Associated Papers
Prenatal-onset of congenital neuronal ceroid lipofuscinosis with a novel CTSD mutation.
Chartier S et al.
Birth Defects Research, 2021
Cathepsin D Variants Associated With Neurodegenerative Diseases Show Dysregulated Functionality and Modified α-Synuclein Degradation Properties.
Bunk J et al.
Frontiers in Cell and Developmental Biology, 2021
Corrigendum: Cathepsin D Variants Associated With Neurodegenerative Diseases Show Dysregulated Functionality and Modified α-Synuclein Degradation Properties.
Bunk J et al.
Frontiers in Cell and Developmental Biology, 2021
Cathepsins in the Pathophysiology of Mucopolysaccharidoses: New Perspectives for Therapy.
De Pasquale V et al.
Cells, 2020
Inherited diseases caused by mutations in cathepsin protease genes.
Ketterer S et al.
The Febs Journal, 2017
The Role of Cathepsin D in the Pathogenesis of Human Neurodegenerative Disorders.
Vidoni C et al.
Medicinal Research Reviews, 2016
Cell biology of the NCL proteins: What they do and don't do.
Cárcel-Trullols J et al.
Biochimica Et Biophysica Acta, 2015
Cathepsin D deficiency induces cytoskeletal changes and affects cell migration pathways in the brain.
Koch S et al.
Neurobiology of Disease, 2013
Cathepsin D expression level affects alpha-synuclein processing, aggregation, and toxicity in vivo.
Cullen V et al.
Molecular Brain, 2009
Novel mutation and the first prenatal screening of cathepsin D deficiency (CLN10).
Fritchie K et al.
Acta Neuropathologica, 2009
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