CA2346155A1 - Synthese enzymatique d'adn simple brin - Google Patents
Synthese enzymatique d'adn simple brin Download PDFInfo
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- CA2346155A1 CA2346155A1 CA002346155A CA2346155A CA2346155A1 CA 2346155 A1 CA2346155 A1 CA 2346155A1 CA 002346155 A CA002346155 A CA 002346155A CA 2346155 A CA2346155 A CA 2346155A CA 2346155 A1 CA2346155 A1 CA 2346155A1
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- C12N2310/11—Antisense
- C12N2310/111—Antisense spanning the whole gene, or a large part of it
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- C12N2310/00—Structure or type of the nucleic acid
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- C12N2310/12—Type of nucleic acid catalytic nucleic acids, e.g. ribozymes
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Abstract
L'invention concerne des méthodes et compositions de production d'ADN complémentaire simple brin grâce à un système vectoriel dans des cellules eucaryotes. Le vecteur contient toutes les instructions de signalisation et le fonctions enzymatiques nécessaires pour permettre à la cellule hôte de produire l'ADN simple brin codant pour une séquence d'acide nucléique voulue (une <= séquence intéressante >=). L'invention concerne également les composants compris dans le vecteur et destinés à synthétiser l'ADN simple brin in vivo. Ces composants comprennent: (1) un gène de transcriptase inverse, (2) un élément génétique fournissant la matrice de la séquence d'ADN simple brin intéressante et (3) un deuxième élément génétique situé à proximité de l'élément génétique codant pour la séquence intéressante qui fournit le site d'amorçage de la transcription inverse par la molécule de transcriptase inverse. Le vecteur contient également des promoteurs/séquences activatrices appropriées. L'invention concerne enfin une méthode de mise au point d'un vecteur comprenant ces composants.
Applications Claiming Priority (5)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US16979398A | 1998-10-09 | 1998-10-09 | |
| US09/169,793 | 1998-10-09 | ||
| US39778399A | 1999-09-16 | 1999-09-16 | |
| US09/397,783 | 1999-09-16 | ||
| PCT/US1999/023933 WO2000022113A1 (fr) | 1998-10-09 | 1999-10-12 | Synthese enzymatique d'adn simple brin |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| CA2346155A1 true CA2346155A1 (fr) | 2000-04-20 |
Family
ID=26865381
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| CA002346155A Abandoned CA2346155A1 (fr) | 1998-10-09 | 1999-10-12 | Synthese enzymatique d'adn simple brin |
Country Status (9)
| Country | Link |
|---|---|
| EP (1) | EP1117776A1 (fr) |
| JP (1) | JP2002527061A (fr) |
| KR (1) | KR20010099682A (fr) |
| AU (1) | AU6430599A (fr) |
| BR (1) | BR9914772A (fr) |
| CA (1) | CA2346155A1 (fr) |
| IL (1) | IL142490A0 (fr) |
| MX (1) | MXPA01003642A (fr) |
| WO (1) | WO2000022113A1 (fr) |
Families Citing this family (177)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE19956568A1 (de) | 1999-01-30 | 2000-08-17 | Roland Kreutzer | Verfahren und Medikament zur Hemmung der Expression eines vorgegebenen Gens |
| US7419964B2 (en) * | 1999-09-16 | 2008-09-02 | Cytogenix, Inc. | Treatment of HSV-related pathologies using ssDNA |
| CA2386246A1 (fr) * | 1999-10-04 | 2001-04-12 | Cytogenix, Inc. | Modification de l'expression genetique a l'aide d'adn monocatenaire produit in vivo |
| DE10100586C1 (de) | 2001-01-09 | 2002-04-11 | Ribopharma Ag | Verfahren zur Hemmung der Expression eines Ziegens |
| US7423142B2 (en) | 2001-01-09 | 2008-09-09 | Alnylam Pharmaceuticals, Inc. | Compositions and methods for inhibiting expression of anti-apoptotic genes |
| US7767802B2 (en) | 2001-01-09 | 2010-08-03 | Alnylam Pharmaceuticals, Inc. | Compositions and methods for inhibiting expression of anti-apoptotic genes |
| US7745418B2 (en) | 2001-10-12 | 2010-06-29 | Alnylam Pharmaceuticals, Inc. | Compositions and methods for inhibiting viral replication |
| CN1620503A (zh) * | 2001-12-14 | 2005-05-25 | 耶鲁大学 | 细胞内制备单链dna |
| AU2005222902B2 (en) | 2004-03-12 | 2010-06-10 | Alnylam Pharmaceuticals, Inc. | iRNA agents targeting VEGF |
| WO2006037127A2 (fr) * | 2004-09-28 | 2006-04-06 | Cytogenix, Inc. | Oligonucleotides antimicrobiens monocatenaires et leurs utilisations |
| CA2626690A1 (fr) | 2005-11-09 | 2007-05-18 | Alnylam Pharmaceuticals, Inc. | Compositions et procedes destines a inhiber l'expression de la mutation du gene du facteur v leiden |
| US8658608B2 (en) | 2005-11-23 | 2014-02-25 | Yale University | Modified triple-helix forming oligonucleotides for targeted mutagenesis |
| KR101462874B1 (ko) | 2006-03-31 | 2014-11-18 | 알닐람 파마슈티칼스 인코포레이티드 | Ｅｇ5 유전자의 발현을 억제하는 이본쇄 리보핵산 |
| JP4812874B2 (ja) | 2006-04-28 | 2011-11-09 | アルナイラム ファーマシューティカルズ， インコーポレイテッド | Ｊｃウイルス遺伝子の発現を抑制するための組成物および方法 |
| CN101484588B (zh) | 2006-05-11 | 2013-11-06 | 阿尔尼拉姆医药品有限公司 | 抑制pcsk9基因表达的组合物和方法 |
| CN101489566B (zh) | 2006-05-19 | 2012-04-18 | 阿尔尼拉姆医药品有限公司 | Aha基因的RNAi调控及其治疗性应用 |
| EP2018443A4 (fr) | 2006-05-22 | 2009-11-11 | Alnylam Pharmaceuticals Inc | Compositions et méthodes inhibant l'expression du gène ikk-b |
| KR20090083338A (ko) | 2006-09-18 | 2009-08-03 | 알닐람 파마슈티칼스 인코포레이티드 | ＳＣＡＰ의 ＲＮＡｉ 조절 및 이들의 치료적 용도 |
| WO2008036933A2 (fr) | 2006-09-21 | 2008-03-27 | Alnylam Pharmaceuticals, Inc. | Compositions et procédés servant à inhiber l'expression du gène hamp |
| PE20090064A1 (es) | 2007-03-26 | 2009-03-02 | Novartis Ag | Acido ribonucleico de doble cadena para inhibir la expresion del gen e6ap humano y composicion farmaceutica que lo comprende |
| JP5558346B2 (ja) | 2007-07-05 | 2014-07-23 | ノバルティス アーゲー | ウイルス感染を処置するためのｄｓＲＮＡ |
| EP2245159A2 (fr) | 2007-12-10 | 2010-11-03 | Alnylam Pharmaceuticals Inc. | Compositions et procédés permettant l'inhibition de l'expression du gène du facteur vii |
| NZ588280A (en) | 2008-03-05 | 2012-11-30 | Alnylam Pharmaceuticals Inc | Compositions and methods for inhibiting expression of eg5 and vegf genes |
| EP2690175B1 (fr) | 2008-09-02 | 2016-12-28 | Alnylam Pharmaceuticals, Inc. | Compositions et procédés d'inhibition combinée d'expression du gène mutant EGFR et IL-6 |
| CA2739170A1 (fr) | 2008-09-25 | 2010-04-01 | Alnylam Pharmaceuticals, Inc. | Compositions a base de preparation lipidique et methodes destinees a inhiber l'expression d'un gene de serum amyloide a |
| IL310600A (en) | 2008-10-20 | 2024-04-01 | Alnylam Pharmaceuticals Inc | Compounds and methods for inhibiting transthyretin expression |
| US8324368B2 (en) | 2008-12-10 | 2012-12-04 | Alnylam Pharmaceuticals, Inc. | GNAQ targeted dsRNA compositions and methods for inhibiting expression |
| SG173182A1 (en) | 2009-02-03 | 2011-09-29 | Hoffmann La Roche | Compositions and methods for inhibiting expression of ptp1b genes |
| WO2010099341A1 (fr) | 2009-02-26 | 2010-09-02 | Alnylam Pharmaceuticals, Inc. | Composition et procédés d'inhibition de l'expression du gène mig-12 |
| JP6032724B2 (ja) | 2009-03-12 | 2016-11-30 | アルナイラム ファーマシューティカルズ， インコーポレイテッドＡｌｎｙｌａｍ Ｐｈａｒｍａｃｅｕｔｉｃａｌｓ， Ｉｎｃ． | 脂質製剤組成物およびＥｇ５遺伝子とＶＥＧＦ遺伝子の発現を阻害する方法 |
| WO2010147992A1 (fr) | 2009-06-15 | 2010-12-23 | Alnylam Pharmaceuticals, Inc. | Procédés pour augmenter l'efficacité d'arnsi dans une formulation lipidique |
| CA2764832A1 (fr) | 2009-06-15 | 2010-12-23 | Alnylam Pharmaceuticals, Inc. | Arn double brin en formulation lipidique ciblant le gene pcsk9 |
| WO2011054939A2 (fr) | 2009-11-09 | 2011-05-12 | F. Hoffmann-La Roche Ag | Compositions et procédés pour inhiber l'expression de gènes kif10 |
| US20110152349A1 (en) | 2009-12-18 | 2011-06-23 | Anke Geick | Compositions and methods for inhibiting expression of il-18 genes |
| TW201129365A (en) | 2010-02-05 | 2011-09-01 | Hoffmann La Roche | Compositions and methods for inhibiting expression of IKK2 genes |
| EP3329924B1 (fr) | 2010-03-29 | 2021-05-05 | Alnylam Pharmaceuticals, Inc. | Thérapie d'arndb pour amylose oculaire associée à la transthyrétine (ttr) |
| CA2792561C (fr) | 2010-04-06 | 2021-10-26 | Alnylam Pharmaceuticals, Inc. | Compositions et procedes permettant d'inhiber l'expression du gene cd274/pd-l1 |
| CA3102008A1 (fr) | 2010-06-02 | 2011-12-08 | Alnylam Pharmaceuticals, Inc. | Compositions et methodes pour traiter une fibrose hepatique |
| EP2630240A1 (fr) | 2010-10-18 | 2013-08-28 | Arrowhead Research Corporation | Compositions et procédés d'inhibition de l'expression de gènes rrm2 |
| EP2649182A4 (fr) | 2010-12-10 | 2015-05-06 | Alnylam Pharmaceuticals Inc | Compositions et procédés pour l'augmentation de la production d'érythropoïétine (epo) |
| US9127275B2 (en) | 2010-12-10 | 2015-09-08 | Alnylam Pharmaceuticals, Inc. | Compositions and methods for inhibiting expression of klf-1 and bcl11a genes |
| CN113736782B (zh) | 2011-03-29 | 2024-07-16 | 阿尔尼拉姆医药品有限公司 | 用于抑制tmprss6基因表达的组合物和方法 |
| US9068184B2 (en) | 2011-06-21 | 2015-06-30 | Alnylam Pharmaceuticals, Inc. | Compositions and methods for inhibition of expression of protein C (PROC) genes |
| WO2012177921A2 (fr) | 2011-06-21 | 2012-12-27 | Alnylam Pharmaceuticals, Inc | Compositions et procédés d'inhibition de l'expression du peptide antimicrobien hepcidine (hamp) ou du gène lié à hamp |
| MX344807B (es) | 2011-06-21 | 2017-01-09 | Alnylam Pharmaceuticals Inc | Composiciones y metodos para inhibicion de genes para alipoproteina c-iii (apoc3). |
| JP2014526882A (ja) | 2011-06-21 | 2014-10-09 | アルナイラム ファーマシューティカルズ， インコーポレイテッド | 対象中の治療剤の活性を判定するアッセイおよび方法 |
| MX345095B (es) | 2011-06-21 | 2017-01-17 | Alnylam Pharmaceuticals Inc | Composiciones de arni similares a angiopoyetina 3 (angptl3) y metodos para su uso. |
| US20140235693A1 (en) | 2011-06-23 | 2014-08-21 | Alnylam Pharmaceuticals, Inc. | Serpina1 sirnas: compositions of matter and methods of treatment |
| TWI695066B (zh) | 2011-06-30 | 2020-06-01 | 美商艾羅海德製藥公司 | 用於抑制b型肝炎病毒基因表現之組合物及方法 |
| JP2014526887A (ja) | 2011-08-01 | 2014-10-09 | アルナイラム ファーマシューティカルズ， インコーポレイテッド | 造血幹細胞移植の成功率を改善する方法 |
| US9133461B2 (en) | 2012-04-10 | 2015-09-15 | Alnylam Pharmaceuticals, Inc. | Compositions and methods for inhibiting expression of the ALAS1 gene |
| US9127274B2 (en) | 2012-04-26 | 2015-09-08 | Alnylam Pharmaceuticals, Inc. | Serpinc1 iRNA compositions and methods of use thereof |
| CN104854242B (zh) | 2012-12-05 | 2018-03-16 | 阿尔尼拉姆医药品有限公司 | PCSK9 iRNA组合物及其使用方法 |
| WO2014130922A1 (fr) | 2013-02-25 | 2014-08-28 | Trustees Of Boston University | Compositions et procédés pour le traitement d'infections fongiques |
| EP2968424B1 (fr) | 2013-03-13 | 2020-01-22 | Geneweave Biosciences Inc. | Particules de transduction non réplicative et systèmes rapporteurs à base de particules de transduction |
| IL288931B1 (en) | 2013-03-14 | 2025-01-01 | Alnylam Pharmaceuticals Inc | Compositions comprising a complementary portion of C5 IRNA and methods of using them |
| WO2014160871A2 (fr) | 2013-03-27 | 2014-10-02 | The General Hospital Corporation | Procédés et agents pour le traitement de la maladie d'alzheimer |
| US10246708B2 (en) | 2013-05-06 | 2019-04-02 | Alnylam Pharmaceuticals, Inc. | Dosages and methods for delivering lipid formulated nucleic acid molecules |
| KR102463973B1 (ko) | 2013-05-22 | 2022-11-07 | 알닐람 파마슈티칼스 인코포레이티드 | ＳＥＲＰＩＮＡ1 ｉＲＮＡ 조성물 및 이의 사용 방법 |
| BR112015029276B1 (pt) | 2013-05-22 | 2022-07-12 | Alnylam Pharmaceuticals, Inc | Agente de irna fita dupla capaz de inibir a expressão de tmprss6, composição farmacêutica e uso dos mesmos |
| MX2016004230A (es) | 2013-10-02 | 2016-10-21 | Alnylam Pharmaceuticals Inc | Composiciones y metodos para inhibir la expresion del gen lect2. |
| US10519446B2 (en) | 2013-10-04 | 2019-12-31 | Novartis Ag | Organic compounds to treat hepatitis B virus |
| WO2015051045A2 (fr) | 2013-10-04 | 2015-04-09 | Novartis Ag | Extrémités 3' pour agents arni destinés à être utilisés dans l'interférence arn |
| BR122020001264B1 (pt) | 2013-10-04 | 2022-11-22 | Icahn School Of Medicine At Mount Sinai | Ácido ribonucleico de fita dupla (dsrna) para inibição da expressão de alas1, composição farmacêutica para inibição da expressão de um gene alas1, métodos de inibição da expressão de alas1 em uma célula e para diminuir um nível de uma porfirina ou de um precursor de porfirina em uma célula, usos de um dsrna, método para avaliar o nível de mrna de alas1 extracelular em circulação em um indivíduo, composição e uso da mesma |
| WO2015051366A2 (fr) | 2013-10-04 | 2015-04-09 | Novartis Ag | Formats inédits pour composés organiques utilisables en interférence arn |
| CA2931090A1 (fr) | 2013-12-12 | 2015-06-18 | Alnylam Pharmaceuticals, Inc. | Composition d'arni d'element de complement et procedes pour les utiliser |
| EP3960860A3 (fr) | 2014-02-11 | 2022-06-08 | Alnylam Pharmaceuticals, Inc. | Compositions d'arni de cétohexokinase (khk) et leurs procédés d'utilisation |
| WO2015175510A1 (fr) | 2014-05-12 | 2015-11-19 | Alnylam Pharmaceuticals, Inc. | Méthodes et compositions pour le traitement d'un trouble associé à serpinc1 |
| CN112852809A (zh) | 2014-05-22 | 2021-05-28 | 阿尔尼拉姆医药品有限公司 | 血管紧张素原(AGT)iRNA组合物及其使用方法 |
| JOP20200115A1 (ar) | 2014-10-10 | 2017-06-16 | Alnylam Pharmaceuticals Inc | تركيبات وطرق لتثبيط التعبير الجيني عن hao1 (حمض أوكسيداز هيدروكسيلي 1 (أوكسيداز جليكولات)) |
| JOP20200092A1 (ar) | 2014-11-10 | 2017-06-16 | Alnylam Pharmaceuticals Inc | تركيبات iRNA لفيروس الكبد B (HBV) وطرق لاستخدامها |
| EP3221451A1 (fr) | 2014-11-17 | 2017-09-27 | Alnylam Pharmaceuticals, Inc. | Compositions d'arni d'apolipoprotéine c3 (apoc3) et procédés d'utilisation de ces compositions |
| WO2016130806A2 (fr) | 2015-02-13 | 2016-08-18 | Alnylam Pharmaceuticals, Inc. | Compositions d'arni du gène codant pour la protéine 3 contenant un domaine phospholipase de type patatine (pnpla3) et leurs procédés d'utilisation |
| EP3283631A1 (fr) | 2015-04-13 | 2018-02-21 | Alnylam Pharmaceuticals, Inc. | Compositions d'arni faisant intervenir la protéine 3 de type angiopoïétine (angptl3) et leurs procédés d'utilisation |
| CA2984636A1 (fr) | 2015-05-06 | 2016-11-10 | Alnylam Pharmaceuticals, Inc. | Compositions d'arni de facteur xii (facteur hageman) (f12), de la kallicreine b plasmatique (facteur fletcher) 1 (klkb1) et de kininogene 1 (kng1) et procedes d'utilisation associ es |
| EP4365291A3 (fr) | 2015-06-12 | 2024-08-14 | Alnylam Pharmaceuticals, Inc. | Compositions d'arni c5 de composant du complément et leurs procédés d'utilisation |
| WO2016209862A1 (fr) | 2015-06-23 | 2016-12-29 | Alnylam Pharmaceuticals, Inc. | Compositions d'arndb contre un gène de glucokinase (gck) et leurs procédés d'utilisation |
| US10494632B2 (en) | 2015-07-10 | 2019-12-03 | Alnylam Pharmaceuticals, Inc. | Insulin-like growth factor binding protein, acid labile subunit (IGFALS) compositions and methods of use thereof |
| WO2017027350A2 (fr) | 2015-08-07 | 2017-02-16 | Arrowhead Pharmaceuticals, Inc. | Thérapie par interférence arn pour l'infection par le virus de l'hépatite b |
| CN108368507B (zh) | 2015-09-02 | 2022-03-22 | 阿尔尼拉姆医药品有限公司 | 程序性细胞死亡1配体1(PD-L1)的iRNA组合物及其使用方法 |
| TW201718857A (zh) | 2015-09-14 | 2017-06-01 | 艾爾妮蘭製藥公司 | 用於抑制alas1基因表現之組合物及方法 |
| IL259795B2 (en) | 2015-12-07 | 2024-04-01 | Genzyme Corp | Methods and preparations for the treatment of diseases related to SERPINC1 |
| WO2017100542A1 (fr) | 2015-12-10 | 2017-06-15 | Alnylam Pharmaceuticals, Inc. | Compositions d'arni chaperon (scap) de la protéine srebp (sterol regulatory element binding protein), et procédés d'utilisation associés |
| EP3416976A2 (fr) | 2016-02-16 | 2018-12-26 | Yale University | Compositions permettant d'améliorer l'édition ciblée de gènes et leurs procédés d'utilisation |
| MA45295A (fr) | 2016-04-19 | 2019-02-27 | Alnylam Pharmaceuticals Inc | Composition d'arni de protéine de liaison de lipoprotéines haute densité (hdlbp/vigiline) et procédés pour les utiliser |
| EP3469083A1 (fr) | 2016-06-10 | 2019-04-17 | Alnylam Pharmaceuticals, Inc. | Compositions d'arni du composant c5 du complément et leurs méthodes d'utilisation pour traiter l'hémoglobinurie paroxystique nocturne (hpn) |
| JOP20170161A1 (ar) | 2016-08-04 | 2019-01-30 | Arrowhead Pharmaceuticals Inc | عوامل RNAi للعدوى بفيروس التهاب الكبد ب |
| TW202313978A (zh) | 2016-11-23 | 2023-04-01 | 美商阿尼拉製藥公司 | 絲胺酸蛋白酶抑制因子Ａ１ ｉＲＮＡ組成物及其使用方法 |
| SG10201913552UA (en) | 2016-12-16 | 2020-03-30 | Alnylam Pharmaceuticals Inc | Methods for treating or preventing ttr-associated diseases using transthyretin (ttr) irna compositions |
| BR112019021852A2 (pt) | 2017-04-18 | 2020-06-02 | Alnylam Pharmaceuticals, Inc. | Agente de rnai e uma vacina contra hbv, uso ou método e kit para tratamento |
| WO2019014530A1 (fr) | 2017-07-13 | 2019-01-17 | Alnylam Pharmaceuticals Inc. | Compositions d'arni de lactate déshydrogénase a (ldha) et leurs procédés d'utilisation |
| EP3704252A1 (fr) | 2017-11-01 | 2020-09-09 | Alnylam Pharmaceuticals, Inc. | Compositions d'arni de composant du complément c3 et leurs procédés d'utilisation |
| WO2019099610A1 (fr) | 2017-11-16 | 2019-05-23 | Alnylam Pharmaceuticals, Inc. | Compositions d'arni de kisspeptine 1 (kiss1) et leurs méthodes d'utilisation |
| EP3714054A1 (fr) | 2017-11-20 | 2020-09-30 | Alnylam Pharmaceuticals, Inc. | Compositions d'arni de composant p amyloïde serique et leurs procédés d'utilisation |
| AU2018388484A1 (en) | 2017-12-18 | 2020-07-30 | Alnylam Pharmaceuticals, Inc. | High mobility group box-1 (HMGB1) iRNA compositions and methods of use thereof |
| US11008602B2 (en) | 2017-12-20 | 2021-05-18 | Roche Molecular Systems, Inc. | Non-replicative transduction particles and transduction particle-based reporter systems |
| TWI851574B (zh) | 2018-05-14 | 2024-08-11 | 美商阿尼拉製藥公司 | 血管收縮素原（ＡＧＴ）ｉＲＮＡ組成物及其使用方法 |
| EP3837367A1 (fr) | 2018-08-16 | 2021-06-23 | Alnylam Pharmaceuticals, Inc. | Compositions et procédés d'inhibition de l'expression du gène lect2 |
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| US11572595B2 (en) | 2018-12-31 | 2023-02-07 | Roche Molecular Systems, Inc. | Non-replicative transduction particles with one or more non-native tail fibers and transduction particle-based reporter systems |
| EP4007812A1 (fr) | 2019-08-01 | 2022-06-08 | Alnylam Pharmaceuticals, Inc. | Compositions d'arni de la famille des serpines 2 (serpinf2) et leurs procedes d'utilisation |
| EP4007811A2 (fr) | 2019-08-01 | 2022-06-08 | Alnylam Pharmaceuticals, Inc. | Compositions d'arni de carboxypeptidase b2 (cpb2) et leurs procédés d'utilisation |
| WO2021030522A1 (fr) | 2019-08-13 | 2021-02-18 | Alnylam Pharmaceuticals, Inc. | Compositions d'agent d'arni à sous-unité de protéine ribosomale 25 (rps25) et leurs procédés d'utilisation |
| WO2021037972A1 (fr) | 2019-08-27 | 2021-03-04 | Sanofi | Compositions et procédés d'inhibition de pcsk9 |
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| WO2021061815A1 (fr) | 2019-09-23 | 2021-04-01 | Omega Therapeutics, Inc. | Compositions et procédés de modulation de l'expression génique du facteur nucléaire hépatocytaire 4-alpha (hnf4α) |
| JP2022548320A (ja) | 2019-09-23 | 2022-11-17 | オメガ セラピューティクス， インコーポレイテッド | アポリポタンパク質ｂ（ａｐｏｂ）遺伝子発現をモジュレートするための組成物および方法 |
| US20220389429A1 (en) | 2019-10-04 | 2022-12-08 | Alnylam Pharmaceuticals, Inc. | Compositions and methods for silencing ugt1a1 gene expression |
| EP4041308A1 (fr) | 2019-10-07 | 2022-08-17 | University of Virginia Patent Foundation | Modulation de vaisseaux lymphatiques dans une maladie neurologique |
| US20240141358A1 (en) | 2019-10-18 | 2024-05-02 | Alnylam Pharmaceuticals, Inc. | Solute carrier family member irna compositions and methods of use thereof |
| TW202134435A (zh) | 2019-10-22 | 2021-09-16 | 美商阿尼拉製藥公司 | 補體成分ｃ３ ｉｒｎａ組成物及其使用方法 |
| KR20220094213A (ko) | 2019-11-01 | 2022-07-05 | 알닐람 파마슈티칼스 인코포레이티드 | 헌팅틴 (HTT) iRNA 제제 조성물 및 이의 사용 방법 |
| EP4051796A1 (fr) | 2019-11-01 | 2022-09-07 | Alnylam Pharmaceuticals, Inc. | Compositions et méthodes pour rendre silencieuse l'expression du gène de fusion dnajb1-prkaca |
| TW202132568A (zh) | 2019-11-13 | 2021-09-01 | 美商阿尼拉製藥公司 | 用於治療血管收縮素原相關病症之方法及組成物 |
| EP4061945A1 (fr) | 2019-11-22 | 2022-09-28 | Alnylam Pharmaceuticals, Inc. | Compositions d'agent arni d'ataxine 3 (atxn3) et leurs procédés d'utilisation |
| AU2020402885A1 (en) | 2019-12-13 | 2022-06-16 | Alnylam Pharmaceuticals, Inc. | Human chromosome 9 open reading frame 72 (C9orf72) iRNA agent compositions and methods of use thereof |
| WO2021126734A1 (fr) | 2019-12-16 | 2021-06-24 | Alnylam Pharmaceuticals, Inc. | Compositions d'arni du gène codant pour la protéine 3 contenant un domaine phospholipase de type patatine (pnpla3) et leurs méthodes d'utilisation |
| EP4085156B1 (fr) | 2019-12-31 | 2023-10-25 | F. Hoffmann-La Roche AG | Criblage par pcr quantitative de prophages inductibles à partir d'isolats bactériens |
| US20230067811A1 (en) | 2020-01-24 | 2023-03-02 | University Of Virginia Patent Foundation | Modulating lymphatic vessels in neurological disease |
| WO2021154941A1 (fr) | 2020-01-31 | 2021-08-05 | Alnylam Pharmaceuticals, Inc. | Compositions d'arni du composant c5 du complément destinées à être utilisées dans le traitement de la sclérose latérale amyotrophique (sla) |
| US20230136787A1 (en) | 2020-02-10 | 2023-05-04 | Alnylam Pharmaceuticals, Inc. | Compositions and methods for silencing vegf-a expression |
| JP2023514336A (ja) | 2020-02-18 | 2023-04-05 | アルナイラム ファーマシューティカルズ， インコーポレイテッド | アポリポタンパク質Ｃ３（ＡＰＯＣ３）ｉＲＮＡ組成物およびその使用法 |
| EP4114948A1 (fr) | 2020-03-06 | 2023-01-11 | Alnylam Pharmaceuticals, Inc. | Compositions d'arni de cétohexokinase (khk) et leurs procédés d'utilisation |
| EP4118207A1 (fr) | 2020-03-11 | 2023-01-18 | Omega Therapeutics, Inc. | Compositions et procédés de modulation de l'expression génique de forkhead box p3 (foxp3) |
| EP4121534A1 (fr) | 2020-03-18 | 2023-01-25 | Alnylam Pharmaceuticals, Inc. | Compositions et méthodes pour traiter des sujets ayant un variant de gène d'alanine-glyoxylate aminotransférase hétérozygote (agxt) |
| CN116209759A (zh) | 2020-03-26 | 2023-06-02 | 阿尔尼拉姆医药品有限公司 | 冠状病毒iRNA组合物及其使用方法 |
| EP4127171A2 (fr) | 2020-03-30 | 2023-02-08 | Alnylam Pharmaceuticals, Inc. | Compositions et procédés de silençage de l'expression du gène dnajc15 |
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| BR112022020227A2 (pt) | 2020-04-07 | 2022-11-22 | Alnylam Pharmaceuticals Inc | Composições e métodos para silenciamento da expressão de scn9a |
| EP4133077A1 (fr) | 2020-04-07 | 2023-02-15 | Alnylam Pharmaceuticals, Inc. | Compositions d'arni de la serine protease 2 transmembranaire (tmprss2) et leurs procédés d'utilisation |
| EP4133076A1 (fr) | 2020-04-07 | 2023-02-15 | Alnylam Pharmaceuticals, Inc. | Compositions arni d'enzyme de conversion de l'angiotensine 2 (eca2) et procédés d'utilisation associés |
| MX2022013525A (es) | 2020-04-27 | 2023-01-24 | Alnylam Pharmaceuticals Inc | Composiciones de agentes de ácido ribonucleico de interferencia (arni) de apolipoproteína e (apoe) y métodos de uso de las mismas. |
| KR20230017789A (ko) | 2020-04-30 | 2023-02-06 | 알닐람 파마슈티칼스 인코포레이티드 | 보체 인자 B (CFB) iRNA 조성물 및 이의 사용 방법 |
| EP4153746A1 (fr) | 2020-05-21 | 2023-03-29 | Alnylam Pharmaceuticals, Inc. | Compositions et procédés d'inhibition de l'expression du gène marc1 |
| TW202214856A (zh) | 2020-06-18 | 2022-04-16 | 美商阿尼拉製藥公司 | 黃嘌呤脫氫酶（ＸＤＨ）ｉＲＮＡ組成物及其使用之方法 |
| EP4217489A1 (fr) | 2020-09-24 | 2023-08-02 | Alnylam Pharmaceuticals, Inc. | Compositions d'arni de dipeptidyle peptidase 4 (dpp4) et leurs procédés d'utilisation |
| TW202229552A (zh) | 2020-10-05 | 2022-08-01 | 美商艾拉倫製藥股份有限公司 | Ｇ蛋白－偶合受體７５（ＧＰＲ７５）ｉＲＮＡ組成物及其使用方法 |
| JP2023546103A (ja) | 2020-10-16 | 2023-11-01 | サノフイ | Ａｎｇｐｔｌ３を阻害するための新規のｒｎａ組成物および方法 |
| JP2023545502A (ja) | 2020-10-16 | 2023-10-30 | サノフイ | リポタンパク質（ａ）を阻害するためのｒｎａ組成物および方法 |
| WO2022087041A1 (fr) | 2020-10-21 | 2022-04-28 | Alnylam Pharmaceuticals, Inc. | Méthodes et compositions pour le traitement de l'hyperoxalurie primaire |
| EP4232582A1 (fr) | 2020-10-23 | 2023-08-30 | Alnylam Pharmaceuticals, Inc. | Compositions d'arni de la mucine 5b (muc5b) et leurs méthodes d'utilisation |
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| EP4259795A1 (fr) | 2020-12-08 | 2023-10-18 | Alnylam Pharmaceuticals, Inc. | Compositions d'arni du facteur de coagulation x (f10) et leurs méthodes d'utilisation |
| WO2022150260A1 (fr) | 2021-01-05 | 2022-07-14 | Alnylam Pharmaceuticals, Inc. | Compositions d'arni du composant du complément 9 (c9) et leurs méthodes d'utilisation |
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| WO2022192519A1 (fr) | 2021-03-12 | 2022-09-15 | Alnylam Pharmaceuticals, Inc. | Compositions d'arni de la glycogène synthase kinase 3 alpha (gsk3a) et leurs procédés d'utilisation |
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| EP4314293A1 (fr) | 2021-04-01 | 2024-02-07 | Alnylam Pharmaceuticals, Inc. | Compositions d'arni de proline déshydrogénase 2 (prodh2) et procédés d'utilisation associés |
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| JP2024523000A (ja) | 2021-06-08 | 2024-06-25 | アルナイラム ファーマシューティカルズ， インコーポレイテッド | シュタルガルト病及び／又は網膜結合タンパク質４（ｒｂｐ４）関連障害を治療又は予防するための組成物及び方法 |
| EP4363580A1 (fr) | 2021-06-30 | 2024-05-08 | Alnylam Pharmaceuticals, Inc. | Procédés et compositions pour le traitement d'un trouble associé à l'angiotensinogène (agt) |
| WO2023283359A2 (fr) | 2021-07-07 | 2023-01-12 | Omega Therapeutics, Inc. | Compositions et procédés de modulation de l'expression génique de la protéine 1 du récepteur frizzled secrété (sfrp1) |
| WO2023003805A1 (fr) | 2021-07-19 | 2023-01-26 | Alnylam Pharmaceuticals, Inc. | Méthodes et compositions pour traiter des sujets ayant ou ayant un risque de développer une maladie ou un trouble d'hyperoxalurie non primaire |
| TW202421169A (zh) | 2021-07-21 | 2024-06-01 | 美商艾拉倫製藥股份有限公司 | 代謝疾患相關的標靶基因ｉＲＮＡ組成物及其使用方法 |
| IL309905A (en) | 2021-07-23 | 2024-03-01 | Alnylam Pharmaceuticals Inc | IRNA compositions in β-catenin (CTNNB1) and methods of using them |
| WO2023009687A1 (fr) | 2021-07-29 | 2023-02-02 | Alnylam Pharmaceuticals, Inc. | Compositions d'arni de 3-hydroxy-3-méthylglutaryle-coa réductase (hmgcr) et leurs procédés d'utilisation |
| CN117795074A (zh) | 2021-08-03 | 2024-03-29 | 阿尔尼拉姆医药品有限公司 | 转甲状腺素蛋白（TTR）iRNA组合物和其使用方法 |
| KR20240042016A (ko) | 2021-08-04 | 2024-04-01 | 알닐람 파마슈티칼스 인코포레이티드 | 안지오텐시노겐(AGT)을 침묵화하기 위한 iRNA 조성물 및 방법 |
| EP4384617A1 (fr) | 2021-08-13 | 2024-06-19 | Alnylam Pharmaceuticals, Inc. | Compositions d'arni du facteur xii (f12) et leurs procédés d'utilisation |
| WO2023044370A2 (fr) | 2021-09-17 | 2023-03-23 | Alnylam Pharmaceuticals, Inc. | Compositions d'arni et procédés de silençage de composant du complément 3 (c3) |
| AU2022345881A1 (en) | 2021-09-20 | 2024-03-21 | Alnylam Pharmaceuticals, Inc. | Inhibin subunit beta e (inhbe) modulator compositions and methods of use thereof |
| AU2022364838A1 (en) | 2021-10-15 | 2024-04-11 | Alnylam Pharmaceuticals, Inc. | Extra-hepatic delivery irna compositions and methods of use thereof |
| KR20240095325A (ko) | 2021-10-29 | 2024-06-25 | 알닐람 파마슈티칼스 인코포레이티드 | 보체 인자 b (cfb) irna 조성물 및 이의 사용 방법 |
| EP4423272A2 (fr) | 2021-10-29 | 2024-09-04 | Alnylam Pharmaceuticals, Inc. | Compositions d'agent d'arni de la huntingtine (htt) et leurs procédés d'utilisation |
| EP4469575A2 (fr) | 2022-01-24 | 2024-12-04 | Alnylam Pharmaceuticals, Inc. | Compositions d'agent d'arni d'enzyme de voie de biosynthèse de sulfate d'héparine et leurs méthodes d'utilisation |
| WO2024059165A1 (fr) | 2022-09-15 | 2024-03-21 | Alnylam Pharmaceuticals, Inc. | Compositions d'arni de 17b-hydroxystéroïde déshydrogénase de type 13 (hsd17b13) et leurs procédés d'utilisation |
| WO2024243438A2 (fr) | 2023-05-23 | 2024-11-28 | Omega Therapeutics, Inc. | Compositions et procédés de réduction de l'expression du gène cxcl9, cxcl10 et cxcl11 |
Family Cites Families (8)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US5434070A (en) * | 1989-02-24 | 1995-07-18 | The University Of Medicine And Dentistry Of New Jersey | Reverse transcriptases from Escherichia coli and Myxococcus xanthus |
| US5436141A (en) * | 1989-02-24 | 1995-07-25 | University Of Medicine And Dentistry Of New Jersey | Method for synthesizing stable single-stranded CDNA in eukaryotes by means of a bacterial retron and products |
| DE69433352T2 (de) * | 1991-08-30 | 2004-09-16 | University Of Medicine And Dentistry Of New Jersey | Überexpression von einzelsträngigen dna molekülen |
| CA2073630C (fr) * | 1991-08-30 | 2007-12-11 | Atsushi Ohshima | Methode de synthese de l'adn simple brin "stem-loop", les produits obtenus et leur utilisation |
| AU4770093A (en) * | 1992-07-02 | 1994-01-31 | Hybridon, Inc. | Self-stabilized oligonucleotides as therapeutic agents |
| AU5871094A (en) * | 1992-12-09 | 1994-07-04 | Jeffrey E. Miller | Methods and compositions for cdna synthesis |
| FR2703053B1 (fr) * | 1993-03-26 | 1995-06-16 | Genset Sa | Oligonucleotides agrafes et semi-agrafes, procede de preparation et applications . |
| CA2193487A1 (fr) * | 1994-06-22 | 1995-12-28 | Jeffrey E. Miller | Procedes et compositions permettant la synthese d'adn complementaire |
-
1999
- 1999-10-12 IL IL14249099A patent/IL142490A0/xx unknown
- 1999-10-12 CA CA002346155A patent/CA2346155A1/fr not_active Abandoned
- 1999-10-12 KR KR1020017004474A patent/KR20010099682A/ko not_active Application Discontinuation
- 1999-10-12 BR BR9914772-6A patent/BR9914772A/pt not_active IP Right Cessation
- 1999-10-12 AU AU64305/99A patent/AU6430599A/en not_active Abandoned
- 1999-10-12 MX MXPA01003642A patent/MXPA01003642A/es unknown
- 1999-10-12 EP EP99951989A patent/EP1117776A1/fr not_active Withdrawn
- 1999-10-12 JP JP2000576004A patent/JP2002527061A/ja active Pending
- 1999-10-12 WO PCT/US1999/023933 patent/WO2000022113A1/fr not_active Application Discontinuation
Also Published As
| Publication number | Publication date |
|---|---|
| EP1117776A1 (fr) | 2001-07-25 |
| KR20010099682A (ko) | 2001-11-09 |
| WO2000022113A1 (fr) | 2000-04-20 |
| JP2002527061A (ja) | 2002-08-27 |
| AU6430599A (en) | 2000-05-01 |
| IL142490A0 (en) | 2002-03-10 |
| WO2000022113A9 (fr) | 2000-08-24 |
| BR9914772A (pt) | 2001-12-11 |
| MXPA01003642A (es) | 2003-07-21 |
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