| Missing Links?: 57 Citation Matrix | Graphs | Glossary HistCite Guide About |
Nodes: 640,
Authors: 911,
Journals: 148,
Outer References: 6859,
Words: 1343
Yearly output |
Document Type |
Language |
Institution |
Institution with Subdivision |
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Collection span: 1965 - 2006
| View: Overview | Sorted by journal name. |
Page 1 of 7: [ 1 2 3 4 5 6 7 ]
| # | LCR | NCR | Node / Date / Journal / Author | LCS | GCS |
|---|---|---|---|---|---|
| 1 | 0 | 0 | 16 1972 ABSTRACTS OF PAPERS OF THE AMERICAN CHEMICAL SOCIETY 164 (AUG-S): 124-& Prusiner SB REGULATION OF GLUTAMINASE ISOENZYMES IN E-COLI | 0 | 0 |
| 2 | 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 |
| 3 | 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 |
| 4 | 0 | 0 | 604 2003 ABSTRACTS OF PAPERS OF THE AMERICAN CHEMICAL SOCIETY 226: U102-U103 Safar JG; Prusiner SB New generation of prion tests: Conformation-dependent immunoassay (CDI). | 0 | 0 |
| 5 | 45 | 145 | 181 1987 ACTA NEUROPATHOLOGICA 72 (4): 299-314 PRUSINER SB; GABIZON R; MCKINLEY MP ON THE BIOLOGY OF PRIONS | 1 | 30 |
| 6 | 13 | 41 | 236 1989 ACTA NEUROPATHOLOGICA 77 (4): 337-342 SNOW AD; KISILEVSKY R; WILLMER J; PRUSINER SB; DEARMOND SJ SULFATED GLYCOSAMINOGLYCANS IN AMYLOID PLAQUES OF PRION DISEASES | 9 | 63 |
| 7 | 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 |
| 8 | 29 | 283 | 114 1984 ADVANCES IN VIRUS RESEARCH 29: 1-56 PRUSINER SB PRIONS - NOVEL INFECTIOUS PATHOGENS | 12 | 36 |
| 9 | 63 | 221 | 214 1988 ADVANCES IN VIRUS RESEARCH 35: 83-136 PRUSINER SB MOLECULAR-STRUCTURE, BIOLOGY, AND GENETICS OF PRIONS | 1 | 19 |
| 10 | 69 | 236 | 305 1992 ADVANCES IN VIRUS RESEARCH 41: 241-280 PRUSINER SB MOLECULAR-BIOLOGY AND GENETICS OF NEURODEGENERATIVE DISEASES CAUSED BY PRIONS | 7 | 13 |
| # | LCR | NCR | Node / Date / Journal / Author | LCS | GCS |
| 11 | 0 | 26 | 1 1965 AEROSPACE MEDICINE 36 (2S1): 123-& BLACKSCH.B; PRUSINER SB; ESPARZA H TOLERANCE OF VESTIBULAR APPARATUS OF HYPOTHERMIC HAMSTER TO 840 G ACCELERATION | 0 | 0 |
| 12 | 0 | 0 | 351 1994 AIDS RESEARCH AND HUMAN RETROVIRUSES 10: S99-S99 PRUSINER SB MOLECULAR-BIOLOGY AND GENETICS OF PRION DISEASES | 0 | 0 |
| 13 | 0 | 0 | 384 1995 AIDS RESEARCH AND HUMAN RETROVIRUSES 11: S71-S71 PRUSINER SB; PAN KM; BALDWIN MA; TELLING GC; SCOTT M THE PRION DISEASES | 0 | 0 |
| 14 | 20 | 67 | 282 1991 ALZHEIMER DISEASE & ASSOCIATED DISORDERS 5 (3): 155-162 HSIAO K; PRUSINER SB MOLECULAR-GENETICS AND TRANSGENIC MODEL OF GERTSMANN-STRAUSSLER-SCHEINKER DISEASE | 0 | 6 |
| 15 | 3 | 34 | 182 1987 AMERICAN JOURNAL OF HUMAN GENETICS 40 (5): 387-400 BOYLAN KB; TAKAHASHI N; DIAMOND M; HOOD LE; PRUSINER SB DNA LENGTH POLYMORPHISM LOCATED 5' TO THE HUMAN MYELIN BASIC-PROTEIN GENE | 2 | 15 |
| 16 | 0 | 0 | 283 1991 AMERICAN JOURNAL OF HUMAN GENETICS 49 (4): 188-188 GABIZON R; MEINER Z; HALIMI M; PRUSINER SB PRION PROTEINS IN FIBROBLASTS AND LEUKOCYTES OF PATIENTS WITH FAMILIAL CREUTZFELDT-JAKOB DISEASE CARRYING A MUTATION AT CODON-200 OF THE PRP GENE | 0 | 0 |
| 17 | 10 | 31 | 326 1993 AMERICAN JOURNAL OF HUMAN GENETICS 53 (4): 828-835 GABIZON R; ROSENMANN H; MEINER Z; KAHANA I; KAHANA E; et al. MUTATION AND POLYMORPHISM OF THE PRION PROTEIN GENE IN LIBYAN JEWS WITH CREUTZFELDT-JAKOB-DISEASE (CJD) | 12 | 61 |
| 18 | 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 |
| 19 | 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 |
| 20 | 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 |
| # | LCR | NCR | Node / Date / Journal / Author | LCS | GCS |
| 21 | 63 | 219 | 385 1995 AMERICAN JOURNAL OF PATHOLOGY 146 (4): 785-811 DEARMOND SJ; PRUSINER SB ETIOLOGY AND PATHOGENESIS OF PRION DISEASES | 6 | 116 |
| 22 | 84 | 254 | 386 1995 AMYLOID-INTERNATIONAL JOURNAL OF EXPERIMENTAL AND CLINICAL INVESTIGATION 2 (1): 39-65 PRUSINER SB; DEARMOND SJ PRION PROTEIN AMYLOID AND NEURODEGENERATION | 2 | 14 |
| 23 | 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 |
| 24 | 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 |
| 25 | 1 | 9 | 19 1973 ANALYTICAL BIOCHEMISTRY 54 (1): 272-275 DAVIS JN; Prusiner SB STAIN FOR GLUTAMINASE ACTIVITY | 1 | 10 |
| 26 | 0 | 7 | 38 1978 ANALYTICAL BIOCHEMISTRY 89 (2): 324-331 HITTELMAN K; MAMELOK RD; PRUSINER SB PRESERVATION BY FREEZING OF GLUCOSE AND ALANINE TRANSPORT INTO KIDNEY MEMBRANE-VESICLES | 2 | 13 |
| 27 | 5 | 35 | 249 1990 ANALYTICAL BIOCHEMISTRY 191 (1): 174-182 BALDWIN MA; STAHL N; REINDERS LG; GIBSON BW; PRUSINER SB; et al. PERMETHYLATION AND TANDEM MASS-SPECTROMETRY OF OLIGOSACCHARIDES HAVING FREE HEXOSAMINE - ANALYSIS OF THE GLYCOINOSITOL PHOSPHOLIPID ANCHOR GLYCAN FROM THE SCRAPIE PRION PROTEIN | 10 | 42 |
| 28 | 0 | 0 | 39 1978 ANNALS OF NEUROLOGY 4 (2): 168-168 PRUSINER SB; GARFIN DE; COCHRAN SP; BARINGER JR; HADLOW WJ; et al. EVIDENCE FOR HYDROPHOBIC DOMAINS ON SURFACE OF SCRAPIE AGENT | 0 | 0 |
| 29 | 0 | 19 | 40 1978 ANNALS OF NEUROLOGY 4 (3): 205-211 BARINGER JR; PRUSINER SB EXPERIMENTAL SCRAPIE IN MICE - ULTRASTRUCTURAL OBSERVATIONS | 23 | 46 |
| 30 | 0 | 9 | 58 1980 ANNALS OF NEUROLOGY 8 (6): 628-631 HADLOW WJ; PRUSINER SB; KENNEDY RC; RACE RE BRAIN-TISSUE FROM PERSONS DYING OF CREUTZFELDT-JAKOB DISEASE CAUSES SCRAPIE-LIKE ENCEPHALOPATHY IN GOATS | 19 | 36 |
| # | LCR | NCR | Node / Date / Journal / Author | LCS | GCS |
| 31 | 0 | 0 | 72 1981 ANNALS OF NEUROLOGY 10 (1): 98-99 MCKINLEY MP; MASIARZ FR; PRUSINER SB CHEMICAL MODIFICATION OF A SCRAPIE AGENT PROTEIN BY DIETHYL PYROCARBONATE | 0 | 0 |
| 32 | 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 |
| 33 | 5 | 32 | 89 1982 ANNALS OF NEUROLOGY 12 (1): 1-9 PRUSINER SB; GAJDUSEK DC; ALPERS MP KURU WITH INCUBATION PERIODS EXCEEDING 2 DECADES | 10 | 28 |
| 34 | 0 | 0 | 115 1984 ANNALS OF NEUROLOGY 16 (1): 152-153 BENDHEIM PE; BOCKMAN JM; BARRY RA; KINGSBURY DT; PRUSINER SB ANTIBODIES TO SCRAPIE PRION PROTEINS RECOGNIZE PROTEINS IN MURINE CREUTZFELDT-JAKOB DISEASE INFECTED BRAIN | 0 | 0 |
| 35 | 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 |
| 36 | 20 | 49 | 183 1987 ANNALS OF NEUROLOGY 21 (6): 589-595 BOCKMAN JM; PRUSINER SB; TATEISHI J; KINGSBURY DT IMMUNOBLOTTING OF CREUTZFELDT-JAKOB DISEASE PRION PROTEINS - HOST SPECIES-SPECIFIC EPITOPES | 45 | 71 |
| 37 | 0 | 0 | 184 1987 ANNALS OF NEUROLOGY 22 (1): 139-139 BOYLAN K; TAKAHASHI N; POPKO B; DIAMOND M; HOOD L; et al. A HIGHLY VARIABLE REGION OF DNA LENGTH POLYMORPHISM LOCATED ADJACENT TO THE HUMAN MYELIN BASIC-PROTEIN GENE | 0 | 0 |
| 38 | 0 | 0 | 185 1987 ANNALS OF NEUROLOGY 22 (1): 155-155 BORCHELT DR; MCKINLEY MP; MOBLEY WC; PRUSINER SB EXPRESSION OF PRION PROTEIN IN PRIMARY CULTURES OF NEONATAL HAMSTER BRAIN | 0 | 0 |
| 39 | 0 | 0 | 186 1987 ANNALS OF NEUROLOGY 22 (1): 156-156 SCOTT M; BORCHELT D; BREDESEN D; BUTLER D; HSIAO K; et al. EXPRESSION OF THE HAMSTER PRION PROTEIN GENE USING EUKARYOTIC EXPRESSION VECTORS | 0 | 0 |
| 40 | 0 | 0 | 187 1987 ANNALS OF NEUROLOGY 22 (1): 157-157 GABIZON R; MCKINLEY MP; GROTH D; KENAGA L; PRUSINER SB PROPERTIES OF SCRAPIE PRION PROTEINS INTO DETERGENT-LIPID-PROTEIN COMPLEXES | 0 | 0 |
| # | LCR | NCR | Node / Date / Journal / Author | LCS | GCS |
| 41 | 2 | 2 | 188 1987 ANNALS OF NEUROLOGY 22 (1): 157-157 WESTAWAY D; GOODMAN P; MIRENDA C; CARLSON G; PRUSINER SB NUCLEOTIDE-SEQUENCE ANALYSIS OF PRN-P GENES FROM SHORT AND LONG SCRAPIE PRION INCUBATION PERIOD MICE | 0 | 0 |
| 42 | 0 | 3 | 237 1989 ANNALS OF NEUROLOGY 26 (1): 137-137 HSIAO K; DOHURA K; KITAMOTO T; TATEISHI J; PRUSINER SB A PRION PROTEIN AMINO-ACID SUBSTITUTION IN ATAXIC GERSTMANN-STRAUSSLER SYNDROME | 28 | 35 |
| 43 | 3 | 36 | 250 1990 ANNALS OF NEUROLOGY 27 (3): 291-297 BOYLAN KB; TAKAHASHI N; PATY DW; SADOVNICK AD; DIAMOND M; et al. DNA LENGTH POLYMORPHISM-5' TO THE MYELIN BASIC-PROTEIN GENE IS ASSOCIATED WITH MULTIPLE-SCLEROSIS | 0 | 63 |
| 44 | 2 | 10 | 284 1991 ANNALS OF NEUROLOGY 29 (1): 95-97 EPSTEIN CJ; FOSTER DB; DEARMOND SJ; PRUSINER SB ACCELERATION OF SCRAPIE IN TRISOMY-16-REVERSIBLE-DIPLOID AGGREGATION CHIMERAS | 0 | 3 |
| 45 | 38 | 122 | 352 1994 ANNALS OF NEUROLOGY 35 (4): 385-395 PRUSINER SB; HSIAO KK HUMAN PRION DISEASES | 19 | 163 |
| 46 | 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 |
| 47 | 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 |
| 48 | 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 |
| 49 | 17 | 25 | 285 1991 ANNALS OF THE NEW YORK ACADEMY OF SCIENCES 640: 166-170 HSIAO K; SCOTT M; FOSTER D; DEARMOND SJ; GROTH D; et al. SPONTANEOUS NEURODEGENERATION IN TRANSGENIC MICE WITH PRION PROTEIN CODON-101 PROLINE-]LEUCINE SUBSTITUTION | 2 | 9 |
| 50 | 73 | 146 | 495 1998 ANNUAL REVIEW OF BIOCHEMISTRY 67: 793-+ Cohen FE; Prusiner SB Pathologic conformations of prion proteins | 28 | 213 |
| # | LCR | NCR | Node / Date / Journal / Author | LCS | GCS |
| 51 | 72 | 220 | 462 1997 ANNUAL REVIEW OF GENETICS 31: 139-175 Prusiner SB; Scott MR Genetics of prions | 2 | 64 |
| 52 | 6 | 160 | 73 1981 ANNUAL REVIEW OF MEDICINE 32: 521-542 PRUSINER SB DISORDERS OF GLUTAMATE METABOLISM AND NEUROLOGICAL DYSFUNCTION | 1 | 9 |
| 53 | 30 | 94 | 189 1987 ANNUAL REVIEW OF MEDICINE 38: 381-398 PRUSINER SB PRIONS CAUSING DEGENERATIVE NEUROLOGICAL DISEASES | 2 | 26 |
| 54 | 49 | 167 | 238 1989 ANNUAL REVIEW OF MICROBIOLOGY 43: 345-374 PRUSINER SB SCRAPIE PRIONS | 62 | 183 |
| 55 | 79 | 251 | 353 1994 ANNUAL REVIEW OF MICROBIOLOGY 48: 655-686 PRUSINER SB BIOLOGY AND GENETICS OF PRION DISEASES | 12 | 116 |
| 56 | 59 | 135 | 354 1994 ANNUAL REVIEW OF NEUROSCIENCE 17: 311-339 PRUSINER SB; DEARMOND SJ PRION DISEASES AND NEURODEGENERATION | 5 | 101 |
| 57 | 0 | 5 | 53 1979 APPLIED AND ENVIRONMENTAL MICROBIOLOGY 38 (5): 934-939 CHATIGNY MA; DUNN S; ISHIMARU K; EAGLESON JA; PRUSINER SB EVALUATION OF A CLASS-III BIOLOGICAL SAFETY CABINET FOR ENCLOSURE OF AN ULTRA-CENTRIFUGE | 0 | 2 |
| 58 | 0 | 47 | 4 1968 ARCHIVES OF BIOCHEMISTRY AND BIOPHYSICS 123 (2): 368-& Prusiner SB; WILLIAMS.JR; CHANCE B; PADDLE BM PYRIDINE NUCLEOTIDE CHANGES DURING THERMOGENESIS IN BROWN FAT TISSUE IN VIVO | 4 | 32 |
| 59 | 14 | 47 | 239 1989 ARCHIVES OF BIOCHEMISTRY AND BIOPHYSICS 274 (1): 1-13 HARAGUCHI T; FISHER S; OLOFSSON S; ENDO T; GROTH D; et al. ASPARAGINE-LINKED GLYCOSYLATION OF THE SCRAPIE AND CELLULAR PRION PROTEINS | 46 | 112 |
| 60 | 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 |
| # | LCR | NCR | Node / Date / Journal / Author | LCS | GCS |
| 61 | 14 | 37 | 616 2004 ARCHIVES OF BIOCHEMISTRY AND BIOPHYSICS 432 (2): 188-195 Requena JR; Dimitrova MN; Legname G; Teijeira S; Prusiner SB; et al. Oxidation of methionine residues in the prion protein by hydrogen peroxide | 0 | 3 |
| 62 | 1 | 38 | 5 1968 ARCHIVES OF NEUROLOGY 19 (6): 623-& Prusiner SB; WOLFSON SK HYPOTHERMIC PROTECTION AGAINST CEREBRAL EDEMA OF ISCHEMIA - PREVENTION OF CEREBRAL EDEMA IN RAT AFTER PROLONGED CIRCULATORY ARREST | 0 | 9 |
| 63 | 71 | 322 | 327 1993 ARCHIVES OF NEUROLOGY 50 (11): 1129-1153 PRUSINER SB GENETIC AND INFECTIOUS PRION DISEASES | 11 | 138 |
| 64 | 0 | 10 | 617 2004 ARCHIVES OF NEUROLOGY 61 (2): 213-216 Goldman JS; Miller BL; Safar J; de Tourreil S; Martindale JL; et al. When Sporadic disease is not Sporadic - The potential for genetic etiology | 0 | 3 |
| 65 | 0 | 8 | 2 1965 ARCHIVES OF SURGERY 91 (6): 902-& PRUSINER SB; MOSKOVIT.PA; WOLFSON SK RELATIONSHIP OF ACIDEMIA TO CEREBRAL EDEMA | 1 | 2 |
| 66 | 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 |
| 67 | 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 |
| 68 | 0 | 22 | 6 1968 BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS 30 (5): 508-& PRUSINER SB; EISENHAR.RH; RYLANDER E; LINDBERG O REGULATION OF OXIDATIVE METABOLISM OF ISOLATED BROWN FAT CELLS | 5 | 31 |
| 69 | 2 | 23 | 13 1971 BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS 45 (6): 1474-& Prusiner SB; STADTMAN ER REGULATION OF GLUTAMINASE IN E-COLI - METABOLITE CONTROL | 7 | 19 |
| 70 | 51 | 191 | 251 1990 BIOCHEMICAL JOURNAL 266 (1): 1-14 GABIZON R; PRUSINER SB PRION LIPOSOMES | 27 | 53 |
| # | LCR | NCR | Node / Date / Journal / Author | LCS | GCS |
| 71 | 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 |
| 72 | 3 | 35 | 41 1978 BIOCHEMISTRY 17 (23): 4987-4992 PRUSINER SB; HADLOW WJ; EKLUND CM; RACE RE; COCHRAN SP SEDIMENTATION CHARACTERISTICS OF SCRAPIE AGENT FROM MURINE SPLEEN AND BRAIN | 27 | 43 |
| 73 | 3 | 38 | 42 1978 BIOCHEMISTRY 17 (23): 4993-4999 PRUSINER SB; HADLOW WJ; GARFIN DE; COCHRAN SP; BARINGER JR; et al. PARTIAL-PURIFICATION AND EVIDENCE FOR MULTIPLE MOLECULAR-FORMS OF SCRAPIE AGENT | 56 | 78 |
| 74 | 3 | 40 | 59 1980 BIOCHEMISTRY 19 (11): 2367-2373 MAMELOK RD; GROTH DF; PRUSINER SB SEPARATION OF MEMBRANE-BOUND GAMMA-GLUTAMYL-TRANSFERASE TRANSPEPTIDASE FROM BRUSH-BORDER TRANSPORT AND ENZYME-ACTIVITIES | 3 | 25 |
| 75 | 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 |
| 76 | 3 | 34 | 61 1980 BIOCHEMISTRY 19 (21): 4892-4898 PRUSINER SB; GROTH DF; COCHRAN SP; MCKINLEY MP; MASIARZ FR GEL-ELECTROPHORESIS AND GLASS PERMEATION CHROMATOGRAPHY OF THE HAMSTER SCRAPIE AGENT AFTER ENZYMATIC DIGESTION AND DETERGENT EXTRACTION | 21 | 27 |
| 77 | 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 |
| 78 | 16 | 43 | 116 1984 BIOCHEMISTRY 23 (25): 5898-5906 BOLTON DC; MCKINLEY MP; PRUSINER SB MOLECULAR CHARACTERISTICS OF THE MAJOR SCRAPIE PRION PROTEIN | 44 | 116 |
| 79 | 13 | 28 | 190 1987 BIOCHEMISTRY 26 (25): 8110-8115 HAY B; PRUSINER SB; LINGAPPA VR EVIDENCE FOR A SECRETORY FORM OF THE CELLULAR PRION PROTEIN | 24 | 78 |
| 80 | 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 |
| # | LCR | NCR | Node / Date / Journal / Author | LCS | GCS |
| 81 | 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 |
| 82 | 15 | 60 | 253 1990 BIOCHEMISTRY 29 (24): 5848-5855 OESCH B; TEPLOW DB; STAHL N; SERBAN D; HOOD LE; et al. IDENTIFICATION OF CELLULAR PROTEINS BINDING TO THE SCRAPIE PRION PROTEIN | 17 | 55 |
| 83 | 24 | 60 | 254 1990 BIOCHEMISTRY 29 (38): 8879-8884 STAHL N; BALDWIN MA; BURLINGAME AL; PRUSINER SB IDENTIFICATION OF GLYCOINOSITOL PHOSPHOLIPID LINKED AND TRUNCATED FORMS OF THE SCRAPIE PRION PROTEIN | 20 | 88 |
| 84 | 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 |
| 85 | 51 | 147 | 307 1992 BIOCHEMISTRY 31 (49): 12277-12288 PRUSINER SB CHEMISTRY AND BIOLOGY OF PRIONS | 6 | 87 |
| 86 | 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 |
| 87 | 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 |
| 88 | 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 |
| 89 | 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 |
| 90 | 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 |
| # | LCR | NCR | Node / Date / Journal / Author | LCS | GCS |
| 91 | 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 |
| 92 | 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 |
| 93 | 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 |
| 94 | 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 |
| 95 | 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 |
| 96 | 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 |
| 97 | 9 | 43 | 605 2003 BIOCHEMISTRY 42 (22): 6794-6803 Burns CS; Aronoff-Spencer E; Legname G; Prusiner SB; Antholine WE; et al. Copper coordination in the full-length, recombinant prion protein | 1 | 37 |
| 98 | 34 | 77 | 148 1986 BIOESSAYS 5 (6): 281-286 PRUSINER SB PRIONS ARE NOVEL INFECTIOUS PATHOGENS CAUSING SCRAPIE AND CREUTZFELDT-JAKOB DISEASE | 0 | 1 |
| 99 | 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 |
| 100 | 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 |
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