Pro----leu change at position 102 of prion protein is the most common but not the sole mutation related to Gerstmann-Sträussler syndrome.
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[1] H. Wiśniewski,et al. A PvuII RFLP detected in the human prion protein (PrP) gene. , 1987, Nucleic acids research.
[2] S. Prusiner,et al. Scrapie and cellular PrP isoforms are encoded by the same chromosomal gene , 1986, Cell.
[3] J. Tateishi,et al. EXPERIMENTAL TRANSMISSION OF CREUTZFELDT‐JAKOB DISEASE , 1981, Acta pathologica japonica.
[4] S. Prusiner,et al. Prions and neurodegenerative diseases. , 1987, The New England journal of medicine.
[5] S. Prusiner,et al. Scrapie prions aggregate to form amyloid-like birefringent rods , 1983, Cell.
[6] Ruedi Aebersold,et al. A cellular gene encodes scrapie PrP 27-30 protein , 1985, Cell.
[7] C. Masters,et al. Creutzfeldt-Jakob disease virus isolations from the Gerstmann-Sträussler syndrome with an analysis of the various forms of amyloid plaque deposition in the virus-induced spongiform encephalopathies. , 1981, Brain : a journal of neurology.
[8] M. Nakazato,et al. Biochemical and genetic characterization of type I familial amyloidotic polyneuropathy , 1987, Annals of neurology.
[9] T. Kitamoto,et al. Immunohistochemical confirmation of Creutzfeldt-Jakob disease with a long clinical course with amyloid plaque core antibodies. , 1988, The American journal of pathology.
[10] M. Hattori,et al. Dideoxy sequencing method using denatured plasmid templates. , 1986, Analytical biochemistry.
[11] B. Chesebro,et al. Identification of scrapie prion protein-specific mRNA in scrapie-infected and uninfected brain , 1985, Nature.
[12] S. Fucharoen,et al. A novel ochre mutation in the beta-thalassemia gene of a Thai. Identification by direct cloning of the entire beta-globin gene amplified using polymerase chain reactions. , 1989, The Journal of biological chemistry.
[13] S. Prusiner,et al. Molecular cloning of a human prion protein cDNA. , 1986, DNA.
[14] P. Daniel,et al. Creutzfeldt-Jakob Disease (Spongiform Encephalopathy): Transmission to the Chimpanzee , 1968, Science.
[15] Jurg Ott,et al. Linkage of a prion protein missense variant to Gerstmann–Sträussler syndrome , 1989, Nature.
[16] M. Ohta,et al. Transmission of chronic spongiform encephalopathy with kuru plaques from humans to small rodents , 1979, Annals of neurology.
[17] K. Mullis,et al. Primer-directed enzymatic amplification of DNA with a thermostable DNA polymerase. , 1988, Science.
[18] T. Kitamoto,et al. Gerstmann‐Sträussler‐Scheinker disease: Immunohistological and experimental studies , 1988, Annals of neurology.
[19] M. Alpers,et al. Experimental Transmission of a Kuru-like Syndrome to Chimpanzees , 1966, Nature.
[20] S. Prusiner. Novel proteinaceous infectious particles cause scrapie. , 1982, Science.
[21] D. Barker,et al. Restriction sites containing CpG show a higher frequency of polymorphism in human DNA , 1984, Cell.