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Journal Abstract Search
250 related items for PubMed ID: 19812735
1. Chemical chaperone and inhibitor discovery: potential treatments for protein conformational diseases. Zhao JH, Liu HL, Lin HY, Huang CH, Fang HW, Chen SS, Ho Y, Tsai WB, Chen WY. Perspect Medicin Chem; 2007 Dec 11; 1():39-48. PubMed ID: 19812735 [Abstract] [Full Text] [Related]
2. Protein-misfolding diseases and chaperone-based therapeutic approaches. Chaudhuri TK, Paul S. FEBS J; 2006 Apr 11; 273(7):1331-49. PubMed ID: 16689923 [Abstract] [Full Text] [Related]
3. Protein conformational diseases: from mechanisms to drug designs. Lin JC, Liu HL. Curr Drug Discov Technol; 2006 Jun 11; 3(2):145-53. PubMed ID: 16925522 [Abstract] [Full Text] [Related]
4. Mechanistic Insights into the Role of Molecular Chaperones in Protein Misfolding Diseases: From Molecular Recognition to Amyloid Disassembly. Hervás R, Oroz J. Int J Mol Sci; 2020 Dec 02; 21(23):. PubMed ID: 33276458 [Abstract] [Full Text] [Related]
5. Molecular chaperones biochemistry and role in neurodegenerative diseases. Chaari A. Int J Biol Macromol; 2019 Jun 15; 131():396-411. PubMed ID: 30853582 [Abstract] [Full Text] [Related]
6. Mechanisms of disease II: cellular protein quality control. Outeiro TF, Tetzlaff J. Semin Pediatr Neurol; 2007 Mar 15; 14(1):15-25. PubMed ID: 17331880 [Abstract] [Full Text] [Related]
7. Protein misfolding, aggregation and mechanism of amyloid cytotoxicity: An overview and therapeutic strategies to inhibit aggregation. Zaman M, Khan AN, Wahiduzzaman, Zakariya SM, Khan RH. Int J Biol Macromol; 2019 Aug 01; 134():1022-1037. PubMed ID: 31128177 [Abstract] [Full Text] [Related]
8. New insights into the mechanisms of protein misfolding and aggregation in amyloidogenic diseases derived from pressure studies. Foguel D, Silva JL. Biochemistry; 2004 Sep 14; 43(36):11361-70. PubMed ID: 15350123 [Abstract] [Full Text] [Related]
9. Conformational changes and aggregation of expanded polyglutamine proteins as therapeutic targets of the polyglutamine diseases: exposed beta-sheet hypothesis. Nagai Y, Popiel HA. Curr Pharm Des; 2008 Sep 14; 14(30):3267-79. PubMed ID: 19075705 [Abstract] [Full Text] [Related]
10. 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 14; 61(2):237-50. PubMed ID: 21573992 [Abstract] [Full Text] [Related]
11. [Neurodegenerative conformational disease and its molecular bases]. Li WW, Cai DF, Ren HM. Sheng Li Ke Xue Jin Zhan; 2006 Apr 14; 37(2):97-102. PubMed ID: 16850610 [Abstract] [Full Text] [Related]
12. The Hsp70/Hsp90 Chaperone Machinery in Neurodegenerative Diseases. Lackie RE, Maciejewski A, Ostapchenko VG, Marques-Lopes J, Choy WY, Duennwald ML, Prado VF, Prado MAM. Front Neurosci; 2017 Apr 14; 11():254. PubMed ID: 28559789 [Abstract] [Full Text] [Related]
13. Protein Quality Control by Molecular Chaperones in Neurodegeneration. Ciechanover A, Kwon YT. Front Neurosci; 2017 Apr 14; 11():185. PubMed ID: 28428740 [Abstract] [Full Text] [Related]
14. Targeting chaperones, heat shock factor-1, and unfolded protein response: Promising therapeutic approaches for neurodegenerative disorders. Bose S, Cho J. Ageing Res Rev; 2017 May 14; 35():155-175. PubMed ID: 27702699 [Abstract] [Full Text] [Related]
15. Protein denaturation and aggregation: Cellular responses to denatured and aggregated proteins. Meredith SC. Ann N Y Acad Sci; 2005 Dec 14; 1066():181-221. PubMed ID: 16533927 [Abstract] [Full Text] [Related]
16. [Molecular therapy targeting protein misfolding and aggregation for the polyglutamine diseases]. Nagai Y. Rinsho Shinkeigaku; 2009 Nov 14; 49(11):913-6. PubMed ID: 20030247 [Abstract] [Full Text] [Related]
17. Chemical chaperones: mechanisms of action and potential use. Papp E, Csermely P. Handb Exp Pharmacol; 2006 Nov 14; (172):405-16. PubMed ID: 16610368 [Abstract] [Full Text] [Related]