Peter G. Gillespie
Affiliations: | Johns Hopkins University, Baltimore, MD |
Area:
Cell Biology, Molecular Biology, Neuroscience BiologyGoogle:
"Peter Gillespie"Mean distance: 53433
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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 |
| Ren T, Gillespie PG. (2012) Probing the cochlear amplifier by immobilizing molecular motors of sensory hair cells. Neuron. 76: 868-70 |
| 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 |
| Zheng QY, Scarborough JD, Zheng Y, et al. (2012) Digenic inheritance of deafness caused by 8J allele of myosin-VIIA and mutations in other Usher I genes. Human Molecular Genetics. 21: 2588-98 |
| 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 |
| Maravillas-Montero JL, Gillespie PG, Patiño-López G, et al. (2011) Myosin 1c participates in B cell cytoskeleton rearrangements, is recruited to the immunologic synapse, and contributes to antigen presentation. Journal of Immunology (Baltimore, Md. : 1950). 187: 3053-63 |
| 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 |