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BMC Medical Genetics|November 26, 2014
Cryptic FMR1 mosaic deletion in a phenotypically normal mother of a boy with fragile X syndrome: case reportShiyu Luo, Wen Huang, Qiuping Xia, et al.BMC Medical Genetics|July 7, 2014
Whole exome sequencing identifies a novel EMD mutation in a Chinese family with dilated cardiomyopathyMingqiu Zhang, Jia Chen, Dayong Si, et al.FASEB Journal : Official Publication of the Federation of American Societies for Experimental Biology|June 13, 2022
Loss of Drosophila NUS1 results in cholesterol accumulation and Parkinson's disease-related neurodegenerationJin Xue, Yingbao Zhu, Liyi Wei, et al.Neuroscience Bulletin|April 15, 2021
Dysregulated CRMP Mediates Circadian Deficits in a Drosophila Model of Fragile X SyndromeJuan Zhao, Jin Xue, Tengfei Zhu, et al.Nucleic Acids Research|December 17, 2025
Genome-wide modulation of alternative splicing by a predicted alpha helix in U2AF2Dingwu Xue, Liqiang Ai, Xiaoqin Wang, et al.Development (Cambridge, England)|November 13, 2007
Argonaute 1 regulates the fate of germline stem cells in DrosophilaLele Yang, Dongsheng Chen, Ranhui Duan, et al.Science in China. Series C, Life Sciences|February 5, 2008
Mitochondrial DNA analysis of human remains from the Yuansha site in Xinjiang, ChinaShiZhu Gao, YinQiu Cui, YiDai Yang, et al.Neuron|August 19, 2007
RNA-binding proteins hnRNP A2/B1 and CUGBP1 suppress fragile X CGG premutation repeat-induced neurodegeneration in a Drosophila model of FXTASOyinkan A Sofola, Peng Jin, Yunlong Qin, et al.Journal of Medical Genetics|November 29, 2013
Correlation between FMR1 expression and clinical phenotype in discordant dichorionic-diamniotic monozygotic twin sisters with the fragile X mutationWen Huang, Shiyu Luo, Jianjun Ou, et al.FASEB Journal : Official Publication of the Federation of American Societies for Experimental Biology|January 10, 2020
The UFM1 cascade times mitosis entry associated with microcephalyLi Yu, Guangxu Li, Jing Deng, et al.Pageof 7