Dendritic spines: Revisiting the physiological role

SB Chidambaram, AG Rathipriya, SR Bolla… - Progress in Neuro …, 2019 - Elsevier
Dendritic spines are small, thin, specialized protrusions from neuronal dendrites, primarily
localized in the excitatory synapses. Sophisticated imaging techniques revealed that …

Dementia in Down's syndrome

C Ballard, W Mobley, J Hardy, G Williams… - The Lancet …, 2016 - thelancet.com
Down's syndrome is the most common genetic cause of learning difficulties, and individuals
with this condition represent the largest group of people with dementia under the age of 50 …

[HTML][HTML] Microglia require CD4 T cells to complete the fetal-to-adult transition

E Pasciuto, OT Burton, CP Roca, V Lagou, WD Rajan… - Cell, 2020 - cell.com
The brain is a site of relative immune privilege. Although CD4 T cells have been reported in
the central nervous system, their presence in the healthy brain remains controversial, and …

Down syndrome and Alzheimer's disease: Common pathways, common goals

D Hartley, T Blumenthal, M Carrillo, G DiPaolo… - Alzheimer's & …, 2015 - Elsevier
Abstract In the United States, estimates indicate there are between 250,000 and 400,000
individuals with Down syndrome (DS), and nearly all will develop Alzheimer's disease (AD) …

Down syndrome: the brain in trisomic mode

M Dierssen - Nature Reviews Neuroscience, 2012 - nature.com
Down syndrome is the most common form of intellectual disability and results from one of the
most complex genetic perturbations that is compatible with survival, trisomy 21. The study of …

OLIG2 drives abnormal neurodevelopmental phenotypes in human iPSC-based organoid and chimeric mouse models of down syndrome

R Xu, AT Brawner, S Li, JJ Liu, H Kim, H Xue, ZP Pang… - Cell stem cell, 2019 - cell.com
Down syndrome (DS) is a common neurodevelopmental disorder, and cognitive defects in
DS patients may arise from imbalances in excitatory and inhibitory neurotransmission …

The genetic architecture of Down syndrome phenotypes revealed by high-resolution analysis of human segmental trisomies

JO Korbel, T Tirosh-Wagner… - Proceedings of the …, 2009 - National Acad Sciences
Down syndrome (DS), or trisomy 21, is a common disorder associated with several complex
clinical phenotypes. Although several hypotheses have been put forward, it is unclear as to …

Role of astroglia in Down's syndrome revealed by patient-derived human-induced pluripotent stem cells

C Chen, P Jiang, H Xue, SE Peterson, HT Tran… - Nature …, 2014 - nature.com
Abstract Down's syndrome (DS), caused by trisomy of human chromosome 21, is the most
common genetic cause of intellectual disability. Here we use induced pluripotent stem cells …

Dendritic spine dysgenesis in autism related disorders

M Phillips, L Pozzo-Miller - Neuroscience letters, 2015 - Elsevier
The activity-dependent structural and functional plasticity of dendritic spines has led to the
long-standing belief that these neuronal compartments are the subcellular sites of learning …

DYRK1A, a Dosage-Sensitive Gene Involved in Neurodevelopmental Disorders, Is a Target for Drug Development in Down Syndrome

A Duchon, Y Herault - Frontiers in behavioral neuroscience, 2016 - frontiersin.org
Down syndrome (DS) is one of the leading causes of intellectual disability, and patients with
DS face various health issues, including learning and memory deficits, congenital heart …