Lipid profiling of parkin-mutant human skin fibroblasts. (Q36256274)

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9 April 2020

title

Lipid profiling of parkin-mutant human skin fibroblasts (English)

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3

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Tiziana Cocco

5

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9 April 2020

author name string

Simona Lobasso

1

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9 April 2020

Paola Tanzarella

2

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Michele Maffia

4

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Angela Corcelli

6

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publication date

10 February 2017

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Journal of Cellular Physiology

9 April 2020

published in

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volume

232

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issue

12

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page(s)

3540-3551

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Parkin reinvents itself to regulate fatty acid metabolism by tagging CD36.

9 April 2020

cites work

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Cardiolipin fingerprinting of leukocytes by MALDI-TOF/MS as a screening tool for Barth syndrome

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Primary skin fibroblasts as a model of Parkinson's disease

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A RAPID METHOD OF TOTAL LIPID EXTRACTION AND PURIFICATION

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Loss of parkin promotes lipid rafts-dependent endocytosis through accumulating caveolin-1: implications for Parkinson's disease

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A biomarker that identifies senescent human cells in culture and in aging skin in vivo

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Pink1, Parkin, DJ-1 and mitochondrial dysfunction in Parkinson's disease

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Parkin and CASK/LIN-2 associate via a PDZ-mediated interaction and are co-localized in lipid rafts and postsynaptic densities in brain

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Major Alterations of Phosphatidylcholine and Lysophosphotidylcholine Lipids in the Substantia Nigra Using an Early Stage Model of Parkinson's Disease

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No evidence for substrate accumulation in Parkinson brains with GBA mutations

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Mutant Parkin impairs mitochondrial function and morphology in human fibroblasts

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Acceleration of α-synuclein aggregation by exosomes

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Altered membrane fluidity and lipid raft composition in presenilin-deficient cells

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Alzheimer's disease: the lipid connection

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Mitochondrial dysfunction, peroxidation damage and changes in glutathione metabolism in PARK6.

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Genome-wide RNAi screen identifies the Parkinson disease GWAS risk locus SREBF1 as a regulator of mitophagy

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Gangliosides' analysis by MALDI-ion mobility MS.

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PINK1- and Parkin-mediated mitophagy at a glance

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Parkin is a lipid-responsive regulator of fat uptake in mice and mutant human cells

21 January 2018

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Mutations in the parkin gene cause autosomal recessive juvenile parkinsonism

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Considerations regarding the etiology and future treatment of autosomal recessive versus idiopathic Parkinson disease.

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The genetics of Parkinson disease: Implications for neurological care

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Parkin is associated with cellular vesicles

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Disease-causing mutations in parkin impair mitochondrial ubiquitination, aggregation, and HDAC6-dependent mitophagy

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Glucocerebrosidase mutations in subjects with parkinsonism

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Biochemical consequences of mutations causing the GM2 gangliosidoses

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Mutation of the GM2 activator protein in a feline model of GM2 gangliosidosis

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Glucocerebrosidase gene mutations: a risk factor for Lewy body disorders

21 January 2018

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Gaucher disease glucocerebrosidase and α-synuclein form a bidirectional pathogenic loop in synucleinopathies

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Plasma ceramide and glucosylceramide metabolism is altered in sporadic Parkinson's disease and associated with cognitive impairment: a pilot study

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Mitochondrial function and morphology are impaired in parkin-mutant fibroblasts

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Glucocerebrosidase mutations in clinical and pathologically proven Parkinson's disease

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Mitochondrial defect and PGC-1α dysfunction in parkin-associated familial Parkinson's disease.

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Systemic LPS causes chronic neuroinflammation and progressive neurodegeneration

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Parkin protects mitochondrial genome integrity and supports mitochondrial DNA repair

21 January 2018

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iPSC-derived neurons from GBA1-associated Parkinson's disease patients show autophagic defects and impaired calcium homeostasis

21 January 2018

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Immunohistochemical and subcellular localization of Parkin protein: absence of protein in autosomal recessive juvenile parkinsonism patients

21 January 2018

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Familial Parkinson disease gene product, parkin, is a ubiquitin-protein ligase

21 January 2018

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The link between the GBA gene and parkinsonism

21 January 2018

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Lipid rafts and signal transduction

21 January 2018

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Infantile-onset symptomatic epilepsy syndrome caused by a homozygous loss-of-function mutation of GM3 synthase.

21 January 2018

1 reference

α-Synuclein in Lewy bodies

21 January 2018

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Molecular pathways in sporadic PD.

21 January 2018

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Cytoskeletal Alterations and Biomechanical Properties of parkin-Mutant Human Primary Fibroblasts.

21 January 2018

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MALDI-TOF MS lipid profiles of cytochrome c oxidases: cardiolipin is not an essential component of the Paracoccus denitrificans oxidase.

21 January 2018

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Parkin, PINK1, and DJ-1 form a ubiquitin E3 ligase complex promoting unfolded protein degradation

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Mechanisms of mitophagy

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The role of glycosphingolipid metabolism in the developing brain

21 January 2018

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Cardiolipin content in mitochondria from cultured skin fibroblasts harboring mutations in the mitochondrial ATP6 gene

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21 January 2018

Identifiers

DOI

10.1002/JCP.25815

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:28109117 AND SRC:MED&resulttype=core&format=json

9 April 2020

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