Patents for A61K 48 - Medicinal preparations containing genetic material which is inserted into cells of the living body to treat genetic diseases; Gene therapy (86,964) |
---|
12/22/1994 | WO1994029440A1 Generation, concentration and efficient transfer of vsv-g pseudotyped retroviral vectors |
12/22/1994 | WO1994029438A1 Method for production of high titer virus and high efficiency retroviral mediated transduction of mammalian cells |
12/22/1994 | WO1994029436A1 Methods for selectively stimulating proliferation of t cells |
12/22/1994 | WO1994029330A1 Myeloid cell leukemia associated gene mcl-1 |
12/22/1994 | WO1994028938A1 Adenovirus vectors for gene therapy sponsorship |
12/22/1994 | WO1994028797A1 Methods of preparing gas-filled liposomes |
12/22/1994 | WO1994028721A1 Treatment of vascular degenerative diseases by modulation of endogenous nitric oxide production or activity |
12/22/1994 | WO1994025588A3 ANTISENSE-OLIGONUCLEOTIDES FOR THE TREATMENT OF IMMUNOSUPPRESSIVE EFFECTS OF TRANSFORMING GROWTH FACTOR-β (TGF-β) |
12/22/1994 | WO1994025477A3 Novel peptide nucleic acids |
12/22/1994 | CA2164953A1 Retroviral vectors for transducing beta-globin gene and beta-locus control region derivatives |
12/22/1994 | CA2164632A1 Treatment of vascular degenerative diseases by modulation of endogenous nitric oxide production or activity |
12/22/1994 | CA2164288A1 Method for treating kaposi's sarcoma with antisense oligonucleotides |
12/22/1994 | CA2163905A1 Inhibiting protein interactions |
12/22/1994 | CA2162497A1 Adenoviral vectors for treatment of hemophilia |
12/21/1994 | EP0629129A1 Method for kidney tubulogenesis |
12/21/1994 | CN1096584A Method for identifying individuals suffering from a cellular abnormality some of whose abnormal cells present complexes of hla-c-clone 10/mage-1 derived peptides, and method for treating said......... |
12/08/1994 | WO1994028391A1 Ligands for flt3 receptors |
12/08/1994 | WO1994028152A1 Defective adenoviruses and corresponding complementation lines |
12/08/1994 | WO1994028151A1 Gene therapy for haemophilia |
12/08/1994 | WO1994028128A1 Test and model for polycystic ovary syndrome and male pattern baldness |
12/08/1994 | WO1994027612A1 Genetic therapy for cardiovascular disease |
12/08/1994 | WO1994027435A1 Genetic immunization with cationic lipids |
12/08/1994 | WO1994027426A1 Methods of using bcl-2 for the therapeutic treatment and prevention of diseases |
12/07/1994 | EP0627489A1 Methods and compositions for the treatment of malignancies in which a protein kinase is associated |
12/07/1994 | EP0627487A2 Ligands for FLT3 receptors |
12/07/1994 | EP0627001A1 MAMMALIAN Sos - A REGULATOR/EFFECTOR OF TYROSINE KINASE SIGNALLING |
12/07/1994 | EP0626852A1 Method for making universal donor cells |
12/06/1994 | US5371009 Enhancers |
11/30/1994 | EP0626012A1 Homogenotization of gene-targeting events |
11/28/1994 | EP0663013A4 Method for delivering nucleic acids into cells. |
11/24/1994 | WO1994026915A1 Gene transfer into pancreatic and biliary epithelial cells |
11/24/1994 | WO1994026914A1 Adenoviral vectors of animal origin and use thereof in gene therapy |
11/24/1994 | WO1994026888A1 Inhibition of proliferation of vascular smooth muscle cell |
11/24/1994 | WO1994026887A1 Antisense oligonucleotides which combat aberrant splicing and methods of using the same |
11/24/1994 | WO1994026877A1 Ribozyme gene therapy for hiv infection and aids |
11/24/1994 | WO1994026307A1 Inhibition of migration inhibitory factor in the treatment of diseases involving cytokine-mediated toxicity |
11/24/1994 | WO1994026289A1 Allogeneic and xenogeneic transplantation |
11/24/1994 | WO1994026285A1 Xenograft thymus |
11/24/1994 | WO1994016073A3 Methods and reagents for inhibiting furin endoprotease |
11/24/1994 | CA2500213A1 Gene transfer into pancreatic and biliary epithelial cells |
11/24/1994 | CA2163234A1 Inhibition of proliferation of vascular smooth muscle cell |
11/24/1994 | CA2163129A1 Ribozyme gene therapy for hiv infection and aids |
11/24/1994 | CA2162602A1 Gene transfer into pancreatic and biliary epithelial cells |
11/24/1994 | CA2162496A1 Allogeneic and xenogeneic transplatation |
11/24/1994 | CA2161797A1 Xenograft thymus |
11/23/1994 | EP0625207A1 Gene therapy for cystic fibrosis transmembrane conductance regulator activity (cftr) |
11/23/1994 | EP0625206A1 Human epidermal gene promoter |
11/23/1994 | EP0625204A1 Hepatitis therapeutics |
11/23/1994 | EP0625195A1 Therapy of central nervous system by genetically modified cells |
11/23/1994 | EP0625192A1 Nucleozymes |
11/23/1994 | EP0625049A1 Ex vivo gene transfer |
11/23/1994 | EP0625007A1 Gene transfer in birds by introduction of dna into muscle in ovo |
11/22/1994 | US5367056 Endothelial cell-leukocyte adhesion molecules (ELAMs) and molecules involved in leukocyte adhesion (MILAs) |
11/17/1994 | EP0624195A1 Novel biologically active polypeptides, preparation thereof and pharmaceutical composition containing said polypeptides |
11/17/1994 | EP0624100A1 Dna encoding a human serotonin receptor (5-ht 4b?) and uses thereof |
11/10/1994 | WO1994025608A1 Natural or recombinant dna binding proteins as carriers for gene transfer or gene therapy |
11/10/1994 | WO1994025601A2 New sequences of hepatitis c virus genotypes and their use as therapeutic and diagnostic agents |
11/10/1994 | WO1994025588A2 ANTISENSE-OLIGONUCLEOTIDES FOR THE TREATMENT OF IMMUNOSUPPRESSIVE EFFECTS OF TRANSFORMING GROWTH FACTOR-β (TGF-β) |
11/10/1994 | WO1994025477A2 Novel peptide nucleic acids |
11/10/1994 | WO1994025073A1 Recombinant viruses and their use in gene therapy |
11/10/1994 | WO1994024870A1 Retroviral vectors capable of expressing multimeric proteins from multiple translational initiation sites |
11/10/1994 | WO1994024864A1 Methods of preventing viral replication |
11/10/1994 | WO1994023048A3 Gibbon ape leukemia virus-based retroviral vectors |
11/10/1994 | WO1994021781A3 Extracellular signal-regulated kinase, sequences, and methods of production and use |
11/10/1994 | WO1994012649A3 Gene therapy for cystic fibrosis |
11/10/1994 | WO1994003075A3 Morphogen-enriched dietary composition |
11/10/1994 | CA2662090A1 New sequences of hepatitis c virus genotypes and their use as therapeutic and diagnostic agents |
11/10/1994 | CA2162056A1 Retroviral vectors capable of expressing multimeric proteins from multiple translational initiation sites |
11/10/1994 | CA2161679A1 Recombinant virus and their use in genic therapy |
11/10/1994 | CA2161230A1 Novel peptide nucleic acids |
11/09/1994 | EP0623628A1 Muscular dystrophy gene products, antibodies thereto and methods for immunodiagnosis of muscular dystrophy |
11/09/1994 | EP0623171A1 Enzymatic rna molecules |
11/09/1994 | EP0623025A1 Vaccination and methods against diseases resulting from pathogenic responses by specific t cell populations |
11/02/1994 | EP0621786A1 Induced tolerance to xenografts |
11/01/1994 | US5360735 DNA encoding a human 5-HT1F receptor, vectors, and host cells |
10/27/1994 | WO1994024300A1 Transposition assembly for gene transfer in eukaryotes |
10/27/1994 | WO1994024299A1 Adenovirus for the transfer of foreign dna into higher eucaryotic cells |
10/27/1994 | WO1994024298A1 Biocompatible implant for the expression and secretion in vivo of a therapeutical compound |
10/27/1994 | WO1994024297A1 Defective recombinant adenoviruses for gene therapy of tumours |
10/27/1994 | WO1994024277A1 Protection of human bone marrow from high dose antifolate therapy using mutated human dihydrofolate reductase dna |
10/27/1994 | WO1994024143A1 Method of forming oligonucleotides |
10/27/1994 | WO1994023756A1 Neural thread protein gene expression and detection of alzheimer's disease |
10/27/1994 | WO1994023754A1 Use of neuro-derived fetal cell lines for transplantation therapy |
10/27/1994 | WO1994023738A1 Encapsulation of nucleic acids with conjugates that facilitate and target cellular uptake and gene expression |
10/27/1994 | WO1994023701A1 Particulate vector and pharmaceutical composition containing such vector |
10/27/1994 | WO1994023699A1 Long-acting treatment by slow-release delivery of antisense oligodeoxyribonucleotides from biodegradable microparticles |
10/27/1994 | WO1994023582A1 Adenoviral vectors including dna encoding lung surfactant protein |
10/27/1994 | CA2161122A1 Biocompatible implant for expression and secretion of a therapeutic compound in vivo |
10/27/1994 | CA2161121A1 Particulate vector and pharmaceutical composition containing the same |
10/27/1994 | CA2161097A1 Neural thread protein gene expression and detection of alzheimer's disease |
10/27/1994 | CA2160878A1 Encapsulation of nucleic acids with conjugates that facilitate and target cellular uptake and gene expression |
10/27/1994 | CA2160877A1 Long-acting treatment by slow-release delivery of antisense oligodeoxyribonucleotides from biodegradable microparticles |
10/27/1994 | CA2160697A1 Transposition kit for gene transfer in eukaryotes |
10/27/1994 | CA2160136A1 Adenoviral vectors including dna encoding lung surfactant protein |
10/27/1994 | CA2159738A1 Use of neuro-derived fetal cell lines for transplantation therapy |
10/26/1994 | EP0620741A1 Cytotoxic drug therapy |
10/25/1994 | US5359051 Compounds useful in the synthesis of nucleic acids capable of cleaning RNA |
10/25/1994 | US5358866 Using cytosine deaminase as marker |
10/19/1994 | EP0620277A1 Nucleic acid pharmaceuticals |
10/19/1994 | EP0619838A1 Repopulation of testicular seminiferous tubules with foreign cells |