Related Experiment Video
Updated: Jul 9, 2026

Histological Examination of Mitochondrial Morphology in a Parkinson's Disease Model
Published on: June 23, 2023
The contribution of mitochondrial dysfunction to a gene-environment model of Guamanian ALS and PD
Daniel Lynch1, Christian Wanglund, Rita Spathis
1Laboratory of Biomedical Anthropology and Neurosciences, State University of New York, PO Box 6000, Binghamton, NY 13902-6000, USA.
Abstract:
Scientific investigations of amyotrophic lateral sclerosis (ALS) and parkinsonism-dementia (PD) of Guam have implicated genetic and environmental risk factors in their etiology. Using brain tissue, we investigated mitochondrial dysfunction and report a higher frequency of somatic mutations in the light strand promoter (LSP) of the mitochondrial control region in Guam ALS and PD patients than in Guam controls, along with the presence of inherited mutations that may contribute to a novel gene-environment interaction risk model. Along with other risk factors, they demonstrate both the importance and significance of genetic and environmental contributions to Guam ALS and PD etiology.
Related Concept Videos
Parkinson Disease ll: Pathophysiology
Animal Mitochondrial Genetics
Human Genetics
The complex relationship between genetics and psychology is observable through common biological components such...
ATP Synthase: Mechanism
Parkinson Disease l: Introduction

