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NPJ Parkinson'S Disease|January 20, 2024
Early-stage idiopathic Parkinson's disease is associated with reduced circular RNA expressionBenjamin J Whittle, Osagie G Izuogu, Hannah Lowes, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|June 6, 2014
Accurate mitochondrial DNA sequencing using off-target reads provides a single test to identify pathogenic point mutationsHelen R Griffin, Angela Pyle, Emma L Blakely, et al.
JIMD Reports|February 23, 2013
NDUFS8-related Complex I Deficiency Extends Phenotype from "PEO Plus" to Leigh SyndromeAdela Della Marina, Ulrike Schara, Angela Pyle, et al.
Frontiers in Immunology|October 16, 2018
Exposure of Monocytic Cells to Lipopolysaccharide Induces Coordinated Endotoxin Tolerance, Mitochondrial Biogenesis, Mitophagy, and Antioxidant DefensesJohn D Widdrington, Aurora Gomez-Duran, Angela Pyle, et al.
Annals of Neurology|March 24, 2005
Mitochondrial DNA haplogroup cluster UKJT reduces the risk of PDAngela Pyle, Thomas Foltynie, Watcharee Tiangyou, et al.
Biochimica Et Biophysica Acta|December 9, 2010
POLG mutations cause decreased mitochondrial DNA repopulation rates following induced depletion in human fibroblastsJoanna D Stewart, Susanne Schoeler, Kamil S Sitarz, et al.
Brain : a Journal of Neurology|December 16, 2014
Exome sequencing in undiagnosed inherited and sporadic ataxiasAngela Pyle, Tania Smertenko, David Bargiela, et al.
Clinical Genetics|August 12, 2020
Homozygous TAF1C variants are associated with a novel childhood-onset neurological phenotypeOula Knuutinen, Angela Pyle, Maria Suo-Palosaari, et al.
Trends in Neuroscience and Education|September 12, 2024
Applying the science of learning to teacher professional development and back again: Lessons from 3 country contextsJennifer M Zosh, Angela Pyle, Nikhit D'Sa, et al.
Human Molecular Genetics|March 9, 2018
Defective mitochondrial protease LonP1 can cause classical mitochondrial diseaseBradley Peter, Christie L Waddington, Monika Oláhová, et al.
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