Selective cochlear degeneration in mice lacking the F-box protein, Fbx2, a glycoprotein-specific ubiquitin ligase subunit. (Q48171841)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:17494702%20AND%20SRC:MED&resulttype=core&format=json

30 December 2019

title

Selective cochlear degeneration in mice lacking the F-box protein, Fbx2, a glycoprotein-specific ubiquitin ligase subunit (English)

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:17494702%20AND%20SRC:MED&resulttype=core&format=json

30 December 2019

2

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:17494702%20AND%20SRC:MED&resulttype=core&format=json

30 December 2019

Richard J Smith

10

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:17494702%20AND%20SRC:MED&resulttype=core&format=json

30 December 2019

author name string

Rick F Nelson

1

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:17494702%20AND%20SRC:MED&resulttype=core&format=json

30 December 2019

Yuzhou Zhang

3

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:17494702%20AND%20SRC:MED&resulttype=core&format=json

30 December 2019

Hsiang Wen

4

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:17494702%20AND%20SRC:MED&resulttype=core&format=json

30 December 2019

Tina Knutson

5

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:17494702%20AND%20SRC:MED&resulttype=core&format=json

30 December 2019

Cynthia M Gouvion

6

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:17494702%20AND%20SRC:MED&resulttype=core&format=json

30 December 2019

Barbara K Robinson

7

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:17494702%20AND%20SRC:MED&resulttype=core&format=json

30 December 2019

Zouping Zhou

8

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:17494702%20AND%20SRC:MED&resulttype=core&format=json

30 December 2019

Baoli Yang

9

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:17494702%20AND%20SRC:MED&resulttype=core&format=json

30 December 2019

Henry L Paulson

11

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:17494702%20AND%20SRC:MED&resulttype=core&format=json

30 December 2019

language of work or name

English

0 references

publication date

1 May 2007

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:17494702%20AND%20SRC:MED&resulttype=core&format=json

30 December 2019

published in

Journal of Neuroscience

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:17494702%20AND%20SRC:MED&resulttype=core&format=json

30 December 2019

volume

27

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:17494702%20AND%20SRC:MED&resulttype=core&format=json

30 December 2019

issue

19

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:17494702%20AND%20SRC:MED&resulttype=core&format=json

30 December 2019

page(s)

5163-5171

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:17494702%20AND%20SRC:MED&resulttype=core&format=json

describes a project that uses

30 December 2019

ImageJ

1 reference

11 June 2022

https://www.ebi.ac.uk/europepmc/webservices/rest/PMC6672365/fullTextXML

inferred from PubMed Central ID database lookup

cites work

KCNQ4, a novel potassium channel expressed in sensory outer hair cells, is mutated in dominant deafness

1 reference

12 December 2020

Targeted disruption of the Kvlqt1 gene causes deafness and gastric hyperplasia in mice

1 reference

12 December 2020

The origin of annular junctions: a mechanism of gap junction internalization

1 reference

12 December 2020

Neuronal KCNQ potassium channels: physiology and role in disease.

1 reference

12 December 2020

Skp1p and the F-box protein Rcy1p form a non-SCF complex involved in recycling of the SNARE Snc1p in yeast

1 reference

12 December 2020

OCP1, an F-box protein, co-localizes with OCP2/SKP1 in the cochlear epithelial gap junction region.

1 reference

12 December 2020

Targeted ablation of connexin26 in the inner ear epithelial gap junction network causes hearing impairment and cell death

1 reference

12 December 2020

E3 ubiquitin ligase that recognizes sugar chains

1 reference

12 December 2020

CUL7: A DOC domain-containing cullin selectively binds Skp1.Fbx29 to form an SCF-like complex

1 reference

12 December 2020

Connexin30 (Gjb6)-deficiency causes severe hearing impairment and lack of endocochlear potential

1 reference

12 December 2020

Physical map of 1p36, placement of breakpoints in monosomy 1p36, and clinical characterization of the syndrome

1 reference

12 December 2020

Association of cadherin 23 with polygenic inheritance and genetic modification of sensorineural hearing loss

1 reference

12 December 2020

Fbs2 is a new member of the E3 ubiquitin ligase family that recognizes sugar chains

1 reference

12 December 2020

Distribution of glycoconjugates during cochlea development in mice: light microscopic lectin study

1 reference

12 December 2020

Quality control in the endoplasmic reticulum protein factory

1 reference

12 December 2020

Ubiquitination-mediated regulation of biosynthesis of the adhesion receptor SHPS-1 in response to endoplasmic reticulum stress

1 reference

12 December 2020

Pathways for degradation of connexins and gap junctions.

1 reference

12 December 2020

The cochlear F-box protein OCP1 associates with OCP2 and connexin 26.

1 reference

12 December 2020

Roles of N-linked glycans in the endoplasmic reticulum

1 reference

12 December 2020

Mutations of ESPN cause autosomal recessive deafness and vestibular dysfunction

1 reference

12 December 2020

TRPA1 is a candidate for the mechanosensitive transduction channel of vertebrate hair cells

1 reference

12 December 2020

Impaired permeability to Ins(1,4,5)P3 in a mutant connexin underlies recessive hereditary deafness

1 reference

12 December 2020

ER stress and the unfolded protein response

1 reference

12 December 2020

Function and regulation of cullin-RING ubiquitin ligases

1 reference

12 December 2020

Activity-dependent NMDA receptor degradation mediated by retrotranslocation and ubiquitination

1 reference

12 December 2020

Thermodynamic analysis of interactions between N-linked sugar chains and F-box protein Fbs1.

1 reference

12 December 2020

ERAD: the long road to destruction

1 reference

12 December 2020

Identification of mutations in CUL7 in 3-M syndrome

1 reference

12 December 2020

A haplotype map of the human genome

1 reference

12 December 2020

A novel route for F-box protein-mediated ubiquitination links CHIP to glycoprotein quality control

1 reference

12 December 2020

Identification of N-glycan-binding proteins for E3 ubiquitin ligases

1 reference

12 December 2020

A neural-specific F-box protein Fbs1 functions as a chaperone suppressing glycoprotein aggregation.

1 reference

12 December 2020

The gap junction protein connexin43 is degraded via the ubiquitin proteasome pathway

1 reference

12 December 2020

Gap junction endocytosis and lysosomal degradation of connexin43-P2 in WB-F344 rat liver epithelial cells treated with DDT and lindane

1 reference

12 December 2020

Specific Proteins of the Organ of Corti

1 reference

12 December 2020

Connexin 26 mutations in hereditary non-syndromic sensorineural deafness

1 reference

12 December 2020

Dystroglycan is essential for early embryonic development: disruption of Reichert's membrane in Dag1-null mice

1 reference

12 December 2020

Behavioral and functional analysis of mouse phenotype: SHIRPA, a proposed protocol for comprehensive phenotype assessment

1 reference

12 December 2020

Chromosome 1p36 deletions: the clinical phenotype and molecular characterization of a common newly delineated syndrome

1 reference

12 December 2020

Human CUL-1, but not other cullin family members, selectively interacts with SKP1 to form a complex with SKP2 and cyclin A

1 reference

12 December 2020

A novel F box protein, NFB42, is highly enriched in neurons and induces growth arrest

1 reference

12 December 2020

10.1523/JNEUROSCI.0206-07.2007

Identifiers

DOI

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:17494702%20AND%20SRC:MED&resulttype=core&format=json

30 December 2019

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:17494702%20AND%20SRC:MED&resulttype=core&format=json

30 December 2019

1 reference