(Q40443093)

20 September 2017

title

Training and aging modulate the loss-of-balance phenotype observed in a new ENU-induced allele of Otopetrin1. (English)

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20 September 2017

9

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20 September 2017

Vanessa Besson

1

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20 September 2017

Valérie Nalesso

2

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20 September 2017

Alexandre Herpin

3

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20 September 2017

Jean-Charles Bizot

4

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20 September 2017

Nadia Messaddeq

5

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20 September 2017

Raymond Romand

6

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20 September 2017

Anne Puech

7

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20 September 2017

Véronique Blanquet

8

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20 September 2017

language of work or name

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1 October 2005

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20 September 2017

number of pages

12

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based on heuristic

inferred from page(s)

published in

Biology of the Cell

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20 September 2017

volume

97

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20 September 2017

issue

10

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20 September 2017

page(s)

787-798

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Retinal degeneration in the rd mouse is caused by a defect in the beta subunit of rod cGMP-phosphodiesterase

20 September 2017

cites work

1 reference

https://api.crossref.org/works/10.1042%2FBC20040525

Man in motion. Historical and clinical aspects of vestibular function. A review

21 January 2018

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Cappuccino, a mouse model of Hermansky-Pudlak syndrome, encodes a novel protein that is part of the pallidin-muted complex (BLOC-1)

21 January 2018

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Partial behavioral compensation is revealed in balance tasked mutant mice lacking otoconia.

21 January 2018

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A proposed test battery and constellations of specific behavioral paradigms to investigate the behavioral phenotypes of transgenic and knockout mice

21 January 2018

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Vestibular compensation and substitution

21 January 2018

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Spatiotemporal expression of otogelin in the developing and adult mouse inner ear.

21 January 2018

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Diagnosis and initiating treatment for peripheral system disorders: imbalance and dizziness with normal hearing

21 January 2018

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Targeted disruption of mouse Pds provides insight about the inner-ear defects encountered in Pendred syndrome.

21 January 2018

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Extracellular matrices associated with the apical surfaces of sensory epithelia in the inner ear: Molecular and structural diversity

21 January 2018

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Development of SHIRPA to characterise the phenotype of gene-targeted mice

21 January 2018

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Efficient generation and mapping of recessive developmental mutations using ENU mutagenesis

21 January 2018

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Genome-wide, large-scale production of mutant mice by ENU mutagenesis.

21 January 2018

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A novel gene involved in zinc transport is deficient in the lethal milk mouse

21 January 2018

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The pallid gene encodes a novel, syntaxin 13-interacting protein involved in platelet storage pool deficiency

21 January 2018

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Non-syndromic vestibular disorder with otoconial agenesis in tilted/mergulhador mice caused by mutations in otopetrin 1

21 January 2018

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Gravity receptor function in mice with graded otoconial deficiencies.

21 January 2018

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Mutation in AP-3 delta in the mocha mouse links endosomal transport to storage deficiency in platelets, melanosomes, and synaptic vesicles

21 January 2018

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Genetic and phenotypic analysis of the mouse mutant mh2J, an Ap3d allele caused by IAP element insertion.

21 January 2018

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Balance and hearing deficits in mice with a null mutation in the gene encoding plasma membrane Ca2+-ATPase isoform 2

21 January 2018

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A targeted deletion in alpha-tectorin reveals that the tectorial membrane is required for the gain and timing of cochlear feedback.

21 January 2018

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Haplo-insufficiency revealed in deafwaddler mice when tested for hearing loss and ataxia

21 January 2018

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Pallidin is a component of a multi-protein complex involved in the biogenesis of lysosome-related organelles

21 January 2018

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A systematic, genome-wide, phenotype-driven mutagenesis programme for gene function studies in the mouse

21 January 2018

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Otoconial agenesis in tilted mutant mice

21 January 2018

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Vestibular defects in head-tilt mice result from mutations in Nox3, encoding an NADPH oxidase

21 January 2018

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Identification of a nonsense mutation in the rod photoreceptor cGMP phosphodiesterase beta-subunit gene of the rd mouse

21 January 2018

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SHIRPA, a protocol for behavioral assessment: validation for longitudinal study of neurological dysfunction in mice.

21 January 2018

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Targeted disruption of otog results in deafness and severe imbalance

21 January 2018

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Development of the mouse vestibular system in the absence of gravity perception

21 January 2018

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Control of crystal size and lattice formation by starmaker in otolith biomineralization.

21 January 2018

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Mutated otopetrin 1 affects the genesis of otoliths and the localization of Starmaker in zebrafish

21 January 2018

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Characterization of otoconin-95, the major protein of murine otoconia, provides insights into the formation of these inner ear biominerals

21 January 2018

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Otoconin-90, the mammalian otoconial matrix protein, contains two domains of homology to secretory phospholipase A2.

21 January 2018

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ENU induced mutations causing congenital cardiovascular anomalies

21 January 2018

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https://api.crossref.org/works/10.1042%2FBC20040525

The gene for the muted (mu) mouse, a model for Hermansky-Pudlak syndrome, defines a novel protein which regulates vesicle trafficking

21 January 2018

1 reference

https://api.crossref.org/works/10.1042%2FBC20040525

Otoancorin, an inner ear protein restricted to the interface between the apical surface of sensory epithelia and their overlying acellular gels, is defective in autosomal recessive deafness DFNB22.

21 January 2018

1 reference

https://api.crossref.org/works/10.1042%2FBC20040525

Influence of visual control, conduction, and central integration on static and dynamic balance in healthy older adults

21 January 2018

1 reference

https://api.crossref.org/works/10.1042%2FBC20040525

21 January 2018

Identifiers

DOI

10.1042/BC20040525

1 reference

20 September 2017

1 reference