SK70598A3 - Methods and compositions for the diagnosis and treatment of cancer - Google Patents
Methods and compositions for the diagnosis and treatment of cancer Download PDFInfo
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- SK70598A3 SK70598A3 SK705-98A SK70598A SK70598A3 SK 70598 A3 SK70598 A3 SK 70598A3 SK 70598 A SK70598 A SK 70598A SK 70598 A3 SK70598 A3 SK 70598A3
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- Pharmacology & Pharmacy (AREA)
- Public Health (AREA)
- Biochemistry (AREA)
- Biophysics (AREA)
- Bioinformatics & Cheminformatics (AREA)
- General Chemical & Material Sciences (AREA)
- Proteomics, Peptides & Aminoacids (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Gastroenterology & Hepatology (AREA)
- Wood Science & Technology (AREA)
- Toxicology (AREA)
- General Engineering & Computer Science (AREA)
- Plant Pathology (AREA)
- Microbiology (AREA)
- Physics & Mathematics (AREA)
- Epidemiology (AREA)
- Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)
- Medicines Containing Material From Animals Or Micro-Organisms (AREA)
- Measuring Or Testing Involving Enzymes Or Micro-Organisms (AREA)
- Medicines Containing Antibodies Or Antigens For Use As Internal Diagnostic Agents (AREA)
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Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
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US781095P | 1995-11-30 | 1995-11-30 | |
PCT/US1996/019083 WO1997020047A1 (en) | 1995-11-30 | 1996-11-27 | Methods and compositions for the diagnosis and treatment of cancer |
Publications (1)
Publication Number | Publication Date |
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SK70598A3 true SK70598A3 (en) | 1999-04-13 |
Family
ID=21728237
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
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SK705-98A SK70598A3 (en) | 1995-11-30 | 1996-11-27 | Methods and compositions for the diagnosis and treatment of cancer |
Country Status (19)
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US (3) | US20020077313A1 (hu) |
EP (1) | EP0863984B1 (hu) |
JP (1) | JP2000501394A (hu) |
KR (1) | KR19990071795A (hu) |
CN (2) | CN1308450C (hu) |
AT (1) | ATE325872T1 (hu) |
AU (1) | AU722042B2 (hu) |
CA (1) | CA2238829A1 (hu) |
CZ (1) | CZ296810B6 (hu) |
DE (1) | DE69636120T2 (hu) |
DK (1) | DK0863984T3 (hu) |
ES (1) | ES2264145T3 (hu) |
HU (1) | HUP9902068A3 (hu) |
NO (1) | NO982481L (hu) |
NZ (1) | NZ324168A (hu) |
PL (1) | PL186018B1 (hu) |
RU (1) | RU2174409C2 (hu) |
SK (1) | SK70598A3 (hu) |
WO (1) | WO1997020047A1 (hu) |
Families Citing this family (59)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
ATE348155T1 (de) * | 1996-11-20 | 2007-01-15 | Introgen Therapeutics Inc | Ein verbessertes verfahren zur produktion und reinigung von adenoviralen vektoren |
US6689600B1 (en) * | 1998-11-16 | 2004-02-10 | Introgen Therapeutics, Inc. | Formulation of adenovirus for gene therapy |
WO2004020971A2 (en) * | 2002-08-28 | 2004-03-11 | Introgen Therapeutics Inc. | Chromatographic methods for adenovirus purification |
US20050032728A1 (en) * | 2002-12-17 | 2005-02-10 | Sidney Kimmel Cancer Center | Tumor suppression through bicistronic co-expression of p53 and p14ARF |
CN1756569A (zh) * | 2002-12-27 | 2006-04-05 | 印屈根治疗学股份有限公司 | 增生性病损中乳头瘤病毒和致癌原转化细胞的p53治疗 |
WO2004078987A1 (fr) * | 2003-03-06 | 2004-09-16 | Zhaohui Peng | Produit de recombinaison construit a partir d'un vecteur viral et d'un gene humain suppresseur de tumeur et utilisation dudit produit de recombinaison |
US20080293652A1 (en) * | 2004-02-24 | 2008-11-27 | Introgen Therapeutics, Inc. | Combination of Ad-P53 and Chemotherapy for the Treatment of Tumours |
CN100333797C (zh) * | 2005-01-26 | 2007-08-29 | 彭朝晖 | 重组腺病毒p53制品在肿瘤治疗中的新用途 |
EP1679065A1 (en) | 2005-01-07 | 2006-07-12 | OctoPlus Sciences B.V. | Controlled release compositions for interferon based on PEGT/PBT block copolymers |
CN101163984A (zh) * | 2005-05-06 | 2008-04-16 | 奥索瑟夫特公司 | 用于跟踪对象的rf系统 |
US20070231304A1 (en) * | 2006-01-30 | 2007-10-04 | Introgen Therapeutics, Inc. | Prognostic factors for anti-hyperproliferative disease gene therapy |
US20090098529A1 (en) | 2006-10-16 | 2009-04-16 | Nanhai Chen | Methods for attenuating virus strains for diagnostic and therapeutic uses |
US20080299182A1 (en) * | 2007-03-01 | 2008-12-04 | Shuyuan Zhang | Methods and formulations for topical gene therapy |
WO2008150496A2 (en) * | 2007-05-31 | 2008-12-11 | Genelux Corporation | Assay for sensitivity to chemotherapeutic agents |
MX2010008168A (es) | 2008-01-25 | 2011-02-24 | P53 Inc | Biomarcadores p53. |
US8314068B2 (en) * | 2008-04-14 | 2012-11-20 | University Hospitals Of Cleveland | P2X7 inhibition of epithelial cancers and papillomas |
US20120052003A9 (en) * | 2008-05-16 | 2012-03-01 | Szalay Aladar A | Microorganisms for preventing and treating neoplasms accompanying cellular therapy |
EP2370582B1 (en) * | 2008-12-04 | 2017-05-10 | CuRNA, Inc. | Treatment of tumor suppressor gene related diseases by inhibition of natural antisense transcript to the gene |
CA3108979A1 (en) * | 2009-02-02 | 2010-08-05 | Glaxosmithkline Biologicals Sa | Simian adenovirus nucleic acid- and amino acid-sequences, vectors containing same, and uses thereof |
US9050276B2 (en) | 2009-06-16 | 2015-06-09 | The Trustees Of Columbia University In The City Of New York | Autism-associated biomarkers and uses thereof |
BR112013009196A2 (pt) | 2010-10-15 | 2020-08-25 | The Trustees Of Columbia University In The City Of New York | usos de polipeptídeo para redução da aquisição de ácido graxo e da ingestão de alimento, bem como para promoção de saciedade relacionados à obesidade |
PT2635299T (pt) | 2010-11-02 | 2019-10-14 | Univ Columbia | Métodos de tratamento de distúrbios de perda de cabelo |
CN114262690A (zh) | 2011-04-15 | 2022-04-01 | 吉恩勒克斯公司 | 减毒的痘苗病毒的克隆毒株及其使用方法 |
CN102352368B (zh) * | 2011-09-29 | 2013-12-04 | 苏州大学 | Ing4与osm双基因共表达载体及其应用 |
WO2013085624A1 (en) * | 2011-12-08 | 2013-06-13 | Virovek, Inc. | Vectors harboring toxic genes, methods and uses therefor |
KR102134490B1 (ko) | 2012-01-12 | 2020-07-16 | 시냅틱스 인코포레이티드 | 단일층 용량성 이미징 센서들 |
WO2013123266A1 (en) * | 2012-02-15 | 2013-08-22 | Aileron Therapeutics, Inc. | Peptidomimetic macrocycles |
US10039777B2 (en) | 2012-03-20 | 2018-08-07 | Neuro-Lm Sas | Methods and pharmaceutical compositions of the treatment of autistic syndrome disorders |
CN104334191A (zh) | 2012-03-29 | 2015-02-04 | 纽约市哥伦比亚大学托管会 | 治疗毛发脱落疾病的方法 |
AU2014236947A1 (en) | 2013-03-15 | 2015-09-03 | The Trustees Of Columbia University In The City Of New York | Fusion proteins and methods thereof |
MX2015013658A (es) * | 2013-03-27 | 2016-02-18 | Ge Healthcare As | Metodo y reactivo para preparar una composicion diagnostica. |
SG10201710528WA (en) * | 2013-06-18 | 2018-01-30 | Dnatrix Inc | Treatment of brain cancer with oncolytic adenovirus |
US9552089B2 (en) | 2013-08-07 | 2017-01-24 | Synaptics Incorporated | Capacitive sensing using a matrix electrode pattern |
US9298325B2 (en) | 2013-09-30 | 2016-03-29 | Synaptics Incorporated | Processing system for a capacitive sensing device |
US20150091842A1 (en) | 2013-09-30 | 2015-04-02 | Synaptics Incorporated | Matrix sensor for image touch sensing |
US10042489B2 (en) | 2013-09-30 | 2018-08-07 | Synaptics Incorporated | Matrix sensor for image touch sensing |
US9459367B2 (en) | 2013-10-02 | 2016-10-04 | Synaptics Incorporated | Capacitive sensor driving technique that enables hybrid sensing or equalization |
US9274662B2 (en) | 2013-10-18 | 2016-03-01 | Synaptics Incorporated | Sensor matrix pad for performing multiple capacitive sensing techniques |
US9081457B2 (en) | 2013-10-30 | 2015-07-14 | Synaptics Incorporated | Single-layer muti-touch capacitive imaging sensor |
US9682123B2 (en) | 2013-12-20 | 2017-06-20 | The Trustees Of Columbia University In The City Of New York | Methods of treating metabolic disease |
US9798429B2 (en) | 2014-02-28 | 2017-10-24 | Synaptics Incorporated | Guard electrodes in a sensing stack |
CN104357408A (zh) * | 2014-03-13 | 2015-02-18 | 哈尔滨博翱生物医药技术开发有限公司 | 一种重组新城疫病毒及其应用 |
US10133421B2 (en) | 2014-04-02 | 2018-11-20 | Synaptics Incorporated | Display stackups for matrix sensor |
US9927832B2 (en) | 2014-04-25 | 2018-03-27 | Synaptics Incorporated | Input device having a reduced border region |
US9690397B2 (en) | 2014-05-20 | 2017-06-27 | Synaptics Incorporated | System and method for detecting an active pen with a matrix sensor |
WO2016050630A1 (en) | 2014-09-30 | 2016-04-07 | Universita' Degli Studi Di Brescia | Antibody binding a linear epitope of human p53 and diagnostic applications thereof |
EP3237452A4 (en) | 2014-12-23 | 2018-12-05 | The Trustees of Columbia University in the City of New York | Fusion proteins and methods thereof |
US10175827B2 (en) | 2014-12-23 | 2019-01-08 | Synaptics Incorporated | Detecting an active pen using a capacitive sensing device |
US9778713B2 (en) | 2015-01-05 | 2017-10-03 | Synaptics Incorporated | Modulating a reference voltage to preform capacitive sensing |
US9939972B2 (en) | 2015-04-06 | 2018-04-10 | Synaptics Incorporated | Matrix sensor with via routing |
US10095948B2 (en) | 2015-06-30 | 2018-10-09 | Synaptics Incorporated | Modulation scheme for fingerprint sensing |
US9715304B2 (en) | 2015-06-30 | 2017-07-25 | Synaptics Incorporated | Regular via pattern for sensor-based input device |
US9720541B2 (en) | 2015-06-30 | 2017-08-01 | Synaptics Incorporated | Arrangement of sensor pads and display driver pads for input device |
CN205028263U (zh) | 2015-09-07 | 2016-02-10 | 辛纳普蒂克斯公司 | 一种电容传感器 |
US10037112B2 (en) | 2015-09-30 | 2018-07-31 | Synaptics Incorporated | Sensing an active device'S transmission using timing interleaved with display updates |
US10067587B2 (en) | 2015-12-29 | 2018-09-04 | Synaptics Incorporated | Routing conductors in an integrated display device and sensing device |
CN106933400B (zh) | 2015-12-31 | 2021-10-29 | 辛纳普蒂克斯公司 | 单层传感器图案和感测方法 |
WO2018071814A1 (en) | 2016-10-14 | 2018-04-19 | The Trustees Of Columbia University In The City Of New York | Methods of treating alcohol abuse disorder |
RU2760993C1 (ru) * | 2021-02-15 | 2021-12-02 | Сергей Александрович Никитин | Способ рентгеновской терапии рака легких |
Family Cites Families (23)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US4740463A (en) * | 1984-04-13 | 1988-04-26 | Massachusetts Institute Of Technology | Methods and artificial genes for antagonizing the function of an oncogene |
ZA858044B (en) * | 1984-11-01 | 1987-05-27 | American Home Prod | Oral vaccines |
US4748022A (en) * | 1985-03-25 | 1988-05-31 | Busciglio John A | Topical composition |
US4822605A (en) * | 1986-02-18 | 1989-04-18 | Exovir, Inc. | Compositions and methods employing the same for the treatment of viral and cancerous skin lesions and the like |
US5055400A (en) * | 1986-11-26 | 1991-10-08 | University Of Guelph | Leukotoxin gene of pasteurella haemolytica |
US5166320A (en) * | 1987-04-22 | 1992-11-24 | University Of Connecticut | Carrier system and method for the introduction of genes into mammalian cells |
US4980289A (en) * | 1987-04-27 | 1990-12-25 | Wisconsin Alumni Research Foundation | Promoter deficient retroviral vector |
US5532220A (en) * | 1987-08-31 | 1996-07-02 | The Regents Of The University Of California | Genetic mechanisms of tumor suppression |
US5017524A (en) * | 1989-02-13 | 1991-05-21 | Iscar Ltd. | Ceramic cutting tool |
US6800617B1 (en) * | 1989-03-29 | 2004-10-05 | The Johns Hopkins University | Methods for restoring wild-type p53 gene function |
US5362623A (en) * | 1991-06-14 | 1994-11-08 | The John Hopkins University | Sequence specific DNA binding by p53 |
US6677312B1 (en) * | 1989-03-29 | 2004-01-13 | The Johns Hopkins University | Methods for restoring wild-type p53 gene function |
US5527676A (en) * | 1989-03-29 | 1996-06-18 | The Johns Hopkins University | Detection of loss of the wild-type P53 gene and kits therefor |
US5328470A (en) * | 1989-03-31 | 1994-07-12 | The Regents Of The University Of Michigan | Treatment of diseases by site-specific instillation of cells or site-specific transformation of cells and kits therefor |
US5585362A (en) * | 1989-08-22 | 1996-12-17 | The Regents Of The University Of Michigan | Adenovirus vectors for gene therapy |
US6410010B1 (en) * | 1992-10-13 | 2002-06-25 | Board Of Regents, The University Of Texas System | Recombinant P53 adenovirus compositions |
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 |
WO1992015680A1 (en) * | 1991-03-06 | 1992-09-17 | Board Of Regents, The University Of Texas System | Methods and compositions for the selective inhibition of gene expression |
US5252479A (en) * | 1991-11-08 | 1993-10-12 | Research Corporation Technologies, Inc. | Safe vector for gene therapy |
FR2688514A1 (fr) * | 1992-03-16 | 1993-09-17 | Centre Nat Rech Scient | Adenovirus recombinants defectifs exprimant des cytokines et medicaments antitumoraux les contenant. |
US5496731A (en) * | 1993-03-25 | 1996-03-05 | Xu; Hong-Ji | Broad-spectrum tumor suppressor genes, gene products and methods for tumor suppressor gene therapy |
TW442569B (en) * | 1993-10-25 | 2001-06-23 | Canji Inc | Recombinant adenoviral vector |
EP0784690B1 (en) * | 1994-06-10 | 2006-08-16 | Genvec, Inc. | Complementary adenoviral vector systems and cell lines |
-
1996
- 1996-11-27 CA CA002238829A patent/CA2238829A1/en not_active Abandoned
- 1996-11-27 CN CNB961995858A patent/CN1308450C/zh not_active Expired - Lifetime
- 1996-11-27 CN CNA2007100051249A patent/CN101028523A/zh active Pending
- 1996-11-27 AT AT96942100T patent/ATE325872T1/de active
- 1996-11-27 KR KR1019980704074A patent/KR19990071795A/ko active Search and Examination
- 1996-11-27 WO PCT/US1996/019083 patent/WO1997020047A1/en active IP Right Grant
- 1996-11-27 PL PL96327009A patent/PL186018B1/pl unknown
- 1996-11-27 DK DK96942100T patent/DK0863984T3/da active
- 1996-11-27 CZ CZ0165798A patent/CZ296810B6/cs not_active IP Right Cessation
- 1996-11-27 EP EP96942100A patent/EP0863984B1/en not_active Expired - Lifetime
- 1996-11-27 SK SK705-98A patent/SK70598A3/sk unknown
- 1996-11-27 NZ NZ324168A patent/NZ324168A/en not_active IP Right Cessation
- 1996-11-27 DE DE69636120T patent/DE69636120T2/de not_active Expired - Lifetime
- 1996-11-27 HU HU9902068A patent/HUP9902068A3/hu unknown
- 1996-11-27 ES ES96942100T patent/ES2264145T3/es not_active Expired - Lifetime
- 1996-11-27 AU AU11263/97A patent/AU722042B2/en not_active Expired
- 1996-11-27 JP JP9520700A patent/JP2000501394A/ja not_active Ceased
- 1996-11-27 RU RU98111928/14A patent/RU2174409C2/ru active
-
1998
- 1998-05-29 NO NO19982481A patent/NO982481L/no not_active Application Discontinuation
-
2001
- 2001-10-01 US US09/968,958 patent/US20020077313A1/en not_active Abandoned
-
2003
- 2003-03-24 US US10/395,864 patent/US20030166603A1/en not_active Abandoned
-
2005
- 2005-08-09 US US11/200,527 patent/US20060035857A1/en not_active Abandoned
Also Published As
Publication number | Publication date |
---|---|
RU2174409C2 (ru) | 2001-10-10 |
ES2264145T3 (es) | 2006-12-16 |
CA2238829A1 (en) | 1997-06-05 |
PL327009A1 (en) | 1998-11-09 |
US20020077313A1 (en) | 2002-06-20 |
HUP9902068A2 (hu) | 1999-10-28 |
CN1308450C (zh) | 2007-04-04 |
NO982481L (no) | 1998-07-29 |
CZ296810B6 (cs) | 2006-06-14 |
CN101028523A (zh) | 2007-09-05 |
WO1997020047A1 (en) | 1997-06-05 |
US20030166603A1 (en) | 2003-09-04 |
US20060035857A1 (en) | 2006-02-16 |
JP2000501394A (ja) | 2000-02-08 |
CZ165798A3 (cs) | 1998-12-16 |
EP0863984A1 (en) | 1998-09-16 |
CN1207771A (zh) | 1999-02-10 |
PL186018B1 (pl) | 2003-09-30 |
KR19990071795A (ko) | 1999-09-27 |
AU1126397A (en) | 1997-06-19 |
ATE325872T1 (de) | 2006-06-15 |
AU722042B2 (en) | 2000-07-20 |
NZ324168A (en) | 2004-11-26 |
DE69636120D1 (de) | 2006-06-14 |
HUP9902068A3 (en) | 2001-02-28 |
DE69636120T2 (de) | 2006-11-30 |
NO982481D0 (no) | 1998-05-29 |
DK0863984T3 (da) | 2006-08-28 |
EP0863984B1 (en) | 2006-05-10 |
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