Abstract: The results presented herein demonstrate the specific expression of CCR3 in CNV endothelial cells in humans with AMD, and despite the expression of its ligands, eotaxin-1, -2, and -3, neither eosinophils nor mast cells are present in human CNV. The genetic or pharmacological targeting of CCR3 or eotaxins as disclosed herein inhibited injury-induced CNV in mice. CNV suppression by CCR3 blockade was due to direct inhibition of endothelial cell proliferation, and was uncoupled from inflammation as it occurred in mice lacking eosinophils or mast cells and was independent of macrophage and neutrophil recruitment. CCR3 blockade was more effective at reducing CNV than vascular endothelial growth factor-A (VEGF-A) neutralization, which is currently in clinical use, and, unlike VEGF-A blockade, not toxic to the mouse retina. In vivo imaging with CCR3-targeting quantum dots located spontaneous CNV invisible to standard fluorescein angiography in mice before retinal invasion.
Type:
Application
Filed:
May 26, 2010
Publication date:
March 15, 2012
Applicant:
University of Kentucky Research Foundation
Inventors:
Jayakrishna Ambati, Mark Ellsworth Kleinman
Abstract: Provided herein are compounds and methods for use in preventing or treating a viral infection mediated by a virus comprising an IRES-containing RNA molecule or cancer related to an increase or decrease in IRES-mediated translation of an RNA molecule. Also provided are methods of inhibiting or promoting IRES-mediated translation. Also provided are methods of screening for an agent that inhibits IRES-mediated translation.
Type:
Application
Filed:
March 26, 2010
Publication date:
March 15, 2012
Applicants:
DiscoveryBiomed, Inc., The UAB Research Foundation
Inventors:
Sunnie R. Thompson, Erik Mills Schwiebert, John H. Streiff
Abstract: The present invention provides isolated Elo1 and Mig3 nucleic acid sequences capable of conferring increased ethanol tolerance on recombinant yeast and methods of using same in biofuel production, particularly ethanol production. Methods of bioengineering yeast using the Elo1 and, or, Mig3 nucleic acid sequences are also provided.
Abstract: The present invention is directed to a method for treating aneurysms in vascular tissue. The method includes administering a bisphosphonate compound to a subject in an amount which is effective against the formation or progression of aneurysm, or which is effective to induce regression of an established aneurysm. In alternative methods, an anti-RANKL neutralizing antibody is administered to the subject to achieve analogous anti-aneurysm effect. The methods of particular advantage in the treatment of subjects having an abdominal aortic aneurysm, a relatively common, and life-threatening, condition.
Abstract: A novel and stable attenuated poliovirus, which replicates in neuroblastoma cells, is produced by engineering an indigenous replication element (cre), into the 5? non-translated genomic region and inactivating the native cre element located in the coding region of 2C (mono-crePV). The stably attenuated poliovirus replicates in a neuroblastoma model (Neuro-2aCD155 tumors) expressing CD155, the poliovirus receptor, and is effective for oncolytic treatment and cure of solid tumors, such as neuroblastoma.
Type:
Application
Filed:
October 7, 2011
Publication date:
March 15, 2012
Applicant:
The Research Foundation of State University of New York
Abstract: The present invention application relates to a pharmaceutical preparation to be administered into respiratory organs for treating or preventing inflammatory respiratory diseases, comprising a peptide which acts on formyl peptide receptors (FPRs) or receptors analogous thereto, in an amount which is effective in suppressing respiratory inflammation. The present invention application also relates to a method for treating or preventing inflammatory respiratory diseases by using the preparation, and to a kit containing the preparation. As compared with systemic administration of the peptide by injection, direct administration of the peptide to respiratory organs remarkedly improves the effect in suppressing respiratory inflammation.
Abstract: An art therapy computer system and a computer-readable storage medium having recorded a program for art therapy are disclosed. An aspect of the present invention provides a computer system that includes a drawing module, which presents a plurality of patterns and in which the drawing module selects a certain pattern, composes and colors a picture according to the working of a person tested for art therapy, an analysis module, which analyzes one or more factors from the colored picture, and a parsing module, which parses the psychological state, symptoms or disorders of the person tested for art therapy from the analyzed factors.
Type:
Application
Filed:
October 30, 2009
Publication date:
March 15, 2012
Applicant:
Korea University Industrial & Academic Collaborative Foundation
Abstract: A flexible microcavity structure made of organic materials using spin-coating technique for allowing large area structures using a roll-to-roll process. The structure includes at least one first polymer layer, at least one second polymer layer, and a cavity layer. The cavity layer has quantum dots embedded therein for realizing an electrically pumped microcavity emitter. The at least one first polymer layer alternates with the at least one second polymer layer, respectively, to form a pair of distributed Bragg reflecting mirrors. The cavity layer is sandwiched between the pair of distributed Bragg reflecting mirrors.
Type:
Grant
Filed:
December 4, 2007
Date of Patent:
March 13, 2012
Assignee:
Research Foundation of the City University of New York
Abstract: The present invention relates to a polypeptide specifically bound to phosphatidylserine and use thereof, and more particularly to a polypeptide having an amino acid sequence designated as sequence number 1 and specifically bound to phosphatidylserine, a phosphatidylserine detecting composition containing the polypeptide as an active ingredient, a detecting method of phosphatidylserine by using polypeptide, a apoptotic cell detecting containing the polypeptide as an active ingredient, a drug delivery composition containing the polypeptide as an active ingredient, a composition for treatment and prevention of a tumorous disease, and a composition for visualization of a tumorous region. A polypeptide having an amino acid sequence designated sequence number 1 is specifically bound to phosphatidylserine.
Type:
Grant
Filed:
February 24, 2009
Date of Patent:
March 13, 2012
Assignee:
Kyungpook National University Industry Academic Cooperation Foundation
Inventors:
Byung-Heon Lee, In-San Kim, Thapa Narendra
Abstract: A transcription factor both necessary and sufficient for human neuroectoderm specification, Pax6, as well as applications thereof, is disclosed.
Abstract: The invention provides method for metallic nanonstructures self-assembly methods and materials testing. Preferred embodiment methods permit for the formation of individual nanostructures and arrays of nanostructures. The nanostructures formed can have a metal alloy crystal structure. Example structures include slender wires, rectangular bars, or plate-like structures. Tips can be shaped, single layer and multiple layer coatings can be formed, tips can be functionalized, molecules can be adhered, and many testing methods are enabled.
Type:
Grant
Filed:
June 2, 2008
Date of Patent:
March 13, 2012
Assignee:
University of Louisville Research Foundation, Inc.
Inventors:
Robert W. Cohn, Mehdi M. Yazdanpanah, Steven A. Harfenist, Frank P. Zamborini, Mahdi Hosseini, Santosh Pabba, Vladimir Dobrokhotov, Abdelilah Safir, Brigitte H. Fasciotto
Abstract: The present invention provides methods, devices and kits for detecting a ligand. The methods involve capturing a ligand from a sample with an affinity substrate that includes a receptor for a ligand, transferring captured ligand to a detection surface and detecting the ligand on the detection surface with a liquid crystal. Accordingly, the capture step is decoupled from the detection step.
Type:
Grant
Filed:
September 23, 2004
Date of Patent:
March 13, 2012
Assignee:
Wisconsin Alumni Research Foundation
Inventors:
Nicholas L. Abbott, Matthew L. Tingey, Brian H. Clare, Chang-Hyun Jang
Abstract: Methods of creating and transferring chemical patterns and physical patterns of deposited materials or molecules using block copolymers are provided. The methods involve providing block copolymer materials blended with one or more transfer molecules or inks. The differences in chemistry of the blocks of the copolymer that result in micro-phase separation (e.g., self-assembly into nanoscale domains) also allow inks to be sequestered into specific blocks. By designing the ink molecules to react, adsorb, or otherwise interact with a second substrate, inks are transferred to the second substrate in a pattern dictated by the pattern of block copolymer domains present at the surface of the block copolymer film.
Abstract: This invention provides for a method for inhibiting new tissue growth in blood vessels in a subject, wherein the subject experienced blood vessel injury, which comprises administering to the subject a pharmaceutically effective amount of an inhibitor of receptor for advanced glycation endproduct (RAGE) so as to inhibit new tissue growth in the subject's blood vessels. The invention also provides for method for inhibiting neointimal formation in blood vessels in a subject, wherein the subject experienced blood vessel injury, which comprises administering to the subject a pharmaceutically effective amount of an inhibitor of receptor for advanced glycation endproduct (RAGE) so as to inhibit neointimal formation in the subject's blood vessels.
Type:
Grant
Filed:
June 7, 2010
Date of Patent:
March 13, 2012
Assignees:
The Trustees of Columbia University in the City of New York, The Cleveland Clinic Foundation
Inventors:
David M. Stern, Ann Marie Schmidt, Steven Marso, Eric Topol, A. Michael Lincoff
Abstract: Provided are method and apparatus of pre-processing in WDR (wide dynamic range) image processing, the method of pre-processing of WDR image processing including: (a) receiving luminance and chrominance signals having different exposure times, and analyzing the correlation between a luminance signal having a first exposure time and a luminance signal having a second exposure time that is longer than the first exposure time; (b) based on the result of the analysis, dividing each of the luminance signal having the first exposure time and the luminance signal having the second exposure signal, into at least one of a bright region, a transition region, and a dark region; and (c) normalizing the regions of the luminance signal having the first exposure time to respectively correspond to the regions of the luminance signal having the second exposure times.
Type:
Grant
Filed:
March 18, 2009
Date of Patent:
March 13, 2012
Assignees:
Samsung Techwin Co., Ltd., Korea University Industrial & Academic Collaboration Foundation
Inventors:
Bong-hyup Kang, Chang-won Jeon, Han-seok Ko
Abstract: The invention relates to a kit comprising MHC Class I and Class II HLA-coated beads containing specific antigenic peptides for binding to antigen-specific T cells and the appropriate negative control peptides. Also provided are methods for making the coated beads and methods for use. The application of these beads go to the stimulation of peripheral blood cell populations and in vitro-stimulated culture for the elicitation of functional activities such as cell activation and signaling, cytokine secretion, proliferation and cytotoxicity activity.
Type:
Grant
Filed:
July 5, 2006
Date of Patent:
March 13, 2012
Assignee:
The Henry M. Jackson Foundation for the Advancement of Military Medicine, Inc.
Inventors:
Sathibalan Ponniah, George E. Peoples, Catherine E. Storrer, Michael Flora
Abstract: The subject invention provides dipeptides useful in promoting healthy muscle tissues as well as effective immune responses. The dipeptides of the subject invention are particularly advantageous because they are stable, bioavailable, and can be formulated in an aqueous solution.
Type:
Grant
Filed:
October 17, 2008
Date of Patent:
March 13, 2012
Assignee:
University of Florida Research Foundation, Inc.
Abstract: A method, apparatus and system for increasing cell capacity through optional signal combining between Relay Stations (RSs) in a cellular system using wired RSs is disclosed.
Type:
Grant
Filed:
December 28, 2007
Date of Patent:
March 13, 2012
Assignees:
Samsung Electronics Co., Ltd., Industry-University Cooperation Foundation Sogang University
Inventors:
Byung-Jik Kim, Seong-Taek Hwang, Won-Jin Sung, Jin-Woo Choe, Jong-Hyun Park, Jong-Hyun Kim
Abstract: A high speed transceiver without using an external clock signal and a communication method used by the high speed transceiver which applies a clock recovery circuit including a coarse code generator, a frequency detector, and a linear phase detector to the receiver so as to solve problems such as skew between a reference clock and data that may occur during data transmission and jitter of a recovered clock while an embedded clock method of applying clock information to data is used.
Type:
Grant
Filed:
July 23, 2008
Date of Patent:
March 13, 2012
Assignee:
Korea University Industrial & Academic Collaboration Foundation
Abstract: A dynamic device for reducing functional mitral regurgitation is described. The device is disposed externally to the heart and effectively acts as a splint for reducing further dilation of the heart in patients diagnosed with cardiomyopathy, and for reducing tethering of the papillary muscle on the mitral valve. The device does not require cardiopulmonary bypass for its installation since it is attached to the outside of the left ventricle, thereby reducing surgical risk, and is not exposed to the patient's blood once installed, thereby reducing the risk of thromboembolic disease.
Type:
Grant
Filed:
September 1, 2006
Date of Patent:
March 13, 2012
Assignee:
Colorado State University Research Foundation
Inventors:
Eric Monnet, E. Christopher Orton, Susan P. James, Kyle Garrett Ordway, John Ordway, legal representative