Ghetti B - Search Results

1

Structure-based classification of tauopathies.

Shi Y, Zhang W, Yang Y, Murzin AG, Falcon B, Kotecha A, van Beers M, Tarutani A, Kametani F, Garringer HJ, Vidal R, Hallinan GI, Lashley T, Saito Y, Murayama S, Yoshida M, Tanaka H, Kakita A, Ikeuchi T, Robinson AC, Mann DMA, Kovacs GG, Revesz T, Ghetti B, Hasegawa M, Goedert M, Scheres SHW. Shi Y, et al. Among authors: ghetti b. Nature. 2021 Oct;598(7880):359-363. doi: 10.1038/s41586-021-03911-7. Epub 2021 Sep 29. Nature. 2021. PMID: 34588692 Free PMC article.

2

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.

3

Frontotemporal dementia and Parkinsonism linked to chromosome 17: a new group of tauopathies.

Spillantini MG, Bird TD, Ghetti B. Spillantini MG, et al. Among authors: ghetti b. Brain Pathol. 1998 Apr;8(2):387-402. doi: 10.1111/j.1750-3639.1998.tb00162.x. Brain Pathol. 1998. PMID: 9546295 Free PMC article. Review.

4

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.

5

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.

6

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

7

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

8

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.

9

Hereditary ferritinopathy.

Vidal R, Delisle MB, Rascol O, Ghetti B. Vidal R, et al. Among authors: ghetti b. J Neurol Sci. 2003 Mar 15;207(1-2):110-1. doi: 10.1016/s0022-510x(02)00435-5. J Neurol Sci. 2003. PMID: 12614943 Review. No abstract available.

10

Comparison of extent of tau pathology in patients with frontotemporal dementia with Parkinsonism linked to chromosome 17 (FTDP-17), frontotemporal lobar degeneration with Pick bodies and early onset Alzheimer's disease.

Shiarli AM, Jennings R, Shi J, Bailey K, Davidson Y, Tian J, Bigio EH, Ghetti B, Murrell JR, Delisle MB, Mirra S, Crain B, Zolo P, Arima K, Iseki E, Murayama S, Kretzschmar H, Neumann M, Lippa C, Halliday G, Mackenzie J, Khan N, Ravid R, Dickson D, Wszolek Z, Iwatsubo T, Pickering-Brown SM, Mann DM. Shiarli AM, et al. Among authors: ghetti b. Neuropathol Appl Neurobiol. 2006 Aug;32(4):374-87. doi: 10.1111/j.1365-2990.2006.00736.x. Neuropathol Appl Neurobiol. 2006. PMID: 16866983

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