway |
AU2007276793B2 (en) | 2006-07-28 | 2014-01-16 | Sanofi | Composition and method for treatment of tumors |
WO2008060813A2 (en) | 2006-10-19 | 2008-05-22 | Merck & Co., Inc. | High affinity antibody antagonists of interleukin-13 receptor alpha 1 |
US8613925B2 (en) | 2006-10-19 | 2013-12-24 | Csl Limited | Anti-IL-13Rα1 antibodies and their uses thereof |
AR064642A1 (es) | 2006-12-22 | 2009-04-15 | Wyeth Corp | Polinucleotido vector que lo comprende celula recombinante que comprende el vector polipeptido , anticuerpo , composicion que comprende el polinucleotido , vector , celula recombinante polipeptido o anticuerpo , uso de la composicion y metodo para preparar la composicion misma y preparar una composi |
WO2009073186A1 (en) | 2007-12-03 | 2009-06-11 | The Regents Of The University Of California | Oxsterols for activation of hedgehog signaling, osteoinduction, antiadipogenesis, and wnt signaling |
ES2648231T3 (es) | 2008-11-05 | 2017-12-29 | Wyeth Llc | Composición inmunogénica de múltiples componentes para la prevención de la enfermedad por estreptococos beta hemolíticos (EBH) |
US20110293608A1 (en) | 2008-12-03 | 2011-12-01 | The Johns Hopkins Univeristy | Annexin a2 as immunological target |
KR101829469B1 (ko) * | 2008-12-04 | 2018-03-30 | 큐알엔에이, 인크. | Epo에 대한 천연 안티센스 전사체의 억제에 의해 에리트로포에틴(epo) 관련된 질환의 치료 |
WO2010096561A1 (en) | 2009-02-18 | 2010-08-26 | The United States Of America, As Represented By The Secretary, Department Of Health And Human Services | Synthetic hiv/siv gag proteins and uses thereof |
EP2547368A4 (en) | 2010-03-19 | 2014-08-06 | Univ South Alabama | METHOD AND COMPOSITIONS FOR CANCER TREATMENT |
ES2664572T3 (es) * | 2010-05-26 | 2018-04-20 | Curna, Inc. | Tratamiento de enfermedades relacionadas con el homólogo atonal 1 (ATOH1) mediante inhibición del transcrito antisentido natural a ATOH1 |
CN103025873B (zh) * | 2010-06-23 | 2018-05-08 | 库尔纳公司 | 通过抑制电压门控钠通道α亚基(SCNA)的天然反义转录物而治疗SCNA相关疾病 |
CN103189071A (zh) | 2010-08-23 | 2013-07-03 | 惠氏有限责任公司 | 脑膜炎萘瑟氏菌rLP2086抗原的稳定制剂 |
EP3056212B1 (en) | 2010-09-10 | 2019-04-03 | Wyeth LLC | Non-lipidated variants of neisseria meningitidis orf2086 antigens |
WO2012135696A2 (en) | 2011-04-01 | 2012-10-04 | University Of South Alabama | Methods and compositions for the diagnosis, classification, and treatment of cancer |
WO2013103401A1 (en) | 2012-01-06 | 2013-07-11 | University Of South Alabama | Methods and compositions for the treatment of cancer |
SA115360586B1 (ar) | 2012-03-09 | 2017-04-12 | فايزر انك | تركيبات لعلاج الالتهاب السحائي البكتيري وطرق لتحضيرها |
MX2018011291A (es) | 2012-03-09 | 2023-01-31 | Pfizer | Composiciones de neisseria meningitidis y metodos de las mismas. |
WO2013169399A1 (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 |
WO2014107739A1 (en) | 2013-01-07 | 2014-07-10 | Eleven Biotherapeutics, Inc. | Antibodies against pcsk9 |
CN105189755A (zh) * | 2013-01-15 | 2015-12-23 | 加利福尼亚大学董事会 | 腺病毒及其用途 |
ES2685894T3 (es) | 2013-03-08 | 2018-10-15 | Pfizer Inc. | Polipéptidos de fusión inmunogénicos |
AU2014249045A1 (en) | 2013-03-11 | 2015-10-29 | University Of Florida Research Foundation, Inc. | Delivery of CARD protein as therapy for occular inflammation |
EP2991652A4 (en) | 2013-05-02 | 2016-12-07 | Univ California | OSSEOUS BONE TARGETING AGENTS BASED ON OSTEOGENOUS OXOGENOUS WITH BONE SELECTIVITY |
MX369534B (es) | 2013-09-08 | 2019-11-11 | Pfizer | Composiciones de neisseria meningitidis y sus metodos. |
MX2016005170A (es) | 2013-10-25 | 2017-02-02 | Psioxus Therapeutics Ltd | Adenovirus oncoliticos armados con genes heterologos. |
EP3107939B1 (en) | 2014-02-19 | 2020-06-17 | University of Florida Research Foundation, Inc. | Delivery of nrf2 as therapy for protection against reactive oxygen species |
BR112016029369B1 (pt) | 2014-06-17 | 2020-12-08 | Nippon Shinyaku Co., Ltd. | oligômero antissentido, composição farmacêutica uso de um oligômero antissentido ou um sal ou hidrato farmaceuticamente aceitável do mesmo, e, métodos para fabricação e para triagem de um oligômero antissentido |
WO2016122791A1 (en) | 2015-01-30 | 2016-08-04 | The Regents Of The University Of California | Spinal subpial gene delivery system |
KR20190049940A (ko) | 2015-02-19 | 2019-05-09 | 화이자 인코포레이티드 | 나이세리아 메닌지티디스 조성물 및 그의 방법 |
SI3288573T1 (sl) | 2015-04-30 | 2020-06-30 | Psioxus Therapeutics Limited | Onkolitični adenovirus, ki kodira protein B7 |
WO2017070237A1 (en) | 2015-10-19 | 2017-04-27 | University Of Maryland, Baltimore | Methods for generating engineered human primary blood dendritic cell lines |
CN108697746A (zh) | 2015-12-17 | 2018-10-23 | 皮斯奥克斯治疗公司 | 编码抗tcr复合体抗体或片段的病毒 |
WO2017172606A1 (en) | 2016-03-28 | 2017-10-05 | The Regents Of The University Of California | Method and composition for treating neuronal hyper-excitability |
US11560412B2 (en) | 2016-04-01 | 2023-01-24 | University Of Maryland, Baltimore | Compositions comprising GRIM-19 therapeutics and methods of use |
CN109641063B (zh) | 2016-04-20 | 2022-11-15 | 能源环境和技术研究中心O.A., M.P. | 用于增强pklr的基因表达的组合物和方法 |
GB201713765D0 (en) | 2017-08-28 | 2017-10-11 | Psioxus Therapeutics Ltd | Modified adenovirus |
EP3515481A1 (en) | 2016-09-20 | 2019-07-31 | Boehringer Ingelheim Vetmedica GmbH | New ehv insertion site orf70 |
BR112019005415A2 (pt) | 2016-09-20 | 2019-10-22 | Boehringer Ingelheim Vetmedica Gmbh | nova vacina contra influenza suína |
EP3515504B1 (en) | 2016-09-20 | 2023-07-12 | Boehringer Ingelheim Vetmedica GmbH | Canine adenovirus vectors |
CN109790550B (zh) | 2016-09-20 | 2024-02-09 | 勃林格殷格翰动物保健有限公司 | 新颖的启动子 |
SG10202111092UA (en) | 2017-01-31 | 2021-11-29 | Pfizer | Neisseria meningitidis compositions and methods thereof |
CN111479924B (zh) | 2017-10-16 | 2024-06-14 | 沃雅戈治疗公司 | 肌萎缩性侧索硬化症(als)的治疗 |
WO2019079242A1 (en) | 2017-10-16 | 2019-04-25 | Voyager Therapeutics, Inc. | TREATMENT OF AMYOTROPHIC LATERAL SCLEROSIS (ALS) |
AU2018352583A1 (en) | 2017-10-16 | 2020-04-09 | Centro de Investigaciones Energeticas, Medioambientales Y Tecnologicas, O.A., M.P. | Lentiviral vectors for delivery of PKLR to treat pyruvate kinase deficiency |
EP3973973A1 (en) | 2017-10-31 | 2022-03-30 | KaliVir Immunotherapeutics, Inc. | Platform oncolytic vector for systemic delivery |
US20210254103A1 (en) | 2018-07-02 | 2021-08-19 | Voyager Therapeutics, Inc. | Treatment of amyotrophic lateral sclerosis and disorders associated with the spinal cord |
WO2020010035A1 (en) | 2018-07-02 | 2020-01-09 | Voyager Therapeutics, Inc. | Cannula system |
WO2021247995A2 (en) | 2020-06-04 | 2021-12-09 | Voyager Therapeutics, Inc. | Compositions and methods of treating neuropathic pain |
CA3185267A1 (en) | 2020-08-07 | 2022-02-10 | Spacecraft Seven, Llc | Plakophilin-2 (pkp2) gene therapy using aav vector |
CN117241813A (zh) | 2021-04-30 | 2023-12-15 | 卡利威尔免疫治疗公司 | 用于修饰的mhc表达的溶瘤病毒 |
AU2022371414A1 (en) | 2021-10-20 | 2024-05-02 | University Of Copenhagen | Isolated glial progenitor cells for use in the competition treatment of age-related white matter loss |
WO2023081633A1 (en) | 2021-11-02 | 2023-05-11 | University Of Rochester | Tcf7l2 mediated remyelination in the brain |
WO2024091824A1 (en) | 2022-10-26 | 2024-05-02 | Ada Forsyth Institute, Inc. | Differentiation and reprogramming of chondrocyte |
Citations (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
WO1991011525A2 (en) * | 1990-01-25 | 1991-08-08 | The University Court Of The University Of Glasgow | Vaccines |
WO1993006223A1 (fr) * | 1991-09-27 | 1993-04-01 | Centre National De La Recherche Scientifique (C.N.R.S.) | Vecteurs recombinants viraux pour l'expression dans des cellules musculaires |
Family Cites Families (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
ZA858044B (en) * | 1984-11-01 | 1987-05-27 | American Home Prod | Oral vaccines |
IE903130A1 (en) * | 1989-09-15 | 1991-03-27 | Regeneron Pharma | Ciliary neurotrophic factor |
FR2688514A1 (fr) * | 1992-03-16 | 1993-09-17 | Centre Nat Rech Scient | Adenovirus recombinants defectifs exprimant des cytokines et medicaments antitumoraux les contenant. |
AU670933B2 (en) * | 1992-03-27 | 1996-08-08 | Collimore Enterprises Pty Ltd | Formwork device |
-
1993
- 1993-05-18 FR FR9305954A patent/FR2705361B1/fr not_active Expired - Lifetime
-
1994
- 1994-05-06 CN CN94192150A patent/CN1067722C/zh not_active Expired - Lifetime
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- 1994-05-06 AU AU67878/94A patent/AU696495B2/en not_active Expired
- 1994-05-06 UA UA95114778A patent/UA66417C2/xx unknown
- 1994-05-06 CA CA002163256A patent/CA2163256C/fr not_active Expired - Lifetime
- 1994-05-06 ES ES94916259T patent/ES2167365T5/es not_active Expired - Lifetime
- 1994-05-06 WO PCT/FR1994/000531 patent/WO1994026914A1/fr active IP Right Grant
- 1994-05-06 BR BR9406720A patent/BR9406720A/pt not_active Application Discontinuation
- 1994-05-06 DK DK94916259T patent/DK0698108T4/da active
- 1994-05-06 PT PT94916259T patent/PT698108E/pt unknown
- 1994-05-06 DE DE69429260T patent/DE69429260T3/de not_active Expired - Lifetime
- 1994-05-06 JP JP52504994A patent/JP3995259B2/ja not_active Expired - Lifetime
- 1994-05-06 KR KR1019950705128A patent/KR100379569B1/ko not_active IP Right Cessation
- 1994-05-06 SK SK1447-95A patent/SK282354B6/sk not_active IP Right Cessation
- 1994-05-06 AT AT94916259T patent/ATE209686T1/de active
- 1994-05-06 RU RU95122419/13A patent/RU2233333C2/ru active
- 1994-05-06 HU HU9503297A patent/HU221340B1/hu unknown
- 1994-05-06 PL PL94311660A patent/PL182814B1/pl unknown
- 1994-05-06 EP EP94916259A patent/EP0698108B2/fr not_active Expired - Lifetime
- 1994-05-06 CZ CZ953028A patent/CZ284903B6/cs not_active IP Right Cessation
- 1994-05-12 IL IL10964494A patent/IL109644A/xx not_active IP Right Cessation
- 1994-05-16 ZA ZA943358A patent/ZA943358B/xx unknown
-
1995
- 1995-11-07 NO NO19954466A patent/NO320818B1/no not_active IP Right Cessation
- 1995-11-17 FI FI955552A patent/FI118538B/fi not_active IP Right Cessation
-
2004
- 2004-02-05 JP JP2004029636A patent/JP2004180689A/ja active Pending
Patent Citations (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
WO1991011525A2 (en) * | 1990-01-25 | 1991-08-08 | The University Court Of The University Of Glasgow | Vaccines |
WO1993006223A1 (fr) * | 1991-09-27 | 1993-04-01 | Centre National De La Recherche Scientifique (C.N.R.S.) | Vecteurs recombinants viraux pour l'expression dans des cellules musculaires |
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