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Results: 1-14 |
Results: 14
MOLECULAR SCREENING OF SHEEP FOR BOVINE SPONGIFORM ENCEPHALOPATHY
Authors: HILL AF SIDLE KCL JOINER S KEYES P MARTIN TC DAWSON M COLLINGE J
Citation: Af. Hill et al., MOLECULAR SCREENING OF SHEEP FOR BOVINE SPONGIFORM ENCEPHALOPATHY, Neuroscience letters, 255(3), 1998, pp. 159-162
THE SAME PRION STRAIN CAUSES VCJD AND BSE
Authors: HILL AF DESBRUSLAIS M JOINER S SIDLE KCL GOWLAND I COLLINGE J DOEY LJ LANTOS P
Citation: Af. Hill et al., THE SAME PRION STRAIN CAUSES VCJD AND BSE, Nature, 389(6650), 1997, pp. 448-450
UNALTERED SUSCEPTIBILITY TO BSE IN TRANSGENIC MICE EXPRESSING HUMAN PRION PROTEIN (VOL 378, PG 779, 1995)
Authors: COLLINGE J PALMER MS SIDLE KCL HILL AF GOWLAND I MEADS J ASANTE E BRADLEY R DOEY LJ LANTOS PL
Citation: J. Collinge et al., UNALTERED SUSCEPTIBILITY TO BSE IN TRANSGENIC MICE EXPRESSING HUMAN PRION PROTEIN (VOL 378, PG 779, 1995), Nature, 389(6650), 1997, pp. 526-526
BIOCHEMICAL TYPING OF SCRAPIE STRAINS - REPLY
Authors: COLLINGE J HILL AF SIDLE KCL IRONSIDE J
Citation: J. Collinge et al., BIOCHEMICAL TYPING OF SCRAPIE STRAINS - REPLY, Nature, 386(6625), 1997, pp. 564-564
TYPING PRION ISOFORMS - REPLY
Authors: COLLINGE J HILL AF SIDLE KCL IRONSIDE J
Citation: J. Collinge et al., TYPING PRION ISOFORMS - REPLY, Nature, 386(6622), 1997, pp. 233-234
GENETIC-BASIS OF CREUTZFELDT-JAKOB-DISEASE IN THE UNITED-KINGDOM - A SYSTEMATIC ANALYSIS OF PREDISPOSING MUTATIONS AND ALLELIC VARIATION INTHE PRNP GENE
Authors: WINDL O DEMPSTER M ESTIBEIRO JP LATHE R DESILVA R ESMONDE T WILL R SPRINGBETT A CAMPBELL TA SIDLE KCL PALMER MS COLLINGE J
Citation: O. Windl et al., GENETIC-BASIS OF CREUTZFELDT-JAKOB-DISEASE IN THE UNITED-KINGDOM - A SYSTEMATIC ANALYSIS OF PREDISPOSING MUTATIONS AND ALLELIC VARIATION INTHE PRNP GENE, Human genetics, 98(3), 1996, pp. 259-264
MOLECULAR ANALYSIS OF PRION STRAIN VARIATION AND THE ETIOLOGY OF NEW VARIANT CJD
Authors: COLLINGE J SIDLE KCL MEADS J IRONSIDE J HILL AF
Citation: J. Collinge et al., MOLECULAR ANALYSIS OF PRION STRAIN VARIATION AND THE ETIOLOGY OF NEW VARIANT CJD, Nature, 383(6602), 1996, pp. 685-690
RESCUE OF NEUROPHYSIOLOGICAL PHENOTYPE SEEN IN PRP NULL MICE BY TRANSGENE ENCODING HUMAN PRION PROTEIN, (VOL 9, PG 197, 1995)
Authors: WHITTINGTON MA SIDLE KCL GOWLAND I MEADS J HILL AF PALMER MS JEFFERYS JGR COLLINGE J
Citation: Ma. Whittington et al., RESCUE OF NEUROPHYSIOLOGICAL PHENOTYPE SEEN IN PRP NULL MICE BY TRANSGENE ENCODING HUMAN PRION PROTEIN, (VOL 9, PG 197, 1995), Nature genetics, 9(4), 1995, pp. 451-451
RESCUE OF NEUROPHYSIOLOGICAL PHENOTYPE SEEN IN PRP NULL MICE BY TRANSGENE ENCODING HUMAN PRION PROTEIN
Authors: WHITTINGTON MA SIDLE KCL GOWLAND I MEADS J HILL AF PALMER MS JEFFERYS JGR COLLINGE J
Citation: Ma. Whittington et al., RESCUE OF NEUROPHYSIOLOGICAL PHENOTYPE SEEN IN PRP NULL MICE BY TRANSGENE ENCODING HUMAN PRION PROTEIN, Nature genetics, 9(2), 1995, pp. 197-201
TRANSMISSION OF FATAL FAMILIAL INSOMNIA TO LABORATORY-ANIMALS
Authors: COLLINGE J PALMER MS SIDLE KCL GOWLAND I MEDORI R IRONSIDE J LANTOS P
Citation: J. Collinge et al., TRANSMISSION OF FATAL FAMILIAL INSOMNIA TO LABORATORY-ANIMALS, Lancet, 346(8974), 1995, pp. 569-570
UNALTERED SUSCEPTIBILITY TO BSE IN TRANSGENIC MICE EXPRESSING HUMAN PRION PROTEIN
Authors: COLLINGE J PALMER MS SIDLE KCL HILL AF GOWLAND I MEADS J ASANTE E BRADLEY R DOEY LJ LANTOS PL
Citation: J. Collinge et al., UNALTERED SUSCEPTIBILITY TO BSE IN TRANSGENIC MICE EXPRESSING HUMAN PRION PROTEIN, Nature, 378(6559), 1995, pp. 779-783
PRION PROTEIN IS NECESSARY FOR NORMAL SYNAPTIC FUNCTION
Authors: COLLINGE J WHITTINGTON MA SIDLE KCL SMITH CJ PALMER MS CLARKE AR JEFFERYS JGR
Citation: J. Collinge et al., PRION PROTEIN IS NECESSARY FOR NORMAL SYNAPTIC FUNCTION, Nature, 370(6487), 1994, pp. 295-297
TRANSMISSION OF CREUTZFELDT-JAKOB-DISEASE FROM HUMANS TO TRANSGENIC MICE EXPRESSING CHIMERIC HUMAN-MOUSE PRION PROTEIN
Authors: TELLING GC SCOTT M HSIAO KK FOSTER D YANG SL TORCHIA M SIDLE KCL COLLINGE J DEARMOND SJ PRUSINER SB
Citation: Gc. Telling et al., TRANSMISSION OF CREUTZFELDT-JAKOB-DISEASE FROM HUMANS TO TRANSGENIC MICE EXPRESSING CHIMERIC HUMAN-MOUSE PRION PROTEIN, Proceedings of the National Academy of Sciences of the United Statesof America, 91(21), 1994, pp. 9936-9940
FAMILIAL PICKS-DISEASE AND DEMENTIA IN FRONTAL-LOBE DEGENERATION OF NON-ALZHEIMER TYPE ARE NOT VARIANTS OF PRION DISEASE
Authors: COLLINGE J PALMER MS SIDLE KCL MAHAL SP CAMPBELL T BROWN J HARDY J BRUN AE GUSTAFSON L BAKKER E ROOS R GROEN JJ
Citation: J. Collinge et al., FAMILIAL PICKS-DISEASE AND DEMENTIA IN FRONTAL-LOBE DEGENERATION OF NON-ALZHEIMER TYPE ARE NOT VARIANTS OF PRION DISEASE, Journal of Neurology, Neurosurgery and Psychiatry, 57(6), 1994, pp. 762-762
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