(Q33756436)

29 July 2017

title

Mouse model for Usher syndrome: linkage mapping suggests homology to Usher type I reported at human chromosome 11p15. (English)

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29 July 2017

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J R Heckenlively

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29 July 2017

B Chang

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29 July 2017

L C Erway

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29 July 2017

C Peng

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29 July 2017

N L Hawes

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29 July 2017

G S Hageman

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29 July 2017

T H Roderick

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29 July 2017

language of work or name

English

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publication date

1 November 1995

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Proceedings of the National Academy of Sciences of the United States of America

29 July 2017

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inferred from page(s)

published in

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29 July 2017

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29 July 2017

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29 July 2017

page(s)

11100-11104

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Defective myosin VIIA gene responsible for Usher syndrome type 1B

29 July 2017

cites work

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https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=40579

Usher syndrome: definition and estimate of prevalence from two high-risk populations

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=40579

Usher's syndrome. Ophthalmic and neuro-otologic findings suggesting genetic heterogeneity

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=40579

Histopathology of the inner ear in Usher's syndrome as observed by light and electron microscopy

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=40579

Clinical findings and common symptoms in retinitis pigmentosa

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=40579

Screening for mouse retinal degenerations. I. Correlation of indirect ophthalmoscopy, electroretinograms, and histology

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=40579

Localization of Usher syndrome type II to chromosome 1q.

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=40579

Mapping recessive ophthalmic diseases: linkage of the locus for Usher syndrome type II to a DNA marker on chromosome 1q.

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=40579

Localization of two genes for Usher syndrome type I to chromosome 11.

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=40579

Linkage of Usher syndrome type I gene (USH1B) to the long arm of chromosome 11

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=40579

Comparative map for mice and humans

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=40579

Purkinje cell degeneration, a new neurological mutation in the mouse

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=40579

A new H-2-linked mutation, rds, causing retinal degeneration in the mouse

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=40579

Usher's Syndrome Type III

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=40579

Genetics of age-related hearing loss in mice: I. Inbred and F1 hybrid strains

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=40579

Embedding in epoxy resins for ultrathin sectioning in electron microscopy

30 October 2018

1 reference

12 December 2020

Screening for mouse retinal degenerations. II. Molossinus MOLC and MOLD strains

1 reference

12 December 2020

Fat (fat) and tubby (tub): two autosomal recessive mutations causing obesity syndromes in the mouse

1 reference

12 December 2020

New mouse primary retinal degeneration (rd-3)

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12 December 2020

RETINAL DEGENERATION IN THE MOUSE: LOCATION OF THE RD LOCUS IN LINKAGE GROUP XVII

1 reference

12 December 2020

Identifiers

DOI

10.1073/PNAS.92.24.11100

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29 July 2017

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29 July 2017

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