Patricia Suaga-Gomez
Granada, AN 18016, Spain
Last Updated: 09/26/2026
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Found 10 publications
Parkinson disease-associated mutations in LRRK2 cause centrosomal defects via Rab8a phosphorylation.
Parkinson disease-associated mutations in LRRK2 cause centrosomal defects via Rab8a phosphorylation.
Journal: Molecular neurodegeneration
Published: June 05, 2017
Iron overload causes endolysosomal deficits modulated by NAADP-regulated 2-pore channels and RAB7A.
Journal: Autophagy
Published: July 08, 2016
Alterations in late endocytic trafficking related to the pathobiology of LRRK2-linked Parkinson's disease.
Journal: Biochemical Society transactions
Published: May 27, 2015
LRRK2 delays degradative receptor trafficking by impeding late endosomal budding through decreasing Rab7 activity.
Journal: Human molecular genetics
Published: August 01, 2014
Upstream deregulation of calcium signaling in Parkinson's disease.
Journal: Frontiers in molecular neuroscience
Published: April 29, 2014
Novel insights into the neurobiology underlying LRRK2-linked Parkinson's disease.
Journal: Neuropharmacology
Published: January 19, 2014
A link between LRRK2, autophagy and NAADP-mediated endolysosomal calcium signalling.
Journal: Biochemical Society transactions
Published: September 20, 2012
A Link between Autophagy and the Pathophysiology of LRRK2 in Parkinson's Disease.
Journal: Parkinson's disease
Published: August 19, 2012
LRRK2 as a modulator of lysosomal calcium homeostasis with downstream effects on autophagy.
Journal: Autophagy
Published: March 24, 2012
Leucine-rich repeat kinase 2 regulates autophagy through a calcium-dependent pathway involving NAADP.
Journal: Human molecular genetics
Published: October 21, 2011
Showing 1-10 of 10
Last Updated: 09/26/2026