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Hippocampal to basal forebrain transport of Mn2+ is impaired by deletion of KLC1, a subunit of the conventional kinesin microtubule-based motor.

Medina CS, Biris O, Falzone TL, Zhang X, Zimmerman AJ, Bearer EL.

Neuroimage. 2017 Jan 15;145(Pt A):44-57. doi: 10.1016/j.neuroimage.2016.09.035. Epub 2016 Oct 14.


In vivo MRI identifies cholinergic circuitry deficits in a Down syndrome model.

Chen Y, Dyakin VV, Branch CA, Ardekani B, Yang D, Guilfoyle DN, Peterson J, Peterhoff C, Ginsberg SD, Cataldo AM, Nixon RA.

Neurobiol Aging. 2009 Sep;30(9):1453-65. doi: 10.1016/j.neurobiolaging.2007.11.026. Epub 2008 Jan 3.


Maternal choline supplementation differentially alters the basal forebrain cholinergic system of young-adult Ts65Dn and disomic mice.

Kelley CM, Powers BE, Velazquez R, Ash JA, Ginsberg SD, Strupp BJ, Mufson EJ.

J Comp Neurol. 2014 Apr 15;522(6):1390-410. doi: 10.1002/cne.23492.


Tracking brain volume changes in C57BL/6J and ApoE-deficient mice in a model of neurodegeneration: a 5-week longitudinal micro-MRI study.

McDaniel B, Sheng H, Warner DS, Hedlund LW, Benveniste H.

Neuroimage. 2001 Dec;14(6):1244-55.


On the cause of mental retardation in Down syndrome: extrapolation from full and segmental trisomy 16 mouse models.

Galdzicki Z, Siarey R, Pearce R, Stoll J, Rapoport SI.

Brain Res Brain Res Rev. 2001 Apr;35(2):115-45. Review.


In vivo 1H MRS study in microlitre voxels in the hippocampus of a mouse model of Down syndrome at 11.7 T.

Santin MD, Valabrègue R, Rivals I, Pénager R, Paquin R, Dauphinot L, Albac C, Delatour B, Potier MC.

NMR Biomed. 2014 Oct;27(10):1143-50. doi: 10.1002/nbm.3155. Epub 2014 Aug 1.


Pharmacotherapy with fluoxetine restores functional connectivity from the dentate gyrus to field CA3 in the Ts65Dn mouse model of down syndrome.

Stagni F, Magistretti J, Guidi S, Ciani E, Mangano C, Calzà L, Bartesaghi R.

PLoS One. 2013 Apr 19;8(4):e61689. doi: 10.1371/journal.pone.0061689. Print 2013.


Manganese-enhanced magnetic resonance imaging of mossy fiber plasticity in vivo.

Nairismägi J, Pitkänen A, Narkilahti S, Huttunen J, Kauppinen RA, Gröhn OH.

Neuroimage. 2006 Mar;30(1):130-5. Epub 2005 Oct 24.


Estrogen alters amyloid precursor protein as well as dendritic and cholinergic markers in a mouse model of Down syndrome.

Granholm AC, Sanders L, Seo H, Lin L, Ford K, Isacson O.

Hippocampus. 2003;13(8):905-14.


Effects of long-term memantine on memory and neuropathology in Ts65Dn mice, a model for Down syndrome.

Lockrow J, Boger H, Bimonte-Nelson H, Granholm AC.

Behav Brain Res. 2011 Aug 10;221(2):610-22. doi: 10.1016/j.bbr.2010.03.036. Epub 2010 Apr 2.


Hippocampal volume and neuronal number in Ts65Dn mice: a murine model of Down syndrome.

Insausti AM, Megías M, Crespo D, Cruz-Orive LM, Dierssen M, Vallina IF, Insausti R, Flórez J.

Neurosci Lett. 1998 Sep 11;253(3):175-8. Erratum in: Neurosci Lett 1998 Dec 24;258(3):190. Vallina TF [corrected to Vallina IF].


Deficits in axonal transport in hippocampal-based circuitry and the visual pathway in APP knock-out animals witnessed by manganese enhanced MRI.

Gallagher JJ, Zhang X, Ziomek GJ, Jacobs RE, Bearer EL.

Neuroimage. 2012 Apr 15;60(3):1856-66. doi: 10.1016/j.neuroimage.2012.01.132. Epub 2012 Feb 10.


In vivo 3D MRI staining of the mouse hippocampal system using intracerebral injection of MnCl2.

Watanabe T, Radulovic J, Spiess J, Natt O, Boretius S, Frahm J, Michaelis T.

Neuroimage. 2004 Jun;22(2):860-7.


The functional nature of synaptic circuitry is altered in area CA3 of the hippocampus in a mouse model of Down's syndrome.

Hanson JE, Blank M, Valenzuela RA, Garner CC, Madison DV.

J Physiol. 2007 Feb 15;579(Pt 1):53-67. Epub 2006 Dec 7.


The Ts65Dn mouse model of Down syndrome shows reduced expression of the Bcl-X(L) antiapoptotic protein in the hippocampus not accompanied by changes in molecular or cellular markers of cell death.

Rueda N, Flórez J, Martínez-Cué C.

Int J Dev Neurosci. 2011 Nov;29(7):711-6. doi: 10.1016/j.ijdevneu.2011.06.001. Epub 2011 Jun 12.


Cholinergic degeneration and memory loss delayed by vitamin E in a Down syndrome mouse model.

Lockrow J, Prakasam A, Huang P, Bimonte-Nelson H, Sambamurti K, Granholm AC.

Exp Neurol. 2009 Apr;216(2):278-89. doi: 10.1016/j.expneurol.2008.11.021. Epub 2008 Dec 10.


Three-dimensional mapping of hippocampal anatomy in adolescents with bipolar disorder.

Bearden CE, Soares JC, Klunder AD, Nicoletti M, Dierschke N, Hayashi KM, Narr KL, Brambilla P, Sassi RB, Axelson D, Ryan N, Birmaher B, Thompson PM.

J Am Acad Child Adolesc Psychiatry. 2008 May;47(5):515-25. doi: 10.1097/CHI.0b013e31816765ab.


Normalization of Dyrk1A expression by AAV2/1-shDyrk1A attenuates hippocampal-dependent defects in the Ts65Dn mouse model of Down syndrome.

Altafaj X, Martín ED, Ortiz-Abalia J, Valderrama A, Lao-Peregrín C, Dierssen M, Fillat C.

Neurobiol Dis. 2013 Apr;52:117-27. doi: 10.1016/j.nbd.2012.11.017. Epub 2012 Dec 5.


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