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Accumulated common variants in the broader fragile X gene family modulate autistic phenotypes.
- Published in:
- EMBO Molecular Medicine, 2015, v. 7, n. 12, p. 1565, doi. 10.15252/emmm.201505696
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- Article
A CAG repeat polymorphism of KCNN3 predicts SK3 channel function and cognitive performance in schizophrenia.
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- EMBO Molecular Medicine, 2011, v. 3, n. 6, p. 309, doi. 10.1002/emmm.201100135
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- Article
Corrigendum to: Two Functional Epithelial Sodium Channel Isoforms Are Present in Rodents despite Pronounced Evolutionary Pseudogenization and Exon Fusion.
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- 2022
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- Correction Notice
Two Functional Epithelial Sodium Channel Isoforms Are Present in Rodents despite Pronounced Evolutionary Pseudogenization and Exon Fusion.
- Published in:
- Molecular Biology & Evolution, 2021, v. 38, n. 12, p. 5704, doi. 10.1093/molbev/msab271
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- Article
Of Humans and Gerbils— Independent Diversification of Neuroligin-4 Into X- and Y-Specific Genes in Primates and Rodents.
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- Frontiers in Molecular Neuroscience, 2022, v. 15, p. 1, doi. 10.3389/fnmol.2022.838262
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- Article
Ca<sup>2+</sup> binding to the C<sub>2</sub>E domain of otoferlin is required for hair cell exocytosis and hearing.
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- Protein & Cell, 2024, v. 15, n. 4, p. 305, doi. 10.1093/procel/pwad058
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- Article
Probing the role of the C<sub>2</sub>F domain of otoferlin.
- Published in:
- Frontiers in Molecular Neuroscience, 2023, p. 1, doi. 10.3389/fnmol.2023.1299509
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- Article