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收藏Neuronal ABCA7 deficiency aggravates mitochondrial dysfunction and neurodegeneration in Alzheimer's disease神经元ABCA7缺乏加剧阿尔茨海默病中的线粒体功能障碍和神经退行性变
Wang, N; Pan, YN; Starling, SC; Haskell, DH; Quintero, AC; Kawatani, K; Inoue, Y; Shue, F; Ma, XY; Aikawa, T; Martens, YA; Kurti, A; Parsons, TM; Perkerson, RB; Roy, B; Raulin, AC; Ren, YX; Deture, M; Dickson, DW; Bao, HM; Han, XL; Bu, GJ; Kanekiyo, T
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收藏Alzheimer's disease risk ABCA7 p.A696S variant disturbs the microglial response to amyloid pathology in mice阿尔茨海默病风险ABCA7 p.A696S变体干扰小鼠小胶质细胞对淀粉样蛋白病理的反应
Ma, Xiaoye; Prokopenko, Dmitry; Wang, Ni; Aikawa, Tomonori; Choi, Younjung; Zhang, Can; Lei, Dan; Ren, Yingxue; Kawatani, Keiji; Starling, Skylar C.; Perkerson, Ralph B.; Roy, Bhaskar; Quintero, Astrid C.; Parsons, Tammee M.; Pan, Yining; Li, Zonghua; Wang, Minghui; Bao, Hanmei; Han, Xianlin; Bu, Guojun; Tanzi, Rudolph E.; Kanekiyo, Takahisa
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收藏lncRNA HIF1A-AS2 acts as an oncogene to regulate malignant phenotypes in cervical cancer
Liu, Yang; Zhang, Yunyan; Chen, Cha; Roy, Bhaskar; Li, Qun; Zhang, Wei; Zhang, Xuan; Pu, Jieying; Li, Yuguang; Liu, Yanli; Liao, Huanlan; Wang, Jingjing; Zhou, Rui; Zhuo, Huiyan; Li, Youqiang
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收藏Amyloid pathology and cognitive impairment in hAβ-KI and APPSAA-KI mouse models of Alzheimer's disease阿尔茨海默病haβ-ki和appsaa-ki小鼠模型的淀粉样蛋白病理和认知障碍
Lu, Wenyan; Shue, Francis; Kurti, Aishe; Jeevaratnam, Suren; Macyczko, Jesse R.; Roy, Bhaskar; Izhar, Taha; Wang, Ni; Bu, Guojun; Kanekiyo, Takahisa; Li, Yonghe
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收藏Genomic landscape and tumor mutational features of resected preinvasive to invasive lung adenocarcinoma
Lin, Yangui; Li, Dan; Hui, Hongliang; Miao, Haoran; Luo, Min; Roy, Bhaskar; Chen, Binbin; Zhang, Wei; Shao, Di; Ma, Di; Jie, Yanbing; Qiu, Fan; Li, Huaming; Jiang, Bo
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收藏CSF biomarkers of immune activation and Alzheimer's disease for predicting cognitive impairment risk in the elderly
Shue, Francis; White, Launia J.; Hendrix, Rachel; Ulrich, Jason; Henson, Rachel L.; Knight, William; Martens, Yuka A.; Wang, Ni; Roy, Bhaskar; Starling, Skylar C.; Ren, Yingxue; Xiong, Chengjie; Asmann, Yan W.; Syrjanen, Jeremy A.; Vassilaki, Maria; Mielke, Michelle M.; Timsina, Jigyasha; Sung, Yun Ju; Cruchaga, Carlos; Holtzman, David M.; Bu, Guojun; Petersen, Ronald C.; Heckman, Michael G.; Kanekiyo, Takahisa
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收藏Biallelic CRELD1 variants cause a multisystem syndrome, including neurodevelopmental phenotypes, cardiac dysrhythmias, and frequent infections
Jeffries, Lauren; Mis, Emily K.; McWalter, Kirsty; Donkervoort, Sandra; Brodsky, Nina N.; Carpier, Jean-Marie; Ji, Weizhen; Ionita, Cristian; Roy, Bhaskar; Morrow, Jon S.; Darbinyan, Armine; Iyer, Krishna; Aul, Ritu B.; Banka, Siddharth; Chao, Katherine R.; Cobbold, Laura; Cohen, Stacey; Custodio, Helena M.; Drummond-Borg, Margaret; Elmslie, Frances; Finanger, Erika; Hainline, Bryan E.; Helbig, Ingo; Hewson, Stacy; Hu, Ying; Jackson, Adam; Josifova, Dragana; Konstantino, Monica; Leach, Meganne E.; Mak, Bryan; McCormick, David; McGee, Elisabeth; Nelson, Stanley; Nguyen, Joanne; Nugent, Kimberly; Ortega, Lucy; Goodkin, Howard P.; Roeder, Elizabeth; Roy, Sani; Sapp, Katie; Saade, Dimah; Sisodiya, Sanjay M.; Stals, Karen; Towner, Shelley; Wilson, William; Khokha, Mustafa K.; Boennemann, Carsten G.; Lucas, Carrie L.; Lakhani, Saquib A.
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