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Connection

David Sherry to Mutation

This is a "connection" page, showing publications David Sherry has written about Mutation.
Connection Strength

0.853
  1. 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.
    View in: PubMed
    Score: 0.542
  2. 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.
    View in: PubMed
    Score: 0.144
  3. 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.
    View in: PubMed
    Score: 0.112
  4. Spontaneous mutation in 2310061I04Rik results in reduced expression of mitochondrial genes and impaired brain myelination. PLoS One. 2024; 19(12):e0290487.
    View in: PubMed
    Score: 0.046
  5. Excitatory amino acid involvement in retinal degeneration. Brain Res. 1990 Oct 29; 531(1-2):350-4.
    View in: PubMed
    Score: 0.004
  6. Immunocytochemical identification of outer segment proteins in the rd chicken. Exp Eye Res. 1990 Aug; 51(2):209-16.
    View in: PubMed
    Score: 0.004
Connection Strength

The connection strength for concepts is the sum of the scores for each matching publication.

Publication scores are based on many factors, including how long ago they were written and whether the person is a first or senior author.

THIS IS A DEVELOPMENT VERSION OF PROFILES. PLEASE GO TO THE PRODUCTION ENVIRONMENT FOR UPDATES