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Fernande Freyermuth
Fernande Freyermuth
Massachusetts General Hospital/ Harvard Medical School
在 mgh.harvard.edu 的电子邮件经过验证
标题
引用次数
引用次数
年份
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
4572019
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
4422018
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
3252011
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
2572013
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
1892016
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
1522018
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
682018
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
342014
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
302017
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
2022
Nuclear-import receptors reverse aberrant phase transitions of disease-linked RNA-binding proteins with prion-like domains.
L Guo, H Kim, H Wang, J Monaghan, F Freyermuth, JC Sung, ...
MOLECULAR BIOLOGY OF THE CELL 29 (26), 2018
2018
Etude des bases moléculaires à l'origine des troubles cardiaques des patients atteints de dystrophies myotoniques
F Freyermuth
Université de Strasbourg, 2013
2013
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