Nicolas Grillet - Publications

Affiliations: 
2014- Stanford University, Palo Alto, CA 
Area:
Molecular Genetics of the inner ear

22 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.

Year Citation  Score
2024 Grillet N, Wang P, Miller K, He E, Dhawan S, Cunningham C. LOXHD1 is indispensable for coupling auditory mechanosensitive channels to the site of force transmission. Research Square. PMID 38260480 DOI: 10.21203/rs.3.rs-3752492/v1  0.584
2021 Trouillet A, Miller KK, George SS, Wang P, Ali NE, Ricci A, Grillet N. mutations cause mechanotransduction defects in cochlear hair cells. The Journal of Neuroscience : the Official Journal of the Society For Neuroscience. PMID 33707295 DOI: 10.1523/JNEUROSCI.0975-20.2021  0.388
2018 Kim J, Xia A, Grillet N, Applegate BE, Oghalai JS. Osmotic stabilization prevents cochlear synaptopathy after blast trauma. Proceedings of the National Academy of Sciences of the United States of America. PMID 29735658 DOI: 10.1073/pnas.1720121115  0.355
2016 Wu Z, Grillet N, Zhao B, Cunningham C, Harkins-Perry S, Coste B, Ranade S, Zebarjadi N, Beurg M, Fettiplace R, Patapoutian A, Müller U. Mechanosensory hair cells express two molecularly distinct mechanotransduction channels. Nature Neuroscience. PMID 27893727 DOI: 10.1038/Nn.4449  0.577
2016 Zeng WZ, Grillet N, Dewey JB, Trouillet A, Krey JF, Barr-Gillespie PG, Oghalai JS, Müller U. Neuroplastin Isoform Np55 Is Expressed in the Stereocilia of Outer Hair Cells and Required for Normal Outer Hair Cell Function. The Journal of Neuroscience : the Official Journal of the Society For Neuroscience. 36: 9201-16. PMID 27581460 DOI: 10.1523/Jneurosci.0093-16.2016  0.366
2016 Lee HY, Raphael PD, Xia A, Kim J, Grillet N, Applegate BE, Ellerbee Bowden AK, Oghalai JS. Two-Dimensional Cochlear Micromechanics Measured In Vivo Demonstrate Radial Tuning within the Mouse Organ of Corti. The Journal of Neuroscience : the Official Journal of the Society For Neuroscience. 36: 8160-73. PMID 27488636 DOI: 10.1523/JNEUROSCI.1157-16.2016  0.293
2014 Zhao B, Wu Z, Grillet N, Yan L, Xiong W, Harkins-Perry S, Müller U. TMIE is an essential component of the mechanotransduction machinery of cochlear hair cells. Neuron. 84: 954-67. PMID 25467981 DOI: 10.1016/j.neuron.2014.10.041  0.481
2014 Xiong W, Wagner T, Yan L, Grillet N, Müller U. Using injectoporation to deliver genes to mechanosensory hair cells. Nature Protocols. 9: 2438-49. PMID 25232939 DOI: 10.1038/nprot.2014.168  0.398
2014 Mendus D, Sundaresan S, Grillet N, Wangsawihardja F, Leu R, Müller U, Jones SM, Mustapha M. Thrombospondins 1 and 2 are important for afferent synapse formation and function in the inner ear. The European Journal of Neuroscience. 39: 1256-67. PMID 24460873 DOI: 10.1111/Ejn.12486  0.38
2012 Xiong W, Grillet N, Elledge HM, Wagner TF, Zhao B, Johnson KR, Kazmierczak P, Müller U. TMHS is an integral component of the mechanotransduction machinery of cochlear hair cells. Cell. 151: 1283-95. PMID 23217710 DOI: 10.1016/j.cell.2012.10.041  0.512
2011 Webb SW, Grillet N, Andrade LR, Xiong W, Swarthout L, Della Santina CC, Kachar B, Müller U. Regulation of PCDH15 function in mechanosensory hair cells by alternative splicing of the cytoplasmic domain. Development (Cambridge, England). 138: 1607-17. PMID 21427143 DOI: 10.1242/Dev.060061  0.374
2011 Borck G, Ur Rehman A, Lee K, Pogoda HM, Kakar N, von Ameln S, Grillet N, Hildebrand MS, Ahmed ZM, Nürnberg G, Ansar M, Basit S, Javed Q, Morell RJ, Nasreen N, et al. Loss-of-function mutations of ILDR1 cause autosomal-recessive hearing impairment DFNB42. American Journal of Human Genetics. 88: 127-37. PMID 21255762 DOI: 10.1016/J.Ajhg.2010.12.011  0.396
2010 Müller U, Grillet N. The genetics of progressive hearing loss: a link between hearing impairment and dysfunction of mechanosensory hair cells. Future Neurology. 5: 9-12. PMID 24436636 DOI: 10.2217/fnl.09.68  0.311
2009 Grillet N, Schwander M, Hildebrand MS, Sczaniecka A, Kolatkar A, Velasco J, Webster JA, Kahrizi K, Najmabadi H, Kimberling WJ, Stephan D, Bahlo M, Wiltshire T, Tarantino LM, Kuhn P, et al. Mutations in LOXHD1, an evolutionarily conserved stereociliary protein, disrupt hair cell function in mice and cause progressive hearing loss in humans. American Journal of Human Genetics. 85: 328-37. PMID 19732867 DOI: 10.1016/J.Ajhg.2009.07.017  0.444
2009 Grillet N, Kazmierczak P, Xiong W, Schwander M, Reynolds A, Sakaguchi H, Tokita J, Kachar B, Müller U. The mechanotransduction machinery of hair cells. Science Signaling. 2: pt5. PMID 19706872 DOI: 10.1126/Scisignal.285Pt5  0.464
2009 Grillet N, Xiong W, Reynolds A, Kazmierczak P, Sato T, Lillo C, Dumont RA, Hintermann E, Sczaniecka A, Schwander M, Williams D, Kachar B, Gillespie PG, Müller U. Harmonin mutations cause mechanotransduction defects in cochlear hair cells. Neuron. 62: 375-87. PMID 19447093 DOI: 10.1016/J.Neuron.2009.04.006  0.496
2008 Iankova I, Chavey C, Clapé C, Colomer C, Guérineau NC, Grillet N, Brunet JF, Annicotte JS, Fajas L. Regulator of G protein signaling-4 controls fatty acid and glucose homeostasis. Endocrinology. 149: 5706-12. PMID 18635652 DOI: 10.1210/En.2008-0717  0.466
2007 Schwander M, Sczaniecka A, Grillet N, Bailey JS, Avenarius M, Najmabadi H, Steffy BM, Federe GC, Lagler EA, Banan R, Hice R, Grabowski-Boase L, Keithley EM, Ryan AF, Housley GD, et al. A forward genetics screen in mice identifies recessive deafness traits and reveals that pejvakin is essential for outer hair cell function. The Journal of Neuroscience : the Official Journal of the Society For Neuroscience. 27: 2163-75. PMID 17329413 DOI: 10.1523/Jneurosci.4975-06.2007  0.434
2007 Herr DR, Grillet N, Schwander M, Rivera R, Müller U, Chun J. Sphingosine 1-phosphate (S1P) signaling is required for maintenance of hair cells mainly via activation of S1P2. The Journal of Neuroscience : the Official Journal of the Society For Neuroscience. 27: 1474-8. PMID 17287522 DOI: 10.1523/JNEUROSCI.4245-06.2007  0.374
2005 Grillet N, Pattyn A, Contet C, Kieffer BL, Goridis C, Brunet JF. Generation and characterization of Rgs4 mutant mice. Molecular and Cellular Biology. 25: 4221-8. PMID 15870291 DOI: 10.1128/Mcb.25.10.4221-4228.2005  0.62
2003 Grillet N, Dubreuil V, Dufour HD, Brunet JF. Dynamic expression of RGS4 in the developing nervous system and regulation by the neural type-specific transcription factor Phox2b. The Journal of Neuroscience : the Official Journal of the Society For Neuroscience. 23: 10613-21. PMID 14627646 DOI: 10.1523/Jneurosci.23-33-10613.2003  0.546
2001 Garcès A, Livet J, Grillet N, Henderson CE, Delapeyrière O. Responsiveness to neurturin of subpopulations of embryonic rat spinal motoneuron does not correlate with expression of GFR alpha 1 or GFR alpha 2. Developmental Dynamics : An Official Publication of the American Association of Anatomists. 220: 189-97. PMID 11241828 DOI: 10.1002/1097-0177(20010301)220:3<189::Aid-Dvdy1106>3.0.Co;2-I  0.528
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