David Sherry to Mutation
This is a "connection" page, showing publications David Sherry has written about Mutation.
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The Elovl4 Spinocerebellar Ataxia-34 Mutation 736T>G (p.W246G) Impairs Retinal Function in the Absence of Photoreceptor Degeneration. Mol Neurobiol. 2020 Nov; 57(11):4735-4753.
Score: 0.542
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W246G Mutant ELOVL4 Impairs Synaptic Plasticity in Parallel and Climbing Fibers and Causes Motor Defects in a Rat Model of SCA34. Mol Neurobiol. 2021 Oct; 58(10):4921-4943.
Score: 0.144
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Homozygous Expression of Mutant ELOVL4 Leads to Seizures and Death in a Novel Animal Model of Very Long-Chain Fatty Acid Deficiency. Mol Neurobiol. 2018 02; 55(2):1795-1813.
Score: 0.112
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Spontaneous mutation in 2310061I04Rik results in reduced expression of mitochondrial genes and impaired brain myelination. PLoS One. 2024; 19(12):e0290487.
Score: 0.046
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Excitatory amino acid involvement in retinal degeneration. Brain Res. 1990 Oct 29; 531(1-2):350-4.
Score: 0.004
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Immunocytochemical identification of outer segment proteins in the rd chicken. Exp Eye Res. 1990 Aug; 51(2):209-16.
Score: 0.004