| MARK2 variants cause autism spectrum disorder via the downregulation of WNT/b-catenin signaling pathway |
| 发表期刊 | AMERICAN JOURNAL OF HUMAN GENETICS
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| 2024-11
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| 卷号 | 111期号:11 |
| Gong, Maolei; Li, Jiayi; Qin, Zailong; Wilke, Matheus Vernet Machado Bressan; Liu, Yijun; Li, Qian; Liu, Haoran; Liang, Chen; Morales-Rosado, Joel A.; Cohen, Ana S. A.; Hughes, Susan S.; Sullivan, Bonnie R.; Waddell, Valerie; van den Boogaard, Marie-Jose H.; van Jaarsveld, Richard H.; van Binsbergen, Ellen; van Gassen, Koen L.; Wang, Tianyun; Hiatt, Susan M.; Amaral, Michelle D.; Kelley, Whitley, V; Zhao, Jianbo; Feng, Weixing; Ren, Changhong; Yu, Yazhen; Boczek, Nicole J.; Ferber, Matthew J.; Lahner, Carrie; Elliott, Sherr; Ruan, Yiyan; Mignot, Cyril; Keren, Boris; Xie, Hua; Wang, Xiaoyan; Popp, Bernt; Zweier, Christiane; Piard, Juliette; Coubes, Christine; Mau-Them, Frederic Tran; Safraou, Hana; Innes, A. Micheil; Gauthier, Julie; Michaud, Jacques L.; Koboldt, Daniel C.; Sylvie, Odent; Willems, Marjolaine; Tan, Wen-Hann; Cogne, Benjamin; Rieubland, Claudine; Braun, Dominique; Mclean, Scott Douglas; Platzer, Konrad; Zacher, Pia; Oppermann, Henry; Evenepoel, Lucie; Blanc, Pierre; El Khattabi, Laila; Haque, Neshatul; Dsouza, Nikita R.; Zimmermann, Michael T.; Urrutia, Raul; Klee, Eric W.; Shen, Yiping; Du, Hongzhen; Rappaport, Leonard; Liu, Chang-Mei; Chen, Xiaoli
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| 关键词 | NEURODEVELOPMENTAL DISORDERS
BIPOLAR DISORDER
BETA-CATENIN
PROTEIN
INDIVIDUALS
NETWORK
GENE
CELL
DIFFERENTIATION
MARK2/PAR-1
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| 文献类型 | 期刊论文
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| 条目标识符 | http://ir.ioz.ac.cn/handle/000000/16197
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| 专题 | 2024年度论文
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推荐引用方式
GB/T 7714 |
Gong, Maolei,Li, Jiayi,Qin, Zailong,et al. MARK2 variants cause autism spectrum disorder via the downregulation of WNT/b-catenin signaling pathway[J]. AMERICAN JOURNAL OF HUMAN GENETICS,2024,111(11).
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| APA |
Gong, Maolei.,Li, Jiayi.,Qin, Zailong.,Wilke, Matheus Vernet Machado Bressan.,Liu, Yijun.,...&Chen, Xiaoli.(2024).MARK2 variants cause autism spectrum disorder via the downregulation of WNT/b-catenin signaling pathway.AMERICAN JOURNAL OF HUMAN GENETICS,111(11).
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| MLA |
Gong, Maolei,et al."MARK2 variants cause autism spectrum disorder via the downregulation of WNT/b-catenin signaling pathway".AMERICAN JOURNAL OF HUMAN GENETICS 111.11(2024).
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