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7105494 Viral and non-viral vectors as vehicles for delivering transgenes for treating bone pathologies  
The present invention relates to a method for treating bone pathologies comprising delivering a viral or non-viral delivery vehicle comprising genetic information (e.g. a transgene) encoding a...
7105493 Methods and compositions for treating flaviviruses and pestiviruses  
A method and composition for treating a host infected with flavivirus or pestivirus comprising administering an effective flavivirus or pestivirus treatment amount of a described 1′, 2′ or...
7105162 Pharmaceutical composition for immunomodulation based on peptides and adjuvants  
Pharmaceutical composition containing at least one peptide or protein (fragment) with an immunomodulatory activity together with an adjuvant. The peptide is derived from a pathogenic agent or a...
7105156 Method of using an adenoviral vector encoding a retinoblastoma protein to treat hyperproliferating cells  
Disclosed are methods of controlling cell cycle progression by introducing into a cell to be controlled a composition selected from the group consisting of p56 RB protein, a fragment of the p56 RB...
7101861 Methods and compositions for treating flaviviruses and pestiviruses  
A method and composition for treating a host infected with flavivirus or pestivirus comprising administering an effective flavivirus or pestivirus treatment amount of a described 1′, 2′ or...
7101542 Cell-mediated targeting of toxins to pathogenic cells  
The invention features vectors encoding immunotoxic fusion proteins containing targeting domains and toxic domains, targeting cells transduced with the vectors, methods of making the targeting...
7101540 Targeted retrograde gene delivery to motor neurons  
Methods are disclosed for delivering a heterologous gene to a cell body of a neuron by contacting a muscle tissue innervated by the neuron with a viral vector comprising a heterologous gene,...
7098192 Antisense oligonucleotide modulation of STAT3 expression  
Compounds, compositions and methods are provided for inhibiting the expression of human STAT3. The compositions comprise antisense oligonucleotides targeted to nucleic acids encoding STAT3. Methods...
7098191 Hyperthermic inducible expression vectors for gene therapy and methods of use thereof  
Expression constructs using an inducible amplification system to drive expression of a therapeutic gene or other genes of interest in mammalian cells are provided, as well as methods of using the...
7098190 Formulations comprising antisense nucleotides to connexins  
A therapeutic and/or cosmetic formulation comprising at least one anti-sense polynucleotide to a connexin protein together with a pharmaceutically acceptable carrier or vehicle is useful in site...
7098030 Polyampholytes for delivering polyions to a cell  
An polyampholyte is utilized in a condensed polynucleotide complex for purposes of nucleic acid delivery to a cell. The complex can be formed with an appropriate amount of positive and/or negative...
7098004 Isolated polypeptide of the stratum corneum and its use  
The invention concerns an isolated polypeptide, of the family of calcium-fixing proteins, a mixture of polypeptides derived from proteolysis of the isolated polypeptide, compositions containing...
7097970 Methods of evaluating viral entry inhibitors using patient derived envelope protein constructs  
The invention provides a method for identifying whether a compound inhibits entry of a virus into a cell which comprises: (a) obtaining nucleic acid encoding a viral envelope protein from a patient...
7097854 Amino alcohol derivatives, process for their production and pharmaceutical preparations and reagents containing these compounds  
The present invention relates to new amino alcohol derivatives, process for the production thereof and medicaments and reagents containing these compounds.
7094767 Polynucleotide herpes virus vaccine  
Genes encoding herpes simplex virus type 2 (HSV-2) proteins were cloned into eukaryotic expression vectors to express the encoded proteins in mammalian muscle cells in vivo. Animals were immunized...
7094766 Use of locally applied DNA fragments  
Methods of treatment or prevention of hyperproliferative diseases or pre-cancerous conditions affecting epithelial cells, such as psoriasis, vitiligo, atopic dermatitis, or hyperproliferative or...
7094765 Antisense restenosis composition and method  
The present invention provides an improved method for reducing the risk or severity of restenosis following cardiac angioplasty. The method includes administering to a target vessel region, a...
7094408 Immunogenicity using a combination of DNA and vaccinia virus vector vaccines  
This invention relates to improved methods of inducing an immune response for the prevention or treatment of HIV-1 infection by using a nucleic acid vaccine in conjunction with a recombinant viral...
7094201 System and method for genetically treating cardiac conduction disturbances  
The present invention provides delivery systems for and methods of delivering conduction protein genetic material to cardiac cells in localized areas of the heart to improve the conductance...
7091040 P450/acetaminophen genetically directed enzyme prodrug therapy (GDEPT)  
The invention hereindescribed relates to a form of cancer therapy which exploits the cytotoxic properties of acetaminophen when converted to NABQI by the metabolic activity of tumour cell specific...
7090846 Method for preparing polycation based bioconjugates suitable for transporting different kinds of active substances within the body  
Polycation bioconjugates and a method for producing them. The polycations are capable of transporting active substances of different types. The polycations function as carrier molecules that...
7090836 Vector for expressing α-L-iduronidase and method of treating MPS I by stereotactic injection into the brain of a mammal  
A purified nucleic acid molecule capable of expressing a lysosomal enzyme, e.g., iduronidase or arylsulphatase, is provided. The molecule includes a promoter of the phosphoglycerate kinase gene to...
7087586 Oligonucleotide compositions and their use to induce differentiation of cells  
The present invention provides compositions comprising a 3′-OH, 5′-OH, chemically unmodified, synthetic phosphodiester nucleotide sequence selected from the group consisting of SEQ ID NO: 1,...
7087585 Tripeptide of FcγRIIA  
The present invention relates, in general, to phagocytosis and phagolysosomal fusion and, in particular, to a tripeptide of FcγRIIA that mediates trafficking of targets phagocytosed via FcγRIIA...
7087584 Detection and modulation of IAPs and NAIP for the diagnosis and treatment of proliferative disease  
Disclosed are diagnostic and prognostic kits for the detection and treatment of proliferative diseases such as ovarian cancer, breast cancer, and lymphoma. Also disclosed are cancer therapeutics...
7087583 Sequence specific DNA binding by p53  
Specific sequences in the human genome are the sites of strong binding of wild-type p53 protein, but not mutant forms of the protein. These sequences are used diagnostically to detect cells in...
7087582 Combination for site-specifically transforming cells in vivo comprising a double-balloon catheter and nucleic acid comprising a gene encoding P21  
The present invention provides a combination including a double-balloon catheter and a nucleic acid encoding the cyclin dependent kinase inhibitor p21. The nucleic acid may also encode HLA-B7, an...
7087581 Method for the treatment of diseases or disorders of the inner ear  
In a process for the treatment of diseases or disorders of the inner ear linked with damage or destruction of sensory cells of the inner ear, for regenerating the sensory cells use is made of at...
7087580 Neuropilin antisense oligonucleotide sequences and methods of using same to modulate cell growth  
This invention relates to oligonucleotides complementary to the neuropilin genes which modulate tumor cell growth and angiogenesis in mammals. This invention is also related to methods of using...
7087433 7SK RNA regulated transcription  
A method for altering transcription in a cell comprising an amount of active CDK9/cyclin, comprises the steps of: (a) introducing in the cell an agent which modulates the amount of active...
7084126 Methods and compositions for enhancing cellular function through protection of tissue components  
Methods and composisions for enhancing cellular function through protection of a tissue components such receptors, proteins, lipids, nucleic acids, carbohydrates, hormones, vitamins, and cofactors,...
7084125 Xylo-LNA analogues  
Based on the above and on the remarkable properties of the 2′-O,4′-C-methylene bridged LNA monomers it was decided to synthesise oligonucleotides comprising one or more...
7081509 Method for producing highly functional, hyper branched polyester by means of enzymatic esterification  
The present invention relates to a process for preparing highly functional hyperbranched polyesters which comprises reacting a reaction solution comprising solvent and (a) one or more dicarboxylic...
7078416 Polypeptides  
The present invention relates to polypeptides, and nucleic acids DNA encoding these polypeptides, capable of eliciting an immune reaction against cancer, methods for generating T lymphocytes...
7078390 Ribozymes to growth factor originating in human platelet  
A ribozyme comprising the following nucleotide sequence (SEQ ID NO:14) (I): 3′-GUGCCCCA GUACGGUG-5′ A C A UGA G AGU N 3 N 1 N 2 ...
7078389 Chemically modified oligonucleotide for site-directed mutagenesis  
A mutagenic, triplex-forming oligonucleotide and methods for use thereof wherein the oligonucleotide is chemically modified to incorporate a mutagen and forms a triple-stranded nucleic acid...
7078388 DNA vaccines for farm animals, in particular bovines and porcines  
DNA vaccine against a pathogen affecting farm animals, in particular bovines or porcines, comprising a plasmid containing a nucleotide sequence encoding an immunogen of a pathogen of the animal...
7078387 Efficient and stable in vivo gene transfer to cardiomyocytes using recombinant adeno-associated virus vectors  
This invention relates to the use of recombinant adeno-associated virus (rAAV) vectors to transduce cardiomyocytes in vivo by infusing the rAAV into a coronary artery or coronary sinus. rAAV...
7078379 Treatment of congenital muscular dystrophies  
The invention provides a method of treating congenital muscular dystrophy due to a mutation in the LAMA2 gene in a mammal. The method comprises administering to the mammal a therapeutically...
7078196 RNA interference mediating small RNA molecules  
Double-stranded RNA (dsRNA) induces sequence-specific post-transcriptional gene silencing in many organisms by a process known as RNA interference (RNAi). Using a Drosophila in vitro system, we...
7078028 Anti-neoplastic viral agents  
A viral DNA construct, and virus encoded thereby, is provided having one or more tumour specific transcription factor binding sites in place of one or more wild type transcription factor binding...
7074772 Design principle for the construction of expression constructs for gene therapy  
The invention concerns an expressible nucleic acid construct, which contains only the sequence information necessary for expressing a gene for RNA or protein synthesis. Expression constructs of...
7074771 Gene encoding MNR2 and uses thereof  
This invention provides an isolated nucleic acid molecule encoding a motor neuron restricted pattern, MNR2, protein. This invention provides an isolated nucleic acid molecule of at least 15...
7074770 Method of DNA vaccination  
A method of vaccinating a mammal against a disease state, comprising administrating to said mammal, within an appropriate vector, a nucleotide sequence encoding an antigenic peptide associated with...
7074769 Oligonucleotide inhibitors of bcl-xL  
This invention provides an antisense oligonucleotide or analog thereof comprising 10 or more contiguous bases or base analogs from the sequence of bases of sequence A, B, C, D, E, F, G, H, I, J, K,...
7074768 Modified protein kinase A-specific oligonucleotides and methods of their use  
Disclosed are synthetic, modified oligonucleotides complementary to, and capable of down-regulating the expression of, nucleic acid encoding protein kinase A subunit RI α . The modified...
7074767 Preparation of a therapeutic composition  
Product R, a novel therapeutic composition for treating viral infections and stimulating the immune system, comprises a unique peptide having 31 amino acids and another unique peptide having 21...
7071172 Secretion signal vectors  
The present invention provides delivery vectors for transferring a nucleic acid sequence to a cell in vitro, ex vivo or in vivo. The delivery vector comprises a segment encoding a secretory signal...
7071171 Unique dendritic cell-associated c-type lectins, dectin-1 and dectin-2 compositions and uses thereof  
Novel genes expressed selectively by long-term dendritic cell (DC) lines (XS series) from murine epidermis which retain important features of resident epidermal Langerhans cells (LC) are provided....
7071163 Compounds for targeting hepatocytes in vivo  
We describe compounds that bind to and are internalized by hepatocytes. Association of these compounds to other molecules or complexes can be used to target the molecules or complexes to...