Joiner S - Search Results

1

2.7 Å cryo-EM structure of ex vivo RML prion fibrils.

Manka SW, Zhang W, Wenborn A, Betts J, Joiner S, Saibil HR, Collinge J, Wadsworth JDF. Manka SW, et al. Among authors: joiner s. Nat Commun. 2022 Jul 13;13(1):4004. doi: 10.1038/s41467-022-30457-7. Nat Commun. 2022. PMID: 35831275 Free PMC article.

2

The same prion strain causes vCJD and BSE.

Hill AF, Desbruslais M, Joiner S, Sidle KC, Gowland I, Collinge J, Doey LJ, Lantos P. Hill AF, et al. Among authors: joiner s. Nature. 1997 Oct 2;389(6650):448-50, 526. doi: 10.1038/38925. Nature. 1997. PMID: 9333232 No abstract available.

3

Strain-specific prion-protein conformation determined by metal ions.

Wadsworth JD, Hill AF, Joiner S, Jackson GS, Clarke AR, Collinge J. Wadsworth JD, et al. Among authors: joiner s. Nat Cell Biol. 1999 May;1(1):55-9. doi: 10.1038/9030. Nat Cell Biol. 1999. PMID: 10559865

4

Species-barrier-independent prion replication in apparently resistant species.

Hill AF, Joiner S, Linehan J, Desbruslais M, Lantos PL, Collinge J. Hill AF, et al. Among authors: joiner s. Proc Natl Acad Sci U S A. 2000 Aug 29;97(18):10248-53. doi: 10.1073/pnas.97.18.10248. Proc Natl Acad Sci U S A. 2000. PMID: 10963685 Free PMC article.

5

Tissue distribution of protease resistant prion protein in variant Creutzfeldt-Jakob disease using a highly sensitive immunoblotting assay.

Wadsworth JD, Joiner S, Hill AF, Campbell TA, Desbruslais M, Luthert PJ, Collinge J. Wadsworth JD, et al. Among authors: joiner s. Lancet. 2001 Jul 21;358(9277):171-80. doi: 10.1016/s0140-6736(01)05403-4. Lancet. 2001. PMID: 11476832

6

Irregular presence of abnormal prion protein in appendix in variant Creutzfeldt-Jakob disease.

Joiner S, Linehan J, Brandner S, Wadsworth JD, Collinge J. Joiner S, et al. J Neurol Neurosurg Psychiatry. 2002 Nov;73(5):597-8. doi: 10.1136/jnnp.73.5.597. J Neurol Neurosurg Psychiatry. 2002. PMID: 12397162 Free PMC article. No abstract available.

7

BSE prions propagate as either variant CJD-like or sporadic CJD-like prion strains in transgenic mice expressing human prion protein.

Asante EA, Linehan JM, Desbruslais M, Joiner S, Gowland I, Wood AL, Welch J, Hill AF, Lloyd SE, Wadsworth JD, Collinge J. Asante EA, et al. Among authors: joiner s. EMBO J. 2002 Dec 2;21(23):6358-66. doi: 10.1093/emboj/cdf653. EMBO J. 2002. PMID: 12456643 Free PMC article.

8

Molecular classification of sporadic Creutzfeldt-Jakob disease.

Hill AF, Joiner S, Wadsworth JD, Sidle KC, Bell JE, Budka H, Ironside JW, Collinge J. Hill AF, et al. Among authors: joiner s. Brain. 2003 Jun;126(Pt 6):1333-46. doi: 10.1093/brain/awg125. Brain. 2003. PMID: 12764055

9

Characterization of two distinct prion strains derived from bovine spongiform encephalopathy transmissions to inbred mice.

Lloyd SE, Linehan JM, Desbruslais M, Joiner S, Buckell J, Brandner S, Wadsworth JDF, Collinge J. Lloyd SE, et al. Among authors: joiner s. J Gen Virol. 2004 Aug;85(Pt 8):2471-2478. doi: 10.1099/vir.0.79889-0. J Gen Virol. 2004. PMID: 15269389

10

Human prion protein with valine 129 prevents expression of variant CJD phenotype.

Wadsworth JD, Asante EA, Desbruslais M, Linehan JM, Joiner S, Gowland I, Welch J, Stone L, Lloyd SE, Hill AF, Brandner S, Collinge J. Wadsworth JD, et al. Among authors: joiner s. Science. 2004 Dec 3;306(5702):1793-6. doi: 10.1126/science.1103932. Epub 2004 Nov 11. Science. 2004. PMID: 15539564

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