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Results:
1-23
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Results: 23
Authors:
KORCZYN AD
SIMON ES
CHAPMAN J
TREVES T
ROSENMANN H
GABIZON R
KAHANA E
Citation: Ad. Korczyn et al., CREUTZFELDT-JAKOB-DISEASE PROFILE IN PATIENTS HOMOZYGOUS FOR THE PRION PROTEIN GENE E200K MUTATION, Annals of neurology, 44(3), 1998, pp. 200-200
Authors:
CASPI S
HALIMI M
YANAI A
BENSASSON S
TARABOULOS A
GABIZON R
Citation: S. Caspi et al., THE ANTI-PRION ACTIVITY OF CONGO RED - PUTATIVE MECHANISM, The Journal of biological chemistry, 273(6), 1998, pp. 3484-3489
Authors:
ROSENMANN H
VARDI J
FINKELSTEIN Y
CHAPMAN J
GABIZON R
Citation: H. Rosenmann et al., IDENTIFICATION IN ISRAEL OF 2 JEWISH CREUTZFELDT-JAKOB-DISEASE PATIENTS WITH A 178 MUTATION AT THEIR PRP GENE, Acta neurologica Scandinavica, 97(3), 1998, pp. 184-187
Authors:
KESHET GI
OVADIA H
GABIZON R
Citation: Gi. Keshet et al., NEURONAL NOS ASSOCIATION TO CAVEOLAE-LIKE DOMAINS IN ADULT MICE DEPENDS ON THE EXPRESSION OF THE CELLULAR PRION PROTEIN, Neuroscience letters, 1997, pp. 28-28
Authors:
SHAKED G
TARABOULOS A
GABIZON R
Citation: G. Shaked et al., DMSO INHIBITS THE AGGREGATION OF THE PRION PROTEIN (PRPSC) INTO AMYLOID RODS, Neuroscience letters, 1997, pp. 45-45
Authors:
GABIZON R
TARABOULOS A
Citation: R. Gabizon et A. Taraboulos, OF MICE AND (MAD) COWS - TRANSGENIC MICE HELP TO UNDERSTAND PRIONS, Trends in genetics, 13(7), 1997, pp. 264-269
Authors:
FRIEDMAN G
GABIZON R
BENYEHUDA A
Citation: G. Friedman et al., APOLIPOPROTEIN E-EPSILON-4 ALLELE, A RISK FACTOR FOR LATE-ONSET NONFAMILIAL ALZHEIMERS-DISEASE AMONG ISRAELI JEWS, Archives of gerontology and geriatrics, 24(2), 1997, pp. 175-181
Authors:
ROSENMANN H
HALIMI M
KAHANA I
BIRAN I
GABIZON R
Citation: H. Rosenmann et al., DIFFERENTIAL ALLELIC EXPRESSION OF PRP MESSENGER-RNA IN CARRIERS OF THE E200K MUTATION, Neurology, 49(3), 1997, pp. 851-856
Authors:
ROSENMANN H
MEINER Z
KAHANA E
HALIMI M
LENETSKY E
ABRAMSKY O
GABIZON R
Citation: H. Rosenmann et al., DETECTION OF 14-3-3-PROTEIN IN THE CSF OF GENETIC CREUTZFELDT-JAKOB-DISEASE, Neurology, 49(2), 1997, pp. 593-595
Authors:
MEINER Z
YANAI A
TELLING G
HALIMI M
TARABOULOS A
PRUSINER SB
GABIZON R
Citation: Z. Meiner et al., PRION PROTEIN WITH THE E200K MUTATION EXHIBITS PROPERTIES SIMILAR TO THE CELLULAR ISOFORM PRPC, Neurology, 48(3), 1997, pp. 5034-5034
Authors:
MEINER Z
GABIZON R
PRUSINER SB
Citation: Z. Meiner et al., FAMILIAL CREUTZFELDT-JAKOB-DISEASE - CODON-200 PRION DISEASE IN LIBYAN JEWS, Medicine, 76(4), 1997, pp. 227-237
Authors:
GABIZON R
TELLING G
MEINER Z
HALIMI H
KAHANA I
PRUSINER SB
Citation: R. Gabizon et al., INSOLUBLE WILD-TYPE AND PROTEASE-RESISTANT MUTANT PRION PROTEIN IN BRAINS OF PATIENTS WITH INHERITED PRION DISEASE, Nature medicine, 2(1), 1996, pp. 59-64
Authors:
TELLING GC
PARCHI P
DEARMOND SJ
CORTELLI P
MONTAGNA P
GABIZON R
MASTRIANNI J
LUGARESI E
GAMBETTI P
PRUSINER SB
Citation: Gc. Telling et al., EVIDENCE FOR THE CONFORMATION OF THE PATHOLOGICAL ISOFORM OF THE PRION PROTEIN ENCIPHERING AND PROPAGATING PRION DIVERSITY, Science, 274(5295), 1996, pp. 2079-2082
Authors:
KANEKO K
PERETZ D
PAN KM
BLOCHBERGER TC
GABIZON R
GRIFFITH OH
COHEN FE
BALDWIN MA
PRUSINER SB
Citation: K. Kaneko et al., PRION PROTEIN (PRP) SYNTHETIC PEPTIDES INDUCE CELLULAR PRP TO ACQUIREPROPERTIES OF THE SCRAPIE ISOFORM, Neurology, 46(2), 1996, pp. 1004-1004
Authors:
OVADIA H
ROSENMANN H
SHEZEN E
HALIMI M
OFRAN I
GABIZON R
Citation: H. Ovadia et al., EFFECT OF SCRAPIE INFECTION ON THE ACTIVITY OF NEURONAL NITRIC-OXIDE SYNTHASE IN BRAIN AND NEUROBLASTOMA-CELLS, The Journal of biological chemistry, 271(28), 1996, pp. 16856-16861
Authors:
SPUDICH S
MASTRIANNI JA
WRENSCH M
GABIZON R
MEINER Z
KAHANA I
ROSENMANN H
KAHANA E
PRUSINER SB
Citation: S. Spudich et al., COMPLETE PENETRANCE OF CREUTZFELDT-JAKOB-DISEASE IN LIBYAN JEWS CARRYING THE E200K MUTATION IN THE PRION PROTEIN GENE, Molecular medicine, 1(6), 1995, pp. 607-613
Authors:
TELLING GC
SCOTT M
MASTRIANNI J
GABIZON R
TORCHIA M
COHEN FE
DEARMOND SJ
PRUSINER SB
Citation: Gc. Telling et al., PRION PROPAGATION IN MICE EXPRESSING HUMAN AND CHIMERIC PRP TRANSGENES IMPLICATES THE INTERACTION OF CELLULAR PRP WITH ANOTHER PROTEIN, Cell, 83(1), 1995, pp. 79-90
Authors:
KANEKO K
PERETZ D
PAN KM
BLOCHBERGER TC
WILLE H
GABIZON R
GRIFFITH OH
COHEN FE
BALDWIN MA
PRUSINER SB
Citation: K. Kaneko et al., PRION PROTEIN (PRP) SYNTHETIC PEPTIDES INDUCE CELLULAR PRP TO ACQUIREPROPERTIES OF THE SCRAPIE ISOFORM, Proceedings of the National Academy of Sciences of the United Statesof America, 92(24), 1995, pp. 11160-11164
Authors:
GABIZON R
ROSENMAN H
MEINER Z
KAHANA I
KAHANA E
SHUGART Y
OTT J
PRUSINER SB
Citation: R. Gabizon et al., MUTATION IN CODON-200 AND POLYMORPHISM IN CODON-129 OF THE PRION PROTEIN GENE IN LIBYAN JEWS WITH CREUTZFELDT-JAKOB-DISEASE, Philosophical transactions-Royal Society of London. Biological sciences, 343(1306), 1994, pp. 385-390
Authors:
GABIZON R
HALIMI M
MEINER Z
Citation: R. Gabizon et al., GENETICS AND BIOCHEMISTRY OF CREUTZFELDT-JAKOB-DISEASE IN LIBYAN JEWS, Biomedicine & pharmacotherapy, 48(8-9), 1994, pp. 385-390
Authors:
GOLDHAMMER Y
GABIZON R
MEINER Z
SADEH M
Citation: Y. Goldhammer et al., AN ISRAELI FAMILY WITH GERSTMANN-STRAUSSLER-SCHEINKER DISEASE MANIFESTING THE CODON-102 MUTATION IN THE PRION PROTEIN GENE, Neurology, 43(12), 1993, pp. 2718-2719
Authors:
GABIZON R
MEINER Z
HALIMI M
BENSASSON SA
Citation: R. Gabizon et al., HEPARIN-LIKE MOLECULES BIND DIFFERENTIALLY TO PRION-PROTEINS AND CHANGE THEIR INTRACELLULAR METABOLIC-FATE, Journal of cellular physiology, 157(2), 1993, pp. 319-325
Authors:
GABIZON R
ROSENMANN H
MEINER Z
KAHANA I
KAHANA E
SHUGART Y
OTT J
PRUSINER SB
Citation: R. Gabizon et al., MUTATION AND POLYMORPHISM OF THE PRION PROTEIN GENE IN LIBYAN JEWS WITH CREUTZFELDT-JAKOB-DISEASE (CJD), American journal of human genetics, 53(4), 1993, pp. 828-835
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