Als Disease Models

ALS disease models are experimental systems used to reproduce key features of amyotrophic lateral sclerosis, a neurodegenerative disease marked by progressive loss of upper and lower motor neurons. These models include patient-derived cells, induced pluripotent stem cell cultures, organoids, and genetically modified animals that can represent mechanisms such as TDP-43 pathology, altered RNA processing, protein aggregation, mitochondrial dysfunction, and neuroinflammation. Researchers use them to investigate disease onset and progression, compare genetic and sporadic forms of ALS, identify biomarkers, and evaluate potential therapies. By linking molecular changes to motor neuron vulnerability, ALS models support therapeutic development while revealing the strengths and limitations of different experimental approaches.

Als Disease Models - Related Videos

Research

JoVE Journal - Medicine

A Quick Phenotypic Neurological Scoring System for Evaluating Disease Progression in the SOD1-G93A Mouse Model of ALS

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Cited by 120 •

2015

This video protocol describes a sensitive, reliable, and quick method for evaluating the neuromuscular deficits in a transgenic mouse model of amyotrophic lateral sclerosis.

Simultaneous Plethysmography and Electromyography Recording in an ALS Mouse Model

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2025

Source: Jensen, V. N., et al. Repeated Measurement of Respiratory Muscle Activity and Ventilation in Mouse Models of Neuromuscular Disease. J. Vis. Exp. (2017).This video demonstrates the method for recording simultaneous plethysmography and electromyography signals in a freely moving ALS mouse model. The procedure involves using implanted electrodes and a transmitter to capture muscle activity, alongside a plethysmography chamber to monitor breathing patterns, to investigate the role of...

ALS - Motor Neuron Disease: Mechanism and Development of New Therapies

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Cited by 1 •

2007

Jeffrey D. Rothstein speaks about the pathology and mechanisms underlying amyotrophic lateral sclerosis or ALS, advances in ALS research, and current strategies towards the development of therapies.

Clinical Testing and Spinal Cord Removal in a Mouse Model for Amyotrophic Lateral Sclerosis (ALS)

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Cited by 20 •

2012

A mouse model for amyotrophic lateral sclerosis (ALS) is examined clinically and behaviorally. As a prerequisite for an accompanying immunohistological analysis the preparation of the spinal cord is depicted in detail.

Research

JoVE Journal - Medicine
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A Protocol for Comprehensive Assessment of Bulbar Dysfunction in Amyotrophic Lateral Sclerosis (ALS)

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Cited by 40 •

2011

Objective assessments of the physiological mechanisms that support speech are needed to monitor disease onset and progression in persons with ALS and to quantify treatment effects in clinical trials. In this video, we present a comprehensive, instrumentation-based protocol for quantifying speech motor performance in clinical populations.

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