関連する実験動画

Updated: Sep 9, 2025

A Novel Strategy Combining Array-CGH, Whole-exome Sequencing and In Utero Electroporation in Rodents to Identify Causative Genes for Brain Malformations
08:22

A Novel Strategy Combining Array-CGH, Whole-exome Sequencing and In Utero Electroporation in Rodents to Identify Causative Genes for Brain Malformations

Published on: December 1, 2017

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YWHAE遺伝子の喪失に関連するフェノタイプを拡大する

Kozue Mori1, Kenichi Maeda1, Yasuhiro Kimoto1

  • 1Division of Pediatrics, Faculty of Medicine, University of Miyazaki, Miyazaki, Japan.

Pediatrics international : official journal of the Japan Pediatric Society
|September 1, 2025
PubMed
まとめ

No abstract available in PubMed .

キーワード:
CRK についてPAFAH1B1についてYWHAEエピレプシー皮質下帯のヘテロトピア

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Investigating the Pathogenesis of MYH7 Mutation Gly823Glu in Familial Hypertrophic Cardiomyopathy using a Mouse Model03:45

Investigating the Pathogenesis of MYH7 Mutation Gly823Glu in Familial Hypertrophic Cardiomyopathy using a Mouse Model

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In Vivo Functional Study of Disease-associated Rare Human Variants Using Drosophila06:41

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

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