Unaltered susceptibility to BSE in transgenic mice expressing human prion protein. [Addendum: Oct 2, 1997, v. 389 (6650), p. 526.] von Collinge, J, Palmer, M.S, Sidle, K.C, Hill, A.F, Gowland, I, Meads, J, Asante, E, Bradley, R, Doey, L.J, Lantos, P.L

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A gene from the human sex-determining region encodes a protein with homology to a conserved DNA-binding motif von Sinclair, Andrew H, Berta, Philippe, Palmer, Mark S, Hawkins, J. Ross, Griffiths, Beatrice L, Smith, Matthijs J, Foster, Jamie W, Frischauf, Anna-Maria, Lovell-Badge, Robin, Goodfellow, Peter N

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Genetic basis of Creutzfeldt-Jakob disease in the United Kingdom : a systematic analysis of predisposing mutations and allelic variation in the PRNP gene von WINDL, O, DEMPSTER, M, PALMER, M. S, COLLINGE, J, ESTIBEIRO, J. P, LATHE, R, DE SILVA, R, ESMONDE, T, WILL, R, SPRINGBETT, A, CAMPBELL, T. A, SIDLE, K. C. L

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Rescue of neurophysiological phenotype seen in PrP null mice by transgene encoding human prion protein von Whittington, Miles A, Sidle, Katie C.L, Gowland, Ian, Meads, Julie, Hill, Andrew F, Palmer, Mark S, Jefferys, John G.R, Collinge, John

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Pathogenic presenilin 1 mutations (P436S & I143F) in early-onset Alzheimer's disease in the UK von Palmer, Mark S., Beck, Jonathan A., Campbell, Tracy A., Humphries, Christine B., Roques, Penelope K., Fox, Nick C., Harvey, Richard, Rossor, Martin N., Collinge, John

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Conformational properties of the prion octa-repeat and hydrophobic sequences von Smith, Corinne J, Drake, Alex F, Banfield, Beaulah A, Bloomberg, Graham B, Palmer, Mark S, Clarke, Anthony R, Collinge, John

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Molecular Genetics of Human Prion Diseases von Collinge, John, Palmer, Mark S.

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Prion protein is necessary for normal synaptic function von Collinge, John, Whittington, Miles A, Sidle, Katie C. L, Smith, Corinne J, Palmer, Mark S, Clarke, Anthony R, Jefferys, John G. R

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Homozygous prion protein genotype predisposes to sporadic Creutzfeldt-Jakob disease von Palmer, Mark S, Dryden, Aidan J, Hughes, J. Trevor, Collinge, John

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Inherited prion disease (PrP lysine 200) in Britain: two case reports von Collinge, J, Palmer, M S, Campbell, T, Sidle, K C, Carroll, D, Harding, A

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Homozygous prion protein genotype predisposes to sporadic Creutzfeldt-Jakob disease von Palmer, M S, Dryden, A J, Hughes, J T, Collinge, J

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Genetic predisposition to iatrogenic Creutzfeldt-Jakob disease von Collinge, J., Palmer, M.S., Dryden, A.J.

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Transmission of fatal familial insomnia to laboratory animals von Collinge, John, Palmer, MarkS, Sidle, KatieC.L., Gowland, Ian, Medori, Rosella, Ironside, James, Lantos, Peter

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Human trophoblast and the choriocarcinoma cell line BeWo express a truncated HLA Class I molecule von Ellis, SA, Palmer, MS, McMichael, AJ

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The human SRY transcript von Clepet, Christian, Schater, Alan J., Sinclair, Andrew H., Palmer, Mark S., Lovell-Badge, Robin, Goodfellow, Peter N.

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Unaltered susceptibility to BSE in transgenic mice expressing human prion protein von Collinge, John, Palmer, Mark S., Sidle, Katie C. L., Hill, Andrew F., Gowland, Ian, Meads, Julie, Asante, Emmanuel, Bradley, Ray, Doey, Lawrence J., Lantos, Peter L.

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Deletions in the prion protein gene are not associated with CJD von Palmer, Mark S., Mahal, Sukhvir P., Campbell, Tracy A., Hill, Andrew F., Sidle, Katie C.L., Laplanche, Jean-Louis, Collinge, John

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Mutations and polymorphisms in the prion protein gene von Palmer, Mark S., Collinge, John

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Molecular biology of prion diseases - Molecular genetics of human prion diseases von Collinge, John, Palmer, Mark S.

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Prion diseases von Collinge, John, Palmer, Mark S

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