| Missing Links?: 57 Citation Matrix | Graphs | Glossary HistCite Guide About |
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 6 of 7: [ 1 2 3 4 5 6 7 ]
| # | LCR | NCR | Node / Date / Journal / Author | LCS | GCS |
|---|---|---|---|---|---|
| 501 | 39 | 94 | 501 1998 CELL 93 (3): 337-348 Prusiner SB; Scott MR; DeArmond SJ; Cohen FE Prion protein biology | 20 | 333 |
| 502 | 0 | 0 | 502 1998 FASEB JOURNAL 12 (8): A1398-A1398 Baldwin M; Whittal R; Ball H; Prusiner SB; Burlingame A Copper binding to the prion protein monitored by ESI-MS | 0 | 0 |
| 503 | 23 | 74 | 503 1998 GENOME RESEARCH 8 (10): 1022-1037 Lee IY; Westaway D; Smit AFA; Wang K; Seto J; et al. Complete genomic sequence and analysis of the prion protein gene region from three mammalian species | 4 | 64 |
| 504 | 20 | 35 | 504 1998 JOURNAL OF VIROLOGY 72 (11): 9413-9418 Williamson RA; Peretz D; Pinilla C; Ball H; Bastidas RB; et al. Mapping the prion protein using recombinant antibodies | 16 | 67 |
| 505 | 0 | 0 | 505 1998 MOLECULAR BIOLOGY OF THE CELL 9: 78A-78A Wille H; Guenebaut V; Kanyo Z; Stroud RM; Agard DA; et al. Crystallization of the scrapie prion protein from reverse micellar solutions. | 0 | 0 |
| 506 | 0 | 0 | 506 1998 MOLECULAR BIOLOGY OF THE CELL 9: 455A-455A Schlumpberger M; Wille H; Herskowitz I; Prusiner SB In vitro amyloid-like fibril formation by yeast Ure2p | 0 | 0 |
| 507 | 0 | 0 | 507 1998 MOLECULAR BIOLOGY OF THE CELL 9: 501A-501A Supattapone S; Muramoto T; Aagaard C; Peretz D; Wille H; et al. Propagation of infectious miniprions in transgenic mice expressing truncated and partially deleted PrP molecules. | 0 | 0 |
| 508 | 31 | 58 | 508 1998 NATURE MEDICINE 4 (10): 1157-1165 Safar J; Wille H; Itrri V; Groth D; Serban H; et al. Eight prion strains have PrPSc molecules with different conformations | 42 | 322 |
| 509 | 21 | 39 | 509 1998 NEUROLOGY 50 (1): A1-A10 DeArmond SJ; Mobley WC; DeMott DL; Barry RA; Beckstead JH; et al. Changes in the localization of brain prion proteins during scrapie infection (Reprinted from Neurology, vol 37, pg 1271-1280, 1987) | 0 | 0 |
| 510 | 0 | 0 | 510 1998 NEUROLOGY 50 (4): A235-A235 Meiner Z; Tremblay P; Heinrich C; Willis L; Galou M; et al. Regulation of the prion protein expression using the tetracycline gene regulatory system | 0 | 0 |
| # | LCR | NCR | Node / Date / Journal / Author | LCS | GCS |
| 511 | 42 | 90 | 511 1998 NEURONAL DEGENERATION AND REGENERATION: FROM BASIC MECHANISMS TO PROSPECTS FOR THERAPY 117: 421-434 Safer J; Prusiner SB Molecular studies of prion diseases | 0 | 0 |
| 512 | 0 | 0 | 512 1998 NEUROSCIENCE LETTERS : S28-S29 Meiner Z; Tremblay P; Gabizon R; Prusiner SB Transgenic mice expressing the E200K mutation of the prion protein develop spontaneous prion disease and produce prions de novo | 0 | 0 |
| 513 | 17 | 32 | 513 1998 PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA 95 (21): 12580-12585 Tremblay P; Meiner Z; Galou M; Heinrich C; Petromilli C; et al. Doxycycline control of prion protein transgene expression modulates prion disease in mice | 4 | 76 |
| 514 | 113 | 346 | 514 1998 PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA 95 (23): 13363-13383 Prusiner SB Prions | 30 | 1181 |
| 515 | 24 | 52 | 515 1998 SCIENCE 279 (5352): 827-834 Hegde RS; Mastrianni JA; Scott MR; DeFea KA; Tremblay P; et al. A transmembrane form of the prion protein in neurodegenerative disease | 17 | 234 |
| 516 | 22 | 78 | 516 1999 BIOCHEMISTRY 38 (17): 5362-5377 Liu H; Farr-Jones S; Ulyanov NB; Llinas M; Marqusee S; et al. Solution structure of Syrian hamster prion protein rPrP(90-231) | 16 | 102 |
| 517 | 0 | 0 | 517 1999 BIOPHYSICAL JOURNAL 76 (1): A258-A258 James TL; Liu H; Farr-Jones S; Ulyanov NB; Llinas M; et al. Solution structure of the cellular prion protein highlighting elements subject to transformation | 0 | 0 |
| 518 | 23 | 73 | 518 1999 BIOPHYSICAL JOURNAL 76 (2): 1048-1062 Wille H; Prusiner SB Ultrastructural studies on scrapie prion protein crystals obtained from reverse micellar solutions | 5 | 19 |
| 519 | 28 | 39 | 519 1999 CELL 96 (6): 869-878 Supattapone S; Bosque P; Muramoto T; Wille H; Aagaard C; et al. Prion protein of 106 residues creates an artificial transmission barrier for prion replication in transgenic mice | 23 | 84 |
| 520 | 0 | 0 | 520 1999 FASEB JOURNAL 13 (7): A1373-A1373 Tremblay P; Meiner Z; Bujard H; DeArmond SJ; Prusiner SB Doxycycline control of prion protein transgene expression modulates prion disease in mice. | 0 | 0 |
| # | LCR | NCR | Node / Date / Journal / Author | LCS | GCS |
| 521 | 0 | 0 | 521 1999 FASEB JOURNAL 13 (7): A1559-A1559 Wille H; Guenebaut V; Stroud RM; Agard DA; Prusiner SB Low resolution projection maps of 2D and 3D scrapie prion protein crystals. | 0 | 0 |
| 522 | 0 | 0 | 522 1999 FASEB JOURNAL 13 (7): A1560-A1560 Peretz D; Williamson AR; Scott MR; Groth D; Burton DR; et al. Four distinct prion protein structures seem to dictate protease resistance of prion strains replicated in syrian hamsters | 0 | 0 |
| 523 | 0 | 0 | 523 1999 FASEB JOURNAL 13 (7): A1582-A1582 Prusiner SB Molecular studies of prion biology and diseases | 0 | 0 |
| 524 | 17 | 53 | 524 1999 JOURNAL OF MOLECULAR BIOLOGY 286 (2): 593-606 Harrison PM; Chan HS; Prusiner SB; Cohen FE Thermodynamics of model prions and its implications for the problem of prion protein folding | 1 | 52 |
| 525 | 28 | 75 | 525 1999 JOURNAL OF MOLECULAR BIOLOGY 292 (4): 797-817 Moore RC; Lee IY; Silverman GL; Harrison PM; Strome R; et al. Ataxia in prion protein (PrP)-deficient mice is associated with upregulation of the novel PrP-like protein Doppel | 10 | 199 |
| 526 | 11 | 39 | 526 1999 JOURNAL OF MOLECULAR BIOLOGY 293 (4): 855-863 Kanyo ZF; Pan KM; Williamson RA; Burton DR; Prusiner SB; et al. Antibody binding defines a structure for an epitope that participates in the PrPC -> PrPSc conformational change | 4 | 22 |
| 527 | 22 | 45 | 527 1999 JOURNAL OF NEUROPATHOLOGY AND EXPERIMENTAL NEUROLOGY 58 (12): 1244-1249 Tatzelt J; Groth DF; Torchia M; Prusiner SB; DeArmond SJ Kinetics of prion protein accumulation in the CNS of mice with experimental scrapie | 3 | 13 |
| 528 | 9 | 39 | 528 1999 LABORATORY INVESTIGATION 79 (6): 689-697 Nishida N; Tremblay P; Sugimoto T; Shigematsu K; Shirabe S; et al. A mouse prion protein transgene rescues mice deficient for the prion protein gene from Purkinje cell degeneration and demyelination | 8 | 75 |
| 529 | 12 | 30 | 529 1999 NATURE 402 (6763): 822-826 Hegde RS; Tremblay P; Groth D; DeArmond SJ; Prusiner SB; et al. Transmissible and genetic prion diseases share a common pathway of neurodegeneration | 6 | 117 |
| 530 | 13 | 37 | 530 1999 NEW ENGLAND JOURNAL OF MEDICINE 340 (21): 1630-1638 Mastrianni JA; Nixon R; Layzer R; Telling GC; Han D; et al. Prion protein conformation in a patient with sporadic fatal insomnia | 10 | 54 |
| # | LCR | NCR | Node / Date / Journal / Author | LCS | GCS |
| 531 | 9 | 34 | 531 1999 PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA 96 (5): 2042-2047 Viles JH; Cohen FE; Prusiner SB; Goodin DB; Wright PE; et al. Copper binding to the prion protein: Structural implications of four identical cooperative binding sites | 17 | 227 |
| 532 | 15 | 40 | 532 1999 PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA 96 (23): 13044-13049 Rudd PM; Endo T; Colominas C; Groth D; Wheeler SF; et al. Glycosylation differences between the normal and pathogenic prion protein isoforms | 6 | 90 |
| 533 | 13 | 47 | 533 1999 PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA 96 (25): 14529-14534 Supattapone S; Nguyen HOB; Cohen FE; Prusiner SB; Scott MR Elimination of prions by branched polyamines and implications for therapeutics | 13 | 86 |
| 534 | 18 | 48 | 534 1999 PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA 96 (26): 15137-15142 Scott MR; Will R; Ironside J; Nguyen HOB; Tremblay P; et al. Compelling transgenetic evidence for transmission of bovine spongiform encephalopathy prions to humans | 16 | 207 |
| 535 | 0 | 0 | 535 2000 ABSTRACTS OF PAPERS OF THE AMERICAN CHEMICAL SOCIETY 219: U277-U277 Prusiner SB; Cohen FE Protein folding in prion replication. | 0 | 0 |
| 536 | 21 | 39 | 536 2000 ARCHIVES OF VIROLOGY : 113-124 Scott MR; Supattapone S; Nguyen HOB; DeArmond SJ; Prusiner SB Transgenic models of prion disease | 0 | 3 |
| 537 | 15 | 31 | 537 2000 ARCHIVES OF VIROLOGY : 227-235 Safar J; Cohen FE; Prusiner SB Quantitative traits of prion strains are enciphered in the conformation of the prion protein | 0 | 0 |
| 538 | 25 | 46 | 538 2000 BIOCHEMISTRY 39 (10): 2792-2804 Baskakov IV; Aagaard C; Mehlhorn I; Wille H; Groth D; et al. Self-assembly of recombinant prion protein of 106 residues | 9 | 33 |
| 539 | 10 | 52 | 539 2000 BIOCHEMISTRY 39 (45): 13760-13771 Aronoff-Spencer E; Burns CS; Avdievich NI; Gerfen GJ; Peisach J; et al. Identification of the Cu2+ binding sites in the N-terminal domain of the prion protein by EPR and CD spectroscopy | 3 | 92 |
| 540 | 4 | 30 | 540 2000 BRAIN RESEARCH 874 (2): 210-215 Bouzamondo E; Milroy AM; Ralston HJ; Prusiner SB; DeArmond SJ Selective neuronal vulnerability during experimental scrapie infection: Insights from an ultrastructural investigation | 2 | 7 |
| # | LCR | NCR | Node / Date / Journal / Author | LCS | GCS |
| 541 | 18 | 44 | 541 2000 GENOMICS 69 (1): 47-53 Stephenson DA; Chiotti K; Ebeling C; Groth D; DeArmond SJ; et al. Quantitative trait loci affecting prion incubation time in mice | 2 | 32 |
| 542 | 11 | 28 | 542 2000 JOURNAL OF BIOLOGICAL CHEMISTRY 275 (35): 26834-26841 Silverman GL; Qin KF; Moore RC; Yang Y; Mastrangelo P; et al. Doppel is an N-glycosylated, glycosylphosphatidylinositol-anchored protein - Expression in testis and ectopic production in the brains of Prnp(o/o) mice predisposed to Purkinje cell loss | 3 | 70 |
| 543 | 19 | 40 | 543 2000 JOURNAL OF GENERAL VIROLOGY 81: 2555-2563 Korth C; Kaneko K; Prusiner SB Expression of unglycosylated mutated prion protein facilitates PrPSc formation in neuroblastoma cells infected with different prion strains | 0 | 18 |
| 544 | 40 | 69 | 544 2000 JOURNAL OF MOLECULAR BIOLOGY 295 (4): 997-1007 Kaneko K; Ball HL; Wille H; Zhang H; Groth D; et al. A synthetic peptide initiates Gerstmann-Straussler-Scheinker (GSS) disease in transgenic mice | 17 | 67 |
| 545 | 18 | 40 | 545 2000 JOURNAL OF MOLECULAR BIOLOGY 300 (5): 1283-1296 Inouye H; Bond J; Baldwin MA; Ball HL; Prusiner SB; et al. Structural changes in a hydrophobic domain of the prion protein induced by hydration and by Ala -> Val and Pro -> Leu substitutions | 1 | 17 |
| 546 | 0 | 0 | 546 2000 JOURNAL OF NEUROCHEMISTRY 74: S12-S12 Inouye H; Bond J; Baldwin MA; Ball HL; Prusiner SB; et al. Structural changes in hydrophobic domain of PrP peptides | 0 | 0 |
| 547 | 35 | 97 | 547 2000 JOURNAL OF STRUCTURAL BIOLOGY 130 (2-3): 323-338 Wille H; Prusiner SB; Cohen FE Scrapie infectivity is independent of amyloid staining properties of the N-terminally truncated prion protein | 1 | 14 |
| 548 | 34 | 65 | 548 2000 JOURNAL OF VIROLOGY 74 (9): 4351-4360 Zulianello L; Kaneko K; Scott M; Erpel S; Han D; et al. Dominant-negative inhibition of prion formation diminished by deletion mutagenesis of the prion protein | 14 | 45 |
| 549 | 16 | 35 | 549 2000 JOURNAL OF VIROLOGY 74 (9): 4377-4386 Bosque PJ; Prusiner SB Cultured cell sublines highly susceptible to prion infection | 3 | 49 |
| 550 | 20 | 32 | 550 2000 JOURNAL OF VIROLOGY 74 (24): 11928-11934 Supattapone S; Nguyen HOB; Muramoto T; Cohen FE; DeArmond SJ; et al. Affinity-tagged miniprion derivatives spontaneously adopt protease-resistant conformations | 1 | 7 |
| # | LCR | NCR | Node / Date / Journal / Author | LCS | GCS |
| 551 | 0 | 0 | 551 2000 MOLECULAR BIOLOGY OF THE CELL 11: 486A-486A Wille H; Guenebaut V; Supattapone S; Latawiec D; Stroud RM; et al. Electron crystallography of the scrapie prion protein and miniprion, projection maps and difference maps. | 0 | 0 |
| 552 | 0 | 0 | 552 2000 NEUROLOGY 54 (7): A412-A412 Supattapone S; Nguyen HOB; Cohen FE; Prusiner SB; Scott M Branched polyamines enhance prion clearance | 0 | 0 |
| 553 | 0 | 0 | 553 2000 NEUROLOGY 54 (7): A414-A414 Perrier V; Wallace AC; Prusiner SB; Cohen FE Mimicking dominant negative inhibition of prion replication through structure based drug design | 0 | 0 |
| 554 | 21 | 50 | 554 2000 PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA 97 (11): 6073-6078 Perrier V; Wallace AC; Kaneko K; Safar J; Prusiner SB; et al. Mimicking dominant negative inhibition of prion replication through structure-based drug design | 8 | 59 |
| 555 | 15 | 55 | 555 2000 PROTEIN SCIENCE 9 (2): 332-343 Whittal RM; Ball HL; Cohen FE; Burlingame AL; Prusiner SB; et al. Copper binding to octarepeat peptides of the prion protein monitored by mass spectrometry | 6 | 99 |
| 556 | 7 | 40 | 556 2000 PROTEIN SCIENCE 9 (3): 440-451 Schlumpberger M; Wille H; Baldwin MA; Butler DA; Herskowitz I; et al. The prion domain of yeast Ure2p induces autocatalytic formation of amyloid fibers by a recombinant fusion protein | 2 | 32 |
| 557 | 3 | 20 | 557 2001 AMERICAN JOURNAL OF HUMAN GENETICS 69 (6): 1385-1388 Moore RC; Xiang FQ; Monaghan J; Han D; Zhang ZP; et al. Huntington disease phenocopy is a familial prion disease | 0 | 13 |
| 558 | 0 | 0 | 558 2001 AMYLOID-JOURNAL OF PROTEIN FOLDING DISORDERS 8: 137-137 Tremblay P; Kociuba K; Safar J; DeArmond SJ; Prusiner SB Doxycycline-regulated Prnp expression modulates development of prion disease in transgenic mice | 0 | 0 |
| 559 | 16 | 57 | 559 2001 BIOCHEMISTRY 40 (9): 2743-2753 Viles JH; Donne D; Kroon G; Prusiner SB; Cohen FE; et al. Local structural plasticity of the prion protein. Analysis of NMR relaxation dynamics | 2 | 42 |
| 560 | 20 | 55 | 560 2001 BIOCHEMISTRY 40 (13): 3759-3766 Rudd PM; Wormald MR; Wing DR; Prusiner SB; Dwek RA Prion glycoprotein: Structure, dynamics, and roles for the sugars | 2 | 37 |
| # | LCR | NCR | Node / Date / Journal / Author | LCS | GCS |
| 561 | 19 | 38 | 561 2001 BIOLOGICAL CHEMISTRY 382 (4): 683-691 Jansen K; Schafer O; Birkmann E; Post K; Serban H; et al. Structural intermediates in the putative pathway from the cellular prion protein to the pathogenic form | 1 | 25 |
| 562 | 26 | 59 | 562 2001 EMBO JOURNAL 20 (7): 1547-1554 Leclerc E; Peretz D; Ball H; Sakurai H; Legname G; et al. Immobilized prion protein undergoes spontaneous rearrangement to a conformation having features in common with the infectious form | 3 | 26 |
| 563 | 6 | 23 | 563 2001 JOURNAL OF BIOLOGICAL CHEMISTRY 276 (23): 19687-19690 Baskakov IV; Legname G; Prusiner SB; Cohen FE Folding of prion protein to its native alpha-helical conformation is under kinetic control | 7 | 66 |
| 564 | 25 | 70 | 564 2001 JOURNAL OF MOLECULAR BIOLOGY 314 (5): 1209-1225 Schmitt-Ulms G; Legname G; Baldwin MA; Ball HL; Bradon N; et al. Binding of neural cell adhesion molecules (N-CAMs) to the cellular prion protein | 6 | 66 |
| 565 | 30 | 63 | 565 2001 JOURNAL OF PEPTIDE RESEARCH 58 (5): 357-374 Ball HL; King DS; Cohen FE; Prusiner SB; Baldwin MA Engineering the prion protein using chemical synthesis | 1 | 6 |
| 566 | 22 | 35 | 566 2001 JOURNAL OF VIROLOGY 75 (3): 1408-1413 Supattapone S; Muramoto T; Legname G; Mehlhorn I; Cohen FE; et al. Identification of two prion protein regions that modify scrapie incubation time | 9 | 27 |
| 567 | 17 | 38 | 567 2001 JOURNAL OF VIROLOGY 75 (7): 3453-3461 Supattapone S; Wille H; Uyechi L; Safar J; Tremblay P; et al. Branched polyamines cure prion-infected neuroblastoma cells | 5 | 52 |
| 568 | 19 | 36 | 568 2001 MOLECULAR AND CELLULAR BIOLOGY 21 (7): 2608-2616 Supattapone S; Bouzamondo E; Ball HL; Wille H; Nguyen HOB; et al. A protease-resistant 61-residue prion peptide causes neurodegeneration in transgenic mice | 3 | 18 |
| 569 | 5 | 56 | 569 2001 MOLECULAR AND CELLULAR BIOLOGY 21 (20): 7035-7046 Schlumpberger M; Prusiner SB; Herskowitz I Induction of distinct [URE3] yeast prion strains | 0 | 23 |
| 570 | 15 | 29 | 570 2001 NATURE 412 (6848): 739-743 Peretz D; Williamson RA; Kaneko K; Vergara J; Leclerc E; et al. Antibodies inhibit prion propagation and clear cell cultures of prion infectivity | 13 | 172 |
| # | LCR | NCR | Node / Date / Journal / Author | LCS | GCS |
| 571 | 14 | 47 | 571 2001 NEUROBIOLOGY OF DISEASE 8 (4): 692-699 Diez M; DeArmond SJ; Groth D; Prusiner SB; Hokfelt T Decreased MK-801 binding in discrete hippocampal regions of prion-infected mice | 1 | 6 |
| 572 | 0 | 0 | 572 2001 NEUROLOGY 56 (8): A421-A421 Bosque PJ; Han D; Lisse T; Gaskin DA; Houser ML; et al. New substitutions in the prion protein gene | 0 | 0 |
| 573 | 12 | 34 | 573 2001 NEUROLOGY 57 (12): 2198-2205 Mastrianni JA; Capellari S; Telling GC; Han D; Bosque P; et al. Inherited prion disease caused by the V210I mutation - Transmission to transgenic mice | 0 | 10 |
| 574 | 25 | 120 | 574 2001 NEW ENGLAND JOURNAL OF MEDICINE 344 (20): 1516-1526 Prusiner SB Shattuck lecture - Neurodegenerative diseases and prions. | 3 | 140 |
| 575 | 17 | 47 | 575 2001 PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA 98 (5): 2352-2357 Mo HP; Moore RC; Cohen FE; Westaway D; Prusiner SB; et al. Two different neurodegenerative diseases caused by proteins with similar structures | 5 | 62 |
| 576 | 6 | 32 | 576 2001 PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA 98 (13): 7170-7175 Requena JR; Groth D; Legname G; Stadtman ER; Prusiner SB; et al. Copper-catalyzed oxidation of the recombinant SHa(29-231) prion protein | 1 | 43 |
| 577 | 13 | 50 | 577 2001 PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA 98 (17): 9836-9841 Korth C; May BCH; Cohen FE; Prusiner SB Acridine and phenothiazine derivatives as pharmacotherapeutics for prion disease | 5 | 152 |
| 578 | 15 | 26 | 578 2001 PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA 98 (20): 11686-11690 Laws DD; Bitter HML; Liu K; Ball HL; Kaneko K; et al. Solid-state NMR studies of the secondary structure of a mutant prion protein fragment of 55 residues that induces neurodegeneration | 1 | 24 |
| 579 | 19 | 35 | 579 2001 PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA 98 (26): 15288-15293 Moore RC; Mastrangelo P; Bouzamondo E; Heinrich C; Legname G; et al. Doppel-induced cerebellar degeneration in transgenic mice | 4 | 39 |
| 580 | 11 | 76 | 580 2001 PROTEIN SCIENCE 10 (4): 819-835 Harrison PM; Chan HS; Prusiner SB; Cohen FE Conformational propagation with prion-like characteristics in a simple model of protein folding | 0 | 39 |
| # | LCR | NCR | Node / Date / Journal / Author | LCS | GCS |
| 581 | 30 | 69 | 581 2001 PROTEIN SCIENCE 10 (4): 854-863 Peretz D; Scott MR; Groth D; Williamson RA; Burton DR; et al. Strain-specified relative conformational stability of the scrapie prion protein | 10 | 32 |
| 582 | 39 | 54 | 582 2001 PROTEINS-STRUCTURE FUNCTION AND GENETICS 44 (2): 110-118 Matsunaga Y; Peretz D; Williamson A; Burton D; Mehlhorn I; et al. Cryptic epitopes in N-terminally truncated prion protein are exposed in the full-length molecule: Dependence of conformation on pH | 0 | 14 |
| 583 | 0 | 0 | 583 2002 ABSTRACTS OF PAPERS OF THE AMERICAN CHEMICAL SOCIETY 223: C35-C35 Wemmer D; Lim KH; Nguyen T; Damo S; Ball H; et al. NMR studies of TTR and PRP peptides - Looking at the beginning and the end of amyloid formation. | 0 | 0 |
| 584 | 0 | 0 | 584 2002 ACTA NEUROPATHOLOGICA 104 (5): 556-556 Korth C; Kaneko K; Groth D; DeArmond S; Prusiner SB A novel transgenic mouse model for Creutzfeldt-Jakob disease (CJD) with abbreviated incubation times for most human prion strains reveals homogeneity of sporadic CJD | 0 | 0 |
| 585 | 0 | 0 | 585 2002 AMERICAN JOURNAL OF HUMAN GENETICS 71 (4): 542-542 Schmidt T; Boy J; Holzmann C; Ibrahim S; Grasshoff U; et al. Inducible mice model of Spinocerebellar Ataxia type 3. | 0 | 0 |
| 586 | 0 | 0 | 586 2002 ARCHIVES OF BIOCHEMISTRY AND BIOPHYSICS 397 (2): 454-455 Prusiner SB Earl R. Stadtman, Ph.D.: Citizen of the world | 0 | 0 |
| 587 | 13 | 34 | 587 2002 BIOCHEMISTRY 41 (41): 12277-12283 Kuwata K; Li H; Yamada H; Legname G; Prusiner SB; et al. Locally disordered conformer of the hamster prion protein: A crucial intermediate to PrPSc? | 1 | 37 |
| 588 | 0 | 0 | 588 2002 BIOPHYSICAL JOURNAL 82 (1): 169A-169A Dyson HJ; Mo HP; Viles JH; Wright PE; Prusiner SB; et al. Structure and dynamics of prion and Doppel proteins | 0 | 0 |
| 589 | 0 | 0 | 589 2002 BIOPHYSICAL JOURNAL 82 (1): 169A-169A Wille H; Michelitsch MD; Guenebaut V; Supattapone S; Segel DJ; et al. Structural studies of the scrapie prion protein by electron crystallography | 0 | 0 |
| 590 | 16 | 46 | 590 2002 JOURNAL OF BIOLOGICAL CHEMISTRY 277 (24): 21140-21148 Baskakov IV; Legname G; Baldwin MA; Prusiner SB; Cohen FE Pathway complexity of prion protein assembly into amyloid | 7 | 71 |
| # | LCR | NCR | Node / Date / Journal / Author | LCS | GCS |
| 591 | 11 | 40 | 591 2002 JOURNAL OF MOLECULAR BIOLOGY 316 (3): 807-815 Nicholson EM; Mo HP; Prusiner SB; Cohen FE; Marqusee S Differences between the prion protein and its homolog Doppel: A partially structured state with implications for scrapie formation | 1 | 24 |
| 592 | 0 | 0 | 592 2002 MOLECULAR BIOLOGY OF THE CELL 13: 368A-368A Latawiec D; Mironov A; Bouzamondo-Bernstein E; Williamson A; Legname G; et al. Localization of the prion protein in scrapie-infected mice | 0 | 0 |
| 593 | 9 | 21 | 593 2002 NATURE BIOTECHNOLOGY 20 (11): 1147-1150 Safar JG; Scott M; Monaghan J; Deering C; Didorenko S; et al. Measuring prions causing bovine spongiform encephalopathy or chronic wasting disease by immunoassays and transgenic mice | 10 | 57 |
| 594 | 0 | 0 | 594 2002 NEUROBIOLOGY OF AGING 23 (1): S427-S427 Prusiner SB Mad cows, demented people, and the biology of neurodegeneration | 0 | 0 |
| 595 | 1 | 3 | 595 2002 NEUROBIOLOGY OF DISEASE 10 (1): 67-68 Yehiely F; Bamborough P; Da Costa M; Perry BJ; Thinakaran G; et al. Identification of candidate proteins binding to prion protein (vol 3, pg 339, 1997) | 0 | 1 |
| 596 | 0 | 0 | 596 2002 NEUROLOGY 58 (7): A135-A135 Geschwind MD; Martindale JL; Young G; DeArmond S; Dillon WP; et al. Flair and diffusion-weighted imaging in neuropathology-confirmed Creutzfeldt Jakob disease | 0 | 0 |
| 597 | 0 | 0 | 597 2002 NEUROLOGY 58 (7): A250-A251 Geschwind MD; Miller D; Martindale JL; DeArmond SJ; Barbaro NM; et al. Challenging the clinical utility of the 14-3-3 protein in cerebrospinal fluid as a diagnostic marker for Creutzfeldt-Jakob disease | 0 | 1 |
| 598 | 25 | 69 | 598 2002 NEURON 34 (6): 921-932 Peretz D; Williamson RA; Legname G; Matsunaga Y; Vergara J; et al. A change in the conformation of prions accompanies the emergence of a new prion strain | 7 | 30 |
| 599 | 22 | 49 | 599 2002 PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA 99 (6): 3563-3568 Wille H; Michelitsch MD; Guenebaut V; Supattapone S; Serban A; et al. Structural studies of the scrapie prion protein by electron crystallography | 11 | 108 |
| 600 | 17 | 50 | 600 2002 PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA 99 (6): 3812-3817 Bosque PJ; Ryou C; Telling G; Peretz D; Legname G; et al. Prions in skeletal muscle | 2 | 53 |
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