Found: 11
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Drosophila model to clarify the pathological significance of OPA1 in autosomal dominant optic atrophy.
- Published in:
- eLife, 2024, p. 1, doi. 10.7554/eLife.87880
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- Article
Functional analysis of RRAS2 pathogenic variants with a Noonan-like phenotype.
- Published in:
- Frontiers in Genetics, 2024, p. 1, doi. 10.3389/fgene.2024.1383176
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- Article
Glial insulin regulates cooperative or antagonistic Golden goal/Flamingo interactions during photoreceptor axon guidance.
- Published in:
- eLife, 2021, p. 1, doi. 10.7554/eLife.66718
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- Article
A Quantitative Model of Sporadic Axonal Degeneration in the Drosophila Visual System.
- Published in:
- Journal of Neuroscience, 2022, v. 42, n. 24, p. 4937, doi. 10.1523/JNEUROSCI.2115-21.2022
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- Article
Inherited C-terminal TREX1 variants disrupt homology-directed repair to cause senescence and DNA damage phenotypes in Drosophila, mice, and humans.
- Published in:
- Nature Communications, 2024, v. 15, n. 1, p. 1, doi. 10.1038/s41467-024-49066-7
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- Article
Publisher Correction: A novel NONO variant that causes developmental delay and cardiac phenotypes.
- Published in:
- 2023
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- Correction Notice
A novel NONO variant that causes developmental delay and cardiac phenotypes.
- Published in:
- Scientific Reports, 2023, v. 13, n. 1, p. 1, doi. 10.1038/s41598-023-27770-6
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- Publication type:
- Article
A novel NONO variant that causes developmental delay and cardiac phenotypes.
- Published in:
- Scientific Reports, 2023, v. 13, n. 1, p. 1, doi. 10.1038/s41598-023-27770-6
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- Publication type:
- Article
Identification of genes regulating stimulus-dependent synaptic assembly in Drosophila using an automated synapse quantification system.
- Published in:
- Genes & Genetic Systems, 2022, v. 97, n. 6, p. 297, doi. 10.1266/ggs.22-00114
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- Article
Direct evaluation of neuroaxonal degeneration with the causative genes of neurodegenerative diseases in Drosophila using the automated axon quantification system, MeDUsA.
- Published in:
- Human Molecular Genetics, 2023, v. 32, n. 9, p. 1524, doi. 10.1093/hmg/ddac307
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- Article
De novo ARF3 variants cause neurodevelopmental disorder with brain abnormality.
- Published in:
- Human Molecular Genetics, 2022, v. 31, n. 1, p. 69, doi. 10.1093/hmg/ddab224
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- Article