Recent

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.
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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
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The alpha tubulin gene TUBA1A in brain development: a key ingredient in the neuronal isotype blend

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