Christine Petit - Publications

Affiliations: 
Institut Pasteur, Paris, Paris, France 

98 high-probability publications. We are testing a new system for linking publications to authors. You can help! If you notice any inaccuracies, please sign in and mark papers as correct or incorrect matches. If you identify any major omissions or other inaccuracies in the publication list, please let us know.

PUBLICATION UPDATES TEMPORARILY DISABLED DURING DATABASE UPDATE, SORRY!

Year Citation  Score
2020 Boucher S, Wong Jun Tai F, Delmaghani S, Lelli A, Singh-Estivalet A, Dupont T, Niasme-Grare M, Michel V, Wolff N, Bahloul A, Bouyacoub Y, Bouccara D, Fraysse B, Deguine O, Collet L, ... ... Petit C, et al. Ultrarare heterozygous pathogenic variants of genes causing dominant forms of early-onset deafness underlie severe presbycusis. Proceedings of the National Academy of Sciences of the United States of America. PMID 33229591 DOI: 10.1073/pnas.2010782117  0.48
2020 Postal O, Dupont T, Bakay W, Dominique N, Petit C, Michalski N, Gourévitch B. Spontaneous Mouse Behavior in Presence of Dissonance and Acoustic Roughness. Frontiers in Behavioral Neuroscience. 14: 588834. PMID 33132864 DOI: 10.3389/fnbeh.2020.588834  0.48
2020 Michel V, Pepermans E, Boutet de Monvel J, England P, Nouaille S, Aghaie A, Delhommel F, Wolff N, Perfettini I, Hardelin JP, Petit C, Bahloul A. Interaction of protocadherin-15 with the scaffold protein whirlin supports its anchoring of hair-bundle lateral links in cochlear hair cells. Scientific Reports. 10: 16430. PMID 33009420 DOI: 10.1038/s41598-020-73158-1  0.4
2019 Avan P, Le Gal S, Michel V, Dupont T, Hardelin JP, Petit C, Verpy E. Otogelin, otogelin-like, and stereocilin form links connecting outer hair cell stereocilia to each other and the tectorial membrane. Proceedings of the National Academy of Sciences of the United States of America. PMID 31776257 DOI: 10.1073/pnas.1902781116  0.4
2019 Dunbar LA, Patni P, Aguilar C, Mburu P, Corns L, Wells HR, Delmaghani S, Parker A, Johnson S, Williams D, Esapa CT, Simon MM, Chessum L, Newton S, Dorning J, ... ... Petit C, et al. Clarin-2 is essential for hearing by maintaining stereocilia integrity and function. Embo Molecular Medicine. e10288. PMID 31448880 DOI: 10.15252/emmm.201910288  0.4
2019 Defourny J, Aghaie A, Perfettini I, Avan P, Delmaghani S, Petit C. Pejvakin-mediated pexophagy protects auditory hair cells against noise-induced damage. Proceedings of the National Academy of Sciences of the United States of America. PMID 30936319 DOI: 10.1073/pnas.1821844116  0.4
2019 Akil O, Dyka F, Calvet C, Emptoz A, Lahlou G, Nouaille S, Boutet de Monvel J, Hardelin JP, Hauswirth WW, Avan P, Petit C, Safieddine S, Lustig LR. Dual AAV-mediated gene therapy restores hearing in a DFNB9 mouse model. Proceedings of the National Academy of Sciences of the United States of America. PMID 30782832 DOI: 10.1073/pnas.1817537116  0.4
2019 Michalski N, Petit C. Genes Involved in the Development and Physiology of Both the Peripheral and Central Auditory Systems. Annual Review of Neuroscience. PMID 30699050 DOI: 10.1146/annurev-neuro-070918-050428  0.48
2018 Dulon D, Papal S, Patni P, Cortese M, Vincent PF, Tertrais M, Emptoz A, Tlili A, Bouleau Y, Michel V, Delmaghani S, Aghaie A, Pepermans E, Allegria-Prevot O, Akil O, ... ... Petit C, et al. Clarin-1 gene transfer rescues auditory synaptopathy in model of Usher syndrome. The Journal of Clinical Investigation. PMID 29985171 DOI: 10.1172/JCI94351  0.4
2018 Trouillet A, Dubus E, Dégardin J, Estivalet A, Ivkovic I, Godefroy D, García-Ayuso D, Simonutti M, Sahly I, Sahel JA, El-Amraoui A, Petit C, Picaud S. Cone degeneration is triggered by the absence of USH1 proteins but prevented by antioxidant treatments. Scientific Reports. 8: 1968. PMID 29386551 DOI: 10.1038/s41598-018-20171-0  0.36
2017 Michalski N, Goutman JD, Auclair SM, Boutet de Monvel J, Tertrais M, Emptoz A, Parrin A, Nouaille S, Guillon M, Sachse M, Ciric D, Bahloul A, Hardelin JP, Sutton RB, Avan P, ... ... Petit C, et al. Otoferlin acts as a Ca sensor for vesicle fusion and vesicle pool replenishment at auditory hair cell ribbon synapses. Elife. 6. PMID 29111973 DOI: 10.7554/eLife.31013  0.48
2017 Michel V, Booth KT, Patni P, Cortese M, Azaiez H, Bahloul A, Kahrizi K, Labbé M, Emptoz A, Lelli A, Dégardin J, Dupont T, Aghaie A, Oficjalska-Pham D, Picaud S, ... ... Petit C, et al. CIB2, defective in isolated deafness, is key for auditory hair cell mechanotransduction and survival. Embo Molecular Medicine. PMID 29084757 DOI: 10.15252/emmm.201708087  0.4
2017 Emptoz A, Michel V, Lelli A, Akil O, Boutet de Monvel J, Lahlou G, Meyer A, Dupont T, Nouaille S, Ey E, Franca de Barros F, Beraneck M, Dulon D, Hardelin JP, Lustig L, ... ... Petit C, et al. Local gene therapy durably restores vestibular function in a mouse model of Usher syndrome type 1G. Proceedings of the National Academy of Sciences of the United States of America. PMID 28835534 DOI: 10.1073/pnas.1708894114  0.4
2017 Libé-Philippot B, Michel V, Boutet de Monvel J, Le Gal S, Dupont T, Avan P, Métin C, Michalski N, Petit C. Auditory cortex interneuron development requires cadherins operating hair-cell mechanoelectrical transduction. Proceedings of the National Academy of Sciences of the United States of America. PMID 28705869 DOI: 10.1073/pnas.1703408114  0.48
2017 Bahloul A, Pepermans E, Raynal B, Wolff N, Cordier F, England P, Nouaille S, Baron B, El-Amraoui A, Hardelin JP, Durand D, Petit C. Conformational switch of harmonin, a submembrane scaffold protein of the hair cell mechanoelectrical transduction machinery. Febs Letters. PMID 28653419 DOI: 10.1002/1873-3468.12729  0.36
2017 Schietroma C, Parain K, Estivalet A, Aghaie A, Boutet de Monvel J, Picaud S, Sahel JA, Perron M, El-Amraoui A, Petit C. Usher syndrome type 1-associated cadherins shape the photoreceptor outer segment. The Journal of Cell Biology. PMID 28495838 DOI: 10.1083/jcb.201612030  0.4
2017 Cortese M, Papal S, Pisciottano F, Elgoyhen AB, Hardelin JP, Petit C, Franchini LF, El-Amraoui A. Spectrin βV adaptive mutations and changes in subcellular location correlate with emergence of hair cell electromotility in mammalians. Proceedings of the National Academy of Sciences of the United States of America. PMID 28179572 DOI: 10.1073/pnas.1618778114  0.4
2016 Potter PK, Bowl MR, Jeyarajan P, Wisby L, Blease A, Goldsworthy ME, Simon MM, Greenaway S, Michel V, Barnard A, Aguilar C, Agnew T, Banks G, Blake A, Chessum L, ... ... Petit C, et al. Novel gene function revealed by mouse mutagenesis screens for models of age-related disease. Nature Communications. 7: 12444. PMID 27534441 DOI: 10.1038/ncomms12444  0.48
2016 Bonnet C, Riahi Z, Chantot-Bastaraud S, Smagghe L, Letexier M, Marcaillou C, Lefèvre GM, Hardelin JP, El-Amraoui A, Singh-Estivalet A, Mohand-Saïd S, Kohl S, Kurtenbach A, Sliesoraityte I, Zobor D, ... ... Petit C, et al. An innovative strategy for the molecular diagnosis of Usher syndrome identifies causal biallelic mutations in 93% of European patients. European Journal of Human Genetics : Ejhg. PMID 27460420 DOI: 10.1038/ejhg.2016.99  0.36
2016 Delmaghani S, Aghaie A, Bouyacoub Y, El Hachmi H, Bonnet C, Riahi Z, Chardenoux S, Perfettini I, Hardelin JP, Houmeida A, Herbomel P, Petit C. Mutations in CDC14A, Encoding a Protein Phosphatase Involved in Hair Cell Ciliogenesis, Cause Autosomal-Recessive Severe to Profound Deafness. American Journal of Human Genetics. 98: 1266-70. PMID 27259055 DOI: 10.1016/j.ajhg.2016.04.015  0.4
2016 Lelli A, Michel V, Boutet de Monvel J, Cortese M, Bosch-Grau M, Aghaie A, Perfettini I, Dupont T, Avan P, El-Amraoui A, Petit C. Class III myosins shape the auditory hair bundles by limiting microvilli and stereocilia growth. The Journal of Cell Biology. 212: 231-44. PMID 26754646 DOI: 10.1083/jcb.201509017  0.4
2016 Lelli A, Michel V, De Monvel JB, Cortese M, Bosch-Grau M, Aghaie A, Perfettini I, Dupont T, Avan P, El-Amraoui A, Petit C. Class III myosins shape the auditory hair bundles by limiting microvilli and stereocilia growth Journal of Cell Biology. 212: 231-244. DOI: 10.1083/jcb.201509017  0.48
2015 Delmaghani S, Defourny J, Aghaie A, Beurg M, Dulon D, Thelen N, Perfettini I, Zelles T, Aller M, Meyer A, Emptoz A, Giraudet F, Leibovici M, Dartevelle S, Soubigou G, ... ... Petit C, et al. Hypervulnerability to Sound Exposure through Impaired Adaptive Proliferation of Peroxisomes. Cell. 163: 894-906. PMID 26544938 DOI: 10.1016/j.cell.2015.10.023  0.48
2015 Ben Halim N, Nagara M, Regnault B, Hsouna S, Lasram K, Kefi R, Azaiez H, Khemira L, Saidane R, Ammar SB, Besbes G, Weil D, Petit C, Abdelhak S, Romdhane L. Estimation of Recent and Ancient Inbreeding in a Small Endogamous Tunisian Community Through Genomic Runs of Homozygosity. Annals of Human Genetics. 79: 402-17. PMID 26420437 DOI: 10.1111/ahg.12131  0.48
2015 Dahmani M, Ammar-Khodja F, Bonnet C, Lefèvre GM, Hardelin JP, Ibrahim H, Mallek Z, Petit C. EPS8L2 is a new causal gene for childhood onset autosomal recessive progressive hearing loss. Orphanet Journal of Rare Diseases. 10: 96. PMID 26282398 DOI: 10.1186/s13023-015-0316-8  0.48
2015 Pepermans E, Petit C. The tip-link molecular complex of the auditory mechano-electrical transduction machinery. Hearing Research. PMID 26049141 DOI: 10.1016/j.heares.2015.05.005  0.48
2015 Zong L, Guan J, Ealy M, Zhang Q, Wang D, Wang H, Zhao Y, Shen Z, Campbell CA, Wang F, Yang J, Sun W, Lan L, Ding D, Xie L, ... ... Petit C, et al. Mutations in apoptosis-inducing factor cause X-linked recessive auditory neuropathy spectrum disorder. Journal of Medical Genetics. 52: 523-31. PMID 25986071 DOI: 10.1136/jmedgenet-2014-102961  0.48
2015 Michalski N, Petit C. Genetics of auditory mechano-electrical transduction. PflüGers Archiv : European Journal of Physiology. 467: 49-72. PMID 24957570 DOI: 10.1007/s00424-014-1552-9  0.48
2014 Vincent PF, Bouleau Y, Safieddine S, Petit C, Dulon D. Exocytotic machineries of vestibular type I and cochlear ribbon synapses display similar intrinsic otoferlin-dependent Ca2+ sensitivity but a different coupling to Ca2+ channels. The Journal of Neuroscience : the Official Journal of the Society For Neuroscience. 34: 10853-69. PMID 25122888 DOI: 10.1523/JNEUROSCI.0947-14.2014  0.48
2014 Wang H, Zhao Y, Yi Y, Gao Y, Liu Q, Wang D, Li Q, Lan L, Li N, Guan J, Yin Z, Han B, Zhao F, Zong L, Xiong W, ... ... Petit C, et al. Targeted high-throughput sequencing identifies pathogenic mutations in KCNQ4 in two large Chinese families with autosomal dominant hearing loss. Plos One. 9: e103133. PMID 25116015 DOI: 10.1371/journal.pone.0103133  0.48
2014 Romdhane L, Ben Halim N, Rejeb I, Kefi R, Bouyacoub Y, Ben Rekaya M, Messai H, Messaoud O, Riahi Z, Bonnet C, Ben Rhouma F, Nagara M, Petit C, McElreavey K, Romeo G, et al. Specific aspects of consanguinity: some examples from the Tunisian population. Human Heredity. 77: 167-74. PMID 25060280 DOI: 10.1159/000362167  0.48
2014 Pepermans E, Michel V, Goodyear R, Bonnet C, Abdi S, Dupont T, Gherbi S, Holder M, Makrelouf M, Hardelin JP, Marlin S, Zenati A, Richardson G, Avan P, Bahloul A, ... Petit C, et al. The CD2 isoform of protocadherin-15 is an essential component of the tip-link complex in mature auditory hair cells. Embo Molecular Medicine. 6: 984-92. PMID 24940003 DOI: 10.15252/emmm.201403976  0.48
2014 Riahi Z, Bonnet C, Zainine R, Louha M, Bouyacoub Y, Laroussi N, Chargui M, Kefi R, Jonard L, Dorboz I, Hardelin JP, Salah SB, Levilliers J, Weil D, McElreavey K, ... ... Petit C, et al. Whole exome sequencing identifies new causative mutations in Tunisian families with non-syndromic deafness. Plos One. 9: e99797. PMID 24926664 DOI: 10.1371/journal.pone.0099797  0.48
2014 Kamiya K, Michel V, Giraudet F, Riederer B, Foucher I, Papal S, Perfettini I, Le Gal S, Verpy E, Xia W, Seidler U, Georgescu MM, Avan P, El-Amraoui A, Petit C. An unusually powerful mode of low-frequency sound interference due to defective hair bundles of the auditory outer hair cells. Proceedings of the National Academy of Sciences of the United States of America. 111: 9307-12. PMID 24920589 DOI: 10.1073/pnas.1405322111  0.48
2014 Behlouli A, Bonnet C, Abdi S, Bouaita A, Lelli A, Hardelin JP, Schietroma C, Rous Y, Louha M, Cheknane A, Lebdi H, Boudjelida K, Makrelouf M, Zenati A, Petit C. EPS8, encoding an actin-binding protein of cochlear hair cell stereocilia, is a new causal gene for autosomal recessive profound deafness. Orphanet Journal of Rare Diseases. 9: 55. PMID 24741995 DOI: 10.1186/1750-1172-9-55  0.48
2014 El-Amraoui A, Petit C. The retinal phenotype of Usher syndrome: pathophysiological insights from animal models. Comptes Rendus Biologies. 337: 167-77. PMID 24702843 DOI: 10.1016/j.crvi.2013.12.004  0.48
2013 Avan P, Büki B, Petit C. Auditory distortions: origins and functions. Physiological Reviews. 93: 1563-619. PMID 24137017 DOI: 10.1152/physrev.00029.2012  0.36
2013 Papal S, Cortese M, Legendre K, Sorusch N, Dragavon J, Sahly I, Shorte S, Wolfrum U, Petit C, El-Amraoui A. The giant spectrin βV couples the molecular motors to phototransduction and Usher syndrome type I proteins along their trafficking route. Human Molecular Genetics. 22: 3773-88. PMID 23704327 DOI: 10.1093/hmg/ddt228  0.4
2013 El-Amraoui A, Petit C. Cadherin defects in inherited human diseases. Progress in Molecular Biology and Translational Science. 116: 361-84. PMID 23481203 DOI: 10.1016/B978-0-12-394311-8.00016-9  0.36
2013 Boulay AC, del Castillo FJ, Giraudet F, Hamard G, Giaume C, Petit C, Avan P, Cohen-Salmon M. Hearing is normal without connexin30. The Journal of Neuroscience : the Official Journal of the Society For Neuroscience. 33: 430-4. PMID 23303923 DOI: 10.1523/JNEUROSCI.4240-12.2013  0.48
2013 Greenspan R, Petit C. Neurogenetics. Current Opinion in Neurobiology. 23: 1-2. PMID 23265962 DOI: 10.1016/j.conb.2012.12.001  0.48
2012 Lukashkin AN, Legan PK, Weddell TD, Lukashkina VA, Goodyear RJ, Welstead LJ, Petit C, Russell IJ, Richardson GP. A mouse model for human deafness DFNB22 reveals that hearing impairment is due to a loss of inner hair cell stimulation. Proceedings of the National Academy of Sciences of the United States of America. 109: 19351-6. PMID 23129639 DOI: 10.1073/pnas.1210159109  0.48
2012 Sahly I, Dufour E, Schietroma C, Michel V, Bahloul A, Perfettini I, Pepermans E, Estivalet A, Carette D, Aghaie A, Ebermann I, Lelli A, Iribarne M, Hardelin JP, Weil D, ... ... Petit C, et al. Localization of Usher 1 proteins to the photoreceptor calyceal processes, which are absent from mice. The Journal of Cell Biology. 199: 381-99. PMID 23045546 DOI: 10.1083/jcb.201202012  0.4
2012 Fakin A, Jarc-Vidmar M, Glavač D, Bonnet C, Petit C, Hawlina M. Fundus autofluorescence and optical coherence tomography in relation to visual function in Usher syndrome type 1 and 2. Vision Research. 75: 60-70. PMID 23000274 DOI: 10.1016/j.visres.2012.08.017  0.48
2012 Safieddine S, El-Amraoui A, Petit C. The auditory hair cell ribbon synapse: from assembly to function. Annual Review of Neuroscience. 35: 509-28. PMID 22715884 DOI: 10.1146/annurev-neuro-061010-113705  0.36
2012 Delmaghani S, Aghaie A, Michalski N, Bonnet C, Weil D, Petit C. Defect in the gene encoding the EAR/EPTP domain-containing protein TSPEAR causes DFNB98 profound deafness. Human Molecular Genetics. 21: 3835-44. PMID 22678063 DOI: 10.1093/hmg/dds212  0.48
2011 Bonnet C, Grati M, Marlin S, Levilliers J, Hardelin JP, Parodi M, Niasme-Grare M, Zelenika D, Délépine M, Feldmann D, Jonard L, El-Amraoui A, Weil D, Delobel B, Vincent C, ... ... Petit C, et al. Complete exon sequencing of all known Usher syndrome genes greatly improves molecular diagnosis. Orphanet Journal of Rare Diseases. 6: 21. PMID 21569298 DOI: 10.1186/1750-1172-6-21  0.48
2011 Reisinger E, Bresee C, Neef J, Nair R, Reuter K, Bulankina A, Nouvian R, Koch M, Bückers J, Kastrup L, Roux I, Petit C, Hell SW, Brose N, Rhee JS, et al. Probing the functional equivalence of otoferlin and synaptotagmin 1 in exocytosis. The Journal of Neuroscience : the Official Journal of the Society For Neuroscience. 31: 4886-95. PMID 21451027 DOI: 10.1523/JNEUROSCI.5122-10.2011  0.48
2011 Caberlotto E, Michel V, Foucher I, Bahloul A, Goodyear RJ, Pepermans E, Michalski N, Perfettini I, Alegria-Prévot O, Chardenoux S, Do Cruzeiro M, Hardelin JP, Richardson GP, Avan P, Weil D, ... Petit C, et al. Usher type 1G protein sans is a critical component of the tip-link complex, a structure controlling actin polymerization in stereocilia. Proceedings of the National Academy of Sciences of the United States of America. 108: 5825-30. PMID 21436032 DOI: 10.1073/pnas.1017114108  0.48
2011 Verpy E, Leibovici M, Michalski N, Goodyear RJ, Houdon C, Weil D, Richardson GP, Petit C. Stereocilin connects outer hair cell stereocilia to one another and to the tectorial membrane. The Journal of Comparative Neurology. 519: 194-210. PMID 21165971 DOI: 10.1002/cne.22509  0.48
2011 Richardson GP, de Monvel JB, Petit C. How the genetics of deafness illuminates auditory physiology. Annual Review of Physiology. 73: 311-34. PMID 21073336 DOI: 10.1146/annurev-physiol-012110-142228  0.48
2010 El-Amraoui A, Petit C. [Stem cell therapy in the inner ear: recent achievements and prospects]. MéDecine Sciences : M/S. 26: 981-5. PMID 21106181 DOI: 10.1051/medsci/20102611981  0.36
2010 Beurg M, Michalski N, Safieddine S, Bouleau Y, Schneggenburger R, Chapman ER, Petit C, Dulon D. Control of exocytosis by synaptotagmins and otoferlin in auditory hair cells. The Journal of Neuroscience : the Official Journal of the Society For Neuroscience. 30: 13281-90. PMID 20926654 DOI: 10.1523/JNEUROSCI.2528-10.2010  0.48
2010 Bahloul A, Michel V, Hardelin JP, Nouaille S, Hoos S, Houdusse A, England P, Petit C. Cadherin-23, myosin VIIa and harmonin, encoded by Usher syndrome type I genes, form a ternary complex and interact with membrane phospholipids. Human Molecular Genetics. 19: 3557-65. PMID 20639393 DOI: 10.1093/hmg/ddq271  0.48
2010 Etournay R, Lepelletier L, Boutet de Monvel J, Michel V, Cayet N, Leibovici M, Weil D, Foucher I, Hardelin JP, Petit C. Cochlear outer hair cells undergo an apical circumference remodeling constrained by the hair bundle shape. Development (Cambridge, England). 137: 1373-83. PMID 20332152 DOI: 10.1242/dev.045138  0.4
2010 El-Amraoui A, Petit C. Cadherins as targets for genetic diseases. Cold Spring Harbor Perspectives in Biology. 2: a003095. PMID 20182609 DOI: 10.1101/cshperspect.a003095  0.36
2010 Petit C, Avan P. WITHDRAWN: Top connectors of the hair bundle are required for waveform distortion and suppression masking but not cochlear amplification. Hearing Research. PMID 20123062 DOI: 10.1016/j.heares.2009.12.007  0.36
2010 del Castillo FJ, Cohen-Salmon M, Charollais A, Caille D, Lampe PD, Chavrier P, Meda P, Petit C. Consortin, a trans-Golgi network cargo receptor for the plasma membrane targeting and recycling of connexins. Human Molecular Genetics. 19: 262-75. PMID 19864490 DOI: 10.1093/hmg/ddp490  0.48
2009 Bahloul A, Simmler MC, Michel V, Leibovici M, Perfettini I, Roux I, Weil D, Nouaille S, Zuo J, Zadro C, Licastro D, Gasparini P, Avan P, Hardelin JP, Petit C. Vezatin, an integral membrane protein of adherens junctions, is required for the sound resilience of cochlear hair cells. Embo Molecular Medicine. 1: 125-38. PMID 20049712 DOI: 10.1002/emmm.200900015  0.48
2009 Avan P, Petit C. WITHDRAWN: Top connectors of the hair bundle are required for waveform distortion and suppression masking but not cochlear amplification. Hearing Research. PMID 19818389 DOI: 10.1016/j.heares.2009.09.014  0.36
2009 Michalski N, Michel V, Caberlotto E, Lefèvre GM, van Aken AF, Tinevez JY, Bizard E, Houbron C, Weil D, Hardelin JP, Richardson GP, Kros CJ, Martin P, Petit C. Harmonin-b, an actin-binding scaffold protein, is involved in the adaptation of mechanoelectrical transduction by sensory hair cells. PflüGers Archiv : European Journal of Physiology. 459: 115-30. PMID 19756723 DOI: 10.1007/s00424-009-0711-x  0.48
2009 Petit C, Richardson GP. Linking genes underlying deafness to hair-bundle development and function. Nature Neuroscience. 12: 703-10. PMID 19471269 DOI: 10.1038/nn.2330  0.48
2009 Legendre K, Petit C, El-Amraoui A. [The outer hair cell of the mammalian cochlea: an outstanding amplifier]. MéDecine Sciences : M/S. 25: 117-20. PMID 19239835 DOI: 10.1051/medsci/2009252117  0.36
2008 Wei D, Levic S, Nie L, Gao WQ, Petit C, Jones EG, Yamoah EN. Cells of adult brain germinal zone have properties akin to hair cells and can be used to replace inner ear sensory cells after damage. Proceedings of the National Academy of Sciences of the United States of America. 105: 21000-5. PMID 19064919 DOI: 10.1073/pnas.0808044105  0.48
2008 Verpy E, Weil D, Leibovici M, Goodyear RJ, Hamard G, Houdon C, Lefèvre GM, Hardelin JP, Richardson GP, Avan P, Petit C. Stereocilin-deficient mice reveal the origin of cochlear waveform distortions. Nature. 456: 255-8. PMID 18849963 DOI: 10.1038/nature07380  0.48
2008 Legendre K, Safieddine S, Küssel-Andermann P, Petit C, El-Amraoui A. alphaII-betaV spectrin bridges the plasma membrane and cortical lattice in the lateral wall of the auditory outer hair cells. Journal of Cell Science. 121: 3347-56. PMID 18796539 DOI: 10.1242/jcs.028134  0.36
2008 Lefèvre G, Michel V, Weil D, Lepelletier L, Bizard E, Wolfrum U, Hardelin JP, Petit C. A core cochlear phenotype in USH1 mouse mutants implicates fibrous links of the hair bundle in its cohesion, orientation and differential growth. Development (Cambridge, England). 135: 1427-37. PMID 18339676 DOI: 10.1242/dev.012922  0.32
2008 Jones C, Roper VC, Foucher I, Qian D, Banizs B, Petit C, Yoder BK, Chen P. Ciliary proteins link basal body polarization to planar cell polarity regulation. Nature Genetics. 40: 69-77. PMID 18066062 DOI: 10.1038/ng.2007.54  0.48
2007 Etournay R, Zwaenepoel I, Perfettini I, Legrain P, Petit C, El-Amraoui A. Shroom2, a myosin-VIIa- and actin-binding protein, directly interacts with ZO-1 at tight junctions. Journal of Cell Science. 120: 2838-50. PMID 17666436 DOI: 10.1242/jcs.002568  0.4
2007 Lévêque M, Marlin S, Jonard L, Procaccio V, Reynier P, Amati-Bonneau P, Baulande S, Pierron D, Lacombe D, Duriez F, Francannet C, Mom T, Journel H, Catros H, Drouin-Garraud V, ... ... Petit C, et al. Whole mitochondrial genome screening in maternally inherited non-syndromic hearing impairment using a microarray resequencing mitochondrial DNA chip. European Journal of Human Genetics : Ejhg. 15: 1145-55. PMID 17637808 DOI: 10.1038/sj.ejhg.5201891  0.48
2007 Michalski N, Michel V, Bahloul A, Lefèvre G, Barral J, Yagi H, Chardenoux S, Weil D, Martin P, Hardelin JP, Sato M, Petit C. Molecular characterization of the ankle-link complex in cochlear hair cells and its role in the hair bundle functioning. The Journal of Neuroscience : the Official Journal of the Society For Neuroscience. 27: 6478-88. PMID 17567809 DOI: 10.1523/JNEUROSCI.0342-07.2007  0.48
2007 Cohen-Salmon M, Regnault B, Cayet N, Caille D, Demuth K, Hardelin JP, Janel N, Meda P, Petit C. Connexin30 deficiency causes instrastrial fluid-blood barrier disruption within the cochlear stria vascularis. Proceedings of the National Academy of Sciences of the United States of America. 104: 6229-34. PMID 17400755 DOI: 10.1073/pnas.0605108104  0.48
2007 Hoskins BE, Cramer CH, Silvius D, Zou D, Raymond RM, Orten DJ, Kimberling WJ, Smith RJ, Weil D, Petit C, Otto EA, Xu PX, Hildebrandt F. Transcription factor SIX5 is mutated in patients with branchio-oto-renal syndrome. American Journal of Human Genetics. 80: 800-4. PMID 17357085 DOI: 10.1086/513322  0.48
2006 Roux I, Safieddine S, Nouvian R, Grati M, Simmler MC, Bahloul A, Perfettini I, Le Gall M, Rostaing P, Hamard G, Triller A, Avan P, Moser T, Petit C. Otoferlin, defective in a human deafness form, is essential for exocytosis at the auditory ribbon synapse. Cell. 127: 277-89. PMID 17055430 DOI: 10.1016/j.cell.2006.08.040  0.48
2006 Delmaghani S, del Castillo FJ, Michel V, Leibovici M, Aghaie A, Ron U, Van Laer L, Ben-Tal N, Van Camp G, Weil D, Langa F, Lathrop M, Avan P, Petit C. Mutations in the gene encoding pejvakin, a newly identified protein of the afferent auditory pathway, cause DFNB59 auditory neuropathy. Nature Genetics. 38: 770-8. PMID 16804542 DOI: 10.1038/ng1829  0.4
2006 Albert S, Blons H, Jonard L, Feldmann D, Chauvin P, Loundon N, Sergent-Allaoui A, Houang M, Joannard A, Schmerber S, Delobel B, Leman J, Journel H, Catros H, Dollfus H, ... ... Petit C, et al. SLC26A4 gene is frequently involved in nonsyndromic hearing impairment with enlarged vestibular aqueduct in Caucasian populations. European Journal of Human Genetics : Ejhg. 14: 773-9. PMID 16570074 DOI: 10.1038/sj.ejhg.5201611  0.48
2005 Adato A, Lefèvre G, Delprat B, Michel V, Michalski N, Chardenoux S, Weil D, El-Amraoui A, Petit C. Usherin, the defective protein in Usher syndrome type IIA, is likely to be a component of interstereocilia ankle links in the inner ear sensory cells. Human Molecular Genetics. 14: 3921-32. PMID 16301217 DOI: 10.1093/hmg/ddi416  0.48
2005 El-Amraoui A, Petit C. Usher I syndrome: unravelling the mechanisms that underlie the cohesion of the growing hair bundle in inner ear sensory cells. Journal of Cell Science. 118: 4593-603. PMID 16219682 DOI: 10.1242/jcs.02636  0.36
2005 Hyenne V, Louvet-Vallée S, El-Amraoui A, Petit C, Maro B, Simmler MC. Vezatin, a protein associated to adherens junctions, is required for mouse blastocyst morphogenesis. Developmental Biology. 287: 180-91. PMID 16199027 DOI: 10.1016/j.ydbio.2005.09.004  0.36
2005 El-Amraoui A, Lefèvre G, Hardelin JP, Petit C. [Usher syndrome type I and the differentiation of inner ear sensory cells' hair bundles]. MéDecine Sciences : M/S. 21: 737-40. PMID 16115459 DOI: 10.1051/medsci/2005218-9737  0.36
2005 del Castillo FJ, Rodríguez-Ballesteros M, Alvarez A, Hutchin T, Leonardi E, de Oliveira CA, Azaiez H, Brownstein Z, Avenarius MR, Marlin S, Pandya A, Shahin H, Siemering KR, Weil D, Wuyts W, ... ... Petit C, et al. A novel deletion involving the connexin-30 gene, del(GJB6-d13s1854), found in trans with mutations in the GJB2 gene (connexin-26) in subjects with DFNB1 non-syndromic hearing impairment. Journal of Medical Genetics. 42: 588-94. PMID 15994881 DOI: 10.1136/jmg.2004.028324  0.48
2005 Etournay R, El-Amraoui A, Bahloul A, Blanchard S, Roux I, Pézeron G, Michalski N, Daviet L, Hardelin JP, Legrain P, Petit C. PHR1, an integral membrane protein of the inner ear sensory cells, directly interacts with myosin 1c and myosin VIIa. Journal of Cell Science. 118: 2891-9. PMID 15976448 DOI: 10.1242/jcs.02424  0.48
2005 Marlin S, Feldmann D, Blons H, Loundon N, Rouillon I, Albert S, Chauvin P, Garabédian EN, Couderc R, Odent S, Joannard A, Schmerber S, Delobel B, Leman J, Journel H, ... ... Petit C, et al. GJB2 and GJB6 mutations: genotypic and phenotypic correlations in a large cohort of hearing-impaired patients. Archives of Otolaryngology--Head & Neck Surgery. 131: 481-7. PMID 15967879 DOI: 10.1001/archotol.131.6.481  0.48
2005 Michel V, Goodyear RJ, Weil D, Marcotti W, Perfettini I, Wolfrum U, Kros CJ, Richardson GP, Petit C. Cadherin 23 is a component of the transient lateral links in the developing hair bundles of cochlear sensory cells. Developmental Biology. 280: 281-94. PMID 15882573 DOI: 10.1016/j.ydbio.2005.01.014  0.48
2005 Leibovici M, Verpy E, Goodyear RJ, Zwaenepoel I, Blanchard S, Lainé S, Richardson GP, Petit C. Initial characterization of kinocilin, a protein of the hair cell kinocilium. Hearing Research. 203: 144-53. PMID 15855039 DOI: 10.1016/j.heares.2004.12.002  0.48
2005 Miao CY, Villeneuve N, Brunel-Jacquemin C, Petit C, Guillaumin JP, Gransagne D, Briant C, Vilaine JP, Vanhoutte PM. Chronic mild hyperhomocysteinemia induces aortic endothelial dysfunction but does not elevate arterial pressure in rats. Journal of Vascular Research. 42: 148-56. PMID 15713986 DOI: 10.1159/000083972  0.48
2005 Adato A, Michel V, Kikkawa Y, Reiners J, Alagramam KN, Weil D, Yonekawa H, Wolfrum U, El-Amraoui A, Petit C. Interactions in the network of Usher syndrome type 1 proteins. Human Molecular Genetics. 14: 347-56. PMID 15590703 DOI: 10.1093/hmg/ddi031  0.4
2005 Delprat B, Michel V, Goodyear R, Yamasaki Y, Michalski N, El-Amraoui A, Perfettini I, Legrain P, Richardson G, Hardelin JP, Petit C. Myosin XVa and whirlin, two deafness gene products required for hair bundle growth, are located at the stereocilia tips and interact directly. Human Molecular Genetics. 14: 401-10. PMID 15590698 DOI: 10.1093/hmg/ddi036  0.48
2004 Feldmann D, Denoyelle F, Chauvin P, Garabédian EN, Couderc R, Odent S, Joannard A, Schmerber S, Delobel B, Leman J, Journel H, Catros H, Le Maréchal C, Dollfus H, Eliot MM, ... ... Petit C, et al. Large deletion of the GJB6 gene in deaf patients heterozygous for the GJB2 gene mutation: genotypic and phenotypic analysis. American Journal of Medical Genetics. Part A. 127: 263-7. PMID 15150777 DOI: 10.1002/ajmg.a.20588  0.48
2004 Ruf RG, Xu PX, Silvius D, Otto EA, Beekmann F, Muerb UT, Kumar S, Neuhaus TJ, Kemper MJ, Raymond RM, Brophy PD, Berkman J, Gattas M, Hyland V, Ruf EM, ... ... Petit C, et al. SIX1 mutations cause branchio-oto-renal syndrome by disruption of EYA1-SIX1-DNA complexes. Proceedings of the National Academy of Sciences of the United States of America. 101: 8090-5. PMID 15141091 DOI: 10.1073/pnas.0308475101  0.48
2004 Sousa S, Cabanes D, El-Amraoui A, Petit C, Lecuit M, Cossart P. Unconventional myosin VIIa and vezatin, two proteins crucial for Listeria entry into epithelial cells. Journal of Cell Science. 117: 2121-30. PMID 15090598 DOI: 10.1242/jcs.01066  0.36
2004 Cohen-Salmon M, Maxeiner S, Krüger O, Theis M, Willecke K, Petit C. Expression of the connexin43- and connexin45-encoding genes in the developing and mature mouse inner ear. Cell and Tissue Research. 316: 15-22. PMID 14986102 DOI: 10.1007/s00441-004-0861-2  0.48
2003 Villeneuve N, Fortuno A, Sauvage M, Fournier N, Breugnot C, Jacquemin C, Petit C, Gosgnach W, Carpentier N, Vanhoutte P, Vilaine JP. Persistence of the nitric oxide pathway in the aorta of hypercholesterolemic apolipoprotein-E-deficient mice. Journal of Vascular Research. 40: 87-96. PMID 12808344 DOI: 10.1159/000070705  0.48
2002 Zwaenepoel I, Mustapha M, Leibovici M, Verpy E, Goodyear R, Liu XZ, Nouaille S, Nance WE, Kanaan M, Avraham KB, Tekaia F, Loiselet J, Lathrop M, Richardson G, Petit C. Otoancorin, an inner ear protein restricted to the interface between the apical surface of sensory epithelia and their overlying acellular gels, is defective in autosomal recessive deafness DFNB22. Proceedings of the National Academy of Sciences of the United States of America. 99: 6240-5. PMID 11972037 DOI: 10.1073/pnas.082515999  0.48
2001 Gillespie PG, Albanesi JP, Bahler M, Bement WM, Berg JS, Burgess DR, Burnside B, Cheney RE, Corey DP, Coudrier E, de Lanerolle P, Hammer JA, Hasson T, Holt JR, Hudspeth AJ, ... ... Petit C, et al. Myosin-I nomenclature. The Journal of Cell Biology. 155: 703-4. PMID 11724811 DOI: 10.1083/jcb.200110032  0.48
2000 Masmoudi S, Elgaied-Boulila A, Kassab I, Ben Arab S, Blanchard S, Bouzouita JE, Drira M, Kassab A, Hachicha S, Petit C, Ayadi H. Determination of the frequency of connexin26 mutations in inherited sensorineural deafness and carrier rates in the Tunisian population using DGGE. Journal of Medical Genetics. 37: E39. PMID 11073548 DOI: 10.1136/JMG.37.11.E39  0.48
2000 Ardouin O, Legouis R, Fasano L, David-Watine B, Korn H, Hardelin J, Petit C. Characterization of the two zebrafish orthologues of the KAL-1 gene underlying X chromosome-linked Kallmann syndrome. Mechanisms of Development. 90: 89-94. PMID 10585565 DOI: 10.1016/S0925-4773(99)00222-1  0.48
1999 Kubisch C, Schroeder BC, Friedrich T, Lütjohann B, El-Amraoui A, Marlin S, Petit C, Jentsch TJ. KCNQ4, a novel potassium channel expressed in sensory outer hair cells, is mutated in dominant deafness. Cell. 96: 437-46. PMID 10025409 DOI: 10.1016/S0092-8674(00)80556-5  0.48
Show low-probability matches.