Published in PLoS One on July 21, 2011
Adaptive aberration correction of GRIN lenses for confocal endomicroscopy. Opt Lett (2011) 0.82
In vivo multiphoton microscopy of deep brain tissue. J Neurophysiol (2003) 3.63
Advances in light microscopy for neuroscience. Annu Rev Neurosci (2009) 2.88
Adaptive wavefront correction in two-photon microscopy using coherence-gated wavefront sensing. Proc Natl Acad Sci U S A (2006) 2.85
In vivo brain imaging using a portable 3.9 gram two-photon fluorescence microendoscope. Opt Lett (2005) 2.82
Ultra-compact fiber-optic two-photon microscope for functional fluorescence imaging in vivo. Opt Express (2008) 2.48
Adaptive optics in microscopy. Philos Trans A Math Phys Eng Sci (2007) 2.14
Miniaturized probe based on a microelectromechanical system mirror for multiphoton microscopy. Opt Lett (2008) 1.39
Miniaturized probe for femtosecond laser microsurgery and two-photon imaging. Opt Express (2008) 1.32
In vivo three-dimensional spectral domain endoscopic optical coherence tomography using a microelectromechanical system mirror. Opt Lett (2007) 1.28
Micromirror-scanned dual-axis confocal microscope utilizing a gradient-index relay lens for image guidance during brain surgery. J Biomed Opt (2010) 1.27
Fiber optic in vivo imaging in the mammalian nervous system. Curr Opin Neurobiol (2004) 1.24
Nonlinear optical endoscope based on a compact two axes piezo scanner and a miniature objective lens. Opt Express (2008) 1.18
Wave front engineering for microscopy of living cells. Opt Express (2005) 1.08
Gradient-index fiber-optic microprobes for minimally invasive in vivo low-coherence interferometry. Opt Lett (2002) 1.01
Correction of low order aberrations using continuous deformable mirrors. Opt Express (2008) 0.82
Application of eigenmode in the adaptive optics system based on a micromachined membrane deformable mirror. Appl Opt (2006) 0.79
Construction and test of a GRIN-based optical objective. J Microsc (2010) 0.79
Impaired permeability to Ins(1,4,5)P3 in a mutant connexin underlies recessive hereditary deafness. Nat Cell Biol (2004) 2.70
A mechanism for sensing noise damage in the inner ear. Curr Biol (2004) 2.07
ATP release through connexin hemichannels and gap junction transfer of second messengers propagate Ca2+ signals across the inner ear. Proc Natl Acad Sci U S A (2008) 2.01
Purinergic signalling and intercellular Ca2+ wave propagation in the organ of Corti. Cell Calcium (2006) 1.21
Permeability and gating properties of human connexins 26 and 30 expressed in HeLa cells. Biochem Biophys Res Commun (2003) 1.15
Unitary permeability of gap junction channels to second messengers measured by FRET microscopy. Nat Methods (2007) 1.14
Pathogenetic role of the deafness-related M34T mutation of Cx26. Hum Mol Genet (2006) 1.14
Coordinated control of connexin 26 and connexin 30 at the regulatory and functional level in the inner ear. Proc Natl Acad Sci U S A (2008) 1.11
The novel mouse mutation Oblivion inactivates the PMCA2 pump and causes progressive hearing loss. PLoS Genet (2008) 1.08
The human deafness-associated connexin 30 T5M mutation causes mild hearing loss and reduces biochemical coupling among cochlear non-sensory cells in knock-in mice. Hum Mol Genet (2010) 1.07
Presynaptic calcium stores modulate afferent release in vestibular hair cells. J Neurosci (2003) 1.03
ATP-mediated cell-cell signaling in the organ of Corti: the role of connexin channels. Purinergic Signal (2010) 1.00
Three-dimensional current flow in a large-scale model of the cochlea and the mechanism of amplification of sound. J R Soc Interface (2009) 0.99
The novel PMCA2 pump mutation Tommy impairs cytosolic calcium clearance in hair cells and links to deafness in mice. J Biol Chem (2010) 0.98
Regulation of outer hair cell cytoskeletal stiffness by intracellular Ca2+: underlying mechanism and implications for cochlear mechanics. Cell Calcium (2003) 0.98
Permeation pathway of homomeric connexin 26 and connexin 30 channels investigated by molecular dynamics. J Biomol Struct Dyn (2012) 0.96
Otoacoustic emissions from residual oscillations of the cochlear basilar membrane in a human ear model. J Assoc Res Otolaryngol (2003) 0.92
BAAV mediated GJB2 gene transfer restores gap junction coupling in cochlear organotypic cultures from deaf Cx26Sox10Cre mice. PLoS One (2011) 0.90
A fully atomistic model of the Cx32 connexon. PLoS One (2008) 0.90
Selective defects in channel permeability associated with Cx32 mutations causing X-linked Charcot-Marie-Tooth disease. Neurobiol Dis (2006) 0.85
The 3.5 ångström X-ray structure of the human connexin26 gap junction channel is unlikely that of a fully open channel. Cell Commun Signal (2013) 0.85
Calcium microdomains at presynaptic active zones of vertebrate hair cells unmasked by stochastic deconvolution. Cell Calcium (2008) 0.85
Reduced phosphatidylinositol 4,5-bisphosphate synthesis impairs inner ear Ca2+ signaling and high-frequency hearing acquisition. Proc Natl Acad Sci U S A (2012) 0.85
No evidence for inositol 1,4,5-trisphosphate-dependent Ca2+ release in isolated fibers of adult mouse skeletal muscle. J Gen Physiol (2012) 0.85
Calcium signaling in the cochlea - Molecular mechanisms and physiopathological implications. Cell Commun Signal (2012) 0.82