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Lina Worpenberg

Showing results (1-10 of 11) with videos related to

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Genome Biology|September 27, 2025
Codon-specific ribosome stalling reshapes translational dynamics during branched-chain amino acid starvationLina Worpenberg, Cédric Gobet, Felix Naef
Bioessays : News and Reviews in Molecular, Cellular and Developmental Biology|December 7, 2021
Functional interplay within the epitranscriptome: Reality or fiction?Lina Worpenberg, Chiara Paolantoni, Jean-Yves Roignant
Biochimica Et Biophysica Acta. Gene Regulatory Mechanisms|November 6, 2018
Mechanistic insights into m<sup>6</sup>A RNA enzymesTina Lence, Chiara Paolantoni, Lina Worpenberg, et al.
Methods in Molecular Biology (Clifton, N.J.)|December 13, 2018
Identification of Methylated Transcripts Using the TRIBE ApproachLina Worpenberg, Tobias Jakobi, Christoph Dieterich, et al.
Communications Biology|November 26, 2025
Conditional deep learning model reveals translation elongation determinants during amino acid deprivationMohan Vamsi Nallapareddy, Francesco Craighero, Lina Worpenberg, et al.
Frontiers in Bioengineering and Biotechnology|May 1, 2018
The Emerging Field of Epitranscriptomics in Neurodevelopmental and Neuronal DisordersMargarita T Angelova, Dilyana G Dimitrova, Nadja Dinges, et al.
Plos One|November 13, 2018
Differential regulation of actin-activated nucleotidyl cyclase virulence factors by filamentous and globular actinDorothée Raoux-Barbot, Alexander Belyy, Lina Worpenberg, et al.
Nature Communications|December 6, 2016
Actin activates Pseudomonas aeruginosa ExoY nucleotidyl cyclase toxin and ExoY-like effector domains from MARTX toxinsAlexander Belyy, Dorothée Raoux-Barbot, Cosmin Saveanu, et al.
Neuroendocrinology|September 15, 2017
Mechanisms of Targeting the MDM2-p53-FOXM1 Axis in Well-Differentiated Intestinal Neuroendocrine TumorsFranziska Briest, Irina Grass, Dagmar Sedding, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|May 25, 2023
Biallelic variants in NSUN6 cause an autosomal recessive neurodevelopmental disorderFrancesca Mattioli, Lina Worpenberg, Cai-Tao Li, et al.
Pageof 2

Showing results (1-10 of 11) with videos related to

Sort By:
Pageof 2
Genome Biology|September 27, 2025
Codon-specific ribosome stalling reshapes translational dynamics during branched-chain amino acid starvationLina Worpenberg, Cédric Gobet, Felix Naef
Bioessays : News and Reviews in Molecular, Cellular and Developmental Biology|December 7, 2021
Functional interplay within the epitranscriptome: Reality or fiction?Lina Worpenberg, Chiara Paolantoni, Jean-Yves Roignant
Biochimica Et Biophysica Acta. Gene Regulatory Mechanisms|November 6, 2018
Mechanistic insights into m<sup>6</sup>A RNA enzymesTina Lence, Chiara Paolantoni, Lina Worpenberg, et al.
Methods in Molecular Biology (Clifton, N.J.)|December 13, 2018
Identification of Methylated Transcripts Using the TRIBE ApproachLina Worpenberg, Tobias Jakobi, Christoph Dieterich, et al.
Communications Biology|November 26, 2025
Conditional deep learning model reveals translation elongation determinants during amino acid deprivationMohan Vamsi Nallapareddy, Francesco Craighero, Lina Worpenberg, et al.
Frontiers in Bioengineering and Biotechnology|May 1, 2018
The Emerging Field of Epitranscriptomics in Neurodevelopmental and Neuronal DisordersMargarita T Angelova, Dilyana G Dimitrova, Nadja Dinges, et al.
Plos One|November 13, 2018
Differential regulation of actin-activated nucleotidyl cyclase virulence factors by filamentous and globular actinDorothée Raoux-Barbot, Alexander Belyy, Lina Worpenberg, et al.
Nature Communications|December 6, 2016
Actin activates Pseudomonas aeruginosa ExoY nucleotidyl cyclase toxin and ExoY-like effector domains from MARTX toxinsAlexander Belyy, Dorothée Raoux-Barbot, Cosmin Saveanu, et al.
Neuroendocrinology|September 15, 2017
Mechanisms of Targeting the MDM2-p53-FOXM1 Axis in Well-Differentiated Intestinal Neuroendocrine TumorsFranziska Briest, Irina Grass, Dagmar Sedding, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|May 25, 2023
Biallelic variants in NSUN6 cause an autosomal recessive neurodevelopmental disorderFrancesca Mattioli, Lina Worpenberg, Cai-Tao Li, et al.
Pageof 2