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Rasmus Hartmann-Petersen

Showing results (81-90 of 95) with videos related to

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Science Advances|February 6, 2026
A near-complete map of human cytosolic degrons and their relevance for diseaseVasileios Voutsinos, Kristoffer E Johansson, Fia B Larsen, et al.
Biomolecules|October 27, 2022
Deciphering the Alphabet of Disorder-Glu and Asp Act Differently on Local but Not Global PropertiesMette Ahrensback Roesgaard, Jeppe E Lundsgaard, Estella A Newcombe, et al.
European Journal of Medical Genetics|August 27, 2019
Novel HARS2 missense variants identified in individuals with sensorineural hearing impairment and Perrault syndromeHelena Gásdal Karstensen, Nanna Dahl Rendtorff, Lone Sandbjerg Hindbæk, et al.
Molecular Cell|October 14, 2014
Dss1 is a 26S proteasome ubiquitin receptorKonstantinos Paraskevopoulos, Franziska Kriegenburg, Michael H Tatham, et al.
Structure (London, England : 1993)|December 20, 2024
Systematic characterization of indel variants using a yeast-based protein folding sensorSven Larsen-Ledet, Søren Lindemose, Aleksandra Panfilova, et al.
Cellular and Molecular Life Sciences : CMLS|January 7, 2023
HSP70-binding motifs function as protein quality control degronsAmanda B Abildgaard, Vasileios Voutsinos, Søren D Petersen, et al.
Biochemistry|September 20, 2018
Random Mutagenesis Analysis of the Influenza A M2 Proton Channel Reveals Novel Resistance MutantsPaul Santner, João Miguel da Silva Martins, Caroline Kampmeyer, et al.
BMC Cell Biology|August 1, 2014
Human ASPL/TUG interacts with p97 and complements the proteasome mislocalization of a yeast ubx4 mutant, but not the ER-associated degradation defectLouise Madsen, Karen Molbæk, Ida B Larsen, et al.
Elife|November 8, 2019
Computational and cellular studies reveal structural destabilization and degradation of MLH1 variants in Lynch syndromeAmanda B Abildgaard, Amelie Stein, Sofie V Nielsen, et al.
Nature Communications|May 13, 2024
Deep mutational scanning reveals a correlation between degradation and toxicity of thousands of aspartoacylase variantsMartin Grønbæk-Thygesen, Vasileios Voutsinos, Kristoffer E Johansson, et al.
Pageof 10

Showing results (81-90 of 95) with videos related to

Sort By:
Pageof 10
Science Advances|February 6, 2026
A near-complete map of human cytosolic degrons and their relevance for diseaseVasileios Voutsinos, Kristoffer E Johansson, Fia B Larsen, et al.
Biomolecules|October 27, 2022
Deciphering the Alphabet of Disorder-Glu and Asp Act Differently on Local but Not Global PropertiesMette Ahrensback Roesgaard, Jeppe E Lundsgaard, Estella A Newcombe, et al.
European Journal of Medical Genetics|August 27, 2019
Novel HARS2 missense variants identified in individuals with sensorineural hearing impairment and Perrault syndromeHelena Gásdal Karstensen, Nanna Dahl Rendtorff, Lone Sandbjerg Hindbæk, et al.
Molecular Cell|October 14, 2014
Dss1 is a 26S proteasome ubiquitin receptorKonstantinos Paraskevopoulos, Franziska Kriegenburg, Michael H Tatham, et al.
Structure (London, England : 1993)|December 20, 2024
Systematic characterization of indel variants using a yeast-based protein folding sensorSven Larsen-Ledet, Søren Lindemose, Aleksandra Panfilova, et al.
Cellular and Molecular Life Sciences : CMLS|January 7, 2023
HSP70-binding motifs function as protein quality control degronsAmanda B Abildgaard, Vasileios Voutsinos, Søren D Petersen, et al.
Biochemistry|September 20, 2018
Random Mutagenesis Analysis of the Influenza A M2 Proton Channel Reveals Novel Resistance MutantsPaul Santner, João Miguel da Silva Martins, Caroline Kampmeyer, et al.
BMC Cell Biology|August 1, 2014
Human ASPL/TUG interacts with p97 and complements the proteasome mislocalization of a yeast ubx4 mutant, but not the ER-associated degradation defectLouise Madsen, Karen Molbæk, Ida B Larsen, et al.
Elife|November 8, 2019
Computational and cellular studies reveal structural destabilization and degradation of MLH1 variants in Lynch syndromeAmanda B Abildgaard, Amelie Stein, Sofie V Nielsen, et al.
Nature Communications|May 13, 2024
Deep mutational scanning reveals a correlation between degradation and toxicity of thousands of aspartoacylase variantsMartin Grønbæk-Thygesen, Vasileios Voutsinos, Kristoffer E Johansson, et al.
Pageof 10