受强制性开放获取政策约束的文章 - Fernande Freyermuth了解详情
可在其他位置公开访问的文章：10 篇
Premature polyadenylation-mediated loss of stathmin-2 is a hallmark of TDP-43-dependent neurodegeneration
Z Melamed, J López-Erauskin, MW Baughn, O Zhang, K Drenner, Y Sun, ...
Nature neuroscience 22 (2), 180-190, 2019
强制性开放获取政策： US National Institutes of Health, Human Frontier Science Program
Nuclear-import receptors reverse aberrant phase transitions of RNA-binding proteins with prion-like domains
L Guo, HJ Kim, H Wang, J Monaghan, F Freyermuth, JC Sung, ...
Cell 173 (3), 677-692. e20, 2018
强制性开放获取政策： US National Institutes of Health, Howard Hughes Medical Institute, American …
Misregulation of miR-1 processing is associated with heart defects in myotonic dystrophy
F Rau, F Freyermuth, C Fugier, JP Villemin, MC Fischer, B Jost, ...
Nature structural & molecular biology 18 (7), 840-845, 2011
强制性开放获取政策： US National Institutes of Health
Sequestration of DROSHA and DGCR8 by expanded CGG RNA repeats alters microRNA processing in fragile X-associated tremor/ataxia syndrome
C Sellier, F Freyermuth, R Tabet, T Tran, F He, F Ruffenach, V Alunni, ...
Cell reports 3 (3), 869-880, 2013
强制性开放获取政策： US National Institutes of Health
Splicing misregulation of SCN5A contributes to cardiac-conduction delay and heart arrhythmia in myotonic dystrophy
F Freyermuth, F Rau, Y Kokunai, T Linke, C Sellier, M Nakamori, Y Kino, ...
Nature communications 7 (1), 1-14, 2016
强制性开放获取政策： US National Institutes of Health, National Institute of Health and Medical …
CUG initiation and frameshifting enable production of dipeptide repeat proteins from ALS/FTD C9ORF72 transcripts
R Tabet, L Schaeffer, F Freyermuth, M Jambeau, M Workman, CZ Lee, ...
Nature communications 9 (1), 1-14, 2018
强制性开放获取政策： US National Institutes of Health
rbFOX1/MBNL1 competition for CCUG RNA repeats binding contributes to myotonic dystrophy type 1/type 2 differences
C Sellier, E Cerro-Herreros, M Blatter, F Freyermuth, A Gaucherot, ...
Nature communications 9 (1), 1-15, 2018
强制性开放获取政策： National Institute of Health and Medical Research, France, European Commission
Tau exon 2 responsive elements deregulated in myotonic dystrophy type I are proximal to exon 2 and synergistically regulated by MBNL1 and MBNL2
C Carpentier, D Ghanem, FJ Fernandez-Gomez, F Jumeau, JV Philippe, ...
Biochimica et Biophysica Acta (BBA)-Molecular Basis of Disease 1842 (4), 654-664, 2014
强制性开放获取政策： National Institute of Health and Medical Research, France
Novel autosomal dominant TNNT1 mutation causing nemaline myopathy
CG Konersman, F Freyermuth, TL Winder, MW Lawlor, ...
Molecular genetics & genomic medicine 5 (6), 678-691, 2017
强制性开放获取政策： US National Institutes of Health
Comprehensive preclinical evaluation of human-derived anti-poly-GA antibodies in cellular and animal models of C9ORF72 disease
M Jambeau, KD Meyer, M Hruska-Plochan, R Tabet, CZ Lee, A Ray-Soni, ...
bioRxiv, 2022
强制性开放获取政策： Swiss National Science Foundation, US National Institutes of Health
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