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1) Arai T, Hasegawa M, Akiyama H, et al. TDP-43 is a component of ubiquitin-positive tau-negative inclusions in frontotemporal lobar degeneration and amyotrophic lateral sclerosis. Biochem Biophys Res Commun. 2006; 351: 602-11
PubMed CrossRef
医中誌リンクサービス
2) Neumann M, Sampathu DM, Kwong LK, et al. Ubiquitinated TDP-43 in frontotemporal lobar degeneration and amyotrophic lateral sclerosis. Science. 2006; 314: 130-3
PubMed CrossRef
医中誌リンクサービス
3) Neumann M, Mackenzie IR, Cairns NJ, et al. TDP-43 in the ubiquitin pathology of frontotemporal dementia with VCP gene mutations. J Neuropathol Exp Neurol. 2007; 66: 152-7
PubMed CrossRef
医中誌リンクサービス
4) Hasegawa M, Arai T, Akiyama H, et al. TDP-43 is deposited in the Guam parkinsonism-dementia complex brains. Brain. 2007; 130: 1386-94
PubMed CrossRef
医中誌リンクサービス
5) Kuzuhara S. [Revisit to Kii ALS-the innovated concept of ALS-Parkinsonism-dementia complex, clinicopathological features, epidemiology and etiology]. Brain Nerve. 2007; 59: 1065-74
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6) Hasegawa M, Arai T, Nonaka T, et al. Phosphorylated TDP-43 in frontotemporal lobar degeneration and amyotrophic lateral sclerosis. Ann Neurol. 2008; 64: 60-70
PubMed CrossRef
医中誌リンクサービス
7) Inukai Y, Nonaka T, Arai T, et al. Abnormal phosphorylation of Ser409/410 of TDP-43 in FTLD-U and ALS. FEBS Lett. 2008; 582: 2899-904
PubMed CrossRef
医中誌リンクサービス
8) Arai T, Mackenzie IR, Hasegawa M, et al. Phosphorylated TDP-43 in Alzheimer's disease and dementia with Lewy bodies. Acta Neuropathol. 2009; 117: 125-36
PubMed CrossRef
医中誌リンクサービス
9) Higashi S, Iseki E, Yamamoto R, et al. Concurrence of TDP-43, tau and alpha-synuclein pathology in brains of Alzheimer's disease and dementia with Lewy bodies. Brain Res. 2007; 1184: 284-94
PubMed CrossRef
医中誌リンクサービス
10) Nakashima-Yasuda H, Uryu K, Robinson J, et al. Co-morbidity of TDP-43 proteinopathy in Lewy body related diseases. Acta Neuropathol. 2007; 114: 221-9
PubMed CrossRef
医中誌リンクサービス
11) Amador-Ortiz C, Lin WL, Ahmed Z, et al. TDP-43 immunoreactivity in hippocampal sclerosis and Alzheimer's disease. Ann Neurol. 2007; 61: 435-45
PubMed CrossRef
医中誌リンクサービス
12) Bigio EH. TAR DNA-binding protein-43 in amyotrophic lateral sclerosis, frontotemporal lobar degeneration, and Alzheimer disease. Acta Neuropathol. 2008; 116: 135-40
PubMed CrossRef
医中誌リンクサービス
13) Uryu K, Nakashima-Yasuda H, Forman MS, et al. Concomitant TAR-DNA-binding protein 43 pathology is present in Alzheimer disease and corticobasal degeneration but not in other tauopathies. J Neuropathol Exp Neurol. 2008; 67: 555-64
PubMed CrossRef
医中誌リンクサービス
14) Farrer MJ, Hulihan MM, Kachergus JM, et al. DCTN1 mutations in Perry syndrome. Nat Genet. 2009; 41: 163-5
PubMed CrossRef
医中誌リンクサービス
15) Schwab C, Arai T, Hasegawa M, et al. Colocalization of transactivation-responsive DNA-binding protein 43 and huntingtin in inclusions of Huntington disease. J Neuropathol Exp Neurol. 2008; 67: 1159-65
PubMed CrossRef
医中誌リンクサービス
16) Schwab C, Arai T, Hasegawa M, et al. TDP-43 pathology in familial British dementia. Acta Neuropathol. 2009; 118: 303-11
PubMed CrossRef
医中誌リンクサービス
17) Nishihira Y, Tan CF, Onodera O, et al. Sporadic amyotrophic lateral sclerosis: two pathological patterns shown by analysis of distribution of TDP-43-immunoreactive neuronal and glial cytoplasmic inclusions. Acta Neuropathol. 2008; 116: 169-82
PubMed CrossRef
医中誌リンクサービス
18) Geser F, Brandmeir NJ, Kwong LK, et al. Evidence of multisystem disorder in whole-brain map of pathological TDP-43 in amyotrophic lateral sclerosis. Arch Neurol. 2008; 65: 636-41
PubMed CrossRef
医中誌リンクサービス
19) Yokoseki A, Shiga A, Tan CF, et al. TDP-43 mutation in familial amyotrophic lateral sclerosis. Ann Neurol. 2008; 63: 538-42
PubMed CrossRef
医中誌リンクサービス
20) Gitcho MA, Baloh RH, Chakraverty S, et al. TDP-43 A315T mutation in familial motor neuron disease. Ann Neurol. 2008; 63: 535-8
PubMed CrossRef
医中誌リンクサービス
21) Kabashi E, Valdmanis PN, Dion P, et al. TARDBP mutations in individuals with sporadic and familial amyotrophic lateral sclerosis. Nat Genet. 2008; 40: 572-4
PubMed CrossRef
医中誌リンクサービス
22) Rutherford NJ, Zhang YJ, Baker M, et al. Novel mutations in TARDBP (TDP-43) in patients with familial amyotrophic lateral sclerosis. PLoS Genet. 2008; 4: e1000193
PubMed CrossRef
医中誌リンクサービス
23) Sreedharan J, Blair IP, Tripathi VB, et al. TDP-43 mutations in familial and sporadic amyotrophic lateral sclerosis. Science. 2008; 319: 1668-72
PubMed CrossRef
医中誌リンクサービス
24) Benajiba L, Le Ber I, Camuzat A, et al. TARDBP mutations in motoneuron disease with frontotemporal lobar degeneration. Ann Neurol. 2009; 65: 470-3
PubMed CrossRef
医中誌リンクサービス
25) Kovacs GG, Murrell JR, Horvath S, et al. TARDBP variation associated with frontotemporal dementia, supranuclear gaze palsy, and chorea. Mov Disord. 2009; 24: 1843-7
PubMed CrossRef
医中誌リンクサービス
26) Piao YS, Wakabayashi K, Kakita A, et al. Neuropathology with clinical correlations of sporadic amyotrophic lateral sclerosis: 102 autopsy cases examined between 1962 and 2000. Brain Pathol. 2003; 13: 10-22
PubMed
医中誌リンクサービス
27) Tan CF, Eguchi H, Tagawa A, et al. TDP-43 immunoreactivity in neuronal inclusions in familial amyotrophic lateral sclerosis with or without SOD1 gene mutation. Acta Neuropathol. 2007; 113: 535-42
PubMed CrossRef
医中誌リンクサービス
28) Mackenzie IR, Bigio EH, Ince PG, et al. Pathological TDP-43 distinguishes sporadic amyotrophic lateral sclerosis from amyotrophic lateral sclerosis with SOD1 mutations. Ann Neurol. 2007; 61: 427-34
PubMed CrossRef
医中誌リンクサービス
29) Nonaka T, Arai T, Buratti E, et al. Phosphorylated and ubiquitinated TDP-43 pathological inclusions in ALS and FTLD-U are recapitulated in SH-SY5Y cells. FEBS Lett. 2009; 583: 394-400
PubMed CrossRef
医中誌リンクサービス
30) Nonaka T, Kametani F, Arai T, et al. Truncation and pathogenic mutations facilitate the formation of intracellular aggregates of TDP-43. Hum Mol Genet. 2009; 18: 3353-64
PubMed CrossRef
医中誌リンクサービス
31) Johnson BS, McCaffery JM, Lindquist S, et al. A yeast TDP-43 proteinopathy model: Exploring the molecular determinants of TDP-43 aggregation and cellular toxicity. Proc Natl Acad Sci U S A. 2008; 105: 6439-44
PubMed CrossRef
医中誌リンクサービス
32) Johnson BS, Snead D, Lee JJ, et al. TDP-43 Is Intrinsically Aggregation-prone, and Amyotrophic Lateral Sclerosis-linked Mutations Accelerate Aggregation and Increase Toxicity. J Biol Chem. 2009; 284: 20329-39
PubMed CrossRef
医中誌リンクサービス
33) Zhang YJ, Xu YF, Cook C, et al. Aberrant cleavage of TDP-43 enhances aggregation and cellular toxicity. Proc Natl Acad Sci U S A. 2009; 106: 7607-12
PubMed CrossRef
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34) Feiguin F, Godena VK, Romano G, et al. Depletion of TDP-43 affects Drosophila motoneurons terminal synapsis and locomotive behavior. FEBS Lett. 2009; 583: 1586-92
PubMed CrossRef
医中誌リンクサービス
35) Yamashita M, Nonaka T, Arai T, et al. Methylene blue and dimebon inhibit aggregation of TDP-43 in cellular models. FEBS Lett. 2009; 583: 2419-24
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