A. Costa

发表

On the Design of Broad-Based Neuropsychological Test Batteries to Assess the Cognitive Abilities of Individuals with Down Syndrome in the Context of Clinical Trials

H. Taylor, K. Koenig, R. Boada, 2018, Brain sciences.

An international survey on the impact of COVID-19 in individuals with Down syndrome

M. Mayer, M. Dierssen, A. Rebillat, 2020, medRxiv.

Microcapillary Reactors via Coaxial Electrospinning: Fabrication of Small Poly(Acrylic Acid) Gel Beads and Thin Threads of Biological Cell Dimensions

G. Wnek, Alberto C. S. Costa, A. Costa, 2021, Gels.

An assessment of optokinetic nystagmus (OKN) in persons with down syndrome

Alberto C. S. Costa, A. Costa, 2011, Experimental Brain Research.

Human Sensory Neurons Derived from Induced Pluripotent Stem Cells Support Varicella-Zoster Virus Infection

M. Levin, C. Freed, G. Cai, 2012, PloS one.

Evidence of Energy Metabolism Alterations in Cultured Neonatal Astrocytes Derived from the Ts65Dn Mouse Model of Down Syndrome

B. L. Zampieri, Alberto C. S. Costa, A. Costa, 2022, Brain sciences.

High resolution structural and functional MRI of the hippocampus in young adults with Down syndrome MRI of the hippocampus in Down syndrome

Z. I. Wang, H. Taylor, S. Oh, 2021 .

Medical vulnerability of individuals with Down syndrome to severe COVID-19–data from the Trisomy 21 Research Society and the UK ISARIC4C survey

M. Mayer, M. Dierssen, A. Rebillat, 2021, EClinicalMedicine.

Deficits in hippocampal CA1 LTP induced by TBS but not HFS in the Ts65Dn mouse: A model of Down syndrome

Alberto C. S. Costa, A. Costa, Michael J. Grybko, 2005, Neuroscience Letters.

Machine Learning Methods Predict Locomotor Response to MK-801 in Mouse Models of Down Syndrome

Cao D. Nguyen, Krzysztof J Cios, K. Cios, 2011, Journal of neurogenetics.

Ultrasonic vocalizations during male–female interaction in the mouse model of Down syndrome Ts65Dn

Fabian Fernandez, B. L. Zampieri, Jennifer N. Pearson, 2014, Physiology & Behavior.

Deletion of the GluR5 subunit of kainate receptors affects cocaine sensitivity and preference

A. Rajadhyaksha, T. Tropea, C. Inturrisi, 2010, Neuroscience Letters.

Sustained hippocampal IL-1β overexpression impairs contextual and spatial memory in transgenic mice

S. Maier, M. O’Banion, J. Olschowka, 2010, Brain, Behavior, and Immunity.

Toward the Identification of Neurophysiological Biomarkers for Alzheimer’s Disease in Down Syndrome: A Potential Role for Cross-Frequency Phase-Amplitude Coupling Analysis

Antônio-Carlos G. Almeida, Daniel J. L. L. Pinheiro, F. Scorza, 2023, Aging and disease.

Pharmacokinetic Properties of Memantine after a Single Intraperitoneal Administration and Multiple Oral Doses in Euploid Mice and in the Ts65Dn Mouse Model of Down's Syndrome

D. B. Victorino, I. Bederman, Alberto C. S. Costa, 2017, Basic & clinical pharmacology & toxicology.

Report of the ninth international workshop on the molecular biology of human chromosome 21 and Down syndrome

K. Gardiner, M. Davisson, Alberto C. S. Costa, 2001, Cytogenetic and Genome Research.

Quantitative Analysis of Retinal Structure and Function in Two Chromosomally Altered Mouse Models of Down Syndrome

Mark W. Johnson, D. B. Victorino, Alberto C. S. Costa, 2020, Investigative ophthalmology & visual science.

The mouse model of Down syndrome Ts65Dn presents visual deficits as assessed by pattern visual evoked potentials.

M. Davisson, B. Chang, R. Hurd, 2010, Investigative ophthalmology & visual science.

History of genetic disease: Down syndrome and genetics — a case of linked histories

D. Patterson, Alberto C. S. Costa, A. Costa, 2005, Nature Reviews Genetics.

Generation of Integration‐Free Induced Pluripotent Stem Cells from Urine‐Derived Cells Isolated from Individuals with Down Syndrome

B. L. Zampieri, Mark W. Johnson, Alberto C. S. Costa, 2017, Stem cells translational medicine.

Deletion of the Glutamate Receptor 5 Subunit of Kainate Receptors Affects the Development of Morphine Tolerance

A. Rajadhyaksha, C. Inturrisi, Alberto C. S. Costa, 2009, Journal of Pharmacology and Experimental Therapeutics.

Protein Profiles Associated With Context Fear Conditioning and Their Modulation by Memantine*

A. Dhanasekaran, K. Gardiner, Suhong Tong, 2014, Molecular & Cellular Proteomics.

Prospects for Improving Brain Function in Individuals with Down Syndrome

Alberto C. S. Costa, A. Costa, J. Scott-McKean, 2013, CNS Drugs.

Protein Dynamics Associated with Failed and Rescued Learning in the Ts65Dn Mouse Model of Down Syndrome

A. Ranjitha Dhanasekaran, A. Dhanasekaran, K. Gardiner, 2015, PloS one.

Genetic analysis of Down syndrome-associated heart defects in mice

Li Zhang, Antonio Baldini, N. Nowak, 2011, Human Genetics.

Fluoxetine rescues deficient neurogenesis in hippocampus of the Ts65Dn mouse model for Down syndrome

P. Yarowsky, S. Clark, Alberto C. S. Costa, 2006, Experimental Neurology.

PERSPECTIVES ON THE USE OF MOUSE MODELS OF DOWN SYNDROME IN TRANSLATIONAL RESEARCH INVOLVING VISUAL AND MOTOR FUNCTIONS

A. Costa, Dafne Herrero, 2014 .

Novel DYRK1A Inhibitor Rescues Learning and Memory Deficits in a Mouse Model of Down Syndrome

U. Rothweiler, R. Engh, W. Stensen, 2021, Pharmaceuticals.

G-Protein-Gated Potassium (GIRK) Channels Containing the GIRK2 Subunit Are Control Hubs for Pharmacologically Induced Hypothermic Responses

M. Stoffel, Alberto C. S. Costa, A. Costa, 2005, The Journal of Neuroscience.

Soluble prion protein and its N-terminal fragment prevent impairment of synaptic plasticity by Aβ oligomers: Implications for novel therapeutic strategy in Alzheimer's disease

W. Surewicz, J. Choi, Alberto C. S. Costa, 2016, Neurobiology of Disease.

Acute Injections of the NMDA Receptor Antagonist Memantine Rescue Performance Deficits of the Ts65Dn Mouse Model of Down Syndrome on a Fear Conditioning Test

Alberto C. S. Costa, A. Costa, M. Stasko, 2008, Neuropsychopharmacology.

On the Promise of Pharmacotherapies Targeted at Cognitive and Neurodegenerative Components of Down Syndrome

Alberto C. S. Costa, A. Costa, 2011, Developmental Neuroscience.

Behavioral validation of the Ts65Dn mouse model for Down syndrome of a genetic background free of the retinal degeneration mutation Pde6b rd1

M. Davisson, Alberto C. S. Costa, A. Costa, 2010, Behavioural Brain Research.

Gait dynamics in trisomic mice: quantitative neurological traits of Down syndrome

I. Amende, T. Hampton, Ivo Amende, 2004, Physiology & Behavior.

Motor dysfunction in a mouse model for Down syndrome

M. Davisson, Alberto C. S. Costa, A. Costa, 1999, Physiology & Behavior.

Cross-Sectional Exploration of Plasma Biomarkers of Alzheimer’s Disease in Down Syndrome: Early Data from the Longitudinal Investigation for Enhancing Down Syndrome Research (LIFE-DSR) Study

Sarah J. Hart, H. D. Rosas, D. Airey, 2021, Journal of clinical medicine.

High resolution structural and functional MRI of the hippocampus in young adults with Down syndrome

Z. I. Wang, H. Taylor, S. Oh, 2021, Brain communications.