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Nature Communications|May 14, 2024
Quantifying 3'UTR length from scRNA-seq data reveals changes independent of gene expressionMervin M Fansler, Sibylle Mitschka, Christine Mayr
Methods in Enzymology|June 29, 2021
Generation of 3'UTR knockout cell lines by CRISPR/Cas9-mediated genome editingSibylle Mitschka, Mervin M Fansler, Christine Mayr
Cell|August 6, 2024
The FXR1 network acts as a signaling scaffold for actomyosin remodelingXiuzhen Chen, Mervin M Fansler, Urška Janjoš, et al.
Biorxiv : the Preprint Server for Biology|November 14, 2023
The FXR1 network acts as signaling scaffold for actomyosin remodelingXiuzhen Chen, Mervin M Fansler, Urška Janjoš, et al.
Nature Communications|May 17, 2022
Enhancers regulate 3' end processing activity to control expression of alternative 3'UTR isoformsBuki Kwon, Mervin M Fansler, Neil D Patel, et al.
Molecular Cell|December 22, 2023
Subcytoplasmic location of translation controls protein outputEllen L Horste, Mervin M Fansler, Ting Cai, et al.
RNA (New York, N.Y.)|October 10, 2023
Extensible benchmarking of methods that identify and quantify polyadenylation sites from RNA-seq dataSam Bryce-Smith, Dominik Burri, Matthew R Gazzara, et al.
Biorxiv : the Preprint Server for Biology|July 10, 2023
Extensible benchmarking of methods that identify and quantify polyadenylation sites from RNA-seq dataSam Bryce-Smith, Dominik Burri, Matthew R Gazzara, et al.
Nature Communications|October 12, 2018
Two high-risk susceptibility loci at 6p25.3 and 14q32.13 for Waldenström macroglobulinemiaMary L McMaster, Sonja I Berndt, Jianqing Zhang, et al.
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