-
1
-
-
0027639817
-
Biogenesis of constitutive secretory vesicles, secretory granules and synaptic vesicles
-
Bauerfeind R, Huttner WB (1993) Biogenesis of constitutive secretory vesicles, secretory granules and synaptic vesicles. Curr Opin Cell Biol 5:628-635
-
(1993)
Curr Opin Cell Biol
, vol.5
, pp. 628-635
-
-
Bauerfeind, R.1
Huttner, W.B.2
-
2
-
-
0026567814
-
Nearly ubiquitous tissue distribution of the scrapie agent precursor protein
-
Bendheim PE, Brown HR, Rudelli RD, Scala LJ Goller NL, Wen GY, Kascsak RJ, Cashman NR, Bolton DC (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
-
-
0028356488
-
Rapid anterograde axonal transport of the cellular prion glycoprotein in the peripheral and central nervous systems
-
Borchelt D R, Koliatsos VE, Guarnieri M, Pardo CA, Sisodia S, Price DL (1994) Rapid anterograde axonal transport of the cellular prion glycoprotein in the peripheral and central nervous systems. J Biol Chem 269:14711-14714
-
(1994)
J Biol Chem
, vol.269
, pp. 14711-14714
-
-
Borchelt, D.R.1
Koliatsos, V.E.2
Guarnieri, M.3
Pardo, C.A.4
Sisodia, S.5
Price, D.L.6
-
4
-
-
0025270288
-
The mRNA encoding the scrapie agent protein is present in a variety of non-neuronal cells
-
Berl
-
Brown HR, Goller N, Rudelli G, Wolfe GC, Wisniewski HM, Robakis NK (1990) The mRNA encoding the scrapie agent protein is present in a variety of non-neuronal cells. Acta Neuropathol (Berl) 80:1-6
-
(1990)
Acta Neuropathol
, vol.80
, pp. 1-6
-
-
Brown, H.R.1
Goller, N.2
Rudelli, G.3
Wolfe, G.C.4
Wisniewski, H.M.5
Robakis, N.K.6
-
5
-
-
0002554696
-
Transmissible human spongiform encephalopathies (infectious cerebral amyloidosis): Creutzfeldt-Jakob disease, Gerstmann-Sträussler-Scheinker syndrome, and kuru
-
Calne DB (ed) Saunders, Philadelphia
-
Brown P (1993) Transmissible human spongiform encephalopathies (infectious cerebral amyloidosis): Creutzfeldt-Jakob disease, Gerstmann-Sträussler-Scheinker syndrome, and kuru. In: Calne DB (ed) Neurodegenerative diseases. Saunders, Philadelphia, pp 839-876
-
(1993)
Neurodegenerative Diseases
, pp. 839-876
-
-
Brown, P.1
-
6
-
-
0022639482
-
Diagnosis of Creutzfeldt-Jakob disease by Western blot identification of marker protein in human brain tissue
-
Brown P, Coker-Vann M, Pomeroy K, Franko M, Asher D, Gibbs C, Gajdusek DC (1988) Diagnosis of Creutzfeldt-Jakob disease by Western blot identification of marker protein in human brain tissue. N Engl J Med 314:547-551
-
(1988)
N Engl J Med
, vol.314
, pp. 547-551
-
-
Brown, P.1
Coker-Vann, M.2
Pomeroy, K.3
Franko, M.4
Asher, D.5
Gibbs, C.6
Gajdusek, D.C.7
-
7
-
-
0027319326
-
Normal development and behaviour of mice lacking the neuronal cell-surface PrP protein
-
Büeler H, Aguzzi A, Sailer A, Greiner RA, Autenried P, Aguet M, Weissmann C (1993) Normal development and behaviour of mice lacking the neuronal cell-surface PrP protein. Cell 73:1339-1347
-
(1993)
Cell
, vol.73
, pp. 1339-1347
-
-
Büeler, H.1
Aguzzi, A.2
Sailer, A.3
Greiner, R.A.4
Autenried, P.5
Aguet, M.6
Weissmann, C.7
-
8
-
-
0022395728
-
Low temperature embedding with Lowicryl resins: Two new formulations and some applications
-
Carlemalm E, Villiger W, Hobot J, Acetarin J, Kellenberger E (1985) Low temperature embedding with Lowicryl resins: two new formulations and some applications. J Microsc 140: 55-72
-
(1985)
J Microsc
, vol.140
, pp. 55-72
-
-
Carlemalm, E.1
Villiger, W.2
Hobot, J.3
Acetarin, J.4
Kellenberger, E.5
-
9
-
-
0025991466
-
The scrapie-associated form of PrP is made from a cell surface precursor that is both protease and phopholipase sensitive
-
Caughey B, Raymond GJ (1991) The scrapie-associated form of PrP is made from a cell surface precursor that is both protease and phopholipase sensitive. J Biol Chem 266:18217-18223
-
(1991)
J Biol Chem
, vol.266
, pp. 18217-18223
-
-
Caughey, B.1
Raymond, G.J.2
-
10
-
-
0027997387
-
Prion protein is necessary for normal synaptic function
-
Collinge J, Whittington M, Sidle K, Smith C, Palmer M, Clarke A, Jefferys J (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.2
Sidle, K.3
Smith, C.4
Palmer, M.5
Clarke, A.6
Jefferys, J.7
-
11
-
-
0023235753
-
Changes in the localization of brain prion proteins during scrapie infection
-
DeArmond SJ, Mobley W, DeMott D, Barry R, Beckstead J, Prusiner SB (1987) Changes in the localization of brain prion proteins during scrapie infection. Neurology 87:1271-1280
-
(1987)
Neurology
, vol.87
, pp. 1271-1280
-
-
DeArmond, S.J.1
Mobley, W.2
DeMott, D.3
Barry, R.4
Beckstead, J.5
Prusiner, S.B.6
-
12
-
-
0025967257
-
-
Diedrich JF, Bendheim PE, Kim YS, Carp RI, Haase HT (1994) Proc Natl Acad Sci USA 88 : 375-379.
-
(1994)
Proc Natl Acad Sci USA
, vol.88
, pp. 375-379
-
-
Diedrich, J.F.1
Bendheim, P.E.2
Kim, Y.S.3
Carp, R.I.4
Haase, H.T.5
-
13
-
-
0026328066
-
Analysis of human mitochondria transcripts using electron microscopic in situ hybridization
-
Escaig-Haye F, Grigoriev V, Peranzi G, Lestienne P, Fournier J-G (1991) Analysis of human mitochondria transcripts using electron microscopic in situ hybridization. J Cell Sci 100:851-862
-
(1991)
J Cell Sci
, vol.100
, pp. 851-862
-
-
Escaig-Haye, F.1
Grigoriev, V.2
Peranzi, G.3
Lestienne, P.4
Fournier, J.-G.5
-
14
-
-
0026936077
-
Ultrastructural localization of HIV-1 RNA and core proteins. Simultaneous visualization using double immunogold labelling after in situ hybridization and immunocytochemistry
-
Escaig-Haye F, Grigoriev V, Sharova I, Rudneva V, Buckrinskaya A, Fournier J-G (1992) Ultrastructural localization of HIV-1 RNA and core proteins. Simultaneous visualization using double immunogold labelling after in situ hybridization and immunocytochemistry. J Submicrosc Cytol Pathol 24:437-443
-
(1992)
J Submicrosc Cytol Pathol
, vol.24
, pp. 437-443
-
-
Escaig-Haye, F.1
Grigoriev, V.2
Sharova, I.3
Rudneva, V.4
Buckrinskaya, A.5
Fournier, J.-G.6
-
15
-
-
0029112533
-
Ultrastructural localization of cellular prion protein (PrPc) in synaptic boutons of normal hamster hippocampus
-
Fournier JG, Escaig-Haye F, Billette de Villemeur T, Robain O (1995) Ultrastructural localization of cellular prion protein (PrPc) in synaptic boutons of normal hamster hippocampus. CR Acad Sci III 318:339-344
-
(1995)
CR Acad Sci III
, vol.318
, pp. 339-344
-
-
Fournier, J.G.1
Escaig-Haye, F.2
Billette De Villemeur, T.3
Robain, O.4
-
16
-
-
0023566948
-
Evidence for a secretory form of the cellular prion protein
-
Hay B, Prusiner SB, Lingappa VR (1987) Evidence for a secretory form of the cellular prion protein. Biochemistry 26:8110-8115
-
(1987)
Biochemistry
, vol.26
, pp. 8110-8115
-
-
Hay, B.1
Prusiner, S.B.2
Lingappa, V.R.3
-
17
-
-
0028874995
-
A cellular form of prion protein PrPc exists in many non-neuronal tissues of sheep
-
Horiuchi M, Yamazaki N, Ikeda T, Ishiguro N, Shinagawa M (1995) A cellular form of prion protein PrPc exists in many non-neuronal tissues of sheep. J Gen Virol 76:2583-2587
-
(1995)
J Gen Virol
, vol.76
, pp. 2583-2587
-
-
Horiuchi, M.1
Yamazaki, N.2
Ikeda, T.3
Ishiguro, N.4
Shinagawa, M.5
-
18
-
-
0026751775
-
Abnormal isoform of prion proteins accumulates in the synaptic structures of the central nervous system in patients with Creutzfeldt-Jakob disease
-
Kitamoto T, Shin RW, Doh-ura K, Tomokane N, Miyazono M, Muramoto T, Tateishi J (1992) Abnormal isoform of prion proteins accumulates in the synaptic structures of the central nervous system in patients with Creutzfeldt-Jakob disease. Am J Pathol 140:1285-1294
-
(1992)
Am J Pathol
, vol.140
, pp. 1285-1294
-
-
Kitamoto, T.1
Shin, R.W.2
Doh-ura, K.3
Tomokane, N.4
Miyazono, M.5
Muramoto, T.6
Tateishi, J.7
-
20
-
-
0025910229
-
Molecular biology of prion diseases
-
Prusiner SB (1991) Molecular biology of prion diseases. Science 252:1515-1522
-
(1991)
Science
, vol.252
, pp. 1515-1522
-
-
Prusiner, S.B.1
-
21
-
-
0028132226
-
Biology and genetics of prion diseases
-
Prusiner SB (1994) Biology and genetics of prion diseases. Annu Rev Microbiol 48:655-686
-
(1994)
Annu Rev Microbiol
, vol.48
, pp. 655-686
-
-
Prusiner, S.B.1
-
22
-
-
13344282734
-
Loss of cerebellar Purkinje cells in aged mice homozygous for a disrupted PrP gene
-
Sakaguchin S, Katamine S, Nishida N, Moriuchi R, Shigenatsu K, Sugimoto T, Nakatari A, Kataoka Y, Houtani T, Shirabe S, Okada H, Hasegawa S, Miyamoto T, Noda T (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
-
-
Sakaguchin, S.1
Katamine, S.2
Nishida, N.3
Moriuchi, R.4
Shigenatsu, K.5
Sugimoto, T.6
Nakatari, A.7
Kataoka, Y.8
Houtani, T.9
Shirabe, S.10
Okada, H.11
Hasegawa, S.12
Miyamoto, T.13
Noda, T.14
-
23
-
-
0028305135
-
A glycolipid-anchored prion protein is endocytosed via clathrin-couted pits
-
Show-Ling, S, Heuser, JE, Harris DA (1994) A glycolipid-anchored prion protein is endocytosed via clathrin-couted pits. J Cell Biol 125:1239-1250
-
(1994)
J Cell Biol
, vol.125
, pp. 1239-1250
-
-
Show-Ling, S.1
Heuser, J.E.2
Harris, D.A.3
-
24
-
-
0025339439
-
Differential release of cellular and scrapie prion protein from cellular membranes by phosphatidylinositol-specific phospholipase C
-
Stahl N, Borchelt DR, Prusiner SB (1990) Differential release of cellular and scrapie prion protein from cellular membranes by phosphatidylinositol-specific phospholipase C. Biochemistry 29:5405-5412
-
(1990)
Biochemistry
, vol.29
, pp. 5405-5412
-
-
Stahl, N.1
Borchelt, D.R.2
Prusiner, S.B.3
-
25
-
-
0026683652
-
A soluble form of prion protein in human cerebrospinal fluid: Implications for prion-relaled encephalopathies
-
Tagliavini F, Pirelli F, Porro M, Salmona M, Bugiani O, Frangione B (1992) A soluble form of prion protein in human cerebrospinal fluid: implications for prion-relaled encephalopathies. Biochem Biophys Res Commun 184:1398-1404
-
(1992)
Biochem Biophys Res Commun
, vol.184
, pp. 1398-1404
-
-
Tagliavini, F.1
Pirelli, F.2
Porro, M.3
Salmona, M.4
Bugiani, O.5
Frangione, B.6
-
26
-
-
0025373111
-
Scrapie prion proteins accumulate in the cytoplasm of persistently infected cultured cells
-
Taraboulos A, Serban D, Prusiner SB (1990) Scrapie prion proteins accumulate in the cytoplasm of persistently infected cultured cells. J Cell Biol 110:2117-2132
-
(1990)
J Cell Biol
, vol.110
, pp. 2117-2132
-
-
Taraboulos, A.1
Serban, D.2
Prusiner, S.B.3
-
27
-
-
0026644090
-
Regional mapping of prion proteins in brains
-
Taraboulos A, Jendroska K, Serban D, Yang S, DeArmond SJ, Prusiner SB (1992) Regional mapping of prion proteins in brains. Proc Natl Acad Sci USA 89:7620-7624
-
(1992)
Proc Natl Acad Sci USA
, vol.89
, pp. 7620-7624
-
-
Taraboulos, A.1
Jendroska, K.2
Serban, D.3
Yang, S.4
DeArmond, S.J.5
Prusiner, S.B.6
-
28
-
-
0028882424
-
Prion propagation in mice expressing human and chimeric PrP transgenes implicates the interaction of cellular PrP with another protein
-
Telling GC, Scott M, Masrianni J, Gabizon R, Torchia M, Cohen FE. DeArmond SJ, Prusiner SB (1995) Prion propagation in mice expressing human and chimeric PrP transgenes implicates the interaction of cellular PrP with another protein. Cell 83:79-90
-
(1995)
Cell
, vol.83
, pp. 79-90
-
-
Telling, G.C.1
Scott, M.2
Masrianni, J.3
Gabizon, R.4
Torchia, M.5
Cohen, F.E.6
DeArmond, S.J.7
Prusiner, S.B.8
|