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Nodes: 640,
Authors: 911,
Journals: 148,
Outer References: 6859,
Words: 1343
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Collection span: 1965 - 2006
| View: Overview | Sorted by year, source, volume, issue, page. |
Page 5 of 7: [ 1 2 3 4 5 6 7 ]
| # | LCR | NCR | Node / Date / Journal / Author | LCS | GCS |
|---|---|---|---|---|---|
| 401 | 0 | 0 | 401 1995 JOURNAL OF CELLULAR BIOCHEMISTRY : 277-277 PRUSINER SB MOLECULAR PATHOGENESIS OF PRION DISEASES | 0 | 0 |
| 402 | 33 | 99 | 402 1995 JOURNAL OF MOLECULAR BIOLOGY 245 (4): 362-374 SCHATZL HM; DACOSTA M; TAYLOR L; COHEN FE; PRUSINER SB PRION PROTEIN GENE VARIATION AMONG PRIMATES | 29 | 142 |
| 403 | 22 | 42 | 403 1995 JOURNAL OF MOLECULAR BIOLOGY 250 (4): 514-526 ZHANG H; KANEKO K; NGUYEN JT; LIVSHITS TL; BALDWIN MA; et al. CONFORMATIONAL TRANSITIONS IN PEPTIDES CONTAINING 2 PUTATIVE ALPHA-HELICES OF THE PRION PROTEIN | 37 | 136 |
| 404 | 21 | 41 | 404 1995 JOURNAL OF MOLECULAR BIOLOGY 252 (4): 412-422 NGUYEN JT; INOUYE H; BALDWIN MA; FLETTERICK RJ; COHEN FE; et al. X-RAY-DIFFRACTION OF SCRAPIE PRION RODS AND PRP PEPTIDES | 14 | 77 |
| 405 | 0 | 0 | 405 1995 JOURNAL OF NEUROPATHOLOGY AND EXPERIMENTAL NEUROLOGY 54 (3): 415-415 QIU Y; NINCHAKCASEY A; YEHIELY F; PRUSINER SB; DEARMOND SJ BRAIN REGION DIFFERENCES IN PRION PROTEIN-STRUCTURE AND SELECTIVE VULNERABILITY OF NEURONS IN SCRAPIE | 0 | 0 |
| 406 | 0 | 0 | 406 1995 JOURNAL OF NEUROPATHOLOGY AND EXPERIMENTAL NEUROLOGY 54 (3): 416-416 WONG K; QIU Y; VANCLEF J; PRUSINER SB; DEARMOND SJ SCRAPIE PRIONS CAUSE DECREASED MEMBRANE FLUIDITY IN CULTURED-CELLS | 0 | 1 |
| 407 | 19 | 52 | 407 1995 MECHANISMS OF DEVELOPMENT 51 (2-3): 317-327 RAEBER AJ; MURAMOTO T; KORNBERG TB; PRUSINER SB EXPRESSION AND TARGETING OF SYRIAN-HAMSTER PRION PROTEIN-INDUCED BY HEAT-SHOCK IN TRANSGENIC DROSOPHILA-MELANOGASTER | 1 | 10 |
| 408 | 5 | 45 | 408 1995 MOLECULAR MEDICINE 1 (6): 607-613 SPUDICH S; MASTRIANNI JA; WRENSCH M; GABIZON R; MEINER Z; et al. COMPLETE PENETRANCE OF CREUTZFELDT-JAKOB-DISEASE IN LIBYAN JEWS CARRYING THE E200K MUTATION IN THE PRION PROTEIN GENE | 15 | 35 |
| 409 | 0 | 0 | 409 1995 NEUROLOGY 45 (4): A201-A201 MASTRIANNI JA; IANNICOLA C; MYERS R; PRUSINER SB IDENTIFICATION OF A NEW MUTATION OF THE PRION PROTEIN GENE AT CODON-208 IN A PATIENT WITH CREUTZFELDT-JAKOB-DISEASE | 0 | 2 |
| 410 | 0 | 0 | 410 1995 NEUROLOGY 45 (4): A308-A308 TELLING GC; FOSTER D; YANG SL; DEARMOND SJ; PRUSINER SB TRANSGENIC MICE EXPRESSING HUMAN AND CHIMERIC HUMAN-MOUSE PRION PROTEINS CARRYING THE CODON-102 MUTATION OF GSS | 0 | 0 |
| # | LCR | NCR | Node / Date / Journal / Author | LCS | GCS |
| 411 | 11 | 43 | 411 1995 NEUROLOGY 45 (11): 2042-2050 MASTRIANNI JA; CURTIS MT; OBERHOLTZER JC; DACOSTA MM; DEARMOND S; et al. PRION DISEASE (PRP-A117V) PRESENTING WITH ATAXIA INSTEAD OF DEMENTIA | 4 | 35 |
| 412 | 17 | 46 | 412 1995 PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA 92 (7): 2944-2948 TATZELT J; ZUO JR; VOELLMY R; SCOTT M; HARTL U; et al. SCRAPIE PRIONS SELECTIVELY MODIFY THE STRESS-RESPONSE IN NEUROBLASTOMA-CELLS | 18 | 63 |
| 413 | 22 | 45 | 413 1995 PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA 92 (24): 11160-11164 KANEKO K; PERETZ D; PAN KM; BLOCHBERGER TC; WILLE H; et al. PRION PROTEIN (PRP) SYNTHETIC PEPTIDES INDUCE CELLULAR PRP TO ACQUIRE PROPERTIES OF THE SCRAPIE ISOFORM | 18 | 82 |
| 414 | 2 | 6 | 414 1995 SCIENTIFIC AMERICAN 272 (1): 48-& PRUSINER SB THE PRION DISEASES | 4 | 47 |
| 415 | 25 | 50 | 415 1996 BIOCHEMISTRY 35 (17): 5528-5537 Mehlhorn I; Groth D; Stockel J; Moffat B; Reilly D; et al. High-level expression and characterization of a purified 142-residue polypeptide of the prion protein | 41 | 115 |
| 416 | 1 | 28 | 416 1996 CHEMICAL PHYSICS LETTERS 251 (3-4): 223-229 Heller J; Larsen R; Ernst M; Kolbert AC; Baldwin M; et al. Application of rotational resonance to inhomogeneously broadened systems | 1 | 15 |
| 417 | 83 | 245 | 417 1996 COLD SPRING HARBOR SYMPOSIA ON QUANTITATIVE BIOLOGY 61: 473-493 Prusiner SB Molecular biology and genetics of prion diseases | 0 | 10 |
| 418 | 45 | 97 | 418 1996 COLD SPRING HARBOR SYMPOSIA ON QUANTITATIVE BIOLOGY 61: 495-509 Bamborough P; Wille H; Telling GC; Yehiely F; Prusiner SB; et al. Prion protein structure and scrapie replication: Theoretical, spectroscopic, and genetic investigations | 14 | 28 |
| 419 | 26 | 57 | 419 1996 COLD SPRING HARBOR SYMPOSIA ON QUANTITATIVE BIOLOGY 61: 531-540 DeArmond SJ; Qiu Y; Wong K; Nixon R; Hyun W; et al. Abnormal plasma membrane properties and functions in prion-infected cell lines | 0 | 2 |
| 420 | 31 | 68 | 420 1996 EMBO JOURNAL 15 (23): 6363-6373 Tatzelt J; Prusiner SB; Welch WJ Chemical chaperones interfere with the formation of scrapie prion protein | 10 | 108 |
| # | LCR | NCR | Node / Date / Journal / Author | LCS | GCS |
| 421 | 26 | 59 | 421 1996 FOLDING & DESIGN 1 (1): 13-19 Huang ZW; Prusiner SB; Cohen FE Scrapie prions: A three-dimensional model of an infectious fragment | 26 | 101 |
| 422 | 1 | 1 | 422 1996 FOLDING & DESIGN 1 (5): 406-406 Huang ZW; Prusiner SB; Cohen FE Scrapie prions: A three-dimensional model of an infectious fragment (vol 1, pg 13, 1996) | 0 | 1 |
| 423 | 27 | 58 | 423 1996 GENES & DEVELOPMENT 10 (14): 1736-1750 Telling GC; Haga T; Torchia M; Tremblay P; DeArmond SJ; et al. Interactions between wild-type and mutant prion proteins modulate neurodegeneration transgenic mice | 42 | 117 |
| 424 | 21 | 61 | 424 1996 JOURNAL OF MOLECULAR BIOLOGY 259 (4): 608-621 Wille H; Zhang GF; Baldwin MA; Cohen FE; Prusiner SB Separation of scrapie prion infectivity from PrP amyloid polymers | 15 | 53 |
| 425 | 15 | 55 | 425 1996 JOURNAL OF NEUROCHEMISTRY 66 (1): 277-285 Guan ZZ; Soderberg M; Sindelar P; Prusiner SB; Kristensson K; et al. Lipid composition in scrapie-infected mouse brain: Prion infection increases the levels of dolichyl phosphate and ubiquinone | 0 | 21 |
| 426 | 0 | 0 | 426 1996 JOURNAL OF NEUROPATHOLOGY AND EXPERIMENTAL NEUROLOGY 55 (5): 122-122 Qiu Y; Nixon R; Mobley WB; Prusiner SB; DeArmond SJ Abnormalities of the plasma membrane and endocytosis in prion-infected cell lines. | 0 | 0 |
| 427 | 0 | 0 | 427 1996 JOURNAL OF NEUROPATHOLOGY AND EXPERIMENTAL NEUROLOGY 55 (5): 225-225 Nixon R; Mastrianni J; Roberts J; Prusiner SB; DeArmond S Sporadic occurrence of fatal thalamic insomnia without a prion protein gene mutation. | 0 | 0 |
| 428 | 21 | 51 | 428 1996 JOURNAL OF VIROLOGY 70 (3): 1714-1722 Riesner D; Kellings K; Post K; Wille H; Serban H; et al. Disruption of prion rods generates 10-nm spherical particles having high alpha-helical content and lacking scrapie infectivity | 11 | 61 |
| 429 | 41 | 131 | 429 1996 MEDICINAL RESEARCH REVIEWS 16 (5): 487-505 Prusiner SB Prion biology and diseases - Laughing cannibals, mad cows, and scientific heresy | 0 | 9 |
| 430 | 0 | 0 | 430 1996 MOLECULAR BIOLOGY OF THE CELL 7: 522-522 Vey M; Pilkuhn S; Wille H; Anderson RGW; Prusiner SB Detergent-resistant, glycosphingolipid-enriched, membranous microdomains contain both the cellular and scrapie prion proteins. | 0 | 0 |
| # | LCR | NCR | Node / Date / Journal / Author | LCS | GCS |
| 431 | 0 | 0 | 431 1996 MOLECULAR BIOLOGY OF THE CELL 7: 1565-1565 Kaneko K; Vey M; Scott M; Pilkuhn S; Prusiner SB COOH-terminal signals of the cellular prion protein direct subcellular trafficking and control conversion into the scrapie isoform. | 0 | 0 |
| 432 | 0 | 0 | 432 1996 MOLECULAR BIOLOGY OF THE CELL 7: 1566-1566 Meiner Z; Vey M; Pilkuhn S; Prusiner SB Fusion of prion protein to green fluorescent protein facilitates subcellular localization. | 0 | 0 |
| 433 | 0 | 0 | 433 1996 MOLECULAR BIOLOGY OF THE CELL 7: 2522-2522 Wille H; Prusiner SB Solubilization of infectious prion rods containing PrP 27-30 using combinations of organic solvents and detergents. | 0 | 0 |
| 434 | 0 | 0 | 434 1996 MOLECULAR BIOLOGY OF THE CELL 7: 3788-3788 Telling GC; Tremblay P; Torchia M; DeArmond SJ; Cohen FE; et al. N-terminally tagged prion protein supports prion propagation in transgenic mice | 0 | 0 |
| 435 | 26 | 55 | 435 1996 NATURE AND ORIGIN OF AMYLOID FIBRILS 199: 181-201 Wille H; Baldwin MA; Cohen FE; DeArmond SJ; Prusiner SB; et al. Prion protein amyloid: Separation of scrapie infectivity from PrP polymers | 1 | 5 |
| 436 | 18 | 47 | 436 1996 NATURE MEDICINE 2 (1): 59-64 Gabizon R; Telling G; Meiner Z; Halimi H; Kahana I; et al. Insoluble wild-type and protease-resistant mutant prion protein in brains of patients with inherited prion disease | 10 | 47 |
| 437 | 0 | 0 | 437 1996 NEUROLOGY 46 (2): 1004-1004 Kaneko K; Peretz D; Pan KM; Blochberger TC; Gabizon R; et al. Prion protein (PrP) synthetic peptides induce cellular PrP to acquire properties of the scrapie isoform | 0 | 0 |
| 438 | 0 | 0 | 438 1996 NEUROLOGY 46 (2): 3085-3085 Telling GC; Mastrianni JA; DeArmond SJ; Prusiner SB Exploring mechanisms of prion propagation using mice expressing human and chimeric mouse human prion protein transgenes | 0 | 0 |
| 439 | 0 | 0 | 439 1996 NEUROLOGY 46 (2): 3086-3086 Scott MR; Groth D; Prusiner SB Differential impact of variations in prion protein (PrP) primary structure on susceptibility to different scrapie prion strains | 0 | 0 |
| 440 | 0 | 0 | 440 1996 NEUROLOGY 46 (2): 4098-4098 Mastrianni JA; Prusiner SB The prevalence of heritable prion disease is underestimated by clinical assessment | 0 | 0 |
| # | LCR | NCR | Node / Date / Journal / Author | LCS | GCS |
| 441 | 0 | 0 | 441 1996 NEUROLOGY 46 (2): 73006-73006 Bosque P; Telling GC; Westaway D; Cayetano J; DeArmond SJ; et al. Prion protein overexpression exclusively in skeletal muscle causes spontaneous myopathy | 0 | 0 |
| 442 | 20 | 56 | 442 1996 NEUROLOGY 47 (2): 449-453 Tatzelt J; Maeda N; Pekny M; Yang SL; Betsholtz C; et al. Scrapie in mice deficient in apolipoprotein E or glial fibrillary acidic protein | 4 | 18 |
| 443 | 23 | 67 | 443 1996 NEUROLOGY 47 (3): 741-750 Wong K; Qiu Y; Hyun W; Nixon R; VanCleff J; et al. Decreased receptor-mediated calcium response in prion-infected cells correlates with decreased membrane fluidity and IP3 release | 7 | 38 |
| 444 | 17 | 54 | 444 1996 NEUROLOGY 47 (5): 1305-1312 Mastrianni JA; Iannicola C; Myers RM; DeArmond S; Prusiner SB Mutation of the prion protein gene at codon 208 in familial Creutzfeldt-Jakob disease | 0 | 23 |
| 445 | 7 | 37 | 445 1996 NEUROREPORT 7 (12): 1887-1892 Diez M; Koistinaho J; DeArmond SJ; Camerino AP; Groth D; et al. Aberrant induction of neuropeptide Y mRNA in hippocampal CA3 pyramidal neurones in scrapie-infected mice | 3 | 5 |
| 446 | 34 | 118 | 446 1996 PRIONS PRIONS PRIONS 207: 1-17 Prusiner SB Human prion diseases and neurodegeneration | 1 | 29 |
| 447 | 23 | 79 | 447 1996 PRIONS PRIONS PRIONS 207: 49-67 Huang Z; Prusiner SB; Cohen FE Structures of prion proteins and conformational models for prion diseases | 1 | 20 |
| 448 | 46 | 134 | 448 1996 PRIONS PRIONS PRIONS 207: 95-123 Scott MRD; Telling GC; Prusiner SB Transgenetics and gene targeting in studies of prion diseases | 0 | 4 |
| 449 | 38 | 80 | 449 1996 PRIONS PRIONS PRIONS 207: 125-146 DeArmond SJ; Prusiner SB Transgenetics and neuropathology of prion diseases | 1 | 3 |
| 450 | 10 | 30 | 450 1996 PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA 93 (6): 2403-2407 Lledo PM; Tremblay P; Dearmond SJ; Prusiner SB; Nicoll RA Mice deficient for prion protein exhibit normal neuronal excitability and synaptic transmission in the hippocampus | 19 | 115 |
| # | LCR | NCR | Node / Date / Journal / Author | LCS | GCS |
| 451 | 17 | 41 | 451 1996 PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA 93 (14): 7279-7282 Williamson RA; Peretz D; Smorodinsky N; Bastidas R; Serban H; et al. Circumventing tolerance to generate autologous monoclonal antibodies to the prion protein | 21 | 57 |
| 452 | 21 | 52 | 452 1996 PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA 93 (25): 14945-14949 Vey M; Pilkuhn S; Wille H; Nixon R; Dearmond SJ; et al. Subcellular colocalization of the cellular and scrapie prion proteins in caveolae-like membranous domains | 30 | 233 |
| 453 | 33 | 59 | 453 1996 PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA 93 (26): 15457-15462 Muramoto T; Scott M; Cohen FE; Prusiner SB Recombinant scrapie-like prion protein of 106 amino acids is soluble | 29 | 94 |
| 454 | 21 | 53 | 454 1996 PROTEIN SCIENCE 5 (8): 1655-1661 Heller J; Kolbert AC; Larsen R; Ernst M; Bekker T; et al. Solid-state NMR studies of the prion protein H1 fragment | 7 | 56 |
| 455 | 15 | 53 | 455 1996 SCIENCE 274 (5295): 2079-2082 Telling GC; Parchi P; DeArmond SJ; Cortelli P; Montagna P; et al. Evidence for the conformation of the pathologic isoform of the prion protein enciphering and propagating prion diversity | 54 | 301 |
| 456 | 0 | 1 | 456 1996 SEMINARS IN VIROLOGY 7 (3): 157-157 Prusiner SB Introduction: Prion diseases | 0 | 6 |
| 457 | 49 | 150 | 457 1996 SEMINARS IN VIROLOGY 7 (3): 159-173 Prusiner SB; Telling G; Cohen FE; DeArmond SJ Prion diseases of humans and animals | 0 | 23 |
| 458 | 45 | 134 | 458 1996 TRANSGENIC MODELS OF HUMAN VIRAL AND IMMUNOLOGICAL DISEASE 206: 275-304 Prusiner SB Transgenetics of prion diseases | 1 | 8 |
| 459 | 35 | 79 | 459 1996 TRENDS IN BIOCHEMICAL SCIENCES 21 (12): 482-487 Prusiner SB Molecular biology and pathogenesis of prion diseases | 5 | 134 |
| 460 | 0 | 0 | 460 1997 ANNALS OF NEUROLOGY 42 (6): 986-986 Bosque PJ; Telling GC; Cayetano J; DeArmond SJ; Prusiner SB Evidence for prion replication in skeletal muscle. | 0 | 1 |
| # | LCR | NCR | Node / Date / Journal / Author | LCS | GCS |
| 461 | 0 | 0 | 461 1997 ANNALS OF NEUROLOGY 42 (6): 986-987 Kaneko K; Zulianello L; Scott M; Cooper CM; Wallace AC; et al. During scrapie prion propagation protein X binds a discontinuous epitope on the cellular prion protein. | 0 | 0 |
| 462 | 72 | 220 | 462 1997 ANNUAL REVIEW OF GENETICS 31: 139-175 Prusiner SB; Scott MR Genetics of prions | 2 | 64 |
| 463 | 20 | 47 | 463 1997 BIOCHEMISTRY 36 (12): 3543-3553 Zhang H; Stockel J; Mehlhorn I; Groth D; Baldwin MA; et al. Physical studies of conformational plasticity in a recombinant prion protein | 19 | 111 |
| 464 | 17 | 40 | 464 1997 CHEMISTRY & BIOLOGY 4 (5): 345-355 Lundberg KM; Stenland CJ; Cohen FE; Prusiner SB; Millhauser GL Kinetics and mechanism of amyloid formation by the prion protein H1 peptide as determined by time-dependent ESR | 0 | 26 |
| 465 | 31 | 51 | 465 1997 CURRENT OPINION IN STRUCTURAL BIOLOGY 7 (1): 53-59 Harrison PM; Bamborough P; Daggett V; Prusiner SB; Cohen FE The prion folding problem | 4 | 101 |
| 466 | 0 | 0 | 466 1997 FASEB JOURNAL 11 (9): A972-A972 Wille H; Prusiner SB Solubilization and crystallization of the N-terminally truncated scrapie prion protein (PrP 27-30) | 0 | 0 |
| 467 | 0 | 0 | 467 1997 JOURNAL OF ALLERGY AND CLINICAL IMMUNOLOGY 99 (1): 902-902 Peretz D; Williamson A; Matsunaga Y; Burton DR; Prusiner SB Isolation of recombinant antibodies to pathogenic PrPSc. | 0 | 0 |
| 468 | 1 | 1 | 468 1997 JOURNAL OF MOLECULAR BIOLOGY 265 (2): 257-257 Schatzl HM; DaCosta M; Taylor L; Cohen FE; Prusiner SB Prion protein gene variation among primates (vol 245, pg 362, 1995) | 0 | 3 |
| 469 | 31 | 56 | 469 1997 JOURNAL OF MOLECULAR BIOLOGY 270 (4): 574-586 Kaneko K; Wille H; Mehlhorn I; Zhang H; Ball H; et al. Molecular properties of complexes formed between the prion protein and synthetic peptides | 9 | 29 |
| 470 | 23 | 43 | 470 1997 JOURNAL OF MOLECULAR BIOLOGY 273 (3): 614-622 Peretz D; Williamson RA; Matsunaga Y; Serban H; Pinilla C; et al. A conformational transition at the N terminus of the prion protein features in formation of the scrapie isoform | 39 | 148 |
| # | LCR | NCR | Node / Date / Journal / Author | LCS | GCS |
| 471 | 0 | 0 | 471 1997 JOURNAL OF NEUROCHEMISTRY 69: S105-S105 Baldwin MA; Prusiner SB Prion diseases as models for therapeutic strategies in amyloid diseases. | 0 | 0 |
| 472 | 0 | 0 | 472 1997 JOURNAL OF NEUROVIROLOGY 3: S21-S21 Prusiner SB Structural biology and genetics of prions | 0 | 1 |
| 473 | 4 | 21 | 473 1997 JOURNAL OF VIROLOGY 71 (3): 2342-2345 Carlson GA; Banks S; Lund D; Reichert C; Groth D; et al. Failure to transmit disease from gray tremor mutant mice | 0 | 0 |
| 474 | 17 | 64 | 474 1997 JOURNAL OF VIROLOGY 71 (11): 8821-8831 Schatzl HM; Laszlo L; Holtzman DM; Tatzelt J; Dearmond SJ; et al. A hypothalamic neuronal cell line persistently infected with scrapie prions exhibits apoptosis | 4 | 75 |
| 475 | 36 | 90 | 475 1997 JOURNAL OF VIROLOGY 71 (12): 9032-9044 Scott MR; Groth D; Tatzelt J; Torchia M; Tremblay P; et al. Propagation of prion strains through specific conformers of the prion protein | 19 | 41 |
| 476 | 21 | 87 | 476 1997 MEDICINE 76 (4): 227-237 Meiner Z; Gabizon R; Prusiner SB Familial Creutzfeldt-Jakob disease - Codon 200 prion disease in Libyan Jews | 1 | 21 |
| 477 | 0 | 0 | 477 1997 MOLECULAR BIOLOGY OF THE CELL 8: 571-571 Kaneko K; Zulianello L; Scott M; Cooper CM; Wallace AC; et al. Protein X binds to a discontinuous epitope on the cellular prion protein during scrapie prion propagation | 0 | 0 |
| 478 | 22 | 40 | 478 1997 NATURE MEDICINE 3 (7): 750-755 Muramoto T; DeArmond SJ; Scott M; Telling GC; Cohen FE; et al. Heritable disorder resembling neuronal storage disease in mice expressing prion protein with deletion of an alpha-helix | 12 | 46 |
| 479 | 24 | 77 | 479 1997 NEUROBIOLOGY OF DISEASE 3 (4): 339-355 Yehiely F; Bamborough P; DaCosta M; Perry BJ; Thinakaran G; et al. Identification of candidate proteins binding to prion protein | 8 | 54 |
| 480 | 0 | 0 | 480 1997 NEUROLOGY 48 (3): 3044-3044 Muramoto T; DeArmond SJ; Scott M; Cohen FE; Prusiner SB Heritable neuronal storage disease in mice expressing prion protein with deletion of an alpha-helix | 0 | 0 |
| # | LCR | NCR | Node / Date / Journal / Author | LCS | GCS |
| 481 | 0 | 0 | 481 1997 NEUROLOGY 48 (3): 5034-5034 Meiner Z; Yanai A; Telling G; Halimi M; Taraboulos A; et al. Prion protein with the E200K mutation exhibits properties similar to the cellular isoform PrPC | 0 | 0 |
| 482 | 0 | 0 | 482 1997 NEUROLOGY 48 (3): 5036-5036 Mastrianni JA; Nixon R; Layzer R; DeArmond SJ; Prusiner SB Fatal sporadic insomnia (FSI): Fatal familial insomnia (FFI) phenotype without a mutation of the prion protein (PrP) gene | 0 | 0 |
| 483 | 40 | 83 | 483 1997 NEURON 19 (6): 1337-1348 DeArmond SJ; Sanchez H; Yehiely F; Qiu Y; Ninchak-Casey A; et al. Selective neuronal targeting in prion disease | 14 | 88 |
| 484 | 0 | 0 | 484 1997 NEUROSCIENCE LETTERS : S35-S35 Meiner Z; Rosental Y; Vey M; Pilkuhn S; Prusiner SB Fusion of prion protein to green-fluorescent protein facilitates subcellular localization | 0 | 0 |
| 485 | 21 | 50 | 485 1997 PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA 94 (6): 2333-2338 Kaneko K; Vey M; Scott M; Pilkuhn S; Cohen FE; et al. COOH-terminal sequence of the cellular prion protein directs subcellular trafficking and controls conversion into the scrapie isoform | 23 | 131 |
| 486 | 21 | 45 | 486 1997 PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA 94 (19): 10069-10074 Kaneko K; Zulianello L; Scott M; Cooper CM; Wallace AC; et al. Evidence for protein X binding to a discontinuous epitope on the cellular prion protein during scrapie prion propagation | 45 | 214 |
| 487 | 24 | 60 | 487 1997 PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA 94 (19): 10086-10091 James TL; Liu H; Ulyanov NB; FarrJones S; Zhang H; et al. Solution structure of a 142-residue recombinant prion protein corresponding to the infectious fragment of the scrapie isoform | 46 | 229 |
| 488 | 8 | 58 | 488 1997 PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA 94 (24): 13267-13272 Diez M; Koistinaho J; Dearmond SJ; Groth D; Prusiner SB; et al. Marked decrease of neuropeptide Y Y2 receptor binding sites in the hippocampus in murine prion disease | 2 | 13 |
| 489 | 12 | 48 | 489 1997 PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA 94 (25): 13452-13457 Donne DG; Viles JH; Groth D; Mehlhorn I; James TL; et al. Structure of the recombinant full-length hamster prion protein PrP(29-231): The N terminus is highly flexible | 42 | 315 |
| 490 | 27 | 69 | 490 1997 PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA 94 (26): 14279-14284 Scott MR; Safar J; Telling G; Nguyen O; Groth D; et al. Identification of a prion protein epitope modulating transmission of bovine spongiform encephalopathy prions to transgenic mice | 10 | 52 |
| # | LCR | NCR | Node / Date / Journal / Author | LCS | GCS |
| 491 | 30 | 80 | 491 1997 PROTEIN ENGINEERING 10 (12): 1465-1473 Blochberger TC; Cooper C; Peretz D; Tatzelt J; Griffith OH; et al. Prion protein expression in Chinese hamster ovary cells using a glutamine synthetase selection and amplification system | 3 | 19 |
| 492 | 28 | 42 | 492 1997 PROTEIN SCIENCE 6 (4): 825-833 Telling GC; Tremblay P; Torchia M; Dearmond SJ; Cohen FE; et al. N-terminally tagged prion protein supports prion propagation in transgenic mice | 1 | 7 |
| 493 | 55 | 181 | 493 1997 SCIENCE 278 (5336): 245-251 Prusiner SB Prion diseases and the BSE crisis | 26 | 402 |
| 494 | 0 | 0 | 494 1998 ANNALS OF NEUROLOGY 44 (6): 990-990 Mastrianni JA; Nixon R; Layzer R; DeArmond S; Prusiner SB Prion protein conformation determines the clinical and pathological phenotype of fatal insomnia | 0 | 0 |
| 495 | 73 | 146 | 495 1998 ANNUAL REVIEW OF BIOCHEMISTRY 67: 793-+ Cohen FE; Prusiner SB Pathologic conformations of prion proteins | 28 | 213 |
| 496 | 40 | 64 | 496 1998 BIOCHEMICAL SOCIETY TRANSACTIONS 26 (3): 481-486 Baldwin MA; James TL; Cohen FE; Prusiner SB The three-dimensional structure of prion protein: implications for prion disease | 0 | 3 |
| 497 | 16 | 56 | 497 1998 BIOCHEMISTRY 37 (20): 7185-7193 Stockel J; Safar J; Wallace AC; Cohen FE; Prusiner SB Prion protein selectively binds copper(II) ions | 22 | 219 |
| 498 | 18 | 50 | 498 1998 BIOLOGICAL CHEMISTRY 379 (11): 1307-1317 Post K; Pitschke M; Schafer O; Wille H; Appel TR; et al. Rapid acquisition of beta-sheet structure in the prion protein prior to multimer formation | 3 | 43 |
| 499 | 57 | 175 | 499 1998 BRAIN PATHOLOGY 8 (3): 499-513 Prusiner SB The prion diseases | 0 | 67 |
| 500 | 3 | 131 | 500 1998 BRAIN RESEARCH REVIEWS 26 (2-3): 154-166 Hokfelt T; Broberger C; Zhang X; Diez M; Kopp J; et al. Neuropeptide Y: some viewpoints on a multifaceted peptide in the normal and diseased nervous system | 0 | 48 |
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