Pathological Trajectory in the Ts65Dn Model of Down Syndrome
Overview
Overview
Authors
Affiliations
Affiliations
Soon will be listed here.
Citing Articles
Ultrasonic vocalization phenotypes in the Ts65Dn and Dp(16)1Yey mouse models of Down syndrome.
Glass T, Lenell C, Fisher E, Yang Q, Connor N Physiol Behav. 2023; 271:114323.
PMID: 37573959 PMC: 10592033. DOI: 10.1016/j.physbeh.2023.114323.
References
1.
Cataldo A, Petanceska S, Peterhoff C, Terio N, Epstein C, Villar A
. App gene dosage modulates endosomal abnormalities of Alzheimer's disease in a segmental trisomy 16 mouse model of down syndrome. J Neurosci. 2003; 23(17):6788-92.
PMC: 6740714.
View
2.
Kelley C, Powers B, Velazquez R, Ash J, Ginsberg S, Strupp B
. Sex differences in the cholinergic basal forebrain in the Ts65Dn mouse model of Down syndrome and Alzheimer's disease. Brain Pathol. 2013; 24(1):33-44.
PMC: 4220609.
DOI: 10.1111/bpa.12073.
View
3.
Tallino S, Winslow W, Bartholomew S, Velazquez R
. Temporal and brain region-specific elevations of soluble Amyloid-β in the Ts65Dn mouse model of Down syndrome and Alzheimer's disease. Aging Cell. 2022; 21(4):e13590.
PMC: 9009111.
DOI: 10.1111/acel.13590.
View
4.
Davisson M, Schmidt C, Reeves R, Irving N, Akeson E, Harris B
. Segmental trisomy as a mouse model for Down syndrome. Prog Clin Biol Res. 1993; 384:117-33.
View
5.
Granholm A, Sanders L, Crnic L
. Loss of cholinergic phenotype in basal forebrain coincides with cognitive decline in a mouse model of Down's syndrome. Exp Neurol. 2000; 161(2):647-63.
DOI: 10.1006/exnr.1999.7289.
View