Abstract: The present invention provides a pharmaceutical composition comprising Protein Kinase C Zeta (PKC-?) inhibitor and therapeutic methods for preventing or treating a pathological condition or symptom or for inducing proliferation of lung progenitor cells in a mammal by administering the PKC-? inhibitor.
Type:
Application
Filed:
October 28, 2015
Publication date:
May 5, 2016
Applicant:
UNIVERSITY OF IOWA RESEARCH FOUNDATION
Inventors:
Alejandro P. Comellas Freymond, Xiaopeng Li, Joseph Zabner, Luis Guillermo Vargas Buonfiglio
Abstract: The present invention relates to methods of reducing ?F508-CFTR ubiquitination or degradation, or increasing ?F508-CFTR processing or function in a CF cell comprising contacting the cell with a therapeutic agent that inhibits NEDD8, FBXO2, and/or SYVN1 expression in the cell.
Abstract: Disclosed are methods and compositions for treating or preventing diseases or disorders associated with mitochondrial calcium uniporter (MCU) activity. The methods may include administering a modulator of MCU activity to a patient in need thereof.
Abstract: The present invention provides in certain embodiments a method of treating autosomal dominant non-syndromic hearing loss (ADNSHL) in a patient in need thereof comprising: (a) identifying a mutation in an ADNSHL-causing gene, (b) preparing a ADNSHL therapeutic miRNA, and (c) administering to the patient a pharmaceutical composition comprising the ADNSHL therapeutic miRNA and a pharmaceutically acceptable carrier.
Abstract: In one aspect, the invention relates to methods for treating muscle atrophy by providing to an animal in need thereof an effective amount of a compound. The compound can modulate the expression levels of multiple mRNA of a muscle atrophy signature. This abstract is intended as a scanning tool for purposes of searching in the particular art and is not intended to be limiting of the present invention.
Type:
Grant
Filed:
June 6, 2012
Date of Patent:
March 29, 2016
Assignee:
UNIVERSITY OF IOWA RESEARCH FOUNDATION
Inventors:
Christopher M. Adams, Steven D. Kunkel, Michael Welsh
Abstract: A method is disclosed for treating nephropathies involving undesired alternative pathway complement activation by administration of a complement inhibitory protein such as soluble complement receptor type I (sCR1).
Type:
Grant
Filed:
September 15, 2011
Date of Patent:
March 29, 2016
Assignees:
CELLDEX THERAPEUTICS, INC., UNIVERSITY OF IOWA RESEARCH FOUNDATION
Inventors:
Richard J. H. Smith, Yuzhou Zhang, Henry C. Marsh
Abstract: The present invention is directed to RNA interference (RNAi) molecules targeted against a Huntington's disease nucleic acid sequence, and methods of using these RNAi molecules to treat Huntington's disease.
Type:
Application
Filed:
May 20, 2015
Publication date:
March 3, 2016
Applicant:
UNIVERSITY OF IOWA RESEARCH FOUNDATION
Inventors:
Beverly L. Davidson, Alejandro Mas Monteys
Abstract: The present invention relates to methods of reducing a level of a target mRNA in a well-differentiated airway epithelial cell by contacting the cell with a sensitizing agent followed by contacting the cell with a therapeutic RNAi agent.
Type:
Grant
Filed:
March 14, 2013
Date of Patent:
March 1, 2016
Assignee:
University of Iowa Research Foundation
Inventors:
Paul B. McCray, Jr., Beverly L. Davidson, Sateesh Krishnamurthy
Abstract: The invention relates to a method for applying a photo-activated layered polymer coating to a substrate material in which one or more layers do not contain photoinitiator, or are not exposed to initiating light, but cure due to migration of cationic active centers. At least two separate monomer layers are applied to the substrate material. At least one of the monomer layers includes a photoinitiator capable of producing cationic active centers. The at least one layer including the photoinitiator is exposed to a source of UV radiation at a desired wavelength forming cationic active centers. The at least two separate monomer layers react in a polymerization reaction forming a cured layered material. The cationic active centers of the exposed monomer layer migrate to the unexposed layer such that both layers cure via the polymerization reaction.
Type:
Grant
Filed:
July 18, 2014
Date of Patent:
March 1, 2016
Assignees:
Toyota Motor Engineering & Manufacturing North America, Inc., University of Iowa Research Foundation
Inventors:
Cynthia G. Templeman, Alec B. Scranton, Beth Ann Rundlett, Cynthia Hoppe
Abstract: The present invention is directed to small interfering RNA molecules (siRNA) targeted against nucleic acid sequence that encodes huntingtin or ataxin-1, and methods of using these siRNA molecules.
Type:
Grant
Filed:
June 18, 2013
Date of Patent:
February 16, 2016
Assignee:
University of Iowa Research Foundation
Inventors:
Beverly L. Davidson, Haibin Xia, Qinwen Mao, Henry Paulson, Ryan Boudreau, Scott Harper
Abstract: Certain embodiments of the present invention provide a method for treating or preventing juvenile neuronal ceroid lipofuscinosis (JNCL) in an animal comprising administering CBX, GRA, or GZA to the animal.
Type:
Application
Filed:
March 17, 2014
Publication date:
February 11, 2016
Applicant:
UNIVERSITY OF IOWA RESEARCH FOUNDATION
Inventors:
Beverly L. Davidson, Colleen S. Stein, Mark Schultz, Luis Tecedor, Tammy L. Kielian
Abstract: In one aspect, the invention relates to methods for promoting muscle hypertrophy or decreasing adiposity by providing to an animal in need thereof an effective amount of a compound. This abstract is intended as a scanning tool for purposes of searching in the particular art and is not intended to be limiting of the present invention.
Type:
Grant
Filed:
February 3, 2015
Date of Patent:
February 9, 2016
Assignee:
UNIVERSITY OF IOWA RESEARCH FOUNDATION
Inventors:
Christopher M. Adams, Michael C. Dyle, Michael Welsh
Abstract: This invention provides a device for implantation directly into the spinal cord for the purpose of treating back pain. Electrodes on a backing that conforms directly to the spinal cord are installed as a source of electrical stimulation and pain relief. The electrode array is maintained on the spinal cord by way of a spring or support structure that is anchored to an anatomical structure outside the spinal cord but near the site of implantation. Suitable anchoring structures include the vertebrae and the dura. Secured in this fashion, the support structure maintains a gentle pressure of the electrode array against the spinal cord so as to stay in electrical contact but minimize injury or inflammation. The device may accommodate and buffer movement of the spinal cord both laterally and in a caudal-rostral fashion so that the electrode array remains in place.
Type:
Grant
Filed:
January 30, 2013
Date of Patent:
February 9, 2016
Assignee:
University of Iowa Research Foundation
Inventors:
Matthew A. Howard, Hiroyuki Oya, Steve Viljoen, Chandan G. Reddy
Abstract: Provided are systems and methods for analyzing images. An exemplary method can comprise receiving at least one image having one or more annotations indicating a feature. The method can comprise generating training images from the at least one image. Each training image can be based on a respective section of the at least one image. The training images can comprise positive images having the feature and negative images without the feature. The method can comprise generating a feature space based on the positive images and the negative images. The method can further comprise identifying the feature in one or more unclassified images based upon the feature space.
Type:
Application
Filed:
March 14, 2014
Publication date:
February 4, 2016
Applicants:
UNIVERSITY OF IOWA RESEARCH FOUNDATION, THE UNITED STATES OF AMERICA, as Represented by THE SECRETARY OF THE DEPT. OF VETERANS AFFAIRS
Inventors:
Michael D. Abramoff, Mona K. Garvin, Hu Qiao
Abstract: Organophosphate (OP) nerve agents and pesticides are potent inhibitors of acetylcholinesterase (AChE). Though oxime nucleophiles can reactivate an AChE-phosphyl adduct, the adduct can undergo a reaction called aging, leading to an aged-AChE adduct. The invention provides compounds and methods that can be used to reactivate an aged-AChE adduct. Such compounds and methods are useful to counteract organophosphorus poisoning.
Type:
Grant
Filed:
January 24, 2014
Date of Patent:
February 2, 2016
Assignee:
University of Iowa Research Foundation
Inventors:
Daniel M. Quinn, Joseph John Topczewski
Abstract: An isolated promoter sequence comprising a nucleic acid of between 600 and 1700 nucleotides in length having at least 90% identity to SEQ ID NO:1, SEQ ID NO:2, SEQ ID NO:3, SEQ ID NO:4, SEQ ID NO:5, SEQ ID NO:6, or SEQ ID NO:7.
Type:
Application
Filed:
March 6, 2014
Publication date:
January 28, 2016
Applicant:
UNIVERSITY OF IOWA RESEARCH FOUNDATION
Inventors:
Beverly L. Davidson, Edgardo Rodriguez, Alejandro Mas Monteys
Abstract: A method for preventing colorectal cancer in a patient possessing human tropomyocin isoform TC22 is disclosed. The method comprises: (a) detecting a serum protein concentration of TC22 in a patient and (b) administering to said patient prior to detecting colorectal cancer in said patient a therapeutically effective amount of a chemotherapeutic composition comprising a chemotherapeutic compound that reduces the level of TC22, wherein the chemotherapeutic compound is selected from the group consisting of sulfasalazine, 5-amino-2-hydroxybenzoic acid, osalazine, and balsalazide.
Type:
Grant
Filed:
May 17, 2006
Date of Patent:
January 19, 2016
Assignees:
RUTGERS, THE STATE UNIVERSITY OF NEW JERSEY, UNIVERSITY OF IOWA RESEARCH FOUNDATION
Abstract: The present disclosure provides targeting peptides and vectors containing a sequence that encodes targeting peptides that deliver agents to the brain.