Flow cytometry as a method for studying effects of stressors on primary rat neurons von Behbahani, H., Rickle, A., Concha, H., Ankarcrona, M., Winblad, B., Cowburn, R.F.

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Expression of presenilin-1 and Notch-1 receptor in human embryonic CNS von Kostyszyn, B, Cowburn, R.F, Seiger, Å, KjÆldgaard, A, Sundström, E

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Alterations in the ryanodine receptor calcium release channel correlate with Alzheimer's disease neurofibrillary and β-amyloid pathologies von Kelliher, M., Fastbom, J., Cowburn, R.F., Bonkale, W., Ohm, T.G., Ravid, R., Sorrentino, V., O'Neill, C.

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PTEN, Akt, and GSK3β signalling in rat primary cortical neuronal cultures following tumor necrosis factor-α and trans-4-hydroxy-2-nonenal treatments von Rickle, A., Behbahani, H., Ankarcrona, M., Winblad, B., Cowburn, R.F.

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Ca2+ stores and capacitative Ca2+ entry in human neuroblastoma (SH-SY5Y) cells expressing a familial Alzheimer's disease presenilin-1 mutation von SMITH, I. F, BOYLE, J. P, VAUGHAN, P. F. T, PEARSON, H. A, COWBURN, R. F, PEERS, C. S

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Regulation of apolipoprotein E secretion in rat primary hippocampal astrocyte cultures von Cedazo-Mı́nguez, A, Hamker, U, Meske, V, Veh, R.W, Hellweg, R, Jacobi, C, Albert, F, Cowburn, R.F, Ohm, T.G

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Abnormalities in Alzheimer’s Disease Fibroblasts Bearing the APP670/671 Mutation von Gibson, G.E, Vestling, M, Zhang, H, Szolosi, S, Alkon, D, Lannfelt, L, Gandy, S, Cowburn, R.F

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Loss of stimulatory effect of guanosine triphosphate on [35S]GTPγS binding correlates with Alzheimer's disease neurofibrillary pathology in entorhinal cortex and CA1 hippocampal su... von García-Jiménez, A., Cowburn, R.F., Ohm, T.G., Lasn, H., Winblad, B., Bogdanovic, N., Fastbom, J.

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A quantitative autoradiographic study of [ [formula omitted]]cAMP binding to cytosolic and particulate protein kinase A in post-mortem brain staged for Alzheimer's disease neurofib... von Bonkale, W.L, Cowburn, R.F, Ohm, T.G, Bogdanovic, N, Fastbom, J

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Quantitative autoradiography of [ [formula omitted]]forskolin binding sites in post-mortem brain staged for Alzheimer's disease neurofibrillary changes and amyloid deposits von Garcı́a-Jiménez, A, Cowburn, R.F, Ohm, T.G, Bogdanovic, N, Winblad, B, Fastbom, J

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Nicergoline stimulates protein kinase C mediated α-secretase processing of the amyloid precursor protein in cultured human neuroblastoma SH-SY5Y cells von Cedazo-Minguez, A., Bonecchi, L., Winblad, B., Post, C., Wong, E.H.F., Cowburn, R.F., Benatti, L.

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Ca 2+ Stores and capacitative Ca 2+ entry in human neuroblastoma (SH-SY5Y) cells expressing a familial Alzheimer’s disease presenilin-1 mutation von Smith, I.F., Boyle, J.P., Vaughan, P.F.T., Pearson, H.A., Cowburn, R.F., Peers, C.S.

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Alzheimer's disease presenilin-1 exon 9 deletion and L250S mutations sensitiZe SH-SY5Y neuroblastoma cells to hyperosmotic stress-induced apoptosis von Tanii, H., Ankarcrona, M., Flood, F., Nilsberth, C., Mehta, N.D., Perez-Tur, J., Winblad, B., Benedikz, E., Cowburn, R.F.

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Distribution of presenilin 1 and 2 and their relation to Notch receptors and ligands in human embryonic/foetal central nervous system von Kostyszyn, B, Cowburn, R.F, Seiger, Å, Kjældgaard, A, Sundström, E

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709 Adenylyl cyclase signal transduction in Alzheimer's disease lymphocytes von Garlind, A., Cowburn, R.F., Winblad, B.

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Autoradiographic characterization of [ 3H]cGMP binding sites in the rat brain von Bonkale, W.L., Cowburn, R.F., Winblad, B., Fastbom, J.

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Amyloid precursor protein heat shock response in lymphoblastoid cell lines bearing presenilin-1 mutations von Johnston, J.A, Lannfelt, L, Wiehager, B, O'Neill, C, Cowburn, R.F

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227 Quantitative solution hybridisation assay of APP and APLP2 mRNA in Alzheimer's disease cerebral cortex von Johnston, J.A., Norgren, S., Ravid, R., Lannfelt, L., Cowburn, R.F.

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226 Effect of fibroblast growth factor and insulin on β-amyloid production in normal and familial Alzheimer's disease fibroblasts von Vigo-Pelfrey, C., Cedazo-Minguez, A., Cowburn, R.F., Jensen, M., Lannfelt, L., Johnston, J.A.

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235 Apolipoprotein E levels in plasma and CSF from members of the Swedish Alzheimer's disease APP 670/671 mutation family and sporadic Alzheimer's disease cases von Lindh, M., Blomberg, M., Jensen, M., Wahlund, L.-O., März, W., Scharnagl, H., Lannfelt, L., Cowburn, R.F.

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