Carolyn H. Ly
Melbourne, VIC 3010, Australia
Last Updated: 09/26/2026
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Found 10 publications
Alloreactivity of Allogeneic Mesenchymal Stem/Stromal Cells and Other Cellular Therapies: A Concise Review.
Journal: Stem cells international
Published: September 16, 2021
Charcot-Marie-tooth disease causing mutation (p.R158H) in pyruvate dehydrogenase kinase 3 (PDK3) affects synaptic transmission, ATP production and causes neurodegeneration in a CMTX6 C. elegans model.
Journal: Human molecular genetics
Published: April 16, 2021
Measuring Mitochondrial Substrate Utilization in Skeletal Muscle Stem Cells.
Journal: Methods in molecular biology (Clifton, N.J.)
Published: August 27, 2017
Characterizing the molecular phenotype of an Atp7a(T985I) conditional knock in mouse model for X-linked distal hereditary motor neuropathy (dHMNX).
Journal: Metallomics : integrated biometal science
Published: June 14, 2016
Pathogenic mechanisms underlying X-linked Charcot-Marie-Tooth neuropathy (CMTX6) in patients with a pyruvate dehydrogenase kinase 3 mutation.
Journal: Neurobiology of disease
Published: March 11, 2016
Improved inherited peripheral neuropathy genetic diagnosis by whole-exome sequencing.
Journal: Molecular genetics & genomic medicine
Published: September 12, 2014
A metabolic link to skeletal muscle wasting and regeneration.
Journal: Frontiers in physiology
Published: November 26, 2013
A new locus for X-linked dominant Charcot-Marie-Tooth disease (CMTX6) is caused by mutations in the pyruvate dehydrogenase kinase isoenzyme 3 (PDK3) gene.
Journal: Human molecular genetics
Published: January 09, 2013
A family with 2 X-linked disorders: Charcot-Marie-Tooth disease and hemophilia A.
Journal: Muscle & nerve
Published: August 22, 2012
Showing 1-10 of 10
Last Updated: 09/26/2026