Patents Assigned to Children's Research Institute
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Patent number: 9861642Abstract: The present invention relates to asthma. Particularly, the present invention relates to clinical screening, diagnosis, prognosis, therapy and prophylaxis, as well as for drug screening and drug development for the treatment of asthma. The present invention relates to a new paradigm in diagnosing, screening, and treating asthma by affecting airway epithelial synchronization.Type: GrantFiled: October 14, 2015Date of Patent: January 9, 2018Assignee: The Children's Research InstituteInventors: Robert J. Freishtat, Eric P. Hoffman
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Patent number: 9789308Abstract: A method of treating a waste evacuation dysfunction comprising administering transcutaneous electrical stimulation (TES) to at least one lower pelvic and/or sacral region for a specific treatment regimens. Also disclosed is a system for configuring a stimulation device to deliver transcutaneous electrical stimulation (TES) the system comprising: a computing device storing or having access to a plurality or TES settings and comprising a user interface to enable authorized selection of at least on of the TES settings for provision of TES by the stimulation device according to the at least one selected TES setting and the stimulation device communicatively coupled to the computing device to receive and store the selected at least one TES setting the stimulation device being of a size to be readily carried on a body and configured to selectively provide current to external electrode according to the one TES setting.Type: GrantFiled: March 2, 2012Date of Patent: October 17, 2017Assignee: MURDOCH CHILDRENS RESEARCH INSTITUTEInventors: Bridget Rae Southwell, John Medwyn Hutson, Andre Yi Feng Tan
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Publication number: 20170267742Abstract: The present invention provides genetic tags operably linked to transgenes. The expression of the genetic tag allows identification, detection, selection, and ablation of cells expressing the transgene and the genetic tag. In some alternatives the genetically modified host cell comprises a transgene comprising a polynucleotide coding for a chimeric antigen receptor comprising a ligand binding domain, a polynucleotide comprising a spacer region, a polynucleotide comprising a transmembrane domain, and a polynucleotide comprising an intracellular signaling domain and a polynucleotide coding for a genetic tag.Type: ApplicationFiled: April 8, 2015Publication date: September 21, 2017Applicant: Seattle Children's Hospital (dba Seattle Children's Research Institute)Inventors: Michael C. Jensen, Adam Johnson
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Patent number: 9687268Abstract: A dermatome including a battery unit, a handle, and a head portion. The head portion includes guards capable of being adjusted to control the width and the depth of the cut without an interruption in the medical procedure.Type: GrantFiled: February 19, 2014Date of Patent: June 27, 2017Assignees: BioVentures, LLC, Arkansas Children's Research InstituteInventors: Gal Shafirstein, Anjay K. Khandelwal, James C. Walker
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Publication number: 20170107285Abstract: The invention is directed to a bispecific chimeric antigen receptor, comprising: (a) at least two antigen-specific targeting regions; (b) an extracellular spacer domain; (c) a transmembrane domain; (d) at least one co-stimulatory domain; and (e) an intracellular signaling domain, wherein each antigen-specific targeting region comprises an antigen-specific single chain Fv (scFv) fragment, and binds a different antigen, and wherein the bispecific chimeric antigen receptor is co-expressed with a therapeutic control. The invention also provides methods and uses of the bispecific chimeric antigen receptors.Type: ApplicationFiled: August 10, 2016Publication date: April 20, 2017Applicant: Seattle Children's Hospital d/b/a Seattle Children's Research InstituteInventor: Michael Jensen
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Publication number: 20170015746Abstract: Aspects of the invention described herein, concern approaches to make genetically modified T-cells comprising a chimeric antigen receptor for human therapy. In some alternatives, the methods utilize a selection and/or isolation of CD4+ and/or CD8+ T-cells from a mixed T-cell population, such as, peripheral blood or apheresis derived mononuclear cells. Once selected/isolated, the CD4+ and/or CD8+ T-cells are then activated, genetically modified, and propagated, preferably, in separate or isolated cultures in the presence of one or more cytokines, which support survival, engraftment and/or proliferation of the cells, as well as, preferably promoting or inducing the retention of cell surface receptors, such as CD62L, CD28, and/or CD27.Type: ApplicationFiled: April 8, 2015Publication date: January 19, 2017Applicant: Seattle Children's Hospital (Dba Seattle Children's Research Institute)Inventor: Michael C. Jensen
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Patent number: 9402896Abstract: The present invention relates generally to the field of allergies. More particularly, the present invention provides a method for treating an allergy in a subject by inducing tolerance to an allergen associated with the allergy. Medicinal kits useful in protocols to induce tolerance or reduce intolerance in a subject also form part of the present invention.Type: GrantFiled: January 30, 2009Date of Patent: August 2, 2016Assignee: MURDOCH CHILDRENS RESEARCH INSTITUTEInventor: Mimi Lai-Kuan Tang
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Patent number: 9006202Abstract: A method for treating latent HIV infection is disclosed. The method includes administering to a subject in need of such treatment an effective amount of an anti-I?B? agent, an anti-I?B? agent or both; and administering to the subject an effective amount of an antiviral agent. A pharmaceutical composition for treating latent HIV infection is also disclosed.Type: GrantFiled: June 27, 2013Date of Patent: April 14, 2015Assignee: Children's Research Institute, Children's National Medical CenterInventors: Steven L. Zeichner, Guerau Fernandez
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Publication number: 20150038684Abstract: The invention is directed to a bispecific chimeric antigen receptor, comprising: (a) at least two antigen-specific targeting regions; (b) an extracellular spacer domain; (c) a transmembrane domain; (d) at least one co-stimulatory domain; and (e) an intracellular signaling domain, wherein each antigen-specific targeting region comprises an antigen-specific single chain Fv (scFv) fragment, and binds a different antigen, and wherein the bispecific chimeric antigen receptor is co-expressed with a therapeutic control. The invention also provides methods and uses of the bispecific chimeric antigen receptors.Type: ApplicationFiled: February 13, 2013Publication date: February 5, 2015Applicant: Seattle Children's Hospital (dba Seattle Children's Research Institute)Inventor: Michael Jensen
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Publication number: 20140275279Abstract: Fibrotic diseases are characterized by the replacement of healthy tissue with scar tissue and extracellular matrix in response to tissue damage. Here we describe the reduction of extracellular matrix (ECM) deposition, interstitial fibroblasts, interstitial volume, expression of Collagen I mRNA and protein, expression of profibrotic cytokines and macrophage infiltration by Cysteamine treatment.Type: ApplicationFiled: October 26, 2011Publication date: September 18, 2014Applicant: SEATTLE CHILDREN'S RESEARCH INSTITUTEInventors: Allison A. Eddy, Daryl M. Okamura
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Publication number: 20140234273Abstract: The present disclosure relates generally to tissue, including organ, transplantation. Taught herein is a genetic-based diagnostic assay to ascertain the status of a tissue transplantation procedure in a recipient based on a characterization of circulating or other cell free nucleic acid material. The instant disclosure enables kits, primers and protocols for ascertaining the status of a transplantation procedure.Type: ApplicationFiled: October 5, 2012Publication date: August 21, 2014Applicant: Muroch Children Research InstituteInventors: Howard Robert Slater, Damien Luis Bruno, Devika Ganesamoorthy
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Publication number: 20140212873Abstract: The present disclosure relates generally to the field of epigenetics and in particular epigenetic profiles associated with a pathological condition. The present specification teaches screening of individuals and populations for epigenetic profiles associated with a pathological condition. Epigenetic profiles are disclosed from the following sites in the FMR1 gene: FREE3, intron 2, an intron, intron/exon boundary and/or splicing region downstream of intron 2, and a site within the FREE2 portion of intron 1 in combination with a FM. Epigenetic profiles are also disclosed from a region in the FMR genetic locus selected from an intron, intron/exon boundary, a splicing region or an intragenic region in combination with an expansion mutation. Kits and diagnostic assays are also taught herein as are computer programs to monitor changes in epigenetic patterns and profiles.Type: ApplicationFiled: June 22, 2012Publication date: July 31, 2014Applicants: LA TROBE UNIVERSITY, MURDOCH CHILDRENS RESEARCH INSTITUTEInventor: David Eugeny Godler
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Patent number: 8673557Abstract: The present disclosure relates to the co-expression of an endonuclease with an end-processing enzyme for the purpose of enhanced processing of the polynucleotide ends generated by endonuclease cleavage.Type: GrantFiled: February 24, 2012Date of Patent: March 18, 2014Assignee: Seattle Children's Research InstituteInventors: Andrew M. Scharenberg, Michael T. Certo, Kamila S. Gwiazda
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Publication number: 20130338032Abstract: The present invention relates generally to an assay for the determination of epigenetic profiles, particularly epigenetic profiles associated with a pathological condition. Even more particularly, the present invention provides an assay to detect epigenetic profiles within the Fragile X Mental Retardation (FMR) genetic locus indicative of a pathoneurological condition such as pathoneurodevelopmental and pathoneurodegenerative conditions. The epigenetic profiles can also identify potential non-neurological conditions. Kits and assays for medicaments also form part of the present invention as do computer programs to monitor changes in epigenetic patterns and methods for screening for agents which modulate epigenetic modification.Type: ApplicationFiled: August 23, 2013Publication date: December 19, 2013Applicant: Murdoch Childrens Research InstituteInventor: DAVID EUGENY GODLER
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Publication number: 20130218196Abstract: A therapeutic ischemic and reperfusion device with an associated monitoring system for generally enhancing the vascular and metabolic environment and wellbeing of a subject. A method for the treatment and prophylaxis of various medical conditions including environmental induced oxidative stress using the therapeutic ischemic and reperfusion device and associated monitoring system is also contemplated herein. The method uses an inflatable cuff around the limb or torso of a subject operated by a controller configured to inflate and deflate the cuff. The monitoring system is used to monitor the physical and metabolic environments of the subject during and subsequent to the ischemia and reperfusion.Type: ApplicationFiled: August 2, 2011Publication date: August 22, 2013Applicant: MURDOCH CHILDRENS RESEARCH INSTITUTEInventor: Michael Cheung
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Publication number: 20130210007Abstract: The present disclosure relates generally to the field of epigenetics and in particular epigenetic profiles associated with a pathological condition. The present specification teaches screening of individuals and populations for epigenetic profiles associated with a pathological condition. The epigenetic profiles can be from an intron, an intron/exon boundary or a splicing region. Epigenetic profiles are disclosed from the following sites in the FMR locus: FREES, intron 2 of FMR1, the genomic FREE2 region as a whole or specific FREE2 fragments including FREE2 (D) or FREE2 (E). Kits and diagnostic assays are also taught herein as are computer programs to monitor changes in epigenetic patterns and profiles. Further enabled herein is a method for screening for agents which can reduce or mask the adverse effects of epigenetic modification and the use of these agents in therapy and prophylaxis.Type: ApplicationFiled: August 11, 2011Publication date: August 15, 2013Applicant: MURDOCH CHILDRENS RESEARCH INSTITUTEInventor: David Eugeny Godler
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Patent number: 8497251Abstract: A method for treating latent HIV infection is disclosed. The method includes administering to a subject in need of such treatment an effective amount of an anti-I?B? agent, an anti-I?B? agent or both; and administering to the subject an effective amount of an antiviral agent. A pharmaceutical composition for treating latent HIV infection is also disclosed.Type: GrantFiled: May 29, 2012Date of Patent: July 30, 2013Assignee: Children's Research Institute, Children's National Medical CenterInventors: Steven L. Zeichner, Guerau Fernandez
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Publication number: 20120276074Abstract: The present disclosure relates to the co-expression of an endonuclease with an end-processing enzyme for the purpose of enhanced processing of the polynucleotide ends generated by endonuclease cleavage.Type: ApplicationFiled: February 24, 2012Publication date: November 1, 2012Applicant: SEATTLE CHILDREN'S RESEARCH INSTITUTEInventors: Andrew M. Scharenberg, Michael T. Certo, Kamila S. Gwiazda
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Publication number: 20120263782Abstract: A method for treating latent HIV infection is disclosed. The method includes administering to a subject in need of such treatment an effective amount of an anti-I?B? agent, an anti-I?B? agent or both; and administering to the subject an effective amount of an antiviral agent. A pharmaceutical composition for treating latent HIV infection is also disclosed.Type: ApplicationFiled: May 29, 2012Publication date: October 18, 2012Applicant: CHILDREN'S RESEARCH INSTITUTE, CHILDREN'S NATIONAL MEDICAL CENTERInventors: STEVEN L. ZEICHNER, GUERAU FERNANDEZ
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Patent number: D757952Type: GrantFiled: April 10, 2014Date of Patent: May 31, 2016Assignee: Murdoch Childrens Research InstituteInventors: Rod Wiebenga, Bridget Rae Southwell