| Year |
Citation |
Score |
| 2023 |
Jean P, Wong Jun Tai F, Singh-Estivalet A, Lelli A, Scandola C, Megharba S, Schmutz S, Roux S, Mechaussier S, Sudres M, Mouly E, Heritier AV, Bonnet C, Mallet A, Novault S, ... ... Michalski N, et al. Single-cell transcriptomic profiling of the mouse cochlea: An atlas for targeted therapies. Proceedings of the National Academy of Sciences of the United States of America. 120: e2221744120. PMID 37339214 DOI: 10.1073/pnas.2221744120 |
0.67 |
|
| 2022 |
Calvet C, Peineau T, Benamer N, Cornille M, Lelli A, Plion B, Lahlou G, Fanchette J, Nouaille S, Boutet de Monvel J, Estivalet A, Jean P, Michel V, Sachse M, Michalski N, et al. The SNARE protein SNAP-25 is required for normal exocytosis at auditory hair cell ribbon synapses. Iscience. 25: 105628. PMID 36483015 DOI: 10.1016/j.isci.2022.105628 |
0.712 |
|
| 2022 |
Postal O, Bakay W, Dupont T, Buck A, Petit C, Michalski N, Gourévitch B. Characterizing subcutaneous cortical auditory evoked potentials in mice. Hearing Research. 422: 108566. PMID 35863162 DOI: 10.1016/j.heares.2022.108566 |
0.651 |
|
| 2021 |
Michalski N, Petit C. Central auditory deficits associated with genetic forms of peripheral deafness. Human Genetics. PMID 34435241 DOI: 10.1007/s00439-021-02339-3 |
0.662 |
|
| 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, ... ... Michalski N, 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 |
0.634 |
|
| 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 |
0.629 |
|
| 2019 |
Tobin M, Chaiyasitdhi A, Michel V, Michalski NA, Martin P. Stiffness and tension gradients of the hair cell's tip-link complex in the mammalian cochlea. Elife. 8. PMID 30932811 DOI: 10.7554/Elife.43473 |
0.734 |
|
| 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 |
0.65 |
|
| 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, 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 |
0.644 |
|
| 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 |
0.672 |
|
| 2017 |
Kronander E, Michalski N, Lebrand C, Hornung JP, Schneggenburger R. An organotypic slice culture to study the formation of calyx of Held synapses in-vitro. Plos One. 12: e0175964. PMID 28419135 DOI: 10.1371/Journal.Pone.0175964 |
0.634 |
|
| 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 |
0.695 |
|
| 2013 |
Bonnet C, Louha M, Loundon N, Michalski N, Verpy E, Smagghe L, Hardelin JP, Rouillon I, Jonard L, Couderc R, Gherbi S, Garabedian EN, Denoyelle F, Petit C, Marlin S. Biallelic nonsense mutations in the otogelin-like gene (OTOGL) in a child affected by mild to moderate hearing impairment. Gene. 527: 537-40. PMID 23850727 DOI: 10.1016/J.Gene.2013.06.044 |
0.627 |
|
| 2013 |
Xiao L, Michalski N, Kronander E, Gjoni E, Genoud C, Knott G, Schneggenburger R. BMP signaling specifies the development of a large and fast CNS synapse. Nature Neuroscience. 16: 856-64. PMID 23708139 DOI: 10.1038/Nn.3414 |
0.726 |
|
| 2013 |
Michalski N, Babai N, Renier N, Perkel DJ, Chédotal A, Schneggenburger R. Robo3-driven axon midline crossing conditions functional maturation of a large commissural synapse. Neuron. 78: 855-68. PMID 23664551 DOI: 10.1016/J.Neuron.2013.04.006 |
0.737 |
|
| 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 |
0.684 |
|
| 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, 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 |
0.706 |
|
| 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 |
0.692 |
|
| 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 |
0.756 |
|
| 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 |
0.694 |
|
| 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 |
0.729 |
|
| 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 |
0.715 |
|
| 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 |
0.672 |
|
| 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 |
0.68 |
|
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