Found: 7
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Gatad2b, associated with the neurodevelopmental syndrome GAND, plays a critical role in neurodevelopment and cortical patterning.
- Published in:
- Translational Psychiatry, 2024, v. 14, n. 1, p. 1, doi. 10.1038/s41398-023-02678-x
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- Article
The Human SCN10A<sup>G1662S</sup> Point Mutation Established in Mice Impacts on Mechanical, Heat, and Cool Sensitivity.
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- Frontiers in Pharmacology, 2021, v. 12, p. 1, doi. 10.3389/fphar.2021.780132
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- Article
Mouse mutant phenotyping at scale reveals novel genes controlling bone mineral density.
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- PLoS Genetics, 2020, v. 16, n. 12, p. 1, doi. 10.1371/journal.pgen.1009190
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- Article
The Human SCN9A <sup> R 185 H </sup> Point Mutation Induces Pain Hypersensitivity and Spontaneous Pain in Mice.
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- Frontiers in Molecular Neuroscience, 2022, v. 15, p. 1, doi. 10.3389/fnmol.2022.913990
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- Article
Changes in social behavior with MAPK2 and KCTD13/CUL3 pathways alterations in two new outbred rat models for the 16p11.2 syndromes with autism spectrum disorders.
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- Frontiers in Neuroscience, 2023, p. 1, doi. 10.3389/fnins.2023.1148683
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- Article
Multi-influential genetic interactions alter behaviour and cognition through six main biological cascades in Down syndrome mouse models.
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- Human Molecular Genetics, 2021, v. 30, n. 9, p. 771, doi. 10.1093/hmg/ddab012
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- Article
Gdaphen, R pipeline to identify the most important qualitative and quantitative predictor variables from phenotypic data.
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- BMC Bioinformatics, 2023, v. 24, n. 1, p. 1, doi. 10.1186/s12859-022-05111-0
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- Article