Patents by Inventor David J. Glass

David J. Glass 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: 7355018
    Abstract: A targeting fusion protein comprising a component that comprises a (i) ligand or derivative or fragment thereof that binds a pre-selected target surface protein, such as a receptor, and (ii) an active agent or therapeutic agent(s), and further optionally (iii) a multimerizing component and/or (iv) a signal sequence. In a preferred embodiment, the targeting fusion polypeptide targets muscle and is useful to treat a muscle-related disease or condition, such as muscle atrophy.
    Type: Grant
    Filed: September 30, 2004
    Date of Patent: April 8, 2008
    Assignee: Regeneron Pharmaceuticals, Inc.
    Inventor: David J. Glass
  • Patent number: 7122648
    Abstract: The present invention provides for nucleic acid sequences that encode novel mammalian intracellular signaling polypeptides, designated MINC102. The invention also provides assay systems that may be used to detect and/or measure agents that bind the MINC102 gene product. The present invention also provides for diagnostic and therapeutic methods for treating muscle atrophy by inhibiting expression or activity of MINC102.
    Type: Grant
    Filed: July 18, 2003
    Date of Patent: October 17, 2006
    Assignee: Regeneron Pharmaceuticals, Inc.
    Inventor: David J. Glass
  • Patent number: 6852838
    Abstract: The present invention provides for a gene, designated as musk, that encodes a novel tyrosine kinase receptor expressed in high levels in denervated muscle. The invention also provides for an isolated polypeptide which activates MuSK receptor. The invention further provides for a polypeptide which is functionally equivalent to the MuSK activating polypeptide. The invention also provides assay systems that may be used to detect and/or measure ligands that bind the musk gene product. The present invention also provides for diagnostic and therapeutic methods based on molecules that activate MuSK.
    Type: Grant
    Filed: November 30, 2001
    Date of Patent: February 8, 2005
    Assignee: Regeneron Pharmaceuticals, Inc.
    Inventors: David M. Valenzuela, David J. Glass, David C. Bowen, George D. Yancopoulos
  • Publication number: 20040214285
    Abstract: A HIV-specific fusion polypeptide, comprising (a) one or more domains which comprise a cellular co-receptor protein, or a fragment, derivative, or functional equivalent thereof; (b) one or more domains which comprise a cellular receptor protein, or a fragment, derivative, or functional equivalent thereof; and optionally (c) a multimerizing component, and (d) one or more domains of a viral protein, or a fragment or derivative thereof. In specific embodiments, the HIV-specific fusion protein is a multimer capable of binding an HIV particle, and is useful for the treatment of HIV infections.
    Type: Application
    Filed: January 30, 2004
    Publication date: October 28, 2004
    Inventors: David J. Glass, Margaret Karow, Eric Smith
  • Publication number: 20040018547
    Abstract: The present invention provides for nucleic acid sequences that encode novel mammalian intracellular signaling polypeptides, designated MINC102. The invention also provides assay systems that may be used to detect and/or measure agents that bind the MINC102 gene product. The present invention also provides for diagnostic and therapeutic methods for treating muscle atrophy by inhibiting expression or activity of MINC102.
    Type: Application
    Filed: July 18, 2003
    Publication date: January 29, 2004
    Inventor: David J. Glass
  • Publication number: 20030219739
    Abstract: The present invention provides for nucleic acid sequences that encode novel mammalian intracellular signaling polypeptides, designated MURF1, MURF3, or MA-61. The invention also provides assay systems that may be used to detect and/or measure agents that bind the MURF1 or MAFBXgene product. The present invention also provides for diagnostic and therapeutic methods based on the interaction between MURF1 or MAFBXand agents that initiate signal transduction or inhibition of ubiqutination through binding to MURF1 or MA-61, inhibiting the mRNA expression of MURF1, MURF3, or MA-61, or inhibiting the MURF, MURF3, or MAFBXpathway.
    Type: Application
    Filed: January 30, 2002
    Publication date: November 27, 2003
    Inventors: David J. Glass, Sue C. Bodine
  • Publication number: 20030129686
    Abstract: The present invention provides for nucleic acid sequences that encode novel mammalian intracellular signaling polypeptides, designated MURF1, MURF3, or MA-61. The invention also provides assay systems that may be used to detect and/or measure agents that bind the MURF1 or MAFBXgene product.
    Type: Application
    Filed: January 30, 2002
    Publication date: July 10, 2003
    Inventors: David J. Glass, Sue C. Bodine
  • Publication number: 20020164702
    Abstract: The present invention provides for a gene, designated as musk, that encodes a novel tyrosine kinase receptor expressed in high levels in denervated muscle. The invention also provides for an isolated polypeptide which activates MuSK receptor. The invention further provides for a polypeptide which is functionally equivalent to the MuSK activating polypeptide. The invention also provides assay systems that may be used to detect and/or measure ligands that bind the musk gene product. The present invention also provides for diagnostic and therapeutic methods based on molecules that activate MuSK.
    Type: Application
    Filed: November 30, 2001
    Publication date: November 7, 2002
    Inventors: David M. Valenzuela, David J. Glass, David C. Bowen, George D. Yancopoulos
  • Publication number: 20020123456
    Abstract: The present invention provides a method for inhibiting atrophy or causing hypertrophy in muscle cells, by inhibiting the action of the phosphatase SHIP2. It further provides a method for inhibiting skeletal muscle atrophy or causing skeletal muscle hypertrophy in vertebrate animals, by inhibiting the Akt pathway through the inhibition of SHIP2. It also provides a method of identifying agents that may be used for inhibiting atrophy or causing hypertrophy in muscle cells, by screening for inhibitors of SHIP2 or inhibitors of the SHIP2 signaling pathway.
    Type: Application
    Filed: February 28, 2002
    Publication date: September 5, 2002
    Inventor: David J. Glass
  • Patent number: 6413740
    Abstract: The present invention provides for a gene, designated as musk, that encodes a novel tyrosine kinase receptor expressed in high levels in denervated muscle. The invention also provides for an isolated polypeptide which activates MuSK receptor. The invention further provides for a polypeptide which is functionally equivalent to the MuSK activating polypeptide. The invention also provides assay systems that may be used to detect and/or measure ligands that bind the musk gene product. The present invention also provides for diagnostic and therapeutic methods based on molecules that activate MuSK.
    Type: Grant
    Filed: September 10, 1998
    Date of Patent: July 2, 2002
    Assignee: Regeneron Pharmaceuticals, Inc.
    Inventors: David M. Valenzuela, David J. Glass, David C. Bowen, George D. Yancopoulos
  • Patent number: 5814478
    Abstract: The present invention provides for a gene, designated as musk, that encodes a novel tyrosine kinase receptor expressed in high levels in denervated muscle. The invention also provides for an isolated and purified polypeptide which activates MuSK receptor. The invention further provides for a polypeptide which is functionally equivalent to the MuSK activating polypeptide. The invention also provides assay systems that may be used to detect and/or measure ligands that bind the musk gene product. The present invention also provides for diagnostic and therapeutic methods based on molecules that activate MuSK.
    Type: Grant
    Filed: May 10, 1996
    Date of Patent: September 29, 1998
    Assignee: Regeneron Pharmaceuticals, Inc.
    Inventors: David M. Valenzuela, David J. Glass, David C. Bowen, George D. Yancopoulos