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Results: 1-14 |
Results: 14
A genomic sequence analysis of the mouse and human microtubule-associated protein tau
Authors: Poorkaj, P Kas, A D'Souza, I Zhou, Y Pham, Q Stone, M Olson, MV Schellenberg, GD
Citation: P. Poorkaj et al., A genomic sequence analysis of the mouse and human microtubule-associated protein tau, MAMM GENOME, 12(9), 2001, pp. 700-712
Frequency of tau gene mutations in familial and sporadic cases of non-Alzheimer dementia
Authors: Poorkaj, P Grossman, M Steinbart, E Payami, H Sadovnick, A Nochlin, D Tabira, T Trojanowski, JQ Borson, S Galasko, D Reich, S Quinn, B Schellenberg, G Bird, TD
Citation: P. Poorkaj et al., Frequency of tau gene mutations in familial and sporadic cases of non-Alzheimer dementia, ARCH NEUROL, 58(3), 2001, pp. 383-387
Impact of DNA testing for early-onset familial Alzheimer disease and frontotemporal dementia
Authors: Steinbart, EJ Smith, CO Poorkaj, P Bird, TD
Citation: Ej. Steinbart et al., Impact of DNA testing for early-onset familial Alzheimer disease and frontotemporal dementia, ARCH NEUROL, 58(11), 2001, pp. 1828-1831
TAU as a susceptibility gene for amyotropic lateral sclerosis-parkinsonismdementia complex of Guam
Authors: Poorkaj, P Tsuang, D Wijsman, E Steinbart, E Garruto, RM Craig, UK Chapman, NH Anderson, L Bird, TD Plato, CC Perl, DP Weiderholt, W Galasko, D Schellenberg, GD
Citation: P. Poorkaj et al., TAU as a susceptibility gene for amyotropic lateral sclerosis-parkinsonismdementia complex of Guam, ARCH NEUROL, 58(11), 2001, pp. 1871-1878
Pro-apoptotic effects of tau mutations in chromosome 17 frontotemporal dementia and parkinsonism
Authors: Furukawa, K D'Souza, I Crudder, CH Onodera, H Itoyama, Y Poorkaj, P Bird, TD Schellenberg, GD
Citation: K. Furukawa et al., Pro-apoptotic effects of tau mutations in chromosome 17 frontotemporal dementia and parkinsonism, NEUROREPORT, 11(1), 2000, pp. 57-60
Single-step conversion of P1 and P1 artificial chromosome clones into yeast artificial chromosomes
Authors: Poorkaj, P Peterson, KR Schellenberg, GD
Citation: P. Poorkaj et al., Single-step conversion of P1 and P1 artificial chromosome clones into yeast artificial chromosomes, GENOMICS, 68(1), 2000, pp. 106-110
A novel mutation at position+12 in the intron following exon 10 of the taugene in familial frontotemporal dementia (FTD-Kumamoto)
Authors: Yasuda, M Takamatsu, J D'Souza, I Crowther, RA Kawamata, T Hasegawa, M Hasegawa, H Spillantini, MG Tanimukai, S Poorkaj, P Varani, L Varani, G Iwatsubo, T Goedert, M Schellenberg, GD Tanaka, C
Citation: M. Yasuda et al., A novel mutation at position+12 in the intron following exon 10 of the taugene in familial frontotemporal dementia (FTD-Kumamoto), ANN NEUROL, 47(4), 2000, pp. 422-429
Familial frontotemporal dementia with ubiquitin-positive, tau-negative inclusions
Authors: Kertesz, A Kawarai, T Rogaeva, E St George-Hyslop, P Poorkaj, P Bird, TD Munoz, DG
Citation: A. Kertesz et al., Familial frontotemporal dementia with ubiquitin-positive, tau-negative inclusions, NEUROLOGY, 54(4), 2000, pp. 818-827
A distinct familial presenile dementia with a novel missense mutation in the tau gene
Authors: Iijima, M Tabira, T Poorkaj, P Schellenberg, GD Trojanowski, JQ Lee, VMY Schmidt, ML Takahashi, K Nabika, T Matsumoto, T Yamashita, Y Yoshioka, S Ishino, H
Citation: M. Iijima et al., A distinct familial presenile dementia with a novel missense mutation in the tau gene, NEUROREPORT, 10(3), 1999, pp. 497-501
Apolipoprotein E genotype does not affect the age of onset of dementia in families with defined tau mutations
Authors: Houlden, H Rizzu, P Stevens, M de Knijff, P van Duijn, CM van Swieten, JC Heutink, P Perez-Tur, J Thomas, V Baker, M Morris, H Rossor, M Jannsen, JC Petersen, RC Dodd, P Dark, F Boeve, B Dickson, D Davies, P Pickering-Brown, S Mann, D Adamson, J Lynch, T Payami, H Poorkaj, P Bird, TD Schellenberg, GD Chakraverty, S Norton, J Morris, JC Goate, A Hutton, M Hardy, J
Citation: H. Houlden et al., Apolipoprotein E genotype does not affect the age of onset of dementia in families with defined tau mutations, NEUROSCI L, 260(3), 1999, pp. 193-195
A mutation in the microtubule-associated protein tau in pallido-nigroluysian degeneration
Authors: Yasuda, M Kawamata, T Komure, O Kuno, S D'Souza, I Poorkaj, P Kawai, J Tanimukai, S Yamamoto, Y Hasegawa, H Sasahara, M Hazama, F Schellenberg, GD Tanaka, C
Citation: M. Yasuda et al., A mutation in the microtubule-associated protein tau in pallido-nigroluysian degeneration, NEUROLOGY, 53(4), 1999, pp. 864-868
Missense and silent tau gene mutations cause frontotemporal dementia with parkinsonism-chromosome 17 type, by affecting multiple alternative RNA splicing regulatory elements
Authors: D'Souza, I Poorkaj, P Hong, M Nochlin, D Lee, VMY Bird, TD Schellenberg, GD
Citation: I. D'Souza et al., Missense and silent tau gene mutations cause frontotemporal dementia with parkinsonism-chromosome 17 type, by affecting multiple alternative RNA splicing regulatory elements, P NAS US, 96(10), 1999, pp. 5598-5603
A clinical pathological comparison of three families with frontotemporal dementia and identical mutations in the tan gene (P301L) (vol 122, pg 741, 1999)
Authors: Bird, TD Nochlin, D Poorkaj, P Cherrier, M Payami, H Peskind, E Lampe, TH Nemens, E Boyer, PJ Schellenberg, GD
Citation: Td. Bird et al., A clinical pathological comparison of three families with frontotemporal dementia and identical mutations in the tan gene (P301L) (vol 122, pg 741, 1999), BRAIN, 122, 1999, pp. 1398-1398
A clinical pathological comparison of three families with frontotemporal dementia and identical mutations in the tau gene (P301L)
Authors: Bird, TD Nochlin, D Poorkaj, P Cherrier, M Kaye, J Payami, H Peskind, E Lampe, TH Nemens, E Boyer, PJ Schellenberg, GD
Citation: Td. Bird et al., A clinical pathological comparison of three families with frontotemporal dementia and identical mutations in the tau gene (P301L), BRAIN, 122, 1999, pp. 741-756
Risultati: 1-14 |