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Keywords: Epilepsy
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Journal Articles

A lissencephaly-associated BAIAP2 variant causes defects in neuronal migration during brain development

Meng-Han Tsai, Wan-Cian Lin, Shih-Ying Chen, Meng-Ying Hsieh, Fang-Shin Nian, Haw-Yuan Cheng, Hong-Jun Zhao, Shih-Shun Hung, Chi-Hsin Hsu, Pei-Shan Hou, Chien-Yi Tung, Mei-Hsuan Lee, Jin-Wu Tsai
Journal: Development
Development (2024) 151 (2): dev201912.
https://doi.org/10.1242/dev.201912
Published: 19 January 2024
.... W. et al. ( 2017 ). DEPDC5 mutations in familial and sporadic focal epilepsy . Clin. Genet. 92 , 397 - 404 . 10.1111/cge.12992 Tsai , M. H. , Nian , F. S. , Hsu , M. H. , Liu , W. S. , Liu , Y. T. , Liu , C. , Lin , P. H. , Hwang , D. Y. , Chuang...
View articletitled, A lissencephaly-associated BAIAP2 variant causes defects in neuronal migration during brain development
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Includes: Supplementary data
Journal Articles

Hippocampal and visuospatial learning defects in mice with a deletion of frizzled 9, a gene in the Williams syndrome deletion interval

Chunjie Zhao, Carmen Avilés, Regina A. Abel, C. Robert Almli, Patrick McQuillen, Samuel J. Pleasure
Journal: Development
Development (2005) 132 (12): 2917–2927.
https://doi.org/10.1242/dev.01871
Published: 15 June 2005
... Epilepsy Mossy cell Apoptosis Wnts regulate the development of dorsal structures (including the hippocampus) in the developing mammalian central nervous system( Muroyama et al., 2002 ). Gain-of-function studies, examining the brains of mice overexpressing a dominant-active version of the Wnt...
View articletitled, Hippocampal and visuospatial learning defects in mice with a deletion of frizzled 9, a gene in the Williams syndrome deletion interval
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Journal Articles

Ccm1 is required for arterial morphogenesis: implications for the etiology of human cavernous malformations

Kevin J. Whitehead, Nicholas W. Plummer, Jennifer A. Adams, Douglas A. Marchuk, Dean Y. Li
Journal: Development
Development (2004) 131 (6): 1437–1448.
https://doi.org/10.1242/dev.01036
Published: 15 March 2004
... rather than neural defects. † Authors for correspondence (e-mail: [email protected] or [email protected] ) * These authors contributed equally to this work 2 12 2003 © 2004. 2004 Ccm1 Gene targeting Mice Angiogenesis Stroke Epilepsy Notch Efnb2...
View articletitled, Ccm1 is required for arterial morphogenesis: implications for the etiology of human cavernous malformations
Open the PDF for Ccm1 is required for arterial morphogenesis: implications for the etiology of human cavernous malformations in another window
Includes: Supplementary data