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Nodes: 640,
Authors: 911,
Journals: 148,
Outer References: 6859,
Words: 1343
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Collection span: 1965 - 2006
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Page 1 of 7: [ 1 2 3 4 5 6 7 ]
| # | LCR | NCR | Node / Date / Journal / Author | LCS | GCS |
|---|---|---|---|---|---|
| 1 | 14 | 174 | 100 1982 SCIENCE 216 (4542): 136-144 PRUSINER SB NOVEL PROTEINACEOUS INFECTIOUS PARTICLES CAUSE SCRAPIE | 183 | 1532 |
| 2 | 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 |
| 3 | 63 | 194 | 303 1991 SCIENCE 252 (5012): 1515-1522 PRUSINER SB MOLECULAR-BIOLOGY OF PRION DISEASES | 121 | 959 |
| 4 | 19 | 78 | 127 1985 CELL 40 (4): 735-746 OESCH B; WESTAWAY D; WALCHLI M; MCKINLEY MP; KENT SBH; et al. A CELLULAR GENE ENCODES SCRAPIE PRP 27-30 PROTEIN | 174 | 948 |
| 5 | 31 | 61 | 349 1993 PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA 90 (23): 10962-10966 PAN KM; BALDWIN M; NGUYEN J; GASSET M; SERBAN A; et al. CONVERSION OF ALPHA-HELICES INTO BETA-SHEETS FEATURES IN THE FORMATION OF THE SCRAPIE PRION PROTEINS | 121 | 901 |
| 6 | 23 | 68 | 315 1992 NATURE 356 (6370): 577-582 BUELER H; FISCHER M; LANG Y; BLUETHMANN H; LIPP HP; et al. NORMAL DEVELOPMENT AND BEHAVIOR OF MICE LACKING THE NEURONAL CELL-SURFACE PRP PROTEIN | 83 | 667 |
| 7 | 18 | 70 | 104 1983 CELL 35 (2): 349-358 PRUSINER SB; MCKINLEY MP; BOWMAN KA; BOLTON DC; BENDHEIM PE; et al. SCRAPIE PRIONS AGGREGATE TO FORM AMYLOID-LIKE BIREFRINGENT RODS | 175 | 649 |
| 8 | 6 | 26 | 101 1982 SCIENCE 218 (4579): 1309-1311 BOLTON DC; MCKINLEY MP; PRUSINER SB IDENTIFICATION OF A PROTEIN THAT PURIFIES WITH THE SCRAPIE PRION | 117 | 621 |
| 9 | 15 | 40 | 245 1989 NATURE 338 (6213): 342-345 HSIAO K; BAKER HF; CROW TJ; POULTER M; OWEN F; et al. LINKAGE OF A PRION PROTEIN MISSENSE VARIANT TO GERSTMANN-STRAUSSLER SYNDROME | 114 | 536 |
| 10 | 21 | 83 | 191 1987 CELL 51 (2): 229-240 STAHL N; BORCHELT DR; HSIAO K; PRUSINER SB SCRAPIE PRION PROTEIN CONTAINS A PHOSPHATIDYLINOSITOL GLYCOLIPID | 114 | 487 |
| # | LCR | NCR | Node / Date / Journal / Author | LCS | GCS |
| 11 | 33 | 88 | 256 1990 CELL 63 (4): 673-686 PRUSINER SB; SCOTT M; FOSTER D; PAN KM; GROTH D; et al. TRANSGENETIC STUDIES IMPLICATE INTERACTIONS BETWEEN HOMOLOGOUS PRP ISOFORMS IN SCRAPIE PRION REPLICATION | 125 | 485 |
| 12 | 16 | 81 | 150 1986 CELL 46 (3): 417-428 BASLER K; OESCH B; SCOTT M; WESTAWAY D; WALCHLI M; et al. SCRAPIE AND CELLULAR PRP ISOFORMS ARE ENCODED BY THE SAME CHROMOSOMAL GENE | 136 | 483 |
| 13 | 8 | 22 | 103 1983 CELL 35 (1): 57-62 MCKINLEY MP; BOLTON DC; PRUSINER SB A PROTEASE-RESISTANT PROTEIN IS A STRUCTURAL COMPONENT OF THE SCRAPIE PRION | 109 | 475 |
| 14 | 18 | 35 | 179 1986 PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA 83 (8): 2310-2314 MEYER RK; MCKINLEY MP; BOWMAN KA; BRAUNFELD MB; BARRY RA; et al. SEPARATION AND PROPERTIES OF CELLULAR AND SCRAPIE PRION PROTEINS | 113 | 421 |
| 15 | 7 | 43 | 204 1987 LABORATORY INVESTIGATION 57 (2): 230-236 KITAMOTO T; OGOMORI K; TATEISHI J; PRUSINER SB METHODS IN LABORATORY INVESTIGATION - FORMIC-ACID PRETREATMENT ENHANCES IMMUNOSTAINING OF CEREBRAL AND SYSTEMIC AMYLOIDS | 13 | 420 |
| 16 | 25 | 56 | 390 1995 CELL 83 (1): 79-90 TELLING GC; SCOTT M; MASTRIANNI J; GABIZON R; TORCHIA M; et al. PRION PROPAGATION IN MICE EXPRESSING HUMAN AND CHIMERIC PRP TRANSGENES IMPLICATES THE INTERACTION OF CELLULAR PRP WITH ANOTHER PROTEIN | 68 | 413 |
| 17 | 55 | 181 | 493 1997 SCIENCE 278 (5336): 245-251 Prusiner SB Prion diseases and the BSE crisis | 26 | 402 |
| 18 | 31 | 89 | 241 1989 CELL 59 (5): 847-857 SCOTT M; FOSTER D; MIRENDA C; SERBAN D; COUFAL F; et al. TRANSGENIC MICE EXPRESSING HAMSTER PRION PROTEIN PRODUCE SPECIES-SPECIFIC SCRAPIE INFECTIVITY AND AMYLOID PLAQUES | 113 | 389 |
| 19 | 18 | 48 | 281 1990 SCIENCE 250 (4987): 1587-1590 HSIAO KK; SCOTT M; FOSTER D; GROTH DF; DEARMOND SJ; et al. SPONTANEOUS NEURODEGENERATION IN TRANSGENIC MICE WITH MUTANT PRION PROTEIN | 78 | 365 |
| 20 | 11 | 49 | 90 1982 BIOCHEMISTRY 21 (26): 6942-6950 PRUSINER SB; BOLTON DC; GROTH DF; BOWMAN KA; COCHRAN SP; et al. FURTHER PURIFICATION AND CHARACTERIZATION OF SCRAPIE PRIONS | 135 | 339 |
| # | LCR | NCR | Node / Date / Journal / Author | LCS | GCS |
| 21 | 39 | 94 | 501 1998 CELL 93 (3): 337-348 Prusiner SB; Scott MR; DeArmond SJ; Cohen FE Prion protein biology | 20 | 333 |
| 22 | 44 | 104 | 328 1993 BIOCHEMISTRY 32 (8): 1991-2002 STAHL N; BALDWIN MA; TEPLOW DB; HOOD L; GIBSON BW; et al. STRUCTURAL STUDIES OF THE SCRAPIE PRION PROTEIN USING MASS-SPECTROMETRY AND AMINO-ACID SEQUENCING | 73 | 331 |
| 23 | 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 |
| 24 | 0 | 40 | 102 1983 CELL 34 (3): 799-806 ROACH A; BOYLAN K; HORVATH S; PRUSINER SB; HOOD LE CHARACTERIZATION OF CLONED CDNA REPRESENTING RAT MYELIN BASIC-PROTEIN - ABSENCE OF EXPRESSION IN BRAIN OF SHIVERER MUTANT MICE | 5 | 320 |
| 25 | 25 | 39 | 258 1990 JOURNAL OF CELL BIOLOGY 110 (3): 743-752 BORCHELT DR; SCOTT M; TARABOULOS A; STAHL N; PRUSINER SB SCRAPIE AND CELLULAR PRION PROTEINS DIFFER IN THEIR KINETICS OF SYNTHESIS AND TOPOLOGY IN CULTURED-CELLS | 106 | 320 |
| 26 | 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 |
| 27 | 18 | 77 | 192 1987 CELL 51 (4): 651-662 WESTAWAY D; GOODMAN PA; MIRENDA CA; MCKINLEY MP; CARLSON GA; et al. DISTINCT PRION PROTEINS IN SHORT AND LONG SCRAPIE INCUBATION PERIOD MICE | 87 | 305 |
| 28 | 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 |
| 29 | 11 | 42 | 117 1984 CELL 38 (1): 127-134 PRUSINER SB; GROTH DF; BOLTON DC; KENT SB; HOOD LE PURIFICATION AND STRUCTURAL STUDIES OF A MAJOR SCRAPIE PRION PROTEIN | 100 | 300 |
| 30 | 22 | 42 | 382 1994 SCIENCE 264 (5158): 530-531 COHEN FE; PAN KM; HUANG Z; BALDWIN M; FLETTERICK RJ; et al. STRUCTURAL CLUES TO PRION REPLICATION | 55 | 268 |
| # | LCR | NCR | Node / Date / Journal / Author | LCS | GCS |
| 31 | 17 | 42 | 151 1986 CELL 46 (4): 503-511 CARLSON GA; KINGSBURY DT; GOODMAN PA; COLEMAN S; MARSHALL ST; et al. LINKAGE OF PRION PROTEIN AND SCRAPIE INCUBATION-TIME GENES | 110 | 267 |
| 32 | 13 | 30 | 146 1986 AMERICAN JOURNAL OF PATHOLOGY 122 (1): 1-5 KRETZSCHMAR HA; PRUSINER SB; STOWRING LE; DEARMOND SJ SCRAPIE PRION PROTEINS ARE SYNTHESIZED IN NEURONS | 54 | 262 |
| 33 | 15 | 51 | 154 1986 DNA-A JOURNAL OF MOLECULAR & CELLULAR BIOLOGY 5 (4): 315-324 KRETZSCHMAR HA; STOWRING LE; WESTAWAY D; STUBBLEBINE WH; PRUSINER SB; et al. MOLECULAR-CLONING OF A HUMAN PRION PROTEIN CDNA | 62 | 258 |
| 34 | 21 | 46 | 323 1992 PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA 89 (22): 10940-10944 GASSET M; BALDWIN MA; LLOYD DH; GABRIEL JM; HOLTZMAN DM; et al. PREDICTED ALPHA-HELICAL REGIONS OF THE PRION PROTEIN WHEN SYNTHESIZED AS PEPTIDES FORM AMYLOID | 60 | 244 |
| 35 | 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 |
| 36 | 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 |
| 37 | 20 | 38 | 209 1987 NEUROLOGY 37 (8): 1271-1280 DEARMOND SJ; MOBLEY WC; DEMOTT DL; BARRY RA; BECKSTEAD JH; et al. CHANGES IN THE LOCALIZATION OF BRAIN PRION PROTEINS DURING SCRAPIE INFECTION | 62 | 231 |
| 38 | 24 | 53 | 348 1993 PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA 90 (22): 10608-10612 PRUSINER SB; GROTH D; SERBAN A; KOEHLER R; FOSTER D; et al. ABLATION OF THE PRION PROTEIN (PRP) GENE IN MICE PREVENTS SCRAPIE AND FACILITATES PRODUCTION OF ANTI-PRP ANTIBODIES | 72 | 231 |
| 39 | 15 | 62 | 128 1985 CELL 41 (1): 221-235 DEARMOND SJ; MCKINLEY MP; BARRY RA; BRAUNFELD MB; MCCOLLOCH JR; et al. IDENTIFICATION OF PRION AMYLOID FILAMENTS IN SCRAPIE-INFECTED BRAIN | 80 | 230 |
| 40 | 31 | 67 | 396 1995 JOURNAL OF CELL BIOLOGY 129 (1): 121-132 TARABOULOS A; SCOTT M; SEMENOV A; AVRAHAM D; LASZLO L; et al. CHOLESTEROL DEPLETION AND MODIFICATION OF COOH-TERMINAL TARGETING SEQUENCE OF THE PRION PROTEIN INHIBIT FORMATION OF THE SCRAPIE ISOFORM | 38 | 230 |
| # | LCR | NCR | Node / Date / Journal / Author | LCS | GCS |
| 41 | 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 |
| 42 | 25 | 64 | 309 1992 JOURNAL OF BIOLOGICAL CHEMISTRY 267 (23): 16188-16199 BORCHELT DR; TARABOULOS A; PRUSINER SB EVIDENCE FOR SYNTHESIS OF SCRAPIE PRION PROTEINS IN THE ENDOCYTIC PATHWAY | 41 | 228 |
| 43 | 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 |
| 44 | 8 | 31 | 124 1984 NATURE 310 (5976): 418-421 BENDHEIM PE; BARRY RA; DEARMOND SJ; STITES DP; PRUSINER SB ANTIBODIES TO A SCRAPIE PRION PROTEIN | 80 | 226 |
| 45 | 10 | 51 | 233 1988 PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA 85 (24): 9811-9815 MOBLEY WC; NEVE RL; PRUSINER SB; MCKINLEY MP NERVE GROWTH-FACTOR INCREASES MESSENGER-RNA LEVELS FOR THE PRION PROTEIN AND THE BETA-AMYLOID PROTEIN-PRECURSOR IN DEVELOPING HAMSTER BRAIN | 28 | 226 |
| 46 | 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 |
| 47 | 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 |
| 48 | 73 | 146 | 495 1998 ANNUAL REVIEW OF BIOCHEMISTRY 67: 793-+ Cohen FE; Prusiner SB Pathologic conformations of prion proteins | 28 | 213 |
| 49 | 1 | 44 | 129 1985 CELL 42 (1): 139-148 TAKAHASHI N; ROACH A; TEPLOW DB; PRUSINER SB; HOOD L CLONING AND CHARACTERIZATION OF THE MYELIN BASIC-PROTEIN GENE FROM MOUSE - ONE GENE CAN ENCODE BOTH 14 KD AND 18.5 KD MBPS BY ALTERNATE USE OF EXONS | 2 | 209 |
| 50 | 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 |
| # | LCR | NCR | Node / Date / Journal / Author | LCS | GCS |
| 51 | 3 | 5 | 244 1989 LANCET 1 (8628): 51-52 OWEN F; LOFTHOUSE R; CROW TJ; BAKER HF; HSIAO K; et al. INSERTION IN PRION PROTEIN GENE IN FAMILIAL CREUTZFELDT-JAKOB DISEASE | 54 | 205 |
| 52 | 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 |
| 53 | 18 | 50 | 357 1994 CELL 76 (1): 117-129 WESTAWAY D; DEARMOND SJ; CAYETANOCANLAS J; GROTH D; FOSTER D; et al. DEGENERATION OF SKELETAL-MUSCLE, PERIPHERAL-NERVES, AND THE CENTRAL-NERVOUS-SYSTEM IN TRANSGENIC MICE OVEREXPRESSING WILD-TYPE PRION PROTEINS | 37 | 187 |
| 54 | 49 | 167 | 238 1989 ANNUAL REVIEW OF MICROBIOLOGY 43: 345-374 PRUSINER SB SCRAPIE PRIONS | 62 | 183 |
| 55 | 25 | 39 | 320 1992 PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA 89 (16): 7620-7624 TARABOULOS A; JENDROSKA K; SERBAN D; YANG SL; DEARMOND SJ; et al. REGIONAL MAPPING OF PRION PROTEINS IN BRAIN | 65 | 183 |
| 56 | 10 | 32 | 88 1982 ANNALS OF NEUROLOGY 11 (4): 353-358 PRUSINER SB; COCHRAN SP; GROTH DF; DOWNEY DE; BOWMAN KA; et al. MEASUREMENT OF THE SCRAPIE AGENT USING AN INCUBATION-TIME INTERVAL ASSAY | 82 | 181 |
| 57 | 26 | 60 | 220 1988 EUROPEAN JOURNAL OF BIOCHEMISTRY 176 (1): 21-30 TURK E; TEPLOW DB; HOOD LE; PRUSINER SB PURIFICATION AND PROPERTIES OF THE CELLULAR AND SCRAPIE HAMSTER PRION PROTEINS | 61 | 177 |
| 58 | 24 | 53 | 259 1990 JOURNAL OF CELL BIOLOGY 110 (6): 2117-2132 TARABOULOS A; SERBAN D; PRUSINER SB SCRAPIE PRION PROTEINS ACCUMULATE IN THE CYTOPLASM OF PERSISTENTLY INFECTED CULTURED-CELLS | 47 | 174 |
| 59 | 19 | 47 | 276 1990 NEUROLOGY 40 (1): 110-117 SERBAN D; TARABOULOS A; DEARMOND SJ; PRUSINER SB RAPID DETECTION OF CREUTZFELDT-JAKOB DISEASE AND SCRAPIE PRION PROTEINS | 78 | 173 |
| 60 | 23 | 38 | 330 1993 CELL 73 (5): 979-988 SCOTT M; GROTH D; FOSTER D; TORCHIA M; YANG SL; et al. PROPAGATION OF PRIONS WITH ARTIFICIAL PROPERTIES IN TRANSGENIC MICE EXPRESSING CHIMERIC PRP GENES | 62 | 172 |
| # | LCR | NCR | Node / Date / Journal / Author | LCS | GCS |
| 61 | 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 |
| 62 | 10 | 38 | 142 1985 NEW ENGLAND JOURNAL OF MEDICINE 312 (2): 73-78 BOCKMAN JM; KINGSBURY DT; MCKINLEY MP; BENDHEIM PE; PRUSINER SB CREUTZFELDT-JAKOB DISEASE PRION PROTEINS IN HUMAN BRAINS | 63 | 171 |
| 63 | 25 | 44 | 228 1988 JOURNAL OF VIROLOGY 62 (5): 1558-1564 BUTLER DA; SCOTT MRD; BOCKMAN JM; BORCHELT DR; TARABOULOS A; et al. SCRAPIE-INFECTED MURINE NEURO-BLASTOMA CELLS PRODUCE PROTEASE-RESISTANT PRION PROTEINS | 56 | 169 |
| 64 | 21 | 42 | 343 1993 PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA 90 (1): 1-5 GASSET M; BALDWIN MA; FLETTERICK RJ; PRUSINER SB PERTURBATION OF THE SECONDARY STRUCTURE OF THE SCRAPIE PRION PROTEIN UNDER CONDITIONS THAT ALTER INFECTIVITY | 59 | 165 |
| 65 | 10 | 40 | 180 1986 PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA 83 (19): 7358-7362 SPARKES RS; SIMON M; COHN VH; FOURNIER REK; LEM J; et al. ASSIGNMENT OF THE HUMAN AND MOUSE PRION PROTEIN GENES TO HOMOLOGOUS CHROMOSOMES | 58 | 163 |
| 66 | 38 | 122 | 352 1994 ANNALS OF NEUROLOGY 35 (4): 385-395 PRUSINER SB; HSIAO KK HUMAN PRION DISEASES | 19 | 163 |
| 67 | 40 | 104 | 210 1987 NEW ENGLAND JOURNAL OF MEDICINE 317 (25): 1571-1581 PRUSINER SB PRIONS AND NEURODEGENERATIVE DISEASES | 38 | 161 |
| 68 | 11 | 40 | 302 1991 NEW ENGLAND JOURNAL OF MEDICINE 324 (16): 1091-1097 HSIAO K; MEINER Z; KAHANA E; CASS C; KAHANA I; et al. MUTATION OF THE PRION PROTEIN IN LIBYAN JEWS WITH CREUTZFELDT-JAKOB DISEASE | 41 | 161 |
| 69 | 8 | 48 | 139 1985 JOURNAL OF VIROLOGY 53 (2): 596-606 BOLTON DC; MEYER RK; PRUSINER SB SCRAPIE PRP 27-30 IS A SIALOGLYCOPROTEIN | 59 | 160 |
| 70 | 19 | 43 | 380 1994 PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA 91 (19): 9126-9130 HSIAO KK; GROTH D; SCOTT M; YANG SL; SERBAN H; et al. SERIAL TRANSMISSION IN RODENTS OF NEURODEGENERATION FROM TRANSGENIC MICE EXPRESSING MUTANT PRION PROTEIN | 44 | 160 |
| # | LCR | NCR | Node / Date / Journal / Author | LCS | GCS |
| 71 | 24 | 61 | 317 1992 NATURE GENETICS 1 (1): 68-71 HSIAO K; DLOUHY SR; FARLOW MR; CASS C; DACOSTA M; et al. MUTANT PRION PROTEINS IN GERSTMANN-STRAUSSLER-SCHEINKER DISEASE WITH NEUROFIBRILLARY TANGLES | 30 | 158 |
| 72 | 32 | 73 | 252 1990 BIOCHEMISTRY 29 (22): 5405-5412 STAHL N; BORCHELT DR; PRUSINER SB DIFFERENTIAL RELEASE OF CELLULAR AND SCRAPIE PRION PROTEINS FROM CELLULAR MEMBRANES BY PHOSPHATIDYLINOSITOL-SPECIFIC PHOSPHOLIPASE-C | 29 | 156 |
| 73 | 16 | 60 | 240 1989 BIOCHEMISTRY 28 (21): 8380-8388 ENDO T; GROTH D; PRUSINER SB; KOBATA A DIVERSITY OF OLIGOSACCHARIDE STRUCTURES LINKED TO ASPARAGINES OF THE SCRAPIE PRION PROTEIN | 56 | 155 |
| 74 | 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 |
| 75 | 24 | 58 | 381 1994 PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA 91 (21): 9936-9940 TELLING GC; SCOTT M; HSIAO KK; FOSTER D; YANG SL; et al. TRANSMISSION OF CREUTZFELDT-JAKOB-DISEASE FROM HUMANS TO TRANSGENIC MICE EXPRESSING CHIMERIC HUMAN-MOUSE PRION PROTEIN | 41 | 149 |
| 76 | 7 | 51 | 85 1981 PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA-BIOLOGICAL SCIENCES 78 (11): 6675-6679 PRUSINER SB; MCKINLEY MP; GROTH DF; BOWMAN KA; MOCK NI; et al. SCRAPIE AGENT CONTAINS A HYDROPHOBIC PROTEIN | 55 | 148 |
| 77 | 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 |
| 78 | 18 | 46 | 324 1992 PROTEIN SCIENCE 1 (8): 986-997 SCOTT MR; KOHLER R; FOSTER D; PRUSINER SB CHIMERIC PRION PROTEIN EXPRESSION IN CULTURED-CELLS AND TRANSGENIC MICE | 47 | 147 |
| 79 | 32 | 79 | 308 1992 GENES & DEVELOPMENT 6 (7): 1213-1228 HECKER R; TARABOULOS A; SCOTT M; PAN KM; YANG SL; et al. REPLICATION OF DISTINCT SCRAPIE PRION ISOLATES IS REGION SPECIFIC IN BRAINS OF TRANSGENIC MICE AND HAMSTERS | 67 | 146 |
| 80 | 4 | 51 | 60 1980 BIOCHEMISTRY 19 (21): 4883-4891 PRUSINER SB; GROTH DF; COCHRAN SP; MASIARZ FR; MCKINLEY MP; et al. MOLECULAR-PROPERTIES, PARTIAL-PURIFICATION, AND ASSAY BY INCUBATION PERIOD MEASUREMENTS OF THE HAMSTER SCRAPIE AGENT | 85 | 145 |
| # | LCR | NCR | Node / Date / Journal / Author | LCS | GCS |
| 81 | 21 | 53 | 387 1995 BIOCHEMISTRY 34 (13): 4186-4192 NGUYEN J; BALDWIN MA; COHEN FE; PRUSINER SB PRION PROTEIN-PEPTIDES INDUCE ALPHA-HELIX TO BETA-SHEET CONFORMATIONAL TRANSITIONS | 23 | 145 |
| 82 | 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 |
| 83 | 18 | 60 | 379 1994 PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA 91 (15): 7139-7143 HUANG ZW; GABRIEL JM; BALDWIN MA; FLETTERICK RJ; PRUSINER SB; et al. PROPOSED 3-DIMENSIONAL STRUCTURE FOR THE CELLULAR PRION PROTEIN | 46 | 141 |
| 84 | 19 | 74 | 358 1994 GENES & DEVELOPMENT 8 (8): 959-969 WESTAWAY D; ZULIANI V; COOPER CM; DACOSTA M; NEUMAN S; et al. HOMOZYGOSITY FOR PRION PROTEIN ALLELES ENCODING GLUTAMINE-171 RENDERS SHEEP SUSCEPTIBLE TO NATURAL SCRAPIE | 24 | 140 |
| 85 | 25 | 120 | 574 2001 NEW ENGLAND JOURNAL OF MEDICINE 344 (20): 1516-1526 Prusiner SB Shattuck lecture - Neurodegenerative diseases and prions. | 3 | 140 |
| 86 | 5 | 20 | 316 1992 NATURE GENETICS 1 (1): 64-67 DLOUHY SR; HSIAO K; FARLOW MR; FOROUD T; CONNEALLY PM; et al. LINKAGE OF THE INDIANA KINDRED OF GERSTMANN-STRAUSSLER-SCHEINKER DISEASE TO THE PRION PROTEIN GENE | 33 | 138 |
| 87 | 71 | 322 | 327 1993 ARCHIVES OF NEUROLOGY 50 (11): 1129-1153 PRUSINER SB GENETIC AND INFECTIOUS PRION DISEASES | 11 | 138 |
| 88 | 23 | 70 | 277 1990 NEUROLOGY 40 (12): 1820-1827 HSIAO K; PRUSINER SB INHERITED HUMAN PRION DISEASES | 36 | 136 |
| 89 | 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 |
| 90 | 35 | 79 | 459 1996 TRENDS IN BIOCHEMICAL SCIENCES 21 (12): 482-487 Prusiner SB Molecular biology and pathogenesis of prion diseases | 5 | 134 |
| # | LCR | NCR | Node / Date / Journal / Author | LCS | GCS |
| 91 | 21 | 40 | 232 1988 PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA 85 (18): 6617-6621 GABIZON R; MCKINLEY MP; GROTH D; PRUSINER SB IMMUNOAFFINITY PURIFICATION AND NEUTRALIZATION OF SCRAPIE PRION INFECTIVITY | 48 | 133 |
| 92 | 11 | 40 | 147 1986 ANNALS OF NEUROLOGY 20 (2): 204-208 KITAMOTO T; TATEISHI J; TASHIMA T; TAKESHITA I; BARRY RA; et al. AMYLOID PLAQUES IN CREUTZFELDT-JAKOB DISEASE STAIN WITH PRION PROTEIN ANTIBODIES | 54 | 132 |
| 93 | 23 | 50 | 297 1991 LABORATORY INVESTIGATION 65 (6): 622-630 MCKINLEY MP; TARABOULOS A; KENAGA L; SERBAN D; STIEBER A; et al. ULTRASTRUCTURAL-LOCALIZATION OF SCRAPIE PRION PROTEINS IN CYTOPLASMIC VESICLES OF INFECTED CULTURED-CELLS | 38 | 132 |
| 94 | 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 |
| 95 | 26 | 65 | 314 1992 MOLECULAR BIOLOGY OF THE CELL 3 (8): 851-863 TARABOULOS A; RAEBER AJ; BORCHELT DR; SERBAN D; PRUSINER SB SYNTHESIS AND TRAFFICKING OF PRION PROTEINS IN CULTURED-CELLS | 29 | 130 |
| 96 | 28 | 48 | 211 1987 PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA 84 (12): 4017-4021 GABIZON R; MCKINLEY MP; PRUSINER SB PURIFIED PRION PROTEINS AND SCRAPIE INFECTIVITY COPARTITION INTO LIPOSOMES | 71 | 129 |
| 97 | 31 | 63 | 290 1991 EMBO JOURNAL 10 (3): 513-519 TAGLIAVINI F; PRELLI F; GHISO J; BUGIANI O; SERBAN D; et al. AMYLOID PROTEIN OF GERSTMANN-STRAUSSLER-SCHEINKER DISEASE (INDIANA KINDRED) IS AN 11-KD FRAGMENT OF PRION PROTEIN WITH AN N-TERMINAL GLYCINE AT CODON-58 | 30 | 128 |
| 98 | 0 | 34 | 10 1970 ANALYTICAL BIOCHEMISTRY 37 (2): 429-& Prusiner SB; MILNER L A RAPID RADIOACTIVE ASSAY FOR GLUTAMINE SYNTHETASE, GLUTAMINASE, ASPARAGINE SYNTHETASE, AND ASPARAGINASE | 7 | 126 |
| 99 | 32 | 84 | 306 1992 BIOCHEMISTRY 31 (21): 5043-5053 STAHL N; BALDWIN MA; HECKER R; PAN KM; BURLINGAME AL; et al. GLYCOSYLINOSITOL PHOSPHOLIPID ANCHORS OF THE SCRAPIE AND CELLULAR PRION PROTEINS CONTAIN SIALIC-ACID | 27 | 126 |
| 100 | 9 | 24 | 299 1991 NEUROLOGY 41 (5): 681-684 HSIAO KK; CASS C; SCHELLENBERG GD; BIRD T; DEVINEGAGE E; et al. A PRION PROTEIN VARIANT IN A FAMILY WITH THE TELENCEPHALIC FORM OF GERSTMANN-STRAUSSLER-SCHEINKER SYNDROME | 35 | 118 |
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