TDP-43 in familial and sporadic frontotemporal lobar degeneration with ubiquitin inclusions.
about
TARDBP mutation analysis in TDP-43 proteinopathies and deciphering the toxicity of mutant TDP-43The genetics and neuropathology of frontotemporal lobar degenerationA harmonized classification system for FTLD-TDP pathologyAccumulation of transactive response DNA binding protein 43 in mild cognitive impairment and Alzheimer diseaseStructural insights into TDP-43 in nucleic-acid binding and domain interactionsA new subtype of frontotemporal lobar degeneration with FUS pathologyFrom animal models to human disease: a genetic approach for personalized medicine in ALSMolecular Pathological Classification of Neurodegenerative Diseases: Turning towards Precision MedicineMouse models of frontotemporal dementiaFrontotemporal dementia and primary progressive aphasia, a reviewCharacterization of Movement Disorder Phenomenology in Genetically Proven, Familial Frontotemporal Lobar Degeneration: A Systematic Review and Meta-Analysis.Frontotemporal dementia: a bridge between dementia and neuromuscular diseaseSpreading of pathology in neurodegenerative diseases: a focus on human studiesTar DNA binding protein-43 (TDP-43) associates with stress granules: analysis of cultured cells and pathological brain tissueTARDBP 3'-UTR variant in autopsy-confirmed frontotemporal lobar degeneration with TDP-43 proteinopathyThe Myoblast C2C12 Transfected with Mutant Valosin-Containing Protein Exhibits Delayed Stress Granule Resolution on Oxidative Stress.Prevalence, laterality, and comorbidity of hippocampal sclerosis in an autopsy sampleFrontotemporal Dementia.Temporoparietal hypometabolism in frontotemporal lobar degeneration and associated imaging diagnostic errors.Common variants at 7p21 are associated with frontotemporal lobar degeneration with TDP-43 inclusions.VCP mutations causing frontotemporal lobar degeneration disrupt localization of TDP-43 and induce cell death.Non-human primate model of amyotrophic lateral sclerosis with cytoplasmic mislocalization of TDP-43Selective forelimb impairment in rats expressing a pathological TDP-43 25 kDa C-terminal fragment to mimic amyotrophic lateral sclerosis.Differential roles of the ubiquitin proteasome system and autophagy in the clearance of soluble and aggregated TDP-43 speciesPedigree with frontotemporal lobar degeneration--motor neuron disease and Tar DNA binding protein-43 positive neuropathology: genetic linkage to chromosome 9.TDP-43 expression in mouse models of amyotrophic lateral sclerosis and spinal muscular atrophy.Transgenic rat model of neurodegeneration caused by mutation in the TDP gene.ALS and FTLD: two faces of TDP-43 proteinopathy.Exaggerated inflammation, impaired host defense, and neuropathology in progranulin-deficient miceNeuropathologic diagnostic and nosologic criteria for frontotemporal lobar degeneration: consensus of the Consortium for Frontotemporal Lobar DegenerationAccumulation of multiple neurodegenerative disease-related proteins in familial frontotemporal lobar degeneration associated with granulin mutation.Neuropathological heterogeneity in frontotemporal lobar degeneration with TDP-43 proteinopathy: a quantitative study of 94 cases using principal components analysisProgranulin is neurotrophic in vivo and protects against a mutant TDP-43 induced axonopathyTDP-43 suppresses tau expression via promoting its mRNA instability.The acoustic cortex in frontotemporal dementia: a Golgi and electron microscope study.A mutation affecting the sodium/proton exchanger, SLC9A6, causes mental retardation with tau deposition.Multiplex SILAC analysis of a cellular TDP-43 proteinopathy model reveals protein inclusions associated with SUMOylation and diverse polyubiquitin chainsFrequency of ubiquitin and FUS-positive, TDP-43-negative frontotemporal lobar degenerationThe role of transactive response DNA-binding protein-43 in amyotrophic lateral sclerosis and frontotemporal dementia.FUS pathology defines the majority of tau- and TDP-43-negative frontotemporal lobar degeneration.
P2860
Q24594172-66D5CB91-E592-4628-8079-5B5A7D7A7BACQ24615201-D2676B5D-917C-4D21-BD50-2B676E8EFE5DQ24630756-1BB0F6B8-7FEF-4802-B6E9-D1CA8FB8BFF7Q24634907-F4430E85-C2E3-40A9-AFCC-71BE7389F91DQ24647225-CF25EFFE-1896-47AF-B91C-0C3200BEB57FQ24647697-D4B4816E-A901-4F36-A435-7EB9EBF6BFA9Q26741250-21624295-D9AE-4746-B31B-253239E041E6Q26768648-6D836CBA-0F32-487C-B6AF-D57DBD762F38Q26829009-59F20ACD-BEB3-4294-AE66-732D860A97F3Q27021040-17BA3E06-3280-43B1-86E6-37E1D405D3D1Q28079852-A8D745EE-62EA-4260-9F3C-8547D9D2387AQ28081198-0BB388F8-A057-480B-9F98-FAD3E88887E7Q28082279-BC3E68E9-AD1E-48AC-B08A-5E746DD14AF3Q28475724-CF6D8814-03CE-44E4-AB0E-8D994EC01666Q28749802-EC2B6539-0595-4794-9119-1ED45FCC20AEQ30008982-813E7C0F-E142-4615-8746-07C09260B3C5Q30051304-FE406F8E-02A4-4B44-9B38-79D69705BD59Q30234793-E112C422-2495-4B94-B2EF-FD30C069C5BEQ30428012-011A09B8-27F0-4A3E-8199-419DB912A6A0Q30434949-49F2145F-2AB0-42CA-B4F5-C39622FCD1A2Q30487226-CBB2442F-A420-4F42-9E1A-271DCE1410ADQ30505515-C035EF3D-BC9A-4DB4-88FA-D5B81DDD6FDEQ30541190-3763BA52-3CC4-4CB4-A801-E1540A6D480FQ30574024-5F4ABA87-657F-49DF-84C5-D7E8247F7254Q33364603-9774CDB3-8C89-4A78-9D6F-F0F695CD7778Q33379948-5C6E838F-FABA-410B-8083-D74C5695F11BQ33548806-E0E59720-E778-41D2-A23D-787691791DB9Q33571116-A15D8BF4-7102-411A-978A-4B032EBFE285Q33615151-30D834DA-2B06-4407-AF87-FEF89BF9AD56Q33685317-B6E1D2ED-C33A-4A22-A817-306BDEAA2817Q33685394-BBEB62EA-1EF4-4B8D-B818-ACA6D5D09FB6Q33694019-6C34CF3F-9FA5-4DA7-8148-209619E96778Q33725391-7F79951D-DFD9-4C25-908B-83FA2D1E4759Q33740999-BF02B8EC-3572-46E2-87B1-4DD4936B67B9Q33781409-316460C3-2659-4505-9BC3-D16B837FC321Q33808422-5037222B-ED3B-4EDD-B06C-BF8FB922C851Q33812891-C59AE609-A3D1-4B57-A8A7-39C9F2D5CC35Q33830991-80EA910E-A1D1-4335-B78F-6EA4C0D59A9FQ33847532-268451B6-BFEA-4697-ABC1-17BE298D4D21Q33922335-C42E1626-6087-4E1D-A463-5821C75D4D44
P2860
TDP-43 in familial and sporadic frontotemporal lobar degeneration with ubiquitin inclusions.
description
2007 nî lūn-bûn
@nan
2007年の論文
@ja
2007年論文
@yue
2007年論文
@zh-hant
2007年論文
@zh-hk
2007年論文
@zh-mo
2007年論文
@zh-tw
2007年论文
@wuu
2007年论文
@zh
2007年论文
@zh-cn
name
TDP-43 in familial and sporadi ...... ion with ubiquitin inclusions.
@ast
TDP-43 in familial and sporadi ...... ion with ubiquitin inclusions.
@en
type
label
TDP-43 in familial and sporadi ...... ion with ubiquitin inclusions.
@ast
TDP-43 in familial and sporadi ...... ion with ubiquitin inclusions.
@en
prefLabel
TDP-43 in familial and sporadi ...... ion with ubiquitin inclusions.
@ast
TDP-43 in familial and sporadi ...... ion with ubiquitin inclusions.
@en
P2093
P2860
P50
P1476
TDP-43 in familial and sporadi ...... ion with ubiquitin inclusions.
@en
P2093
Anna Stieber
Chan Foong
Deborah Carter
Dirk Troost
Eileen H Bigio
Hans A Kretzschmar
Ian R A Mackenzie
Ida E Holm
Jeffrey Strider
Julie A Schneider
P2860
P304
P356
10.2353/AJPATH.2007.070182
P407
P577
2007-07-01T00:00:00Z