Inventor · disambiguated record
Christine Petit
Also filed as: PETIT CHRISTINE
13 granted patents·8 pending applications·60 citations·filing 1992–2023
90Inventor score
Top patents by PatentIndex Score
21 records- 0171US5998147AMutated polynucleotide corresponding to a mutation responsible for prelingual non-syndromic deafness in the connexin 26 gene and method of detecting this hereditary defectPASTEUR INSTITUT·Filed 1998·Granted Dec 7, 1999·25 cites·31 claims
- 0269US9169517B2Mutation within the connexin 26 gene responsible for prelingual non-syndromic deafness and method of detectionPASTEUR INSTITUT·Filed 2013·Granted Oct 27, 2015·0 cites·6 claims
- 0367US2023405085A1Prevention and/or treatment of hearing loss or impairmentPASTEUR INSTITUT·Filed 2023·Application pending·0 cites
- 0466US8143000B2Mutation within the connexin 26 gene responsible for prelingual non-syndromic deafness and method of detectionPETIT CHRISTINE·Filed 2007·Granted Mar 27, 2012·0 cites·16 claims
- 0565US6548475B1Use of the KAL protein and treatment with the KAL protein in treatment of retinal, renal, neuronal and neural injuryPASTEUR INSTITUT·Filed 2000·Granted Apr 15, 2003·3 cites·5 claims
- 0664US8455195B2Mutation within the connexin 26 gene responsible for prelingual non-syndromic deafness and method of detectionPETIT CHRISTINE·Filed 2012·Granted Jun 4, 2013·0 cites·12 claims
- 0763US10751385B2Prevention and/or treatment of hearing loss or impairmentPASTEUR INSTITUT·Filed 2016·Granted Aug 25, 2020·1 cites·7 claims
- 0863US9868989B2Mutation within the connexin 26 gene responsible for prelingual non-syndromic deafness and method of detectionPASTEUR INSTITUT·Filed 2015·Granted Jan 16, 2018·0 cites·11 claims
- 0962US11679140B2Prevention and/or treatment of hearing loss or impairmentPASTEUR INSTITUT·Filed 2020·Granted Jun 20, 2023·0 cites·17 claims
- 1061US7258975B2Mutation within the connexin 26 gene responsible for prelingual non-syndromic deafness and method of detectionPASTEUR INSTITUT·Filed 2002·Granted Aug 21, 2007·0 cites·12 claims
- 1161US6485908B1Mutation within the connexin 26 gene responsible for prelingual non-syndromic deafness and method of detectionPASTEUR INSTITUT·Filed 1998·Granted Nov 26, 2002·13 cites·12 claims
- 1260US6770743B2Use of the KAL protein and treatment with the KAL protein in treatment of retinal, renal, neuronal and neural injuryPASTEUR INSTITUT·Filed 2002·Granted Aug 3, 2004·1 cites·10 claims
- 1357US6121231AUse of the KAL protein and treatment with the KAL protein in treatment of retinal, renal, neuromal and neural injuryPASTEUR INSTITUT·Filed 1996·Granted Sep 19, 2000·13 cites·4 claims
- 1457US2007037736A1Therapeutic composition comprising the KAL protein and use of the KAL protein for the treatment of retinal, renal, neuronal and neural injuryCENTRE NAT RECH SCIENT·Filed 2006·Application pending·0 cites
- 1554US2025295716A1Dual recombinant aav8 vector system encoding isoform 5 of otoferlin and uses thereofPASTEUR INSTITUT·Filed 2022·Application pending·0 cites
- 1652US2024050520A1Gene therapy for treating usher syndromePASTEUR INSTITUT·Filed 2021·Application pending·0 cites
- 1746US2022125875A1Aav-mediated gene therapy restoring the otoferlin genePASTEUR INSTITUT·Filed 2021·Application pending·0 cites
- 1846US2011059855A1Use of adiponectin for the diagnosis and/or treatment of presbycusisPASTEUR INSTITUT·Filed 2009·Application pending·0 cites
- 1941US2002123467A1Therapeutic composition comprising the KAL protein and use of the KAL protein for the treatment of retinal, renal, neuronal and neural injuryPASTEUR INSTITUT·Filed 2002·Application pending·0 cites
- 2040US2003148381A1More protein-protein interactions in the inner earHYBRIGENICS SA·Filed 2002·Application pending·0 cites
- 2130US5763166AGene associated with X linked Kallmann syndrome and diagnostic applications therefromPASTEUR INSTITUT·Filed 1992·Granted Jun 9, 1998·4 cites·16 claims
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