Jiri Lindovsky
Vestec, ST, Czech Republic
Last Updated: 09/26/2026
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Found 17 publications
Searching for New Genes That Cause Usher Syndrome.
Journal: American journal of ophthalmology
Published: January 21, 2026
SEARCHING FOR NEW GENES THAT CAUSE USHER SYNDROME.
Journal: American journal of ophthalmology
Published: January 21, 2026
Characterisation of SLC38A8 and Its Role in Retinal Pathways and Disease.
Journal: Clinical & experimental ophthalmology
Published: June 08, 2024
A review of standardized high-throughput cardiovascular phenotyping with a link to metabolism in mice.
Journal: Mammalian genome : official journal of the International Mammalian Genome Society
Published: April 20, 2023
Metabolic switch from fatty acid oxidation to glycolysis in knock-in mouse model of Barth syndrome.
Journal: EMBO molecular medicine
Published: January 06, 2023
OCT and ERG Techniques in High-Throughput Phenotyping of Mouse Vision.
Journal: Genes
Published: December 02, 2022
Retinitis pigmentosa-associated mutations in mouse Prpf8 cause misexpression of circRNAs and degeneration of cerebellar granule cells.
Journal: Life science alliance
Published: November 25, 2022
Acoustically Enriched Environment during the Critical Period of Postnatal Development Positively Modulates Gap Detection and Frequency Discrimination Abilities in Adult Rats.
Journal: Neural plasticity
Published: December 15, 2020
Myopia disease mouse models: a missense point mutation (S673G) and a protein-truncating mutation of the Zfp644 mimic human disease phenotype.
Journal: Cell & bioscience
Published: January 18, 2019
Fast tonotopy mapping of the rat auditory cortex with a custom-made electrode array.
Journal: Physiological research
Published: September 12, 2018
Last Updated: 09/26/2026