(Q45259091)

11 December 2017

title

Normal lytic granule secretion by cytotoxic T lymphocytes deficient in BLOC-1, -2 and -3 and myosins Va, VIIa and XV. (English)

1 reference

11 December 2017

0 references

11

1 reference

11 December 2017

Giovanna Bossi

1

1 reference

11 December 2017

Sarah Booth

2

1 reference

11 December 2017

Richard Clark

3

1 reference

11 December 2017

E Graham Davis

4

1 reference

11 December 2017

Ri Liesner

5

1 reference

11 December 2017

Katherine Richards

6

1 reference

11 December 2017

Marta Starcevic

7

1 reference

11 December 2017

Jane Stinchcombe

8

1 reference

11 December 2017

Christina Trambas

9

1 reference

11 December 2017

Esteban C Dell'Angelica

10

1 reference

11 December 2017

publication date

1 March 2005

1 reference

11 December 2017

1 reference

11 December 2017

volume

6

1 reference

11 December 2017

issue

3

1 reference

11 December 2017

page(s)

243-251

1 reference

Mutations in RAB27A cause Griscelli syndrome associated with haemophagocytic syndrome

11 December 2017

cites work

1 reference

https://api.crossref.org/works/10.1111%2FJ.1600-0854.2005.00264.X

Complementation of the beige mutation in cultured cells by episomally replicating murine yeast artificial chromosomes.

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1600-0854.2005.00264.X

The Beige/Chediak-Higashi syndrome gene encodes a widely expressed cytosolic protein

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1600-0854.2005.00264.X

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1600-0854.2005.00264.X

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1600-0854.2005.00264.X

Rab27a is required for regulated secretion in cytotoxic T lymphocytes

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1600-0854.2005.00264.X

Rab27a regulates the peripheral distribution of melanosomes in melanocytes

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1600-0854.2005.00264.X

The leaden gene product is required with Rab27a to recruit myosin Va to melanosomes in melanocytes

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1600-0854.2005.00264.X

Synaptotagmin-like protein 5: a novel Rab27A effector with C-terminal tandem C2 domains

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1600-0854.2005.00264.X

The Slp homology domain of synaptotagmin-like proteins 1-4 and Slac2 functions as a novel Rab27A binding domain

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1600-0854.2005.00264.X

Slac2-c (synaptotagmin-like protein homologue lacking C2 domains-c), a novel linker protein that interacts with Rab27, myosin Va/VIIa, and actin

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1600-0854.2005.00264.X

MyRIP, a novel Rab effector, enables myosin VIIa recruitment to retinal melanosomes

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1600-0854.2005.00264.X

Disorders of vesicles of lysosomal lineage: the Hermansky-Pudlak syndromes

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1600-0854.2005.00264.X

Adaptor protein 3-dependent microtubule-mediated movement of lytic granules to the immunological synapse

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1600-0854.2005.00264.X

BLOC-1, a novel complex containing the pallidin and muted proteins involved in the biogenesis of melanosomes and platelet-dense granules

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1600-0854.2005.00264.X

Hermansky-Pudlak syndrome type 7 (HPS-7) results from mutant dysbindin, a member of the biogenesis of lysosome-related organelles complex 1 (BLOC-1)

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1600-0854.2005.00264.X

Cappuccino, a mouse model of Hermansky-Pudlak syndrome, encodes a novel protein that is part of the pallidin-muted complex (BLOC-1)

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1600-0854.2005.00264.X

The building BLOC(k)s of lysosomes and related organelles

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1600-0854.2005.00264.X

Identification of snapin and three novel proteins (BLOS1, BLOS2, and BLOS3/reduced pigmentation) as subunits of biogenesis of lysosome-related organelles complex-1 (BLOC-1)

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1600-0854.2005.00264.X

Reduced pigmentation (rp), a mouse model of Hermansky-Pudlak syndrome, encodes a novel component of the BLOC-1 complex

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1600-0854.2005.00264.X

Ru2 and Ru encode mouse orthologs of the genes mutated in human Hermansky-Pudlak syndrome types 5 and 6

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1600-0854.2005.00264.X

Characterization of BLOC-2, a complex containing the Hermansky-Pudlak syndrome proteins HPS3, HPS5 and HPS6

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1600-0854.2005.00264.X

The Hermansky-Pudlak syndrome 3 (cocoa) protein is a component of the biogenesis of lysosome-related organelles complex-2 (BLOC-2).

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1600-0854.2005.00264.X

Biogenesis of lysosome-related organelles complex 3 (BLOC-3): a complex containing the Hermansky-Pudlak syndrome (HPS) proteins HPS1 and HPS4

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1600-0854.2005.00264.X

BLOC-3, a protein complex containing the Hermansky-Pudlak syndrome gene products HPS1 and HPS4

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1600-0854.2005.00264.X

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1600-0854.2005.00264.X

The Hermansky-Pudlak syndrome 1 (HPS1) and HPS4 proteins are components of two complexes, BLOC-3 and BLOC-4, involved in the biogenesis of lysosome-related organelles

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1600-0854.2005.00264.X

The mouse organellar biogenesis mutant buff results from a mutation in Vps33a, a homologue of yeast vps33 and Drosophila carnation

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1600-0854.2005.00264.X

Defective granule exocytosis in Rab27a-deficient lymphocytes from Ashen mice

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1600-0854.2005.00264.X

Pigment mutations in the mouse which also affect lysosomal functions lead to suppressed natural killer cell activity

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1600-0854.2005.00264.X

Identification of an organelle receptor for myosin-Va

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1600-0854.2005.00264.X

Munc13-4 is a GTP-Rab27-binding protein regulating dense core granule secretion in platelets.

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1600-0854.2005.00264.X

Munc13-4 is essential for cytolytic granules fusion and is mutated in a form of familial hemophagocytic lymphohistiocytosis (FHL3).

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1600-0854.2005.00264.X

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1600-0854.2005.00264.X

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1600-0854.2005.00264.X

Perforin is activated by a proteolytic cleavage during biosynthesis which reveals a phospholipid-binding C2 domain.

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1600-0854.2005.00264.X

Secretory Lysosome Biogenesis in Cytotoxic T Lymphocytes from Normal and Chediak Higashi Syndrome Patients

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1600-0854.2005.00264.X

10.1111/J.1600-0854.2005.00264.X

21 January 2018

Identifiers

DOI

1 reference

11 December 2017

1 reference