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Output Catalog

ASAP is committed to accelerating the pace of discovery and informing a path to a cure for Parkinson’s disease through collaboration, research-enabling resources, and data sharing. We’ve created this catalog to showcase the research outputs and tools developed by ASAP-funded programs.

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Leveraging animal models to understand non-motor symptoms of Parkinson’s disease

Parkinson's disease diagnosis focuses on motor symptoms, but non-motor symptoms like cognitive issues and sleep disorders significantly affect patients. Research on non-motor signs in animals aims to improve understanding of the disease.

Program: Collaborative Research Network
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Preparation of Acute Brain Slices

This protocol describes the steps for preparing acute brain slices.

Program: Collaborative Research Network
Team:
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Postsynaptic adaptations in direct pathway muscarinic M4-receptor signaling follow the temporal and regional pattern of dopaminergic degeneration

Imbalances in dorsal striatum output in Parkinson's disease are driven by dopamine loss and disrupted acetylcholine signaling. These changes occur in response to dopamine loss, affecting M4 receptors in striatal neurons, crucial for PD progression.

Program: Collaborative Research Network
Team:
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Stereotaxic Surgery

This protocol describes the steps for performing mouse stereotaxic surgery. It is applicable to intracranial injections of viruses and drugs.

Program: Collaborative Research Network
Team:
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6-OHDA mouse model of Parkinson’s disease

Protocol for creating a Parkinson's disease mouse model using 6-OHDA involves injecting different doses into the brain to induce varying levels of dopaminergic damage.

Program: Collaborative Research Network
Team:
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Levodopa treatment for low-dose 6-OHDA-treated mice

This protocol describes a one-week levodopa treatment for mice partially depleted of dopamine.

Program: Collaborative Research Network
Team:
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Ex Vivo Electrophysiology – Ford Lab

This protocol describes the steps to perform whole-cell electrophysiology recordings in acute brain slices.

Program: Collaborative Research Network
Team:
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Electrophysiology and 2-photon imaging of Ca+2-transients

Protocol for imaging dendritic calcium transients using 2-photon microscopy with a Ti:Sapphire laser. Fluorescence collected through objective, dichroic mirror, and filters, then detected by a GaAsP PMT. Output digitized for analysis.

Program: Collaborative Research Network
Team:
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Motor Behavioral Assessment

Protocol outlines motor behavior tests for Parkinson's disease in mice using open field, rotarod, cylinder, and balance beam tests. Mice were habituated for 30-40 min before tests conducted 3-4 weeks post-injections.

Program: Collaborative Research Network
Team:
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Data for Jain et al Adaptor Protein-3 Produces Synaptic Vesicles that Release Phasic Dopamine

Primary data for Jain et al "Adaptor protein-3 produces synaptic vesicles that release phasic dopamine" (Proc Natl Acad Sci. 2023; 120(42):e2309843120. doi: 10.1073/pnas.2309843120)

Program: Collaborative Research Network
Team:
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Slow Release Pellet Implantation

This protocol describes how to subcutaneously implant slow-release pellets into mice.

Program: Collaborative Research Network
Team:
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Striatal Punch Collection

This protocol describes how to collect striatal punches from fresh frozen mouse brain tissue for HPLC analysis.

Program: Collaborative Research Network
Team:
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Mouse Behavior – Open Field and T-Maze

This protocol describes two behavioral tasks for mice. The first is the Open Field Test, which is used to asses motor behavior, and the second is the T-Maze, which is used to assess spatial learning.

Program: Collaborative Research Network
Team:
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Live Imaging of Primary Mouse Neuron Cultures

This protocol describes live imaging of primary neuron cultures. Included are methods for preparing hippocampal or dopamine neuronal cultures from neonatal mouse brain tissue. The imaging described involves labeling of dopamine neurons with a…

Program: Collaborative Research Network
Team:
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In Vivo Electrophysiology (Mouse)

This protocol describes the in vivo electrophysiology method for recording neuronal activity in mice.

Program: Collaborative Research Network
Team:
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