Patents by Inventor Dominique Weil

Dominique Weil 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).

  • Mutation within the connexin 26 gene responsible for prelingual non-syndromic deafness and method of detection
    Patent number: 9868989
    Abstract: A purified polynucleotide having a chain of nucleotides corresponding to a mutated sequence, which in a wild form encodes a polypeptide implicated in hereditary sensory defect wherein said mutated purified polynucleotide presents a mutation responsible for prelingual non-syndromic deafness selected from the group consisting of a specific deletion of at least one nucleotide.
    Type: Grant
    Filed: September 18, 2015
    Date of Patent: January 16, 2018
    Assignee: INSTITUT PASTEUR
    Inventors: Christine Petit, Francoise Denoyelle-Gryson, Dominique Weil, Sandrine Marlin, Jean-Luc Guesdon
  • MUTATION WITHIN THE CONNEXIN 26 GENE RESPONSIBLE FOR PRELINGUAL NON-SYNDROMIC DEAFNESS AND METHOD OF DETECTION
    Publication number: 20160076101
    Abstract: A purified polynucleotide having a chain of nucleotides corresponding to a mutated sequence, which in a wild form encodes a polypeptide implicated in hereditary sensory defect wherein said mutated purified polynucleotide presents a mutation responsible for prelingual non-syndromic deafness selected from the group consisting of a specific deletion of at least one nucleotide.
    Type: Application
    Filed: September 18, 2015
    Publication date: March 17, 2016
    Applicant: Institut Pasteur
    Inventors: Christine Petit, Francoise Denoyelle-Gryson, Dominique Weil, Sandrine Marlin, Jean-Luc Guesdon
  • Mutation within the connexin 26 gene responsible for prelingual non-syndromic deafness and method of detection
    Patent number: 9169517
    Abstract: A purified polynucleotide having a chain of nucleotides corresponding to a mutated sequence, which in a wild form encodes a polypeptide implicated in hereditary sensory defect, wherein said mutated purified polynucleotide presents a mutation responsible for prelingual non-syndromic deafness selected from the group consisting of a specific deletion of at least one nucleotide.
    Type: Grant
    Filed: May 22, 2013
    Date of Patent: October 27, 2015
    Assignee: INSTITUT PASTEUR
    Inventors: Christine Petit, Francoise Denoyelle-Gryson, Dominique Weil, Sandrine Marlin, Jean-Luc Guesdon
  • MUTATION WITHIN THE CONNEXIN 26 GENE RESPONSIBLE FOR PRELINGUAL NON-SYNDROMIC DEAFNESS AND METHOD OF DETECTION
    Publication number: 20140113285
    Abstract: A purified polynucleotide having a chain of nucleotides corresponding to a mutated sequence, which in a wild form encodes a polypeptide implicated in hereditary sensory defect, wherein said mutated purified polynucleotide presents a mutation responsible for prelingual non-syndromic deafness selected from the group consisting of a specific deletion of at least one nucleotide.
    Type: Application
    Filed: May 22, 2013
    Publication date: April 24, 2014
    Applicants: Centre National de la Recherche Scientifique, Institut Pasteur
    Inventors: Christine PETIT, Francoise Denoyelle-Gryson, Dominique Weil, Sandrine Marlin-Duvernois, Jean-Luc Guesdon
  • Mutation within the connexin 26 gene responsible for prelingual non-syndromic deafness and method of detection
    Patent number: 8455195
    Abstract: A purified polynucleotide having a chain of nucleotides corresponding to a mutated sequence, which in a wild form encodes a polypeptide implicated in hereditary sensory defect, wherein said mutated purified polynucleotide presents a mutation responsible for prelingual non-syndromic deafness selected from the group consisting of a specific deletion of at least one nucleotide.
    Type: Grant
    Filed: March 26, 2012
    Date of Patent: June 4, 2013
    Assignee: Institut Pasteur
    Inventors: Christine Petit, Françoise Denoyelle-Gryson, Dominique Weil, Sandrine Marlin-Duvernois, Jean-Luc Guesdon
  • MUTATION WITHIN THE CONNEXIN 26 GENE RESPONSIBLE FOR PRELINGUAL NON-SYNDROMIC DEAFNESS AND METHOD OF DETECTION
    Publication number: 20120322059
    Abstract: A purified polynucleotide having a chain of nucleotides corresponding to a mutated sequence, which in a wild form encodes a polypeptide implicated in hereditary sensory defect, wherein said mutated purified polynucleotide presents a mutation responsible for prelingual non-syndromic deafness selected from the group consisting of a specific deletion of at least one nucleotide.
    Type: Application
    Filed: March 26, 2012
    Publication date: December 20, 2012
    Applicant: Institut Pasteur
    Inventors: Christine Petit, Françoise Denoyelle-Gryson, Dominique Weil, Sandrine Marlin-Duvernois, Jean-Luc Guesdon
  • Mutation within the connexin 26 gene responsible for prelingual non-syndromic deafness and method of detection
    Patent number: 8143000
    Abstract: A purified polynucleotide having a chain of nucleotides corresponding to a mutated sequence, which in a wild form encodes a polypeptide implicated in hereditary sensory defect, wherein said mutated purified polynucleotide presents a mutation responsible for prelingual non-syndromic deafness selected from the group consisting of a specific deletion of at least one nucleotide.
    Type: Grant
    Filed: July 12, 2007
    Date of Patent: March 27, 2012
    Assignee: Institut Pasteur
    Inventors: Christine Petit, Françoise Denoyelle-Gryson, Dominique Weil, Sandrine Marlin-Duvernois, Jean-Luc Guesdon
  • Use of adiponectin for the diagnosis and/or treatment of presbycusis
    Publication number: 20110059855
    Abstract: The present invention relates to mutations located within the gene coding for adiponectin, said mutations being associated with presbycusis. The present invention further relates to adiponectin polynucleotides comprising such mutations, to adiponectin polypeptides encoded by such polynucleotides, and to methods of diagnosing and/or treating presbycusis using adiponectin polynucleotides, adiponectin polypeptides and/or ADIPOR2 polypeptides.
    Type: Application
    Filed: February 9, 2009
    Publication date: March 10, 2011
    Applicants: INSTITUT PASTEUR
    Inventors: Christine Petit, Mark Lathrop, Anne Aubois, Christian Kubisch, Dominique Weil, Valerie Franco-Vidal, Arnaud Coez, Jose-Alain Sahel
  • Mutation within the connexin 26 gene responsible for prelingual non-syndromic deafness and method of detection
    Publication number: 20090104600
    Abstract: A purified polynucleotide having a chain of nucleotides corresponding to a mutated sequence, which in a wild form encodes a polypeptide implicated in hereditary sensory defect, wherein said mutated purified polynucleotide presents a mutation responsible for prelingual non-syndromic deafness selected from the group consisting of a specific deletion of at least one nucleotide.
    Type: Application
    Filed: July 12, 2007
    Publication date: April 23, 2009
    Inventors: Christine Petit, Francoise Denoyelle-Gryson, Dominique Weil, Sandrine Marlin-Duvernois, Jean-Luc Guesdon
  • Mutation within the connexin 26 gene responsible for prelingual non-syndromic deafness and method of detection
    Patent number: 7258975
    Abstract: A purified polynucleotide having a chain of nucleotides corresponding to a mutated sequence, which in wildtype form encodes a polypeptide implicated in hereditary sensory defect, wherein said mutated purified polynucleotide presents a mutation responsible for prelingual non-syndromic deafness selected from the group consisting of a specific deletion of at least one nucleotide.
    Type: Grant
    Filed: October 23, 2002
    Date of Patent: August 21, 2007
    Assignee: Institut Pasteur
    Inventors: Christine Petit, Françoise Denoyelle-Gryson, Dominique Weil, Sandrine Marlin-Duvernois, Jean-Luc Guesdon
  • Mutation within the connexin 26 gene responsible for prelingual non-syndromic deafness and method of detection
    Publication number: 20030170676
    Abstract: A purified polynucleotide having a chain of nucleotides corresponding to a mutated sequence, which in a wild form encodes a polypeptide implicated in hereditary sensory defect, wherein said mutated purified polynucleotide presents a mutation responsible for prelingual non-syndromic deafness selected from the group consisting of a specific deletion of at least one nucleotide.
    Type: Application
    Filed: October 23, 2002
    Publication date: September 11, 2003
    Applicant: Institute Pasteur
    Inventors: Christine Petit, Francoise Denoyelle-Gryson, Dominique Weil, Sandrine Marlin-Duvernois, Jean-Luc Guesdon
  • Mutation within the connexin 26 gene responsible for prelingual non-syndromic deafness and method of detection
    Patent number: 6485908
    Abstract: A purified polynucleotide having a chain of nucleotides corresponding to a mutated sequence, which in wild-type form encodes a polypeptide implicated in hereditary sensory defect, wherein the mutated purified polynucleotide presents a mutation responsible for prelingual non-syndromic deafness selected from the group consisting of a specific deletion of at least one nucleotide.
    Type: Grant
    Filed: May 3, 2000
    Date of Patent: November 26, 2002
    Assignee: Institut Pasteur
    Inventors: Christine Petit, Françoise Denoyelle-Gryson, Dominique Weil, Sandrine Marlin-Duvernois, Jean-Luc Guesdon
  • Mutated polynucleotide corresponding to a mutation responsible for prelingual non-syndromic deafness in the connexin 26 gene and method of detecting this hereditary defect
    Patent number: 5998147
    Abstract: A purified polynucleotide having a chain of nucleotides corresponding to a mutated sequence, which in a wild type form encodes a polypeptide implicated in hereditary sensory defect, wherein said mutated purified polynucleotide presents a mutation responsible for prelingual non-syndromic deafness selected from the group consisting of a specific deletion of at least one nucleotide.
    Type: Grant
    Filed: August 14, 1998
    Date of Patent: December 7, 1999
    Assignee: Institut Pasteur
    Inventors: Christine Petit, Francoise Denoyelle-Gryson, Dominique Weil, Sandrine Marlin-Duvernois, Jean-Luc Guesdon