Curtis R. French

300 Prince Phillip Drive
St. John's, NL, Canada

Last Updated: 09/26/2026

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Found 20 publications

Heterozygous Nonsense Mutation in the Nuclear Transport Factor KPNA7, a Maternal Factor Active in Embryonic Tissues, Causes Autosomal Dominant Otosclerosis.

Heterozygous Nonsense Mutation in the Nuclear Transport Factor KPNA7, a Maternal Factor Active in Embryonic Tissues, Causes Autosomal Dominant Otosclerosis.

Journal: International journal of molecular sciences

Published: March 26, 2026

Mutation of the GDP-Fucose Biosynthesis Gene gmds Increases Hair Cell Number and Neuromast Regenerative Capacity in Zebrafish.

Mutation of the GDP-Fucose Biosynthesis Gene gmds Increases Hair Cell Number and Neuromast Regenerative Capacity in Zebrafish.

Journal: International journal of molecular sciences

Published: August 01, 2025

Genetic Diseases of Fucosylation: Insights from Model Organisms.

Genetic Diseases of Fucosylation: Insights from Model Organisms.

Journal: Genes

Published: April 23, 2025

Genomic analysis of glaucoma pathogenesis due to gmds mutation in zebrafish.

Genomic analysis of glaucoma pathogenesis due to gmds mutation in zebrafish.

Journal: Experimental eye research

Published: November 12, 2024

The P4-phospholipid flippase Atp11a is required for maintenance of eye and ear structure in zebrafish.

The P4-phospholipid flippase Atp11a is required for maintenance of eye and ear structure in zebrafish.

Journal: Journal of cell science

Published: May 23, 2024

Pleiotropy in FOXC1-attributable phenotypes involves altered ciliation and cilia-dependent signaling.

Pleiotropy in FOXC1-attributable phenotypes involves altered ciliation and cilia-dependent signaling.

Journal: Scientific reports

Published: February 23, 2024

Phytocannabinoids Reduce Seizures in Larval Zebrafish and Affect Endocannabinoid Gene Expression.

Phytocannabinoids Reduce Seizures in Larval Zebrafish and Affect Endocannabinoid Gene Expression.

Journal: Biomolecules

Published: July 21, 2023

Mutation of foxl1 Results in Reduced Cartilage Markers in a Zebrafish Model of Otosclerosis.

Mutation of foxl1 Results in Reduced Cartilage Markers in a Zebrafish Model of Otosclerosis.

Journal: Genes

Published: April 04, 2022

Mechanistic Insights into Axenfeld-Rieger Syndrome from Zebrafish foxc1 and pitx2 Mutants.

Mechanistic Insights into Axenfeld-Rieger Syndrome from Zebrafish foxc1 and pitx2 Mutants.

Journal: International journal of molecular sciences

Published: July 27, 2021

Autosomal dominant non-syndromic hearing loss maps to DFNA33 (13q34) and co-segregates with splice and frameshift variants in ATP11A, a phospholipid flippase gene.

Autosomal dominant non-syndromic hearing loss maps to DFNA33 (13q34) and co-segregates with splice and frameshift variants in ATP11A, a phospholipid flippase gene.

Journal: Human genetics

Published: May 24, 2021

A pathogenic deletion in Forkhead Box L1 (FOXL1) identifies the first otosclerosis (OTSC) gene.

A pathogenic deletion in Forkhead Box L1 (FOXL1) identifies the first otosclerosis (OTSC) gene.

Journal: Human genetics

Published: May 15, 2021

Protein fucosylation is required for Notch dependent vascular integrity in zebrafish.

Protein fucosylation is required for Notch dependent vascular integrity in zebrafish.

Journal: Developmental biology

Published: February 15, 2021

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Last Updated: 09/26/2026