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PMID:28750690

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Citation

Wang, HY, Trocmé-Thibierge, C, Stucky, A, Shah, SM, Kvasic, J, Khan, A, Morain, P, Guignot, I, Bouguen, E, Deschet, K, Pueyo, M, Mocaer, E, Ousset, PJ, Vellas, B and Kiyasova, V (2017) Increased Aβ-α7-like nicotinic acetylcholine receptor complex level in lymphocytes is associated with apolipoprotein E4-driven Alzheimer's disease pathogenesis. Alzheimers Res Ther 9:54

Abstract

The apolipoprotein E ε4 (APOE4) genotype is a prominent late-onset Alzheimer's disease (AD) risk factor. ApoE4 disrupts memory function in rodents and may contribute to both plaque and tangle formation.

Links

PubMed PMC5530996 Online version:10.1186/s13195-017-0280-8

Keywords

Aged; Aged, 80 and over; Alzheimer Disease/genetics; Alzheimer Disease/pathology; Amyloid beta-Peptides/metabolism; Amyloid beta-Peptides/pharmacology; Animals; Cognitive Dysfunction/genetics; Cognitive Dysfunction/pathology; Dose-Response Relationship, Drug; Female; Frontal Lobe/ultrastructure; Humans; Lymphocytes/drug effects; Lymphocytes/metabolism; Male; Peptide Fragments/metabolism; Peptide Fragments/pharmacology; Phosphorylation/drug effects; Protein Binding/drug effects; Rats; Rats, Sprague-Dawley; Receptors, LDL/metabolism; Statistics as Topic; Synaptosomes/metabolism; Synaptosomes/ultrastructure; alpha7 Nicotinic Acetylcholine Receptor/metabolism; tau Proteins/metabolism

Significance

Annotations

Gene product Qualifier GO Term Evidence Code with/from Aspect Extension Notes Status

HUMAN:A4

enables

GO:0042802: identical protein binding

ECO:0000353: physical interaction evidence used in manual assertion

UniProtKB:P05067:PRO_0000000092

F

Seeded From UniProt

complete

Notes

See also

References

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