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Number of items: 66.

A

Aguzzi, A and Blattler, T and Klein, M and Raber, A and Weissmann, C and Brandner, S (1996) Telencephalic brain grafts in the study of scrapie pathogenesis. In: Court, L and Dodet, B, (eds.) TRANSMISSIBLE SUBACUTE SPONGIFORM ENCEPHALOPATHIES: PRION DISEASES. (pp. 173 - 184). EDITIONS SCIENTIFIQUE & MEDICALES ELSEVIER

Aguzzi, A and Brandner, S and Marino, S and Steinbach, JP (1996) Transgenic and knockout mice in the study of neurodegenerative diseases. J MOL MED-JMM , 74 (3) 111 - 126.

Armstrong, RA and Cairns, NJ and Myers, D and Smith, CUM and Lantos, PL and Rossor, MN (1996) A comparison of beta-amyloid deposition in the medial temporal lobe in sporadic Alzheimer's disease, Down's syndrome and normal elderly brains. NEURODEGENERATION , 5 (1) 35 - 41.

Armstrong, RA and Cairns, NJ and Patel, R and Lantos, PL and Rossor, MN (1996) Relationships between beta-amyloid (A beta) deposits and blood vessels in patients with sporadic and familial Alzheimer's disease. NEUROSCI LETT , 207 (3) 171 - 174.

B

Bermingham, N and Martin, JE and Fisher, EMC (1996) The mouse lysosomal membrane protein 1 gene as a candidate for the motorneuron degeneration (mnd) locus. Genomics , 32 266 - 271.

Bermingham, N and McKay, T and Hoyle, J and Hernandez, D and Martin, JE and Fisher, EMC (1996) The gene encoding tripeptidyl peptidase II maps to chromosome 1 in the mouse. Mamm Genome , 7 390 - ?.

Brandner, S and Isenmann, S and Raeber, A and Fischer, M and Sailer, A and Kobayashi, Y and Marino, S and Weissmann, C and Aguzzi, A (1996) Normal host prion protein necessary for scrapie-induced neurotoxicity. NATURE , 379 (6563) 339 - 343.

Brandner, S and Raeber, A and Sailer, A and Blattler, T and Fischer, M and Weissmann, C and Aguzzi, A (1996) Normal host prion protein (PrPc) is required for scrapie spread within the central nervous system. P NATL ACAD SCI USA , 93 (23) 13148 - 13151.

Brown, J and Lantos, PL and Roques, P and Fidani, L and Rossor, MN (1996) Familial dementia with swollen achromatic neurons and corticobasal inclusion bodies: A clinical and pathological study. J NEUROL SCI , 135 (1) 21 - 30.

Budka, H and Aguzzi, A and Brown, P and Brucher, JM and Bugiani, O and Collinge, J and Diringer, H and Gullotta, F and Haltia, M and Hauw, JJ and Ironside, JW and Kretzschmar, HA and Lantos, PL and Masullo, C and Pocchiari, M and Schlote, W and Tateishi, J and Will, RG (1996) Tissue handling in suspected Creutzfeldt-Jakob disease (CJD) and other human spongiform encephalopathies (prion diseases). PATHOLOGE , 17 (2) 171 - 175.

Budka, H and Aguzzi, A and Brown, P and Brucher, JM and Bugiani, O and Collinge, J and Diringer, H and Gullotta, F and Haltia, M and Hauw, JJ and Ironside, JW and Kretzschmar, HA and Lantos, PL and Masullo, C and Pocchiari, M and Schlote, W and Tateishi, J and Will, RG (1996) [Consensus report: tissue handling in suspected Creutzfeldt-Jakob disease and other spongiform encephalopathies (prion diseases) in the human. European Union Biomed-1 Concerted Action]. Pathologe , 17 (2) 171 - 175.

C

Campbell, TA and Palmer, MS and Will, RG and Gibb, WRG and Luthert, PJ and Collinge, J (1996) A prion disease with a novel 96-base pair insertional mutation in the prion protein gene. NEUROLOGY , 46 (3) 761 - 766.

Colling, SB and Collinge, J and Jefferys, JGR (1996) Hippocampal slices from prion protein null mice: Disrupted Ca2+-activated K+ currents. NEUROSCI LETT , 209 (1) 49 - 52.

Collinge, J (1996) New diagnostic tests for prion diseases. NEW ENGL J MED , 335 (13) 963 - 965.

Collinge, J (1996) Prion diseases. In: Weatherall, DJ and Ledingham, J and Warrell, D, (eds.) Oxford textbook of medicine. (3977 - 3981). Oxford University Press: Oxford, UK.

Collinge, J and Beck, J and Campbell, T and Estibeiro, K and Will, RG (1996) Prion protein gene analysis in new variant cases of Creutzfeldt-Jakob disease. LANCET , 348 (9019) 56 - 56.

Collinge, J and Rossor, M (1996) A new variant of prion disease. LANCET , 347 (9006) 916 - 917.

Collinge, J and Sidle, KCL and Meads, J and Ironside, J and Hill, AF (1996) Molecular analysis of prion strain variation and the aetiology of 'new variant' CJD. NATURE , 383 (6602) 685 - 690.

D

Delabar, JM and Creau, N and Antonarakis, SE and Brahe, C and Estivill, X and Pritchard, M and Fisher, EMC and Kessling, A and Yaspo, ML and Lehrach, H and Nizetic, D and Oliva, R and Petersen, M and Potier, MC and Roizes, G and Van-Broeckhoven, C and Lutfalla, G (1996) Towards an integrated chromosome 21 map: progress of the European chromosome 21 consortium. In: European Journal of Human Genetics.

E

Eastwood, MR (1996) The challenge of the dementias. Lancet , 347 (9011) 1303 - 1307.

F

Fischer, M and Rulicke, T and Raeber, A and Sailer, A and Moser, M and Oesch, B and Brandner, S and Aguzzi, A and Weissmann, C (1996) Prion protein (PrP) with amino-proximal deletions restoring susceptibility of PrP knockout mice to scrapie. EMBO J , 15 (6) 1255 - 1264.

Fox, N and Harvey, RJ and Rossor, MN (1996) Protein folding, nucleation phenomena and delayed neurodegeneration in Alzheimer's disease. REV NEUROSCIENCE , 7 (1) 21 - 28.

Fox, NC and Freeborough, PA and Rossor, MN (1996) Visualisation and quantification of rates of atrophy in Alzheimer's disease. LANCET , 348 (9020) 94 - 97.

Fox, NC and Warrington, EK and Freeborough, PA and Hartikainen, P and Kennedy, AM and Stevens, JM and Rossor, MN (1996) Presymptomatic hippocampal atrophy in Alzheimer's disease - A longitudinal MRI study. BRAIN , 119 2001 - 2007.

Fox, NC and Warrington, EK and Stevens, JM and Rossor, MN (1996) Atrophy of the hippocampal formation in early familial Alzheimer's disease a longitudinal MRI study of at-risk members of a family with an amyloid precursor protein 717(VAL-GLY) mutation. NEUROBIOLOGY OF ALZHEIMER'S DISEASE , 777 226 - 232.

Freeborough, PA and Woods, RP and Fox, NC (1996) Accurate registration of serial 3D MR brain images and its application to visualizing change in neurodegenerative disorders. J COMPUT ASSIST TOMO , 20 (6) 1012 - 1022.

Fritschy, JM and Brandner, S and Aguzzi, A and Koedood, M and Luscher, B and Mitchell, PJ (1996) Brain cell type specificity and gliosis-induced activation of the human cytomegalovirus immediate-early promoter in transgenic mice. J NEUROSCI , 16 (7) 2275 - 2282.

Fukutani, Y and Cairns, NJ and Rossor, MN and Lantos, PL (1996) Cerebellar pathology in sporadic and familial Alzheimer's disease including APP 717 (Val->Ile) mutation cases. NEUROPATH APPL NEURO , 22 (5) 452 - 452.

Fukutani, Y and Cairns, NJ and Rossor, MN and Lantos, PL (1996) Purkinje cell loss and astrocytosis in the cerebellum in familial and sporadic Alzheimer's disease. NEUROSCI LETT , 214 (1) 33 - 36.

G

Gonos, ES and Burns, JS and Mazars, GR and Kobrna, A and Riley, TEW and Barnett, SC and Zafarana, G and Ludwig, RL and Ikram, Z and Powell, AJ and Jat, PS (1996) Rat embryo fibroblasts immortalized with simian virus 40 large T antigen undergo senescence upon its inactivation. MOL CELL BIOL , 16 (9) 5127 - 5138.

H

Harvey, RJ and Roques, P and Fox, NC and Rossor, MN (1996) Non-Alzheimer dementias in young patients. BRIT J PSYCHIAT , 168 (3) 384 - 385.

Hassler, W and Brandner, S and Slansky, I (1996) Microsurgical management of lateral lumbar disc herniations: Combined lateral and interlaminar approach. ACTA NEUROCHIR , 138 (8) 907 - 910.

Hernandez, D and Fisher, EMC (1996) Down syndrome genetics: unravelling a multifactorial disorder. Hum Mol Genet , 5 1411 - 1416.

Hopfer, U and Jacobberger, JW and Gruenert, DC and Eckert, RL and Jat, PS and Whitsett, JA (1996) Immortalization of epithelial cells. AM J PHYSIOL-CELL PH , 39 (1) C1 - C11.

Hoyle, J and Fisher, EMC (1996) Genomic organization and mapping of the mouse P26s4 ATPase gene: a member of the remarkably conserved AAA gene family. Genomics , 31 115 - 118.

Hoyle, J and Phelan, JP and Bermingham, N and Fisher, EMC (1996) Localization of human and mouse N-ethylmaleimide-sensitive factor (NSF) gene: a two domain member of the AAA family which is involved in membrane fusion. Mamm Genome , 7 850 - ?.

Hoyle, J and Yulug, IG and Johnstone, K and Scambler, PJ and Fisher, EMC (1996) Characterisation of a short interspersed repeat (Mermaid) which has family members on human chromosome 21 and elsewhere in the human genome. Hum Genet , 97 117 - 120.

Hutton, M and Busfield, F and Wragg, M and Crook, R and PerezTur, J and Clark, RF and Prihar, G and Talbot, C and Phillips, H and Wright, K and Baker, M and Lendon, C and Duff, K and Martinez, A and Houlden, H and Nichols, A and Karran, E and Roberts, G and Roques, P and Rossor, M and Venter, JC and Adams, MD and Cline, RT and Phillips, CA and Fuldner, RA and Hardy, J and Goate, A (1996) Complete analysis of the presenilin 1 gene in early onset Alzheimer's disease. NEUROREPORT , 7 (3) 801 - 805.

I

Isenmann, S and Brandner, S and Aguzzi, A (1996) Neuroectodermal grafting: A new tool for the study of neurodegenerative diseases. HISTOL HISTOPATHOL , 11 (4) 1063 - 1073.

Isenmann, S and Brandner, S and Kuhne, G and Boner, J and Aguzzi, A (1996) Comparative in vivo and pathological analysis of the blood-brain barrier in mouse telencephalic transplants. NEUROPATH APPL NEURO , 22 (2) 118 - 128.

Isenmann, S and Brandner, S and Sure, U and Aguzzi, A (1996) Telencephalic transplants in mice: Characterization of growth and differentiation patterns. NEUROPATH APPL NEURO , 22 (2) 108 - 117.

K

Katsanis, N and Fisher, EMC (1996) The gene encoding the p60 subunit of chromatin assembly factor I (CAF1P60) maps to human chromosome 21q22.2, a region associated with some of the major features of Down syndrome. Hum Genet , 98 497 - ?.

Katsanis, N and Fitzgibbon, J and Fisher, EMC (1996) Paralogy mapping: identification of a region in the human MHC triplicated onto human chromosomes 1 and 9 allows the prediction and isolation of novel PBX and NOTCH loci. Genomics , 35 101 - 108.

L

Lindberg, RLP and Porcher, C and Grandchamp, B and Ledermann, B and Burki, K and Brandner, S and Aguzzi, A and Meyer, UA (1996) Porphobilinogen deaminase deficiency in mice causes a neuropathy resembling that of human hepatic porphyria. NAT GENET , 12 (2) 195 - 199.

Lovestone, S and Wilcock, G and Rossor, M and Cayton, H and Ragan, I (1996) Apolipoprotein E genotyping in Alzheimer's disease. The UK Alzheimer's Disease Genetic consortium. Lancet , 347 (9017) 1775 - 1776.

M

Mann, DMA and Iwatsubo, T and Cairns, NJ and Lantos, PL and Nochlin, D and Sumi, SM and Bird, TD and Poorkaj, P and Hardy, J and Hutton, M and Prihar, G and Crook, R and Rossor, MN and Haltia, M (1996) Amyloid beta protein (A beta) deposition in chromosome 14-linked Alzheimer's disease: Predominance of A beta(42(43)). ANN NEUROL , 40 (2) 149 - 156.

Mann, DMA and Iwatsubo, T and Ihara, Y and Cairns, NJ and Lantos, PL and Bogdanovic, N and Lannfelt, L and Winblad, B and MaatSchieman, MLC and Rossor, MN (1996) Predominant deposition of amyloid-beta(42(43)) in plaques in cases of Alzheimer's disease and hereditary cerebral hemorrhage associated with mutations in the amyloid precursor protein gene. AM J PATHOL , 148 (4) 1257 - 1266.

Matthews, D and Fry, L and Powles, A and Weber, J and McCarthy, M and Fisher, EMC and Davies, K and Williamson, R (1996) Evidence for a locus for familial psoriasis mapping to chromosome 4q. Nature genetics , 14 231 - 233.

McKeith, IG and Morris, CM and Lovestone, S and Wilcock, G and Rossor, M and Cayton, H and Ragan, I and Humphries, S and Betteridge, DJ and Durrington, PN and Galton, DJ and Nicholls, P (1996) Apolipoprotein E genotyping in Alzheimer's disease [21]. Lancet , 347 (9017) 1775 - 1776.

Moran, TH and Reeves, RH and Rogers, D and Fisher, EMC (1996) Ain't misbehavin' - it's genetic. Nature Genetics , 12 115 - 116.

Muller, U and Cristina, N and Li, ZW and Wolfer, DPY and Lipp, HP and Rulicke, T and Brandner, S and Aguzzi, A and Weissman, C (1996) Mice homozygous for a modified beta-amyloid precursor protein (beta APP) gene show impaired behavior and high incidence of agenesis of the corpus callosum. NEUROBIOLOGY OF ALZHEIMER'S DISEASE , 777 65 - 73.

P

Palmer, MS and vanLeeven, RH and Mahal, SP and Campbell, TA and Humphreys, CB and Collinge, J (1996) Sequence variation of intron of prion protein gene, crucial for complete diagnostic strategies. HUM MUTAT , 7 (3) 280 - 281.

R

Rossor, MN (1996) BSE and human disease. J ROY COLL PHYS LOND , 30 (6) 494 - 495.

Rossor, MN (1996) Degenerative diseases. Current Opinion in Neurology , 9 (4) 251 - 253.

Rossor, MN (1996) Degenerative diseases - Editorial comment. CURR OPIN NEUROL , 9 (4) 251 - 253.

Rossor, MN (1996) Mad cows and demented people. Trans Med Soc Lond , 113 34 - 37.

Rossor, MN and Fox, NC and Beck, J and Campbell, TC and Collinge, J (1996) Incomplete penetrance of familial Alzheimer's disease in a pedigree with a novel presenilin-1 gene mutation. LANCET , 347 (9014) 1560 - 1560.

Rossor, MN and Fox, NC and Freeborough, PA and Harvey, RJ (1996) Clinical features of sporadic and familial Alzheimer's disease. NEURODEGENERATION , 5 (4) 393 - 397.

Rossor, MN and Kennedy, AM and Frackowiak, RSJ (1996) Clinical and neuroimaging features of familial Alzheimer's disease. NEUROBIOLOGY OF ALZHEIMER'S DISEASE , 777 49 - 56.

S

Sweeney, BJ and Rossor, MN (1996) Medial medullary syndrome associated with patent foramen ovale in a weightlifter. EUR NEUROL , 36 (6) 391 - 391.

T

Tabrizi, SJ and Scaravilli, F and Howard, RS and Collinge, J and Rossor, M (1996) Creutzfeldt-Jakob disease in a young woman. LANCET , 347 (9006) 945 - 948.

Thal, LJ and Schwartz, G and Sano, M and Weiner, M and Knopman, D and Harrell, L and Bodenheimer, S and Rossor, M and Philpot, M and Schor, J and Goldberg, A (1996) A multicenter double-blind study of controlled-release physostigmine for the treatment of symptoms secondary to Alzheimer's disease. NEUROLOGY , 47 (6) 1389 - 1395.

Tschopp, RR and Brandner, S and Marino, S and Bothe, K and Horak, I and Rethwilm, A and Aguzzi, A (1996) Analysis of the determinants of neurotropism and neurotoxicity of HFV in transgenic mice. VIROLOGY , 216 (2) 338 - 346.

W

Weissmann, C and Fischer, M and Raeber, A and Bueler, H and Sailer, A and Shmerling, D and Rulicke, T and Brandner, S and Aguzzi, A (1996) The use of transgenic mice in the investigation of transmissible spongiform encephalopathies. INTERNATIONAL JOURNAL OF EXPERIMENTAL PATHOLOGY , 77 (6) 283 - 293.

Weissmann, C and Fischer, M and Raeber, A and Sailer, A and Shmerling, D and Rulicke, T and Brandner, S and Aguzzi, A (1996) The role of PrP in pathogenesis of experimental scrapie. COLD SPRING HARBOR SYMPOSIA ON QUANTITATIVE BIOLOGY , 61 511 - 522.

Windl, O and Dempster, M and Estibeiro, JP and Lathe, R and deSilva, R and Esmonde, T and Will, R and Springbett, A and Campbell, TA and Sidle, KCL and Palmer, MS and Collinge, J (1996) Genetic basis of Creutzfeldt-Jakob disease in the United Kingdom: A systematic analysis of predisposing mutations and allelic variation in the PRNP gene. HUM GENET , 98 (3) 259 - 264.

This list was generated on Fri May 24 10:18:23 2013 BST.