日期:
2020 年 — 2026 年
2020
2021
2022
2023
2024
2025
2026
影响因子:

Decoding neurodegeneration one cell at a time

逐个细胞解码神经退行性疾病

Gautier, Olivia; Nguyen, Thao P; Gitler, Aaron D

TDP-43 is coming to the cottage: A new tool to study neurodegenerative diseases

TDP-43即将走进我们的视野:一种研究神经退行性疾病的新工具

Rayner, Stephanie L; Gitler, Aaron D

TDP-43-mediated alternative polyadenylation is associated with a reduction in VPS35 and VPS29 expression in frontotemporal dementia

TDP-43介导的替代性多聚腺苷酸化与额颞叶痴呆中VPS35和VPS29表达的降低有关

Maheswari Jawahar, Vidhya; Zeng, Yi; Armour, Ellen M; Yue, Mei; Citrano, Kathryn; Lovchykova, Anastasiia; Reeves, Madison M; Rawlinson, Bailey; DeTure, Michael; Dunmore, Judith A; Song, Yuping; Ball, Sophie K; Wszolek, Zbigniew K; Graff-Radford, Neill R; Boeve, Bradley F; Knopman, David S; Day, Gregory S; Small, Scott A; Dickson, Dennis W; Ward, Michael E; Gendron, Tania F; Zhang, Yongjie; Prudencio, Mercedes; Gitler, Aaron D; Petrucelli, Leonard

Whole-genome 3D architectural screen reveals modulators of brain DNA structure

全基因组三维结构筛选揭示大脑DNA结构的调节因子

Parasar, Bibudha; Venkatesh, Achuthan Raja; Perera, Jonathan; Sosnick, Lucas; Moghadami, Siavash; Seo, Yunji; Shi, Jenny; Chan, Lynette; Takenawa, Satoshi; Akiyama, Tetsuya; Sianto, Odilia; Uenaka, Takeshi; Hadjipanayis, Angela; Wernig, Marius; Gitler, Aaron D; Tan, Longzhi

A consensus spinal cord cell type atlas across mouse, macaque, and human

小鼠、猕猴和人类脊髓细胞类型共识图谱

Schmitz, Matthew T; Johansen, Nelson J; Kempynck, Niklas; Kapen, Inkar; Fu, Yuanyuan; Hewitt, Madeleine; Seeman, Stephanie C; Kussick, Emily; Gautier, Olivia; Leone, Michael J; Ding, Song-Lin; Gao, Yuan; Bhandiwad, Ashwin; Ariza, Jeanelle; Ayala, Angela; Barta, Stuard; Blum, Jacob A; Cano-Gomez, Liliana; Cardenas, Trangthanh; Chakka, Anish Bhaswanth; Cuevas, Nasmil Valera; Donadio, Nicholas; Fancher, Katherine A; Thomas, Emma D; Ferrer, Rebecca; Goldy, Jeff; Hastings, Samantha D; Hirschstein, Daniel; Ho, Windy; Huang, Cindy; Juneau, Zoe C; Kim, Sa Rang; Lewis, Zachary R; Liang, Elizabeth; Martin, Naomi X; Nagra, Josh; Newman, Dakota; Noh, Myung-Chul; Olsen, Paul; Oyama, Alana; Pena, Nick; Poldsam, Helen; Ray, Patrick L; Reding, Melissa; Rimorin, Christine; Ruiz, Augustin; Shapovalova, Nadiya V; Shulga, Lyudmila; Sobieski, Cassandra; Torkelson, Amy; Wirthlin, Morgan; Yao, Shenqin; Lai, Helen; Pfenning, Andreas; Pool, Allan-Hermann; Seal, Rebecca; Tasic, Bosiljka; Ting, Jonathan T; Waters, Jack; Yao, Zizhen; Gitler, Aaron D; McMillen, Delissa; Ng, Lydia; Zeng, Hongkui; van Velthoven, Cindy T J; Daigle, Tanya L; Smith, Kimberly A; Hodge, Rebecca D; Lein, Ed S; Bakken, Trygve E

Granulin loss and TMEM106B risk converge on lysosomal C-terminal fragment pathology in frontotemporal dementia.

颗粒蛋白丢失和 TMEM106B 风险在额颞叶痴呆中导致溶酶体 C 端片段病理。

Zeng Yi, Xiong Jian, Lovchykova Anastasiia, Nguyen Thao Phuong, Song Abigail, Gitler Semma W, Abu-Remaileh Monther, Gitler Aaron D

Pathogenic UNC13A variants cause a neurodevelopmental syndrome by impairing synaptic function

致病性UNC13A变异体通过损害突触功能导致神经发育综合征。

Asadollahi, Reza; Ahmad, Aisha; Boonsawat, Paranchai; Shahanoor Hinzen, Jasmine; Lohse, Mareike; Bouazza-Arostegui, Boris; Sun, Siqi; Utesch, Tillmann; Sommer, Jonas D; Ilic, Dragana; Padmanarayana, Murugesh; Fischermanns, Kati; Ranjan, Mrinalini; Boll, Moritz; Ka, Chandran; Piton, Amélie; Mattioli, Francesca; Isidor, Bertrand; Õunap, Katrin; Reinson, Karit; Wojcik, Monica H; Marshall, Christian R; Mercimek-Andrews, Saadet; Matsumoto, Naomichi; Miyake, Noriko; Stephan, Bruno de Oliveira; Honjo, Rachel Sayuri; Bertola, Debora R; Kim, Chong Ae; Yusupov, Roman; Mefford, Heather C; Christodoulou, John; Lee, Joy; Heath, Oliver; Brown, Natasha J; Baker, Naomi; Stark, Zornitza; Delatycki, Martin; Lake, Nicole J; Zeidler, Shimriet; Zuurbier, Linda; Maas, Saskia M; de Kruiff, Chris C; Rajabi, Farrah; Rodan, Lance H; Coury, Stephanie A; Platzer, Konrad; Oppermann, Henry; Abou Jamra, Rami; Beblo, Skadi; Maxton, Caroline; Śmigiel, Robert; Underhill, Hunter; Dubbs, Holly; Rosen, Alyssa; Helbig, Katherine L; Helbig, Ingo; Ruggiero, Sarah McKeown; Fitzgerald, Mark P; Kraemer, Dennis; Prada, Carlos E; Tenney, Jeffrey; Jayakar, Parul; Redon, Sylvia; Lefranc, Jérémie; Uguen, Kevin; Race, Simone; Efthymiou, Stephanie; Maroofian, Reza; Houlden, Henry; Coppens, Sandra; Deconinck, Nicolas; Ashokkumar, Balasubramaniem; Varalakshmi, Perumal; Gowda K, Vykunta Raju; Eghbal, Fatemeh; Ghayoor Karimiani, Ehsan; Heidari, Morteza; Neidhardt, John; Owczarek-Lipska, Marta; Korenke, G Christoph; Bamshad, Michael J; Campeau, Philippe M; Lehman, Anna; Hendon, Laura G; Wentzensen, Ingrid M; Monaghan, Kristin G; Chen, Yanmin; Szuto, Anna; Cohn, Ronald D; Au, Ping Yee Billie; Hübner, Christoph; Boschann, Felix; Manickam, Kandamurugu; Koboldt, Daniel C; Rad, Aboulfazl; Oprea, Gabriela; Bachman, Kristine K; Seeley, Andrea H; Agolini, Emanuele; Terracciano, Alessandra; Carmelo, Piscopo; Bupp, Caleb; Grysko, Bethany; Rein-Rothschild, Annick; Ben Zeev, Bruria; Margolin, Amy; Morrison, Jennifer; Dagli, Aditi; Stolerman, Elliot; Louie, Raymond J; Washington, Camerun; Stevens, Servi J C; Heijligers, Malou; Alkuraya, Fowzan S; Lisfeld, Jasmin; Neu, Axel; Paoli Monteiro, Fabíola; Santos Pessoa, André Luiz; Camelo-Filho, Antonio Edvan; Kok, Fernando; Koeberl, Dwight; Riley, Kacie; Burglen, Lydie; Doummar, Diane; Héron, Bénédicte; Mignot, Cyril; Keren, Boris; Charles, Perrine; Nava, Caroline; Bernhard, Felix P; Kühn, Andrea A; Thoms, Sven; Morrie, Ryan D; Mekhoubad, Shila; Green, Eric M; Barmada, Sami J; Gitler, Aaron D; Jahn, Olaf; Rhee, Jeong Seop; Rosenmund, Christian; Mitkovski, Mišo; Sticht, Heinrich; Sun, Han; Le Gac, Gerald; Taschenberger, Holger; Brose, Nils; Dittman, Jeremy S; Rauch, Anita; Lipstein, Noa

TDP-43 nuclear loss in FTD/ALS causes widespread alternative polyadenylation changes

在额颞叶痴呆/肌萎缩侧索硬化症中,TDP-43 核丢失会导致广泛的替代性多聚腺苷酸化改变。

Zeng, Yi; Lovchykova, Anastasiia; Akiyama, Tetsuya; Rayner, Stephanie L; Maheswari Jawahar, Vidhya; Liu, Chang; Sianto, Odilia; Guo, Caiwei; Calliari, Anna; Prudencio, Mercedes; Dickson, Dennis W; Petrucelli, Leonard; Gitler, Aaron D

Opposing roles of p38α-mediated phosphorylation and PRMT1-mediated arginine methylation in driving TDP-43 proteinopathy

p38α介导的磷酸化和PRMT1介导的精氨酸甲基化在驱动TDP-43蛋白病中发挥相反的作用

Aikio, Mari; Odeh, Hana M; Wobst, Heike J; Lee, Bo Lim; Chan, Úna; Mauna, Jocelyn C; Mack, Korrie L; Class, Bradley; Ollerhead, Thomas A; Ford, Alice F; Barbieri, Edward M; Cupo, Ryan R; Drake, Lauren E; Smalley, Joshua L; Lin, Yuan-Ta; Lam, Stephanie; Thomas, Reuben; Castello, Nicholas; Baral, Ashmita; Beyer, Jenna N; Najar, Mohd A; Dunlop, John; Gitler, Aaron D; Javaherian, Ashkan; Kaye, Julia A; Burslem, George M; Brown, Dean G; Donnelly, Christopher J; Finkbeiner, Steven; Moss, Stephen J; Brandon, Nicholas J; Shorter, James

An emergent disease-associated motor neuron state precedes cell death in a mouse model of ALS

在肌萎缩侧索硬化症(ALS)小鼠模型中,一种与疾病相关的运动神经元新状态先于细胞死亡出现。

Gautier, Olivia; Blum, Jacob A; Nguyen, Thao P; Klemm, Sandy; Yamakawa, Mai; Sinnott-Armstrong, Nasa; Zeng, Yi; Davis, Chung-Ha O; Bombosch, Juliane; Nakayama, Lisa; Guttenplan, Kevin A; Chen, Derek; Kathira, Arwa; Zhao, Luke; Rexach, Jessica E; Greenleaf, William J; Gitler, Aaron D