Multi-organellar disorders of pigmentation: intracellular traffic jams in mammals, flies and yeast (Q33719413)

28 July 2017

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title

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

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28 July 2017

1

Spritz RA

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28 July 2017

1 September 1999

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28 July 2017

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28 July 2017

15

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28 July 2017

9

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28 July 2017

337-340

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Molecular genetics of the Hermansky-Pudlak and Chediak-Higashi syndromes

28 July 2017

1 reference

https://api.crossref.org/works/10.1016%2FS0168-9525%2899%2901785-0

7 January 2021

Multi-organellar disorders of pigmentation: tied up in traffic

1 reference

https://api.crossref.org/works/10.1016%2FS0168-9525%2899%2901785-0

7 January 2021

Genetics, development, and malignancy of melanocytes.

1 reference

https://api.crossref.org/works/10.1016%2FS0168-9525%2899%2901785-0

7 January 2021

Mouse models of Hermansky Pudlak syndrome: a review

1 reference

https://api.crossref.org/works/10.1016%2FS0168-9525%2899%2901785-0

7 January 2021

Not just pretty eyes: Drosophila eye-colour mutations and lysosomal delivery.

1 reference

https://api.crossref.org/works/10.1016%2FS0168-9525%2899%2901785-0

7 January 2021

Protein transport to the yeast vacuole

1 reference

https://api.crossref.org/works/10.1016%2FS0168-9525%2899%2901785-0

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0168-9525%2899%2901785-0

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0168-9525%2899%2901785-0

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0168-9525%2899%2901785-0

7 January 2021

Mutation analysis of patients with Hermansky-Pudlak syndrome: a frameshift hot spot in the HPS gene and apparent locus heterogeneity

1 reference

https://api.crossref.org/works/10.1016%2FS0168-9525%2899%2901785-0

7 January 2021

Three new mutations in a gene causing Hermansky-Pudlak syndrome: clinical correlations.

1 reference

https://api.crossref.org/works/10.1016%2FS0168-9525%2899%2901785-0

7 January 2021

HPS gene mutations in Hermansky-Pudlak syndrome

1 reference

https://api.crossref.org/works/10.1016%2FS0168-9525%2899%2901785-0

7 January 2021

Altered expression of a novel adaptin leads to defective pigment granule biogenesis in the Drosophila eye color mutant garnet

1 reference

https://api.crossref.org/works/10.1016%2FS0168-9525%2899%2901785-0

7 January 2021

Characterization of the adaptor-related protein complex, AP-3

1 reference

https://api.crossref.org/works/10.1016%2FS0168-9525%2899%2901785-0

7 January 2021

AP-3: an adaptor-like protein complex with ubiquitous expression

1 reference

https://api.crossref.org/works/10.1016%2FS0168-9525%2899%2901785-0

7 January 2021

The mammalian AP-3 adaptor-like complex mediates the intracellular transport of lysosomal membrane glycoproteins.

1 reference

https://api.crossref.org/works/10.1016%2FS0168-9525%2899%2901785-0

7 January 2021

Endocytosis and molecular sorting

1 reference

https://api.crossref.org/works/10.1016%2FS0168-9525%2899%2901785-0

7 January 2021

Clathrin-coated vesicle formation and protein sorting: an integrated process

1 reference

https://api.crossref.org/works/10.1016%2FS0168-9525%2899%2901785-0

7 January 2021

The trans-Golgi network: a late secretory sorting station

1 reference

https://api.crossref.org/works/10.1016%2FS0168-9525%2899%2901785-0

7 January 2021

Linking cargo to vesicle formation: receptor tail interactions with coat proteins.

1 reference

https://api.crossref.org/works/10.1016%2FS0168-9525%2899%2901785-0

7 January 2021

Coats and vesicle budding

1 reference

https://api.crossref.org/works/10.1016%2FS0168-9525%2899%2901785-0

7 January 2021

Mechanisms of protein sorting and coat assembly: insights from the clathrin-coated vesicle pathway

1 reference

https://api.crossref.org/works/10.1016%2FS0168-9525%2899%2901785-0

7 January 2021

The AP-3 complex: a coat of many colours

1 reference

https://api.crossref.org/works/10.1016%2FS0168-9525%2899%2901785-0

7 January 2021

A di-leucine-based motif in the cytoplasmic tail of LIMP-II and tyrosinase mediates selective binding of AP-3.

1 reference

https://api.crossref.org/works/10.1016%2FS0168-9525%2899%2901785-0

7 January 2021

Association of the AP-3 adaptor complex with clathrin

1 reference

https://api.crossref.org/works/10.1016%2FS0168-9525%2899%2901785-0

7 January 2021

AP-4, a novel protein complex related to clathrin adaptors

1 reference

https://api.crossref.org/works/10.1016%2FS0168-9525%2899%2901785-0

7 January 2021

Mutation in AP-3 delta in the mocha mouse links endosomal transport to storage deficiency in platelets, melanosomes, and synaptic vesicles

1 reference

https://api.crossref.org/works/10.1016%2FS0168-9525%2899%2901785-0

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0168-9525%2899%2901785-0

7 January 2021

Altered trafficking of lysosomal proteins in Hermansky-Pudlak syndrome due to mutations in the beta 3A subunit of the AP-3 adaptor

1 reference

https://api.crossref.org/works/10.1016%2FS0168-9525%2899%2901785-0

7 January 2021

Receptor-mediated protein sorting to the vacuole in yeast: roles for a protein kinase, a lipid kinase and GTP-binding proteins

1 reference

https://api.crossref.org/works/10.1016%2FS0168-9525%2899%2901785-0

7 January 2021

Molecular characterization of the deep orange (dor) gene of Drosophila melanogaster.

1 reference

https://api.crossref.org/works/10.1016%2FS0168-9525%2899%2901785-0

7 January 2021

Identification and mutation analysis of the complete gene for Chediak-Higashi syndrome

1 reference

https://api.crossref.org/works/10.1016%2FS0168-9525%2899%2901785-0

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0168-9525%2899%2901785-0

7 January 2021

Novel myosin heavy chain encoded by murine dilute coat colour locus

1 reference

https://api.crossref.org/works/10.1016%2FS0168-9525%2899%2901785-0

7 January 2021

Direct interaction of microtubule- and actin-based transport motors

1 reference

https://api.crossref.org/works/10.1016%2FS0168-9525%2899%2901785-0

7 January 2021

10.1016/S0168-9525(99)01785-0

Identifiers

DOI

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28 July 2017

1 reference

PubMed ID

10461199