The pallid gene encodes a novel, syntaxin 13-interacting protein involved in platelet storage pool deficiency
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BLOC-1, a novel complex containing the pallidin and muted proteins involved in the biogenesis of melanosomes and platelet-dense granulesAssembly and architecture of biogenesis of lysosome-related organelles complex-1 (BLOC-1).BLOC-3, a protein complex containing the Hermansky-Pudlak syndrome gene products HPS1 and HPS4Identification of snapin and three novel proteins (BLOS1, BLOS2, and BLOS3/reduced pigmentation) as subunits of biogenesis of lysosome-related organelles complex-1 (BLOC-1)The dysbindin-containing complex (BLOC-1) in brain: developmental regulation, interaction with SNARE proteins and role in neurite outgrowthSystematic discovery of nonobvious human disease models through orthologous phenotypesThe pallidin (Pldn) gene and the role of SNARE proteins in melanosome biogenesisMutations in the clathrin-assembly gene Picalm are responsible for the hematopoietic and iron metabolism abnormalities in fit1 miceThe BLOS1-interacting protein KXD1 is involved in the biogenesis of lysosome-related organellesLarge scale protein identification in intracellular aquaporin-2 vesicles from renal inner medullary collecting ductDysbindin-containing complexes and their proposed functions in brain: from zero to (too) many in a decade.BLOC-1 and BLOC-3 regulate VAMP7 cycling to and from melanosomes via distinct tubular transport carriersMutations in the BLOC-1 subunits dysbindin and muted generate divergent and dosage-dependent phenotypes.BLOC-1 deficiency causes alterations in amino acid profile and in phospholipid and adenosine metabolism in the postnatal mouse hippocampus.Hermansky-Pudlak syndrome and related disorders of organelle formation.Megakaryocytes and beyond: the birth of platelets.The dark side of lysosome-related organelles: specialization of the endocytic pathway for melanosome biogenesis.What is the role of SNARE proteins in membrane fusion?Cell biology of the BLOC-1 complex subunit dysbindin, a schizophrenia susceptibility gene.Mechanisms of protein delivery to melanosomes in pigment cells.Training and aging modulate the loss-of-balance phenotype observed in a new ENU-induced allele of Otopetrin1.Aberrant lung structure, composition, and function in a murine model of Hermansky-Pudlak syndrome.BLOS2 negatively regulates Notch signaling during neural and hematopoietic stem and progenitor cell development.Neurodevelopmental disease mechanisms, primary cilia, and endosomes converge on the BLOC-1 and BORC complexes.Recognition deficits in mice carrying mutations of genes encoding BLOC-1 subunits pallidin or dysbindin.BLOC-1 is required for selective membrane protein trafficking from endosomes to primary cilia.Alpha1-antitrypsin determines the pattern of emphysema and function in tobacco smoke-exposed mice: parallels with human disease.Biogenesis of Melanosomes
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The pallid gene encodes a novel, syntaxin 13-interacting protein involved in platelet storage pool deficiency
description
article
@en
im November 1999 veröffentlichter wissenschaftlicher Artikel
@de
wetenschappelijk artikel
@nl
наукова стаття, опублікована в листопаді 1999
@uk
ലേഖനം
@ml
name
The pallid gene encodes a nove ...... atelet storage pool deficiency
@en
The pallid gene encodes a nove ...... atelet storage pool deficiency
@nl
type
label
The pallid gene encodes a nove ...... atelet storage pool deficiency
@en
The pallid gene encodes a nove ...... atelet storage pool deficiency
@nl
prefLabel
The pallid gene encodes a nove ...... atelet storage pool deficiency
@en
The pallid gene encodes a nove ...... atelet storage pool deficiency
@nl
P2093
P356
P1433
P1476
The pallid gene encodes a nove ...... atelet storage pool deficiency
@en
P2093
Jane Gitschier
Liping Huang
Yien-Ming Kuo
P2888
P304
P356
10.1038/15507
P407
P577
1999-11-01T00:00:00Z
P5875
P6179
1027796271