Abstract: Disclosed herein is an isolated nucleic acid molecule comprising a first nucleic acid sequence 5?-ACCCTGCCGCCTGGACTCCGCCTGT-3? (SEQ ID NO: 22), or a functional variant thereof, operably linked to a second, heterologous nucleic acid sequence. The isolated nucleic acid molecule can be DNA (in an expression vector) and RNA (mRNA, shRNA, orncRNA). Also disclosed is a microvesicle comprising the nucleic acid molecule and a microvesicle preparation comprising the microvesicle. Also disclosed is an in vitro method of producing a microvesicle preparation enriched for a specific RNA sequence by transfecting cells with the nucleic acid sequence, and isolating microvesicles generated therefrom. Methods of delivering therapeutic RNA to a subject are also disclosed.
Type:
Grant
Filed:
January 17, 2013
Date of Patent:
January 30, 2018
Assignee:
THE GENERAL HOSPTIAL CORPORATION
Inventors:
Okay Saydam, Mehmet Fatih Bolukbasi, Arda Mizrak, Xandra O. Breakefield
Abstract: A magnetic resonance imaging (MRT) method for jointly estimating an image degradation and reconstructing an image of a subject in which that image degradation is mitigated is provided. The MRI system is operated to acquire multiple different k-space data sets that are acquired with different acquisition parameters so as to modulate the image degradation to be estimated. Using an iterative process, the image degradation is estimated while jointly reconstructing an image in which the estimated image degradation is mitigated.
Abstract: One aspect of the present invention relates to compounds, compositions and methods for diagnosis and/or treatment of a subject suffering from an amyloidosis-associated pathological condition. In certain embodiments, the imaging and/or therapeutic agents of the instant invention may be administered to a subject for identification and/or treatment of amyloid deposits. A specific imaging method detects amyloid deposits by administering the imaging agent to the subject and detecting the spatial distribution of the agent. Differential accumulation of the agent is indicative of AD or an amyloidosis-associated pathological condition and can be monitored by using a PET or SPECT camera.
Type:
Grant
Filed:
March 23, 2009
Date of Patent:
May 28, 2013
Assignees:
The General Hosptial Corporation, Fluoropharma, Inc.
Inventors:
David R. Elmaleh, Timothy M. Shoup, Hongning Fu
Abstract: Certain isolated motile cells spontaneously migrate unidirectionally through a mechanically confined space, such as a microcapillary channel, in the absence of an external gradient (e.g., a chemical gradient). Assays and methods for detecting motile cells, and identifying chemical agents that inhibit cell migration, can include detecting the movement of motile cancer cells through a microcapillary channel.
Abstract: The present invention provides microparticles that create permanent tissue markings, such as tattoos, designed in advance for change and/or removal on demand, as well as methods for implanting the microparticles in tissue and changing and/or removing the resulting markings. Colored microparticles are constructed with specific electromagnetic absorption and/or structural properties that facilitate changing and/or removing tissue markings made using the microparticles by applying specific energy (such as electromagnetic radiation from a laser or flash-lamp) to the tissue marking site.
Type:
Grant
Filed:
October 22, 2007
Date of Patent:
October 14, 2008
Assignees:
The General Hosptial Corporation, Freedom-2, Inc.
Inventors:
Richard Rox Anderson, Susanna K. Mlynarczyk-Evans, Craig A. Drill
Abstract: The invention provides methods for treating neuropsychiatric disorders such as schizophrenia, Alzheimer's Disease, autism, depression, benign forgetfulness, childhood learning disorders, close head injury, and attention deficit disorder. The methods entail administering to a patient diagnosed as having a neuropsychiatric disorder a pharmaceutical composition containing (i) a therapeutically effective amount of D- or L-phosphoserine.
Abstract: Disclosed are sets of DNA molecules, and cell containing such molecules, each molecule encoding a candidate interacting protein fused to either a DNA binding domain or a gene activating domain to which it is not naturally bonded.