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Molecular genetic dissection of mouse unconventional myosin-VA: head region mutations
scientific journal article
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instance of
scholarly article
1 reference
stated in
PubMed
PubMed ID
9560408
retrieved
31 January 2017
title
Molecular genetic dissection of mouse unconventional myosin-VA: head region mutations
(English)
1 reference
stated in
PubMed
PubMed ID
9560408
retrieved
31 January 2017
main subject
Myosin VA
1 reference
stated in
GOA release 2020-03-11
author name string
J. D. Huang
series ordinal
1
1 reference
stated in
PubMed
PubMed ID
9560408
retrieved
31 January 2017
M. J. Cope
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2
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PubMed
PubMed ID
9560408
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31 January 2017
V. Mermall
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3
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stated in
PubMed
PubMed ID
9560408
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31 January 2017
M. C. Strobel
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4
1 reference
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PubMed
PubMed ID
9560408
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31 January 2017
J. Kendrick-Jones
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5
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PubMed
PubMed ID
9560408
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31 January 2017
L. B. Russell
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6
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PubMed
PubMed ID
9560408
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31 January 2017
M. S. Mooseker
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7
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PubMed
PubMed ID
9560408
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31 January 2017
N. G. Copeland
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8
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PubMed
PubMed ID
9560408
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31 January 2017
N. A. Jenkins
series ordinal
9
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PubMed
PubMed ID
9560408
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31 January 2017
language of work or name
English
0 references
publication date
1 April 1998
1 reference
stated in
PubMed
PubMed ID
9560408
retrieved
31 January 2017
published in
Genetics
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stated in
PubMed
PubMed ID
9560408
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31 January 2017
volume
148
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PubMed
PubMed ID
9560408
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31 January 2017
page(s)
1951–1961
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PubMed
PubMed ID
9560408
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31 January 2017
issue
4
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PubMed
PubMed ID
9560408
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31 January 2017
cites work
Molecular genetic dissection of mouse unconventional myosin-VA: tail region mutations
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1460099
retrieved
17 March 2017
The autosomal recessive isolated deafness, DFNB2, and the Usher 1B syndrome are allelic defects of the myosin-VIIA gene
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1460099
retrieved
17 March 2017
Mutations in the myosin VIIA gene cause non-syndromic recessive deafness
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1460099
retrieved
17 March 2017
Myosin V associates with melanosomes in mouse melanocytes: evidence that myosin V is an organelle motor
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1460099
retrieved
17 March 2017
Cultured melanocytes from dilute mutant mice exhibit dendritic morphology and altered melanosome distribution
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1460099
retrieved
17 March 2017
Myosin VIIA mutation screening in 189 Usher syndrome type 1 patients
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1460099
retrieved
17 March 2017
The dilute-lethal (dl) gene attacks a Ca2+ store in the dendritic spine of Purkinje cells in mice
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1460099
retrieved
17 March 2017
Contractile protein mutations and heart disease
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1460099
retrieved
17 March 2017
X-ray structure of the magnesium(II).ADP.vanadate complex of the Dictyostelium discoideum myosin motor domain to 1.9 A resolution
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1460099
retrieved
17 March 2017
Structure of the actin-myosin complex and its implications for muscle contraction
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1460099
retrieved
17 March 2017
Three-dimensional structure of myosin subfragment-1: a molecular motor
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1460099
retrieved
17 March 2017
Structure of the regulatory domain of scallop myosin at 2.8 A resolution
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1460099
retrieved
17 March 2017
A type VII myosin encoded by the mouse deafness gene shaker-1
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1460099
retrieved
17 March 2017
Defective myosin VIIA gene responsible for Usher syndrome type 1B
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1460099
retrieved
17 March 2017
Retroviral sequences located within an intron of the dilute gene alter dilute expression in a tissue-specific manner
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1460099
retrieved
17 March 2017
X-ray structure of the magnesium(II)-pyrophosphate complex of the truncated head of Dictyostelium discoideum myosin to 2.7 A resolution
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1460099
retrieved
17 March 2017
X-ray structures of the myosin motor domain of Dictyostelium discoideum complexed with MgADP.BeFx and MgADP.AlF4-
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1460099
retrieved
17 March 2017
The mouse Snell's waltzer deafness gene encodes an unconventional myosin required for structural integrity of inner ear hair cells
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1460099
retrieved
17 March 2017
Genomic sequencing
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1460099
retrieved
17 March 2017
Cleavage of Structural Proteins during the Assembly of the Head of Bacteriophage T4
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1460099
retrieved
17 March 2017
Novel myosin heavy chain encoded by murine dilute coat colour locus
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1460099
retrieved
17 March 2017
Electrophoretic transfer of proteins from polyacrylamide gels to nitrocellulose sheets: procedure and some applications
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1460099
retrieved
17 March 2017
A Study of the Physiological Genetics of Coat Color in the Mouse by Means of the Dopa Reaction in Frozen Sections of Skin.
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1460099
retrieved
29 September 2017
Spectrum of Bmp5 mutations from germline mutagenesis experiments in mice
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1460099
retrieved
29 September 2017
Missense mutations in the beta-myosin heavy-chain gene cause central core disease in hypertrophic cardiomyopathy
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1460099
retrieved
29 September 2017
Porcine myosin-VI: characterization of a new mammalian unconventional myosin
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1460099
retrieved
29 September 2017
Actin- and microtubule-dependent organelle motors: interrelationships between the two motility systems.
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1460099
retrieved
29 September 2017
Structural interpretation of the mutations in the beta-cardiac myosin that have been implicated in familial hypertrophic cardiomyopathy
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1460099
retrieved
29 September 2017
A review of the genotoxicity of 1-ethyl-1-nitrosourea
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1460099
retrieved
29 September 2017
Molecular analysis of two mouse dilute locus deletion mutations: spontaneous dilute lethal20J and radiation-induced dilute prenatal lethal Aa2 alleles
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1460099
retrieved
29 September 2017
Differences in clinical expression of hypertrophic cardiomyopathy associated with two distinct mutations in the beta-myosin heavy chain gene. A 908Leu----Val mutation and a 403Arg----Gln mutation
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1460099
retrieved
29 September 2017
Primary structure and cellular localization of chicken brain myosin-V (p190), an unconventional myosin with calmodulin light chains
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1460099
retrieved
29 September 2017
Endoplasmic reticulum is missing in dendritic spines of Purkinje cells of the ataxic mutant rat.
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1460099
retrieved
3 June 2018
In vitro motilities of the unconventional myosins, brush border myosin-I, and chick brain myosin-V exhibit assay-dependent differences in velocity
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1460099
retrieved
27 November 2018
Subcellular localization of myosin V in nerve growth cones and outgrowth from dilute-lethal neurons
1 reference
stated in
PubMed
reference URL
https://pubmed.ncbi.nlm.nih.gov/9560408
retrieved
12 December 2020
based on heuristic
inferred from PubMed ID database lookup
Brain myosin-V is a two-headed unconventional myosin with motor activity
1 reference
stated in
PubMed
reference URL
https://pubmed.ncbi.nlm.nih.gov/9560408
retrieved
12 December 2020
based on heuristic
inferred from PubMed ID database lookup
Definition of functional units in a small chromosomal segment of the mouse and its use in interpreting the nature of radiation-induced mutations
1 reference
stated in
PubMed
reference URL
https://pubmed.ncbi.nlm.nih.gov/9560408
retrieved
12 December 2020
based on heuristic
inferred from PubMed ID database lookup
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PMCID
1460099
0 references
PubMed ID
9560408
1 reference
stated in
PubMed
PubMed ID
9560408
retrieved
31 January 2017
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