A mutation in Rab27a causes the vesicle transport defects observed in ashen mice (Q28594384)

31 January 2017

title

A mutation in Rab27a causes the vesicle transport defects observed in ashen mice (English)

1 reference

RAB27A, member RAS oncogene family

31 January 2017

main subject

1 reference

GOA release 2020-03-11

author name string

S. M. Wilson

1

1 reference

31 January 2017

R. Yip

2

1 reference

31 January 2017

D. A. Swing

3

1 reference

31 January 2017

T. N. O'Sullivan

4

1 reference

31 January 2017

Y. Zhang

5

1 reference

31 January 2017

E. K. Novak

6

1 reference

31 January 2017

R. T. Swank

7

1 reference

31 January 2017

L. B. Russell

8

1 reference

31 January 2017

N. G. Copeland

9

1 reference

31 January 2017

N. A. Jenkins

10

1 reference

31 January 2017

language of work or name

English

0 references

publication date

5 July 2000

1 reference

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

31 January 2017

published in

1 reference

31 January 2017

volume

97

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31 January 2017

issue

14

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31 January 2017

page(s)

7933–7938

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Cloning and characterization of a novel RING finger protein that interacts with class V myosins

31 January 2017

cites work

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17 March 2017

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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

17 March 2017

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17 March 2017

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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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Molecular cloning and characterization of rab27a and rab27b, novel human rab proteins shared by melanocytes and platelets

17 March 2017

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

17 March 2017

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17 March 2017

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

17 March 2017

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Positional cloning of a gene for Hermansky-Pudlak syndrome, a disorder of cytoplasmic organelles

17 March 2017

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cDNA cloning of component A of Rab geranylgeranyl transferase and demonstration of its role as a Rab escort protein

17 March 2017

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17 March 2017

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Dilute suppressor dsu acts semidominantly to suppress the coat color phenotype of a deletion mutation, dl20J, of the murine dilute locus

17 March 2017

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17 March 2017

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17 March 2017

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7 April 2017

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Multi-organellar disorders of pigmentation: intracellular traffic jams in mammals, flies and yeast

29 September 2017

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Direct interaction of microtubule- and actin-based transport motors

29 September 2017

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Visualization of melanosome dynamics within wild-type and dilute melanocytes suggests a paradigm for myosin V function In vivo

29 September 2017

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The mouse pale ear (ep) mutation is the homologue of human Hermansky-Pudlak syndrome

29 September 2017

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Griscelli disease maps to chromosome 15q21 and is associated with mutations in the myosin-Va gene

29 September 2017

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29 September 2017

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Functional identification of the mouse circadian Clock gene by transgenic BAC rescue

29 September 2017

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The role of Myo2, a yeast class V myosin, in vesicular transport

29 September 2017

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29 September 2017

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Melanosomes are specialized members of the lysosomal lineage of organelles.

29 September 2017

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Deficient geranylgeranylation of Ram/Rab27 in choroideremia.

29 September 2017

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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

29 September 2017

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Organization, distribution, and stability of endogenous ecotropic murine leukemia virus DNA sequences in chromosomes of Mus musculus

29 September 2017

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The murine dilute suppressor gene dsu suppresses the coat-color phenotype of three pigment mutations that alter melanocyte morphology, d, ash and ln

29 September 2017

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Cocoa: a new mouse model for platelet storage pool deficiency

29 September 2017

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Molecular genetic analysis of the dilute-short ear (d-se) region of the mouse

29 September 2017

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The ram: a novel low molecular weight GTP-binding protein cDNA from a rat megakaryocyte library

29 September 2017

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Mouse coat colour mutations: a molecular genetic resource which spans the centuries.

29 September 2017

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Topography And Thickness Of Air-Dried Human Platelets Measured By Correlative Transmission And Scanning Electron Microscopy

29 September 2017

1 reference

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An easy method to determine the serotonin content of human platelets

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=16648

Unconventional myosins in cell movement, membrane traffic, and signal transduction

3 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=16648

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

3 June 2018

1 reference

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A cloned, immortal line of murine melanoblasts inducible to differentiate to melanocytes.

3 June 2018

1 reference

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Association of kinesin with characterized membrane-bounded organelles

3 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=16648

The lysosomal granule membrane protein, LAMP-2, is also present in platelet dense granule membranes.

3 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=16648

Mouse choroideremia gene mutation causes photoreceptor cell degeneration and is not transmitted through the female germline.

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=16648

Mouse pale ear (ep) is homologous to human Hermansky-Pudlak syndrome and contains a rare 'AT-AC' intron

27 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=16648

Definition of functional units in a small chromosomal segment of the mouse and its use in interpreting the nature of radiation-induced mutations

27 November 2018

1 reference

12 December 2020

Dilute (d) coat colour mutation of DBA/2J mice is associated with the site of integration of an ecotropic MuLV genome

1 reference

12 December 2020

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

12 December 2020

1 reference

12 December 2020

Identifiers

DOI

10.1073/PNAS.140212797

1 reference

31 January 2017

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0 references

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