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Updated: Jun 13, 2026

In Vivo Functional Study of Disease-associated Rare Human Variants Using Drosophila
06:41

In Vivo Functional Study of Disease-associated Rare Human Variants Using Drosophila

Published on: August 20, 2019

DCCの変異は先天的な鏡の動きを引き起こす

Myriam Srour1, Jean-Baptiste Rivière, Jessica M T Pham

  • 1Center of Excellence in Neuromics, Université de Montréal, Montréal, QC H2L 2W5, Canada.

Science (New York, N.Y.)
|May 1, 2010
PubMed
まとめ

生まれながらの鏡の動きは,しばしば神経系の発達の問題と関連しており,2つの家族で研究されました. 研究者らは,神経の誘導に不可欠なDCC遺伝子の変異が,これらの非自発的な動きを引き起こし,人間の神経系の横行化におけるその役割を強調した.

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