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

Live imaging of the extracellular matrix with a glycan-binding fluorophore.

利用糖结合荧光染料对细胞外基质进行活体成像

Fiore Antonio, Yu Guoqiang, Northey Jason J, Patel Ronak, Ravenscroft Thomas A, Ikegami Richard, Kolkman Wiert, Kumar Pratik, Dilan Tanya L, Ruetten Virginia M S, Ahrens Misha B, Shroff Hari, Wang Shaohe, Weaver Valerie M, Pedram Kayvon

Heterozygous loss-of-function variants significantly expand the phenotypes associated with loss of GDF11

杂合功能缺失变异显著扩展了与 GDF11 缺失相关的表型

Ravenscroft, Thomas A; Phillips, Jennifer B; Fieg, Elizabeth; Bajikar, Sameer S; Peirce, Judy; Wegner, Jeremy; Luna, Alia A; Fox, Eric J; Yan, Yi-Lin; Rosenfeld, Jill A; Zirin, Jonathan; Kanca, Oguz; Benke, Paul J; Cameron, Eric S; Strehlow, Vincent; Platzer, Konrad; Jamra, Rami Abou; Klöckner, Chiara; Osmond, Matthew; Licata, Thomas; Rojas, Samantha; Dyment, David; Chong, Josephine S C; Lincoln, Sharyn; Stoler, Joan M; Postlethwait, John H; Wangler, Michael F; Yamamoto, Shinya; Krier, Joel; Westerfield, Monte; Bellen, Hugo J

Lipidomic and Transcriptomic Basis of Lysosomal Dysfunction in Progranulin Deficiency

前粒蛋白缺乏症溶酶体功能障碍的脂质组学和转录组学基础

Evers, Bret M; Rodriguez-Navas, Carlos; Tesla, Rachel J; Prange-Kiel, Janine; Wasser, Catherine R; Yoo, Kyoung Shin; McDonald, Jeffrey; Cenik, Basar; Ravenscroft, Thomas A; Plattner, Florian; Rademakers, Rosa; Yu, Gang; White, Charles L 3rd; Herz, Joachim

TYROBP genetic variants in early-onset Alzheimer's disease

TYROBP基因变异与早发性阿尔茨海默病

Pottier, Cyril; Ravenscroft, Thomas A; Brown, Patricia H; Finch, NiCole A; Baker, Matt; Parsons, Meeia; Asmann, Yan W; Ren, Yingxue; Christopher, Elizabeth; Levitch, Denise; van Blitterswijk, Marka; Cruchaga, Carlos; Campion, Dominique; Nicolas, Gaël; Richard, Anne-Claire; Guerreiro, Rita; Bras, Jose T; Zuchner, Stephan; Gonzalez, Michael A; Bu, Guojun; Younkin, Steven; Knopman, David S; Josephs, Keith A; Parisi, Joseph E; Petersen, Ronald C; Ertekin-Taner, Nilüfer; Graff-Radford, Neill R; Boeve, Bradley F; Dickson, Dennis W; Rademakers, Rosa

Mutations in protein N-arginine methyltransferases are not the cause of FTLD-FUS

蛋白质N-精氨酸甲基转移酶的突变并非FTLD-FUS的病因。

Ravenscroft, Thomas A; Baker, Matt C; Rutherford, Nicola J; Neumann, Manuela; Mackenzie, Ian R; Josephs, Keith A; Boeve, Bradley F; Petersen, Ronald; Halliday, Glenda M; Kril, Jillian; van Swieten, John C; Seeley, William W; Dickson, Dennis W; Rademakers, Rosa