NO861553L - Angiogen faktor og fremgangsmaate for frembringelse av angiogenese. - Google Patents
Angiogen faktor og fremgangsmaate for frembringelse av angiogenese.Info
- Publication number
- NO861553L NO861553L NO861553A NO861553A NO861553L NO 861553 L NO861553 L NO 861553L NO 861553 A NO861553 A NO 861553A NO 861553 A NO861553 A NO 861553A NO 861553 L NO861553 L NO 861553L
- Authority
- NO
- Norway
- Prior art keywords
- preparation
- angiogenic
- lipid
- neovascularization
- tissue
- Prior art date
Links
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Classifications
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K38/00—Medicinal preparations containing peptides
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K35/00—Medicinal preparations containing materials or reaction products thereof with undetermined constitution
- A61K35/12—Materials from mammals; Compositions comprising non-specified tissues or cells; Compositions comprising non-embryonic stem cells; Genetically modified cells
- A61K35/37—Digestive system
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K31/00—Medicinal preparations containing organic active ingredients
Landscapes
- Health & Medical Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Public Health (AREA)
- Chemical & Material Sciences (AREA)
- Pharmacology & Pharmacy (AREA)
- Veterinary Medicine (AREA)
- Epidemiology (AREA)
- General Health & Medical Sciences (AREA)
- Animal Behavior & Ethology (AREA)
- Medicinal Chemistry (AREA)
- Immunology (AREA)
- Engineering & Computer Science (AREA)
- Biotechnology (AREA)
- Biomedical Technology (AREA)
- Virology (AREA)
- Physiology (AREA)
- Developmental Biology & Embryology (AREA)
- Cell Biology (AREA)
- Nutrition Science (AREA)
- Zoology (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Proteomics, Peptides & Aminoacids (AREA)
- Medicines Containing Material From Animals Or Micro-Organisms (AREA)
- Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)
- Compositions Of Oxide Ceramics (AREA)
- Inorganic Insulating Materials (AREA)
- Peptides Or Proteins (AREA)
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US06/642,624 US4699788A (en) | 1984-08-20 | 1984-08-20 | Angiogenic factor methods of extraction and method for producing angiogenesis |
Publications (1)
Publication Number | Publication Date |
---|---|
NO861553L true NO861553L (no) | 1986-04-18 |
Family
ID=24577348
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
NO861553A NO861553L (no) | 1984-08-20 | 1986-04-18 | Angiogen faktor og fremgangsmaate for frembringelse av angiogenese. |
Country Status (12)
Country | Link |
---|---|
US (1) | US4699788A (fr) |
EP (1) | EP0191804A1 (fr) |
JP (1) | JPS62500026A (fr) |
KR (1) | KR870700359A (fr) |
AU (1) | AU584914B2 (fr) |
BR (1) | BR8506887A (fr) |
CA (1) | CA1261258A (fr) |
DK (1) | DK179086A (fr) |
FI (1) | FI861654A (fr) |
NO (1) | NO861553L (fr) |
RO (1) | RO94021B (fr) |
WO (1) | WO1986001111A1 (fr) |
Families Citing this family (46)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US4897464A (en) * | 1985-04-17 | 1990-01-30 | President And Fellows Of Harvard College | Purified protein having angiogenic activity and methods of preparation |
US4710490A (en) * | 1985-10-01 | 1987-12-01 | Angio Medical Corporation | Compositions containing ganglioside molecules with enhanced angiogenic activity |
US4767746A (en) * | 1985-12-04 | 1988-08-30 | Trustees Of Boston University | Method for enhancement of healing of epithelial wounds in mammals |
US4879114A (en) * | 1985-12-20 | 1989-11-07 | Angio-Medical Corporation | Lipids from omentum and methods for cosmetic use |
US4990333A (en) * | 1985-12-20 | 1991-02-05 | Angio Medical Corporation | Method for healing bone damage |
US4778787A (en) * | 1985-12-20 | 1988-10-18 | Trustees Of Boston University | Method for treatment of angina and myocardial infarctions with omental lipids |
EP0274547A1 (fr) * | 1986-12-18 | 1988-07-20 | Trustees Of Boston University | Méthode pour augmenter la guérison de blessures épithéliales chez les mammifères |
IL84864A0 (en) * | 1986-12-31 | 1988-06-30 | Univ Boston | Composition for promoting hair growth containing omental lipids and process for promoting hair growth utilizing the same |
GB8708009D0 (en) * | 1987-04-03 | 1987-05-07 | Clayton Found Res | Injectable soft tissue augmentation materials |
US4952403A (en) * | 1987-06-19 | 1990-08-28 | President And Fellows Of Harvard College | Implants for the promotion of healing of meniscal tissue |
US4952404A (en) * | 1987-06-19 | 1990-08-28 | President And Fellows Of Harvard College | Promotion of healing of meniscal tissue |
US4853219A (en) * | 1987-08-06 | 1989-08-01 | President And Fellows Of Harvard College | Antibodies to angiogenin: immunotherapeutic agents |
US4940730A (en) * | 1987-10-29 | 1990-07-10 | Takeda Chemical Industries, Ltd. | Angiogenesis enhancer |
US4879312A (en) * | 1988-03-07 | 1989-11-07 | Angio Medical Corporation | Method for enhancing or provoking angiogenesis using angiogenically active omega-3 polyunsaturated fatty acids |
IE891173L (en) * | 1988-04-18 | 1989-10-18 | Univ Utrecht | Composition for promoting hair growth in androgenetic¹alopecia and method thereof |
US5837235A (en) * | 1994-07-08 | 1998-11-17 | Sulzer Medizinaltechnik Ag | Process for regenerating bone and cartilage |
US5733884A (en) * | 1995-11-07 | 1998-03-31 | Nestec Ltd. | Enteral formulation designed for optimized wound healing |
AU721034B2 (en) | 1996-02-15 | 2000-06-22 | Biosense, Inc. | Catheter based surgery |
US6443974B1 (en) | 1996-07-28 | 2002-09-03 | Biosense, Inc. | Electromagnetic cardiac biostimulation |
WO1998005307A1 (fr) * | 1996-08-08 | 1998-02-12 | Localmed, Inc. | Procede et appareil d'administration transmurale de medicaments |
AU7000398A (en) * | 1996-11-05 | 1998-05-29 | Localmed, Inc. | Method and device for continuous intralumenal delivery of bioactive substances |
US20030129750A1 (en) * | 1998-02-05 | 2003-07-10 | Yitzhack Schwartz | Homing of donor cells to a target zone in tissue using active therapeutics or substances |
ES2255155T3 (es) | 1998-02-05 | 2006-06-16 | Biosense Webster, Inc. | Dispositivo para la administracion intracardiaca de farmacos. |
US20030113303A1 (en) * | 1998-02-05 | 2003-06-19 | Yitzhack Schwartz | Homing of embryonic stem cells to a target zone in tissue using active therapeutics or substances |
EP1071445A2 (fr) * | 1998-04-17 | 2001-01-31 | Angiogenix, Incorporated | Facteurs angiogeniques therapeutiques et procedes d'utilisation |
US6211157B1 (en) | 1998-05-01 | 2001-04-03 | Sulzer Biologics, Inc. | Protein mixtures to induce therapeutic angiogenesis |
US7087577B2 (en) * | 1998-10-16 | 2006-08-08 | Zimmer Orthobiologies, Inc. | Method of promoting natural bypass |
US6992066B2 (en) * | 1998-10-16 | 2006-01-31 | Zimmer Orthobiologics, Inc. | Povidone-containing carriers for polypeptide growth factors |
US9597395B2 (en) | 2001-12-07 | 2017-03-21 | Cytori Therapeutics, Inc. | Methods of using adipose tissue-derived cells in the treatment of cardiovascular conditions |
US20050095228A1 (en) | 2001-12-07 | 2005-05-05 | Fraser John K. | Methods of using regenerative cells in the treatment of peripheral vascular disease and related disorders |
US20050048035A1 (en) | 2001-12-07 | 2005-03-03 | Fraser John K. | Methods of using regenerative cells in the treatment of stroke and related diseases and disorders |
US7651684B2 (en) | 2001-12-07 | 2010-01-26 | Cytori Therapeutics, Inc. | Methods of using adipose tissue-derived cells in augmenting autologous fat transfer |
US20030161816A1 (en) | 2001-12-07 | 2003-08-28 | Fraser John K. | Systems and methods for treating patients with processed lipoaspirate cells |
US7514075B2 (en) | 2001-12-07 | 2009-04-07 | Cytori Therapeutics, Inc. | Systems and methods for separating and concentrating adipose derived stem cells from tissue |
US7771716B2 (en) | 2001-12-07 | 2010-08-10 | Cytori Therapeutics, Inc. | Methods of using regenerative cells in the treatment of musculoskeletal disorders |
US7585670B2 (en) | 2001-12-07 | 2009-09-08 | Cytori Therapeutics, Inc. | Automated methods for isolating and using clinically safe adipose derived regenerative cells |
US7595043B2 (en) | 2001-12-07 | 2009-09-29 | Cytori Therapeutics, Inc. | Method for processing and using adipose-derived stem cells |
US7232802B2 (en) * | 2001-12-21 | 2007-06-19 | Zimmer Orthobiologics, Inc. | Compositions and methods for promoting myocardial and peripheral angiogenesis |
US7622562B2 (en) | 2002-06-26 | 2009-11-24 | Zimmer Orthobiologics, Inc. | Rapid isolation of osteoinductive protein mixtures from mammalian bone tissue |
US7241874B2 (en) * | 2002-06-26 | 2007-07-10 | Zimmer Ortho Biologics, Inc. | Rapid isolation of osteoinductive protein mixtures from mammalian bone tissue |
JP2011511769A (ja) * | 2008-01-26 | 2011-04-14 | シン サイニ サリンダー | 大網及びその用途 |
WO2010021993A1 (fr) | 2008-08-19 | 2010-02-25 | Cytori Therapeutics, Inc. | Procédés d'utilisation de cellules issues du tissu adipeux dans le traitement du système lymphatique et d'une maladie maligne |
ES2625893T3 (es) | 2009-05-01 | 2017-07-20 | Bimini Technologies Llc | Sistemas, procedimientos y composiciones para optimizar injertos enriquecidos con tejido y células |
EP2688576A4 (fr) * | 2011-03-25 | 2014-12-03 | Cooperlabs Ltd | Extraits d'épiploon extraits à la chaleur, compositions, procédés de préparation et leurs utilisations |
IL250881A0 (en) | 2017-03-01 | 2017-06-29 | Pali Nazir | A process of instant creation of artificial bone tissue |
IL257853A (en) | 2018-03-04 | 2019-03-31 | Pali Nazir | Process for building artificial multifunctional injectable filler |
Family Cites Families (12)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US4229532A (en) * | 1978-12-29 | 1980-10-21 | Monsanto Company | Production of tumor angiogenesis factor by cell culture |
US4229531A (en) * | 1978-12-29 | 1980-10-21 | Monsanto Company | Production of tumor angiogenesis factor by cell culture |
US4209587A (en) * | 1978-12-29 | 1980-06-24 | Monsanto Company | Production of tumor angiogenesis factor by cell culture |
US4210718A (en) * | 1978-12-29 | 1980-07-01 | Monsanto Company | Production of tumor angiogenesis factor by cell culture |
US4210719A (en) * | 1978-12-29 | 1980-07-01 | Monsanto Company | Production of tumor angiogenesis factor by cell culture |
US4225670A (en) * | 1978-12-29 | 1980-09-30 | Monsanto Company | Production of tumor angiogenesis factor by cell culture |
US4217412A (en) * | 1979-04-25 | 1980-08-12 | President And Fellows Of Harvard College | Production of tumor angiogenesis factor by cell culture |
US4268629A (en) * | 1980-03-03 | 1981-05-19 | Monsanto Company | Production of angiogenic factor by cell culture |
US4273871A (en) * | 1980-03-03 | 1981-06-16 | Monsanto Company | Production of angiogenic factor by cell culture |
CA1168980A (fr) * | 1980-04-17 | 1984-06-12 | Rolf Schafer | Compositions cicatrisantes |
ZA833446B (en) * | 1982-05-28 | 1984-02-29 | Solco Basel Ag | Process for the preparation of cell-and tissue-regenerating substances |
US4529590A (en) * | 1982-12-27 | 1985-07-16 | Leveen Robert F | Production of angiogenetic factor |
-
1984
- 1984-08-20 US US06/642,624 patent/US4699788A/en not_active Expired - Fee Related
-
1985
- 1985-08-01 WO PCT/US1985/001445 patent/WO1986001111A1/fr not_active Application Discontinuation
- 1985-08-01 JP JP60503442A patent/JPS62500026A/ja active Pending
- 1985-08-01 AU AU46387/85A patent/AU584914B2/en not_active Ceased
- 1985-08-01 EP EP85903953A patent/EP0191804A1/fr not_active Withdrawn
- 1985-08-01 BR BR8506887A patent/BR8506887A/pt unknown
- 1985-08-19 CA CA000488992A patent/CA1261258A/fr not_active Expired
-
1986
- 1986-04-18 FI FI861654A patent/FI861654A/fi not_active Application Discontinuation
- 1986-04-18 DK DK179086A patent/DK179086A/da not_active Application Discontinuation
- 1986-04-18 NO NO861553A patent/NO861553L/no unknown
- 1986-04-19 KR KR860700224A patent/KR870700359A/ko not_active Application Discontinuation
- 1986-04-21 RO RO123075A patent/RO94021B/ro unknown
Also Published As
Publication number | Publication date |
---|---|
DK179086D0 (da) | 1986-04-18 |
RO94021B (ro) | 1988-03-31 |
AU4638785A (en) | 1986-03-07 |
EP0191804A1 (fr) | 1986-08-27 |
US4699788A (en) | 1987-10-13 |
FI861654A0 (fi) | 1986-04-18 |
JPS62500026A (ja) | 1987-01-08 |
DK179086A (da) | 1986-04-18 |
AU584914B2 (en) | 1989-06-08 |
RO94021A (fr) | 1988-03-30 |
CA1261258A (fr) | 1989-09-26 |
FI861654A (fi) | 1986-04-18 |
BR8506887A (pt) | 1986-12-09 |
WO1986001111A1 (fr) | 1986-02-27 |
KR870700359A (ko) | 1987-12-28 |
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