(Q30494485)

21 September 2017

Function of MYO7A in the human RPE and the validity of shaker1 mice as a model for Usher syndrome 1B (English)

1 reference

21 September 2017

1 reference

Daniel Gibbs

1

1 reference

21 September 2017

Tanja Diemer

2

1 reference

21 September 2017

Kornnika Khanobdee

3

1 reference

21 September 2017

Jane Hu

4

1 reference

21 September 2017

Dean Bok

5

1 reference

21 September 2017

David S Williams

6

1 reference

21 September 2017

language of work or name

English

0 references

publication date

30 July 2009

1 reference

Investigative Ophthalmology Visual Science

21 September 2017

1 reference

21 September 2017

51

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21 September 2017

2

1 reference

21 September 2017

1130-1135

1 reference

describes a project that uses

21 September 2017

ImageJ

1 reference

11 June 2022

https://www.ebi.ac.uk/europepmc/webservices/rest/PMC2868451/fullTextXML

inferred from PubMed Central ID database lookup

cites work

Harmonin in the murine retina and the retinal phenotypes of Ush1c-mutant mice and human USH1C.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2868451

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

14 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2868451

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

14 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2868451

The ternary Rab27a-Myrip-Myosin VIIa complex regulates melanosome motility in the retinal pigment epithelium

14 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2868451

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

14 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2868451

Lentiviral gene replacement therapy of retinas in a mouse model for Usher syndrome type 1B.

14 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2868451

Ames Waltzer deaf mice have reduced electroretinogram amplitudes and complex alternative splicing of Pcdh15 transcripts

14 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2868451

Characterization of Usher syndrome type I gene mutations in an Usher syndrome patient population

14 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2868451

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

14 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2868451

Isolation and culture of primary mouse retinal pigmented epithelial cells.

14 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2868451

The role of Rab27a in the regulation of melanosome distribution within retinal pigment epithelial cells

14 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2868451

Cdh23 mutations in the mouse are associated with retinal dysfunction but not retinal degeneration

14 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2868451

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

14 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2868451

A cell culture medium that supports the differentiation of human retinal pigment epithelium into functionally polarized monolayers

14 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2868451

Genetic heterogeneity of Usher syndrome: analysis of 151 families with Usher type I.

14 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2868451

Myosin VIIa participates in opsin transport through the photoreceptor cilium

14 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2868451

Mutation analysis of the mouse myosin VIIA deafness gene

14 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2868451

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

14 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2868451

Myosin VIIa, the product of the Usher 1B syndrome gene, is concentrated in the connecting cilia of photoreceptor cells.

14 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2868451

Human Usher 1B/mouse shaker-1: the retinal phenotype discrepancy explained by the presence/absence of myosin VIIA in the photoreceptor cells

14 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2868451

ARPE-19, a human retinal pigment epithelial cell line with differentiated properties

14 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2868451

Clinical diagnosis of the Usher syndromes. Usher Syndrome Consortium

14 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2868451

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

14 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2868451

Defective myosin VIIA gene responsible for Usher syndrome type 1B

14 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2868451

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

14 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2868451

Mouse models for Usher syndrome 1B.

14 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2868451

Assessment of retinal structure and function in Ames waltzer mice.

26 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2868451

Myosin VIIa as a common component of cilia and microvilli

26 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2868451

Rhodopsin transport in the membrane of the connecting cilium of mammalian photoreceptor cells

26 November 2018

1 reference

12 December 2020

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

1 reference

12 December 2020

Cochlear implantation in individuals with Usher type 1 syndrome

1 reference

12 December 2020

Evaluation of the myosin VIIA gene and visual function in patients with Usher syndrome type I

1 reference

12 December 2020

Identifiers

DOI

10.1167/IOVS.09-4032

1 reference

21 September 2017

1 reference

21 September 2017

PubMed publication ID

19643958

1 reference