Activation of Tyrosine Phosphorylation Signaling in Erythrocytes of Patients with Alzheimer’s Disease

Neuroscience ◽  
2020 ◽  
Vol 433 ◽  
pp. 36-41
Author(s):  
Cinzia Mallozzi ◽  
Alessio Crestini ◽  
Carmen D'Amore ◽  
Paola Piscopo ◽  
Marisa Cappella ◽  
...  
Keyword(s):  
Alzheimer’S Disease ◽  
Alzheimer's Disease ◽  
Tyrosine Phosphorylation

scholarly journals c-Abl Stabilizes HDAC2 Levels by Tyrosine Phosphorylation Repressing Neuronal Gene Expression in Alzheimer’s Disease

2014 ◽  
Vol 56 (1) ◽  
pp. 163-173 ◽  
Author(s):  
Marcelo Gonzalez-Zuñiga ◽  
Pablo S. Contreras ◽  
Lisbell D. Estrada ◽  
David Chamorro ◽  
Alejandro Villagra ◽  
...  
Keyword(s):  
Gene Expression ◽  
Alzheimer’S Disease ◽  
Alzheimer's Disease ◽  
Tyrosine Phosphorylation ◽  
Neuronal Gene

scholarly journals A novel DYRK1A (Dual specificity tyrosine phosphorylation-regulated kinase 1A) inhibitor for the treatment of Alzheimer's disease: effect on Tau and amyloid pathologies in vitro

2015 ◽  
Vol 133 (3) ◽  
pp. 440-451 ◽  
Author(s):  
Séverine Coutadeur ◽  
Hélène Benyamine ◽  
Laurence Delalonde ◽  
Catherine de Oliveira ◽  
Bertrand Leblond ◽  
...  
Keyword(s):  
Alzheimer’S Disease ◽  
Alzheimer's Disease ◽  
Tyrosine Phosphorylation ◽  
Dual Specificity ◽  
Disease Effect

scholarly journals cdc-Like/Dual-Specificity Tyrosine Phosphorylation–Regulated Kinases Inhibitor Leucettine L41 Induces mTOR-Dependent Autophagy: Implication for Alzheimer’s Disease

2013 ◽  
Vol 85 (3) ◽  
pp. 441-450 ◽  
Author(s):  
Xavier Fant ◽  
Emilie Durieu ◽  
Gaëtan Chicanne ◽  
Bernard Payrastre ◽  
Diego Sbrissa ◽  
...  
Keyword(s):  
Alzheimer’S Disease ◽  
Alzheimer's Disease ◽  
Tyrosine Phosphorylation ◽  
Dual Specificity

Cognitive control constrains memory attributions

2019 ◽  
Vol 42 ◽  
Author(s):  
Colleen M. Kelley ◽  
Larry L. Jacoby
Keyword(s):  
Alzheimer’S Disease ◽  
Older Adults ◽  
Alzheimer's Disease ◽  
Traumatic Brain Injury ◽  
Brain Injury ◽  
Cognitive Control

Abstract Cognitive control constrains retrieval processing and so restricts what comes to mind as input to the attribution system. We review evidence that older adults, patients with Alzheimer's disease, and people with traumatic brain injury exert less cognitive control during retrieval, and so are susceptible to memory misattributions in the form of dramatic levels of false remembering.

Formation of paired helical filaments in Alzheimer's disease

1984 ◽  
Vol 42 ◽  
pp. 302-303
Author(s):  
J. Metuzals ◽  
D. F. Clapin ◽  
V. Montpetit
Keyword(s):  
Alzheimer’S Disease ◽  
Alzheimer's Disease ◽  
Frontal Lobe ◽  
Giant Axon ◽  
Paired Helical Filaments ◽  
Normal Brain ◽  
Protein Assemblies ◽  
Electron Microscopic ◽  
Helical Symmetry ◽  
Structural Levels

Information on the conformation of paired helical filaments (PHF) and the neurofilamentous (NF) network is essential for an understanding of the mechanisms involved in the formation of the primary lesions of Alzheimer's disease (AD): tangles and plaques. The structural and chemical relationships between the NF and the PHF have to be clarified in order to discover the etiological factors of this disease. We are investigating by stereo electron microscopic and biochemical techniques frontal lobe biopsies from patients with AD and squid giant axon preparations. The helical nature of the lesion in AD is related to pathological alterations of basic properties of the nervous system due to the helical symmetry that exists at all hierarchic structural levels in the normal brain. Because of this helical symmetry of NF protein assemblies and PHF, the employment of structure reconstruction techniques to determine the conformation, particularly the handedness of these structures, is most promising. Figs. 1-3 are frontal lobe biopsies.

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