Biogenesis of lysosome-related organelles complex 3 (BLOC-3): a complex containing the Hermansky-Pudlak syndrome (HPS) proteins HPS1 and HPS4
about
Association of the Hermansky-Pudlak syndrome type-3 protein with clathrin.Characterization of BLOC-2, a complex containing the Hermansky-Pudlak syndrome proteins HPS3, HPS5 and HPS6Identification of snapin and three novel proteins (BLOS1, BLOS2, and BLOS3/reduced pigmentation) as subunits of biogenesis of lysosome-related organelles complex-1 (BLOC-1)Reinvestigation of the dysbindin subunit of BLOC-1 (biogenesis of lysosome-related organelles complex-1) as a dystrobrevin-binding proteinClinical and cellular characterisation of Hermansky-Pudlak syndrome type 6Melanocyte-specific proteins are aberrantly trafficked in melanocytes of Hermansky-Pudlak syndrome-type 3The BLOC-1 complex promotes endosomal maturation by recruiting the Rab5 GTPase-activating protein Msb3.Assembly of the biogenesis of lysosome-related organelles complex-3 (BLOC-3) and its interaction with Rab9BLOC-3 mutated in Hermansky-Pudlak syndrome is a Rab32/38 guanine nucleotide exchange factorRUTBC1 Functions as a GTPase-activating Protein for Rab32/38 and Regulates Melanogenic Enzyme Trafficking in MelanocytesThe BLOS1-interacting protein KXD1 is involved in the biogenesis of lysosome-related organellesBLOC-1 interacts with BLOC-2 and the AP-3 complex to facilitate protein trafficking on endosomesBLOC-1 and BLOC-3 regulate VAMP7 cycling to and from melanosomes via distinct tubular transport carriersEpithelial stress and apoptosis underlie Hermansky-Pudlak syndrome-associated interstitial pneumoniaCellular, molecular and clinical characterization of patients with Hermansky-Pudlak syndrome type 5.Hermansky-Pudlak syndrome: a disease of protein trafficking and organelle function.Platelet alpha granules in BLOC-2 and BLOC-3 subtypes of Hermansky-Pudlak syndrome.Melanocytic galectin-3 is associated with tyrosinase-related protein-1 and pigment biosynthesis.Association of the Hermansky-Pudlak syndrome type 4 (HPS4) gene variants with cognitive function in patients with schizophrenia and healthy subjects.Cargo sorting to lysosome-related organelles regulates siRNA-mediated gene silencing.Clinical, molecular, and cellular features of non-Puerto Rican Hermansky-Pudlak syndrome patients of Hispanic descent.Interstitial lung disease and pulmonary fibrosis in Hermansky-Pudlak syndrome type 2, an adaptor protein-3 complex diseaseIntermediate filaments and vesicular membrane traffic: the odd couple's first dance?The cell biology of Hermansky-Pudlak syndrome: recent advances.Cellular and molecular defects in a patient with Hermansky-Pudlak syndrome type 5An immunoblotting assay to facilitate the molecular diagnosis of Hermansky-Pudlak syndromeA divalent interaction between HPS1 and HPS4 is required for the formation of the biogenesis of lysosome-related organelle complex-3 (BLOC-3).MAP1LC3B overexpression protects against Hermansky-Pudlak syndrome type-1-induced defective autophagy in vitroSnapin associates with late endocytic compartments and interacts with late endosomal SNAREsDisorders of lysosome-related organelle biogenesis: clinical and molecular genetics.Identifying putative promoter regions of Hermansky-Pudlak syndrome genes by means of phylogenetic footprintingAlveolar macrophage dysregulation in Hermansky-Pudlak syndrome type 1.The endo-lysosomal sorting machinery interacts with the intermediate filament cytoskeleton.Caenorhabditis elegans HOPS and CCZ-1 mediate trafficking to lysosome-related organelles independently of RAB-7 and SAND-1.Cell type-specific Rab32 and Rab38 cooperate with the ubiquitous lysosome biogenesis machinery to synthesize specialized lysosome-related organelles.Hypopigmentation in Hermansky-Pudlak syndrome.The Hermansky-Pudlak syndrome 3 (cocoa) protein is a component of the biogenesis of lysosome-related organelles complex-2 (BLOC-2).Storage pool diseases illuminate platelet dense granule biogenesis.Structure Dependence of Lysosomal Transit of Chitosan-Based Polyplexes for Gene Delivery.A Novel Splice Site Mutation in HPS1 Gene is Associated with Hermansky-Pudlak Syndrome-1 (HPS1) in an Iranian Family.
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P2860
Biogenesis of lysosome-related organelles complex 3 (BLOC-3): a complex containing the Hermansky-Pudlak syndrome (HPS) proteins HPS1 and HPS4
description
2003 nî lūn-bûn
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2003 թուականի Յուլիսին հրատարակուած գիտական յօդուած
@hyw
2003 թվականի հուլիսին հրատարակված գիտական հոդված
@hy
2003年の論文
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2003年論文
@yue
2003年論文
@zh-hant
2003年論文
@zh-hk
2003年論文
@zh-mo
2003年論文
@zh-tw
2003年论文
@wuu
name
Biogenesis of lysosome-related ...... e (HPS) proteins HPS1 and HPS4
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Biogenesis of lysosome-related ...... e (HPS) proteins HPS1 and HPS4
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Biogenesis of lysosome-related ...... e (HPS) proteins HPS1 and HPS4
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Biogenesis of lysosome-related ...... e (HPS) proteins HPS1 and HPS4
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Biogenesis of lysosome-related ...... e (HPS) proteins HPS1 and HPS4
@en
Biogenesis of lysosome-related ...... e (HPS) proteins HPS1 and HPS4
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Biogenesis of lysosome-related ...... e (HPS) proteins HPS1 and HPS4
@ast
Biogenesis of lysosome-related ...... e (HPS) proteins HPS1 and HPS4
@en
Biogenesis of lysosome-related ...... e (HPS) proteins HPS1 and HPS4
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Biogenesis of lysosome-related ...... e (HPS) proteins HPS1 and HPS4
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P2093
Esteban C Dell'Angelica
Ramin Nazarian
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P304
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P356
10.1073/PNAS.1532040100
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P577
2003-07-22T00:00:00Z