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A mutation in Rab27a causes the vesicle transport defects observed in ashen mice
scientific journal article
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scholarly article
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stated in
PubMed
PubMed ID
10859366
retrieved
31 January 2017
title
A mutation in Rab27a causes the vesicle transport defects observed in ashen mice
(English)
1 reference
stated in
PubMed
PubMed ID
10859366
retrieved
31 January 2017
main subject
RAB27A, member RAS oncogene family
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GOA release 2020-03-11
author name string
S. M. Wilson
series ordinal
1
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PubMed
PubMed ID
10859366
retrieved
31 January 2017
R. Yip
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2
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PubMed
PubMed ID
10859366
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31 January 2017
D. A. Swing
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3
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PubMed
PubMed ID
10859366
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31 January 2017
T. N. O'Sullivan
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4
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PubMed
PubMed ID
10859366
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31 January 2017
Y. Zhang
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PubMed
PubMed ID
10859366
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31 January 2017
E. K. Novak
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6
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PubMed
PubMed ID
10859366
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31 January 2017
R. T. Swank
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7
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PubMed
PubMed ID
10859366
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31 January 2017
L. B. Russell
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PubMed
PubMed ID
10859366
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31 January 2017
N. G. Copeland
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9
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PubMed
PubMed ID
10859366
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31 January 2017
N. A. Jenkins
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10
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PubMed
PubMed ID
10859366
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31 January 2017
language of work or name
English
0 references
publication date
5 July 2000
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PubMed
PubMed ID
10859366
retrieved
31 January 2017
published in
Proceedings of the National Academy of Sciences of the United States of America
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PubMed
PubMed ID
10859366
retrieved
31 January 2017
volume
97
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PubMed
PubMed ID
10859366
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31 January 2017
page(s)
7933–7938
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PubMed
PubMed ID
10859366
retrieved
31 January 2017
issue
14
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PubMed
PubMed ID
10859366
retrieved
31 January 2017
cites work
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Altered trafficking of lysosomal proteins in Hermansky-Pudlak syndrome due to mutations in the beta 3A subunit of the AP-3 adaptor
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The beta3A subunit gene (Ap3b1) of the AP-3 adaptor complex is altered in the mouse hypopigmentation mutant pearl, a model for Hermansky-Pudlak syndrome and night blindness
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Interaction of a Golgi-associated kinesin-like protein with Rab6
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Myosin V associates with melanosomes in mouse melanocytes: evidence that myosin V is an organelle motor
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Molecular cloning and characterization of rab27a and rab27b, novel human rab proteins shared by melanocytes and platelets
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Cultured melanocytes from dilute mutant mice exhibit dendritic morphology and altered melanosome distribution
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17 March 2017
Absence epilepsy in tottering mutant mice is associated with calcium channel defects
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The dilute-lethal (dl) gene attacks a Ca2+ store in the dendritic spine of Purkinje cells in mice
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PubMed Central
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Positional cloning of a gene for Hermansky-Pudlak syndrome, a disorder of cytoplasmic organelles
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PubMed Central
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17 March 2017
cDNA cloning of component A of Rab geranylgeranyl transferase and demonstration of its role as a Rab escort protein
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PubMed Central
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The murine dilute suppressor gene encodes a cell autonomous suppressor
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17 March 2017
Dilute suppressor dsu acts semidominantly to suppress the coat color phenotype of a deletion mutation, dl20J, of the murine dilute locus
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The Saccharomyces cerevisiae MYO2 gene encodes an essential myosin for vectorial transport of vesicles
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17 March 2017
Novel myosin heavy chain encoded by murine dilute coat colour locus
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17 March 2017
A ras-like protein is required for a post-Golgi event in yeast secretion
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PubMed Central
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Cloning, mapping and characterization of the human RAB27A gene.
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Multi-organellar disorders of pigmentation: intracellular traffic jams in mammals, flies and yeast
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29 September 2017
Direct interaction of microtubule- and actin-based transport motors
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PubMed Central
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29 September 2017
Visualization of melanosome dynamics within wild-type and dilute melanocytes suggests a paradigm for myosin V function In vivo
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PubMed Central
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29 September 2017
The mouse pale ear (ep) mutation is the homologue of human Hermansky-Pudlak syndrome
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PubMed Central
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29 September 2017
Griscelli disease maps to chromosome 15q21 and is associated with mutations in the myosin-Va gene
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PubMed Central
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29 September 2017
Brain myosin V is a synaptic vesicle-associated motor protein: evidence for a Ca2+-dependent interaction with the synaptobrevin-synaptophysin complex
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29 September 2017
Functional identification of the mouse circadian Clock gene by transgenic BAC rescue
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The role of Myo2, a yeast class V myosin, in vesicular transport
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Melanosomes are specialized members of the lysosomal lineage of organelles.
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PubMed Central
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Deficient geranylgeranylation of Ram/Rab27 in choroideremia.
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29 September 2017
Relationship between a retroviral germ line reintegration and a new mutation at the ashen locus in B10.F mice. Retroviral integration and an ashen mutation
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PubMed Central
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29 September 2017
Organization, distribution, and stability of endogenous ecotropic murine leukemia virus DNA sequences in chromosomes of Mus musculus
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PubMed Central
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https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=16648
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29 September 2017
The murine dilute suppressor gene dsu suppresses the coat-color phenotype of three pigment mutations that alter melanocyte morphology, d, ash and ln
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PubMed Central
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https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=16648
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29 September 2017
Cocoa: a new mouse model for platelet storage pool deficiency
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PubMed Central
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29 September 2017
Molecular genetic analysis of the dilute-short ear (d-se) region of the mouse
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PubMed Central
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https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=16648
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29 September 2017
The ram: a novel low molecular weight GTP-binding protein cDNA from a rat megakaryocyte library
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PubMed Central
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https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=16648
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29 September 2017
Mouse coat colour mutations: a molecular genetic resource which spans the centuries.
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29 September 2017
Topography And Thickness Of Air-Dried Human Platelets Measured By Correlative Transmission And Scanning Electron Microscopy
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PubMed Central
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29 September 2017
An easy method to determine the serotonin content of human platelets
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3 June 2018
Unconventional myosins in cell movement, membrane traffic, and signal transduction
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3 June 2018
Endoplasmic reticulum is missing in dendritic spines of Purkinje cells of the ataxic mutant rat.
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PubMed Central
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3 June 2018
A cloned, immortal line of murine melanoblasts inducible to differentiate to melanocytes.
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3 June 2018
Association of kinesin with characterized membrane-bounded organelles
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PubMed Central
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3 June 2018
The lysosomal granule membrane protein, LAMP-2, is also present in platelet dense granule membranes.
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PubMed Central
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https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=16648
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20 June 2018
Mouse choroideremia gene mutation causes photoreceptor cell degeneration and is not transmitted through the female germline.
1 reference
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PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=16648
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27 November 2018
Mouse pale ear (ep) is homologous to human Hermansky-Pudlak syndrome and contains a rare 'AT-AC' intron.
1 reference
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PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=16648
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27 November 2018
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/10859366
retrieved
12 December 2020
based on heuristic
inferred from PubMed ID database lookup
Dilute (d) coat colour mutation of DBA/2J mice is associated with the site of integration of an ecotropic MuLV genome
1 reference
stated in
PubMed
reference URL
https://pubmed.ncbi.nlm.nih.gov/10859366
retrieved
12 December 2020
based on heuristic
inferred from PubMed ID database lookup
The predominant defect in dilute melanocytes is in melanosome distribution and not cell shape, supporting a role for myosin V in melanosome transport
1 reference
stated in
PubMed
reference URL
https://pubmed.ncbi.nlm.nih.gov/10859366
retrieved
12 December 2020
based on heuristic
inferred from PubMed ID database lookup
Rab proteins
1 reference
stated in
PubMed
reference URL
https://pubmed.ncbi.nlm.nih.gov/10859366
retrieved
12 December 2020
based on heuristic
inferred from PubMed ID database lookup
Identifiers
DOI
10.1073/PNAS.140212797
1 reference
stated in
PubMed
PubMed ID
10859366
retrieved
31 January 2017
ADS bibcode
2000PNAS...97.7933W
0 references
PMCID
16648
0 references
PubMed ID
10859366
1 reference
stated in
PubMed
PubMed ID
10859366
retrieved
31 January 2017
ResearchGate publication ID
12460033
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