Patents by Inventor Iori Ohmori

Iori Ohmori 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: 11970706
    Abstract: Provided is a nonhuman animal model that is obtained by modifying a gene encoding thioredoxin and useful as a disease model of aging, kidney diseases, cardiovascular diseases, hypertension, aortic dissection, chronic obstructive lung disease, age-dependent epilepsy, abnormality of lipid metabolism, anemia, osteoporosis, abnormal immunity, etc. These variety of phenotypes are caused by the fact that a modification of a gene encoding thioredoxin induces hypofunction of thioredoxin expressed in multiple organs throughout the body. The gene encoding thioredoxin is a gene selected from among TXN, TRX, TRX1, RRDX, Txn1, Txn, Trx1 and ADF.
    Type: Grant
    Filed: December 6, 2018
    Date of Patent: April 30, 2024
    Assignees: HAMAMATSU PHOTONICS K.K.
    Inventors: Iori Ohmori, Mamoru Ouchida, Tomoji Mashimo
  • Publication number: 20210171978
    Abstract: Provided is a nonhuman animal model that is obtained by modifying a gene encoding thioredoxin and useful as a disease model of aging, kidney diseases, cardiovascular diseases, hypertension, aortic dissection, chronic obstructive lung disease, age-dependent epilepsy, abnormality of lipid metabolism, anemia, osteoporosis, abnormal immunity, etc. These variety of phenotypes are caused by the fact that a modification of a gene encoding thioredoxin induces hypofunction of thioredoxin expressed in multiple organs throughout the body. The gene encoding thioredoxin is a gene selected from among TXN, TRX, TRX1, RRDX, Txn1, Txn, Trx1 and ADF.
    Type: Application
    Filed: December 6, 2018
    Publication date: June 10, 2021
    Applicant: HAMAMATSU PHOTONICS K.K.
    Inventors: Iori OHMORI, Mamoru OUCHIDA, Tomoji MASHIMO
  • Publication number: 20190160093
    Abstract: Provided is an inhalation gas device for a therapy of a disease accompanied by epileptiform discharges comprising a medical gas bottle, and a medical inhalation gas device connected to the medical gas bottle, the inhalation gas device for a therapy of a disease accompanied by epileptiform discharges including the following 1) and 2): 1) a therapeutic agent for a disease accompanied by epileptiform discharges containing carbon dioxide as an active ingredient being filled in the medical gas bottle; and 2) the medical inhalation gas device being provided with a gas inhalation mask.
    Type: Application
    Filed: February 1, 2019
    Publication date: May 30, 2019
    Inventors: Mamoru Ouchida, Iori Ohmori, Yuko Kaida, Hirotsugu Takeuchi, Mitsuhiro Ogawa, Toshie Furuumi
  • Publication number: 20160166605
    Abstract: Provided is a therapeutic agent for a disease accompanied by epileptiform discharges, which is easily-handled, has a low side effect, and has a fast acting property. By controlling the concentration of carbon dioxide of inhaled air, it is possible to change the pH in body fluids to an acidic side to reduce epileptiform discharges. Carbon dioxide is an active ingredient of a therapeutic agent for a disease accompanied by epileptiform discharges.
    Type: Application
    Filed: July 12, 2011
    Publication date: June 16, 2016
    Applicant: National University Corporation Okayama University
    Inventors: Mamoru OUCHIDA, Iori OHMORI, Yuko KAIDA
  • Patent number: 8916743
    Abstract: Provided is a method of assessing a potential for development of Dravet syndrome with high accuracy, and use thereof. The method according to the present invention of assessing a potential for development of Dravet syndrome includes, with use of a sample taken from a subject, detecting whether or not a mutation is on ?-subunit type 1 of voltage-gated sodium ion channel NaV1.1, and detecting whether or not a mutation is on ?-subunit type 1 of voltage-gated calcium ion channel CaV2.1.
    Type: Grant
    Filed: June 23, 2014
    Date of Patent: December 23, 2014
    Assignee: National University Corporation Okayama University
    Inventors: Iori Ohmori, Mamoru Ouchida
  • Publication number: 20140304843
    Abstract: Provided is a method of assessing a potential for development of Dravet syndrome with high accuracy, and use thereof. The method according to the present invention of assessing a potential for development of Dravet syndrome includes, with use of a sample taken from a subject, detecting whether or not a mutation is on ?-subunit type 1 of voltage-gated sodium ion channel NaV1.1, and detecting whether or not a mutation is on ?-subunit type 1 of voltage-gated calcium ion channel CaV2.1.
    Type: Application
    Filed: June 23, 2014
    Publication date: October 9, 2014
    Inventors: Iori Ohmori, Mamoru Ouchida
  • Publication number: 20130036482
    Abstract: Provided is a method of assessing a potential for development of Dravet syndrome with high accuracy, and use thereof. The method according to the present invention of assessing a potential for development of Dravet syndrome includes, with use of a sample taken from a subject, detecting whether or not a mutation is on ?-subunit type 1 of voltage-gated sodium ion channel NaV1.1, and detecting whether or not a mutation is on ?-subunit type 1 of voltage-gated calcium ion channel CaV2.1.
    Type: Application
    Filed: January 27, 2011
    Publication date: February 7, 2013
    Applicant: NATIONAL UNIVERSITY CORPORATION OKAYAMA UNIVERSITY
    Inventors: Iori Ohmori, Mamoru Ouchida