-
1
-
-
0023837236
-
Characterization of prion proteins with monospecific antisera to synthetic peptides
-
Barry, R.A., Vincent, M.T., Kent, S.B., Hood, L.E., and Prusiner, S.B. (1988). Characterization of prion proteins with monospecific antisera to synthetic peptides. J. Immunol. 140, 1188-1193.
-
(1988)
J. Immunol.
, vol.140
, pp. 1188-1193
-
-
Barry, R.A.1
Vincent, M.T.2
Kent, S.B.3
Hood, L.E.4
Prusiner, S.B.5
-
2
-
-
0026567814
-
Nearly ubiquitous tissue distribution of the scrapie agent precursor protein
-
Bendheim, P.E., Brown, H.R., Rudelli, R.D., Scala, L.J., Goller, N.L., Wen, G.Y., Kascsak, R.J., Cashman, N.R., and Bolton, D.C. (1992). Nearly ubiquitous tissue distribution of the scrapie agent precursor protein. Neurology 42, 149-156.
-
(1992)
Neurology
, vol.42
, pp. 149-156
-
-
Bendheim, P.E.1
Brown, H.R.2
Rudelli, R.D.3
Scala, L.J.4
Goller, N.L.5
Wen, G.Y.6
Kascsak, R.J.7
Cashman, N.R.8
Bolton, D.C.9
-
3
-
-
0030054010
-
Normal host prion protein necessary for scrapie-induced neurotoxicity
-
Brandner, S., Isenmann, S., Raeber, A., Fischer, M., Sailer, A., Kobayashi, Y., Marino, S., Weissmann, C., and Aguzzi, A. (1996). Normal host prion protein necessary for scrapie-induced neurotoxicity. Nature 379, 339-343.
-
(1996)
Nature
, vol.379
, pp. 339-343
-
-
Brandner, S.1
Isenmann, S.2
Raeber, A.3
Fischer, M.4
Sailer, A.5
Kobayashi, Y.6
Marino, S.7
Weissmann, C.8
Aguzzi, A.9
-
4
-
-
0001305936
-
Factors affecting the efficiency of introducing foreign DNA into mice by microinjecting eggs
-
Brinster, R.L., Chen, H.Y., Trumbauer, M.E., Yagle, M.K., and Palmiter, A.D. (1985). Factors affecting the efficiency of introducing foreign DNA into mice by microinjecting eggs. Proc. Natl. Acad. Sci. USA 82, 4438-4442.
-
(1985)
Proc. Natl. Acad. Sci. USA
, vol.82
, pp. 4438-4442
-
-
Brinster, R.L.1
Chen, H.Y.2
Trumbauer, M.E.3
Yagle, M.K.4
Palmiter, A.D.5
-
5
-
-
0031444294
-
The cellular prion protein binds copper in vivo
-
Brown, D.R., Qin, K., Herms, J.W., Madlung, A., Manson, J., Strome, R., Fraser, P.E., Kruck, T., von Bohlen, A., Schulz-Schaeffer, W., et al. (1997). The cellular prion protein binds copper in vivo. Nature 390, 684-687.
-
(1997)
Nature
, vol.390
, pp. 684-687
-
-
Brown, D.R.1
Qin, K.2
Herms, J.W.3
Madlung, A.4
Manson, J.5
Strome, R.6
Fraser, P.E.7
Kruck, T.8
Von Bohlen, A.9
Schulz-Schaeffer, W.10
-
6
-
-
0026600865
-
Normal development and behaviour of mice lacking the neuronal cell-surface PrP protein
-
Büeler, H., Fischer, M., Lang, Y., Bluethmann, H., Lipp, H.-P., DeArmond, S.J., Prusiner, S.B., Aguet, M., and Weissmann, C. (1992). Normal development and behaviour of mice lacking the neuronal cell-surface PrP protein. Nature 356, 577-582.
-
(1992)
Nature
, vol.356
, pp. 577-582
-
-
Büeler, H.1
Fischer, M.2
Lang, Y.3
Bluethmann, H.4
Lipp, H.-P.5
DeArmond, S.J.6
Prusiner, S.B.7
Aguet, M.8
Weissmann, C.9
-
7
-
-
0029027854
-
Truncated forms of the human prion protein in normal brain and in prion diseases
-
Chen, S.G., Teplow, D.B., Parchi, P., Teller, J.K., Gambetti, P., and Autilio-Gambetti, L. (1995). Truncated forms of the human prion protein in normal brain and in prion diseases. J. Biol. Chem. 270, 19173-19180.
-
(1995)
J. Biol. Chem.
, vol.270
, pp. 19173-19180
-
-
Chen, S.G.1
Teplow, D.B.2
Parchi, P.3
Teller, J.K.4
Gambetti, P.5
Autilio-Gambetti, L.6
-
8
-
-
0023277545
-
Single-step method of RNA isolation by acid guanidinium thiocyanate-phenol-chloroform extraction
-
Chomczynski, P., and Sacchi, N. (1987). Single-step method of RNA isolation by acid guanidinium thiocyanate-phenol-chloroform extraction. Anal. Biochem. 162, 156-159.
-
(1987)
Anal. Biochem.
, vol.162
, pp. 156-159
-
-
Chomczynski, P.1
Sacchi, N.2
-
9
-
-
0029971378
-
Hippocampal slices from prion protein null mice: Disrupted Ca(2+)-activated K+ currents
-
Colling, S.B., Collinge, J., and Jefferys, J.G. (1996). Hippocampal slices from prion protein null mice: disrupted Ca(2+)-activated K+ currents. Neurosci. Lett. 209, 49-52.
-
(1996)
Neurosci. Lett.
, vol.209
, pp. 49-52
-
-
Colling, S.B.1
Collinge, J.2
Jefferys, J.G.3
-
10
-
-
0027997387
-
Prion protein is necessary for normal synaptic function
-
Collinge, J., Whittington, M.A., Sidle, K.C.L., Smith, C.J., Palmer, M.S., Clarke, A.R., and Jefferys, J.G.R. (1994). Prion protein is necessary for normal synaptic function. Nature 370, 295-297.
-
(1994)
Nature
, vol.370
, pp. 295-297
-
-
Collinge, J.1
Whittington, M.A.2
Sidle, K.C.L.3
Smith, C.J.4
Palmer, M.S.5
Clarke, A.R.6
Jefferys, J.G.R.7
-
11
-
-
0031456947
-
Structure of the recombinant full-length hamster prion protein PrP(29-231): The N terminus is highly flexible
-
Donne, D.G., Viles, J.H., Groth, D., Mehlhorn, I., James, T.L., Cohen, F.E., Prusiner, S.B., Wright, P.E., and Dyson, H.J. (1997). Structure of the recombinant full-length hamster prion protein PrP(29-231): the N terminus is highly flexible. Proc. Natl. Acad. Sci. USA 94, 13452-13457.
-
(1997)
Proc. Natl. Acad. Sci. USA
, vol.94
, pp. 13452-13457
-
-
Donne, D.G.1
Viles, J.H.2
Groth, D.3
Mehlhorn, I.4
James, T.L.5
Cohen, F.E.6
Prusiner, S.B.7
Wright, P.E.8
Dyson, H.J.9
-
13
-
-
0029863648
-
Prion protein (PrP) with amino-proximal deletions restoring susceptibility of PrP knockout mice to scrapie
-
Fischer, M., Rülicke, T., Raeber, A., Sailer, A., Moser, M., Oesch, B., Brandner, S., Aguzzi, A.L, and Weissmann, C. (1996). Prion protein (PrP) with amino-proximal deletions restoring susceptibility of PrP knockout mice to scrapie. EMBO J. 15, 1255-1264.
-
(1996)
EMBO J.
, vol.15
, pp. 1255-1264
-
-
Fischer, M.1
Rülicke, T.2
Raeber, A.3
Sailer, A.4
Moser, M.5
Oesch, B.6
Brandner, S.7
Aguzzi, A.L.8
Weissmann, C.9
-
14
-
-
0022423216
-
Various rat adult tissues express only one major mRNA species from the glyceraldehyde-3-phosphate-dehydrogenase multigenic family
-
Fort, P., Marty, L., Piechaczyk, M., el Sabrouty, S., Dani, C., Jeanteur, P., and Blanchard, J.M. (1985). Various rat adult tissues express only one major mRNA species from the glyceraldehyde-3-phosphate-dehydrogenase multigenic family. Nucleic Acids Res. 13, 1431-1442.
-
(1985)
Nucleic Acids Res.
, vol.13
, pp. 1431-1442
-
-
Fort, P.1
Marty, L.2
Piechaczyk, M.3
El Sabrouty, S.4
Dani, C.5
Jeanteur, P.6
Blanchard, J.M.7
-
15
-
-
0027516363
-
Infantile cerebello-optic atrophy. Neuropathology of the progressive encephalopathy syndrome with edema, hypsarrhythmia and optic atrophy (the PEHO syndrome)
-
Haltia, M., and Somer, M. (1993). Infantile cerebello-optic atrophy. Neuropathology of the progressive encephalopathy syndrome with edema, hypsarrhythmia and optic atrophy (the PEHO syndrome). Acta Neuropathol. 85, 241-247.
-
(1993)
Acta Neuropathol.
, vol.85
, pp. 241-247
-
-
Haltia, M.1
Somer, M.2
-
16
-
-
0027405573
-
Processing of a cellular prion protein: Identification of N-and C-terminal cleavage sites
-
Harris, D.A., Huber, M.T., van Dijken, P., Shyng, S.L., Chait, B.T., and Wang, R. (1993). Processing of a cellular prion protein: identification of N-and C-terminal cleavage sites. Biochemistry 32, 1009-1016.
-
(1993)
Biochemistry
, vol.32
, pp. 1009-1016
-
-
Harris, D.A.1
Huber, M.T.2
Van Dijken, P.3
Shyng, S.L.4
Chait, B.T.5
Wang, R.6
-
17
-
-
0028793453
-
Patch-clamp analysis of synaptic transmission to cerebellar Purkinje cells of prion protein knockout mice
-
Herms, J.W., Kretzschmar, H.A., Titz, S., and Keller, B.U. (1995). Patch-clamp analysis of synaptic transmission to cerebellar Purkinje cells of prion protein knockout mice. Eur. J. Neurosci. 7, 2508-2512.
-
(1995)
Eur. J. Neurosci.
, vol.7
, pp. 2508-2512
-
-
Herms, J.W.1
Kretzschmar, H.A.2
Titz, S.3
Keller, B.U.4
-
18
-
-
0028608963
-
Serial transmission in rodents of neurodegeneration from transgenic mice expressing mutant prion protein
-
Hsiao, K.K., Groth, D., Scott, M., Yang, S.L., Serban, H., Rapp, D., Foster, D., Torchia, M., Dearmond, S.J., and Prusiner, S.B. (1994). Serial transmission in rodents of neurodegeneration from transgenic mice expressing mutant prion protein. Proc. Natl. Acad. Sci. USA 91, 9126-9130.
-
(1994)
Proc. Natl. Acad. Sci. USA
, vol.91
, pp. 9126-9130
-
-
Hsiao, K.K.1
Groth, D.2
Scott, M.3
Yang, S.L.4
Serban, H.5
Rapp, D.6
Foster, D.7
Torchia, M.8
Dearmond, S.J.9
Prusiner, S.B.10
-
19
-
-
0029916617
-
Mice deficient for prion protein exhibit normal neuronal excitability and synaptic transmission in the hippocampus
-
Lledo, P.-M., Tremblay, P., DeArmond, S.J., Prusiner, S.B., and Nicoll, R.A. (1996). Mice deficient for prion protein exhibit normal neuronal excitability and synaptic transmission in the hippocampus. Proc. Natl. Acad. Sci. USA 93, 2403-2407.
-
(1996)
Proc. Natl. Acad. Sci. USA
, vol.93
, pp. 2403-2407
-
-
Lledo, P.-M.1
Tremblay, P.2
DeArmond, S.J.3
Prusiner, S.B.4
Nicoll, R.A.5
-
20
-
-
0028420937
-
129/Ola mice carrying a null mutation in PrP that abolishes mRNA production are developmentally normal
-
Manson, J.C., Clarke, A.R., Hooper, M.L., Aitchison, L., McConnell, I., and Hope, J. (1994). 129/Ola mice carrying a null mutation in PrP that abolishes mRNA production are developmentally normal. Mol. Neurobiol. 8, 121-127.
-
(1994)
Mol. Neurobiol.
, vol.8
, pp. 121-127
-
-
Manson, J.C.1
Clarke, A.R.2
Hooper, M.L.3
Aitchison, L.4
McConnell, I.5
Hope, J.6
-
21
-
-
0031466157
-
Complementary hydropathy identifies a cellular prion priotein receptor
-
Martins, V.R., Graner, E., Garcia-Abreu, J., de Souza, S.J., Mercadante, A.F., Veiga, S.S., Zanata, S.M., Moura Neto, V., and Brentani, R.R. (1997). Complementary hydropathy identifies a cellular prion priotein receptor. Nat. Med. 3, 1376-1382.
-
(1997)
Nat. Med.
, vol.3
, pp. 1376-1382
-
-
Martins, V.R.1
Graner, E.2
Garcia-Abreu, J.3
De Souza, S.J.4
Mercadante, A.F.5
Veiga, S.S.6
Zanata, S.M.7
Moura Neto, V.8
Brentani, R.R.9
-
22
-
-
0029122724
-
Targeting of transforming growth factor-alpha expression to pituitary lactotrophs in transgenic mice results in selective lactotroph proliferation and adenomas
-
McAndrew, J., Paterson, A.J., Asa, S.I., McCarthy, K.J., and Kudlow, J.E. (1995). Targeting of transforming growth factor-alpha expression to pituitary lactotrophs in transgenic mice results in selective lactotroph proliferation and adenomas. Endocrinology 136, 4479-4488.
-
(1995)
Endocrinology
, vol.136
, pp. 4479-4488
-
-
McAndrew, J.1
Paterson, A.J.2
Asa, S.I.3
McCarthy, K.J.4
Kudlow, J.E.5
-
23
-
-
0003436550
-
-
Baltimore, MD: The Johns Hopkins University Press
-
McKusick, V.A. (1988). Mendelian Inheritance in Man (Baltimore, MD: The Johns Hopkins University Press).
-
(1988)
Mendelian Inheritance in Man
-
-
McKusick, V.A.1
-
24
-
-
0030811015
-
Heritable disorder resembling neuronal storage disease in mice expressing prion protein with deletion of an alpha-helix
-
Muramoto, T., DeArmond, S.J., Scott, M., Telling, G.C., Cohen, F.E., and Prusiner, S.B. (1997). Heritable disorder resembling neuronal storage disease in mice expressing prion protein with deletion of an alpha-helix. Nat. Med. 3, 750-755.
-
(1997)
Nat. Med.
, vol.3
, pp. 750-755
-
-
Muramoto, T.1
DeArmond, S.J.2
Scott, M.3
Telling, G.C.4
Cohen, F.E.5
Prusiner, S.B.6
-
25
-
-
0001676883
-
Primary degeneration of the granular layer of the cerebellum: An unusual form of familial cerebellar atrophy occurring in early life
-
Norman, R.M. (1940). Primary degeneration of the granular layer of the cerebellum: an unusual form of familial cerebellar atrophy occurring in early life. Brain 63, 365-379.
-
(1940)
Brain
, vol.63
, pp. 365-379
-
-
Norman, R.M.1
-
26
-
-
0022005315
-
A cellular gene encodes scrapie PrP 27-30 protein
-
Oesch, B., Westaway, D., Wälchli, M., McKinley, M.P., Kent, S.B., Aebersold, R., Barry, R.A., Tempst, P., Teplow, D.B., Hood, L.E., et al. (1985). A cellular gene encodes scrapie PrP 27-30 protein. Cell 40, 735-746.
-
(1985)
Cell
, vol.40
, pp. 735-746
-
-
Oesch, B.1
Westaway, D.2
Wälchli, M.3
McKinley, M.P.4
Kent, S.B.A.R.5
Barry, R.A.6
Tempst, P.7
Teplow, D.B.8
Hood, L.E.9
-
27
-
-
0027980424
-
Primary degeneration of the granular layer of the cerebellum. A study of 14 patients and review of the literature
-
Pascual-Castroviejo, I., Gutierrez, M., Morales, C., Gonzalez-Mediero, I., Martinez-Bermejo, A., and Pascual-Pascual, S.I. (1994). Primary degeneration of the granular layer of the cerebellum. A study of 14 patients and review of the literature. Neuropediatrics 25, 183-190.
-
(1994)
Neuropediatrics
, vol.25
, pp. 183-190
-
-
Pascual-Castroviejo, I.1
Gutierrez, M.2
Morales, C.3
Gonzalez-Mediero, I.4
Martinez-Bermejo, A.5
Pascual-Pascual, S.I.6
-
28
-
-
0003195421
-
Metal chelate affinity chromatography
-
J.E. Coligan, B.M. Dunn, H.L. Ploegh, D.W. Speicher, and P.T. Wingfield, eds. (New York: John Wiley and Sons)
-
Petty, K.J. (1996). Metal chelate affinity chromatography. In Current Protocols in Protein Science, J.E. Coligan, B.M. Dunn, H.L. Ploegh, D.W. Speicher, and P.T. Wingfield, eds. (New York: John Wiley and Sons), pp. 9.4.1-9.4.16.
-
(1996)
Current Protocols in Protein Science
, pp. 941-9416
-
-
Petty, K.J.1
-
29
-
-
0020321767
-
Novel proteinaceous infectious particles cause scrapie
-
Prusiner, S.B. (1982). Novel proteinaceous infectious particles cause scrapie. Science 216, 136-144.
-
(1982)
Science
, vol.216
, pp. 136-144
-
-
Prusiner, S.B.1
-
30
-
-
0031436335
-
The human 37-kDa laminin receptor precursor interacts with the prion protein in eukaryotic cells
-
Rieger, R., Edenhofer, F., Lasmézas, C.I., and Weiss, S. (1997). The human 37-kDa laminin receptor precursor interacts with the prion protein in eukaryotic cells. Nat. Med. 3, 1383-1388.
-
(1997)
Nat. Med.
, vol.3
, pp. 1383-1388
-
-
Rieger, R.1
Edenhofer, F.2
Lasmézas, C.I.3
Weiss, S.4
-
31
-
-
0030836511
-
NMR characterization of the full-length recombinant murine prion protein, mPrP(23-231)
-
Riek, R., Hornemann, S., Wider, G., Glockshuber, R., and Wüthrich, K. (1997). NMR characterization of the full-length recombinant murine prion protein, mPrP(23-231). FEBS Lett. 413, 282-288.
-
(1997)
FEBS Lett.
, vol.413
, pp. 282-288
-
-
Riek, R.1
Hornemann, S.2
Wider, G.3
Glockshuber, R.4
Wüthrich, K.5
-
32
-
-
0028820122
-
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
-
Sakaguchi, S., Katamine, S., Shigematsu, K., Nakatani, A., Moriuchi, R., Nishida, N., Kurokawa, K., Nakaoke, R., Sato, H., Jishage, K., et al. (1995). 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)
J. Virol.
, vol.69
, pp. 7586-7592
-
-
Sakaguchi, S.1
Katamine, S.2
Shigematsu, K.3
Nakatani, A.4
Moriuchi, R.5
Nishida, N.6
Kurokawa, K.7
Nakaoke, R.8
Sato, H.9
Jishage, K.10
-
33
-
-
13344282734
-
Loss of cerebellar Purkinje cells in aged mice homozygous for a disrupted PrP gene
-
Sakaguchi, S., Katamine, S., Nishida, N., Moriuchi, R., Shigematsu, K., Sugimoto, T., Nakatani, A., Kataoka, Y., Houtani, T., Shirabe, S., et al. (1996). Loss of cerebellar Purkinje cells in aged mice homozygous for a disrupted PrP gene. Nature 380, 528-531.
-
(1996)
Nature
, vol.380
, pp. 528-531
-
-
Sakaguchi, S.1
Katamine, S.2
Nishida, N.3
Moriuchi, R.4
Shigematsu, K.5
Sugimoto, T.6
Nakatani, A.7
Kataoka, Y.8
Houtani, T.9
Shirabe, S.10
-
34
-
-
0029910845
-
Hepatocyte growth factor/scatter factor overexpression induces growth, abnormal development, and tumor formation in transgenic mouse livers
-
Sakata, H., Takayama, H., Sharp, R., Rubin, J.S., Merlino, G., and LaRochelle, W.J. (1996). Hepatocyte growth factor/scatter factor overexpression induces growth, abnormal development, and tumor formation in transgenic mouse livers. Cell Growth Differ. 7, 1513-1523.
-
(1996)
Cell Growth Differ.
, vol.7
, pp. 1513-1523
-
-
Sakata, H.1
Takayama, H.2
Sharp, R.3
Rubin, J.S.4
Merlino, G.5
LaRochelle, W.J.6
-
35
-
-
0003903343
-
-
Cold Spring Harbor, NY: Cold Spring Harbor Laboratory Press
-
Sambrook, J., Fritsch, E.F., and Maniatis, T. (1989). Molecular Cloning: A Laboratory Manual (Cold Spring Harbor, NY: Cold Spring Harbor Laboratory Press).
-
(1989)
Molecular Cloning: A Laboratory Manual
-
-
Sambrook, J.1
Fritsch, E.F.2
Maniatis, T.3
-
36
-
-
0017681196
-
DNA sequencing with chain-terminating inhibitors
-
Sanger, F., Nicklen, S., and Coulson, A.R. (1977). DNA sequencing with chain-terminating inhibitors. Proc. Natl. Acad. Sci. USA 74, 5463-5467.
-
(1977)
Proc. Natl. Acad. Sci. USA
, vol.74
, pp. 5463-5467
-
-
Sanger, F.1
Nicklen, S.2
Coulson, A.R.3
-
37
-
-
0028104332
-
Histopathology of lymphatic tissues in transgenic mice expressing human tissue kallikrein gene
-
Simson, J.A., Wang, J., Chao, J., and Chao, L. (1994). Histopathology of lymphatic tissues in transgenic mice expressing human tissue kallikrein gene. Lab. Invest. 71, 680-687.
-
(1994)
Lab. Invest.
, vol.71
, pp. 680-687
-
-
Simson, J.A.1
Wang, J.2
Chao, J.3
Chao, L.4
-
38
-
-
0029740354
-
Interactions between wild-type and mutant prion proteins modulate neurodegeneration in transgenic mice
-
Telling, G.G., Haga, T., Torchia, M., Tremblay, P., DeArmond, S.J., and Prusiner, S.B. (1996). Interactions between wild-type and mutant prion proteins modulate neurodegeneration in transgenic mice. Genes Dev. 10, 1736-1750.
-
(1996)
Genes Dev.
, vol.10
, pp. 1736-1750
-
-
Telling, G.G.1
Haga, T.2
Torchia, M.3
Tremblay, P.4
DeArmond, S.J.5
Prusiner, S.B.6
-
39
-
-
15844421385
-
Altered circadian activity rhythms and sleep in mice devoid of prion protein
-
Tobler, I., Gaus, S.E., Deboer, T., Achermann, P., Fischer, M., Rülicke, T., Moser, M., Oesch, B., McBride, P.A., and Manson, J.C. (1996). Altered circadian activity rhythms and sleep in mice devoid of prion protein. Nature 380, 639-642.
-
(1996)
Nature
, vol.380
, pp. 639-642
-
-
Tobler, I.1
Gaus, S.E.2
Deboer, T.3
Achermann, P.4
Fischer, M.5
Rülicke, T.6
Moser, M.7
Oesch, B.8
McBride, P.A.9
Manson, J.C.10
-
40
-
-
0030280747
-
PrP effects clarified
-
Weissmann, C. (1996). PrP effects clarified. Curr. Biol. 6, 1359.
-
(1996)
Curr. Biol.
, vol.6
, pp. 1359
-
-
Weissmann, C.1
-
41
-
-
0028052363
-
Degeneration of skeletal muscle, peripheral nerves, and the central nervous system in transgenic mice overexpressing wild-type prion proteins
-
Westaway, D., DeArmond, S.J., Cayetano, C.J., Groth, D., Foster, D., Yang, S.L., Torchia, M., Carlson, G.A., and Prusiner, S.B. (1994). Degeneration of skeletal muscle, peripheral nerves, and the central nervous system in transgenic mice overexpressing wild-type prion proteins. Cell 76, 117-129.
-
(1994)
Cell
, vol.76
, pp. 117-129
-
-
Westaway, D.1
DeArmond, S.J.2
Cayetano, C.J.3
Groth, D.4
Foster, D.5
Yang, S.L.6
Torchia, M.7
Carlson, G.A.8
Prusiner, S.B.9
-
42
-
-
0028802150
-
Rescue of neurophysiological phenotype seen in PrP null mice by transgene encoding human prion protein
-
Whittington, M.A., Sidle, K.C., Gowland, I., Meads, J., Hill, A.F., Palmer, M.S., Jefferys, J.G., and Collinge, J. (1995). Rescue of neurophysiological phenotype seen in PrP null mice by transgene encoding human prion protein. Nat. Genet. 9, 197-201.
-
(1995)
Nat. Genet.
, vol.9
, pp. 197-201
-
-
Whittington, M.A.1
Sidle, K.C.2
Gowland, I.3
Meads, J.4
Hill, A.F.5
Palmer, M.S.6
Jefferys, J.G.7
Collinge, J.8
-
43
-
-
0025781492
-
Genetic manipulation of mammals and its application in reproductive biology
-
Wilmut, I., Hooper, M.L., and Simons, J.P. (1991). Genetic manipulation of mammals and its application in reproductive biology. J. Reprod. Fertil. 92, 245-279.
-
(1991)
J. Reprod. Fertil.
, vol.92
, pp. 245-279
-
-
Wilmut, I.1
Hooper, M.L.2
Simons, J.P.3
-
44
-
-
0030940607
-
Identification of candidate proteins binding to prion protein
-
Yehiely, F., Bamborough, P., Da Costa, M., Perry, B.J., Thinakaran, G., Cohen, F.E., Carlson, G.A., and Prusiner, S.B. (1997). Identification of candidate proteins binding to prion protein. Neurobiol. Dis. 3, 339-355.
-
(1997)
Neurobiol. Dis.
, vol.3
, pp. 339-355
-
-
Yehiely, F.1
Bamborough, P.2
Da Costa, M.3
Perry, B.J.4
Thinakaran, G.5
Cohen, F.E.6
Carlson, G.A.7
Prusiner, S.B.8
-
45
-
-
0027410516
-
Increased expression of neurofilament subunit NF-L produces morphological alterations that resemble the pathology of human motor neuron disease
-
Xu, Z., Cork, L.C., Griffin, J.W., and Cleveland, D.W. (1993). Increased expression of neurofilament subunit NF-L produces morphological alterations that resemble the pathology of human motor neuron disease. Cell 73, 23-33.
-
(1993)
Cell
, vol.73
, pp. 23-33
-
-
Xu, Z.1
Cork, L.C.2
Griffin, J.W.3
Cleveland, D.W.4
|