Patents by Inventor Michael Chopp

Michael Chopp has filed for patents to protect the following inventions. This listing includes patent applications that are pending as well as patents that have already been granted by the United States Patent and Trademark Office (USPTO).

  • Patent number: 11957705
    Abstract: Provided herein are methods for the prevention and treatment of cardiovascular diseases and disorders in a subject diagnosed as having suffered a cerebrovascular injury by administering agents that contain or induce the expression of microRNA-126.
    Type: Grant
    Filed: February 24, 2023
    Date of Patent: April 16, 2024
    Assignee: Henry Ford Health System
    Inventors: Jieli Chen, Michael Chopp
  • Publication number: 20230241091
    Abstract: Provided herein are methods for the prevention and treatment of cardiovascular diseases and disorders in a subject diagnosed as having suffered a cerebrovascular injury by administering agents that contain or induce the expression of microRNA-126.
    Type: Application
    Filed: February 24, 2023
    Publication date: August 3, 2023
    Applicant: Henry Ford Health System
    Inventors: Jieli CHEN, Michael CHOPP
  • Patent number: 11665031
    Abstract: A method for tuning an analog front end response is provided. The method includes determining a peaking control value for an analog front end (AFE) of a receiver, determining an attribute corresponding to the peaking control value, selecting the peaking control value as the operating peaking control value for the AFE based on the attribute being determined to be higher than a previous attribute, and performing a receiver adaptation using the peaking control for a one or more transmitter configurations.
    Type: Grant
    Filed: October 5, 2021
    Date of Patent: May 30, 2023
    Assignee: SYNOPSYS, INC.
    Inventors: Srinivas Perisetty, Jayabharath Reddy Madi Reddy, Suresh Nagula, Philip Michael Chopp
  • Patent number: 11612618
    Abstract: Provided herein are methods for the prevention and treatment of cardiovascular diseases and disorders in a subject diagnosed as having suffered a cerebrovascular injury by administering agents that contain or induce the expression of microRNA-126.
    Type: Grant
    Filed: November 14, 2018
    Date of Patent: March 28, 2023
    Assignee: Henry Ford Health System
    Inventors: Jieli Chen, Michael Chopp
  • Publication number: 20220347227
    Abstract: Without limitation, a method for preventing and/or treating neuropathic pain in a subject/patient comprising administering a therapeutically effective amount of exosomes derived and isolated from mammalian cells to the subject/patient and a method of treating cancer in a subject/patient in need thereof, comprises administering a combination comprising a therapeutically effective amount of exosomes derived and isolated from mammalian cells and a chemotherapeutic agent.
    Type: Application
    Filed: May 17, 2022
    Publication date: November 3, 2022
    Applicant: Henry Ford Health System
    Inventors: Zhenggang Zhang, Yi Zhang, Michael Chopp
  • Patent number: 11357800
    Abstract: Without limitation, a method for preventing and/or treating neuropathic pain in a subject/patient comprising administering a therapeutically effective amount of exosomes derived and isolated from mammalian cells to the subject/patient and a method of treating cancer in a subject/patient in need thereof, comprises administering a combination comprising a therapeutically effective amount of exosomes derived and isolated from mammalian cells and a chemotherapeutic agent.
    Type: Grant
    Filed: August 16, 2017
    Date of Patent: June 14, 2022
    Assignee: Henry Ford Health System
    Inventors: Zhenggang Zhang, Yi Zhang, Michael Chopp
  • Publication number: 20220000932
    Abstract: Some embodiments comprise a method and kit for the treatment and prevention of stroke by administering a therapeutically effective combination of mammalian exosomes and/or microvesicles, collectively referred to as extracellular vesicles, and Tissue Plasminogen Activator (tPA), and/or a thrombectomy procedure, to a subject in need thereof. Some embodiments comprise a method and kit for the treatment and prevention of cerebrovascular injury caused by a stroke by administering a therapeutically effective combination of mammalian exosomes, Tissue Plasminogen Activator (tPA), and/or a thrombectomy procedure, to a subject in need thereof. Some embodiments also comprise the administration a therapeutically effective amount of a combination comprising mammalian exosomes and Tissue Plasminogen Activator (tPA) to a subject in need thereof; the mammalian exosomes containing one or more microRNAs selected from miR-19a, miR-21, and miR-146a.
    Type: Application
    Filed: September 27, 2019
    Publication date: January 6, 2022
    Applicant: Henry Ford Health System
    Inventors: Zhenggang Zhang, Li Zhang, Michael Chopp, Benjamin Buller
  • Publication number: 20200297779
    Abstract: Some embodiments comprise methods, systems, and/or compositions comprising the production and/or use of one or agents selected from a group comprising microRNA-126, a promoter of microRNA-126 expression, a microRNA-126 mimic, cells such as human umbilical cord blood cells (“HUCBCs”), endothelial cells (“EC”), endothelial progenitor cells (“EPC”), and microRNA-126-enriched Exosomes/Microvesicles (“EMVs”) to promote, increase, or improve recovery from conditions, diseases, or injuries and/or function or outcome in a patient in need thereof.
    Type: Application
    Filed: May 28, 2020
    Publication date: September 24, 2020
    Inventors: Jieli CHEN, Michael CHOPP
  • Publication number: 20200297750
    Abstract: Provided herein are methods for the prevention and treatment of cardiovascular diseases and disorders in a subject diagnosed as having suffered a cerebrovascular injury by administering agents that contain or induce the expression of microRNA-126.
    Type: Application
    Filed: November 14, 2018
    Publication date: September 24, 2020
    Inventors: Jieli CHEN, Michael CHOPP
  • Patent number: 10548983
    Abstract: Methods for treating a subject in need thereof are provided which include administering a pharmaceutical composition comprising a protein transduction reagent-modified reprogramming protein to the subject, wherein the protein transduction reagent is non-covalently bound to the reprogramming protein and wherein the protein transduction reagent comprises a cation reagent and a lipid. According to aspects, such methods provide delivery of protein-transduction reagent-modified reprogramming proteins to cancer cells, such as tumor cells, as well as diseased cells of diseased tissues and provide in vivo conversion of diseased cells into normal cells via protein-induced in situ cell reprogramming without administration of nucleic acids to the subject.
    Type: Grant
    Filed: September 4, 2018
    Date of Patent: February 4, 2020
    Assignee: Wayne State University
    Inventors: Jianjun Wang, Qianqian Li, Michael Chopp, Feng Jiang, Guojun Wu
  • Publication number: 20190175661
    Abstract: Without limitation, a method for preventing and/or treating neuropathic pain in a subject/patient comprising administering a therapeutically effective amount of exosomes derived and isolated from mammalian cells to the subject/patient and a method of treating cancer in a subject/patient in need thereof, comprises administering a combination comprising a therapeutically effective amount of exosomes derived and isolated from mammalian cells and a chemotherapeutic agent.
    Type: Application
    Filed: August 16, 2017
    Publication date: June 13, 2019
    Inventors: Zhenggang ZHANG, Yi ZHANG, Michael CHOPP
  • Patent number: 10308959
    Abstract: Some embodiments comprise methods, systems, and compositions to promote, improve and/or increase neuronal differentiation, oligodendrocyte differentiation, or neurological outcome or function in a patient in need thereof. Some embodiments also comprise the administration a composition comprising a pharmaceutically effective amount of one or more of a group comprising microRNA-146a, exosomes comprising microRNA-146a, a promoter of microRNA-146a expression, a microRNA-146a thymosin beta 4, and a phosphodiesterase 5 inhibitor to treat neurological conditions, diseases, or injuries in mammals, including in human beings.
    Type: Grant
    Filed: May 19, 2017
    Date of Patent: June 4, 2019
    Assignee: Henry Ford Health System
    Inventors: Xianshuang Liu, Zhenggang Zhang, Michael Chopp, Lei Wang, Benjamin A. L. Buller
  • Patent number: 10227593
    Abstract: Some embodiments comprise methods, systems, and compositions to produce and/or administer modified exosomes or other vesicles containing one or more selected microRNAs, including but not limited to, miR-146b. Some embodiments also comprise the therapeutic administration and use of such modified exosomes and/or producer cells to treat mammalian brain or neurologic injuries and diseases, including in human beings.
    Type: Grant
    Filed: December 23, 2016
    Date of Patent: March 12, 2019
    Assignee: Henry Ford Health System
    Inventors: Mark E. Katakowski, Benjamin A. L. Buller, Michael Chopp
  • Publication number: 20190060367
    Abstract: Described herein is a method for treating and/or ameliorating at least one symptom associated with traumatic brain injury in a subject, the method comprises administering a safe and therapeutically effective amount of a composition comprising exosomes generated from hMSCs in 2D or 3D cultures.
    Type: Application
    Filed: March 3, 2017
    Publication date: February 28, 2019
    Applicant: Henry Ford Health System
    Inventors: Zheng Gang Zhang, Ye Xiong, Michael Chopp
  • Publication number: 20190000982
    Abstract: Methods for treating a subject in need thereof are provided which include administering a pharmaceutical composition comprising a protein transduction reagent-modified reprogramming protein to the subject, wherein the protein transduction reagent is non-covalently bound to the reprogramming protein and wherein the protein transduction reagent comprises a cation reagent and a lipid. According to aspects, such methods provide delivery of protein-transduction reagent-modified reprogramming proteins to cancer cells, such as tumor cells, as well as diseased cells of diseased tissues and provide in vivo conversion of diseased cells into normal cells via protein-induced in situ cell reprogramming without administration of nucleic acids to the subject.
    Type: Application
    Filed: September 4, 2018
    Publication date: January 3, 2019
    Applicant: Qurgen, Inc.
    Inventors: Jianjun Wang, Qianqian Li, Michael Chopp, Feng Jiang, Guojun Wu
  • Patent number: 10076574
    Abstract: Methods for treating a subject in need thereof are provided which include administering a pharmaceutical composition comprising a protein transduction reagent-modified reprogramming protein to the subject, wherein the protein transduction reagent is non-covalently bound to the reprogramming protein and wherein the protein transduction reagent comprises a cation reagent and a lipid. According to aspects, such methods provide delivery of protein-transduction reagent-modified reprogramming proteins to cancer cells, such as tumor cells, as well as diseased cells of diseased tissues and provide in vivo conversion of diseased cells into normal cells via protein-induced in situ cell reprogramming without administration of nucleic acids to the subject.
    Type: Grant
    Filed: October 27, 2014
    Date of Patent: September 18, 2018
    Assignee: Wayne State University
    Inventors: Jianjun Wang, Qianqian Li, Michael Chopp, Feng Jiang, Guojun Wu
  • Publication number: 20170321225
    Abstract: Some embodiments comprise methods, systems, and compositions to promote, improve and/or increase neuronal differentiation, oligodendrocyte differentiation, or neurological outcome or function in a patient in need thereof. Some embodiments also comprise the administration a composition comprising a pharmaceutically effective amount of one or more of a group comprising microRNA-146a, exosomes comprising microRNA-146a, a promoter of microRNA-146a expression, a microRNA-146a thymosin beta 4, and a phosphodiesterase 5 inhibitor to treat neurological conditions, diseases, or injuries in mammals, including in human beings.
    Type: Application
    Filed: May 19, 2017
    Publication date: November 9, 2017
    Inventors: Xianshuang Liu, Zhenggang Zhang, Michael Chopp, Lei Wang, Benjamin A.L. Buller
  • Patent number: 9775883
    Abstract: Without limitation, some embodiments comprise a method of treatment for promoting recovery of peripheral neuropathy in a subject, including administering to a subject in need of such treatment a therapeutically effective amount of a composition comprised of thymosin beta 4, amino acid sequences LKKTET or LKKTNT, and/or any conservative variants thereof, or an agent that stimulates production of any of those materials, or a conservative variant thereof.
    Type: Grant
    Filed: December 21, 2012
    Date of Patent: October 3, 2017
    Assignee: Henry Ford Health System
    Inventors: Michael Chopp, Zhenggang Zhang, Daniel C. Morris, Lei Wang
  • Publication number: 20170247708
    Abstract: Some embodiments comprise methods, systems, and compositions to produce and/or administer modified exosomes or other vesicles containing one or more selected microRNAs, including but not limited to, miR-146b. Some embodiments also comprise the therapeutic administration and use of such modified exosomes and/or producer cells to treat mammalian brain or neurologic injuries and diseases, including in human beings.
    Type: Application
    Filed: December 23, 2016
    Publication date: August 31, 2017
    Applicant: Henry Ford Health System
    Inventors: Mark E. Katakowski, Benjamin A.L. Buller, Michael Chopp
  • Patent number: 9670490
    Abstract: Some embodiments comprise methods, systems, and compositions to promote, improve and/or increase neuronal differentiation, oligodendrocyte differentiation, or neurological outcome or function in a patient in need thereof. Some embodiments also comprise the administration a composition comprising a pharmaceutically effective amount of one or more of a group comprising microRNA-146a, a promoter of microRNA-146a expression, a microRNA-146a mimic, thymosin beta 4, and a phosphodiesterase 5 inhibitor to treat neurological conditions, disease, or injury in mammals, including in human beings.
    Type: Grant
    Filed: January 22, 2014
    Date of Patent: June 6, 2017
    Assignee: Henry Ford Health System
    Inventors: Xianshuang Liu, Zhenggang Zhang, Michael Chopp, Lei Wang