Rlip overexpression reduces oxidative stress and mitochondrial dysfunction in Alzheimer's disease: Mechanistic insights
PH Reddy, S Kshirsagar, C Bose… - … et Biophysica Acta (BBA …, 2023 - Elsevier
Alzheimer's disease (AD) is a neurodegenerative disease that affects a large proportion of
the aging population. RalBP1 (Rlip) is a stress-activated protein that plays a crucial role in …
the aging population. RalBP1 (Rlip) is a stress-activated protein that plays a crucial role in …
[HTML][HTML] Rlip reduction induces oxidative stress and mitochondrial dysfunction in mutant tau-expressed immortalized hippocampal neurons: mechanistic insights
RalBP1 (Rlip) is a stress-activated protein that is believed to play a large role in aging and
neurodegenerative diseases such as Alzheimer's disease (AD) and other tauopathies. The …
neurodegenerative diseases such as Alzheimer's disease (AD) and other tauopathies. The …
[HTML][HTML] RALBP1 in oxidative stress and mitochondrial dysfunction in Alzheimer's disease
The purpose of our study is to understand the role of the RALBP1 gene in oxidative stress
(OS), mitochondrial dysfunction and cognition in Alzheimer's disease (AD) pathogenesis …
(OS), mitochondrial dysfunction and cognition in Alzheimer's disease (AD) pathogenesis …
The role of RLIP76 in oxidative stress and mitochondrial dysfunction: Evidence based on autopsy brains from Alzheimer's disease patients
Several converging lines of evidence from our group support a potential role of RLIP76 (AKA
Rlip) in neurodegenerative disorders, including Alzheimer's Disease (AD). However, the role …
Rlip) in neurodegenerative disorders, including Alzheimer's Disease (AD). However, the role …
[HTML][HTML] Rlip76: an unexplored player in neurodegeneration and Alzheimer's disease?
A Hindle, SP Singh, JA Pradeepkiran, C Bose… - International Journal of …, 2022 - mdpi.com
Alzheimer's disease (AD) is a progressive neurodegenerative disorder and is the most
common cause of dementia in older people. AD is associated with the loss of synapses …
common cause of dementia in older people. AD is associated with the loss of synapses …
Abnormal interaction of Rlip with mutant APP/Abeta and phosphorylated tau reduces wild-type Rlip levels and disrupt Rlip function in Alzheimer's disease
Alzheimer's disease (AD) is a neurodegenerative disease that affects a large proportion of
the aging population. RalBP1 (Rlip) is a stress-activated protein, that plays an important role …
the aging population. RalBP1 (Rlip) is a stress-activated protein, that plays an important role …
[HTML][HTML] Correction: Reddy et al. Rlip Reduction Induces Oxidative Stress and Mitochondrial Dysfunction in Mutant Tau-Expressed Immortalized Hippocampal Neurons …
PH Reddy, S Kshirsagar, C Bose, JA Pradeepkiran… - Cells, 2024 - mdpi.com
Cells | Free Full-Text | Correction: Reddy et al. Rlip Reduction Induces Oxidative Stress and
Mitochondrial Dysfunction in Mutant Tau-Expressed Immortalized Hippocampal Neurons …
Mitochondrial Dysfunction in Mutant Tau-Expressed Immortalized Hippocampal Neurons …
[HTML][HTML] Autophagy and LRRK2 in the aging brain
F Albanese, S Novello, M Morari - Frontiers in neuroscience, 2019 - frontiersin.org
Autophagy is a highly conserved process by which long-lived macromolecules, protein
aggregates and dysfunctional/damaged organelles are delivered to lysosomes for …
aggregates and dysfunctional/damaged organelles are delivered to lysosomes for …
[HTML][HTML] Low density lipoprotein receptor-related protein 1 promotes anti-apoptotic signaling in neurons by activating Akt survival pathway
The low density lipoprotein receptor-related protein 1 (LRP1) is a multi-ligand receptor
abundantly expressed in neurons. Previous work has shown that brain LRP1 levels are …
abundantly expressed in neurons. Previous work has shown that brain LRP1 levels are …
Redox Proteomics Analyses of the Influence of Co-Expression of Wild-Type or Mutated LRRK2 and Tau on C. elegans Protein Expression and Oxidative Modification …
F Di Domenico, R Sultana, A Ferree… - Antioxidants & redox …, 2012 - liebertpub.com
Aims: The human LRRK2 gene has been identified as the most common causative gene of
autosomal-dominantly inherited and idiopathic Parkinson disease (PD). The G2019S …
autosomal-dominantly inherited and idiopathic Parkinson disease (PD). The G2019S …
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