BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

312 related articles for article (PubMed ID: 22444587)

  • 1. Protein misfolded oligomers: experimental approaches, mechanism of formation, and structure-toxicity relationships.
    Bemporad F; Chiti F
    Chem Biol; 2012 Mar; 19(3):315-27. PubMed ID: 22444587
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Oligomeric intermediates in amyloid formation: structure determination and mechanisms of toxicity.
    Fändrich M
    J Mol Biol; 2012 Aug; 421(4-5):427-40. PubMed ID: 22248587
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Common mechanisms of amyloid oligomer pathogenesis in degenerative disease.
    Glabe CG
    Neurobiol Aging; 2006 Apr; 27(4):570-5. PubMed ID: 16481071
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Structure of amyloid oligomers and their mechanisms of toxicities: Targeting amyloid oligomers using novel therapeutic approaches.
    Salahuddin P; Fatima MT; Abdelhameed AS; Nusrat S; Khan RH
    Eur J Med Chem; 2016 May; 114():41-58. PubMed ID: 26974374
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Structural properties and dynamic behavior of nonfibrillar oligomers formed by PrP(106-126).
    Walsh P; Neudecker P; Sharpe S
    J Am Chem Soc; 2010 Jun; 132(22):7684-95. PubMed ID: 20465257
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Generic cell dysfunction in neurodegenerative disorders: role of surfaces in early protein misfolding, aggregation, and aggregate cytotoxicity.
    Stefani M
    Neuroscientist; 2007 Oct; 13(5):519-31. PubMed ID: 17901260
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Preparation and characterization of neurotoxic tau oligomers.
    Lasagna-Reeves CA; Castillo-Carranza DL; Guerrero-Muoz MJ; Jackson GR; Kayed R
    Biochemistry; 2010 Nov; 49(47):10039-41. PubMed ID: 21047142
    [TBL] [Abstract][Full Text] [Related]  

  • 8. [Neurodegenerative conformational disease and its molecular bases].
    Li WW; Cai DF; Ren HM
    Sheng Li Ke Xue Jin Zhan; 2006 Apr; 37(2):97-102. PubMed ID: 16850610
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Protein-misfolding diseases and chaperone-based therapeutic approaches.
    Chaudhuri TK; Paul S
    FEBS J; 2006 Apr; 273(7):1331-49. PubMed ID: 16689923
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Glycosaminoglycans (GAGs) suppress the toxicity of HypF-N prefibrillar aggregates.
    Saridaki T; Zampagni M; Mannini B; Evangelisti E; Taddei N; Cecchi C; Chiti F
    J Mol Biol; 2012 Aug; 421(4-5):616-30. PubMed ID: 22326346
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Proteopathy: the next therapeutic frontier?
    Walker LC; LeVine H
    Curr Opin Investig Drugs; 2002 May; 3(5):782-7. PubMed ID: 12090553
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Targeting oligomers in neurodegenerative disorders: lessons from α-synuclein, tau, and amyloid-β peptide.
    Gadad BS; Britton GB; Rao KS
    J Alzheimers Dis; 2011; 24 Suppl 2():223-32. PubMed ID: 21460436
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Amyloid oligomer conformation in a group of natively folded proteins.
    Yoshiike Y; Minai R; Matsuo Y; Chen YR; Kimura T; Takashima A
    PLoS One; 2008 Sep; 3(9):e3235. PubMed ID: 18800165
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Generalization of the prion hypothesis to other neurodegenerative diseases: an imperfect fit.
    Guest WC; Silverman JM; Pokrishevsky E; O'Neill MA; Grad LI; Cashman NR
    J Toxicol Environ Health A; 2011; 74(22-24):1433-59. PubMed ID: 22043906
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Defective protein folding and aggregation as the basis of neurodegenerative diseases: the darker aspect of proteins.
    Naeem A; Fazili NA
    Cell Biochem Biophys; 2011 Nov; 61(2):237-50. PubMed ID: 21573992
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Amyloid peptides and proteins in review.
    Harrison RS; Sharpe PC; Singh Y; Fairlie DP
    Rev Physiol Biochem Pharmacol; 2007; 159():1-77. PubMed ID: 17846922
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Structural features and cytotoxicity of amyloid oligomers: implications in Alzheimer's disease and other diseases with amyloid deposits.
    Stefani M
    Prog Neurobiol; 2012 Dec; 99(3):226-45. PubMed ID: 22450705
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Amino acid sequence determinants and molecular chaperones in amyloid fibril formation.
    Nerelius C; Fitzen M; Johansson J
    Biochem Biophys Res Commun; 2010 May; 396(1):2-6. PubMed ID: 20494101
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Oligomerization preceding amyloid fibril formation: a process in common to intrinsically disordered and globular proteins.
    Zerovnik E
    Network; 2011; 22(1-4):154-61. PubMed ID: 22149676
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Amyloid oligomers: dynamics and toxicity in the cytosol and nucleus.
    Kitamura A; Kubota H
    FEBS J; 2010 Mar; 277(6):1369-79. PubMed ID: 20148962
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 16.