PRUSINER

Your search request has found 221 STORIES through Level 1

                             LEVEL 1 - 221 STORIES                              
1.   Science, October 4, 1996, Vol. 274 ; No. 5284 ; Pg. 99; ISSN: 0036-8075,
3188 words, Correlative memory deficits, A-beta elevation, and amyloid plaques
in transgenic mice., Hsiao, Karen ; Chapman, Paul ; Nilsen, Steven ; Eckman,
Chris ; Harigaya, Yasuo ; Younkin, Steven ; Yang, Fusheng ; Cole, Greg, IAC
18781874

2.   PR Newswire, September 22, 1996, Sunday, Financial News, 469 words, First
Keio Medical Science Prize To Professor Stanley B.Prusiner, TOKYO, Sept. 22

3.  PR Newswire, September 21, 1996, Saturday, Domestic News, 467 words,
First Keio Medical Science Prize To Professor Stanley B. Prusiner, TOKYO,
Sept. 21

4.   Japan Economic Newswire, SEPTEMBER 20, 1996, FRIDAY, 219 words, U.S.,
Japanese doctors to get Keio medical awards, TOKYO, Sept. 20 Kyodo

5.  PR Newswire, September 5, 1996, Thursday, Financial News, 773 words,
UCSF Professor Stanley Prusiner Wins ICN's $50,000 International Prize In
Virology, COSTA MESA, Calif., Sept. 5

6.  The Tampa Tribune, August 18, 1996, Sunday, METRO EDITION, Pg. 1, 1301
words, Rare brain disorder grips Mulberry woman, CRAIG S. PALOSKY; of The
Tampa Tribune

7.   Morbidity and Mortality Weekly Report, August 9, 1996, Vol. 45 ; No. 31 ;
Pg. 665; ISSN: 0149-2195, 2013 words, Surveillance for Creudtzfeldt-Jakob
disease - United States., IAC 18654068

8.   Lancet, August 3, 1996, VOL. 348; No. 23; Pg. 326, 971 words, Keeping an
open mind about prions, Finkel, Elizabeth, IAC 06140651

9.  The Lancet, August 3, 1996, Vol. 348 ; No. 9023 ; Pg. 326; ISSN:
0099-5355, 973 words, Keeping an open mind about prions., Finkel,
Elizabeth, IAC 18566422

10.   Science, August 2, 1996, Vol. 273 ; No. 5275 ; Pg. 622; ISSN: 0036-8075,
4047 words, Support for the prion hypothesis for inheritance of a phenotype
trait in yeast., Patino, Maria M. ; Liu, Jia-Jia ; Glover, John ; Lindquist,
Susan, IAC 18599672

11.   Science, July 12, 1996, Vol. 273 ; No. 5272 ; Pg. 184; ISSN: 0036-8075,
5165 words, Putting prions to the test; proteinaceous infectious particles,
infectious proteins; includes related article on neurologist Stanley Prusiner,
Mestel, Rosie, IAC 18500947

12.   Science, July 12, 1996, Vol. 273 ; No. 5272 ; Pg. 186; ISSN: 0036-8075,
1008 words, Flipping yeast; malformed proteins, prions, Mestel, Rosie, IAC
18500948

13.  The Guardian, July 4, 1996, THE GUARDIAN ONLINE PAGE; Pg. 13, 1867
words, OFF LINE: BSE: IS BRITISH SCIENCE TO BLAME? Jeffrey Almond

14.  Lewiston Morning Tribune, June 17, 1996, Local/Regional; Pg. 5A, 867
words Cows aren't the only ones going loco

15.   Newsday, June 13, 1996, Thursday, NASSAU EDITION, Page A42, 529 words,
TESTS BEING DEVELOPED FOR MAD COW DISEASE, By Robert Cooke. STAFF WRITER 

16.  Food Chemical News, June 3, 1996, No. 15, Vol. 38; ISSN: 0015-6337,
394 words, MAD COW DISEASE MUST BE FOUND IN U.S. COWS IN LOW LEVELS, SAYS
RESEARCH, 3323653

17.  The Daily Telegraph, May 29, 1996, Wednesday, Pg. 18, 668 words,
Science:  THREE DISEASES WITH ONE CAUSE Long hunt for the deadly agent

18.  Los Angeles Times, May 26, 1996, Sunday, Home Edition, Page 3, 1616
words, 'MAD COW' DISEASE: IS IT A PRION OR A VIRUS?;  MEDICINE: A UC
SCIENTIST THEORIZES THAT A RUNAWAY PROTEIN CAUSES THE FATAL BRAIN DISEASE,
THOUGH NOTHING IS CONCLUSIVE., KENNETH CHANG, TIMES STAFF WRITER

19.   Lancet, May 11, 1996, VOL. 347; No. 11; Pg. 1332, 2466 words,
Creutzfeldt-Jakob disease, Foncin, Jean-Franois, IAC 06100287

20. FDCH Federal Department and Agency Documents , May 10, 1996; Friday ,
1602 words, DEPARTMENT OF HEALTH AND HUMAN SERVICES , 02 - Food, Drug and
Health , BOVINE SPONGIFORM ENCEPHALOPATHY AND CREUTZFELDT-JAKOB DISEASE ,
202/ 690 6343

21.  Federal Document Clearing House Congressional Testimony, May 10,
1996, Friday, CAPITOL HILL HEARING TESTIMONY, 3532 words, TESTIMONY May
10, 1996 DON A. FRANCO, DVM DIRECTOR OF SCIENTIFIC SERVICES NATIONAL
RENDERERS ASSOCIATION, INC.  HOUSE GOVERNMENT REFORM AND OVERSIGHT HUMAN
RESOURCES AND INTERGOVERNMENTAL RELATIONS FDA CENTER FOR VETERINARY MEDICINE

22.  The Buffalo News, May 5, 1996, Sunday, FINAL EDITION, VIEWPOINTS, Pg.
12F, 1410 words, THE MYSTERIOUS 'PRION' -- 'STRANGEST THING IN ALL
BIOLOGY'; IT'S IMPLICATED IN SCRAPIE SICKNESS OF SHEEP, 'MAD-COW DISEASE,'
AND; 'LAUGHING DEATH' IN CANNIBALS, LAURA BEIL; Dallas Morning News

23.  Lancet, April 20, 1996, VOL. 347; No. 9008; Pg. 1114, 1077 words,
Mites as vectors for scrapie, Wisniewski, Henryk MSigurdarson,
SigurdurRubenstein, RichardCarp., Richard I Kascsak, Richard J, IAC
06094307

24.  THE DALLAS MORNING NEWS, April 15, 1996, Monday, HOME FINAL EDITION,
DISCOVERIES; Pg. 8D, 1744 words, WHAT'S THE BEEF?; Unusual type of
infectious agent is likely suspect in mad cow' disease, Laura Beil, Public
Health Writer of The Dallas Morning News

25.  BIOWORLD Today, April 8, 1996, VOL. 7; No. 69, 918 words, CAN
BRITAIN'S 'MAD COWS' BE CAUSING HUMAN PRION DISEASE? NEUROLOGISTS WONDER
ABOUT CREUTZFELDT-JAKOB OUTBREAK, IAC 06085990

26.  Business Week, April 8, 1996, NEWS; Analysis & Commentary:
COMMENTARY; Number 3470; Pg. 35, 707 words, COMMENTARY: JUNK SCIENCE AND
MASS HYSTERIA, By Paul Raeburn; Raeburn is BUSINESS WEEK’s senior
editor for science and technology. 

27.  Newsweek, April 8, 1996 , UNITED STATES EDITION, LIFESTYLE; Medicine;
Pg.  58, 968 words, 'Mad Cow Disease' in the U.S.?, BY MARY HAGER AND MARK
HOSENBALL With SHARON BEGLEY

28.  The Washington Post, April 08, 1996, Monday, Final Edition, A
SECTION; Pg. A03; SCIENCE: BIOLOGY, 1235 words, At Cow Scare's Core: An
Odd Protein, David Brown, Washington Post Staff Writer

29.  Pittsburgh Post-Gazette, April 7, 1996, Sunday, FIVE STAR EDITION,
Pg. A-13, 882 words, CALIF. TEAM IDENTIFIED 'MAD COW' 15 YEARS AGO, LISA
M. KRIEGER, SAN FRANCISCO EXAMINER, SAN FRANCISCO

30.  Pittsburgh Post-Gazette, April 7, 1996, Sunday, TWO STAR EDITION, Pg.
A-12 396 words, U.S. DOCTORS SAW MAD-COW THREAT LONG AGO, LISA M. KRIEGER,
SAN FRANCISCO EXAMINER, SAN FRANCISCO

31.  The Lancet, April 6, 1996, Vol. 347 ; No. 9006 ; Pg. 917; ISSN:
0099-5355, 1211 words, A dreadful challenge.route of human infection from
bovine spongiform encephalopathy; Commentary, Collee, J. Gerald, IAC
18214449

32.  The Lancet, April 6, 1996, Vol. 347 ; No. 9006 ; Pg. 945; ISSN:
0099-5355, 4202 words, Creutzfeldt-Jacob disease in a young woman.Report
of a Meeting of Physicians and Scientists, St Thomas' Hospital, London;
Grand Round, Tabrizi, S.J. ; Scaravilli, F. ; Howard, R.S. ; Collinge,
John ; Rossor, M.N., IAC 18214460

33.  The Richmond Times Dispatch, April 4, 1996, Thursday, CITY EDITION,
Pg. E-1, 607 words, AGENT IN MAD COW DISEASE MULTIPLIES IN UNUSUAL WAY,
Beverly Orndorff

PRUSINER

Your search request has found 306 REFERENCES through Level 1

                            LEVEL 1 - 306 REFERENCES                        
1. Interactions between wild-type and mutant prion proteins modulate
neurodegeneration in transgenic mice., Telling GC; Haga T; Torchia M; Tremblay
P; DeArmond SJ; Prusiner SB, Genes Dev 1996 Jul 15; 10 (14): 1736-50

2. Circumventing tolerance to generate autologous monoclonal antibodies to the
prion protein., Williamson RA; Peretz D; Smorodinsky N; Bastidas R; Serban H;
Mehlhorn I; DeArmond SJ; Prusiner SB; Burton DR, Proc Natl Acad Sci U S A 1996
Jul 9; 93 (14): 7279-82

3. Separation of scrapie prion infectivity from PrP amyloid polymers.,
Wille H;  Zhang GF; Baldwin MA; Cohen FE; Prusiner SB, J Mol Biol 1996 Jun
21; 259 (4): 608-21

4. High-level expression and characterization of a purified 142-residue
polypeptide of the prion protein., Mehlhorn I; Groth D; Stockel J; Moffat B;
Reilly D; Yansura D; Willett WS; Baldwin M; Fletterick R; Cohen FE; Vandlen R;
Henner D; Prusiner SB, Biochemistry 1996 Apr 30; 35 (17): 5528-37

5. Mice deficient for prion protein exhibit normal neuronal excitability and
synaptic transmission in the hippocampus., Lledo PM; Tremblay P; DeArmond SJ;
Prusiner SB; Nicoll RA, Proc Natl Acad Sci U S A 1996 Mar 19; 93 (6): 2403-7

6. Disruption of prion rods generates 10-nm spherical particles having high
alpha-helical content and lacking scrapie infectivity., Riesner D; Kellings K;
Post K; Wille H; Serban H; Groth D; Baldwin MA; Prusiner SB, J Virol 1996 Mar;
70 (3): 1714-22

7. Human prion diseases and neurodegeneration., 118 REFS, Prusiner SB,
Curr Top Microbiol Immunol 1996; 207: 1-17

8. Transgenetics and neuropathology of prion diseases., 80 REFS, DeArmond SJ;
Prusiner SB, Curr Top Microbiol Immunol 1996; 207: 125-46

9. Structures of prion proteins and conformational models for prion diseases.,
Huang Z; Prusiner SB; Cohen FE, Curr Top Microbiol Immunol 1996; 207: 49-67

10. Transgenetics and gene targeting in studies of prion diseases., 134
REFS, Scott MR; Telling GC; Prusiner SB, Curr Top Microbiol Immunol 1996;
207: 95-123 11. Transgenetics of prion diseases., 134 REFS, Prusiner SB,
Curr Top Microbiol Immunol 1996; 206: 275-304

12. Lipid composition in scrapie-infected mouse brain: prion infection
increases the levels of dolichyl phosphate and ubiquinone., Guan Z;
Soderberg M; P; Prusiner SB; Kristensson K; Dallner G, J Neurochem 1996
Jan; 66 (1): 277-85

13. Insoluble wild-type and protease-resistant mutant prion protein in
brains of patients with inherited prion disease., Gabizon R; Telling G;
Meiner Z; Halimi M; Kahana I; Prusiner SB, Nat Med 1996 Jan; 2 (1): 59-64

14. Prion disease (PrP-A117V) presenting with ataxia instead of dementia.,
Mastrianni JA; Curtis MT; Oberholtzer JC; Da Costa MM; DeArmond S;
Prusiner SB;  Garbern JY, Neurology 1995 Nov; 45 (11): 2042-50

15. Scanning for mutations in the human prion protein open reading frame
by temporal temperature gradient gel electrophoresis., Wiese U; Wulfert M;
Prusiner SB; Riesner D, Electrophoresis 1995 Oct; 16 (10): 1851-60

16. Complete penetrance of Creutzfeldt-Jakob disease in Libyan Jews
carrying the E200K mutation in the prion protein gene., Spudich S;
Mastrianni JA; Wrensch M;  Gabizon R; Meiner Z; Kahana I; Rosenmann H;
Kahana E; Prusiner SB, Mol Med 1995 Sep; 1 (6): 607-13

17. Prion protein isoforms, a convergence of biological and structural
investigations., 80 REFS, Baldwin MA; Cohen FE; Prusiner SB, J Biol Chem 1995
Aug 18; 270 (33): 19197-200

18. Conformational transitions in peptides containing two putative
alpha-helices of the prion protein., Zhang H; Kaneko K; Nguyen JT;
Livshits TL; Baldwin MA; Cohen FE; James TL; Prusiner SB, J Mol Biol 1995
Jul 21; 250 (4): 514-26

19. Prion protein peptides induce alpha-helix to beta-sheet conformational
transitions., Nguyen J; Baldwin MA; Cohen FE; Prusiner SB, Biochemistry
1995 Apr 4; 34 (13): 4186-92

20. Etiology and pathogenesis of prion diseases., 219 REFS, DeArmond SJ;
Prusiner SB, Am J Pathol 1995 Apr; 146 (4): 785-811

21. Cholesterol depletion and modification of COOH-terminal targeting
sequence of the prion protein inhibit formation of the scrapie isoform
[published erratum appears in J Cell Biol 1995 Jul;130(2):501].,
Taraboulos A; Scott M; Semenov A;  Avrahami D; Laszlo L; Prusiner SB;
Avraham D /[corrected to Avrahami D], J Cell Biol 1995 Apr; 129 (1): 121-32

22. On safari with PrP: prion diseases of animals., 84 REFS, Westaway D;
Carlson GA; Prusiner SB, Trends Microbiol 1995 Apr; 3 (4): 141-7

23. Scrapie prions selectively modify the stress response in neuroblastoma
cells., Tatzelt J; Zuo J; Voellmy R; Scott M; Hartl U; Prusiner SB; Welch WJ,
Proc Natl Acad Sci U S A 1995 Mar 28; 92 (7): 2944-8

24. Prion protein gene variation among primates., Schatzl HM; Da Costa M;
Taylor L; Cohen FE; Prusiner SB, J Mol Biol 1995 Jan 27; 245 (4): 362-74

25. Prion protein gene variation among primates., Schatzl HM; Da Costa M;
Taylor L; Cohen FE; Prusiner SB, J Mol Biol 1995 Jan 27; 245 (4): 362-74

26. Prion protein transgenes and the neuropathology in prion diseases., 80
REFS, DeArmond SJ; Prusiner SB, Brain Pathol 1995 Jan; 5 (1): 77-89

27. The prion diseases., 6 REFS, Prusiner SB, Sci Am 1995 Jan; 272 (1): 48-51,
54-7

28. Serial transmission in rodents of neurodegeneration from transgenic
mice expressing mutant prion protein., Hsiao KK; Groth D; Scott M; Yang
SL; Serban H; Rapp D; Foster D; Torchia M; Dearmond SJ; Prusiner SB, Proc
Natl Acad Sci U S A 1994 Sep 13; 91 (19): 9126-30

29. Neurodegeneration in humans caused by prions., 114 REFS, Prusiner SB,
West J Med 1994 Sep; 161 (3): 264-72

30. Proposed three-dimensional structure for the cellular prion protein.,
Huang Z; Gabriel JM; Baldwin MA; Fletterick RJ; Prusiner SB; Cohen FE,
Proc Natl Acad Sci U S A 1994 Jul 19; 91 (15): 7139-43

31. Structure and polymorphism of the mouse prion protein gene., Westaway
D; Cooper C; Turner S; Da Costa M; Carlson GA; Prusiner SB, Proc Natl Acad
Sci U S A 1994 Jul 5; 91 (14): 6418-22

32. Determinants of carboxyl-terminal domain translocation during prion
protein biogenesis., De Fea KA; Nakahara DH; Calayag MC; Yost CS; Mirels
LF; Prusiner SB; Lingappa VR, J Biol Chem 1994 Jun 17; 269 (24): 16810-20

33. Prion isolate specified allotypic interactions between the cellular
and scrapie prion proteins in congenic and transgenic mice., Carlson GA;
Ebeling C;  Yang SL; Telling G; Torchia M; Groth D; Westaway D; DeArmond
SJ; Prusiner SB, Proc Natl Acad Sci U S A 1994 Jun 7; 91 (12): 5690-4

34. PrP-deficient mice are resistant to scrapie., Weissmann C; Bueler H;
Fischer M; Sailer A; Aguzzi A; Aguet M, Ann N Y Acad Sci 1994 Jun 6; 724:
235-40

35. Inherited prion diseases., 68 REFS, Prusiner SB, Proc Natl Acad Sci U S A
1994 May 24; 91 (11): 4611-4

36. [Natural history of transmissible subacute spongiform encephalopathy
(TSSE)]., Histoire naturelle des encephalopathies subaigues spongiformes
transmissibles (ESST)., 41 REFS, Constantin A, Bull Acad Natl Med 1994
May; 178 (5): 859-71

37. Structural clues to prion replication [see comments]., Cohen FE; Pan
KM; Huang Z; Baldwin M; Fletterick RJ; Prusiner SB, Science 1994 Apr 22;
264 (5158): 530-1

38. Homozygosity for prion protein alleles encoding glutamine-171 renders
sheep susceptible to natural scrapie., Westaway D; Zuliani V; Cooper CM;
Da Costa M; Neuman S; Jenny AL; Detwiler L; Prusiner SB, Genes Dev 1994
Apr 15; 8 (8): 959-69

39. Human prion diseases., 122 REFS, Prusiner SB; Hsiao KK, Ann Neurol
1994 Apr; 35 (4): 385-95

40. Genetics of prion diseases and prion diversity in mice., 32 REFS,
Carlson GA; DeArmond SJ; Torchia M; Westaway D; Prusiner SB, Philos Trans
R Soc Lond B Biol Sci 1994 Mar 29; 343 (1306): 363-9

41. Mutation in codon 200 and polymorphism in codon 129 of the prion
protein gene in Libyan Jews with Creutzfeldt-Jakob disease., Gabizon R;
Rosenman H; Meiner Z; Kahana I; Kahana E; Shugart Y; Ott J; Prusiner SB,
Philos Trans R Soc Lond B Biol Sci 1994 Mar 29; 343 (1306): 385-90

42. The neuropathological phenotype in transgenic mice expressing different
prion protein constructs., 49 REFS, DeArmond SJ; Yang SL; Cayetano-Canlas J;
Groth D; Prusiner SB, Philos Trans R Soc Lond B Biol Sci 1994 Mar 29; 343
(1306): 415-23

43. Nucleic acids in prion preparations: unspecific background or
essential component?., Kellings K; Prusiner SB; Riesner D, Philos Trans R
Soc Lond B Biol Sci 1994 Mar 29; 343 (1306): 425-30

44. Molecular biology and genetics of prion diseases., 218 REFS, Prusiner SB,
Philos Trans R Soc Lond B Biol Sci 1994 Mar 29; 343 (1306): 447-63

45. Biosynthesis of the prion proteins in scrapie-infected cells in culture.,
Taraboulos A; Scott M; Semenov A; Avrahami D; Prusiner SB, Braz J Med Biol Res
1994 Feb; 27 (2): 303-7

46. Prion protein (PrP) is not involved in the pathogenesis of spongiform
encephalopathy in zitter rats., Gomi H; Ikeda T; Kunieda T; Itohara S;
Prusiner SB; Yamanouchi K, Neurosci Lett 1994 Jan 31; 166 (2): 171-4

47. Degeneration of skeletal muscle, peripheral nerves, and the central
nervous system in transgenic mice overexpressing wild-type prion
proteins., Westaway D;  DeArmond SJ; Cayetano-Canlas J; Groth D; Foster D;
Yang SL; Torchia M; Carlson GA; Prusiner SB, Cell 1994 Jan 14; 76 (1):
117-29

48. Prion diseases and neurodegeneration., 135 REFS, Prusiner SB; DeArmond SJ,
Annu Rev Neurosci 1994; 17: 311-39

49. Biology and genetics of prion diseases., 249 REFS, Prusiner SB, Annu Rev
Microbiol 1994; 48: 655-86

50. Detecting prion protein gene mutations by denaturing gradient gel
electrophoresis., Fink JK; Peacock ML; Warren JT Jr; Roses AD; Prusiner
SB, Hum Mutat 1994; 4 (1): 42-50

51. A national strategy for development of effective methods for the
prevention and treatment of Alzheimer's disease and related
neurodegenerative disorders., 0 REFS, Prusiner SB, Neurobiol Aging 1994;
15 Suppl 2: S29-32

52. Ablation of the prion protein (PrP) gene in mice prevents scrapie and
facilitates production of anti-PrP antibodies., Prusiner SB; Groth D;
Serban A;  Koehler R; Foster D; Torchia M; Burton D; Yang SL; DeArmond SJ,
Proc Natl Acad Sci U S A 1993 Nov 15; 90 (22): 10608-12

53. Genetic and infectious prion diseases., 324 REFS, Prusiner SB, Arch Neurol
1993 Nov; 50 (11): 1129-53

54. The neurochemistry of prion diseases., 84 REFS, DeArmond SJ; Prusiner
SB, J Neurochem 1993 Nov; 61 (5): 1589-601

55. Mutation and polymorphism of the prion protein gene in Libyan Jews
with Creutzfeldt-Jakob disease (CJD)., Gabizon R; Rosenmann H; Meiner Z;
Kahana I; Kahana E; Shugart Y; Ott J; Prusiner SB, Am J Hum Genet 1993
Oct; 53 (4): 828-35 56. Transgenetics and cell biology of prion diseases:
investigations of PrPSc synthesis and diversity., 125 REFS, Prusiner SB,
Br Med Bull 1993 Oct; 49 (4): 873-912

57. Release of the cellular prion protein from cultured cells after loss
of its glycoinositol phospholipid anchor., Borchelt DR; Rogers M; Stahl N;
Telling G; Prusiner SB, Glycobiology 1993 Aug; 3 (4): 319-29

58. Three scrapie prion isolates exhibit different accumulation patterns
of the prion protein scrapie isoform., DeArmond SJ; Yang SL; Lee A; Bowler
R; Taraboulos A; Groth D; Prusiner SB, Proc Natl Acad Sci U S A 1993 Jul
15; 90 (14): 6449-53

59. Mice devoid of PrP are resistant to scrapie., Bueler H; Aguzzi A;
Sailer A;  Greiner RA; Autenried P; Aguet M; Weissmann C, Cell 1993 Jul 2;
73 (7): 1339-47 60. Propagation of prions with artificial properties in
transgenic mice expressing chimeric PrP genes., Scott M; Groth D; Foster
D; Torchia M; Yang SL;  DeArmond SJ; Prusiner SB, Cell 1993 Jun 4; 73 (5):
979-88

61. Biology of prion diseases., 30 REFS, Prusiner SB, J Acquir Immune Defic
Syndr 1993 Jun; 6 (6): 663-5

62. Conversion of truncated and elongated prion proteins into the scrapie
isoform in cultured cells., Rogers M; Yehiely F; Scott M; Prusiner SB,
Proc Natl Acad Sci U S A 1993 Apr 15; 90 (8): 3182-6

63. Delimiting the location of the scrapie prion incubation time gene on
chromosome 2 of the mouse., Carlson GA; Ebeling C; Torchia M; Westaway D;
Prusiner SB, Genetics 1993 Apr; 133 (4): 979-88

64. Attempts to restore scrapie prion infectivity after exposure to
protein denaturants., Prusiner SB; Groth D; Serban A; Stahl N; Gabizon R,
Proc Natl Acad Sci U S A 1993 Apr 1; 90 (7): 2793-7

65. Structural studies of the scrapie prion protein using mass
spectrometry and amino acid sequencing., Stahl N; Baldwin MA; Teplow DB;
Hood L; Gibson BW; Burlingame AL; Prusiner SB, Biochemistry 1993 Mar 2; 32
(8): 1991-2002

66. Immunologic and molecular biologic studies of prion proteins in bovine
spongiform encephalopathy., Prusiner SB; Fuzi M; Scott M; Serban D; Serban
H; Taraboulos A; Gabriel JM; Wells GA; Wilesmith JW; Bradley R; et al, J
Infect Dis 1993 Mar; 167 (3): 602-13

67. Transgenetic investigations of prion diseases of humans and animals., 136
REFS, Prusiner SB, Philos Trans R Soc Lond B Biol Sci 1993 Feb 27; 339 (1288):
239-54

68. Prions and nucleic acids: search for "residual" nucleic acids and
screening for mutations in the PrP-gene., Riesner D; Kellings K; Wiese U;
Wulfert M; Mirenda C; Prusiner SB, Dev Biol Stand 1993; 80: 173-81

69. Prion encephalopathies of animals and humans., 118 REFS, Prusiner SB, Dev
Biol Stand 1993; 80: 31-44

70. Role of the PrP gene in transmissible spongiform encephalopathies., 88
REFS, Weissmann C; Bueler H; Fischer M; Aguet M, Intervirology 1993; 35
(1-4): 164-75

71. Perturbation of the secondary structure of the scrapie prion protein under
conditions that alter infectivity., Gasset M; Baldwin MA; Fletterick RJ;
Prusiner SB, Proc Natl Acad Sci U S A 1993 Jan 1; 90 (1): 1-5

72. Chemistry and biology of prions., 169 REFS, Prusiner SB, Biochemistry 1992
Dec 15; 31 (49): 12277-88

73. Predicted alpha-helical regions of the prion protein when synthesized
as peptides form amyloid., Gasset M; Baldwin MA; Lloyd DH; Gabriel JM;
Holtzman DM; Cohen F; Fletterick R; Prusiner SB, Proc Natl Acad Sci U S A
1992 Nov 15; 89 (22): 10940-4

74. Natural and experimental prion diseases of humans and animals., 115 REFS,
Prusiner SB, Curr Opin Neurobiol 1992 Oct; 2 (5): 638-47

75. Molecular cloning of a mink prion protein gene., Kretzschmar HA;
Neumann M;  Riethmuller G; Prusiner SB, J Gen Virol 1992 Oct; 73 ( Pt 10):
2757-61

76. Attempts to convert the cellular prion protein into the scrapie isoform in
cell-free systems., Raeber AJ; Borchelt DR; Scott M; Prusiner SB, J Virol 1992
Oct; 66 (10): 6155-63

77. Molecular cloning of a candidate chicken prion protein., Gabriel JM;
Oesch B; Kretzschmar H; Scott M; Prusiner SB, Proc Natl Acad Sci U S A
1992 Oct 1; 89 (19): 9097-101

78. Prion protein preamyloid and amyloid deposits in
Gerstmann-Straussler-Scheinker disease, Indiana kindred [published erratum
appears in Proc Natl Acad Sci U S A 1993 Jan 1;90(1):302]., Giaccone G;
Verga L; Bugiani O; Frangione B; Serban D; Prusiner SB; Farlow MR; Ghetti
B; Tagliavini F Proc Natl Acad Sci U S A 1992 Oct 1; 89 (19): 9349-53

79. Purification and properties of the cellular prion protein from Syrian
hamster brain., Pan KM; Stahl N; Prusiner SB, Protein Sci 1992 Oct; 1 (10):
1343-52

80. Evidence for synthesis of scrapie prion proteins in the endocytic
pathway., Borchelt DR; Taraboulos A; Prusiner SB, J Biol Chem 1992 Aug 15;
267 (23): 16188-99

81. Regional mapping of prion proteins in brain., Taraboulos A; Jendroska K;
Serban D; Yang SL; DeArmond SJ; Prusiner SB, Proc Natl Acad Sci U S A 1992 Aug
15; 89 (16): 7620-4

82. Synthesis and trafficking of prion proteins in cultured cells.,
Taraboulos A; Raeber AJ; Borchelt DR; Serban D; Prusiner SB, Mol Biol Cell
1992 Aug; 3 (8): 851-63

83. Chimeric prion protein expression in cultured cells and transgenic mice.,
Scott MR; Kohler R; Foster D; Prusiner SB, Protein Sci 1992 Aug; 1 (8): 986-97

84. Replication of distinct scrapie prion isolates is region specific in
brains of transgenic mice and hamsters., Hecker R; Taraboulos A; Scott M;
Pan KM; Yang SL; Torchia M; Jendroska K; DeArmond SJ; Prusiner SB, Genes
Dev 1992 Jul; 6 (7): 1213-28

85. Presence of prion protein in peripheral tissues of Libyan Jews with
Creutzfeldt-Jakob disease [see comments]., Meiner Z; Halimi M; Polakiewicz RD;
Prusiner SB; Gabizon R, Neurology 1992 Jul; 42 (7): 1355-60

86. Glycosylinositol phospholipid anchors of the scrapie and cellular
prion proteins contain sialic acid., Stahl N; Baldwin MA; Hecker R; Pan
KM; Burlingame AL; Prusiner SB, Biochemistry 1992 Jun 2; 31 (21): 5043-53

87. Normal development and behaviour of mice lacking the neuronal
cell-surface PrP protein [see comments]., Bueler H; Fischer M; Lang Y;
Bluethmann H; Lipp HP; DeArmond SJ; Prusiner SB; Aguet M; Weissmann C,
Nature 1992 Apr 16; 356 (6370):  577-82

88. Further analysis of nucleic acids in purified scrapie prion
preparations by improved return refocusing gel electrophoresis., Kellings
K; Meyer N; Mirenda C; Prusiner SB; Riesner D, J Gen Virol 1992 Apr; 73 (
Pt 4): 1025-9

89. Linkage of the Indiana kindred of Gerstmann-Straussler-Scheinker
disease to the prion protein gene., Dlouhy SR; Hsiao K; Farlow MR; Foroud
T; Conneally PM;  Johnson P; Prusiner SB; Hodes ME; Ghetti B, Nat Genet
1992 Apr; 1 (1): 64-7

90. Mutant prion proteins in Gerstmann-Straussler-Scheinker disease with
neurofibrillary tangles., Hsiao K; Dlouhy SR; Farlow MR; Cass C; Da Costa M;
Conneally PM; Hodes ME; Ghetti B; Prusiner SB, Nat Genet 1992 Apr; 1 (1):

91. Prion protein mutation at codon 102 in an Italian family with
Gerstmann-Straussler-Scheinker syndrome., Kretzschmar HA; Kufer P; Riethmuller
G; DeArmond S; Prusiner SB; Schiffer D, Neurology 1992 Apr; 42 (4): 809-10

92. Molecular biology and genetics of neurodegenerative diseases caused by
prions., 228 REFS, Prusiner SB, Adv Virus Res 1992; 41: 241-80

93. Ultrastructural localization of scrapie prion proteins in cytoplasmic
vesicles of infected cultured cells., McKinley MP; Taraboulos A; Kenaga L;
Serban D; Stieber A; DeArmond SJ; Prusiner SB; Gonatas N, Lab Invest 1991 Dec;
65 (6): 622-30

94. Epitope mapping of the Syrian hamster prion protein utilizing chimeric
and mutant genes in a vaccinia virus expression system., Rogers M; Serban
D; Gyuris T; Scott M; Torchia T; Prusiner SB, J Immunol 1991 Nov 15; 147
(10): 3568-74

95. [Prions and Trypanosoma as a source of knowledge of the brain].,
Prioner och trypanosomer ger kunskaper om hjarnan., 15 REFS, Kristensson
K, Lakartidningen 1991 Oct 9; 88 (41): 3387-90

96. Prions and prion proteins., 114 REFS, Stahl N; Prusiner SB, FASEB J 1991
Oct; 5 (13): 2799-807

97. Electrospray mass spectrometry of the glycosylinositol phospholipid of
the scrapie prion protein., Stahl N; Baldwin MA; Prusiner SB, Cell Biol
Int Rep 1991 Sep; 15 (9): 853-62

98. Proteinase-resistant prion protein accumulation in Syrian hamster
brain correlates with regional pathology and scrapie infectivity.,
Jendroska K; Heinzel FP; Torchia M; Stowring L; Kretzschmar HA; Kon A;
Stern A; Prusiner SB;  DeArmond SJ, Neurology 1991 Sep; 41 (9): 1482-90

99. Molecular biology and pathology of scrapie and the prion diseases of
humans. 153 REFS, Prusiner SB; DeArmond SJ, Brain Pathol 1991 Jul; 1 (4):
297-310

100. Molecular biology of prion diseases., 83 REFS, Prusiner SB, Science 1991
Jun 14; 252 (5012): 1515-22

101. Infectious and genetic manifestations of prion diseases., 127 REFS,
Prusiner SB; Westaway D, Mol Plant Microbe Interact 1991 May-Jun; 4 (3):
226-33

102. A prion protein variant in a family with the telencephalic form of
Gerstmann-Straussler-Scheinker syndrome., Hsiao KK; Cass C; Schellenberg GD;
Bird T; Devine-Gage E; Wisniewski H; Prusiner SB, Neurology 1991 May; 41 (5):
681-4

103. Mutation of the prion protein in Libyan Jews with Creutzfeldt-Jakob
disease., Hsiao K; Meiner Z; Kahana E; Cass C; Kahana I; Avrahami D;
Scarlato G; Abramsky O; Prusiner SB; Gabizon R, N Engl J Med 1991 Apr 18;
324 (16): 1091-7

104. Molecular biology and genetics of prions -- implications for sheep
scrapie, "mad cows" and the BSE epidemic. Historical background
[editorial]., Prusiner SB; Torchia M; Westaway D, Cornell Vet 1991 Apr; 81
(2): 85-101

105. 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., Tagliavini F; Prelli F; Ghiso J; Bugiani O; Serban D;
Prusiner SB; Farlow MR; Ghetti B; Frangione B, EMBO J 1991 Mar; 10 (3):
513-9

106. Scrapie prion rod formation in vitro requires both detergent
extraction and limited proteolysis., McKinley MP; Meyer RK; Kenaga L;
Rahbar F; Cotter R; Serban A; Prusiner SB, J Virol 1991 Mar; 65 (3):
1340-51

107. Genetics of prion infections., 41 REFS, Carlson GA; Hsiao K; Oesch B;
Westaway D; Prusiner SB, Trends Genet 1991 Feb; 7 (2): 61-5

108. Spontaneous neurodegeneration in transgenic mice with prion protein codon
101 proline -- -- leucine substitution., Hsiao K; Scott M; Foster D; DeArmond
SJ; Groth D; Serban H; Prusiner SB, Ann N Y Acad Sci 1991; 640: 166-70

109. Acceleration of scrapie in trisomy 16 -- -- diploid aggregation
chimeras., Epstein CJ; Foster DB; DeArmond SJ; Prusiner SB, Ann Neurol
1991 Jan; 29 (1): 95-7

110. Molecular biology and transgenetics of prion diseases., 336 REFS,
Prusiner SB, Crit Rev Biochem Mol Biol 1991; 26 (5-6): 397-438

111. Prion protein genes: evolutionary and functional aspects., 78 REFS, Oesch
B; Westaway D; Prusiner SB, Curr Top Microbiol Immunol 1991; 172: 109-24

112. Novel properties and biology of scrapie prions., 183 REFS, Prusiner SB,
Curr Top Microbiol Immunol 1991; 172: 233-57

113. Ultrastructural studies of prions., 60 REFS, McKinley MP; Prusiner
SB, Curr Top Microbiol Immunol 1991; 172: 75-91

114. Molecular biology of prions causing infectious and genetic
encephalopathies of humans as well as scrapie of sheep and BSE of cattle.,
159 REFS, Prusiner SB, Dev Biol Stand 1991; 75: 55-74

115. Prion biology and diseases., 203 REFS, Prusiner SB, Harvey Lect 1991-92;
87: 85-114

116. Search for a putative scrapie genome in purified prion fractions
reveals a paucity of nucleic acids., Meyer N; Rosenbaum V; Schmidt B;
Gilles K; Mirenda C; Groth D; Prusiner SB; Riesner D, J Gen Virol 1991
Jan; 72 ( Pt 1): 37-49

117. Spontaneous neurodegeneration in transgenic mice with mutant prion
protein [see comments]., Hsiao KK; Scott M; Foster D; Groth DF; DeArmond
SJ; Prusiner SB Science 1990 Dec 14; 250 (4987): 1587-90

118. Inherited human prion diseases., 70 REFS, Hsiao K; Prusiner SB,
Neurology 1990 Dec; 40 (12): 1820-7

119. Transgenetic studies implicate interactions between homologous PrP
isoforms in scrapie prion replication., Prusiner SB; Scott M; Foster D;
Pan KM; Groth D;  Mirenda C; Torchia M; Yang SL; Serban D; Carlson GA; et
al, Cell 1990 Nov 16; 63 (4): 673-86

120. Permethylation and tandem mass spectrometry of oligosaccharides
having free hexosamine: analysis of the glycoinositol phospholipid anchor
glycan from the scrapie prion protein., Baldwin MA; Stahl N; Reinders LG;
Gibson BW; Prusiner SB; Burlingame AL, Anal Biochem 1990 Nov 15; 191 (1):
174-82

121. Immunolocalization of heparan sulfate proteoglycans to the prion
protein amyloid plaques of Gerstmann-Straussler syndrome,
Creutzfeldt-Jakob disease and scrapie., Snow AD; Wight TN; Nochlin D;
Koike Y; Kimata K; DeArmond SJ; Prusiner SB, Lab Invest 1990 Nov; 63 (5):
601-11

122. Acquisition of protease resistance by prion proteins in
scrapie-infected cells does not require asparagine-linked glycosylation.,
Taraboulos A; Rogers M; Borchelt DR; McKinley MP; Scott M; Serban D;
Prusiner SB, Proc Natl Acad Sci U S A 1990 Nov; 87 (21): 8262-6

123. Novel structure and genetics of prions causing neurodegeneration in
humans and animals., 181 REFS, Prusiner SB, Biologicals 1990 Oct; 18 (4):
247-62

124. Identification of glycoinositol phospholipid linked and truncated
forms of the scrapie prion protein., Stahl N; Baldwin MA; Burlingame AL;
Prusiner SB, Biochemistry 1990 Sep 25; 29 (38): 8879-84

125. Intracellular accumulation of the cellular prion protein after
mutagenesis of its Asn-linked glycosylation sites., Rogers M; Taraboulos
A; Scott M; Groth D; Prusiner SB, Glycobiology 1990 Sep; 1 (1): 101-9

126. Link between scrapie and BSE? [letter]., Westaway D; Prusiner SB, Nature
1990 Jul 12; 346 (6280): 113

127. Identification of cellular proteins binding to the scrapie prion
protein., Oesch B; Teplow DB; Stahl N; Serban D; Hood LE; Prusiner SB,
Biochemistry 1990 Jun 19; 29 (24): 5848-55

128. Differential release of cellular and scrapie prion proteins from cellular
membranes by phosphatidylinositol-specific phospholipase C., Stahl N; Borchelt
DR; Prusiner SB, Biochemistry 1990 Jun 5; 29 (22): 5405-12

129. Scrapie prion proteins accumulate in the cytoplasm of persistently
infected cultured cells., Taraboulos A; Serban D; Prusiner SB, J Cell Biol
1990 Jun; 110 (6): 2117-32

130. Unusual topogenic sequence directs prion protein biogenesis., Lopez CD;
Yost CS; Prusiner SB; Myers RM; Lingappa VR, Science 1990 Apr 13; 248 (4952):
226-9

131. DNA length polymorphism 5' to the myelin basic protein gene is
associated with multiple sclerosis., Boylan KB; Takahashi N; Paty DW;
Sadovnick AD; Diamond M; Hood LE; Prusiner SB, Ann Neurol 1990 Mar; 27
(3): 291-7

132. Scrapie and cellular prion proteins differ in their kinetics of synthesis
and topology in cultured cells., Borchelt DR; Scott M; Taraboulos A; Stahl N;
Prusiner SB, J Cell Biol 1990 Mar; 110 (3): 743-52

133. Three hamster species with different scrapie incubation times and
neuropathological features encode distinct prion proteins., Lowenstein DH;
Butler DA; Westaway D; McKinley MP; DeArmond SJ; Prusiner SB, Mol Cell
Biol 1990 Mar; 10 (3): 1153-63

134. Prion liposomes [published erratum appears in Biochem J 1991 Mar
15;274(Pt 3):903]., 193 REFS, Gabizon R; Prusiner SB, Biochem J 1990 Feb
15; 266 (1): 1-14 135. Non-hydrophobic extracytoplasmic determinant of
stop transfer in the prion protein., Yost CS; Lopez CD; Prusiner SB; Myers
RM; Lingappa VR, Nature 1990 Feb 15; 343 (6259): 669-72

136. Repetitive DNA (TGGA)n 5' to the human myelin basic protein gene: a
new form of oligonucleotide repetitive sequence showing length
polymorphism., Boylan KB; Ayres TM; Popko B; Takahashi N; Hood LE;
Prusiner SB, Genomics 1990 Jan; 6 (1): 16-22

137. Prion diseases of the central nervous system., 171 REFS, Prusiner SB;
DeArmond SJ, Monogr Pathol 1990; (32): 86-122

138. Rapid detection of Creutzfeldt-Jakob disease and scrapie prion proteins.,
Serban D; Taraboulos A; DeArmond SJ; Prusiner SB, Neurology 1990 Jan; 40 (1):
110-7

139. Nerve growth factor induces gene expression of the prion protein and
beta-amyloid protein precursor in the developing hamster central nervous
system. McKinley MP; Longo FM; Valletta JS; Rahbar F; Neve RL; Prusiner
SB; Mobley WC, Prog Brain Res 1990; 86: 227-38

140. [Encephalopathy caused by prions]., Les encephalopathies dues aux
prions., 94 REFS, Michel B, Rev Neurol (Paris) 1990; 146 (1): 1-11

141. Diversity of oligosaccharide structures linked to asparagines of the
scrapie prion protein., Endo T; Groth D; Prusiner SB; Kobata A, Biochemistry
1989 Oct 17; 28 (21): 8380-8

142. Acceleration of scrapie in neonatal Syrian hamsters., McKinley MP;
DeArmond SJ; Torchia M; Mobley WC; Prusiner SB, Neurology 1989 Oct; 39
(10): 1319-24

143. Primary structure of prion protein may modify scrapie isolate
properties., Carlson GA; Westaway D; DeArmond SJ; Peterson-Torchia M;
Prusiner SB, Proc Natl Acad Sci U S A 1989 Oct; 86 (19): 7475-9

144. Unraveling prion diseases through molecular genetics., 96 REFS,
Westaway D; Carlson GA; Prusiner SB, Trends Neurosci 1989 Jun; 12 (6):
221-7

145. Linkage of a prion protein missense variant to Gerstmann-Straussler
syndrome., Hsiao K; Baker HF; Crow TJ; Poulter M; Owen F; Terwilliger JD;
Westaway D; Ott J; Prusiner SB, Nature 1989 Mar 23; 338 (6213): 342-5

146. Insertion in prion protein gene in familial Creutzfeldt-Jakob disease
[letter]., Owen F; Poulter M; Lofthouse R; Collinge J; Crow TJ; Risby D; Baker
HF; Ridley RM; Hsiao K; Prusiner SB, Lancet 1989 Jan 7; 1 (8628): 51-2

147. Sulfated glycosaminoglycans in amyloid plaques of prion diseases.,
Snow AD; Kisilevsky R; Willmer J; Prusiner SB; DeArmond SJ, Acta
Neuropathol (Berl) 1989; 77 (4): 337-42

148. Scrapie prions., 167 REFS, Prusiner SB, Annu Rev Microbiol 1989; 43:
345-74

149. Immunoaffinity purification and neutralization of scrapie prions., 47
REFS, Gabizon R; McKinley MP; Groth D; Westaway D; DeArmond SJ; Carlson
GA; Prusiner SB, Prog Clin Biol Res 1989; 317: 583-600

150. PrPSc in scrapie-infected hamster brain is spatially and temporally
related to histopathology and infectivity titer., 22 REFS, De Armond SJ;
Gonzales M; Mobley WC; Kon AA; Stern A; Prusiner H; Prusiner SB, Prog Clin
Biol Res 1989; 317: 601-18

151. Genetics and polymorphism of the mouse prion gene complex: control of
scrapie incubation time., Carlson GA; Goodman PA; Lovett M; Taylor BA;
Marshall ST; Peterson-Torchia M; Westaway D; Prusiner SB, Mol Cell Biol
1988 Dec; 8 (12): 5528-40

152. Nerve growth factor increases mRNA levels for the prion protein and
the beta-amyloid protein precursor in developing hamster brain., Mobley
WC; Neve RL; Prusiner SB; McKinley MP, Proc Natl Acad Sci U S A 1988 Dec;
85 (24): 9811-5

153. CNS amyloid proteins in neurodegenerative diseases., Roberts GW;
Lofthouse R; Allsop D; Landon M; Kidd M; Prusiner SB; Crow TJ, Neurology
1988 Oct; 38 (10): 1534-40

154. Purification and properties of the cellular and scrapie hamster prion
proteins., Turk E; Teplow DB; Hood LE; Prusiner SB, Eur J Biochem 1988 Sep 1;
176 (1): 21-30

155. Immunoaffinity purification and neutralization of scrapie prion
infectivity [published erratum appears in Proc Natl Acad Sci U S A 1989
Feb;86(4):1223]., Gabizon R; McKinley MP; Groth D; Prusiner SB, Proc Natl
Acad Sci U S A 1988 Sep; 85 (18): 6617-21

156. Scrapie prion liposomes and rods exhibit target sizes of 55,000 Da.,
Bellinger-Kawahara CG; Kempner E; Groth D; Gabizon R; Prusiner SB,
Virology 1988 Jun; 164 (2): 537-41

157. Scrapie-infected murine neuroblastoma cells produce protease-resistant
prion proteins., Butler DA; Scott MR; Bockman JM; Borchelt DR; Taraboulos A;
Hsiao KK; Kingsbury DT; Prusiner SB, J Virol 1988 May; 62 (5): 1558-64

158. Properties of scrapie prion protein liposomes., Gabizon R; McKinley MP;
Groth DF; Kenaga L; Prusiner SB, J Biol Chem 1988 Apr 5; 263 (10): 4950-5

159. Prion protein gene expression in cultured cells., Scott MR; Butler DA;
Bredesen DE; Walchli M; Hsiao KK; Prusiner SB, Protein Eng 1988 Apr; 2 (1):
69-76

160. Characterization of prion proteins with monospecific antisera to
synthetic peptides., Barry RA; Vincent MT; Kent SB; Hood LE; Prusiner SB,
J Immunol 1988 Feb 15; 140 (4): 1188-93

161. Molecular structure, biology, and genetics of prions., 220 REFS, Prusiner
SB, Adv Virus Res 1988; 35: 83-136

162. Search for a scrapie-specific nucleic acid: a progress report., 25 REFS,
Oesch B; Groth DF; Prusiner SB; Weissmann C, Ciba Found Symp 1988; 135: 209-23

163. Developmental regulation of prion protein mRNA in brain., McKinley MP;
Lingappa VR; Prusiner SB, Ciba Found Symp 1988; 135: 101-16

164. Properties of scrapie prion proteins in liposomes and amyloid rods., 36
REFS, Gabizon R; McKinley MP; Prusiner SB, Ciba Found Symp 1988; 135: 182-96

165. Novel mechanisms of degeneration of the central nervous system -- prion
structure and biology., 98 REFS, Prusiner SB; Stahl N; DeArmond SJ, Ciba Found
Symp 1988; 135: 239-60

166. Genetic control of prion incubation period in mice., 27 REFS, Carlson GA;
Westaway D; Goodman PA; Peterson M; Marshall ST; Prusiner SB, Ciba Found Symp
1988; 135: 84-99

167. Prions and neurodegenerative diseases., 105 REFS, Prusiner SB, N Engl
J Med 1987 Dec 17; 317 (25): 1571-81

168. Evidence for a secretory form of the cellular prion protein., Hay B;
Prusiner SB; Lingappa VR, Biochemistry 1987 Dec 15; 26 (25): 8110-5

169. The burden of proof in linking AIDS to scrapie [letter]., Braun MJ;
Gonda MA; George DG; Bazan JF; Fletterick RJ; Prusiner SB, Nature 1987 Dec
10-16; 330 (6148): 525-6

170. Immuno-gold localization of prion filaments in scrapie-infected
hamster brains., Wiley CA; Burrola PG; Buchmeier MJ; Wooddell MK; Barry
RA; Prusiner SB; Lampert PW, Lab Invest 1987 Dec; 57 (6): 646-56

171. Distinct prion proteins in short and long scrapie incubation period
mice., Westaway D; Goodman PA; Mirenda CA; McKinley MP; Carlson GA;
Prusiner SB, Cell 1987 Nov 20; 51 (4): 651-62

172. Isolation and structural studies of the intact scrapie agent protein.,
Bolton DC; Bendheim PE; Marmorstein AD; Potempska A, Arch Biochem Biophys 1987
Nov 1; 258 (2): 579-90

173. Scrapie prion protein contains a phosphatidylinositol glycolipid.,
Stahl N; Borchelt DR; Hsiao K; Prusiner SB, Cell 1987 Oct 23; 51 (2):
229-40

174. Purified scrapie prions resist inactivation by procedures that hydrolyze,

modify, or shear nucleic acids., Bellinger-Kawahara C; Diener TO; McKinley MP;
Groth DF; Smith DR; Prusiner SB, Virology 1987 Sep; 160 (1): 271-4

175. Formic acid pretreatment enhances immunostaining of cerebral and
systemic amyloids., Kitamoto T; Ogomori K; Tateishi J; Prusiner SB, Lab
Invest 1987 Aug;  57 (2): 230-6

176. Changes in the localization of brain prion proteins during scrapie
infection [published erratum appears in Neurology 1987 Nov;37(11):1770].,
DeArmond SJ; Mobley WC; DeMott DL; Barry RA; Beckstead JH; Prusiner SB,
Neurology 1987 Aug; 37 (8): 1271-80

177. Scrapie infection diminishes spines and increases varicosities of
dendrites in hamsters: a quantitative Golgi analysis., Hogan RN; Baringer
JR; Prusiner J Neuropathol Exp Neurol 1987 Jul; 46 (4): 461-73

178. Immunoblotting of Creutzfeldt-Jakob disease prion proteins: host
species-specific epitopes., Bockman JM; Prusiner SB; Tateishi J; Kingsbury DT,
Ann Neurol 1987 Jun; 21 (6): 589-95

179. Purified prion proteins and scrapie infectivity copartition into
liposomes. Gabizon R; McKinley MP; Prusiner SB, Proc Natl Acad Sci U S A
1987 Jun; 84 (12): 4017-21

180. DNA length polymorphism located 5' to the human myelin basic protein
gene., Boylan KB; Takahashi N; Diamond M; Hood LE; Prusiner SB, Am J Hum
Genet 1987 May; 40 (5): 387-400

181. Developmental expression of prion protein gene in brain., McKinley
MP; Hay B; Lingappa VR; Lieberburg I; Prusiner SB, Dev Biol 1987 May; 121
(1): 105-10

182. Prion diseases and central nervous system degeneration., 143 REFS,
Prusiner SB, Clin Res 1987 Apr; 35 (3): 177-91

183. Prions causing nervous system degeneration., 161 REFS, Prusiner SB;
DeArmond SJ, Lab Invest 1987 Apr; 56 (4): 349-63

184. AIDS virus and scrapie protein genes [letter]., Fernando Bazan J;
Fletterick RJ; Prusiner SB, Nature 1987 Feb 12-18; 325 (6105): 581

185. Biogenesis and transmembrane orientation of the cellular isoform of the
scrapie prion protein [published errratum appears in Mol Cell Biol 1987
May;7(5):2035]., Hay B; Barry RA; Lieberburg I; Prusiner SB; Lingappa VR, Mol
Cell Biol 1987 Feb; 7 (2): 914-20

186. Predicted secondary structure and membrane topology of the scrapie prion
protein., Bazan JF; Fletterick RJ; McKinley MP; Prusiner SB, Protein Eng 1987
Feb-Mar; 1 (2): 125-35

187. On the biology of prions., 147 REFS, Prusiner SB; Gabizon R; McKinley MP,
Acta Neuropathol (Berl) 1987; 72 (4): 299-314

188. Prions causing degenerative neurological diseases., 95 REFS, Prusiner SB,
Annu Rev Med 1987; 38: 381-98

189. Purified scrapie prions resist inactivation by UV irradiation.,
Bellinger-Kawahara C; Cleaver JE; Diener TO; Prusiner SB, J Virol 1987 Jan; 61
(1): 159-66

190. Prions are novel infectious pathogens causing scrapie and
Creutzfeldt-Jakob disease., 77 REFS, Prusiner SB, Bioessays 1986 Dec; 5
(6): 281-6

191. Prion-protein immunoreactivity in human transmissible dementias
[letter]., Roberts GW; Lofthouse R; Brown R; Crow TJ; Barry RA; Prusiner
SB, N Engl J Med 1986 Nov 6; 315 (19): 1231-3

192. Vasoactive intestinal peptide stimulates cyclic AMP metabolism in
choroid plexus epithelial cells., Crook RB; Prusiner SB, Brain Res 1986
Oct 1; 384 (1):  138-44

193. Monoclonal antibodies to the cellular and scrapie prion proteins., Barry
RA; Prusiner SB, J Infect Dis 1986 Sep; 154 (3): 518-21

194. Linkage of prion protein and scrapie incubation time genes., Carlson GA;
Kingsbury DT; Goodman PA; Coleman S; Marshall ST; DeArmond S; Westaway D;
Prusiner SB, Cell 1986 Aug 15; 46 (4): 503-11

195. Amyloid plaques in Creutzfeldt-Jakob disease stain with prion protein
antibodies., Kitamoto T; Tateishi J; Tashima T; Takeshita I; Barry RA;
DeArmond SJ; Prusiner SB, Ann Neurol 1986 Aug; 20 (2): 204-8

196. Scrapie and cellular PrP isoforms are encoded by the same chromosomal
gene. Basler K; Oesch B; Scott M; Westaway D; Walchli M; Groth DF;
McKinley MP; Prusiner SB; Weissmann C, Cell 1986 Aug 1; 46 (3): 417-28

197. Molecular cloning of a human prion protein cDNA., Kretzschmar HA;
Stowring LE; Westaway D; Stubblebine WH; Prusiner SB; Dearmond SJ, DNA
1986 Aug; 5 (4): 315-24

198. Molecular characteristics of prion rods purified from
scrapie-infected hamster brains., McKinley MP; Braunfeld MB; Bellinger CG;
Prusiner SB, J Infect Dis 1986 Jul; 154 (1): 110-20

199. Scrapie and cellular prion proteins share polypeptide epitopes.,
Barry RA;  Kent SB; McKinley MP; Meyer RK; DeArmond SJ; Hood LE; Prusiner
SB, J Infect Dis 1986 May; 153 (5): 848-54

200. Separation and properties of cellular and scrapie prion proteins.,
Meyer RK; McKinley MP; Bowman KA; Braunfeld MB; Barry RA; Prusiner SB,
Proc Natl Acad Sci U S A 1986 Apr; 83 (8): 2310-4

201. Conservation of the cellular gene encoding the scrapie prion protein.,
Westaway D; Prusiner SB, Nucleic Acids Res 1986 Mar 11; 14 (5): 2035-44

202. H2 histamine receptors on the epithelial cells of choroid plexus., Crook
RB; Farber MB; Prusiner SB, J Neurochem 1986 Feb; 46 (2): 489-93

203. Scrapie prion proteins are synthesized in neurons., Kretzschmar HA;
Prusiner SB; Stowring LE; DeArmond SJ, Am J Pathol 1986 Jan; 122 (1): 1-5

204. Biology and structure of scrapie prions., 110 REFS, McKinley MP; Prusiner
SB, Int Rev Neurobiol 1986; 28: 1-57

205. Replication of scrapie prions in hamster eyes precedes retinal
degeneration., Hogan RN; Bowman KA; Baringer JR; Prusiner SB, Ophthalmic Res
1986; 18 (4): 230-5

206. Transmission of scrapie in hamsters., Prusiner SB; Cochran SP; Alpers
MP, J Infect Dis 1985 Nov; 152 (5): 971-8

207. 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.,
Takahashi N; Roach A; Teplow DB; Prusiner SB; Hood L, Cell 1985 Aug; 42 (1):
139-48

208. A microangiopathic syndrome of encephalopathy, hearing loss, and
retinal arteriolar occlusions., Monteiro ML; Swanson RA; Coppeto JR; Cuneo
RA; DeArmond SJ; Prusiner SB, Neurology 1985 Aug; 35 (8): 1113-21

209. Antibodies to the scrapie protein decorate prion rods., Barry RA;
McKinley MP; Bendheim PE; Lewis GK; DeArmond SJ; Prusiner SB, J Immunol
1985 Jul; 135 (1): 603-13

210. Identification of prion amyloid filaments in scrapie-infected brain.,
DeArmond SJ; McKinley MP; Barry RA; Braunfeld MB; McColloch JR; Prusiner SB,
Cell 1985 May; 41 (1): 221-35

211. Scrapie PrP 27-30 is a sialoglycoprotein., Bolton DC; Meyer RK;
Prusiner SB J Virol 1985 Feb; 53 (2): 596-606

212. Scrapie and Creutzfeldt-Jakob disease prion proteins share physical
properties and antigenic determinants., Bendheim PE; Bockman JM; McKinley MP;
Kingsbury DT; Prusiner SB, Proc Natl Acad Sci U S A 1985 Feb; 82 (4): 997-1001

213. Creutzfeldt-Jakob disease prion proteins in human brains., Bockman JM;
Kingsbury DT; McKinley MP; Bendheim PE; Prusiner SB, N Engl J Med 1985 Jan 10;
312 (2): 73-8

214. Prions -- infectious pathogens causing the spongiform encephalopathies.,
110 REFS, Prusiner SB; Kingsbury DT, CRC Crit Rev Clin Neurobiol 1985; 1 (3):
181-200

215. Scrapie prions, brain amyloid, and senile dementia., Prusiner SB,
Curr Top Cell Regul 1985; 26: 79-95

216. Scrapie and Creutzfeldt-Jakob disease prions., 54 REFS, Prusiner SB;
Barry RA; McKinley MP; Bellinger CG; Meyer RK; DeArmond SJ; Kingsbury DT,
Microbiol Sci 1985; 2 (2): 33-9

217. Molecular characteristics of the major scrapie prion protein., Bolton DC;
McKinley MP; Prusiner SB, Biochemistry 1984 Dec 4; 23 (25): 5898-906

218. Bitemporal hypometabolism in Creutzfeldt-Jakob disease measured by
positron emission tomography with [18F]-2-fluorodeoxyglucose., Friedland
RP; Prusiner SB; Jagust WJ; Budinger TF; Davis RL, J Comput Assist Tomogr
1984 Oct; 8 (5): 978-81

219. Prions., Prusiner SB, Sci Am 1984 Oct; 251 (4): 50-9

220. Antibodies to a scrapie prion protein., Bendheim PE; Barry RA;
DeArmond SJ; Stites DP; Prusiner SB, Nature 1984 Aug 2-8; 310 (5976):
418-21

221. Purification and structural studies of a major scrapie prion protein.,
Prusiner SB; Groth DF; Bolton DC; Kent SB; Hood LE, Cell 1984 Aug; 38 (1):
127-34

222. Some speculations about prions, amyloid, and Alzheimer's disease.,
Prusiner SB, N Engl J Med 1984 Mar 8; 310 (10): 661-3

223. Hormones and neurotransmitters control cyclic AMP metabolism in choroid
plexus epithelial cells., Crook RB; Farber MB; Prusiner SB, J Neurochem 1984
Feb; 42 (2): 340-50

224. Prions: novel infectious pathogens., 283 REFS, Prusiner SB, Adv Virus Res
1984; 29: 1-56

225. Scrapie prions aggregate to form amyloid-like birefringent rods.,
Prusiner SB; McKinley MP; Bowman KA; Bolton DC; Bendheim PE; Groth DF;
Glenner GG, Cell 1983 Dec; 35 (2 Pt 1): 349-58

226. Retinal degeneration in experimental Creutzfeldt-Jakob disease.,
Hogan RN;  Kingsbury DT; Baringer JR; Prusiner SB, Lab Invest 1983 Dec; 49
(6): 708-15

227. Scrapie infectivity, fibrils and low molecular weight protein.,
Diringer H; Gelderblom H; Hilmert H; Ozel M; Edelbluth C; Kimberlin RH,
Nature 1983 Dec 1-7; 306 (5942): 476-8

228. A protease-resistant protein is a structural component of the scrapie
prion., McKinley MP; Bolton DC; Prusiner SB, Cell 1983 Nov; 35 (1): 57-62

229. Characterization of cloned cDNA representing rat myelin basic protein:
absence of expression in brain of shiverer mutant mice., Roach A; Boylan K;
Horvath S; Prusiner SB; Hood LE, Cell 1983 Oct; 34 (3): 799-806

230. Replication of the scrapie agent in hamster brain precedes neuronal
vacuolation., Baringer JR; Bowman KA; Prusiner SB, J Neuropathol Exp
Neurol 1983 Sep; 42 (5): 539-47

231. Metastatic adenocarcinoma presenting as bilateral blindness.,
Prusiner PE;  Butler A; Yavitz EQ; Stern WH, Ann Ophthalmol 1983 Jul; 15
(7): 653-6

232. Genetic control of scrapie and Creutzfeldt-Jakob disease in mice.,
Kingsbury DT; Kasper KC; Stites DP; Watson JD; Hogan RN; Prusiner SB, J
Immunol 1983 Jul; 131 (1): 491-6

233. Resistance of the scrapie agent to inactivation by psoralens.,
McKinley MP; Masiarz FR; Isaacs ST; Hearst JE; Prusiner SB, Photochem
Photobiol 1983 May; 37 (5): 539-45

234. Protein replication by amino acid pairing., Root-Bernstein RS, J
Theor Biol 1983 Jan 7; 100 (1): 99-106

235. Identification of a protein that purifies with the scrapie prion.,
Bolton DC; McKinley MP; Prusiner SB, Science 1982 Dec 24; 218 (4579):
1309-11

236. Further purification and characterization of scrapie prions.,
Prusiner SB;  Bolton DC; Groth DF; Bowman KA; Cochran SP; McKinley MP,
Biochemistry 1982 Dec 21; 21 (26): 6942-50

237. Immunological studies of scrapie infection., Kasper KC; Stites DP; Bowman
KA; Panitch H; Prusiner SB, J Neuroimmunol 1982 Nov; 3 (3): 187-201

238. Viroids and prions., Diener TO; McKinley MP; Prusiner SB, Proc Natl Acad
Sci U S A 1982 Sep; 79 (17): 5220-4

239. Research on scrapie [letter]., Prusiner SB, Lancet 1982 Aug 28; 2 (8296):
494-5

240. Kuru with incubation periods exceeding two decades., Prusiner SB;
Gajdusek C; Alpers MP, Ann Neurol 1982 Jul; 12 (1): 1-9

241. Novel proteinaceous infectious particles cause scrapie., Prusiner SB,
Science 1982 Apr 9; 216 (4542): 136-44

242. Measurement of the scrapie agent using an incubation time interval
assay., Prusiner SB; Cochran SP; Groth DF; Downey DE; Bowman KA; Martinez
HM, Ann Neurol 1982 Apr; 11 (4): 353-8

243. Reversible chemical modification of the scrapie agent., McKinley MP;
Masiarz FR; Prusiner SB, Science 1981 Dec 11; 214 (4526): 1259-61

244. Scrapie agent contains a hydrophobic protein., Prusiner SB; McKinley MP;
Groth DF; Bowman KA; Mock NI; Cochran SP; Masiarz FR, Proc Natl Acad Sci U S A
1981 Nov; 78 (11): 6675-9

245. Culture and characterization of epithelial cells from bovine choroid
plexus., Crook RB; Kasagami H; Prusiner SB, J Neurochem 1981 Oct; 37 (4):
845-54

246. Membrane populations of bovine choroid plexus: separation by density
gradient centrifugation in modified colloidal silica., Mamelok RD; Macrae DR;
Benet LZ; Prusiner SB, J Neurochem 1981 Sep; 37 (3): 768-74

247. Thiocyanate and hydroxyl ions inactivate the scrapie agent., Prusiner
SB; Groth DF; McKinley MP; Cochran SP; Bowman KA; Kasper KC, Proc Natl
Acad Sci U S A 1981 Jul; 78 (7): 4606-10

248. Scrapie-associated particles in postsynaptic processes. Further
ultrastructural studies., Baringer JR; Prusiner SB; Wong JS, J Neuropathol Exp
Neurol 1981 May; 40 (3): 281-8

249. Kinetics of D-glucose transport into renal membrane vesicles:
measurements using a vacuum manifold apparatus., Mamelok RD; Macrae DR;
Hittelman K; Hoefer JP; Prusiner SB, J Biochem Biophys Methods 1981 Mar; 4
(3-4): 147-53

250. Determination of scrapie agent titer from incubation period
measurements in hamsters., Prusiner SB; Cochran SP; Downey DE; Groth DF,
Adv Exp Med Biol 1981;  134: 385-99

251. Toward development of assays for scrapie-specific antibodies., Kasper KC;
Bowman K; Stites DP; Prusiner SB, Adv Exp Med Biol 1981; 134: 401-13

252. Disorders of glutamate metabolism and neurological dysfunction., 161
REFS, Prusiner SB, Annu Rev Med 1981; 32: 521-42

253. Progressive retinal degeneration in scrapie-infected hamsters: a
light and electron microscopic analysis., Hogan RN; Baringer JR; Prusiner
SB, Lab Invest 1981 Jan; 44 (1): 34-42

254. Brain tissue from persons dying of Creutzfeldt-Jakob disease causes
scrapie-like encephalopathy in goats., Hadlow WJ; Prusiner SB; Kennedy RC;
Race RE, Ann Neurol 1980 Dec; 8 (6): 628-32

255. Molecular properties, partial purification, and assay by incubation
period measurements of the hamster scrapie agent., Prusiner SB; Groth DF;
Cochran SP; Masiarz FR; McKinley MP; Martinez HM, Biochemistry 1980 Oct
14; 19 (21): 4883-91

256. Gel electrophoresis and glass permeation chromatography of the
hamster scrapie agent after enzymatic digestion and detergent extraction.,
Prusiner SB;  Groth DF; Cochran SP; McKinley MP; Masiarz FR, Biochemistry
1980 Oct 14; 19 (21): 4892-8

257. Experimental scrapie in the mouse: electrophoretic and sedimentation
properties of the partially purified agent., Prusiner SB; Garfin DE; Cochran
McKinley MP; Groth DF; Hadlow WJ; Race RE; Eklund CM, J Neurochem 1980 Sep; 35
(3): 574-82

258. Biohazards of investigations on the transmissible spongiform
encephalopathies., 63 REFS, Chatigny MA; Prusiner SB, Rev Infect Dis 1980
Sep-Oct; 2 (5): 713-24

259. Separation of membrane-bound gamma-glutamyl transpeptidase from brush
border transport and enzyme activities., Mamelok RD; Groth DF; Prusiner SB,
Biochemistry 1980 May 27; 19 (11): 2367-73

260. Electrophoretic properties of the scrapie agent in agarose gels.,
Prusiner SB; Groth DF; Bildstein C; Masiarz FR; McKinley MP; Cochran SP,
Proc Natl Acad Sci U S A 1980 May; 77 (5): 2984-8

261. Slow viruses: molecular properties of the agents causing scrapie in
mice and hamsters., Prusiner SB; Cochran SP; Baringer JR; Groth D; Masiarz
F; McKinley M; Bildstein C; Garfin D; Hadlow WJ; Race RE; Eklund CM, Prog
Clin Biol Res 1980; 39: 73-89

262. Evaluation of a class III biological safety cabinet for enclosure of an
ultracentrifuge., Chatigny MA; Dunn S; Ishimaru K; Eagleson JA; Prusiner SB,
Appl Environ Microbiol 1979 Nov; 38 (5): 934-9

263. Partial purification and evidence for multiple molecular forms of the
scrapie agent., Prusiner SB; Hadlow WJ; Garfin DE; Cochran SP; Baringer
JR; Race RE; Eklund CM, Biochemistry 1978 Nov 14; 17 (23): 4993-9

264. Sedimentation characteristics of the scrapie agent from murine spleen and
brain., Prusiner SB; Hadlow WJ; Eklund CM; Race RE; Cochran SP, Biochemistry
1978 Nov 14; 17 (23): 4987-92

265. Zwitterionic character of nucleotides: possible significance in the
evolution of nucleic acids., Sundaralingam M; Prusiner P, Nucleic Acids
Res 1978 Nov; 5 (11): 4375-83

266. Preservation by freezing of glucose and alanine transport into kidney
membrane vesicles., Hittelman K; Mamelok RD; Prusiner SB, Anal Biochem
1978 Sep; 89 (2): 324-31

267. Experimental scrapie in mice: ultrastructural observations., Baringer JR;
Prusiner SB, Ann Neurol 1978 Sep; 4 (3): 205-11

268. Mitogen stimulation of splenocytes from mice infected with scrapie
agent., Garfin DE; Stites DP; Perlman JD; Cochran SP; Prusiner SB, J
Infect Dis 1978 Sep; 138 (3): 396-400

269. Suppression of polyclonal B cell activation in scrapie-infected C3H/HeJ
mice., Garfin DE; Stites DP; Zitnik LA; Prusiner SB, J Immunol 1978 Jun; 120
(6): 1986-90

270. Partial purification and kinetics of gamma-glutamyl transpeptidase
from bovine choroid plexus., Prusiner PE; Prusiner SB, J Neurochem 1978
Jun; 30 (6):  1253-9

271. Modulation of gamma-glutamyl transpeptidase activity from bovine choroid
plexus., Prusiner PE; Prusiner SB, J Neurochem 1978 Jun; 30 (6): 1261-7

272. An approach to the isolation of biological particles using sedimentation
analysis., Prusiner SB, J Biol Chem 1978 Feb 10; 253 (3): 916-21

273. Evidence for hydrophobic domains on the surface of the scrapie
agent., Prusiner SB; Garfin DE; Cochran SP; Baringer JR; Hadlow WJ; Eklund
CM; Race RE, Trans Am Neurol Assoc 1978; 103: 62-4

274. Sedimentation properties of the scrapie agent., Prusiner SB; Hadlow WJ;
Eklund CM; Race RE, Proc Natl Acad Sci U S A 1977 Oct; 74 (10): 4656-60

275. Comparative studies on membranes from bovine choroid plexus and rat
kidney cortex., Kirk G; Prusiner SB, Life Sci 1977 Sep 15; 21 (6): 833-40

276. Carotidynia., Raskin NH; Prusiner S, Neurology 1977 Jan; 27 (1): 43-6

277. A novel mechanism for group translocation: substrate-product
reutilization by gamma-glutamyl transpeptidase in peptide and amino acid
transport., Prusiner S; Doak CW; Kirk G, J Cell Physiol 1976 Dec; 89 (4):
853-63

278. Regulation of glutaminase B in Escherichia coli. II. Modulaltion of
activity by carbosylate and borate ions., Prusiner S; Stadtman ER, J Biol Chem
1976 Jun 10; 251 (11): 3457-62

279. Regulation of glutaminase B in Escherichia coli. III. Control by
nucleotides and divalent cations., Prusiner S; Stadtman ER, J Biol Chem
1976 Jun 10; 251 (11): 3463-9

280. Regulation of glutaminase B in Escherichia coli. I. Purification,
properties, and cold lability., Prusiner S; Davis JN; Stadtman ER, J Biol Chem
1976 Jun 10; 251 (11): 3447-56

281. Regulation of glutaminase levels in Escherichia coli., Prusiner S, J
Bacteriol 1975 Sep; 123 (3): 992-9

282. Effect of ribose O(2')-methylation on the conformation of nucleosides and
nucleotides., Prusiner P; Yathindra N; Sundaralingam M, Biochim Biophys Acta
1974 Oct 11; 366 (2): 115-23

283. Regulation of glutamine synthetase from Bacillus subtilis by divalent
cations, feedback inhibitors, and L-glutamine., Deuel TF; Prusiner S, J Biol
Chem 1974 Jan 10; 249 (1): 257-64

284. A new class of synthetic nucleoside analogues with broad-spectrum
antiviral properties., Prusiner P; Sundaralingam M, Nature New Biol 1973
Jul 25; 244 (134): 116-8

285. Stain for glutaminase activity., Davis JN; Prusiner S, Anal Biochem 1973
Jul; 54 (1): 272-5

286. The space-time distribution of Hodgkin's disease in Connecticut,
1940-69., Kryscio RJ; Myers MH; Prusiner ST; Heise HW; Christine BW, J
Natl Cancer Inst 1973 May; 50 (5): 1107-10

287. Crystal structure and molecular conformation of formycin
monohydrates. Possible origin of the anomalous circular dichroic spectra
in formycin mono- and polynucleotides., Prusiner P; Brennan T;
Sundaralingam M, Biochemistry 1973 Mar 13; 12 (6): 1196-202

288. Adenosine 3':5'-cyclic monophosphate control of the enzymes of
glutamine metabolism in Escherichia coli., Prusiner S; Miller RE;
Valentine RC, Proc Natl Acad Sci U S A 1972 Oct; 69 (10): 2922-6

289. On the regulation of glutaminase in E. coli: metabolite control.,
Prusiner S; Stadtman ER, Biochem Biophys Res Commun 1971 Dec 17; 45 (6):
1474-81

290. Vacuum manifold for rapid assay of enzymes using radioactive tracers
and ion exchange chromatography., Prusiner SB; Milner LS; Long CW; Myers
ML, Rev Sci Instrum 1971 Apr; 42 (4): 493-4

291. A rapid radioactive assay for glutamine synthetase, glutaminase,
asparagine synthetase, and asparaginase., Prusiner S; Milner L, Anal
Biochem 1970 Oct; 37 (2): 429-38

292. Metabolic control in isolated brown fat cells., Lindberg O; Prusiner SB;
Cannon B; Ching TM; Eisenhardt RH, Lipids 1970 Feb; 5 (2): 204-9

293. Spectroscopic evidence for the control of respiration prior to
phosphorylation in hamster brown fat cells., Prusiner S, J Biol Chem 1970 Jan
25; 245 (2): 382-9

294. [Energetic disturbance of cation transport as a cause of
intracellular brain edema]., Energetische Storung des Kationentransports
als Ursache des intrazellularen Hirnodems., Reulen HJ; Steude U; Brendel
W; Hilber C; Prusiner S Acta Neurochir (Wien) 1970; 22 (2): 129-66

295. Control of metabolism in brown adipose tissue., Williamson JR;
Prusiner S;  Olson MS; Fukami M, Lipids 1970 Jan; 5 (1): 1-14

296. Hypothermic protection against cerebral edema of ischemia., Prusiner S;
Wolfson SK Jr, Arch Neurol 1968 Dec; 19 (6): 623-7

297. Oxidative metabolism in cells isolated from brown adipose tissue. 2.
Catecholamine regulated respiratory control., Prusiner SB; Cannon B; Ching TM;
Lindberg O, Eur J Biochem 1968 Dec; 7 (1): 51-7

298. Thermodynamic cosiderations of mammalian thermogenesis., Prusiner S;
Poe M, Nature 1968 Oct 19; 220 (164): 235-7

299. Oxidative metabolism in cells isolated from brown adipose tissue. 1.
Catecholamine and fatty acid stimulation of respiration., Prusiner SB;
Cannon B; Lindberg O, Eur J Biochem 1968 Oct 17; 6 (1): 15-22

300. The regulation of oxidative metabolism of isolated brown fat cells.,
Prusiner SB; Eisenhardt RH; Rylander E; Lindberg O, Biochem Biophys Res Commun
1968 Mar 12; 30 (5): 508-15

301. Pyridine nucleotide changes during thermogenesis in brown fat tissue
in vivo., Prusiner S; Williamson JR; Chance B; Paddle BM, Arch Biochem
Biophys 1968 Feb; 123 (2): 368-77

302. The bioautofuel cell: a device for pacemaker power from direct energy
conversion consuming autogenous fuel., Wolfson SK Jr; Gofberg SL; Prusiner P;
Nanis L, Trans Am Soc Artif Intern Organs 1968; 14: 198-203

303. Relationship of acidemia to cerebral edema., Prusiner SB; Moskovitz PA;
Wolfson SK Jr, Arch Surg 1965 Dec; 91 (6): 902-5

304. Evidence for multiple molecular forms of the scrapie agent.  pp.
591-613., Prusiner SB; Garfin DE; Baringer JR; Cochran SP, In: Stevens JG,
et al., ed. Persistent viruses. New York, Academic Press, 1978.  W3 I322
v.11 1978. 591-613

305. Creutzfeldt-Jakob disease and scrapie prions., 124 REFS, Prusiner SB,
Alzheimer Dis Assoc Disord 1989 Spring-Summer; 3 (1-2): 52-78

306. Molecular genetics and transgenic model of
Gertsmann-Straussler-Scheinker disease., 70 REFS, Hsiao K; Prusiner SB,
Alzheimer Dis Assoc Disord 1991 Fall; 5 (3): 155-62