Abstract: A method is provided for inducing cell death comprising administering to said cell a composition comprising tempo or a functional derivative of tempo.
Abstract: Epstein-Barr virus (EBV) specific polypeptides are disclosed. Also disclosed are the use of these polypeptides for the production of polypeptide-specific antibodies and the diagnosis and treatment of EBV-associated disease.
Type:
Application
Filed:
May 21, 2003
Publication date:
January 22, 2004
Applicants:
Ortho Diagnostic Systems, Inc., Georgetown University
Inventors:
Richard S. Smith, Gary R. Pearson, D. Elliot Parks, Susan Pothen Varghese
Abstract: The present invention relates to a method of inhibiting carcinoma progression wherein matriptase plays a role in a subject in need of such inhibition including administering to a subject an effective amount of a compound comprising two positively charged groups, which are the same or different. The groups are linked by a chemical group having a length of between 5 and 30 A, and preferably between 15 and 24 A. Diagnostic methods based on matriptase action and therapeutic methods involving inhibition of matriptase activity are provided.
Type:
Grant
Filed:
June 21, 2001
Date of Patent:
January 13, 2004
Assignee:
Georgetown University School of Medicine
Inventors:
Chen-Yong Lin, Robert B. Dickson, Shaomeng Wang, Istvan Enyedy, Sheau-Ling Lee
Abstract: The invention provides a SHINC-3 polynucleotide, which can be a nucleic acid encoding all or a portion of a SHINC-3 protein, or a complementary polynucleotide or antisense polynucleotide. In another aspect, the invention provides a SHINC-3 polypeptide, which can be a full-length SHINC-3 protein or a fragment thereof or an analog or homolog thereof. Desirably, the SHINC-3 polypeptide modulates apoptosis. In another aspect, the invention provides an antibody that specifically binds a SHINC-3 polypeptide.
Abstract: A method for the treatment for hepatitis delta infection in a host, that includes administering an effective amount of a nucleoside or a nucleoside analog that suppresses the expression of the hepatitis B surface or preS1 antigen in the host 100-fold or more relative to pretreatment values in vivo; or to not more than 1 microgram per milliliter in vivo. In a preferred embodiment, the nucleoside is L-FMAU, or a pharmaceutically acceptable salt or prodrug thereof.
Type:
Grant
Filed:
March 29, 2001
Date of Patent:
December 30, 2003
Assignees:
Georgetown University, Cornell Research Foundation, Inc., University of Georgia Research Foundation, Inc.
Inventors:
John L. Casey, Brent E. Korba, Paul J. Cote, John L. Gerin, Bud C. Tennant, Chung K. Chu
Abstract: The present invention relates to the preparation and biological activity of 3-deoxy-Dmyo-inositol ether lipid analogs as inhibitors of phosphatidylinositol-3-kinase signaling and cancer cell growth. The compounds of the present invention are useful as anti-tumor 5 agents which effectively inhibit the growth of mammalian cells.
Type:
Grant
Filed:
June 12, 2001
Date of Patent:
December 23, 2003
Assignees:
Arizona Board of Regents on behalf of the University of
Arizona, Georgetown University School of Medicine
Inventors:
Alan P. Kozikowski, Lixin Qiao, Garth Powis
Abstract: A system for delivery of high dosage of radiation to a targeted spinal area is provided. This is accomplished by a system which provides for precise immobilization and positioning of the treated spinal area during dose planning and treatment via stereotactic radiosurgery. Advantages of the system include convenience to the patient, enhanced efficacy, and reduced risk of radiotoxicity to non-target tissues.
Type:
Grant
Filed:
April 5, 2001
Date of Patent:
December 16, 2003
Assignee:
Georgetown University School of Medicine
Inventors:
Fraser C. Henderson, James Rodgers, Azam Niroomand-Rad, Kevin Cleary, Anatoly Dritschilo, Leon Der
Abstract: The invention relates to novel cationic lipid formulations and use thereof for treatment of cancer, especially in combination with radiation.
Abstract: The invention provides a SHINC-2 polynucleotide, which can be a nucleic acid encoding all or a portion of a SHINC-2 protein, or a complementary polynucleotide or antisense polynucleotide. In another aspect, the invention provides a SHINC-2 polypeptide, which can be a full-length SHINC-2 protein or a fragment thereof or an analog or homolog thereof Desirably, the SHINC-2 polypeptide modulates apoptosis. In another aspect, the invention provides an antibody that specifically binds a SHINC-2 polypeptide.
Abstract: The invention relates to the use of oliognucleotide containing cationic liposomal formulations to enhance the efficacy of chemotherapy and/or radiotherapy, particularly as a means to chemosensitize cancer are tumor tissues to the efficiencies of chemotherapy. This is particularly advantageous in the context of treatment of ras expressing tumors such as breast, lung, pancreatic and prostate cancer.
Abstract: The present invention encompasses methods of treating patients for essential hypertension. The invention also includes related pharmaceutical compositions of nitroxides. Specific drugs, such as 4-hydroxy-2,2,6,6-tetramethyl-1-piperidinyloxy (Tempol) are disclosed. These compositions are also contemplated for use in the treatment of oxidative stress and modulation of blood pressure.
Abstract: A method of detecting an enzyme-mediated DNA cleavage reaction in a fluorometric assay is provided. The method can be used to detect DNA cleavage caused by restriction endonucleases, retroviral integrase enzymes, DNases, RNases, or enzymes utilized in other strand separating processes in molecular biology.
Type:
Application
Filed:
July 10, 2002
Publication date:
September 4, 2003
Applicant:
Georgetown University
Inventors:
Myun Ki Han, S. Paul Lee, Jack G. Chirikjian
Abstract: The present invention provides bicyclic metabotropic glutamate receptor ligands, as well as compositions comprising such ligands, and and methods for their use.
Type:
Grant
Filed:
March 6, 2002
Date of Patent:
August 26, 2003
Assignee:
Georgetown University
Inventors:
Alan P. Kozikowski, Darryl Hugh Steensma, Werner Tueckmantel, Gian Luca Araldi
Abstract: The invention provides compounds of formula(I):
X—L—X1 (I)
wherein X, L, and X1 have any of the meanings defined in the specification; as well a pharmaceutical composition comprising a compound of formula I; intermediates and methods useful for preparing a compound of formula I; and therapeutic methods for treating drug addiction, Parkinson's disease, depression, or a disease wherein the administration of cocaine is indicated, comprising administering a compound of formula I or a pharmaceutically acceptable salt thereof to a mammal in need of such treatment.
Type:
Grant
Filed:
July 30, 2002
Date of Patent:
August 12, 2003
Assignee:
Georgetown University
Inventors:
Alan P. Kozikowski, Gian Luca Araldi, Amir P. Tamiz
Abstract: One aspect of the present invention relates to 2-hydroxymethylglutamic acid and congeners thereof. A second aspect of the invention relates to a method of synthesizing 2-hydroxymethylglutamic acid and congeners thereof.
Abstract: The invention relates to novel cationic lipid formulations and use thereof for treatment of cancer, especially in combination with radiation.
Abstract: The present invention relates to an expression vector which expresses a malaria MSA1 peptide in combination with a signal peptide and anchor peptide in a host animal. The MSA1 peptide is combined with a signal peptide and anchor peptide for expression. Chimeric peptides being expressed with both signal peptides and anchor peptides were the most effective in eliciting an immunogenic response from a vaccinated host.
Abstract: The present invention relates to novel compounds and formulations thereof which compounds are ligands, e.g., agonists or antagonists, for a metabotropic glutamate receptor or a NAALADase enzyme or both. The present invention also relates to methods of modulating the activity of a metabotropic glutamate receptor or a NAALADase enzyme or both, e.g., in a subject in need thereof, using a compound or formulation of the present invention. The present invention also relates to methods of treating a subject suffering from a chronic or acute disease, malady or condition due at least in part to an abnormality in the activity of an endogenous metabotropic glutamate receptor or a NAALADase enzyme or both, using a compound or formulation of the present invention.
Type:
Grant
Filed:
September 15, 2000
Date of Patent:
March 4, 2003
Assignee:
Georgetown University
Inventors:
Alan P. Kozikowski, Jarda T. Wroblewski, Fajun Nan