Rab27a: A key to melanosome transport in human melanocytes (Q24290970)

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5 November 2019

title

Rab27a: A key to melanosome transport in human melanocytes (English)

1 reference

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RAB27A, member RAS oncogene family

5 November 2019

main subject

1 reference

GOA release 2020-03-11

author

Philippe Bahadoran

1

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Geneviève de Saint Basile

5 November 2019

7

1 reference

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Ricardo P Casaroli-Marano

5 November 2019

8

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5 November 2019

Robert Ballotti

10

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5 November 2019

author name string

E Aberdam

2

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5 November 2019

F Mantoux

3

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5 November 2019

R Buscà

4

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5 November 2019

K Bille

5

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5 November 2019

N Yalman

6

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5 November 2019

J P Ortonne

9

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5 November 2019

language of work or name

English

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publication date

1 February 2001

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5 November 2019

number of pages

8

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inferred from page(s)

published in

Journal of Cell Biology

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5 November 2019

volume

152

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5 November 2019

page(s)

843-850

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5 November 2019

issue

4

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Interaction of a Golgi-associated kinesin-like protein with Rab6

5 November 2019

cites work

1 reference

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Retinal degeneration in choroideremia: deficiency of rab geranylgeranyl transferase

19 March 2017

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Immuno-localization of the insulin regulatable glucose transporter in brown adipose tissue of the rat

19 March 2017

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The COOH-terminal domain of Myo2p, a yeast myosin V, has a direct role in secretory vesicle targeting

19 March 2017

1 reference

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

19 March 2017

1 reference

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A syndrome associating partial albinism and immunodeficiency

19 March 2017

1 reference

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

19 March 2017

1 reference

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

19 March 2017

1 reference

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Novel myosin heavy chain encoded by murine dilute coat colour locus

19 March 2017

1 reference

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Mutations in RAB27A cause Griscelli syndrome associated with haemophagocytic syndrome

19 March 2017

1 reference

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Two genes are responsible for Griscelli syndrome at the same 15q21 locus.

7 April 2017

1 reference

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Cloning, mapping and characterization of the human RAB27A gene.

27 September 2017

1 reference

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Rab5 regulates motility of early endosomes on microtubules

27 September 2017

1 reference

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Genetic basis of hemophagocytic lymphohistiocytosis syndrome (Review).

27 September 2017

1 reference

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

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2195788

Subcellular localization of myosin-V in the B16 melanoma cells, a wild-type cell line for the dilute gene

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2195788

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

27 September 2017

1 reference

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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

27 September 2017

1 reference

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Griscelli disease with cerebral involvement

27 September 2017

1 reference

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Partial albinism with immunodeficiency: Griscelli syndrome: report of a case and review of the literature

27 September 2017

1 reference

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

30 May 2018

1 reference

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Repeated UVB irradiations do not have the same potential to promote stimulation of melanogenesis in cultured normal human melanocytes.

30 May 2018

1 reference

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Specific identification of an authentic clone for mammalian tyrosinase.

30 May 2018

1 reference

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Myosin V colocalizes with melanosomes and subcortical actin bundles not associated with stress fibers in human epidermal melanocytes.

30 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2195788

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

29 November 2018

1 reference

12 December 2020

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

1 reference

12 December 2020

Partial albinism with immunodeficiency (Griscelli syndrome)

1 reference

12 December 2020

The mutation Gly142-->Glu in human lipoprotein lipase produces a missorted protein that is diverted to lysosomes

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

Identifiers

DOI

10.1083/JCB.152.4.843

2 references

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5 November 2019

1 reference

2 references

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5 November 2019

2 references