Tau protein aggregation in Alzheimer's disease: An attractive target for the development of novel therapeutic agents.Eur J Med Chem. 2017 Oct 20; 139:153-167.EJ
Abstract
Alzheimer's Disease (AD) is a neurodegenerative brain disorder in which many biological dysfunctions are involved. Among them, two main types of lesions were discovered and widely studied: the amyloid plaques and the neurofibrillary tangles (NFTs). These two lesions are caused by the dysfunction and the accumulation of two proteins which are, respectively, the beta-amyloid peptide and the tau protein. The process that leads these two proteins to aggregate is complex and is the subject of current studies. After a brief description of the aggregation mechanisms, we will provide an overview of new therapeutic agents targeting the different dysfunctions and toxic species found during aggregation.
Links
Pub Type(s)
Journal Article
Review
Language
eng
PubMed ID
28800454
Citation
Jouanne, Marie, et al. "Tau Protein Aggregation in Alzheimer's Disease: an Attractive Target for the Development of Novel Therapeutic Agents." European Journal of Medicinal Chemistry, vol. 139, 2017, pp. 153-167.
Jouanne M, Rault S, Voisin-Chiret AS. Tau protein aggregation in Alzheimer's disease: An attractive target for the development of novel therapeutic agents. Eur J Med Chem. 2017;139:153-167.
Jouanne, M., Rault, S., & Voisin-Chiret, A. S. (2017). Tau protein aggregation in Alzheimer's disease: An attractive target for the development of novel therapeutic agents. European Journal of Medicinal Chemistry, 139, 153-167. https://doi.org/10.1016/j.ejmech.2017.07.070
Jouanne M, Rault S, Voisin-Chiret AS. Tau Protein Aggregation in Alzheimer's Disease: an Attractive Target for the Development of Novel Therapeutic Agents. Eur J Med Chem. 2017 Oct 20;139:153-167. PubMed PMID: 28800454.
* Article titles in AMA citation format should be in sentence-case
TY - JOUR
T1 - Tau protein aggregation in Alzheimer's disease: An attractive target for the development of novel therapeutic agents.
AU - Jouanne,Marie,
AU - Rault,Sylvain,
AU - Voisin-Chiret,Anne-Sophie,
Y1 - 2017/07/29/
PY - 2017/07/12/received
PY - 2017/07/27/revised
PY - 2017/07/28/accepted
PY - 2017/8/12/pubmed
PY - 2017/11/1/medline
PY - 2017/8/12/entrez
KW - Aggregation
KW - Alzheimer's disease
KW - Tau protein
KW - Therapeutic agents
SP - 153
EP - 167
JF - European journal of medicinal chemistry
JO - Eur J Med Chem
VL - 139
N2 - Alzheimer's Disease (AD) is a neurodegenerative brain disorder in which many biological dysfunctions are involved. Among them, two main types of lesions were discovered and widely studied: the amyloid plaques and the neurofibrillary tangles (NFTs). These two lesions are caused by the dysfunction and the accumulation of two proteins which are, respectively, the beta-amyloid peptide and the tau protein. The process that leads these two proteins to aggregate is complex and is the subject of current studies. After a brief description of the aggregation mechanisms, we will provide an overview of new therapeutic agents targeting the different dysfunctions and toxic species found during aggregation.
SN - 1768-3254
UR - https://www.unboundmedicine.com/medline/citation/28800454/Tau_protein_aggregation_in_Alzheimer's_disease:_An_attractive_target_for_the_development_of_novel_therapeutic_agents_
L2 - https://linkinghub.elsevier.com/retrieve/pii/S0223-5234(17)30592-5
DB - PRIME
DP - Unbound Medicine
ER -