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David Vilchez

Researcher at University of Cologne

Publications -  54
Citations -  2981

David Vilchez is an academic researcher from University of Cologne. The author has contributed to research in topics: Proteostasis & Induced pluripotent stem cell. The author has an hindex of 21, co-authored 43 publications receiving 2390 citations. Previous affiliations of David Vilchez include Salk Institute for Biological Studies & University of Barcelona.

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The role of protein clearance mechanisms in organismal ageing and age-related diseases

TL;DR: Modulation of either proteasome activity or autophagic-lysosomal potential extends lifespan and protects organisms from symptoms associated with proteostasis disorders, suggesting that protein clearance mechanisms are directly linked to ageing and age-associated diseases.
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RPN-6 determines C. elegans longevity under proteotoxic stress conditions

TL;DR: It is found that the forced re-investment of resources from the germ line to the soma in Caenorhabditis elegans results in elevated somatic proteasome activity, clearance of damaged proteins and increased longevity.
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Increased proteasome activity in human embryonic stem cells is regulated by PSMD11.

TL;DR: The results suggest a new regulation of proteostasis in hESCs that links longevity and stress resistance in invertebrates to hESC function and identity and that is correlated with increased levels of the 19S proteasome subunit PSMD11.
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Mechanism suppressing glycogen synthesis in neurons and its demise in progressive myoclonus epilepsy.

TL;DR: It is shown that mouse neurons have the enzymatic machinery for synthesizing glycogen, but that it is suppressed by retention of muscle glycogen synthase in the phosphorylated, inactive state, and that the malin-laforin complex ensures a blockade of neuronal glycogen synthesis even under intense glycogenic conditions.
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The Mechanistic Links Between Proteasome Activity, Aging and Age-related Diseases.

Isabel Saez, +1 more
- 31 Jan 2014 - 
TL;DR: Modulation of proteasomesome activity extends lifespan and protects organisms from symptoms associated with proteostasis disorders, and strategies to modulate proteasome activity and delay the onset of diseases associated to proteasomal dysfunction are discussed herein.