Powers B, Velazquez R, Strawderman M, Ginsberg S, Mufson E, Strupp B
Front Aging Neurosci. 2021; 13:723046.
PMID: 34690739
PMC: 8527982.
DOI: 10.3389/fnagi.2021.723046.
Avila J, Memos N, Aslan A, Andrejewski T, Luine V, Serrano P
J Psychopharmacol. 2021; 35(10):1240-1252.
PMID: 34587831
PMC: 9083019.
DOI: 10.1177/02698811211048285.
Lauterborn J, Schultz M, Le A, Amani M, Friedman A, Leach P
Transl Psychiatry. 2019; 9(1):166.
PMID: 31182707
PMC: 6557858.
DOI: 10.1038/s41398-019-0495-5.
Sathyanesan A, Zhou J, Scafidi J, Heck D, Sillitoe R, Gallo V
Nat Rev Neurosci. 2019; 20(5):298-313.
PMID: 30923348
PMC: 7236620.
DOI: 10.1038/s41583-019-0152-2.
Powers B, Santiago N, Strupp B
Behav Neurosci. 2018; 132(1):51-56.
PMID: 29553775
PMC: 5938627.
DOI: 10.1037/bne0000227.
Opposite phenotypes of muscle strength and locomotor function in mouse models of partial trisomy and monosomy 21 for the proximal Hspa13-App region.
Brault V, Duchon A, Romestaing C, Sahun I, Pothion S, Karout M
PLoS Genet. 2015; 11(3):e1005062.
PMID: 25803843
PMC: 4372517.
DOI: 10.1371/journal.pgen.1005062.
Chronic up-regulation of the SHH pathway normalizes some developmental effects of trisomy in Ts65Dn mice.
Dutka T, Hallberg D, Reeves R
Mech Dev. 2014; 135:68-80.
PMID: 25511459
PMC: 4297701.
DOI: 10.1016/j.mod.2014.11.004.
Timing of muscle response to a sudden leg perturbation: comparison between adolescents and adults with Down syndrome.
Valle M, Cioni M, Pisasale M, Panto M, Casabona A
PLoS One. 2013; 8(11):e81053.
PMID: 24278374
PMC: 3835738.
DOI: 10.1371/journal.pone.0081053.
Size does not always matter: Ts65Dn Down syndrome mice show cerebellum-dependent motor learning deficits that cannot be rescued by postnatal SAG treatment.
Gutierrez-Castellanos N, Winkelman B, Tolosa-Rodriguez L, Devenney B, Reeves R, De Zeeuw C
J Neurosci. 2013; 33(39):15408-13.
PMID: 24068809
PMC: 3858639.
DOI: 10.1523/JNEUROSCI.2198-13.2013.
Hedgehog agonist therapy corrects structural and cognitive deficits in a Down syndrome mouse model.
Das I, Park J, Shin J, Jeon S, Lorenzi H, Linden D
Sci Transl Med. 2013; 5(201):201ra120.
PMID: 24005160
PMC: 4006719.
DOI: 10.1126/scitranslmed.3005983.
Weaker control of the electrical properties of cerebellar granule cells by tonically active GABAA receptors in the Ts65Dn mouse model of Down's syndrome.
Szemes M, Davies R, Garden C, Usowicz M
Mol Brain. 2013; 6:33.
PMID: 23870245
PMC: 3723448.
DOI: 10.1186/1756-6606-6-33.
Down syndrome: the brain in trisomic mode.
Dierssen M
Nat Rev Neurosci. 2012; 13(12):844-58.
PMID: 23165261
DOI: 10.1038/nrn3314.
LRRK2 knockout mice have an intact dopaminergic system but display alterations in exploratory and motor co-ordination behaviors.
Hinkle K, Yue M, Behrouz B, Dachsel J, Lincoln S, Bowles E
Mol Neurodegener. 2012; 7:25.
PMID: 22647713
PMC: 3441373.
DOI: 10.1186/1750-1326-7-25.
Increased excitability and altered action potential waveform in cerebellar granule neurons of the Ts65Dn mouse model of Down syndrome.
Usowicz M, Garden C
Brain Res. 2012; 1465:10-7.
PMID: 22627164
PMC: 3389345.
DOI: 10.1016/j.brainres.2012.05.027.
Cognitive and sensorimotor tasks for assessing functional impairments in mouse models of Alzheimer's disease and related disorders.
Boutajangout A, Li Y, Quartermain D, Sigurdsson E
Methods Mol Biol. 2012; 849:529-40.
PMID: 22528113
PMC: 3859369.
DOI: 10.1007/978-1-61779-551-0_35.
Trisomy 21 and early brain development.
Haydar T, Reeves R
Trends Neurosci. 2011; 35(2):81-91.
PMID: 22169531
PMC: 3273608.
DOI: 10.1016/j.tins.2011.11.001.
Comprehensive behavioral phenotyping of Ts65Dn mouse model of Down syndrome: activation of β1-adrenergic receptor by xamoterol as a potential cognitive enhancer.
Faizi M, Bader P, Tun C, Encarnacion A, Kleschevnikov A, Belichenko P
Neurobiol Dis. 2011; 43(2):397-413.
PMID: 21527343
PMC: 3539757.
DOI: 10.1016/j.nbd.2011.04.011.
A new mouse model for the trisomy of the Abcg1-U2af1 region reveals the complexity of the combinatorial genetic code of down syndrome.
Lopes Pereira P, Magnol L, Sahun I, Brault V, Duchon A, Prandini P
Hum Mol Genet. 2009; 18(24):4756-69.
PMID: 19783846
PMC: 2778371.
DOI: 10.1093/hmg/ddp438.
Impairments in motor coordination without major changes in cerebellar plasticity in the Tc1 mouse model of Down syndrome.
Galante M, Jani H, Vanes L, Daniel H, Fisher E, Tybulewicz V
Hum Mol Genet. 2009; 18(8):1449-63.
PMID: 19181682
PMC: 2664148.
DOI: 10.1093/hmg/ddp055.
Effects of aneuploidy on skull growth in a mouse model of Down syndrome.
Hill C, Reeves R, Richtsmeier J
J Anat. 2007; 210(4):394-405.
PMID: 17428201
PMC: 2100298.
DOI: 10.1111/j.1469-7580.2007.00705.x.