Home
Random
Nearby
Log in
Settings
Donate
About Wikidata
Disclaimers
Search
(Q28591690)
Watch
English
Mutant myosin VIIa causes defective melanosome distribution in the RPE of shaker-1 mice
scientific journal article
In more languages
edit
Statements
instance of
scholarly article
1 reference
stated in
PubMed
PubMed ID
9620764
retrieved
31 January 2017
title
Mutant myosin VIIa causes defective melanosome distribution in the RPE of shaker-1 mice
(English)
1 reference
stated in
PubMed
PubMed ID
9620764
retrieved
31 January 2017
main subject
Myosin VIIA
1 reference
stated in
GOA release 2020-03-11
author name string
X. Liu
series ordinal
1
1 reference
stated in
PubMed
PubMed ID
9620764
retrieved
31 January 2017
B. Ondek
series ordinal
2
1 reference
stated in
PubMed
PubMed ID
9620764
retrieved
31 January 2017
D. S. Williams
series ordinal
3
1 reference
stated in
PubMed
PubMed ID
9620764
retrieved
31 January 2017
language of work or name
English
0 references
publication date
1 June 1998
1 reference
stated in
PubMed
PubMed ID
9620764
retrieved
31 January 2017
published in
Nature Genetics
1 reference
stated in
PubMed
PubMed ID
9620764
retrieved
31 January 2017
volume
19
1 reference
stated in
PubMed
PubMed ID
9620764
retrieved
31 January 2017
page(s)
117–118
1 reference
stated in
PubMed
PubMed ID
9620764
retrieved
31 January 2017
issue
2
1 reference
stated in
PubMed
PubMed ID
9620764
retrieved
31 January 2017
cites work
Defective myosin VIIA gene responsible for Usher syndrome type 1B
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2F470
retrieved
21 January 2018
A type VII myosin encoded by the mouse deafness gene shaker-1
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2F470
retrieved
21 January 2018
Mutation analysis of the mouse myosin VIIA deafness gene
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2F470
retrieved
21 January 2018
Expression in cochlea and retina of myosin VIIa, the gene product defective in Usher syndrome type 1B
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2F470
retrieved
21 January 2018
Human Usher 1B/mouse shaker-1: the retinal phenotype discrepancy explained by the presence/absence of myosin VIIA in the photoreceptor cells
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2F470
retrieved
21 January 2018
Cultured melanocytes from dilute mutant mice exhibit dendritic morphology and altered melanosome distribution
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2F470
retrieved
21 January 2018
Brain myosin-V is a two-headed unconventional myosin with motor activity
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2F470
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Identifiers
DOI
10.1038/470
1 reference
stated in
PubMed
PubMed ID
9620764
retrieved
31 January 2017
PubMed ID
9620764
1 reference
stated in
PubMed
PubMed ID
9620764
retrieved
31 January 2017
Springer Nature article ID
10.1038/470
0 references
Sitelinks
Wikipedia
(0 entries)
edit
Wikibooks
(0 entries)
edit
Wikinews
(0 entries)
edit
Wikiquote
(0 entries)
edit
Wikisource
(0 entries)
edit
Wikiversity
(0 entries)
edit
Wikivoyage
(0 entries)
edit
Wiktionary
(0 entries)
edit
Multilingual sites
(0 entries)
edit
