PHF8 activates transcription of rRNA genes through H3K4me3 binding and H3K9me1/2 demethylation von Jenuwein, Thomas, Ye, Jing, Yonezawa, Masato, Grummt, Ingrid, Feng, Weijun

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Global Navigation Satellite System Signal Phase Combining and Performance of Distributed Antenna Arrays von GUO, Wenfei, ZHANG, Jun, GUO, Chi, FENG, Weijun

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Editorial: Molecular characteristics and personalized treatment for pediatric brain tumors von Feng, Weijun, Kawauchi, Daisuke, Wan, Feng

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Chd7 is indispensable for mammalian brain development through activation of a neuronal differentiation programme von Feng, Weijun, Kawauchi, Daisuke, Körkel-Qu, Huiqin, Deng, Huan, Serger, Elisabeth, Sieber, Laura, Lieberman, Jenna Ariel, Jimeno-González, Silvia, Lambo, Sander, Hanna, Bola S., Harim, Yassin, Jansen, Malin, Neuerburg, Anna, Friesen, Olga, Zuckermann, Marc, Rajendran, Vijayanad, Gronych, Jan, Ayrault, Olivier, Korshunov, Andrey, Jones, David T. W., Kool, Marcel, Northcott, Paul A., Lichter, Peter, Cortés-Ledesma, Felipe, Pfister, Stefan M., Liu, Hai-Kun

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chromatin remodeling complex NuRD establishes the poised state of rRNA genes characterized by bivalent histone modifications and altered nucleosome positions von Xie, Wenbing, Ling, Te, Zhou, Yonggang, Feng, Weijun, Zhu, Qiaoyun, Stunnenberg, Henk G, Grummt, Ingrid, Tao, Wei

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Activation of RNA Polymerase I Transcription by Cockayne Syndrome Group B Protein and Histone Methyltransferase G9a von Yuan, Xuejun, Feng, Weijun, Imhof, Axel, Grummt, Ingrid, Zhou, Yonggang

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Multipath extraction and mitigation for static relative positioning based on adaptive layer wavelet packets, bootstrapped searches and CNR constraints von Su, Mingkun, Yang, Yanxi, Qiao, Lei, Ma, Hao, Feng, WeiJun, Qiu, Zhaoyang, Zheng, Jiansheng

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A single-cell atlas reveals the heterogeneity of meningeal immunity in a mouse model of Methyl CpG binding protein 2 deficiency von Li, Huiping, Hu, Meixin, Huang, Zhuxi, Wang, Yi, Xu, Ying, Deng, Jingxin, Zhu, Ming, Feng, Weijun, Xu, Xiu

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Versatile Roles of the Chromatin Remodeler CHD7 during Brain Development and Disease von Feng, Weijun, Shao, Chunxuan, Liu, Hai-Kun

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Novel compound heterozygous mutation in STAMBP causes a neurodevelopmental disorder by disrupting cortical proliferation von Hu, Meixin, Li, Huiping, Huang, Zhuxi, Li, Dongyun, Xu, Ying, Xu, Qiong, Chen, Bo, Wang, Yi, Deng, Jingxin, Zhu, Ming, Feng, Weijun, Xu, Xiu

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Cholix protein domain I functions as a carrier element for efficient apical to basal epithelial transcytosis von Taverner, Alistair, MacKay, Julia, Laurent, Floriane, Hunter, Tom, Liu, Keyi, Mangat, Khushdeep, Song, Lisa, Seto, Elbert, Postlethwaite, Sally, Alam, Aatif, Chandalia, Apurva, Seung, Minji, Saberi, Mazi, Feng, Weijun, Mrsny, Randall J.

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CRISPR-mediated Loss of Function Analysis in Cerebellar Granule Cells Using In Utero Electroporation-based Gene Transfer von Feng, Weijun, Herbst, Lena, Lichter, Peter, Pfister, Stefan M, Liu, Hai-Kun, Kawauchi, Daisuke

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Lead exposure leads to premature neural differentiation via inhibiting Wnt signaling von Li, Jun, Hu, Meixin, Liu, Yingying, Lu, Rongrong, Feng, Weijun

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Hormone-Dependent Coactivator Binding to a Hydrophobic Cleft on Nuclear Receptors von Feng, Weijun, Ralff C. J. Ribeiro, Wagner, Richard L., Nguyen, Hoa, Apriletti, James W., Fletterick, Robert J., Baxter, John D., Kushner, Peter J., West, Brian L.

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Activation of NF-κ B via a Src-Dependent Ras-MAPK-pp90rsk Pathway is Required for Pseudomonas aeruginosa-Induced Mucin Overproduction in Epithelial Cells von Li, Jian-Dong, Feng, Weijun, Gallup, Marianne, Kim, Jae-Ho, Gum, James, Kim, Young, Basbaum, Carol

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Generation and characterization of Chd7‐iCreERT2‐tdTomato mice von Han, Zi'ang, Wang, Ze, Huang, Zhuxi, Feng, Weijun

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Three-dimensional hierarchical microstructures of the suture of turtle shell and its effect on the mechanical properties von Peng, Zhilong, Feng, Weijun, Huang, Jiawei, Li, Peiran, Chen, Shaohua

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A spectrum of AKT3 activating mutations cause focal malformations of cortical development (FMCDs) in cortical organoids von Xu, Ying, Lu, Rongrong, Li, Hao, Feng, Weijun, Zhao, Rui

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AAV-mediated Stambp gene replacement therapy rescues neurological defects in a mouse model of microcephaly-capillary malformation syndrome von Hu, Meixin, Li, Jun, Deng, Jingxin, Liu, Chunxue, Liu, Yingying, Li, Huiping, Feng, Weijun, Xu, Xiu

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Potentiation of Estrogen Receptor Activation Function 1 (AF-1) by Src/JNK through a Serine 118-Independent Pathway von Feng, Weijun, Webb, Paul, Nguyen, Phuong, Liu, Xiaohong, Li, Jiandong, Karin, Michael, Kushner, Peter J

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