Ghetti B - Search Results

1

Brain homogenates from human tauopathies induce tau inclusions in mouse brain.

Clavaguera F, Akatsu H, Fraser G, Crowther RA, Frank S, Hench J, Probst A, Winkler DT, Reichwald J, Staufenbiel M, Ghetti B, Goedert M, Tolnay M. Clavaguera F, et al. Among authors: ghetti b. Proc Natl Acad Sci U S A. 2013 Jun 4;110(23):9535-40. doi: 10.1073/pnas.1301175110. Epub 2013 May 20. Proc Natl Acad Sci U S A. 2013. PMID: 23690619 Free PMC article.

2

Vascular variant of prion protein cerebral amyloidosis with tau-positive neurofibrillary tangles: the phenotype of the stop codon 145 mutation in PRNP.

Ghetti B, Piccardo P, Spillantini MG, Ichimiya Y, Porro M, Perini F, Kitamoto T, Tateishi J, Seiler C, Frangione B, Bugiani O, Giaccone G, Prelli F, Goedert M, Dlouhy SR, Tagliavini F. Ghetti B, et al. Proc Natl Acad Sci U S A. 1996 Jan 23;93(2):744-8. doi: 10.1073/pnas.93.2.744. Proc Natl Acad Sci U S A. 1996. PMID: 8570627 Free PMC article.

3

Familial multiple system tauopathy with presenile dementia: a disease with abundant neuronal and glial tau filaments.

Spillantini MG, Goedert M, Crowther RA, Murrell JR, Farlow MR, Ghetti B. Spillantini MG, et al. Among authors: ghetti b. Proc Natl Acad Sci U S A. 1997 Apr 15;94(8):4113-8. doi: 10.1073/pnas.94.8.4113. Proc Natl Acad Sci U S A. 1997. PMID: 9108114 Free PMC article.

4

Familial multiple-system tauopathy with presenile dementia is localized to chromosome 17.

Murrell JR, Koller D, Foroud T, Goedert M, Spillantini MG, Edenberg HJ, Farlow MR, Ghetti B. Murrell JR, et al. Among authors: ghetti b. Am J Hum Genet. 1997 Nov;61(5):1131-8. doi: 10.1086/301594. Am J Hum Genet. 1997. PMID: 9345089 Free PMC article.

5

Mutation in the tau gene in familial multiple system tauopathy with presenile dementia.

Spillantini MG, Murrell JR, Goedert M, Farlow MR, Klug A, Ghetti B. Spillantini MG, et al. Among authors: ghetti b. Proc Natl Acad Sci U S A. 1998 Jun 23;95(13):7737-41. doi: 10.1073/pnas.95.13.7737. Proc Natl Acad Sci U S A. 1998. PMID: 9636220 Free PMC article.

6

Tau pathology in a family with dementia and a P301L mutation in tau.

Mirra SS, Murrell JR, Gearing M, Spillantini MG, Goedert M, Crowther RA, Levey AI, Jones R, Green J, Shoffner JM, Wainer BH, Schmidt ML, Trojanowski JQ, Ghetti B. Mirra SS, et al. Among authors: ghetti b. J Neuropathol Exp Neurol. 1999 Apr;58(4):335-45. doi: 10.1097/00005072-199904000-00004. J Neuropathol Exp Neurol. 1999. PMID: 10218629

7

Structure of tau exon 10 splicing regulatory element RNA and destabilization by mutations of frontotemporal dementia and parkinsonism linked to chromosome 17.

Varani L, Hasegawa M, Spillantini MG, Smith MJ, Murrell JR, Ghetti B, Klug A, Goedert M, Varani G. Varani L, et al. Among authors: ghetti b. Proc Natl Acad Sci U S A. 1999 Jul 6;96(14):8229-34. doi: 10.1073/pnas.96.14.8229. Proc Natl Acad Sci U S A. 1999. PMID: 10393977 Free PMC article.

8

Tau gene mutation G389R causes a tauopathy with abundant pick body-like inclusions and axonal deposits.

Murrell JR, Spillantini MG, Zolo P, Guazzelli M, Smith MJ, Hasegawa M, Redi F, Crowther RA, Pietrini P, Ghetti B, Goedert M. Murrell JR, et al. Among authors: ghetti b. J Neuropathol Exp Neurol. 1999 Dec;58(12):1207-26. doi: 10.1097/00005072-199912000-00002. J Neuropathol Exp Neurol. 1999. PMID: 10604746

9

Progress in hereditary tauopathies: a mutation in the Tau gene (G389R) causes a Pick disease-like syndrome.

Ghetti B, Murrell JR, Zolo P, Spillantini MG, Goedert M. Ghetti B, et al. Ann N Y Acad Sci. 2000;920:52-62. doi: 10.1111/j.1749-6632.2000.tb06905.x. Ann N Y Acad Sci. 2000. PMID: 11193177

10

Tau gene mutations in frontotemporal dementia and parkinsonism linked to chromosome 17 (FTDP-17). Their relevance for understanding the neurogenerative process.

Goedert M, Ghetti B, Spillantini MG. Goedert M, et al. Among authors: ghetti b. Ann N Y Acad Sci. 2000;920:74-83. doi: 10.1111/j.1749-6632.2000.tb06907.x. Ann N Y Acad Sci. 2000. PMID: 11193179 Review.

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