Editorial: Proteomic alterations by mutations involved in Parkinson's disease and related disorders

Curr Protein Pept Sci. 2017;18(7):654-655. doi: 10.2174/138920371807170508185242.

Authors

F Cardona¹, J Perez-Tur¹

Affiliation

¹ Instituto de Biomedicina de Valencia Consejo Superior de Investigaciones Científicas (IBV-CSIC) Calle Jaime Roig 11 Valencia E46010, Spain.

PMID: 28879817
DOI: 10.2174/138920371807170508185242

No abstract available

Publication types

Editorial
Introductory Journal Article

MeSH terms

F-Box Proteins / genetics
High-Temperature Requirement A Serine Peptidase 2 / genetics
Humans
Leucine-Rich Repeat Serine-Threonine Protein Kinase-2 / genetics
Mutation*
Neurodegenerative Diseases / genetics*
Parkinson Disease / genetics*
Proteomics*
Ubiquitin Thiolesterase / genetics
Vesicular Transport Proteins / genetics
alpha-Synuclein / genetics

Substances

F-Box Proteins
FBXO7 protein, human
SNCA protein, human
UCHL1 protein, human
VPS35 protein, human
Vesicular Transport Proteins
alpha-Synuclein
LRRK2 protein, human
Leucine-Rich Repeat Serine-Threonine Protein Kinase-2
Ubiquitin Thiolesterase
HTRA2 protein, human
High-Temperature Requirement A Serine Peptidase 2