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Journal Abstract Search

114 related items for PubMed ID: 33640796

  • 1. Characterisation of the structural, dynamic and aggregation properties of the W64R amyloidogenic variant of human lysozyme.
    Vettore N, Moray J, Brans A, Herman R, Charlier P, Kumita JR, Kerff F, Dobson CM, Dumoulin M.
    Biophys Chem; 2021 Apr; 271():106563. PubMed ID: 33640796
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  • 2. Reduced global cooperativity is a common feature underlying the amyloidogenicity of pathogenic lysozyme mutations.
    Dumoulin M, Canet D, Last AM, Pardon E, Archer DB, Muyldermans S, Wyns L, Matagne A, Robinson CV, Redfield C, Dobson CM.
    J Mol Biol; 2005 Feb 25; 346(3):773-88. PubMed ID: 15713462
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  • 4. A non-natural variant of human lysozyme (I59T) mimics the in vitro behaviour of the I56T variant that is responsible for a form of familial amyloidosis.
    Hagan CL, Johnson RJ, Dhulesia A, Dumoulin M, Dumont J, De Genst E, Christodoulou J, Robinson CV, Dobson CM, Kumita JR.
    Protein Eng Des Sel; 2010 Jul 25; 23(7):499-506. PubMed ID: 20382744
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  • 6. Rationalising lysozyme amyloidosis: insights from the structure and solution dynamics of T70N lysozyme.
    Johnson RJ, Christodoulou J, Dumoulin M, Caddy GL, Alcocer MJ, Murtagh GJ, Kumita JR, Larsson G, Robinson CV, Archer DB, Luisi B, Dobson CM.
    J Mol Biol; 2005 Sep 30; 352(4):823-36. PubMed ID: 16126226
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  • 11. Engineering a camelid antibody fragment that binds to the active site of human lysozyme and inhibits its conversion into amyloid fibrils.
    Chan PH, Pardon E, Menzer L, De Genst E, Kumita JR, Christodoulou J, Saerens D, Brans A, Bouillenne F, Archer DB, Robinson CV, Muyldermans S, Matagne A, Redfield C, Wyns L, Dobson CM, Dumoulin M.
    Biochemistry; 2008 Oct 21; 47(42):11041-54. PubMed ID: 18816062
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  • 12. Formation of amyloid aggregates from human lysozyme and its disease-associated variants using hydrostatic pressure.
    De Felice FG, Vieira MN, Meirelles MN, Morozova-Roche LA, Dobson CM, Ferreira ST.
    FASEB J; 2004 Jul 21; 18(10):1099-101. PubMed ID: 15155566
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  • 15. Amyloid fibril formation and seeding by wild-type human lysozyme and its disease-related mutational variants.
    Morozova-Roche LA, Zurdo J, Spencer A, Noppe W, Receveur V, Archer DB, Joniau M, Dobson CM.
    J Struct Biol; 2000 Jun 21; 130(2-3):339-51. PubMed ID: 10940237
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  • 16. Local cooperativity in an amyloidogenic state of human lysozyme observed at atomic resolution.
    Dhulesia A, Cremades N, Kumita JR, Hsu ST, Mossuto MF, Dumoulin M, Nietlispach D, Akke M, Salvatella X, Dobson CM.
    J Am Chem Soc; 2010 Nov 10; 132(44):15580-8. PubMed ID: 20958028
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  • 17. Mechanistic studies of the folding of human lysozyme and the origin of amyloidogenic behavior in its disease-related variants.
    Canet D, Sunde M, Last AM, Miranker A, Spencer A, Robinson CV, Dobson CM.
    Biochemistry; 1999 May 18; 38(20):6419-27. PubMed ID: 10350460
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  • 18. Local cooperativity in the unfolding of an amyloidogenic variant of human lysozyme.
    Canet D, Last AM, Tito P, Sunde M, Spencer A, Archer DB, Redfield C, Robinson CV, Dobson CM.
    Nat Struct Biol; 2002 Apr 18; 9(4):308-15. PubMed ID: 11887182
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  • 19. Instability, unfolding and aggregation of human lysozyme variants underlying amyloid fibrillogenesis.
    Booth DR, Sunde M, Bellotti V, Robinson CV, Hutchinson WL, Fraser PE, Hawkins PN, Dobson CM, Radford SE, Blake CC, Pepys MB.
    Nature; 1997 Feb 27; 385(6619):787-93. PubMed ID: 9039909
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  • 20. A highly amyloidogenic region of hen lysozyme.
    Frare E, Polverino De Laureto P, Zurdo J, Dobson CM, Fontana A.
    J Mol Biol; 2004 Jul 23; 340(5):1153-65. PubMed ID: 15236974
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