Chromosome 17 and hereditary dementia: linkage studies in three non-Alzheimer families and kindreds with late-onset FAD.
about
Frontotemporal dementia and parkinsonism linked to chromosome 17 (FTDP-17)Cloning and characterization of PRAX-1. A new protein that specifically interacts with the peripheral benzodiazepine receptorFour decades of neurodegenerative disease research: how far we have come!Tra2 beta, SF2/ASF and SRp30c modulate the function of an exonic splicing enhancer in exon 10 of tau pre-mRNAProgranulin: normal function and role in neurodegenerationProgranulin and frontotemporal lobar degenerationAlternative splicing of exon 10 in the tau gene as a target for treatment of tauopathies.Prediction of psychosis onset in Alzheimer disease: the role of depression symptom severity and the HTR2A T102C polymorphism.Genetics of psychosis in Alzheimer's disease: a reviewThe role of tau (MAPT) in frontotemporal dementia and related tauopathies.A new molecular link between the fibrillar and granulovacuolar lesions of Alzheimer's disease.No association of psychosis in Alzheimer disease with neurodegenerative pathway genes.Psychotic symptoms in Alzheimer disease: evidence for a distinct phenotype.Mapping the onset and progression of atrophy in familial frontotemporal lobar degeneration.Missense and silent tau gene mutations cause frontotemporal dementia with parkinsonism-chromosome 17 type, by affecting multiple alternative RNA splicing regulatory elementsMutation in the tau gene in familial multiple system tauopathy with presenile dementia.The molecular genetics and neuropathology of frontotemporal lobar degeneration: recent developments.The tauopathy associated with mutation +3 in intron 10 of Tau: characterization of the MSTD family.Review: Recent progress in frontotemporal lobar degeneration.Neuropsychiatric features of C9orf72-associated behavioral variant frontotemporal dementia and frontotemporal dementia with motor neuron disease.Frontotemporal dementia in a large Swedish family is caused by a progranulin null mutation.Unusually long duration and delayed penetrance in a family with FTD and mutation in MAPT (V337M).Efficacy of acetylcholinesterase inhibitors versus nootropics in Alzheimer's disease: a retrospective, longitudinal study.Frontotemporal dementia with the V337M MAPT mutation: Tau-PET and pathology correlations.Rivastigmine reverses cognitive deficit and acetylcholinesterase activity induced by ketamine in an animal model of schizophrenia.A clinical pathological comparison of three families with frontotemporal dementia and identical mutations in the tau gene (P301L)Segregation of a missense mutation in the microtubule-associated protein tau gene with familial frontotemporal dementia and parkinsonism.Tau negative frontal lobe dementia at 17q21: significant finemapping of the candidate region to a 4.8 cM interval.Is there a familial overlap between dementia and other psychiatric disorders?Mutations in tau reduce its microtubule binding properties in intact cells and affect its phosphorylation
P2860
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P2860
Chromosome 17 and hereditary dementia: linkage studies in three non-Alzheimer families and kindreds with late-onset FAD.
description
1997 nî lūn-bûn
@nan
1997年の論文
@ja
1997年論文
@yue
1997年論文
@zh-hant
1997年論文
@zh-hk
1997年論文
@zh-mo
1997年論文
@zh-tw
1997年论文
@wuu
1997年论文
@zh
1997年论文
@zh-cn
name
Chromosome 17 and hereditary d ...... kindreds with late-onset FAD.
@en
Chromosome 17 and hereditary d ...... kindreds with late-onset FAD.
@nl
type
label
Chromosome 17 and hereditary d ...... kindreds with late-onset FAD.
@en
Chromosome 17 and hereditary d ...... kindreds with late-onset FAD.
@nl
prefLabel
Chromosome 17 and hereditary d ...... kindreds with late-onset FAD.
@en
Chromosome 17 and hereditary d ...... kindreds with late-onset FAD.
@nl
P2093
P356
P1433
P1476
Chromosome 17 and hereditary d ...... kindreds with late-onset FAD.
@en
P2093
Schellenberg GD
Wijsman EM
P304
P356
10.1212/WNL.48.4.949
P407
P577
1997-04-01T00:00:00Z