Yeh S. Lau
Kuala Lumpur, Malaysia
Last Updated: 09/26/2026
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Found 24 publications
Correction: Development of muscular dystrophy in a CRISPR-engineered mutant rabbit model with frame-disrupting ANO5 mutations.
Journal: Cell death & disease
Published: June 20, 2020
Genome-wide CRISPR screen identifies LGALS2 as an oxidative stress-responsive gene with an inhibitory function on colon tumor growth.
Journal: Oncogene
Published: June 18, 2020
Genetic disruption of the inflammasome adaptor ASC has minimal impact on the pathogenesis of Duchenne muscular dystrophy in mdx mice.
Journal: Life sciences
Published: December 11, 2019
Life-Long AAV-Mediated CRISPR Genome Editing in Dystrophic Heart Improves Cardiomyopathy without Causing Serious Lesions in mdx Mice.
Journal: Molecular therapy : the journal of the American Society of Gene Therapy
Published: February 22, 2019
Adeno-Associated Virus-Mediated Delivery of CRISPR for Cardiac Gene Editing in Mice.
Journal: Journal of visualized experiments : JoVE
Published: August 21, 2018
Co-administration of conjugated linoleic acid and rosiglitazone increases atherogenic co-efficient and alters isoprenaline-induced vasodilatation in rats fed high fat diet.
Journal: Physiological research
Published: May 12, 2018
Automated muscle histopathology analysis using CellProfiler.
Journal: Skeletal muscle
Published: April 20, 2018
A novel ANO5 splicing variant in a LGMD2L patient leads to production of a truncated aggregation-prone Ano5 peptide.
Journal: The journal of pathology. Clinical research
Published: October 19, 2017
A novel rabbit model of Duchenne muscular dystrophy generated by CRISPR/Cas9.
Journal: Disease models & mechanisms
Published: September 25, 2017
Paeonol Attenuates LPS-Induced Endothelial Dysfunction and Apoptosis by Inhibiting BMP4 and TLR4 Signaling Simultaneously but Independently.
Journal: The Journal of pharmacology and experimental therapeutics
Published: September 25, 2017
Last Updated: 09/26/2026