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Sandra M. Cardoso

Researcher at University of Coimbra

Publications -  121
Citations -  16605

Sandra M. Cardoso is an academic researcher from University of Coimbra. The author has contributed to research in topics: Mitochondrion & Neurodegeneration. The author has an hindex of 44, co-authored 110 publications receiving 13613 citations.

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Mitochondria as a therapeutic target in Alzheimer's disease and diabetes.

TL;DR: Clinical and biochemical features shared by AD and diabetes, giving special attention to the involvement of mitochondria are discussed, particularly mitochondrial target antioxidants and Szeto-Schiller peptides.
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Novel tacrine-benzofuran hybrids as potential multi-target drug candidates for the treatment of Alzheimer's Disease.

TL;DR: Design, synthesis and evaluation of new tacrine-benzofuran hybrids as multitargeting anti- Alzheimer’s disease agents; high AChE inhibition associated with other relevant properties; structure–activity relationship analysis.
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Hydroxypyridinone-benzofuran hybrids with potential protective roles for Alzheimer´s disease therapy.

TL;DR: Eleven new hybrid compounds developed and evaluated for chemical and biological properties showed neuroprotective effects in neuronal cells subjected to model stressors of AD, but not significant dependence on the substituent groups, and evidenced drug-likeness properties, including good membrane permeability.
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LRRK2 at the Crossroad Between Autophagy and Microtubule Trafficking Insights into Parkinson’s Disease

TL;DR: The literature is reviewed and discussed on how LRRK2 affects mitochondrial function, autophagy, and microtubule dynamics and how this is implicated in the PD etiology.
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Mitochondrial control of autophagic lysosomal pathway in Alzheimer's disease

TL;DR: Evidence suggesting a clear association between mitochondrial dysfunction, autophagy impairment and amyloid-beta accumulation in Alzheimer's disease pathophysiology is discussed and an innovative window for new therapeutic strategies aimed to activate or ameliorate macroautophagy may be opened.