Emanuela Kerschbamer

Publication Activity (10 Years)

Years Active: 2019-2023
Publications (10 Years): 4

Top Topics

Duchenne Muscular Dystrophy

Intellectual Disability

Top Venues

Nucleic acids research

This page only lists publications with an associated author ORCID identifier.

Publications

Dilara Ayyildiz, Guendalina Bergonzoni, Alan Monziani, Takshashila Tripathi, Jessica Döring, Emanuela Kerschbamer, Francesca Di Leva, Elia Pennati, Luisa Donini, Marina Kovalenko, Jacopo Zasso, Luciano Conti, Vanessa C Wheeler, Christoph Dieterich, Silvano Piazza, Erik Dassi, Marta Biagioli
CAG repeat expansion in the Huntington's disease gene shapes linear and circular RNAs biogenesis. PLoS genetics 19 (10) (2023)
Martina Minisini, Eros Di Giorgio, Emanuela Kerschbamer, Emiliano Dalla, Massimo Faggiani, Elisa Franforte, Franz-Josef Meyer-Almes, Rino Ragno, Lorenzo Antonini, Antonello Mai, Francesco Fiorentino, Dante Rotili, Monica Chinellato, Stefano Perin, Laura Cendron, Christian X Weichenberger, Alessandro Angelini, Claudio Brancolini
Transcriptomic and genomic studies classify NKL54 as a histone deacetylase inhibitor with indirect influence on MEF2-dependent transcription. Nucleic acids research 50 (5) (2022)
Aurora Irene Idilli, Francesca Pagani, Emanuela Kerschbamer, Francesco Berardinelli, Manuel Bernabé, Maria Luisa Cayuela, Silvano Piazza, Pietro Luigi Poliani, Emilio Cusanelli, Maria Caterina Mione
Changes in the Expression of Pre-Replicative Complex Genes in hTERT and ALT Pediatric Brain Tumors. Cancers 12 (4) (2020)
Vidya Murthy, Toma Tebaldi, Yeguang Hu, Serkan Erdin, Teresa Calzonetti, Ravi Vijayvargia, Takshashila Tripathi, Emanuela Kerschbamer, Ihn Sik Seong, Alessandro Quattrone, Michael E Talkowski, James F Gusella, Katia Georgopoulos, Marcy E MacDonald, Marta Biagioli
Hypomorphic mutation of the mouse Huntington's disease gene orthologue. PLoS genetics 15 (3) (2019)