Associated Papers
The ChinaMAP analytics of deep whole genome sequences in 10,588 individuals.
Cao Y et al.
Cell Research, 2020
32355288 (PubMed )
Supplement: 41422_2020_322_MOESM14_ESM.xlsx › S7
modPDZpep: a web resource for structure based analysis of human PDZ-mediated interaction networks.
Sain N et al.
Biology Direct, 2016
27655048 (PubMed )
Supplement: 13062_2016_151_MOESM1_ESM.xls › Sheet4
HTRA2 variations in Taiwanese Parkinson's disease.
Chen CM et al.
Journal of Neural Transmission (vienna, Austria : 1996), 2014
Phosphorylation of HtrA2 by cyclin-dependent kinase-5 is important for mitochondrial function.
Fitzgerald JC et al.
Cell Death and Differentiation, 2012
Novel variant Pro143Ala in HTRA2 contributes to Parkinson's disease by inducing hyperphosphorylation of HTRA2 protein in mitochondria.
Lin CH et al.
Human Genetics, 2011
Genetic variations of Omi/HTRA2 in Chinese patients with Parkinson's disease.
Wang CY et al.
Brain Research, 2011
Drosophila HtrA2 is dispensable for apoptosis but acts downstream of PINK1 independently from Parkin.
Tain LS et al.
Cell Death and Differentiation, 2009
Parkinson's disease: from monogenic forms to genetic susceptibility factors.
Lesage S et al.
Human Molecular Genetics, 2009
Genetic variation of Omi/HtrA2 and Parkinson's disease.
Ross OA et al.
Parkinsonism & Related Disorders, 2008
Genetic variability in the mitochondrial serine protease HTRA2 contributes to risk for Parkinson disease.
Bogaerts V et al.
Human Mutation, 2008
Genetic findings in Parkinson's disease and translation into treatment: a leading role for mitochondria?
Bogaerts V et al.
Genes, Brain, and Behavior, 2008
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