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Disruption of endocytic trafficking in frontotemporal dementia with CHMP2B mutations.
Urwin H, Authier A, Nielsen JE, Metcalf D, Powell C, Froud K, Malcolm DS, Holm I, Johannsen P, Brown J, Fisher EM, van der Zee J, Bruyland M; FReJA Consortium; Van Broeckhoven C, Collinge J, Brandner S, Futter C, Isaacs AM. Urwin H, et al. Among authors: collinge j. Hum Mol Genet. 2010 Jun 1;19(11):2228-38. doi: 10.1093/hmg/ddq100. Epub 2010 Mar 10. Hum Mol Genet. 2010. PMID: 20223751 Free PMC article.
Genetic characterization of a novel familial dementia.
Brown J, Smith S, Brun A, Collinge J, Gydesen S, Hardy J, Mullan M, Goate A. Brown J, et al. Among authors: collinge j. Ann N Y Acad Sci. 1991;640:181-3. doi: 10.1111/j.1749-6632.1991.tb00213.x. Ann N Y Acad Sci. 1991. PMID: 1776737
G/T polymorphism in CRYA2 gene.
Ashworth A, Campbell T, Palmer M, Collinge J, Brown J. Ashworth A, et al. Among authors: collinge j. Hum Mol Genet. 1994 Sep;3(9):1712. doi: 10.1093/hmg/3.9.1712. Hum Mol Genet. 1994. PMID: 7833944 No abstract available.
Familial non-specific dementia maps to chromosome 3.
Brown J, Ashworth A, Gydesen S, Sorensen A, Rossor M, Hardy J, Collinge J. Brown J, et al. Among authors: collinge j. Hum Mol Genet. 1995 Sep;4(9):1625-8. doi: 10.1093/hmg/4.9.1625. Hum Mol Genet. 1995. PMID: 8541850
Prions and the prion disorders.
Fisher E, Telling G, Collinge J. Fisher E, et al. Among authors: collinge j. Mamm Genome. 1998 Jul;9(7):497-502. doi: 10.1007/s003359900807. Mamm Genome. 1998. PMID: 9657843 Review.
Molecular genetic characterisation of frontotemporal dementia on chromosome 3.
Ashworth A, Lloyd S, Brown J, Gydesen S, Sorensen SA, Brun A, Englund E, Humphreys C, Housman D, Badura M, Stanton V Jr, Taylor K, Cameron J, Munroe D, Johansson J, Rossor M, Fisher EM, Collinge J. Ashworth A, et al. Among authors: collinge j. Dement Geriatr Cogn Disord. 1999;10 Suppl 1:93-101. doi: 10.1159/000051222. Dement Geriatr Cogn Disord. 1999. PMID: 10436350
512 results