蛋白质构象病 (Chinese Wikipedia)

Analysis of information sources in references of the Wikipedia article "蛋白质构象病" in Chinese language version.

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21doi.org

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17nih.gov

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2archive.org

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archive.org

Glabe CG. Common mechanisms of amyloid oligomer pathogenesis in degenerative disease. Neurobiol Aging. 2006, 27 (4): 570–575. PMID 16481071. doi:10.1016/j.neurobiolaging.2005.04.017.
Jucker, M; Walker, LC. Self-propagation of pathogenic protein aggregates in neurodegenerative diseases. Nature. 2013, 501: 45–51. doi:10.1038/nature12481.

doi.org

Walker LC, LeVine III H. The cerebral proteopathies. Neurobiol Aging. 2000, 21 (4): 559–561. PMID 10924770. doi:10.1016/S0197-4580(00)00160-3.
Walker LC, LeVine III H. The cerebral proteopathies: Neurodegenerative disorders of protein conformation and assembly. Mol Neurobiol. 2000, 21 (1–2): 83–95. PMID 11327151. doi:10.1385/MN:21:1-2:083.
Luheshi M, Crowther DC, Dobson CM. Protein misfolding and disease: from the test tube to the organism. Current Opinion in Chemical Biology. 2008, 12 (1): 25–31. PMID 18295611. doi:10.1016/j.cbpa.2008.02.011.
Chiti F, Dobson CM. Protein misfolding, functional amyloid, and human disease. Annu Rev Biochem. 2006, 75 (1): 333–366. PMID 16756495. doi:10.1146/annurev.biochem.75.101304.123901.
Carrell RW, Lomas DA. Conformational disease. Lancet. 1997, 350 (9071): 134–138. PMID 9228977. doi:10.1016/S0140-6736(97)02073-4.
Westermark P, et al. A primer of amyloid nomenclature. Amyloid. 2007, 14 (3): 179–183. PMID 17701465. doi:10.1080/13506120701460923.
Westermark, GT; et al. Noncerebral Amyloidoses: Aspects on Seeding, Cross-Seeding, and Transmission. Cold Spring Harb Perspect Med. 2017, 8: a024323. PMID 28108533. doi:10.1101/cshperspect.a024323.
Prusiner, SB. Biology and genetics of prions causing neurodegeneration. Annu Rev Genet. 2013, 47: 601–623. PMC 4010318 . PMID 24274755. doi:10.1146/annurev-genet-110711-155524.
Sipe JD, Cohen AS. Review: History of the amyloid fibril. J Struct Biol. 2000, 130 (2–3): 88–98. PMID 10940217. doi:10.1006/jsbi.2000.4221.
Wisniewski HM, Sadowski M, Jakubowska-Sadowska K, Tarnawski M, Wegiel J. Diffuse, lake-like amyloid-beta deposits in the parvopyramidal layer of the presubiculum in Alzheimer disease. J Neuropath Exp Neurol. 1998, 57 (7): 674–683. PMID 9690671. doi:10.1097/00005072-199807000-00004.
Glabe CG. Common mechanisms of amyloid oligomer pathogenesis in degenerative disease. Neurobiol Aging. 2006, 27 (4): 570–575. PMID 16481071. doi:10.1016/j.neurobiolaging.2005.04.017.
Gadad BS, Britton GB, Rao KS. Targeting oligomers in neurodegenerative disorders: lessons from α-synuclein, tau, and amyloid-β peptide. Journal of Alzheimer's disease : JAD. 2011,. 24 Suppl 2: 223–232. PMID 21460436. doi:10.3233/JAD-2011-110182.
Ito D, Suzuki N. Conjoint pathologic cascades mediated by ALS/FTLD-U linked RNA-binding proteins TDP-43 and FUS. Neurology. 2011, 77 (17): 1636–43. PMC 3198978 . PMID 21956718. doi:10.1212/WNL.0b013e3182343365.
Wolozin, B; Apicco, D. RNA binding proteins and the genesis of neurodegenerative diseases. Adv Exp Med Biol. 2015, 822: 11–15. doi:10.1007/978-3-319-08927-0_3.
Dobson CM. Protein misfolding, evolution and disease. TIBS. 1999, 24 (9): 329–332. PMID 10470028. doi:10.1016/S0968-0004(99)01445-0.
Jucker, M; Walker, LC. Self-propagation of pathogenic protein aggregates in neurodegenerative diseases. Nature. 2013, 501: 45–51. doi:10.1038/nature12481.
Selkoe DJ. Folding proteins in fatal ways. Nature. 2003, 426 (6968): 900–904. PMID 14685251. doi:10.1038/nature02264.
Eisenberg, D; Jucker, M. The amyloid state of proteins in human diseases. Cell. 2012, 148: 1188–1203. doi:10.1016/j.cell.2012.02.022.
Walker, LC. Proteopathic Strains and the Heterogeneity of Neurodegenerative Diseases. Annu Rev Genet. 2016, 50: 329–346. doi:10.1146/annurev-genet-120215-034943.
Collinge J, Clarke AR. A general model of prion strains and their pathogenicity. Science. 2007, 318 (5852): 930–936. PMID 17991853. doi:10.1126/science.1138718.
Colby DW, Prusiner SB. De novo generation of prion strains. Nature Reviews Microbiology. 2011, 9 (11): 771–7. PMID 21947062. doi:10.1038/nrmicro2650.

nih.gov

ncbi.nlm.nih.gov

Walker LC, LeVine III H. The cerebral proteopathies. Neurobiol Aging. 2000, 21 (4): 559–561. PMID 10924770. doi:10.1016/S0197-4580(00)00160-3.
Walker LC, LeVine III H. The cerebral proteopathies: Neurodegenerative disorders of protein conformation and assembly. Mol Neurobiol. 2000, 21 (1–2): 83–95. PMID 11327151. doi:10.1385/MN:21:1-2:083.
Luheshi M, Crowther DC, Dobson CM. Protein misfolding and disease: from the test tube to the organism. Current Opinion in Chemical Biology. 2008, 12 (1): 25–31. PMID 18295611. doi:10.1016/j.cbpa.2008.02.011.
Chiti F, Dobson CM. Protein misfolding, functional amyloid, and human disease. Annu Rev Biochem. 2006, 75 (1): 333–366. PMID 16756495. doi:10.1146/annurev.biochem.75.101304.123901.
Carrell RW, Lomas DA. Conformational disease. Lancet. 1997, 350 (9071): 134–138. PMID 9228977. doi:10.1016/S0140-6736(97)02073-4.
Westermark P, et al. A primer of amyloid nomenclature. Amyloid. 2007, 14 (3): 179–183. PMID 17701465. doi:10.1080/13506120701460923.
Westermark, GT; et al. Noncerebral Amyloidoses: Aspects on Seeding, Cross-Seeding, and Transmission. Cold Spring Harb Perspect Med. 2017, 8: a024323. PMID 28108533. doi:10.1101/cshperspect.a024323.
Prusiner, SB. Biology and genetics of prions causing neurodegeneration. Annu Rev Genet. 2013, 47: 601–623. PMC 4010318 . PMID 24274755. doi:10.1146/annurev-genet-110711-155524.
Sipe JD, Cohen AS. Review: History of the amyloid fibril. J Struct Biol. 2000, 130 (2–3): 88–98. PMID 10940217. doi:10.1006/jsbi.2000.4221.
Wisniewski HM, Sadowski M, Jakubowska-Sadowska K, Tarnawski M, Wegiel J. Diffuse, lake-like amyloid-beta deposits in the parvopyramidal layer of the presubiculum in Alzheimer disease. J Neuropath Exp Neurol. 1998, 57 (7): 674–683. PMID 9690671. doi:10.1097/00005072-199807000-00004.
Glabe CG. Common mechanisms of amyloid oligomer pathogenesis in degenerative disease. Neurobiol Aging. 2006, 27 (4): 570–575. PMID 16481071. doi:10.1016/j.neurobiolaging.2005.04.017.
Gadad BS, Britton GB, Rao KS. Targeting oligomers in neurodegenerative disorders: lessons from α-synuclein, tau, and amyloid-β peptide. Journal of Alzheimer's disease : JAD. 2011,. 24 Suppl 2: 223–232. PMID 21460436. doi:10.3233/JAD-2011-110182.
Ito D, Suzuki N. Conjoint pathologic cascades mediated by ALS/FTLD-U linked RNA-binding proteins TDP-43 and FUS. Neurology. 2011, 77 (17): 1636–43. PMC 3198978 . PMID 21956718. doi:10.1212/WNL.0b013e3182343365.
Dobson CM. Protein misfolding, evolution and disease. TIBS. 1999, 24 (9): 329–332. PMID 10470028. doi:10.1016/S0968-0004(99)01445-0.
Selkoe DJ. Folding proteins in fatal ways. Nature. 2003, 426 (6968): 900–904. PMID 14685251. doi:10.1038/nature02264.
Collinge J, Clarke AR. A general model of prion strains and their pathogenicity. Science. 2007, 318 (5852): 930–936. PMID 17991853. doi:10.1126/science.1138718.
Colby DW, Prusiner SB. De novo generation of prion strains. Nature Reviews Microbiology. 2011, 9 (11): 771–7. PMID 21947062. doi:10.1038/nrmicro2650.