PMEL: a pigment cell-specific model for functional amyloid formation
about
Emerging roles of extracellular vesicles in the nervous systemPMEL Amyloid Fibril Formation: The Bright Steps of PigmentationMorphological Characters and Transcriptome Profiles Associated with Black Skin and Red Skin in Crimson Snapper (Lutjanus erythropterus)The Human Disease-Associated Aβ Amyloid Core Sequence Forms Functional Amyloids in a Fungal AdhesinThe Kringle-like Domain Facilitates Post-endoplasmic Reticulum Changes to Premelanosome Protein (PMEL) Oligomerization and Disulfide Bond Configuration and Promotes Amyloid Formation.Pharmacological BACE1 and BACE2 inhibition induces hair depigmentation by inhibiting PMEL17 processing in mice.The PKD domain distinguishes the trafficking and amyloidogenic properties of the pigment cell protein PMEL and its homologue GPNMB.BACE2 processes PMEL to form the melanosome amyloid matrix in pigment cells.Lysosome-related organelles: unusual compartments become mainstream.Melanosomal formation of PMEL core amyloid is driven by aromatic residues.Fold modulating function: bacterial toxins to functional amyloids.Amyloidosis in alkaptonuria.Study of Exosomes Shed New Light on Physiology of Amyloidogenesis.Cellular Regulation of Amyloid Formation in Aging and Disease.Toll-like receptor 9 regulates melanogenesis through NF-κB activation.Regulation of melanosome number, shape and movement in the zebrafish retinal pigment epithelium by OA1 and PMEL.Amyloids, melanins and oxidative stress in melanomagenesis.Reduced Abundance and Subverted Functions of Proteins in Prion-Like Diseases: Gained Functions Fascinate but Lost Functions Affect Aetiology.Why are Functional Amyloids Non-Toxic in Humans?Melanomagenesis: multifaceted attacks on the genome.Loss of GPNMB Causes Autosomal-Recessive Amyloidosis Cutis Dyschromica in Humans.Functional amyloid: widespread in Nature, diverse in purpose.PIKfyve regulates melanosome biogenesis.A β-solenoid model of the Pmel17 repeat domain: insights to the formation of functional amyloid fibrils.Neuromelanin organelles are specialized autolysosomes that accumulate undegraded proteins and lipids in aging human brain and are likely involved in Parkinson's disease.Trial watch: DNA-based vaccines for oncological indicationsAmyloid assembly and disassemblyLength variations within the retrotransposon of canine : correlating genotype with phenotype
P2860
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P2860
PMEL: a pigment cell-specific model for functional amyloid formation
description
2013 nî lūn-bûn
@nan
2013年の論文
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2013年論文
@yue
2013年論文
@zh-hant
2013年論文
@zh-hk
2013年論文
@zh-mo
2013年論文
@zh-tw
2013年论文
@wuu
2013年论文
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2013年论文
@zh-cn
name
PMEL: a pigment cell-specific model for functional amyloid formation
@en
type
label
PMEL: a pigment cell-specific model for functional amyloid formation
@en
prefLabel
PMEL: a pigment cell-specific model for functional amyloid formation
@en
P2093
P2860
P356
P1476
PMEL: a pigment cell-specific model for functional amyloid formation
@en
P2093
Brenda Watt
Graça Raposo
Michael S Marks
P2860
P304
P356
10.1111/PCMR.12067
P577
2013-02-19T00:00:00Z