Peter G. Gillespie

Affiliations: 
Johns Hopkins University, Baltimore, MD 
Area:
Cell Biology, Molecular Biology, Neuroscience Biology
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"Peter Gillespie"
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Publications

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Spinelli KJ, Gillespie PG. (2012) Monitoring intracellular calcium ion dynamics in hair cell populations with Fluo-4 AM. Plos One. 7: e51874
Grati M, Shin JB, Weston MD, et al. (2012) Localization of PDZD7 to the stereocilia ankle-link associates this scaffolding protein with the Usher syndrome protein network. The Journal of Neuroscience : the Official Journal of the Society For Neuroscience. 32: 14288-93
Zhao H, Avenarius MR, Gillespie PG. (2012) Improved biolistic transfection of hair cells. Plos One. 7: e46765
Zhao H, Williams DE, Shin JB, et al. (2012) Large membrane domains in hair bundles specify spatially constricted radixin activation. The Journal of Neuroscience : the Official Journal of the Society For Neuroscience. 32: 4600-9
Powers RJ, Roy S, Atilgan E, et al. (2012) Stereocilia membrane deformation: implications for the gating spring and mechanotransduction channel. Biophysical Journal. 102: 201-10
Spinelli KJ, Klimek JE, Wilmarth PA, et al. (2012) Distinct energy metabolism of auditory and vestibular sensory epithelia revealed by quantitative mass spectrometry using MS2 intensity. Proceedings of the National Academy of Sciences of the United States of America. 109: E268-77
Yang Y, Dai M, Wilson TM, et al. (2011) Na+/K+-ATPase α1 identified as an abundant protein in the blood-labyrinth barrier that plays an essential role in the barrier integrity. Plos One. 6: e16547
Borck G, Ur Rehman A, Lee K, et al. (2011) Loss-of-function mutations of ILDR1 cause autosomal-recessive hearing impairment DFNB42. American Journal of Human Genetics. 88: 127-37
Shin JB, Longo-Guess CM, Gagnon LH, et al. (2010) The R109H variant of fascin-2, a developmentally regulated actin crosslinker in hair-cell stereocilia, underlies early-onset hearing loss of DBA/2J mice. The Journal of Neuroscience : the Official Journal of the Society For Neuroscience. 30: 9683-94
Grillet N, Xiong W, Reynolds A, et al. (2009) Harmonin mutations cause mechanotransduction defects in cochlear hair cells. Neuron. 62: 375-87
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