Biomedical Engineering Reference
In-Depth Information
30. Dyson HJ, Wright PE (2005) Intrinsically
unstructured proteins and their functions.
Nat Rev Mol Cell Biol 6:197-208
31. Surguchov A (2008) Molecular and cellular
biology of synucleins. Int Rev Cell Mol Biol
270:225-317
32. Uversky VN (2008) Alpha-synuclein misfold-
ing and neurodegenerative diseases. Curr
Protein Pept Sci 9:507-540
33. Bross P, Corydon TJ, Andresen BS, Jorgensen
MM, Bolund L, Gregersen N (1999) Protein
misfolding and degradation in genetic dis-
eases. Hum Mutat 14:186-198
34. Cooper DN, Ball EV, Krawczak M (1998)
The human gene mutation database. Nucleic
Acids Res 26:285-287
35. Carrell RW, Lomas DA (1997) Conformational
disease. Lancet 350:134-138
36. Beissinger M, Buchner J (1998) How chap-
erones fold proteins. Biol Chem 379:
245-259
37. Thomas PJ, Qu BH, Pedersen PL (1995)
Defective protein folding as a basis of human
disease. Trends Biochem Sci 20:456-459
38. Amaral MD (2004) CFTR and chaperones:
processing and degradation. J Mol Neurosci
23:41-48
39. Holliday R (1996) The current status of the
protein error theory of ageing. Exp Gerontol
31:449-452
40. Rattan SIS (2006) Theories of biological age-
ing: genes, proteins and free radicals. Free
Rad Res 40:1230-1238
41. Westermark P, Benson MD, Buxbaum JN,
Cohen AS, Frangione B, Ikeda S, Masters CL,
Merlini G, Saraiva MJ, Sipe JD (2005)
Amyloid: toward terminology clarification.
Report from the Nomenclature Committee of
the International Society of Amyloidosis.
Amyloid 12:1-4
42. Bucciantini M, Giannoni E, Chiti F, Baroni F,
Formigli L, Zurdo J, Taddei N, Ramponi G,
Dobson CM, Stefani M (2002) Inherent tox-
icity of aggregates implies a common mecha-
nism for protein misfolding diseases. Nature
416:507-511
43. Isaacs AM, Senn DB, Yuan M, Shine JP,
Yankner BA (2006) Acceleration of amyloid
beta-peptide aggregation by physiological
concentrations of calcium. J Biol Chem
281:27916-27923
44. Lansbury PT, Lashuel HA (2006) A century-old
debate on protein aggregation and neurodegen-
eration enters the clinic. Nature 443:774-779
45. Cohen E, Bieschke J, Perciavalle RM, Kelly
JW, Dillin A (2006) Opposing activities pro-
tect against age-onset proteotoxicity. Science
313:1604-1610
46. Malgaroli A, Vallar L, Zimarino V (2006)
Protein homeostasis in neurons and its patho-
logical alterations. Curr Opin Neurobiol
16:270-274
47. Rattan SIS (2008) Hormesis in ageing. Ageing
Res Rev 7:63-78
48. Maisonneuve E, Fraysse L, Moinier D, Dukan
S (2008) Existence of abnormal protein
aggregates in healthy Escherichia coli cells.
J Bacteriol 190:887-893
49. Maisonneuve E, Ezraty B, Dukan S (2008)
Protein aggregates: an ageing factor involved
in cell death. J Bacteriol 190:6070-6075
50. Caughey B, Lansbury PT (2003) Protofibrils,
pores, fibrils, and neurodegeneration: separat-
ing the responsible protein aggregates from
the innocent bystanders. Annu Rev Neurosci
26:267-298
51. Uversky VN (2003) A protein-chameleon: con-
formational plasticity of alpha-synuclein, a dis-
ordered protein involved in neurodegenerative
disorders. J Biomol Struct Dyn 21:211-234
Search WWH ::




Custom Search