Multiplexed assays reveal effects of missense variants in MSH2 and cancer predisposition von Nielsen, Sofie V, Hartmann-Petersen, Rasmus, Stein, Amelie, Lindorff-Larsen, Kresten

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Molecular Basis and Regulation of OTULIN-LUBAC Interaction von Elliott, Paul R., Nielsen, Sofie V., Marco-Casanova, Paola, Fiil, Berthe Katrine, Keusekotten, Kirstin, Mailand, Niels, Freund, Stefan M.V., Gyrd-Hansen, Mads, Komander, David

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Folliculin variants linked to Birt-Hogg-Dubé syndrome are targeted for proteasomal degradation von Clausen, Lene, Stein, Amelie, Grønbæk-Thygesen, Martin, Nygaard, Lasse, Søltoft, Cecilie L, Nielsen, Sofie V, Lisby, Michael, Ravid, Tommer, Lindorff-Larsen, Kresten, Hartmann-Petersen, Rasmus

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Predicting the impact of Lynch syndrome-causing missense mutations from structural calculations von Nielsen, Sofie V, Stein, Amelie, Dinitzen, Alexander B, Papaleo, Elena, Tatham, Michael H, Poulsen, Esben G, Kassem, Maher M, Rasmussen, Lene J, Lindorff-Larsen, Kresten, Hartmann-Petersen, Rasmus

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Computational and cellular studies reveal structural destabilization and degradation of MLH1 variants in Lynch syndrome von Abildgaard, Amanda B, Stein, Amelie, Nielsen, Sofie V, Schultz-Knudsen, Katrine, Papaleo, Elena, Shrikhande, Amruta, Hoffmann, Eva R, Bernstein, Inge, Gerdes, Anne-Marie, Takahashi, Masanobu, Ishioka, Chikashi, Lindorff-Larsen, Kresten, Hartmann-Petersen, Rasmus

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Co-Chaperones in Targeting and Delivery of Misfolded Proteins to the 26S Proteasome von Abildgaard, Amanda B, Gersing, Sarah K, Larsen-Ledet, Sven, Nielsen, Sofie V, Stein, Amelie, Lindorff-Larsen, Kresten, Hartmann-Petersen, Rasmus

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Understanding the Origins of Loss of Protein Function by Analyzing the Effects of Thousands of Variants on Activity and Abundance von Cagiada, Matteo, Johansson, Kristoffer E, Valanciute, Audrone, Nielsen, Sofie V, Hartmann-Petersen, Rasmus, Yang, Jun J, Fowler, Douglas M, Stein, Amelie, Lindorff-Larsen, Kresten

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Lynch syndrome, molecular mechanisms and variant classification von Abildgaard, Amanda B., Nielsen, Sofie V., Bernstein, Inge, Stein, Amelie, Lindorff-Larsen, Kresten, Hartmann-Petersen, Rasmus

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Bioinformatics analysis identifies several intrinsically disordered human E3 ubiquitin-protein ligases von Boomsma, Wouter, Nielsen, Sofie V, Lindorff-Larsen, Kresten, Hartmann-Petersen, Rasmus, Ellgaard, Lars

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Protein quality control in the nucleus von Nielsen, Sofie V, Poulsen, Esben G, Rebula, Caio A, Hartmann-Petersen, Rasmus

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Systematic characterization of indel variants using a yeast-based protein folding sensor von Larsen-Ledet, Sven, Lindemose, Søren, Panfilova, Aleksandra, Gersing, Sarah, Suhr, Caroline H., Genzor, Aitana Victoria, Lanters, Heleen, Nielsen, Sofie V., Lindorff-Larsen, Kresten, Winther, Jakob R., Stein, Amelie, Hartmann-Petersen, Rasmus

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Disease-linked mutations cause exposure of a protein quality control degron von Kampmeyer, Caroline, Larsen-Ledet, Sven, Wagnkilde, Morten Rose, Michelsen, Mathias, Iversen, Henriette K.M., Nielsen, Sofie V., Lindemose, Søren, Caregnato, Alberto, Ravid, Tommer, Stein, Amelie, Teilum, Kaare, Lindorff-Larsen, Kresten, Hartmann-Petersen, Rasmus

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Toward mechanistic models for genotype–phenotype correlations in phenylketonuria using protein stability calculations von Scheller, Rasmus, Stein, Amelie, Nielsen, Sofie V., Marin, Frederikke I., Gerdes, Anne‐Marie, Marco, Miriam, Papaleo, Elena, Lindorff‐Larsen, Kresten, Hartmann‐Petersen, Rasmus

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Blocking protein quality control to counter hereditary cancers von Kampmeyer, Caroline, Nielsen, Sofie V., Clausen, Lene, Stein, Amelie, Gerdes, Anne‐Marie, Lindorff‐Larsen, Kresten, Hartmann‐Petersen, Rasmus

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High-Throughput siRNA Screening Applied to the Ubiquitin–Proteasome System von Poulsen, Esben G., Nielsen, Sofie V., Pietras, Elin J., Johansen, Jens V., Steinhauer, Cornelia, Hartmann-Petersen, Rasmus

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Human ASPL/TUG interacts with p97 and complements the proteasome mislocalization of a yeast ubx4 mutant, but not the ER-associated degradation defect von Madsen, Louise, Molbæk, Karen, Larsen, Ida B, Nielsen, Sofie V, Poulsen, Esben G, Walmod, Peter S, Hofmann, Kay, Seeger, Michael, Chien, Chen-Ying, Chen, Rey-Huei, Kriegenburg, Franziska, Hartmann-Petersen, Rasmus

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Multiplexed assays reveal effects of missense variants in MSH2 and cancer predisposition von Nielsen, Sofie V, Hartmann-Petersen, Rasmus, Stein, Amelie, Lindorff-Larsen, Kresten

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Multiplexed assays reveal effects of missense variants in MSH2 and cancer predisposition von Nielsen, Sofie V, Hartmann-Petersen, Rasmus, Stein, Amelie, Lindorff-Larsen, Kresten

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Multiplexed assays reveal effects of missense variants in MSH2 and cancer predisposition von Nielsen, Sofie V, Hartmann-Petersen, Rasmus, Stein, Amelie, Lindorff-Larsen, Kresten

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Multiplexed assays reveal effects of missense variants in MSH2 and cancer predisposition von Nielsen, Sofie V, Hartmann-Petersen, Rasmus, Stein, Amelie, Lindorff-Larsen, Kresten

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