(Q30481050)

English

A novel allele of myosin VIIa reveals a critical function for the C-terminal FERM domain for melanosome transport in retinal pigment epithelial cells

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scholarly article

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Europe PubMed Central

PMC publication ID

12 September 2017

A novel allele of myosin VIIa reveals a critical function for the C-terminal FERM domain for melanosome transport in retinal pigment epithelial cells (English)

1 reference

Europe PubMed Central

PMC publication ID

12 September 2017

author name string

Martin Schwander

1

1 reference

Europe PubMed Central

PMC publication ID

12 September 2017

Vanda Lopes

2

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Europe PubMed Central

PMC publication ID

12 September 2017

Anna Sczaniecka

3

1 reference

Europe PubMed Central

PMC publication ID

12 September 2017

Daniel Gibbs

4

1 reference

Europe PubMed Central

PMC publication ID

12 September 2017

Concepcion Lillo

5

1 reference

Europe PubMed Central

PMC publication ID

12 September 2017

David Delano

6

1 reference

Europe PubMed Central

PMC publication ID

12 September 2017

Lisa M Tarantino

7

1 reference

Europe PubMed Central

PMC publication ID

12 September 2017

Tim Wiltshire

8

1 reference

Europe PubMed Central

PMC publication ID

12 September 2017

David S Williams

9

1 reference

Europe PubMed Central

PMC publication ID

12 September 2017

Ulrich Müller

10

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Europe PubMed Central

PMC publication ID

12 September 2017

language of work or name

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publication date

1 December 2009

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Europe PubMed Central

PMC publication ID

12 September 2017

Journal of Neuroscience

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Europe PubMed Central

PMC publication ID

12 September 2017

29

1 reference

Europe PubMed Central

PMC publication ID

12 September 2017

50

1 reference

Europe PubMed Central

PMC publication ID

12 September 2017

15810-15818

1 reference

Europe PubMed Central

PMC publication ID

12 September 2017

describes a project that uses

1 reference

Europe PubMed Central

11 June 2022

https://www.ebi.ac.uk/europepmc/webservices/rest/PMC2834289/fullTextXML

based on heuristic

inferred from PubMed Central ID database lookup

Impacts of Usher syndrome type IB mutations on human myosin VIIa motor function

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2834289

20 June 2018

The multiple lives of NMD factors: balancing roles in gene and genome regulation

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2834289

20 June 2018

Usher syndromes due to MYO7A, PCDH15, USH2A or GPR98 mutations share retinal disease mechanism

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2834289

20 June 2018

Usher syndrome: animal models, retinal function of Usher proteins, and prospects for gene therapy

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2834289

20 June 2018

Analysis of the linkage of MYRIP and MYO7A to melanosomes by RAB27A in retinal pigment epithelial cells

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2834289

20 June 2018

A forward genetics screen in mice identifies recessive deafness traits and reveals that pejvakin is essential for outer hair cell function

1 reference

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20 June 2018

The cargo-binding domain regulates structure and activity of myosin 5

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2834289

20 June 2018

A mutant mouse with a highly specific contextual fear-conditioning deficit found in an N-ethyl-N-nitrosourea (ENU) mutagenesis screen

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2834289

20 June 2018

Physical and functional interaction between protocadherin 15 and myosin VIIa in mechanosensory hair cells

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2834289

20 June 2018

The unconventional myosin-VIIa associates with lysosomes

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2834289

20 June 2018

Role of myosin VIIa and Rab27a in the motility and localization of RPE melanosomes

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2834289

20 June 2018

Abnormal phagocytosis by retinal pigmented epithelium that lacks myosin VIIa, the Usher syndrome 1B protein

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2834289

20 June 2018

Genome-wide single-nucleotide polymorphism analysis defines haplotype patterns in mouse

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2834289

20 June 2018

Slac2-c (synaptotagmin-like protein homologue lacking C2 domains-c), a novel linker protein that interacts with Rab27, myosin Va/VIIa, and actin

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2834289

20 June 2018

Stereocilia defects in waltzer (Cdh23), shaker1 (Myo7a) and double waltzer/shaker1 mutant mice

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2834289

20 June 2018

MyRIP, a novel Rab effector, enables myosin VIIa recruitment to retinal melanosomes

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2834289

20 June 2018

Reduced climbing and increased slipping adaptation in cochlear hair cells of mice with Myo7a mutations

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2834289

20 June 2018

Map Manager QTX, cross-platform software for genetic mapping

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2834289

20 June 2018

Ca(2 )-dependent regulation of the motor activity of myosin V.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2834289

20 June 2018

Exonic splicing enhancers: mechanism of action, diversity and role in human genetic diseases

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2834289

20 June 2018

Effect of ADP and ionic strength on the kinetic and motile properties of recombinant mouse myosin V

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2834289

20 June 2018

Myosin VIIa participates in opsin transport through the photoreceptor cilium

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2834289

20 June 2018

Assessment of hearing in 80 inbred strains of mice by ABR threshold analyses

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2834289

20 June 2018

N-ethyl-N-nitrosourea mutagenesis of a 6- to 11-cM subregion of the Fah-Hbb interval of mouse chromosome 7: Completed testing of 4557 gametes and deletion mapping and complementation analysis of 31 mutations.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2834289

20 June 2018

Mutation analysis of the mouse myosin VIIA deafness gene

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2834289

20 June 2018

Mutant myosin VIIa causes defective melanosome distribution in the RPE of shaker-1 mice

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2834289

20 June 2018

Shaker-1 mutations reveal roles for myosin VIIA in both development and function of cochlear hair cells

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2834289

20 June 2018

Mutations in the myosin VIIA gene cause non-syndromic recessive deafness

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2834289

20 June 2018

Integrin alpha8beta1 is critically important for epithelial-mesenchymal interactions during kidney morphogenesis

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2834289

20 June 2018

Lack of neurotrophin-3 results in death of spinal sensory neurons and premature differentiation of their precursors

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2834289

20 June 2018

Molecular cloning and domain structure of human myosin-VIIa, the gene product defective in Usher syndrome 1B

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2834289

20 June 2018

A type VII myosin encoded by the mouse deafness gene shaker-1

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2834289

20 June 2018

Defective myosin VIIA gene responsible for Usher syndrome type 1B

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2834289

20 June 2018

Expression in cochlea and retina of myosin VIIa, the gene product defective in Usher syndrome type 1B

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2834289

20 June 2018

Splice junctions, branch point sites, and exons: sequence statistics, identification, and applications to genome project

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2834289

20 June 2018

A strategy for fine-structure functional analysis of a 6- to 11-centimorgan region of mouse chromosome 7 by high-efficiency mutagenesis

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2834289

20 June 2018

Mutation spectrum of MYO7A and evaluation of a novel nonsyndromic deafness DFNB2 allele with residual function

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2834289

26 November 2018

Single base-pair substitutions in exon-intron junctions of human genes: nature, distribution, and consequences for mRNA splicing

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2834289

26 November 2018

Functional analysis of Slac2-c/MyRIP as a linker protein between melanosomes and myosin VIIa.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2834289

26 November 2018

Mouse models for Usher syndrome 1B.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2834289

26 November 2018

Kinetic characterization of a monomeric unconventional myosin V construct

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2834289

26 November 2018

Myosin VIIa as a common component of cilia and microvilli

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2834289

26 November 2018

Effects of shaker-1 mutations on myosin-VIIa protein and mRNA expression

1 reference

https://pubmed.ncbi.nlm.nih.gov/20016096

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Mutation profile of the MYO7A gene in Spanish patients with Usher syndrome type I

1 reference

https://pubmed.ncbi.nlm.nih.gov/20016096

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.1523/JNEUROSCI.4876-09.2009

1 reference

Europe PubMed Central

PMC publication ID

12 September 2017

PMC publication ID

1 reference

Europe PubMed Central

PMC publication ID

12 September 2017

PubMed publication ID

1 reference

Europe PubMed Central

PMC publication ID

12 September 2017

ResearchGate publication ID

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