Tubulin mutations in brain development disorders: Why haploinsufficiency does not explain TUBA1A tubulinopathies.
Ion Channel Contributions to Wing Development in Drosophila melanogaster.
TUBA1A mutations identified in lissencephaly patients dominantly disrupts neuronal migration and impair dyne activity.
Inwardly Rectifying Potassium Channels influences Drosophila wing morphogenesis by regulating Dpp release
Kir2.1 is important for BMP signaling to correctly pattern the mammalian face
A potential molecular target for morphological defects of fetal alcohol syndrome: Kir2.1
Ion channels in Development and Cancer
The alpha tubulin gene TUBA1A in brain development: a key ingredient in the neuronal isotype blend
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