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References
54
Referenced
144
-
Wells, G.A.H. et al. A novel progressuve sponigform encephalopathy in cattle. Vet. Rec. 121, 419–420 (1987).
(
10.1136/vr.121.18.419
) / Vet. Rec. by GAH Wells (1987) -
Creutzfeldt, H.G. Über eine eigenartige herdformige Erkrankung des Zentralnervensystems. Z. Gesamte Neurol. Psychiatrie 57, 247–250 (1920).
(
10.1007/BF02866081
) / Z. Gesamte Neurol. Psychiatrie by HG Creutzfeldt (1920) -
Jakob, A. Über eigenartige Erkrankungen des Zentralnervensystems mit bemerkenswertem anatomischen Befunden (spastische Pseudosklerose-Encephalomyopathie mit diseminierten Degenerationsherden). Z. Gesamte Neurol. Psychiatrie 64, 147–228 (1921).
(
10.1007/BF02870932
) / Z. Gesamte Neurol. Psychiatrie by A Jakob (1921) - Gerstmann, J., Straussler, E. & Scheinker, I. Über eine eigenartige herediatar-familare Erkankung des Zentralnervensystems zugleich ein Beitrag zur Frage des vorzeitigen lokalen Alterns. Z. Neurol. 154, 736–762 (1936). / Z. Neurol. by J Gerstmann (1936)
-
Gadjusek, D.C. & Zigas, V. Degenerative disease of the central nervous system in New Guinea: epidemic occurrence of “ Kuru rdquo; in the native population. New Engl. J. Med. 257, 974–978 (1957).
(
10.1056/NEJM195711142572005
) / New Engl. J. Med. by DC Gadjusek (1957) -
Lugaresi, E. et al Fatal Familial Insomnia and dysautonomia with selective degeneration of thalamic nuclei. New Engl. J. Med. 315, 997–1003 (1986).
(
10.1056/NEJM198610163151605
) / New Engl. J. Med. by E Lugaresi (1986) -
DeArmond, S.J. et al Identification of prion amyloid filaments in scrapie-infected brain. Cell 41, 221–235 (1985).
(
10.1016/0092-8674(85)90076-5
) / Cell by SJ DeArmond (1985) -
Hope, J. et al The major polypeptide of scrapie associated fibrils (SAF) has the same size, charge distribution and N-terminal protein sequence as predicted for the normal brain protein (PrP). EMBOJ. 10, 2591–2597 (1986).
(
10.1002/j.1460-2075.1986.tb04539.x
) / EMBOJ. by J Hope (1986) -
Bell, J.E. & Ironside, J.W. Neuropathology of spongiform encephalopathies in humans. B. Med. Bull. 49, 738–777 (1993).
(
10.1093/oxfordjournals.bmb.a072645
) / B. Med. Bull. by JE Bell (1993) -
Hainfellner, J.A. et al Pathology and immunocytochemistry of a Kuru Brain. Brain Pathology 7, 547–553 (1997).
(
10.1111/j.1750-3639.1997.tb01072.x
) / Brain Pathology by JA Hainfellner (1997) -
Basler, K. et al. Scrapie and cellular PrP isoforms are encoded by the same chromosomal gene. Cell 46, 417–428 (1986).
(
10.1016/0092-8674(86)90662-8
) / Cell by K Basler (1986) -
Chandler, R.L. Encephalopathy in mice produced with scrapie brain material. Lancet 1. 1378–1379 (1961).
(
10.1016/S0140-6736(61)92008-6
) / Lancet by RL Chandler (1961) -
Dickinson, A.G. & MacKay, J.M.K. Genetical control of the incubation period in mice of the neurological disease, scrapie. Heredity 19, 279–288 (1964).
(
10.1038/hdy.1964.31
) / Heredity by AG Dickinson (1964) -
Dickinson, A.G., Meikle, V. & Fraser, H. Identification of a gene which controls the incubation period of some strains of scrapie agent in mice. J. Comp. Path. 78, 293–299 (1968).
(
10.1016/0021-9975(68)90005-4
) / J. Comp. Path. by AG Dickinson (1968) -
Carlson, G. et al. Linkage of prion protein and scrapie incubation time genes. Cell 46, 503–511 (1986).
(
10.1016/0092-8674(86)90875-5
) / Cell by G Carlson (1986) -
Carlson, G. et al Genetics and polymorphism of the mouse prion gene complex: the control of scrapie incubation time. Mol. Cell. Biol. 8, 5528–5540 (1988).
(
10.1128/MCB.8.12.5528
) / Mol. Cell. Biol. by G Carlson (1988) -
Hunter, N., Hope, J., McConnell, I. & Dickinson, A.G. Linkage of the scrapie associated fibril protein (PrP) gene and Sine using congenic mice and restriction fragment length polymorphism analysis. J. Gen. Virol. 68, 2711–2716 (1987).
(
10.1099/0022-1317-68-10-2711
) / J. Gen. Virol. by N Hunter (1987) -
Westaway, D. et al Distinct prion proteins in short and long scrapie incubation period mice. Cell 51, 561–662 (1987).
(
10.1016/0092-8674(87)90134-6
) / Cell by D Westaway (1987) -
Carlson, G., Ebeling, C., Torchia, M., Westaway, D. & Prusiner, S.B. Delimiting the location of the scrapie prion incubation time gene on chromosome 2 of the mouse. Genetics 133, 979–988 (1993).
(
10.1093/genetics/133.4.979
) / Genetics by G Carlson (1993) -
Race, R.E., Graham, K., Ernst, D. & Chesebro, B. Analysis of linkage between scrapie incubation period and the prion protein gene in mice. J. Gen. Virol. 71, 493–497 (1990).
(
10.1099/0022-1317-71-2-493
) / J. Gen. Virol. by RE Race (1990) -
Bruce, M.E., McConnell, I., Fraser, H. & Dickinson, A.G. The disease characteristics of different strains of scrapie in Sine congenic mouse lines: implications for the nature of the agent and host control of pathogenesis. J. Gen. Virol. 72, 595–603 (1991).
(
10.1099/0022-1317-72-3-595
) / J. Gen. Virol. by ME Bruce (1991) -
Hunter, N. et al Are Sine and the PrP gene congruent -evidence from PrP gene analysis in Sine congenic mice. J. Gen. Virol 73, 2751–2755 (1992).
(
10.1099/0022-1317-73-10-2751
) / J. Gen. Virol by N Hunter (1992) -
Westaway, D. et al Paradoxical shortening of scrapie incubation times by expression of prion protein transgenes derived from long incubation period mice. Neuron 7, 59–68 (1991).
(
10.1016/0896-6273(91)90074-A
) / Neuron by D Westaway (1991) -
Carlson, G. et al Prion isolate specified allotype interactions between the cellular and scrapie prion proteins in congenic and transgenic mice. Proc Natl. Acad. Sci. USA 91, 5690–5694 (1994).
(
10.1073/pnas.91.12.5690
) / Proc Natl. Acad. Sci. USA by G Carlson (1994) -
Bruce, M.E. & Dickinson, A.G. Genetic control of amyloid plaque production and incubation period in scrapie infected mice. J. Neuropath. Exp. Neurol. 44, 285–294 (1985).
(
10.1097/00005072-198505000-00006
) / J. Neuropath. Exp. Neurol. by ME Bruce (1985) - Moore, R.C. et al Double replacement gene targetting for the production of a series of mouse strains with different prion protein gene alterations Biotechnology 13, 999–1004 (1995). / Biotechnology by RC Moore (1995)
-
Magin, T.M., McWhir, J. & Melton, D.W. A new mouse embryonic stem cell line with good germ line contribution and targetting frequency. Nucleic Acids Res. 20, 3795–3796 (1992).
(
10.1093/nar/20.14.3795
) / Nucleic Acids Res. by TM Magin (1992) -
Simpson, E.M. et al Genetic variation among 129 substrains and its importance fortargetted mutagenesis in mice. Nature Genet. 16, 19–27 (1997).
(
10.1038/ng0597-19
) / Nature Genet. by EM Simpson (1997) - Manson, J.C., Clarke, A.R., McBride, P.A., McConnell, I. & Hope, J. PrP gene dosage determines the timing but not the final intensity or distribution of lesions in scrapie pathology. Neurodegeneration 13, 331–340 (1994). / Neurodegeneration by JC Manson (1994)
-
Westaway, D. et al. Structure and polymorphism of the mouse prion protein gene. Proc. Natal. Acad. Sci. USA 91, 6418–6422 (1994).
(
10.1073/pnas.91.14.6418
) / Proc. Natal. Acad. Sci. USA by D Westaway (1994) -
Baybutt, H. & Manson, J. Characterisation of two promoters for prion protein (PrP) gene expression in neuronal cells. Gene 184, 125–131 (1997).
(
10.1016/S0378-1119(96)00600-2
) / Gene by H Baybutt (1997) -
Prusiner, S.B. et al Transgenic studies implicate interactions between homologous PrP isoforms in scrapie prion replication. Cell 63, 673–686 (1990).
(
10.1016/0092-8674(90)90134-Z
) / Cell by SB Prusiner (1990) -
Telling, G.C. et al. Interactions between wild-type and mutant prion proteins modulate neurodegeneration in transgenic mice. Genes Devel. 10, 1736–1750 (1996).
(
10.1101/gad.10.14.1736
) / Genes Devel. by GC Telling (1996) -
Fischer, M. et al. Prion protein (PrP) with amino-proximal deletions restoring susceptibility of PrP knockout mice to scrapie. EMBO J. 15, 1255–1264 (1996).
(
10.1002/j.1460-2075.1996.tb00467.x
) / EMBO J. by M Fischer (1996) -
Bueler, H. et al. Mice devoid of PrP are resistant to scrapie. Cell 73, 1339–1347 (1993).
(
10.1016/0092-8674(93)90360-3
) / Cell by H Bueler (1993) -
Prusiner, S.B. et al Ablation of the prion protein (PrP) gene in mice prevents scrapie and facilitates production of anti-PrP antibodies. Proc. Natal. Acad. Sci. USA 90, 10608–10612 (1993).
(
10.1073/pnas.90.22.10608
) / Proc. Natal. Acad. Sci. USA by SB Prusiner (1993) -
Sakaguchi, S. et al Accumulation of proteinase K-resistant Prion protein (PrP) is restricted by the expression level of normal PrP in mice inoculated with a mouse-adapted strain of the Creutzfeldt-Jakob Disease agent. J. Virol. 69, 7586–7592 (1995).
(
10.1128/JVI.69.12.7586-7592.1995
) / J. Virol. by S Sakaguchi (1995) - Manson, J.C., McBride, P. & Hope, J. Expression of the PrP gene in the brain of Sine congenic mice and its relationship to the development of scrapie. Neurodegeneration 1, 45–52 (1992). / Neurodegeneration by JC Manson (1992)
-
Meyer, R.K. et al Separation and properties of cellular and scrapie prion proteins. Proc Natal. Acad. Sci. USA 83, 2310–2314 (1986).
(
10.1073/pnas.83.8.2310
) / Proc Natal. Acad. Sci. USA by RK Meyer (1986) -
Farquhar, C.F. et al Protease resistant PrP deposition in brain and non-central nervous system tissues of a murine model of bovine spongiform encephalopathy. J. Gen. Virol 77, 1941–1946 (1996).
(
10.1099/0022-1317-77-8-1941
) / J. Gen. Virol by CF Farquhar (1996) -
Fraser, H. & Dickinson, A.G. Distribution of experimentally induced scrapie lesions in the brain. Nature 216, 1310–1311 (1967).
(
10.1038/2161310a0
) / Nature by H Fraser (1967) -
Fraser, H. & Dickinson, A.G. The sequential development of the brain lesions of scrapie in three strains of mice. J. Comp. Path. 78, 301–311 (1968).
(
10.1016/0021-9975(68)90006-6
) / J. Comp. Path. by H Fraser (1968) -
Kingsbury, D.T. et al. Genetic control of scrapie and Creutzfeldt-Jakob disease in mice. J. Immunology 131, 491–496 (1983).
(
10.4049/jimmunol.131.1.491
) / J. Immunology by DT Kingsbury (1983) -
Bruce, M., Chree, A., McConnell, I. & Wells, G.A.H. Transmission of bovine spongiform encephalopathy and scrapie to mice: strain variation and the species barrier. Phil. Trans. R. Soc. Lond. B 343, 405–411 (1994).
(
10.1098/rstb.1994.0036
) / Phil. Trans. R. Soc. Lond. B by M Bruce (1994) - Fraser, H. The pathology of natural and experimental scrapie. In: Slow Virus Diseases of Animals and Man (ed. R.H. Kimberlin. Amsterdam) 267–305 (1976).
-
Bruce, M.E., McBride, P.A. & Farquhar, C.F. Precise targetting of the pathology of the sialoglycoprotein, PrP, and vacuolar degeneration in mouse scrapie. Neurosci. Lett. 102, 1–6 (1989).
(
10.1016/0304-3940(89)90298-X
) / Neurosci. Lett. by ME Bruce (1989) -
Hecker, R. et al Replication of distinct scrapie prion isolates is region specific in brains of transgenic mice and hamsters. Genes Devel 6, 1213–1228 (1992).
(
10.1101/gad.6.7.1213
) / Genes Devel by R Hecker (1992) -
Kunkel, T.A., Roberts, J.D. & Zakour, R.A. Rapid and efficient site-specific mutagenesis without phenotypic selection. Meth. Enzymol. 154, 367–382 (1987).
(
10.1016/0076-6879(87)54085-X
) / Meth. Enzymol. by TA Kunkel (1987) -
Thompson, S., Clarke, A.R., Pow, A.M., Hooper, M.L. & Melton, D.W. Germline transmission and expression of a corrected HPRT gene produced by gene targetting in embryonic stem cells. Cell 56, 313–321 (1989).
(
10.1016/0092-8674(89)90905-7
) / Cell by S Thompson (1989) -
Fraser, H., Bruce, M.E., Chree, A., McConnell, I. & Wells, G.A.H. Transmission of bovine spongiform encephalopathy and scrapie to mice. J. Gen. Virol. 73, 1891–1897 (1992).
(
10.1099/0022-1317-73-8-1891
) / J. Gen. Virol. by H Fraser (1992) -
Sternberger, L.A., Hardy, P.H., Cuculis, J.J. & Meyer, H. The unlabelled antibody-enzyme method of immunohistochemistry. Preparation of soluble antigen-antibody complex (horse-radish peroxidase-antihorseradish peroxidase) and its use in identifying spirochetes. J. Histochem. Cytochem. 18, 315–333 (1970).
(
10.1177/18.5.315
) / J. Histochem. Cytochem. by LA Sternberger (1970) -
Farquhar, C.F., Somerville, R.A. & Ritchie, L.A. Postmortem immunodiagnosis of scrapie and bovine spongiform encephalopathy J. Virol. Meth. 24, 215–222 (1989).
(
10.1016/0166-0934(89)90023-2
) / J. Virol. Meth. by CF Farquhar (1989) - Farquhar, C.F. et al A review of the detection of PrPSc. In: Proceedings of a Consultation on BSE with the Scientific Veterinary Committee of the Commission of the European Communities 301–313 (European Commission, Brussels, 1993).
-
Laemmli, U.K. Cleavage of structural proteins during the assembly of the head of bacteriophage T4. Nature 227, 680–685 (1970).
(
10.1038/227680a0
) / Nature by UK Laemmli (1970)
Dates
Type | When |
---|---|
Created | 21 years ago (Aug. 18, 2004, 4:37 p.m.) |
Deposited | 2 years, 3 months ago (May 18, 2023, 4:22 p.m.) |
Indexed | 2 months ago (July 2, 2025, 2:31 p.m.) |
Issued | 27 years, 7 months ago (Feb. 1, 1998) |
Published | 27 years, 7 months ago (Feb. 1, 1998) |
Published Print | 27 years, 7 months ago (Feb. 1, 1998) |
@article{Moore_1998, title={Mice with gene targetted prion protein alterations show that Prnp, Sine and Prni are congruent}, volume={18}, ISSN={1546-1718}, url={http://dx.doi.org/10.1038/ng0298-118}, DOI={10.1038/ng0298-118}, number={2}, journal={Nature Genetics}, publisher={Springer Science and Business Media LLC}, author={Moore, Richard C. and Hope, James and McBride, Patricia A. and McConnell, Irene and Selfridge, James and Melton, David W. and Manson, Jean C.}, year={1998}, month=feb, pages={118–125} }