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7344872 Method for rapid screening of bacterial transformants and novel simian adenovirus proteins  
Chimpanzee serotype C68 proteins, peptides, and polypeptide are provided. Also provided are novel adenoviruses derived from these proteins, as well as compositions containing these proteins and...
7344711 Use of adenoviruses mutated in the VA genes for cancer treatment  
This invention refers to the use of an adenovirus for cancer treatment, being this adenovirus defective in its virus-associated (VA) RNAs. Said adenovirus has a mutation in the VAI or VAII gene...
7344710 Combination bacteriolytic therapy for the treatment of tumors  
Current chemotherapeutic approaches for cancer are in part limited by the inability of drugs to destroy neoplastic cells within poorly vascularized compartments of tumors. We have here...
7342002 Molecular vaccine linking an endoplasmic chaperone polypeptide to an antigen  
This invention provides compositions and methods for inducing and enhancing immune responses, such as antigen-specific cytotoxic T lymphocyte (CTL) responses, using chimeric molecules comprising...
7341718 Neuronal gene transfer of adenovirus and herpes virus vectors  
The present invention is related to compositions and methods for the delivery of nucleic acids to neurons in a mammal, and uses thereof. The present invention specifically discloses the use of...
7338655 Gene therapy using TGF-β  
The subject invention is related to a cell-mediated gene therapy treatment for orthopedic disease using a member belonging to the transforming growth factor-β (TGF-β) superfamily. TGF-β gene th...
7338656 Composition and method to alter lean body mass and bone properties in a subject  
A method for decreasing the body fat proportion, increasing lean body mass, increasing bone density, or improving the rate of bone healing, or all, of a subject. Embodiments of the invention...
7335505 Materials and methods relating to protein aggregation in neurodegenerative disease  
The present invention provides methods of proteolytically converting a precursor protein (e.g. tau) to a product fragment (e.g., a 12 kd fragment) in a stable cell line, wherein the precursor...
7332324 Attenuated vaccine useful for immunizations against Coccidioides spp. infections  
A Coccidioides spp. fungus that is attenuated by the loss of endosporulation potential of the fungus wherein said fungus does not replicate when transformed into the parasitic phase.
7332337 Viral vectors having tissue tropism for T-lymphocytes, B- and mast cells  
The present invention relates to methods of introducing an expressible non-viral nucleic acid sequence into a T lymphocyte cell, a B-cell, or a mast cell, comprising contacting the cell with a...
7329807 High-efficiency fusogenic vesicles, methods of producing them, and pharmaceutical compositions containing them  
The present invention relates to novel fusogenic vesicles as highly efficient and versatile encapsulation systems for delivering a substance of choice, such as nucleic acids, proteins, peptides,...
7326692 Induction of immunity using inhibitors of granzymes  
The present invention provides methods for enhancing host immunity to a virus and/or a cancer and methods for enhancing the cytotoxic T-cell (CTL) mediated immune responses by providing granzyme B...
7323165 Production of pancreatic islet cells and delivery of insulin  
The present invention relates to the production of islet cells and insulin in a subject by providing for expression of an islet transcription factors in the pancreas of the subject, by for example,...
7323623 RHIZOC3 nucleic acid molecules  
The present invention is directed to nucleic acid molecules tat encode defensive polypeptides and methods of their use in enhancing disease resistance of a plant to a fungal pathogen. Vectors,...
7320787 Redirection of cellular immunity by protein tyrosine kinase chimeras  
Disclosed is a method of directing a cellular response in a mammal by expressing in a cell of the mammal a chimeric receptor which causes the cells to specifically recognize and destroy an...
7318919 Adenovirus vectors for gene therapy  
Gene Therapy vectors, which are especially useful for cystic fibrosis, and methods for using the vectors are disclosed.
7316812 Cells expressing anti-Fc receptor binding components  
Cells transformed to express on their surface a component which binds to an Fc receptor of an effector cell are disclosed. Also disclosed are expression vectors used to transform the cells. Once...
7314912 AAv scleroprotein, production and use thereof  
The invention relates to a structural protein of adeno-associated virus (AAV) which comprises at least one mutation which brings about an increase in the infectivity of the virus.
7311907 Lentiviral packaging cells  
Novel packaging cell lines which produce recombinant retrovirus, free of detectable helper-virus are disclosed. Also disclosed are methods of making the cell lines and methods of producing...
7309814 Nucleic acid molecules encoding bacterial autoinducer inactivation protein as targets for engineering disease resistance  
The present invention relates to isolated nucleic acid molecules encoding a bacterial autoinactivation protein and methods for increasing disease resistance and preventing or reducing bacterial...
7306792 Tumor therapy with alphavirus-based and high affinity laminin receptor-targeted vectors  
The present invention relates to methods and compositions for treating tumors using vectors that preferentially target tumor cells. In particular, the invention relates to Sindbis virus vectors...
7306794 Methods and compositions for the treatment of defects in lipoprotein metabolism  
The invention provides a recombinant viral vector comprising the DNA of, or corresponding to, at least a portion of the genome of an adenovirus, which portion is capable of infecting a hepatic...
7306793 Defective recombinant adenoviruses expressing cytokines for antitumor treatment  
A recombinant nucleic acid used for the production of a defective adenovirus containing an inserted sequence coding for a cytokine under the control of a promoter in the genomic sequence of the...
7297685 Use of pro-apoptotic factors in treatment of atherosclerosis  
The present invention features a novel method of treating vascular disease that involves modifying smooth muscle cells to express a gene encoding a protein having both anti-inflammatory and...
7297540 Methods of generating tissue using devitalized, acellular scaffold matrices derived from micro-organs  
Methods of generating, and isolating adult stem cells and utilizing such cells and/or embryonic stem cells in generating tissue of a specific function and micro-architecture are provided.
7294334 Methods and compositions to treat myocardial conditions  
Methods, devices, kits and compositions to treat a myocardial infarction. In one embodiment, the method includes the prevention of remodeling of the infarct zone of the ventricle using a...
7291325 Method for producing target proteins by deleting or amplifying ibpA and/or ibpB gene coding for inclusion body-associated proteins  
A method for producing target proteins by deleting or amplifying ibpA and/or ibpB genes coding for inclusion body-associated proteins. Two methods for producing target proteins using ibpA and/or...
7291454 Transgenic animals and cell lines for screening drugs effective for the treatment or prevention of Alzheimer's disease  
Disclosed are transgenic animals and transfected cell lines expressing a protein associated with Alzheimer's Disease, neuroectodermal tumors, malignant astrocytomas, and glioblastomas. Also...
7285265 Stable adenoviral vectors and methods for propagation thereof  
The present invention provides methods and means to increase the stability and/or the packaging capacity of recombinant adenoviruses, by overexpression of pIX in an adenoviral packaging cell, by...
7282199 Adeno-associated virus (AAV) serotype 8 sequences, vectors containing same, and uses therefor  
Sequences of a serotype 8 adeno-associated virus and vectors and host cells containing these sequences are provided. Also described are methods of using such host cells and vectors in production of...
7276333 Viral infection inhibitor targeting integrase N-terminal domain  
The object of the present invention is to provide a screening method of a new integrase inhibitor being able to inhibit an HIV infection before the reverse transcription step and having a...
7276233 Methods of treating neoplasia with combinations of target cell-specific adenovirus and chemotherapy  
The invention provides methods of treating neoplasia using combinations of target cell-specific replication competent adenoviral vectors and chemotherapy, radiation therapy or combinations thereof....
7276234 Method of acquiring immunological tolerance  
The aim of the present invention is to provide a method of acquiring immunological tolerance to a foreign DNA or its expression product whereby the foreign DNA such as a vector carrying a foreign...
7273605 Vaccine  
The present invention relates to a fowlpox virus genome which has modifications in one or more wild-type FPV genes. The present invention also relates to a viral particle comprising such a genome...
7273855 Use of prohibitin RNA in treatment of cancer  
It has now been found that the introduction of single stranded oligonucleotides of DNA or RNA, particularly RNA transcribed from portions of wild type prohibitin 3′UTR, into tumors leads to a...
7270811 Serotype of adenovirus and uses thereof  
The invention provides a gene delivery vehicle and a gene of interest comprising at least one Ad35 element or a functional equivalent thereof, responsible for avoiding or diminishing neutralizing...
7270812 Pharmaceutical composition for treatment of cancers  
The present invention relates to a pharmaceutical composition for treatment of cancers containing Sindbis virus as an active ingredient, a method for treatment of cancers, which comprises...
7268120 Methods for treating cancer using cytokine-expressing polynucleotides  
The present invention provides a pharmaceutical composition, comprising a non-infectious, non-integrating polynucleotide construct comprising a polynucleotide encoding an interferon ω and one or ...
7265268 Insecticidal proteins derived from Bacillus thuringiensis  
The present invention relates to the field of plant pest control, particularly insect control. Provided are nucleotide sequences from Bacillus thuringiensis encoding insecticidal proteins. Further...
7262342 FUS6 nucleic acid molecules and methods of their use in enhancing disease resistance in plants  
The present invention is directed to nucleic acid molecules that encode Fus6 defensive polypeptides and methods of their use in enhancing disease resistance of a plant to a fungal pathogen....
7261887 Leishmania as carriers for the delivery of proteins and peptides  
Methods for delivering potentially therapeutic or prophylactic protein and peptide agents to mammalian cells are provided. The agents are delivered by mutant trypanosomatid protozoa that have been...
7261885 Adenoviral vector with replication-dependent transgene expression  
The invention provides an adenoviral vector comprising (a) at least a portion of an adenoviral genome comprising a major late transcription unit containing a terminal exon, wherein the terminal...
7261884 Live genetically attenuated malaria vaccine  
Method for inoculating a vertebrate host against malaria, by administering to the host a live Plasmodium organism that is genetically engineered to disrupt a liver-stage-specific gene function.
7261886 Insect larva aerosol infection method for producing recombinant proteins and baculovirus bio-insecticides  
An insect larva aerosol infection method for producing recombinant proteins and baculovirus bio-insecticides is disclosed. A liquid spray of budded form baculoviruses are employed to infect insect...
7261899 Method of producing thy A-strains of Vibrio cholerae, such strains and their use  
A method of producing a thy A−strain of vibrio cholerae comprising the step of site-directed mutagenesis in the V. cholerae chromosome at the locus of the thy A gene SEQ ID NO: 1 of FIG. 1, is d...
RE39788 Gene therapy  
Primary human cells which are genetically engineered with DNA (RNA) encoding a marker or therapeutic which is expressed to be expressed in vivo. Such engineered cells may be used in gene therapy.
RE39789 Tumor therapy  
Neoplasia is treated by administering to a mammalian host a composition comprising ligands for the NKG2D receptor. In addition, other NKG2D ligands, proteins specific for the neoplastic cells and...
7258854 Targeted chromosomal genomic alterations with modified single stranded oligonucleotides  
Presented are methods and compositions for targeted chromosomal genomic alterations using modified single-stranded oligonucleotides. The oligonucleotides of the invention have at least one modified...
7259151 AAV virions with decreased immunoreactivity and uses therefor  
Methods of making and using recombinant AAV virions with decreased immunoreactivity are described. The recombinant AAV virions include mutated capsid proteins or are derived from non-primate...
7255855 Surface expression method of peptides P5 and Anal3 using the gene encoding poly-gamma-glutamate synthetase  
The present invention relates to a method for expressing each of peptide antibiotics P5 3 and Ana13 35 having amphiphilicity and showing antibacterial, antifungal and anticancer activities 61, 63,...