(Q34874723)

5 August 2017

1 reference

title

The molecular machinery for the biogenesis of lysosome-related organelles: lessons from Hermansky-Pudlak syndrome (English)

1 reference

5 August 2017

Marta Starcevic

1

1 reference

PubMed ID

12243726

5 August 2017

Ramin Nazarian

series ordinal

2

1 reference

PubMed ID

12243726

5 August 2017

Esteban C Dell'Angelica

series ordinal

3

1 reference

5 August 2017

1 August 2002

1 reference

5 August 2017

8

1 reference

Seminars in Cell & Developmental Biology

inferred from page(s)

published in

1 reference

5 August 2017

13

1 reference

5 August 2017

4

1 reference

5 August 2017

271-278

1 reference

The melanosome: membrane dynamics in black and white

5 August 2017

1 reference

https://api.crossref.org/works/10.1016%2FS1084952102000563

7 January 2021

Development of platelet secretory granules

1 reference

https://api.crossref.org/works/10.1016%2FS1084952102000563

7 January 2021

Hermansky-Pudlak syndrome and related disorders of organelle formation

1 reference

https://api.crossref.org/works/10.1016%2FS1084952102000563

7 January 2021

Mutation of a new gene causes a unique form of Hermansky-Pudlak syndrome in a genetic isolate of central Puerto Rico

1 reference

https://api.crossref.org/works/10.1016%2FS1084952102000563

7 January 2021

Mouse models of Hermansky Pudlak syndrome: a review

1 reference

https://api.crossref.org/works/10.1016%2FS1084952102000563

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%2FS1084952102000563

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%2FS1084952102000563

7 January 2021

Molecular characterization of the protein encoded by the Hermansky-Pudlak syndrome type 1 gene

1 reference

https://api.crossref.org/works/10.1016%2FS1084952102000563

7 January 2021

The Hermansky-Pudlak syndrome (HPS) protein is part of a high molecular weight complex involved in biogenesis of early melanosomes

1 reference

https://api.crossref.org/works/10.1016%2FS1084952102000563

7 January 2021

Abnormal translocation of tyrosinase and tyrosinase-related protein 1 in cutaneous melanocytes of Hermansky-Pudlak Syndrome and in melanoma cells transfected with anti-sense HPS1 cDNA.

1 reference

https://api.crossref.org/works/10.1016%2FS1084952102000563

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%2FS1084952102000563

7 January 2021

Adaptor-related proteins

1 reference

https://api.crossref.org/works/10.1016%2FS1084952102000563

7 January 2021

Beta-NAP, a cerebellar degeneration antigen, is a neuron-specific vesicle coat protein

1 reference

https://api.crossref.org/works/10.1016%2FS1084952102000563

7 January 2021

Accessory factors in clathrin-dependent synaptic vesicle endocytosis

1 reference

https://api.crossref.org/works/10.1016%2FS1084952102000563

7 January 2021

Adaptors for clathrin-mediated traffic

1 reference

https://api.crossref.org/works/10.1016%2FS1084952102000563

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%2FS1084952102000563

7 January 2021

Assembly and function of AP-3 complexes in cells expressing mutant subunits.

1 reference

https://api.crossref.org/works/10.1016%2FS1084952102000563

7 January 2021

AP-3 mediates tyrosinase but not TRP-1 trafficking in human melanocytes

1 reference

https://api.crossref.org/works/10.1016%2FS1084952102000563

7 January 2021

AP-3 adaptor functions in targeting P-selectin to secretory granules in endothelial cells

1 reference

https://api.crossref.org/works/10.1016%2FS1084952102000563

7 January 2021

A function for the AP3 coat complex in synaptic vesicle formation from endosomes

1 reference

https://api.crossref.org/works/10.1016%2FS1084952102000563

7 January 2021

The neuronal form of adaptor protein-3 is required for synaptic vesicle formation from endosomes.

1 reference

https://api.crossref.org/works/10.1016%2FS1084952102000563

7 January 2021

The medium subunits of adaptor complexes recognize distinct but overlapping sets of tyrosine-based sorting signals

1 reference

https://api.crossref.org/works/10.1016%2FS1084952102000563

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%2FS1084952102000563

7 January 2021

ADP-Ribosylation factor 1 (ARF1) regulates recruitment of the AP-3 adaptor complex to membranes.

1 reference

https://api.crossref.org/works/10.1016%2FS1084952102000563

7 January 2021

Functional and physical interactions of the adaptor protein complex AP-4 with ADP-ribosylation factors (ARFs).

1 reference

https://api.crossref.org/works/10.1016%2FS1084952102000563

7 January 2021

The assembly of AP-3 adaptor complex-containing clathrin-coated vesicles on synthetic liposomes

1 reference

https://api.crossref.org/works/10.1016%2FS1084952102000563

7 January 2021

Beta3A-adaptin, a subunit of the adaptor-like complex AP-3

1 reference

https://api.crossref.org/works/10.1016%2FS1084952102000563

7 January 2021

The AP-3 complex required for endosomal synaptic vesicle biogenesis is associated with a casein kinase Ialpha-like isoform

1 reference

https://api.crossref.org/works/10.1016%2FS1084952102000563

7 January 2021

A novel adaptor-related protein complex

1 reference

https://api.crossref.org/works/10.1016%2FS1084952102000563

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS1084952102000563

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS1084952102000563

7 January 2021

A dileucine-like sorting signal directs transport into an AP-3-dependent, clathrin-independent pathway to the yeast vacuole

1 reference

https://api.crossref.org/works/10.1016%2FS1084952102000563

7 January 2021

Association of the AP-3 adaptor complex with clathrin

1 reference

https://api.crossref.org/works/10.1016%2FS1084952102000563

7 January 2021

Peptide-in-groove interactions link target proteins to the beta-propeller of clathrin

1 reference

https://api.crossref.org/works/10.1016%2FS1084952102000563

7 January 2021

A novel clathrin homolog that co-distributes with cytoskeletal components functions in the trans-Golgi network

1 reference

https://api.crossref.org/works/10.1016%2FS1084952102000563

7 January 2021

Formation of AP-3 transport intermediates requires Vps41 function

1 reference

https://api.crossref.org/works/10.1016%2FS1084952102000563

7 January 2021

Vps41p function in the alkaline phosphatase pathway requires homo-oligomerization and interaction with AP-3 through two distinct domains

1 reference

https://api.crossref.org/works/10.1016%2FS1084952102000563

7 January 2021

hVPS41 is expressed in multiple isoforms and can associate with vesicles through a RING-H2 finger motif

1 reference

https://api.crossref.org/works/10.1016%2FS1084952102000563

7 January 2021

The gene mutated in cocoa mice, carrying a defect of organelle biogenesis, is a homologue of the human Hermansky-Pudlak syndrome-3 gene

1 reference

https://api.crossref.org/works/10.1016%2FS1084952102000563

7 January 2021

The pallid gene encodes a novel, syntaxin 13-interacting protein involved in platelet storage pool deficiency

1 reference

https://api.crossref.org/works/10.1016%2FS1084952102000563

7 January 2021

The gene for the muted (mu) mouse, a model for Hermansky-Pudlak syndrome, defines a novel protein which regulates vesicle trafficking

1 reference

https://api.crossref.org/works/10.1016%2FS1084952102000563

7 January 2021

Hermansky-Pudlak syndrome is caused by mutations in HPS4, the human homolog of the mouse light-ear gene

1 reference

https://api.crossref.org/works/10.1016%2FS1084952102000563

7 January 2021

Rab proteins as membrane organizers

1 reference

https://api.crossref.org/works/10.1016%2FS1084952102000563

7 January 2021

Rab geranylgeranyl transferase alpha mutation in the gunmetal mouse reduces Rab prenylation and platelet synthesis

1 reference

https://api.crossref.org/works/10.1016%2FS1084952102000563

7 January 2021

10.1016/S1084952102000563

Identifiers

DOI

1 reference

5 August 2017

1 reference

PubMed ID

12243726