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

Transition of Néel-Type and Bloch-Néel Hybrid Skyrmion in a Metallic Multilayer Material System

金属多层材料体系中尼尔型和布洛赫-尼尔混合型斯格明子的转变

Wang, Binbin; Bagués, Núria; Cheng, Shuyu; Das, Shekhar; Selcu, Camelia; Li, Ziling; Freyermuth, Jacob B; Pelekhov, Denis V; Hammel, P Chris; Randeria, Mohit; Kawakami, Roland K; McComb, David W

Comprehensive evaluation of human-derived anti-poly-GA antibodies in cellular and animal models of C9orf72 disease

在C9orf72疾病的细胞和动物模型中对人源抗poly-GA抗体进行全面评估

Jambeau, Melanie; Meyer, Kevin D; Hruska-Plochan, Marian; Tabet, Ricardos; Lee, Chao-Zong; Ray-Soni, Ananya; Aguilar, Corey; Savage, Kitty; Mishra, Nibha; Cavegn, Nicole; Borter, Petra; Lin, Chun-Chia; Jansen-West, Karen R; Jiang, Jie; Freyermuth, Fernande; Li, Nan; De Rossi, Pierre; Pérez-Berlanga, Manuela; Jiang, Xin; Daughrity, Lilian M; Pereira, João; Narayanan, Sarav; Gu, Yuanzheng; Dhokai, Shekhar; Dalkilic-Liddle, Isin; Maniecka, Zuzanna; Weber, Julien; Workman, Michael; McAlonis-Downes, Melissa; Berezovski, Eugene; Zhang, Yong-Jie; Berry, James; Wainger, Brian J; Kankel, Mark W; Rushe, Mia; Hock, Christoph; Nitsch, Roger M; Cleveland, Don W; Petrucelli, Leonard; Gendron, Tania F; Montrasio, Fabio; Grimm, Jan; Polymenidou, Magdalini; Lagier-Tourenne, Clotilde

Premature polyadenylation-mediated loss of stathmin-2 is a hallmark of TDP-43-dependent neurodegeneration

过早多聚腺苷酸化介导的 stathmin-2 丢失是 TDP-43 依赖性神经退行性疾病的标志

Ze'ev Melamed, Jone López-Erauskin, Michael W Baughn, Ouyang Zhang, Kevin Drenner, Ying Sun, Fernande Freyermuth, Moira A McMahon, Melinda S Beccari, Jon W Artates, Takuya Ohkubo, Maria Rodriguez, Nianwei Lin, Dongmei Wu, C Frank Bennett, Frank Rigo, Sandrine Da Cruz, John Ravits, Clotilde Lagier-To

Diagonal nematicity in the pseudogap phase of HgBa(2)CuO(4+δ)

HgBa(2)CuO(4+δ)赝能隙相中的对角向列性

Murayama, H; Sato, Y; Kurihara, R; Kasahara, S; Mizukami, Y; Kasahara, Y; Uchiyama, H; Yamamoto, A; Moon, E-G; Cai, J; Freyermuth, J; Greven, M; Shibauchi, T; Matsuda, Y

Nuclear-Import Receptors Reverse Aberrant Phase Transitions of RNA-Binding Proteins with Prion-like Domains

核输入受体逆转具有朊病毒样结构域的 RNA 结合蛋白的异常相变

Lin Guo, Hong Joo Kim, Hejia Wang, John Monaghan, Fernande Freyermuth, Julie C Sung, Kevin O'Donovan, Charlotte M Fare, Zamia Diaz, Nikita Singh, Zi Chao Zhang, Maura Coughlin, Elizabeth A Sweeny, Morgan E DeSantis, Meredith E Jackrel, Christopher B Rodell, Jason A Burdick, Oliver D King, Aaron D Gi

Rational design of silicon structures for optically controlled multiscale biointerfaces

光控多尺度生物界面硅结构的合理设计

Yuanwen Jiang, Xiaojian Li, Bing Liu, Jaeseok Yi, Yin Fang, Fengyuan Shi, Xiang Gao, Edward Sudzilovsky, Ramya Parameswaran, Kelliann Koehler, Vishnu Nair, Jiping Yue, KuangHua Guo, Yin Fang, Hsiu-Ming Tsai, George Freyermuth, Raymond C S Wong, Chien-Min Kao, Chin-Tu Chen, Alan W Nicholls, Xiaoyang

rbFOX1/MBNL1 competition for CCUG RNA repeats binding contributes to myotonic dystrophy type 1/type 2 differences

rbFOX1/MBNL1 竞争 CCUG RNA 重复序列结合导致 1 型/2 型强直性肌营养不良症的差异

Chantal Sellier, Estefanía Cerro-Herreros, Markus Blatter, Fernande Freyermuth, Angeline Gaucherot, Frank Ruffenach, Partha Sarkar, Jack Puymirat, Bjarne Udd, John W Day, Giovanni Meola, Guillaume Bassez, Harutoshi Fujimura, Masanori P Takahashi, Benedikt Schoser, Denis Furling, Ruben Artero, Frédér

CUG initiation and frameshifting enable production of dipeptide repeat proteins from ALS/FTD C9ORF72 transcripts

CUG 启动和移码使 ALS/FTD C9ORF72 转录本能够产生二肽重复蛋白

Ricardos Tabet, Laure Schaeffer, Fernande Freyermuth, Melanie Jambeau, Michael Workman, Chao-Zong Lee, Chun-Chia Lin, Jie Jiang, Karen Jansen-West, Hussein Abou-Hamdan, Laurent Désaubry, Tania Gendron, Leonard Petrucelli, Franck Martin, Clotilde Lagier-Tourenne

Novel autosomal dominant TNNT1 mutation causing nemaline myopathy

导致线粒体肌病的新型常染色体显性 TNNT1 突变

Chamindra G Konersman, Fernande Freyermuth, Thomas L Winder, Michael W Lawlor, Clotilde Lagier-Tourenne, Shailendra B Patel

Splicing misregulation of SCN5A contributes to cardiac-conduction delay and heart arrhythmia in myotonic dystrophy

SCN5A 剪接失调导致强直性肌营养不良症患者的心脏传导延迟和心律失常

Fernande Freyermuth, Frédérique Rau, Yosuke Kokunai, Thomas Linke, Chantal Sellier, Masayuki Nakamori, Yoshihiro Kino, Ludovic Arandel, Arnaud Jollet, Christelle Thibault, Muriel Philipps, Serge Vicaire, Bernard Jost, Bjarne Udd, John W Day, Denis Duboc, Karim Wahbi, Tsuyoshi Matsumura, Harutoshi Fu