Age-dependent gait abnormalities in mice lacking the Rnf170 gene linked to human autosomal-dominant sensory ataxia. (Q51698376)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:26433933%20AND%20SRC:MED&resulttype=core&format=json

25 February 2020

title

Age-dependent gait abnormalities in mice lacking the Rnf170 gene linked to human autosomal-dominant sensory ataxia (English)

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:26433933%20AND%20SRC:MED&resulttype=core&format=json

25 February 2020

8

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:26433933%20AND%20SRC:MED&resulttype=core&format=json

25 February 2020

author name string

Youngsoo Kim

1

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:26433933%20AND%20SRC:MED&resulttype=core&format=json

25 February 2020

Seong Hun Kim

2

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:26433933%20AND%20SRC:MED&resulttype=core&format=json

25 February 2020

Kook Hwan Kim

3

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:26433933%20AND%20SRC:MED&resulttype=core&format=json

25 February 2020

Sujin Chae

4

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:26433933%20AND%20SRC:MED&resulttype=core&format=json

25 February 2020

Chanki Kim

5

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:26433933%20AND%20SRC:MED&resulttype=core&format=json

25 February 2020

Jeongjin Kim

6

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:26433933%20AND%20SRC:MED&resulttype=core&format=json

25 February 2020

Hee-Sup Shin

7

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:26433933%20AND%20SRC:MED&resulttype=core&format=json

25 February 2020

Daesoo Kim

9

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:26433933%20AND%20SRC:MED&resulttype=core&format=json

25 February 2020

publication date

3 October 2015

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:26433933%20AND%20SRC:MED&resulttype=core&format=json

25 February 2020

published in

Human Molecular Genetics

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:26433933%20AND%20SRC:MED&resulttype=core&format=json

25 February 2020

volume

24

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:26433933%20AND%20SRC:MED&resulttype=core&format=json

25 February 2020

issue

25

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:26433933%20AND%20SRC:MED&resulttype=core&format=json

25 February 2020

page(s)

7196-7206

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:26433933%20AND%20SRC:MED&resulttype=core&format=json

Progression of gait disorder and rigidity and risk of death in older persons.

25 February 2020

cites work

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDV417

Gait disorders in older adults

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDV417

Gluten ataxia in perspective: epidemiology, genetic susceptibility and clinical characteristics

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDV417

Gait analysis of spinal cord injured subjects: effects of injury level and spasticity.

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDV417

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDV417

RNF170 protein, an endoplasmic reticulum membrane ubiquitin ligase, mediates inositol 1,4,5-trisphosphate receptor ubiquitination and degradation

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDV417

IP3 receptor/Ca2+ channel: from discovery to new signaling concepts

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDV417

The Role of the Transmembrane RING Finger Proteins in Cellular and Organelle Function

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDV417

A mutation in the RNF170 gene causes autosomal dominant sensory ataxia

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDV417

A founder haplotype for autosomal dominant sensory ataxia in Eastern Canada.

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDV417

A novel neurodegenerative disease characterised by posterior column ataxia and pyramidal tract involvement maps to chromosome 8p12-8q12.1.

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDV417

A Point Mutation in the Ubiquitin Ligase RNF170 That Causes Autosomal Dominant Sensory Ataxia Destabilizes the Protein and Impairs Inositol 1,4,5-Trisphosphate Receptor-mediated Ca2+ Signaling

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDV417

Dynamics of Insulin Secretion by the Perfused Rat Pancreas

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDV417

CatWalk-assisted gait analysis in the assessment of spinal cord injury

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDV417

Assessing gait impairment following experimental traumatic brain injury in mice

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDV417

Ataxic gait analysis in a mouse model of the olivocerebellar degeneration

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDV417

Bace1 and Neuregulin-1 cooperate to control formation and maintenance of muscle spindles

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDV417

Friedreich ataxia mouse models with progressive cerebellar and sensory ataxia reveal autophagic neurodegeneration in dorsal root ganglia

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDV417

Proprioceptive sensory neuropathy in mice with a mutation in the cytoplasmic Dynein heavy chain 1 gene

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDV417

Chronic suppression of inositol 1,4,5-triphosphate receptor-mediated calcium signaling in cerebellar purkinje cells alleviates pathological phenotype in spinocerebellar ataxia 2 mice

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDV417

Autosomal dominant cerebellar ataxia (SCA6) associated with small polyglutamine expansions in the alpha 1A-voltage-dependent calcium channel

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDV417

Progressive ataxia due to a missense mutation in a calcium-channel gene

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDV417

HECT and RING finger families of E3 ubiquitin ligases at a glance

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDV417

Compensatory strategies for reaching in stroke.

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDV417

Dynamic arm swinging in human walking.

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDV417

The how and why of arm swing during human walking

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDV417

Intrinsic function of a neuronal network — a vertebrate central pattern generator1Published on the World Wide Web on 8 April 1998.1

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDV417

Dual-mode operation of neuronal networks involved in left-right alternation

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDV417

Rac-GAP alpha-chimerin regulates motor-circuit formation as a key mediator of EphrinB3/EphA4 forward signaling

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDV417

Autosomal dominant sensory ataxia: a neuroaxonal dystrophy

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDV417