(Q28587966)

31 January 2017

title

Molecular genetic dissection of mouse unconventional myosin-VA: head region mutations (English)

1 reference

31 January 2017

1 reference

GOA release 2020-03-11

author name string

J. D. Huang

1

1 reference

31 January 2017

M. J. Cope

2

1 reference

31 January 2017

V. Mermall

3

1 reference

31 January 2017

M. C. Strobel

4

1 reference

31 January 2017

J. Kendrick-Jones

5

1 reference

31 January 2017

L. B. Russell

6

1 reference

31 January 2017

M. S. Mooseker

7

1 reference

31 January 2017

N. G. Copeland

8

1 reference

31 January 2017

N. A. Jenkins

9

1 reference

31 January 2017

language of work or name

English

0 references

publication date

1 April 1998

1 reference

31 January 2017

1 reference

31 January 2017

volume

148

1 reference

31 January 2017

issue

4

1 reference

31 January 2017

page(s)

1951–1961

1 reference

Molecular genetic dissection of mouse unconventional myosin-VA: tail region mutations

31 January 2017

cites work

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1460099

The autosomal recessive isolated deafness, DFNB2, and the Usher 1B syndrome are allelic defects of the myosin-VIIA gene

17 March 2017

1 reference

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

17 March 2017

1 reference

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Myosin V associates with melanosomes in mouse melanocytes: evidence that myosin V is an organelle motor

17 March 2017

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Cultured melanocytes from dilute mutant mice exhibit dendritic morphology and altered melanosome distribution

17 March 2017

1 reference

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Myosin VIIA mutation screening in 189 Usher syndrome type 1 patients

17 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1460099

The dilute-lethal (dl) gene attacks a Ca2+ store in the dendritic spine of Purkinje cells in mice

17 March 2017

1 reference

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Contractile protein mutations and heart disease

17 March 2017

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X-ray structure of the magnesium(II).ADP.vanadate complex of the Dictyostelium discoideum myosin motor domain to 1.9 A resolution

17 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1460099

Structure of the actin-myosin complex and its implications for muscle contraction

17 March 2017

1 reference

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Three-dimensional structure of myosin subfragment-1: a molecular motor

17 March 2017

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Structure of the regulatory domain of scallop myosin at 2.8 A resolution

17 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1460099

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

17 March 2017

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Defective myosin VIIA gene responsible for Usher syndrome type 1B

17 March 2017

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Retroviral sequences located within an intron of the dilute gene alter dilute expression in a tissue-specific manner

17 March 2017

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X-ray structure of the magnesium(II)-pyrophosphate complex of the truncated head of Dictyostelium discoideum myosin to 2.7 A resolution

17 March 2017

1 reference

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X-ray structures of the myosin motor domain of Dictyostelium discoideum complexed with MgADP.BeFx and MgADP.AlF4-

17 March 2017

1 reference

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The mouse Snell's waltzer deafness gene encodes an unconventional myosin required for structural integrity of inner ear hair cells

17 March 2017

1 reference

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17 March 2017

1 reference

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Cleavage of Structural Proteins during the Assembly of the Head of Bacteriophage T4

17 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1460099

Novel myosin heavy chain encoded by murine dilute coat colour locus

17 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1460099

Electrophoretic transfer of proteins from polyacrylamide gels to nitrocellulose sheets: procedure and some applications

17 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1460099

A Study of the Physiological Genetics of Coat Color in the Mouse by Means of the Dopa Reaction in Frozen Sections of Skin.

17 March 2017

1 reference

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Spectrum of Bmp5 mutations from germline mutagenesis experiments in mice

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1460099

Missense mutations in the beta-myosin heavy-chain gene cause central core disease in hypertrophic cardiomyopathy

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1460099

Porcine myosin-VI: characterization of a new mammalian unconventional myosin

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1460099

Actin- and microtubule-dependent organelle motors: interrelationships between the two motility systems.

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1460099

Structural interpretation of the mutations in the beta-cardiac myosin that have been implicated in familial hypertrophic cardiomyopathy

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1460099

A review of the genotoxicity of 1-ethyl-1-nitrosourea

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1460099

Molecular analysis of two mouse dilute locus deletion mutations: spontaneous dilute lethal20J and radiation-induced dilute prenatal lethal Aa2 alleles

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1460099

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

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1460099

Primary structure and cellular localization of chicken brain myosin-V (p190), an unconventional myosin with calmodulin light chains

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1460099

Endoplasmic reticulum is missing in dendritic spines of Purkinje cells of the ataxic mutant rat.

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1460099

In vitro motilities of the unconventional myosins, brush border myosin-I, and chick brain myosin-V exhibit assay-dependent differences in velocity

3 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1460099

Subcellular localization of myosin V in nerve growth cones and outgrowth from dilute-lethal neurons

27 November 2018

1 reference

https://pubmed.ncbi.nlm.nih.gov/9560408

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Brain myosin-V is a two-headed unconventional myosin with motor activity

1 reference

https://pubmed.ncbi.nlm.nih.gov/9560408

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

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

https://pubmed.ncbi.nlm.nih.gov/9560408

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Identifiers

PMC publication ID

1460099

0 references

1 reference