Found: 12
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Spatiotemporal expression of foxo4, foxo6a, and foxo6b in the developing brain and retina are transcriptionally regulated by PI3K signaling in zebrafish.
- Published in:
- Development Genes & Evolution, 2017, v. 227, n. 3, p. 219, doi. 10.1007/s00427-017-0575-6
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- Article
Cnr2 Is Important for Ribbon Synapse Maturation and Function in Hair Cells and Photoreceptors.
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- Frontiers in Molecular Neuroscience, 2021, v. 13, p. N.PAG, doi. 10.3389/fnmol.2021.624265
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- Article
Zebrafish rgs4 is essential for motility and axonogenesis mediated by Akt signaling.
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- Cellular & Molecular Life Sciences, 2013, v. 70, n. 5, p. 935, doi. 10.1007/s00018-012-1178-z
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- Article
Bi-allelic ACBD6 variants lead to a neurodevelopmental syndrome with progressive and complex movement disorders.
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- Brain: A Journal of Neurology, 2024, v. 147, n. 4, p. 1436, doi. 10.1093/brain/awad380
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- Article
Evaluating the association of biallelic OGDHL variants with significant phenotypic heterogeneity.
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- Genome Medicine, 2023, v. 15, n. 1, p. 1, doi. 10.1186/s13073-023-01258-4
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- Article
The epigenetic factor Kmt2a/Mll1 regulates neural progenitor proliferation and neuronal and glial differentiation.
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- Developmental Neurobiology (19328451), 2015, v. 75, n. 5, p. 452, doi. 10.1002/dneu.22235
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- Article
Bmp5 Regulates Neural Crest Cell Survival and Proliferation via Two Different Signaling Pathways.
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- Stem Cells, 2017, v. 35, n. 4, p. 1003, doi. 10.1002/stem.2533
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- Article
A biallelic variant in CLRN2 causes non-syndromic hearing loss in humans.
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- Human Genetics, 2021, v. 140, n. 6, p. 915, doi. 10.1007/s00439-020-02254-z
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- Article
ABE-ultramax for high-efficiency biallelic adenine base editing in zebrafish.
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- Nature Communications, 2024, v. 15, n. 1, p. 1, doi. 10.1038/s41467-024-49943-1
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- Article
Front Cover, Volume 43, Issue 10.
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- Human Mutation, 2022, v. 43, n. 10, p. i, doi. 10.1002/humu.24464
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- Article
WARS1 and SARS1: Two tRNA synthetases implicated in autosomal recessive microcephaly.
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- Human Mutation, 2022, v. 43, n. 10, p. 1454, doi. 10.1002/humu.24430
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- Article
Biallelic variants in WARS1 cause a highly variable neurodevelopmental syndrome and implicate a critical exon for normal auditory function.
- Published in:
- Human Mutation, 2022, v. 43, n. 10, p. 1472, doi. 10.1002/humu.24435
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- Article