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Abbreviated incubation times for human prions in mice expressing a chimeric mouse-human prion protein transgene.
Proc Natl Acad Sci U S A. 2003 Apr 15;100(8):4784-9. doi: 10.1073/pnas.2627989100. Epub 2003 Apr 8.
2
A traceback phenomenon can reveal the origin of prion infection.
Neuropathology. 2009 Oct;29(5):619-24. doi: 10.1111/j.1440-1789.2008.00973.x. Epub 2009 Jul 29.
3
Mouse-adapted sporadic human Creutzfeldt-Jakob disease prions propagate in cell culture.
Int J Biochem Cell Biol. 2008;40(12):2793-801. doi: 10.1016/j.biocel.2008.05.024. Epub 2008 Jun 11.
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Human prion strain selection in transgenic mice.
Ann Neurol. 2010 Aug;68(2):151-61. doi: 10.1002/ana.22104.
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Prion encephalopathies of animals and humans.
Dev Biol Stand. 1993;80:31-44.
7
The neuropathological phenotype in transgenic mice expressing different prion protein constructs.
Philos Trans R Soc Lond B Biol Sci. 1994 Mar 29;343(1306):415-23. doi: 10.1098/rstb.1994.0038.
8
Prion protein transgenes and the neuropathology in prion diseases.
Brain Pathol. 1995 Jan;5(1):77-89. doi: 10.1111/j.1750-3639.1995.tb00579.x.
9
Molecular biology and genetics of prion diseases.
Philos Trans R Soc Lond B Biol Sci. 1994 Mar 29;343(1306):447-63. doi: 10.1098/rstb.1994.0043.
10
Transmission of Creutzfeldt-Jakob disease from humans to transgenic mice expressing chimeric human-mouse prion protein.
Proc Natl Acad Sci U S A. 1994 Oct 11;91(21):9936-40. doi: 10.1073/pnas.91.21.9936.

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3
Prion protein E219K polymorphism: from the discovery of the KANNO blood group to interventions for human prion disease.
Front Neurol. 2024 Jul 10;15:1392984. doi: 10.3389/fneur.2024.1392984. eCollection 2024.
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Efficient transmission of human prion diseases to a glycan-free prion protein-expressing host.
Brain. 2024 Apr 4;147(4):1539-1552. doi: 10.1093/brain/awad399.
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Phenotypic diversity of genetic Creutzfeldt-Jakob disease: a histo-molecular-based classification.
Acta Neuropathol. 2021 Oct;142(4):707-728. doi: 10.1007/s00401-021-02350-y. Epub 2021 Jul 29.
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Environmental and host factors that contribute to prion strain evolution.
Acta Neuropathol. 2021 Jul;142(1):5-16. doi: 10.1007/s00401-021-02310-6. Epub 2021 Apr 25.
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Two distinct prions in fatal familial insomnia and its sporadic form.
Brain Commun. 2019 Dec 9;1(1):fcz045. doi: 10.1093/braincomms/fcz045. eCollection 2019.

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3
Dominant-negative inhibition of prion replication in transgenic mice.
Proc Natl Acad Sci U S A. 2002 Oct 1;99(20):13079-84. doi: 10.1073/pnas.182425299. Epub 2002 Sep 23.
4
A change in the conformation of prions accompanies the emergence of a new prion strain.
Neuron. 2002 Jun 13;34(6):921-32. doi: 10.1016/s0896-6273(02)00726-2.
5
Doppel-induced cerebellar degeneration in transgenic mice.
Proc Natl Acad Sci U S A. 2001 Dec 18;98(26):15288-93. doi: 10.1073/pnas.251550798. Epub 2001 Dec 4.
6
A protease-resistant 61-residue prion peptide causes neurodegeneration in transgenic mice.
Mol Cell Biol. 2001 Apr;21(7):2608-16. doi: 10.1128/MCB.21.7.2608-2616.2001.
8
Identification of two prion protein regions that modify scrapie incubation time.
J Virol. 2001 Feb;75(3):1408-13. doi: 10.1128/JVI.75.3.1408-1413.2001.
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Compelling transgenetic evidence for transmission of bovine spongiform encephalopathy prions to humans.
Proc Natl Acad Sci U S A. 1999 Dec 21;96(26):15137-42. doi: 10.1073/pnas.96.26.15137.

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