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Charlotte M. Dobson, Ph.D. - Publications

Affiliations: 
2004 University of Calgary, Calgary, Alberta, Canada 
Area:
Molecular Biology, Animal Physiology Biology, Pathology
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23 high-probability publications. We are testing a new system for linking publications to authors. You can help! If you notice any inaccuracies, please sign in and mark papers as correct or incorrect matches. If you identify any major omissions or other inaccuracies in the publication list, please let us know.

Year Citation  Score
2021 Vettore N, Moray J, Brans A, Herman R, Charlier P, Kumita JR, Kerff F, Dobson CM, Dumoulin M. Characterisation of the structural, dynamic and aggregation properties of the W64R amyloidogenic variant of human lysozyme. Biophysical Chemistry. 271: 106563. PMID 33640796 DOI: 10.1016/j.bpc.2021.106563  0.336
2020 Ruggeri FS, Flagmeier P, Kumita JR, Meisl G, Chirgadze DY, Bongiovanni MN, Knowles TPJ, Dobson CM. The Influence of Pathogenic Mutations in α-Synuclein on Biophysical and Structural Characteristics of Amyloid Fibrils. Acs Nano. PMID 32159944 DOI: 10.1021/Acsnano.9B09676  0.304
2016 Ahn M, Hagan CL, Bernardo-Gancedo A, De Genst E, Newby FN, Christodoulou J, Dhulesia A, Dumoulin M, Robinson CV, Dobson CM, Kumita JR. The Significance of the Location of Mutations for the Native-State Dynamics of Human Lysozyme. Biophysical Journal. 111: 2358-2367. PMID 27926837 DOI: 10.1016/J.Bpj.2016.10.028  0.324
2011 Raimondi S, Guglielmi F, Giorgetti S, Di Gaetano S, Arciello A, Monti DM, Relini A, Nichino D, Doglia SM, Natalello A, Pucci P, Mangione P, Obici L, Merlini G, Stoppini M, ... ... Dobson CM, et al. Effects of the known pathogenic mutations on the aggregation pathway of the amyloidogenic peptide of apolipoprotein A-I. Journal of Molecular Biology. 407: 465-76. PMID 21296086 DOI: 10.1016/J.Jmb.2011.01.044  0.319
2009 Froese DS, Dobson CM, White AP, Wu X, Padovani D, Banerjee R, Haller T, Gerlt JA, Surette MG, Gravel RA. Sleeping beauty mutase (sbm) is expressed and interacts with ygfd in Escherichia coli Microbiological Research. 164: 1-8. PMID 18950999 DOI: 10.1016/J.Micres.2008.08.006  0.655
2008 Calamai M, Tartaglia GG, Vendruscolo M, Chiti F, Dobson CM. Mutational analysis of the aggregation-prone and disaggregation-prone regions of acylphosphatase. Journal of Molecular Biology. 387: 965-74. PMID 18809411 DOI: 10.1016/J.Jmb.2008.09.003  0.305
2006 Dobson CM, Gradinger A, Longo N, Wu X, Leclerc D, Lerner-Ellis J, Lemieux M, Belair C, Watkins D, Rosenblatt DS, Gravel RA. Homozygous nonsense mutation in the MCEE gene and siRNA suppression of methylmalonyl-CoA epimerase expression: a novel cause of mild methylmalonic aciduria. Molecular Genetics and Metabolism. 88: 327-33. PMID 16697227 DOI: 10.1016/j.ymgme.2006.03.009  0.709
2006 Kumita JR, Johnson RJ, Alcocer MJ, Dumoulin M, Holmqvist F, McCammon MG, Robinson CV, Archer DB, Dobson CM. Impact of the native-state stability of human lysozyme variants on protein secretion by Pichia pastoris. The Febs Journal. 273: 711-20. PMID 16441658 DOI: 10.1111/J.1742-4658.2005.05099.X  0.325
2006 Zhang J, Dobson CM, Wu X, Lerner-Ellis J, Rosenblatt DS, Gravel RA. Impact of cblB mutations on the function of ATP:cob(I)alamin adenosyltransferase in disorders of vitamin B12 metabolism. Molecular Genetics and Metabolism. 87: 315-22. PMID 16439175 DOI: 10.1016/j.ymgme.2005.12.003  0.716
2006 Lerner-Ellis JP, Gradinger AB, Watkins D, Tirone JC, Villeneuve A, Dobson CM, Montpetit A, Lepage P, Gravel RA, Rosenblatt DS. Mutation and biochemical analysis of patients belonging to the cblB complementation class of vitamin B12-dependent methylmalonic aciduria. Molecular Genetics and Metabolism. 87: 219-25. PMID 16410054 DOI: 10.1016/J.Ymgme.2005.11.011  0.705
2006 Lerner-Ellis JP, Tirone JC, Pawelek PD, Doré C, Atkinson JL, Watkins D, Morel CF, Fujiwara TM, Moras E, Hosack AR, Dunbar GV, Antonicka H, Forgetta V, Dobson CM, Leclerc D, et al. Identification of the gene responsible for methylmalonic aciduria and homocystinuria, cblC type. Nature Genetics. 38: 93-100. PMID 16311595 DOI: 10.1038/Ng1683  0.696
2005 Dumoulin M, Canet D, Last AM, Pardon E, Archer DB, Muyldermans S, Wyns L, Matagne A, Robinson CV, Redfield C, Dobson CM. Reduced global cooperativity is a common feature underlying the amyloidogenicity of pathogenic lysozyme mutations. Journal of Molecular Biology. 346: 773-88. PMID 15713462 DOI: 10.1016/J.Jmb.2004.11.020  0.352
2004 Calloni G, Zoffoli S, Stefani M, Dobson CM, Chiti F. Investigating the effects of mutations on protein aggregation in the cell. The Journal of Biological Chemistry. 280: 10607-13. PMID 15611128 DOI: 10.1074/Jbc.M412951200  0.355
2004 Lerner-Ellis JP, Dobson CM, Wai T, Watkins D, Tirone JC, Leclerc D, Doré C, Lepage P, Gravel RA, Rosenblatt DS. Mutations in the MMAA gene in patients with the cblA disorder of vitamin B12 metabolism. Human Mutation. 24: 509-16. PMID 15523652 DOI: 10.1002/humu.20104  0.705
2003 Chiti F, Stefani M, Taddei N, Ramponi G, Dobson CM. Rationalization of the effects of mutations on peptide and protein aggregation rates. Nature. 424: 805-8. PMID 12917692 DOI: 10.1038/Nature01891  0.318
2003 Dumoulin M, Last AM, Desmyter A, Decanniere K, Canet D, Larsson G, Spencer A, Archer DB, Sasse J, Muyldermans S, Wyns L, Redfield C, Matagne A, Robinson CV, Dobson CM. A camelid antibody fragment inhibits the formation of amyloid fibrils by human lysozyme. Nature. 424: 783-8. PMID 12917687 DOI: 10.1038/Nature01870  0.345
2002 Dobson CM, Wai T, Leclerc D, Kadir H, Narang M, Lerner-Ellis JP, Hudson TJ, Rosenblatt DS, Gravel RA. Identification of the gene responsible for the cblB complementation group of vitamin B12-dependent methylmalonic aciduria. Human Molecular Genetics. 11: 3361-9. PMID 12471062 DOI: 10.1093/hmg/11.26.3361  0.72
2002 Dobson CM, Wai T, Leclerc D, Wilson A, Wu X, Doré C, Hudson T, Rosenblatt DS, Gravel RA. Identification of the gene responsible for the cblA complementation group of vitamin B12-responsive methylmalonic acidemia based on analysis of prokaryotic gene arrangements. Proceedings of the National Academy of Sciences of the United States of America. 99: 15554-9. PMID 12438653 DOI: 10.1073/Pnas.242614799  0.706
2002 Sandilands A, Hutcheson AM, Long HA, Prescott AR, Vrensen G, Löster J, Klopp N, Lutz RB, Graw J, Masaki S, Dobson CM, MacPhee CE, Quinlan RA. Altered aggregation properties of mutant gamma-crystallins cause inherited cataract. The Embo Journal. 21: 6005-14. PMID 12426373 DOI: 10.1093/Emboj/Cdf609  0.302
2002 Chiti F, Calamai M, Taddei N, Stefani M, Ramponi G, Dobson CM. Studies of the aggregation of mutant proteins in vitro provide insights into the genetics of amyloid diseases. Proceedings of the National Academy of Sciences of the United States of America. 16419-26. PMID 12374855 DOI: 10.1073/Pnas.212527999  0.323
2002 Chiti F, Taddei N, Baroni F, Capanni C, Stefani M, Ramponi G, Dobson CM. Kinetic partitioning of protein folding and aggregation. Nature Structural Biology. 9: 137-43. PMID 11799398 DOI: 10.1038/Nsb752  0.319
2002 Chamberlain AK, Receveur V, Spencer A, Redfield C, Dobson CM. Characterization of the structure and dynamics of amyloidogenic variants of human lysozyme by NMR spectroscopy. Protein Science : a Publication of the Protein Society. 10: 2525-30. PMID 11714920 DOI: 10.1110/Ps.28101  0.303
2000 Taddei N, Chiti F, Fiaschi T, Bucciantini M, Capanni C, Stefani M, Serrano L, Dobson CM, Ramponi G. Stabilisation of alpha-helices by site-directed mutagenesis reveals the importance of secondary structure in the transition state for acylphosphatase folding. Journal of Molecular Biology. 300: 633-47. PMID 10884358 DOI: 10.1006/Jmbi.2000.3870  0.319
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