Antonio Mollica
Toronto, ON M5S1A8, Canada
Last Updated: 09/26/2026
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Found 8 publications
Precise template-free correction restores gene function in Tay-Sachs disease while reframing is ineffective.
Journal: Molecular therapy. Nucleic acids
Published: May 25, 2024
Mutations in the β-tubulin TUBB impair ciliogenesis and are associated with ciliopathy-like phenotypes.
Journal: Nature communications
Published: June 16, 2023
DPCD is a regulator of R2TP in ciliogenesis initiation through Akt signaling.
Journal: Cell reports
Published: February 23, 2023
Efficient prime editing in two-cell mouse embryos using PEmbryo.
Journal: Nature biotechnology
Published: June 14, 2022
Phenotype Driven Analysis of Whole Genome Sequencing Identifies Deep Intronic Variants that Cause Retinal Dystrophies by Aberrant Exonization.
Journal: Investigative ophthalmology & visual science
Published: September 04, 2020
DYNC2H1 hypomorphic or retina-predominant variants cause nonsyndromic retinal degeneration.
Journal: Genetics in medicine : official journal of the American College of Medical Genetics
Published: February 03, 2020
Acyldepsipeptide Analogs Dysregulate Human Mitochondrial ClpP Protease Activity and Cause Apoptotic Cell Death.
Journal: Cell chemical biology
Published: December 08, 2017
Showing 1-8 of 8
Last Updated: 09/26/2026