Otoferlin interacts with myosin VI: implications for maintenance of the basolateral synaptic structure of the inner hair cell. (Q43779285)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:19417007%20AND%20SRC:MED&resulttype=core&format=json

27 January 2020

title

Otoferlin interacts with myosin VI: implications for maintenance of the basolateral synaptic structure of the inner hair cell (English)

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:19417007%20AND%20SRC:MED&resulttype=core&format=json

27 January 2020

6

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:19417007%20AND%20SRC:MED&resulttype=core&format=json

27 January 2020

author name string

Paulina Heidrych

1

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:19417007%20AND%20SRC:MED&resulttype=core&format=json

27 January 2020

Ulrike Zimmermann

2

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:19417007%20AND%20SRC:MED&resulttype=core&format=json

27 January 2020

Stephanie Kuhn

3

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:19417007%20AND%20SRC:MED&resulttype=core&format=json

27 January 2020

Christoph Franz

4

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:19417007%20AND%20SRC:MED&resulttype=core&format=json

27 January 2020

Jutta Engel

5

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:19417007%20AND%20SRC:MED&resulttype=core&format=json

27 January 2020

Bernhard Hirt

7

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:19417007%20AND%20SRC:MED&resulttype=core&format=json

27 January 2020

Carsten M Pusch

8

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:19417007%20AND%20SRC:MED&resulttype=core&format=json

27 January 2020

Peter Ruth

9

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:19417007%20AND%20SRC:MED&resulttype=core&format=json

27 January 2020

Markus Pfister

10

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:19417007%20AND%20SRC:MED&resulttype=core&format=json

27 January 2020

Walter Marcotti

11

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:19417007%20AND%20SRC:MED&resulttype=core&format=json

27 January 2020

Nikolaus Blin

12

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:19417007%20AND%20SRC:MED&resulttype=core&format=json

27 January 2020

Marlies Knipper

13

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:19417007%20AND%20SRC:MED&resulttype=core&format=json

27 January 2020

publication date

5 May 2009

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:19417007%20AND%20SRC:MED&resulttype=core&format=json

27 January 2020

published in

Human Molecular Genetics

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:19417007%20AND%20SRC:MED&resulttype=core&format=json

27 January 2020

volume

18

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:19417007%20AND%20SRC:MED&resulttype=core&format=json

27 January 2020

issue

15

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:19417007%20AND%20SRC:MED&resulttype=core&format=json

27 January 2020

page(s)

2779-2790

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:19417007%20AND%20SRC:MED&resulttype=core&format=json

A mutation in OTOF, encoding otoferlin, a FER-1-like protein, causes DFNB9, a nonsyndromic form of deafness

27 January 2020

cites work

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDP213

Substitutions in the conserved C2C domain of otoferlin cause DFNB9, a form of nonsyndromic autosomal recessive deafness

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDP213

Non-syndromic recessive auditory neuropathy is the result of mutations in the otoferlin (OTOF) gene

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDP213

OTOF encodes multiple long and short isoforms: genetic evidence that the long ones underlie recessive deafness DFNB9.

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDP213

Otoferlin, defective in a human deafness form, is essential for exocytosis at the auditory ribbon synapse

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDP213

Direct interaction of otoferlin with syntaxin 1A, SNAP-25, and the L-type voltage-gated calcium channel Cav1.3.

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDP213

Differential expression of otoferlin in brain, vestibular system, immature and mature cochlea of the rat

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDP213

Thyroid hormone deficiency affects postnatal spiking activity and expression of Ca2+ and K+ channels in rodent inner hair cells.

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDP213

Tonotopic variation in the calcium dependence of neurotransmitter release and vesicle pool replenishment at mammalian auditory ribbon synapses

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDP213

Hair cell afferent synapses

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDP213

The mouse Snell's waltzer deafness gene encodes an unconventional myosin required for structural integrity of inner ear hair cells

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDP213

Role of myosin VI in the differentiation of cochlear hair cells

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDP213

Porcine myosin-VI: characterization of a new mammalian unconventional myosin

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDP213

Characterization of unconventional MYO6, the human homologue of the gene responsible for deafness in Snell's waltzer mice

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDP213

Mutations of MYO6 are associated with recessive deafness, DFNB37

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDP213

MYO6, the human homologue of the gene responsible for deafness in Snell's waltzer mice, is mutated in autosomal dominant nonsyndromic hearing loss

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDP213

Random mutagenesis of proximal mouse chromosome 5 uncovers predominantly embryonic lethal mutations

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDP213

A missense mutation in the conserved C2B domain of otoferlin causes deafness in a new mouse model of DFNB9

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDP213

How are the cellular functions of myosin VI regulated within the cell?

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDP213

Myosin VI is required for sorting of AP-1B-dependent cargo to the basolateral domain in polarized MDCK cells

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDP213

Myosin VI is an actin-based motor that moves backwards

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDP213

Myosin VI: cellular functions and motor properties

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDP213

Myosin VI, an actin motor for membrane traffic and cell migration

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDP213

Deletion of the Ca2+-activated potassium (BK) alpha-subunit but not the BKbeta1-subunit leads to progressive hearing loss

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDP213

Extrasynaptic localization of inactivating calcium-activated potassium channels in mouse inner hair cells.

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDP213

Increase in efficiency and reduction in Ca2+ dependence of exocytosis during development of mouse inner hair cells.

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDP213

Persistence of Ca(v)1.3 Ca2+ channels in mature outer hair cells supports outer hair cell afferent signaling.

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDP213

Regulation of myosin-VI targeting to endocytic compartments

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDP213

Congenital deafness and sinoatrial node dysfunction in mice lacking class D L-type Ca2+ channels

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDP213

Kinetics of exocytosis and endocytosis at the cochlear inner hair cell afferent synapse of the mouse

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDP213

Few CaV1.3 channels regulate the exocytosis of a synaptic vesicle at the hair cell ribbon synapse.

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDP213

Synaptotagmins: why so many?

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDP213

Bruchpilot promotes active zone assembly, Ca2+ channel clustering, and vesicle release

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDP213

A Myo6 mutation destroys coordination between the myosin heads, revealing new functions of myosin VI in the stereocilia of mammalian inner ear hair cells

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDP213

Loss of myosin VI reduces secretion and the size of the Golgi in fibroblasts from Snell's waltzer mice

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDP213

Aminoglycoside-induced phosphatidylserine externalization in sensory hair cells is regionally restricted, rapid, and reversible.

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDP213

Rab8b GTPase, a protein transport regulator, is an interacting partner of otoferlin, defective in a human autosomal recessive deafness form

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDP213

The vesicle docking protein p115 binds GM130, a cis-Golgi matrix protein, in a mitotically regulated manner

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDP213

Rab8 regulates basolateral secretory, but not recycling, traffic at the recycling endosome

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDP213

Membrane traffic in polarized epithelial cells

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDP213

Transport Protein Trafficking in Polarized Cells

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDP213