PETIT; Christine

Patent Applications and Registrations

Patent applications and USPTO patent grants for PETIT; Christine.The latest application filed is for "aav-mediated gene therapy restoring the otoferlin gene".

Company Profile

3.9.14

PETIT; Christine - Paris FR
Petit; Christine - Le Plessis-Robinson FR

*profile and listings may contain filings by different individuals or companies with the same name. Review application materials to confirm ownership/assignment.

Patent Activity

Patent	Date
Aav-mediated Gene Therapy Restoring The Otoferlin Gene App 20220125875 - SAFIEDDINE; Saaid ; et al.	2022-04-28
Prevention And/or Treatment Of Hearing Loss Or Impairment App 20200353039 - PETIT; Christine ; et al.	2020-11-12
Prevention and/or treatment of hearing loss or impairment Grant 10,751,385 - Petit , et al. A	2020-08-25
Prevention And/or Treatment Of Hearing Loss Or Impairment App 20180055908 - PETIT; Christine ; et al.	2018-03-01
Mutation within the connexin 26 gene responsible for prelingual non-syndromic deafness and method of detection Grant 9,868,989 - Petit , et al. January 16, 2	2018-01-16
Mutation Within The Connexin 26 Gene Responsible For Prelingual Non-syndromic Deafness And Method Of Detection App 20160076101 - Petit; Christine ; et al.	2016-03-17
Mutation within the connexin 26 gene responsible for prelingual non-syndromic deafness and method of detection Grant 9,169,517 - Petit , et al. October 27, 2	2015-10-27
Mutation Within The Connexin 26 Gene Responsible For Prelingual Non-syndromic Deafness And Method Of Detection App 20140113285 - PETIT; Christine ; et al.	2014-04-24
Mutation within the connexin 26 gene responsible for prelingual non-syndromic deafness and method of detection Grant 8,455,195 - Petit , et al. June 4, 2	2013-06-04
Mutation Within The Connexin 26 Gene Responsible For Prelingual Non-syndromic Deafness And Method Of Detection App 20120322059 - Petit; Christine ; et al.	2012-12-20
Mutation within the connexin 26 gene responsible for prelingual non-syndromic deafness and method of detection Grant 8,143,000 - Petit , et al. March 27, 2	2012-03-27
Use of adiponectin for the diagnosis and/or treatment of presbycusis App 20110059855 - Petit; Christine ; et al.	2011-03-10
Mutation within the connexin 26 gene responsible for prelingual non-syndromic deafness and method of detection App 20090104600 - Petit; Christine ; et al.	2009-04-23
Mutation within the connexin 26 gene responsible for prelingual non-syndromic deafness and method of detection Grant 7,258,975 - Petit , et al. August 21, 2	2007-08-21
Therapeutic composition comprising the KAL protein and use of the KAL protein for the treatment of retinal, renal, neuronal and neural injury App 20070037736 - Petit; Christine ; et al.	2007-02-15
Use of the KAL protein and treatment with the KAL protein in treatment of retinal, renal, neuronal and neural injury Grant 6,770,743 - Petit , et al. August 3, 2	2004-08-03
Mutation within the connexin 26 gene responsible for prelingual non-syndromic deafness and method of detection App 20030170676 - Petit, Christine ; et al.	2003-09-11
More protein-protein interactions in the inner ear App 20030148381 - Daviet, Laurent ; et al.	2003-08-07
Use of the KAL protein and treatment with the KAL protein in treatment of retinal, renal, neuronal and neural injury App 20030060401 - Petit, Christine ; et al.	2003-03-27
Therapeutic composition comprising the KAL protein and use of the KAL protein for the treatment of retinal, renal, neuronal and neural injury App 20020123467 - Petit, Christine ; et al.	2002-09-05
Mutated polynucleotide corresponding to a mutation responsible for prelingual non-syndromic deafness in the connexin 26 gene and method of detecting this hereditary defect Grant 5,998,147 - Petit , et al. December 7, 1	1999-12-07

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