Related references
Note: Only part of the references are listed.Calcium- and otoferlin-dependent exocytosis by immature outer hair cells
Maryline Beurg et al.
JOURNAL OF NEUROSCIENCE (2008)
The interaction of JRAB/MICAL-L2 with Rab8 and Rab13 coordinates the assembly of tight junctions and adherens junctions
Rie Yamamura et al.
MOLECULAR BIOLOGY OF THE CELL (2008)
Rab8 regulates basolateral secretory, but not recycling, traffic at the recycling endosome
Lauren Henry et al.
MOLECULAR BIOLOGY OF THE CELL (2008)
A missense mutation in the conserved C2B domain of otoferlin causes deafness in a new mouse model of DFNB9
Chantal Longo-Guess et al.
HEARING RESEARCH (2007)
Thyroid hormone deficiency affects postnatal spiking activity and expression of Ca2+ and K+ channels in rodent inner hair cells
Niels Brandt et al.
JOURNAL OF NEUROSCIENCE (2007)
Differential expression of otoferlin in brain, vestibular system, immature and mature cochlea of the rat
Nicola Schug et al.
EUROPEAN JOURNAL OF NEUROSCIENCE (2006)
Thyroid hormone receptors TRα1 and TRβ differentially regulate gene expression of Kcnq4 and prestin during final differentiation of outer hair cells
Harald Winter et al.
JOURNAL OF CELL SCIENCE (2006)
Bardet-Biedl syndrome: an emerging pathomechanism of intracellular transport
O. E. Blacque et al.
CELLULAR AND MOLECULAR LIFE SCIENCES (2006)
Optineurin links myosin VI to the Golgi complex and is involved in Golgi organization and exocytosis
DA Sahlender et al.
JOURNAL OF CELL BIOLOGY (2005)
Deletion of the Ca2+-activated potassium (BK) α-subunit but not the BKβ1-subunit leads to progressive hearing loss
L Rüttiger et al.
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA (2004)
Local control of AMPA receptor trafficking at the postsynaptic terminal by a small GTPase of the Rab family
NZ Gerges et al.
JOURNAL OF BIOLOGICAL CHEMISTRY (2004)
The Rab8 GTPase selectively regulates AP-1B-dependent basolateral transport in polarized Madin!Darby canine kidney cells
AL Ang et al.
JOURNAL OF CELL BIOLOGY (2003)
Non-syndromic recessive auditory neuropathy is the result of mutations in the otoferlin (OTOF) gene
R Varga et al.
JOURNAL OF MEDICAL GENETICS (2003)
Substitutions in the conserved C2C domain of otoferlin cause DFNB9, a form of nonsyndromic autosomal recessive deafness
F Mirghomizadeh et al.
NEUROBIOLOGY OF DISEASE (2002)
Mutant rab8 impairs docking and fusion of rhodopsin-bearing post-Golgi membranes and causes cell death of transgenic Xenopus rods
OL Moritz et al.
MOLECULAR BIOLOGY OF THE CELL (2001)
Rab8b and its interacting partner TRIP8b are involved in regulated secretion in AtT20 cells
S Chen et al.
JOURNAL OF BIOLOGICAL CHEMISTRY (2001)
OTOF encodes multiple long and short isoforms: Genetic evidence that the long ones underlie recessive deafness DFNB9
S Yasunaga et al.
AMERICAN JOURNAL OF HUMAN GENETICS (2000)
Share Paper
