The most common type of FTLD-FUS (aFTLD-U) is associated with a distinct clinical form of frontotemporal dementia but is not related to mutations in the FUS gene.
about
Pathogenesis of FUS-associated ALS and FTD: insights from rodent modelsFrontotemporal Dementia.Neuropathology of Amyotrophic Lateral Sclerosis and Its Variants.FET proteins TAF15 and EWS are selective markers that distinguish FTLD with FUS pathology from amyotrophic lateral sclerosis with FUS mutations.Familial behavioral variant frontotemporal dementia associated with astrocyte-predominant tauopathyFrontotemporal lobar degeneration: defining phenotypic diversity through personalized medicine.Distinct clinical and pathological characteristics of frontotemporal dementia associated with C9ORF72 mutationsAmnesia in frontotemporal dementia: shedding light on the Geneva historical data.Clinico-pathological correlations of the most common neurodegenerative dementias.Imaging signatures of molecular pathology in behavioral variant frontotemporal dementiaSevere respiratory changes at end stage in a FUS-induced disease state in adult rats.New approaches to genetic counseling and testing for Alzheimer's disease and frontotemporal degenerationMechanisms of disease in frontotemporal lobar degeneration: gain of function versus loss of function effectsAmyotrophic lateral sclerosis: update and new developments.Nuclear carrier and RNA-binding proteins in frontotemporal lobar degeneration associated with fused in sarcoma (FUS) pathological changes.Arginine methylation next to the PY-NLS modulates Transportin binding and nuclear import of FUS.The molecular basis of the frontotemporal lobar degeneration-amyotrophic lateral sclerosis spectrumChorea as a clinical feature of the basophilic inclusion body disease subtype of fused-in-sarcoma-associated frontotemporal lobar degenerationMutations in protein N-arginine methyltransferases are not the cause of FTLD-FUS.A 44-year-old man with profound behavioural changes.Neuropathological background of phenotypical variability in frontotemporal dementia.Modeling ALS and FTLD proteinopathies in yeast: an efficient approach for studying protein aggregation and toxicity.Molecular pathology and genetic advances in amyotrophic lateral sclerosis: an emerging molecular pathway and the significance of glial pathology.Neuroimaging in frontotemporal lobar degeneration--predicting molecular pathology.Genetics of dementia: update and guidelines for the clinician.Schizophrenia and frontotemporal dementia: shared causation?Rapidly progressive Fronto-temporal dementia (FTD) associated with Frontotemporal lobar degeneration (FTLD) in the presence of Fused in Sarcoma (FUS) protein: a rare, sporadic, and aggressive form of FTD.Frontotemporal lobar degeneration: Pathogenesis, pathology and pathways to phenotype.Role of FET proteins in neurodegenerative disorders.Nuclear trafficking in amyotrophic lateral sclerosis and frontotemporal lobar degeneration.An autopsy case of frontotemporal lobar degeneration with the appearance of fused in sarcoma inclusions (basophilic inclusion body disease) clinically presenting corticobasal syndrome.Genetic mutations in RNA-binding proteins and their roles in ALS.Clinicopathological correlations in behavioural variant frontotemporal dementia.Transportin 1 accumulates specifically with FET proteins but no other transportin cargos in FTLD-FUS and is absent in FUS inclusions in ALS with FUS mutations.Neuropathology of frontotemporal lobar degeneration: a review.Rare Neurodegenerative Diseases: Clinical and Genetic Update.Mislocated FUS is sufficient for gain-of-toxic-function amyotrophic lateral sclerosis phenotypes in mice.Fused in Sarcoma Neuropathology in Neurodegenerative Disease.Neuroimaging in Dementia.Early Neurodegeneration in the Brain of a Child Without Functional PKR-like Endoplasmic Reticulum Kinase.
P2860
Q28067147-7CF34044-705C-4221-9061-1D6597EE6880Q30234793-745B805C-B8DA-4E0F-B91C-4048C18CBCD0Q33361835-20BE1435-2A83-4CF5-90B3-D1F768479CDCQ34209561-2E6AE3B4-8524-4CF7-991B-9BEAB3C42DE9Q35196395-1706BD52-2DDC-44A2-9779-250FC0206422Q35204586-6D46DAC6-1366-4443-95FA-E6B500ADCB9DQ35776901-CC1B6F8F-2224-4E79-8136-B19D9053A4A2Q35904467-D17DEACF-CAEB-4559-B418-6AD95648114BQ35923461-0369B976-F4E8-4AE9-B08E-8B7FD04B9195Q36107386-DF32CD43-B8BD-4CC1-865E-36630BF1C5C1Q36177447-036A28CC-9E08-47B9-8142-D3FCA59E32B6Q36218610-DB389B6A-A7EB-4DE5-A543-0EC51BFA0126Q36241872-E57F1154-3271-4712-94FB-FE61BC86FDBDQ36278310-CABBC6E5-0C5B-4A0F-B11C-42D15B10D2B5Q36342066-9E800C39-386C-4285-BEE6-8CEC671F1C8AQ36408540-1AEEC002-2B7F-452F-A762-305128225F53Q36485513-91BD5A1B-4D4D-4E43-8E6B-4225E8DE9FD0Q36765301-2B5EB8F2-75DF-46A7-BD48-8728FF8D40ECQ36932604-CD55DD27-5382-41F0-B7D5-1CA6B638F44AQ37383848-D3F5BA30-F38D-4B9A-A179-71CAFED2C673Q37879961-221AC106-BC1A-42F7-A3F1-7D7DCB345815Q37952582-ECB34651-FCF2-4F48-B4C2-E1A833BF743BQ37959310-4265AE39-6408-4B5A-96E8-3F9B1F620914Q37980047-39791DC4-33BE-4519-A4CD-87F9E402C001Q38027808-51C63F2D-F749-4ECC-B021-6F439536F11FQ38101087-A6CDCC3C-D5B9-4090-9618-2E13DB9CA953Q38374796-9BF563BC-E314-4359-9694-AB038691D5D7Q38382217-2A50DE20-B406-4A80-B72B-55D7FA2A5244Q38896526-CA731C60-6540-4434-BEF5-41501ED5519BQ38920545-91B06664-8818-4B45-B8B7-4F6CC92D81F8Q38979310-D3044B83-800A-4219-A191-11AD950E2BE0Q42278719-07253ADE-63EC-45B6-A114-F66F53625504Q45952280-63CE8027-2631-4F64-A309-93DB4A9C6C4CQ46624207-E270965B-3FBA-4A4A-8640-60FA1D94035DQ47237309-5535B42D-7BA9-400B-AD42-0F291F59EC50Q47928785-1398E02A-108A-40C9-8E53-559D40FDEE3FQ48645659-5D54A259-E3DF-41FA-98C8-E4ACFD0867B3Q51185958-FBAB8293-BB4C-4A77-B2E1-9B57B886A537Q51800676-2040DDC1-3C29-4226-9D9A-5E7621C7BA35Q52152102-7187ABE3-3705-47A2-AC79-F56C30E4C89E
P2860
The most common type of FTLD-FUS (aFTLD-U) is associated with a distinct clinical form of frontotemporal dementia but is not related to mutations in the FUS gene.
description
2011 nî lūn-bûn
@nan
2011年の論文
@ja
2011年論文
@yue
2011年論文
@zh-hant
2011年論文
@zh-hk
2011年論文
@zh-mo
2011年論文
@zh-tw
2011年论文
@wuu
2011年论文
@zh
2011年论文
@zh-cn
name
The most common type of FTLD-F ...... to mutations in the FUS gene.
@en
type
label
The most common type of FTLD-F ...... to mutations in the FUS gene.
@en
prefLabel
The most common type of FTLD-F ...... to mutations in the FUS gene.
@en
P2093
P2860
P50
P1476
The most common type of FTLD-F ...... to mutations in the FUS gene.
@en
P2093
Anna Richardson
Atik Baborie
David M A Mann
David Neary
Evelyn Jaros
Nicola Halliwell
Robert H Perry
Sara Rollinson
Yvonne S Davidson
P2860
P2888
P304
P356
10.1007/S00401-011-0816-0
P577
2011-03-20T00:00:00Z
P6179
1020197641