Holton J - Search Results

1

Abundant pyroglutamate-modified ABri and ADan peptides in extracellular and vascular amyloid deposits in familial British and Danish dementias.

Saul A, Lashley T, Revesz T, Holton J, Ghiso JA, Coomaraswamy J, Wirths O. Saul A, et al. Among authors: holton j. Neurobiol Aging. 2013 May;34(5):1416-25. doi: 10.1016/j.neurobiolaging.2012.11.014. Epub 2012 Dec 20. Neurobiol Aging. 2013. PMID: 23261769 Free PMC article.

2

Cytoskeletal pathology in familial cerebral amyloid angiopathy (British type) with non-neuritic amyloid plaque formation.

Revesz T, Holton JL, Doshi B, Anderton BH, Scaravilli F, Plant GT. Revesz T, et al. Among authors: holton jl. Acta Neuropathol. 1999 Feb;97(2):170-6. doi: 10.1007/s004010050970. Acta Neuropathol. 1999. PMID: 9928828

3

A decamer duplication in the 3' region of the BRI gene originates an amyloid peptide that is associated with dementia in a Danish kindred.

Vidal R, Revesz T, Rostagno A, Kim E, Holton JL, Bek T, Bojsen-Møller M, Braendgaard H, Plant G, Ghiso J, Frangione B. Vidal R, et al. Among authors: holton jl. Proc Natl Acad Sci U S A. 2000 Apr 25;97(9):4920-5. doi: 10.1073/pnas.080076097. Proc Natl Acad Sci U S A. 2000. PMID: 10781099 Free PMC article.

4

Variant Alzheimer's disease with spastic paraparesis and cotton wool plaques is caused by PS-1 mutations that lead to exceptionally high amyloid-beta concentrations.

Houlden H, Baker M, McGowan E, Lewis P, Hutton M, Crook R, Wood NW, Kumar-Singh S, Geddes J, Swash M, Scaravilli F, Holton JL, Lashley T, Tomita T, Hashimoto T, Verkkoniemi A, Kalimo H, Somer M, Paetau A, Martin JJ, Van Broeckhoven C, Golde T, Hardy J, Haltia M, Revesz T. Houlden H, et al. Among authors: holton jl. Ann Neurol. 2000 Nov;48(5):806-8. Ann Neurol. 2000. PMID: 11079548

5

A pathogenic presenilin-1 deletion causes abberrant Abeta 42 production in the absence of congophilic amyloid plaques.

Steiner H, Revesz T, Neumann M, Romig H, Grim MG, Pesold B, Kretzschmar HA, Hardy J, Holton JL, Baumeister R, Houlden H, Haass C. Steiner H, et al. Among authors: holton jl. J Biol Chem. 2001 Mar 9;276(10):7233-9. doi: 10.1074/jbc.M007183200. Epub 2000 Nov 17. J Biol Chem. 2001. PMID: 11084029 Free article.

6

Regional distribution of amyloid-Bri deposition and its association with neurofibrillary degeneration in familial British dementia.

Holton JL, Ghiso J, Lashley T, Rostagno A, Guerin CJ, Gibb G, Houlden H, Ayling H, Martinian L, Anderton BH, Wood NW, Vidal R, Plant G, Frangione B, Revesz T. Holton JL, et al. Am J Pathol. 2001 Feb;158(2):515-26. doi: 10.1016/S0002-9440(10)63993-4. Am J Pathol. 2001. PMID: 11159188 Free PMC article.

7

Amyloidogenesis in familial British dementia is associated with a genetic defect on chromosome 13.

Ghiso J, Vidal R, Rostagno A, Miravalle L, Holton JL, Mead S, Révész T, Plant G, Frangione B. Ghiso J, et al. Among authors: holton jl. Ann N Y Acad Sci. 2000;920:84-92. doi: 10.1111/j.1749-6632.2000.tb06908.x. Ann N Y Acad Sci. 2000. PMID: 11193180

8

Systemic amyloid deposits in familial British dementia.

Ghiso JA, Holton J, Miravalle L, Calero M, Lashley T, Vidal R, Houlden H, Wood N, Neubert TA, Rostagno A, Plant G, Revesz T, Frangione B. Ghiso JA, et al. Among authors: holton j. J Biol Chem. 2001 Nov 23;276(47):43909-14. doi: 10.1074/jbc.M105956200. Epub 2001 Sep 13. J Biol Chem. 2001. PMID: 11557758 Free article.

9

Familial cerebral amyloid angiopathy related to stroke and dementia.

Frangione B, Révész T, Vidal R, Holton J, Lashley T, Houlden H, Wood N, Rostagno A, Plant G, Ghiso J. Frangione B, et al. Among authors: holton j. Amyloid. 2001 Jul;8 Suppl 1:36-42. Amyloid. 2001. PMID: 11676288 Review.

10

Chromosome 13 dementia syndromes as models of neurodegeneration.

Ghiso J, Révész T, Holton J, Rostagno A, Lashley T, Houlden H, Gibb G, Anderton B, Bek T, Bojsen-Møller M, Wood N, Vidal R, Braendgaard H, Plant G, Frangione B. Ghiso J, et al. Among authors: holton j. Amyloid. 2001 Dec;8(4):277-84. doi: 10.3109/13506120108993826. Amyloid. 2001. PMID: 11791622 Review.

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