New insights into genetic and molecular mechanisms of brain degeneration in tauopathies (Q34156138)

31 July 2017

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title

New insights into genetic and molecular mechanisms of brain degeneration in tauopathies (English)

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31 July 2017

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3

Trojanowski JQ

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31 July 2017

Forman MS

1

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31 July 2017

Lee VM

series ordinal

2

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31 July 2017

publication date

1 December 2000

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Journal of Chemical Neuroanatomy

31 July 2017

published in

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31 July 2017

volume

20

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31 July 2017

issue

3-4

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31 July 2017

page(s)

225-244

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Hyperphosphorylated tau and neurofilament and cytoskeletal disruptions in mice overexpressing human p25, an activator of cdk5

31 July 2017

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The tau mutation (val337met) disrupts cytoskeletal networks of microtubules

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Two brothers with frontotemporal dementia and parkinsonism with an N279K mutation of the tau gene

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Association of an extended haplotype in the tau gene with progressive supranuclear palsy

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Abnormal Alzheimer-like phosphorylation of tau-protein by cyclin-dependent kinases cdk2 and cdk5

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Direct genetic evidence for involvement of tau in progressive supranuclear palsy

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Corticobasal ganglionic degeneration and progressive supranuclear palsy presenting with cognitive decline

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Phosphorylation of Ser262 strongly reduces binding of tau to microtubules: distinction between PHF-like immunoreactivity and microtubule binding.

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Regulated phosphorylation and dephosphorylation of tau protein: effects on microtubule interaction, intracellular trafficking and neurodegeneration

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The distribution of tau in the mammalian central nervous system

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A clinical pathological comparison of three families with frontotemporal dementia and identical mutations in the tau gene (P301L)

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Abnormal tau phosphorylation at Ser396 in Alzheimer's disease recapitulates development and contributes to reduced microtubule binding

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Transgenic expression of the shortest human tau affects its compartmentalization and its phosphorylation as in the pretangle stage of Alzheimer's disease

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7 January 2021

Hyperphosphorylated tau proteins differentiate corticobasal degeneration and Pick's disease

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7 January 2021

Tau protein isoforms, phosphorylation and role in neurodegenerative disorders11These authors contributed equally to this work

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7 January 2021

Frontotemporal dementia and corticobasal degeneration in a family with a P301S mutation in tau.

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7 January 2021

Tau protein binds to microtubules through a flexible array of distributed weak sites

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7 January 2021

Alzheimer-like neurodegeneration in aged antinerve growth factor transgenic mice

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7 January 2021

Overexpression of four-repeat tau mRNA isoforms in progressive supranuclear palsy but not in Alzheimer's disease

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7 January 2021

Pathogenic implications of mutations in the tau gene in pallido-ponto-nigral degeneration and related neurodegenerative disorders linked to chromosome 17

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7 January 2021

Purification of tau, a microtubule-associated protein that induces assembly of microtubules from purified tubulin

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7 January 2021

Genetic evidence for the involvement of tau in progressive supranuclear palsy

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7 January 2021

Pick's disease. Histological and clinical correlations

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7 January 2021

Gene dose of apolipoprotein E type 4 allele and the risk of Alzheimer's disease in late onset families

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7 January 2021

Primary structure of high molecular weight tau present in the peripheral nervous system

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7 January 2021

Straight and paired helical filaments in Alzheimer disease have a common structural unit

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7 January 2021

Missense and silent tau gene mutations cause frontotemporal dementia with parkinsonism-chromosome 17 type, by affecting multiple alternative RNA splicing regulatory elements

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https://api.crossref.org/works/10.1016%2FS0891-0618%2800%2900100-9

7 January 2021

Determinants of 4-repeat tau expression. Coordination between enhancing and inhibitory splicing sequences for exon 10 inclusion

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7 January 2021

Mutations in tau reduce its microtubule binding properties in intact cells and affect its phosphorylation

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https://api.crossref.org/works/10.1016%2FS0891-0618%2800%2900100-9

7 January 2021

Specific pathological Tau protein variants characterize Pick's disease.

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7 January 2021

A mutation at codon 279 (N279K) in exon 10 of the Tau gene causes a tauopathy with dementia and supranuclear palsy

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7 January 2021

Missense tau mutations identified in FTDP-17 have a small effect on tau-microtubule interactions

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7 January 2021

Corticobasal degeneration shares a common genetic background with progressive supranuclear palsy

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7 January 2021

Pick's disease: a modern approach.

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7 January 2021

Neuropathologic differentiation of progressive supranuclear palsy and corticobasal degeneration

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7 January 2021

Modulation of the dynamic instability of tubulin assembly by the microtubule-associated protein tau

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7 January 2021

MARK, a novel family of protein kinases that phosphorylate microtubule-associated proteins and trigger microtubule disruption

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7 January 2021

Characterization of pathology in transgenic mice over-expressing human genomic and cDNA tau transgenes

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7 January 2021

Segregation of a missense mutation in the microtubule-associated protein tau gene with familial frontotemporal dementia and parkinsonism

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7 January 2021

Identification of a novel polymorphism in the promoter region of the tau gene highly associated to progressive supranuclear palsy in humans.

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7 January 2021

Epitope expression and hyperphosphorylation of tau protein in corticobasal degeneration: differentiation from progressive supranuclear palsy.

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7 January 2021

Neuropathologic overlap of progressive supranuclear palsy, Pick's disease and corticobasal degeneration

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7 January 2021

Abnormal Tau proteins in progressive supranuclear palsy. Similarities and differences with the neurofibrillary degeneration of the Alzheimer type.

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7 January 2021

Frontotemporal dementia and parkinsonism linked to chromosome 17: a consensus conference. Conference Participants

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7 January 2021

Abnormal microtubule packing in processes of SF9 cells expressing the FTDP-17 V337M tau mutation

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https://api.crossref.org/works/10.1016%2FS0891-0618%2800%2900100-9

7 January 2021

Pro-apoptotic effects of tau mutations in chromosome 17 frontotemporal dementia and parkinsonism

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https://api.crossref.org/works/10.1016%2FS0891-0618%2800%2900100-9

7 January 2021

Alzheimer-type neuropathology in transgenic mice overexpressing V717F β-amyloid precursor protein

1 reference

https://api.crossref.org/works/10.1016%2FS0891-0618%2800%2900100-9

7 January 2021

Complex regulation of tau exon 10, whose missplicing causes frontotemporal dementia.

1 reference

https://api.crossref.org/works/10.1016%2FS0891-0618%2800%2900100-9

7 January 2021

p42 map kinase phosphorylation sites in microtubule-associated protein tau are dephosphorylated by protein phosphatase 2A1Implications for Alzheimer's disease

1 reference

https://api.crossref.org/works/10.1016%2FS0891-0618%2800%2900100-9

7 January 2021

Phosphorylation of microtubule-associated protein tau by stress-activated protein kinases

1 reference

https://api.crossref.org/works/10.1016%2FS0891-0618%2800%2900100-9

7 January 2021

Effects of frontotemporal dementia FTDP-17 mutations on heparin-induced assembly of tau filaments

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https://api.crossref.org/works/10.1016%2FS0891-0618%2800%2900100-9

7 January 2021

Cloning of a big tau microtubule-associated protein characteristic of the peripheral nervous system

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https://api.crossref.org/works/10.1016%2FS0891-0618%2800%2900100-9

7 January 2021

Tau gene mutation in familial progressive subcortical gliosis

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https://api.crossref.org/works/10.1016%2FS0891-0618%2800%2900100-9

7 January 2021

Molecular dissection of the paired helical filament

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https://api.crossref.org/works/10.1016%2FS0891-0618%2800%2900100-9

7 January 2021

Multiple isoforms of human microtubule-associated protein tau: sequences and localization in neurofibrillary tangles of Alzheimer's disease

1 reference

https://api.crossref.org/works/10.1016%2FS0891-0618%2800%2900100-9

7 January 2021

Cloning and sequencing of the cDNA encoding a core protein of the paired helical filament of Alzheimer disease: identification as the microtubule-associated protein tau

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https://api.crossref.org/works/10.1016%2FS0891-0618%2800%2900100-9

7 January 2021

Functional interactions between the proline-rich and repeat regions of tau enhance microtubule binding and assembly

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https://api.crossref.org/works/10.1016%2FS0891-0618%2800%2900100-9

7 January 2021

Identification of a novel microtubule binding and assembly domain in the developmentally regulated inter-repeat region of tau.

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https://api.crossref.org/works/10.1016%2FS0891-0618%2800%2900100-9

7 January 2021

A preparation of Alzheimer paired helical filaments that displays distinct tau proteins by polyacrylamide gel electrophoresis

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7 January 2021

Dementia as the most common presentation of cortical-basal ganglionic degeneration.

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7 January 2021

5' splice site mutations in tau associated with the inherited dementia FTDP-17 affect a stem-loop structure that regulates alternative splicing of exon 10.

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https://api.crossref.org/works/10.1016%2FS0891-0618%2800%2900100-9

7 January 2021

Human tau becomes phosphorylated and forms filamentous deposits when overexpressed in lamprey central neurons in situ.

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7 January 2021

Glycogen synthase kinase-3 induces Alzheimer's disease-like phosphorylation of tau: generation of paired helical filament epitopes and neuronal localisation of the kinase

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https://api.crossref.org/works/10.1016%2FS0891-0618%2800%2900100-9

7 January 2021

Altered microtubule organization in small-calibre axons of mice lacking tau protein

1 reference

https://api.crossref.org/works/10.1016%2FS0891-0618%2800%2900100-9

7 January 2021

Genetic classification of primary neurodegenerative disease

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7 January 2021

Tau proteins with FTDP-17 mutations have a reduced ability to promote microtubule assembly

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7 January 2021

FTDP-17 mutations N279K and S305N in tau produce increased splicing of exon 10

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7 January 2021

Preliminary NINDS neuropathologic criteria for Steele-Richardson-Olszewski syndrome (progressive supranuclear palsy).

1 reference

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7 January 2021

Hereditary frontotemporal dementia is linked to chromosome 17q21?q22: A genetic and clinicopathological study of three dutch families

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7 January 2021

Progressive supranuclear gaze palsy is in linkage disequilibrium with the tau and not the alpha-synuclein gene

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7 January 2021

Tau consists of a set of proteins with repeated C-terminal microtubule-binding domains and variable N-terminal domains

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7 January 2021

The tau gene A0 allele and progressive supranuclear palsy.

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7 January 2021

Lithium reduces tau phosphorylation by inhibition of glycogen synthase kinase-3.

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7 January 2021

Insulin and insulin-like growth factor-1 regulate tau phosphorylation in cultured human neurons.

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7 January 2021

Mutation-specific functional impairments in distinct tau isoforms of hereditary FTDP-17.

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7 January 2021

Correlative Memory Deficits, Abeta Elevation, and Amyloid Plaques in Transgenic Mice

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7 January 2021

Neuropathological features of frontotemporal dementia and parkinsonism linked to chromosome 17q21-22 (FTDP-17): Duke Family 1684.

1 reference

https://api.crossref.org/works/10.1016%2FS0891-0618%2800%2900100-9

7 January 2021

Association of missense and 5'-splice-site mutations in tau with the inherited dementia FTDP-17

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7 January 2021

A distinct familial presenile dementia with a novel missense mutation in the tau gene

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7 January 2021

Muscle weakness, hyperactivity, and impairment in fear conditioning in tau-deficient mice.

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7 January 2021

Age-Dependent Emergence and Progression of a Tauopathy in Transgenic Mice Overexpressing the Shortest Human Tau Isoform

1 reference

https://api.crossref.org/works/10.1016%2FS0891-0618%2800%2900100-9

7 January 2021

Aberrant splicing of tau pre-mRNA caused by intronic mutations associated with the inherited dementia frontotemporal dementia with parkinsonism linked to chromosome 17.

1 reference

https://api.crossref.org/works/10.1016%2FS0891-0618%2800%2900100-9

7 January 2021

Altered conformation of recombinant frontotemporal dementia-17 mutant tau proteins

1 reference

https://api.crossref.org/works/10.1016%2FS0891-0618%2800%2900100-9

7 January 2021

Fetal-type phosphorylation of the tau in paired helical filaments

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https://api.crossref.org/works/10.1016%2FS0891-0618%2800%2900100-9

7 January 2021

Paired Helical Filaments in Electron Microscopy of Alzheimer's Disease

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7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0891-0618%2800%2900100-9

7 January 2021

Tau-positive glial inclusions in progressive supranuclear palsy, corticobasal degeneration and Pick's disease

1 reference

https://api.crossref.org/works/10.1016%2FS0891-0618%2800%2900100-9

7 January 2021

The carboxyl third of tau is tightly bound to paired helical filaments.

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https://api.crossref.org/works/10.1016%2FS0891-0618%2800%2900100-9

7 January 2021

Epitopes that span the tau molecule are shared with paired helical filaments.

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https://api.crossref.org/works/10.1016%2FS0891-0618%2800%2900100-9

7 January 2021

Tau polymorphisms are not associated with Alzheimer's disease

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https://api.crossref.org/works/10.1016%2FS0891-0618%2800%2900100-9

7 January 2021

The microtubule binding domain of tau protein.

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7 January 2021

A68: a major subunit of paired helical filaments and derivatized forms of normal Tau.

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7 January 2021

Hereditary dysphasic disinhibition dementia: a frontotemporal dementia linked to 17q21-22.

1 reference

https://api.crossref.org/works/10.1016%2FS0891-0618%2800%2900100-9

7 January 2021

Neurofibrillary tangles, amyotrophy and progressive motor disturbance in mice expressing mutant (P301L) tau protein

1 reference

https://api.crossref.org/works/10.1016%2FS0891-0618%2800%2900100-9

7 January 2021

Protein phosphatase 1 is targeted to microtubules by the microtubule-associated protein Tau.

1 reference

https://api.crossref.org/works/10.1016%2FS0891-0618%2800%2900100-9

7 January 2021

Cognitive, neuroimaging, and pathological studies in a patient with Pick's disease

1 reference

https://api.crossref.org/works/10.1016%2FS0891-0618%2800%2900100-9

7 January 2021

Clinical research criteria for the diagnosis of progressive supranuclear palsy (Steele-Richardson-Olszewski syndrome): report of the NINDS-SPSP international workshop

1 reference

https://api.crossref.org/works/10.1016%2FS0891-0618%2800%2900100-9

7 January 2021

Validity and reliability of the preliminary NINDS neuropathologic criteria for progressive supranuclear palsy and related disorders.

1 reference

https://api.crossref.org/works/10.1016%2FS0891-0618%2800%2900100-9

7 January 2021

Functional implications for the microtubule-associated protein tau: localization in oligodendrocytes

1 reference

https://api.crossref.org/works/10.1016%2FS0891-0618%2800%2900100-9

7 January 2021

Phosphorylation of tau by glycogen synthase kinase-3β in intact mammalian cells: The effects on the organization and stability of microtubules

1 reference

https://api.crossref.org/works/10.1016%2FS0891-0618%2800%2900100-9

7 January 2021

The prolyl isomerase Pin1 restores the function of Alzheimer-associated phosphorylated tau protein

1 reference

https://api.crossref.org/works/10.1016%2FS0891-0618%2800%2900100-9

7 January 2021

Clinical and neuropathological criteria for frontotemporal dementia. The Lund and Manchester Groups

1 reference

https://api.crossref.org/works/10.1016%2FS0891-0618%2800%2900100-9

7 January 2021

Phosphorylation of specific sets of tau isoforms reflects different neurofibrillary degeneration processes.

1 reference

https://api.crossref.org/works/10.1016%2FS0891-0618%2800%2900100-9

7 January 2021

Glycogen synthase kinase-3 and the Alzheimer-like state of microtubule-associated protein tau.

1 reference

https://api.crossref.org/works/10.1016%2FS0891-0618%2800%2900100-9

7 January 2021

Dementia of frontal type and dementias with subcortical gliosis

1 reference

https://api.crossref.org/works/10.1016%2FS0891-0618%2800%2900100-9

7 January 2021

Molecular basis of the neurodegenerative disorders

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https://api.crossref.org/works/10.1016%2FS0891-0618%2800%2900100-9

7 January 2021

Spinal cord neurofibrillary tangles of Guamanian amyotrophic lateral sclerosis and parkinsonism-dementia complex: an immunohistochemical study

1 reference

https://api.crossref.org/works/10.1016%2FS0891-0618%2800%2900100-9

7 January 2021

Stable expression in Chinese hamster ovary cells of mutated tau genes causing frontotemporal dementia and parkinsonism linked to chromosome 17 (FTDP-17)

1 reference

https://api.crossref.org/works/10.1016%2FS0891-0618%2800%2900100-9

7 January 2021

Biopsy-derived adult human brain tau is phosphorylated at many of the same sites as Alzheimer's disease paired helical filament tau.

1 reference

https://api.crossref.org/works/10.1016%2FS0891-0618%2800%2900100-9

7 January 2021

Selective destruction of stable microtubules and axons by inhibitors of protein serine/threonine phosphatases in cultured human neurons.

1 reference

https://api.crossref.org/works/10.1016%2FS0891-0618%2800%2900100-9

7 January 2021

Tau pathology in a family with dementia and a P301L mutation in tau.

1 reference

https://api.crossref.org/works/10.1016%2FS0891-0618%2800%2900100-9

7 January 2021

Progressive supranuclear palsy: earlier age of onset in patients with the tau protein A0/A0 genotype

1 reference

https://api.crossref.org/works/10.1016%2FS0891-0618%2800%2900100-9

7 January 2021

Hyperphosphorylation of tau in PHF

1 reference

https://api.crossref.org/works/10.1016%2FS0891-0618%2800%2900100-9

7 January 2021

The tau gene A0 polymorphism in progressive supranuclear palsy and related neurodegenerative diseases.

1 reference

https://api.crossref.org/works/10.1016%2FS0891-0618%2800%2900100-9

7 January 2021

Familial multiple-system tauopathy with presenile dementia is localized to chromosome 17

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https://api.crossref.org/works/10.1016%2FS0891-0618%2800%2900100-9

7 January 2021

Tau gene mutation G389R causes a tauopathy with abundant pick body-like inclusions and axonal deposits.

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https://api.crossref.org/works/10.1016%2FS0891-0618%2800%2900100-9

7 January 2021

Accelerated filament formation from tau protein with specific FTDP-17 missense mutations.

1 reference

https://api.crossref.org/works/10.1016%2FS0891-0618%2800%2900100-9

7 January 2021

From genotype to phenotype: a clinical pathological, and biochemical investigation of frontotemporal dementia and parkinsonism (FTDP-17) caused by the P301L tau mutation

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7 January 2021

Frontotemporal lobar degeneration: a consensus on clinical diagnostic criteria

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7 January 2021

Identification of cDNA clones for the human microtubule-associated protein tau and chromosomal localization of the genes for tau and microtubule-associated protein 2.

1 reference

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7 January 2021

Conversion of p35 to p25 deregulates Cdk5 activity and promotes neurodegeneration

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7 January 2021

Tau is a candidate gene for chromosome 17 frontotemporal dementia

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7 January 2021

Axonopathy and amyotrophy in mice transgenic for human four-repeat tau protein

1 reference

https://api.crossref.org/works/10.1016%2FS0891-0618%2800%2900100-9

7 January 2021

Pick's disease: hyperphosphorylated tau protein segregates to the somatoaxonal compartment

1 reference

https://api.crossref.org/works/10.1016%2FS0891-0618%2800%2900100-9

7 January 2021

Corticodentatonigral Degeneration With Neuronal Achromasia

1 reference

https://api.crossref.org/works/10.1016%2FS0891-0618%2800%2900100-9

7 January 2021

Autosomal dominant dementia with widespread neurofibrillary tangles.

1 reference

https://api.crossref.org/works/10.1016%2FS0891-0618%2800%2900100-9

7 January 2021

The neuropathology of a chromosome 17-linked autosomal dominant parkinsonism and dementia ("pallido-ponto-nigral degeneration").

1 reference

https://api.crossref.org/works/10.1016%2FS0891-0618%2800%2900100-9

7 January 2021

Reactivating kinase/p38 phosphorylates tau protein in vitro

1 reference

https://api.crossref.org/works/10.1016%2FS0891-0618%2800%2900100-9

7 January 2021

Stress-activated protein kinase/c-jun N-terminal kinase phosphorylates tau protein

1 reference

https://api.crossref.org/works/10.1016%2FS0891-0618%2800%2900100-9

7 January 2021

High prevalence of mutations in the microtubule-associated protein tau in a population study of frontotemporal dementia in the Netherlands

1 reference

https://api.crossref.org/works/10.1016%2FS0891-0618%2800%2900100-9

7 January 2021

Missense point mutations of tau to segregate with FTDP-17 exhibit site-specific effects on microtubule structure in COS cells: a novel action of R406W mutation

1 reference

https://api.crossref.org/works/10.1016%2FS0891-0618%2800%2900100-9

7 January 2021

Neurofibrillary tangles in progressive supranuclear palsy contain the same tau epitopes identified in Alzheimer's disease PHFtau.

1 reference

https://api.crossref.org/works/10.1016%2FS0891-0618%2800%2900100-9

7 January 2021

The origins of Alzheimer disease: a is for amyloid.

1 reference

https://api.crossref.org/works/10.1016%2FS0891-0618%2800%2900100-9

7 January 2021

Splice junctions, branch point sites, and exons: sequence statistics, identification, and applications to genome project

1 reference

https://api.crossref.org/works/10.1016%2FS0891-0618%2800%2900100-9

7 January 2021

Potentiation of GSK-3-catalyzed Alzheimer-like phosphorylation of human tau by cdk5.

1 reference

https://api.crossref.org/works/10.1016%2FS0891-0618%2800%2900100-9

7 January 2021

Different distribution of phosphorylated tau protein isoforms in Alzheimer's and Pick's diseases.

1 reference

https://api.crossref.org/works/10.1016%2FS0891-0618%2800%2900100-9

7 January 2021

Neurofibrillary degeneration in progressive supranuclear palsy and corticobasal degeneration: tau pathologies with exclusively "exon 10" isoforms

1 reference

https://api.crossref.org/works/10.1016%2FS0891-0618%2800%2900100-9

7 January 2021

Detection of Phosphorylated Ser262 in Fetal Tau, Adult Tau, and Paired Helical Filament Tau

1 reference

https://api.crossref.org/works/10.1016%2FS0891-0618%2800%2900100-9

7 January 2021

The exon splicing silencer in human immunodeficiency virus type 1 Tat exon 3 is bipartite and acts early in spliceosome assembly

1 reference

https://api.crossref.org/works/10.1016%2FS0891-0618%2800%2900100-9

7 January 2021

The neuropathology of chromosome 17-linked dementia

1 reference

https://api.crossref.org/works/10.1016%2FS0891-0618%2800%2900100-9

7 January 2021

Modulation of GSK-3-catalyzed phosphorylation of microtubule-associated protein tau by non-proline-dependent protein kinases.

1 reference

https://api.crossref.org/works/10.1016%2FS0891-0618%2800%2900100-9

7 January 2021

Interaction of neuronal Cdc2-like protein kinase with microtubule-associated protein tau.

1 reference

https://api.crossref.org/works/10.1016%2FS0891-0618%2800%2900100-9

7 January 2021

A novel pool of protein phosphatase 2A is associated with microtubules and is regulated during the cell cycle

1 reference

https://api.crossref.org/works/10.1016%2FS0891-0618%2800%2900100-9

7 January 2021

Molecular interactions among protein phosphatase 2A, tau, and microtubules. Implications for the regulation of tau phosphorylation and the development of tauopathies

1 reference

https://api.crossref.org/works/10.1016%2FS0891-0618%2800%2900100-9

7 January 2021

FTDP-17: an early-onset phenotype with parkinsonism and epileptic seizures caused by a novel mutation

1 reference

https://api.crossref.org/works/10.1016%2FS0891-0618%2800%2900100-9

7 January 2021

Comparison of the neurofibrillary pathology in Alzheimer's disease and familial presenile dementia with tangles

1 reference

https://api.crossref.org/works/10.1016%2FS0891-0618%2800%2900100-9

7 January 2021

Tau pathology in two Dutch families with mutations in the microtubule-binding region of tau

1 reference

https://api.crossref.org/works/10.1016%2FS0891-0618%2800%2900100-9

7 January 2021

Mutation in the tau gene in familial multiple system tauopathy with presenile dementia

1 reference

https://api.crossref.org/works/10.1016%2FS0891-0618%2800%2900100-9

7 January 2021

Prominent axonopathy in the brain and spinal cord of transgenic mice overexpressing four-repeat human tau protein

1 reference

https://api.crossref.org/works/10.1016%2FS0891-0618%2800%2900100-9

7 January 2021

Progressive supranuclear palsy pathology caused by a novel silent mutation in exon 10 of the tau gene: expansion of the disease phenotype caused by tau gene mutations.

1 reference

https://api.crossref.org/works/10.1016%2FS0891-0618%2800%2900100-9

7 January 2021

PROGRESSIVE SUPRANUCLEAR PALSY. A HETEROGENEOUS DEGENERATION INVOLVING THE BRAIN STEM, BASAL GANGLIA AND CEREBELLUM WITH VERTICAL GAZE AND PSEUDOBULBAR PALSY, NUCHAL DYSTONIA AND DEMENTIA.

1 reference

https://api.crossref.org/works/10.1016%2FS0891-0618%2800%2900100-9

7 January 2021

Two amyloid precursor protein transgenic mouse models with Alzheimer disease-like pathology

1 reference

https://api.crossref.org/works/10.1016%2FS0891-0618%2800%2900100-9

7 January 2021

Familial presenile dementia with psychosis associated with cortical neurofibrillary tangles and degeneration of the amygdala

1 reference

https://api.crossref.org/works/10.1016%2FS0891-0618%2800%2900100-9

7 January 2021

Involvement of tau protein kinase I in paired helical filament-like phosphorylation of the juvenile tau in rat brain

1 reference

https://api.crossref.org/works/10.1016%2FS0891-0618%2800%2900100-9

7 January 2021

Regional distribution and biochemical characteristics of high molecular weight tau in the nervous system

1 reference

https://api.crossref.org/works/10.1016%2FS0891-0618%2800%2900100-9

7 January 2021

Polypurine sequences within a downstream exon function as a splicing enhancer

1 reference

https://api.crossref.org/works/10.1016%2FS0891-0618%2800%2900100-9

7 January 2021

Ultrastructure of Neurofibrillary Tangles in Steele-Richardson-Olszewski Syndrome

1 reference

https://api.crossref.org/works/10.1016%2FS0891-0618%2800%2900100-9

7 January 2021

Expression of human apolipoprotein E4 in neurons causes hyperphosphorylation of protein tau in the brains of transgenic mice

1 reference

https://api.crossref.org/works/10.1016%2FS0891-0618%2800%2900100-9

7 January 2021

Phenotypic variation in hereditary frontotemporal dementia with tau mutations

1 reference

https://api.crossref.org/works/10.1016%2FS0891-0618%2800%2900100-9

7 January 2021

Structure of tau exon 10 splicing regulatory element RNA and destabilization by mutations of frontotemporal dementia and parkinsonism linked to chromosome 17

1 reference

https://api.crossref.org/works/10.1016%2FS0891-0618%2800%2900100-9

7 January 2021

A protein factor essential for microtubule assembly

1 reference

https://api.crossref.org/works/10.1016%2FS0891-0618%2800%2900100-9

7 January 2021

Localization of the gene for rapidly progressive autosomal dominant parkinsonism and dementia with pallido-ponto-nigral degeneration to chromosome 17q21

1 reference

https://api.crossref.org/works/10.1016%2FS0891-0618%2800%2900100-9

7 January 2021

Isolation of a fragment of tau derived from the core of the paired helical filament of Alzheimer disease

1 reference

https://api.crossref.org/works/10.1016%2FS0891-0618%2800%2900100-9

7 January 2021

Preferential labeling of Alzheimer neurofibrillary tangles with antisera for tau protein kinase (TPK) I/glycogen synthase kinase-3 beta and cyclin-dependent kinase 5, a component of TPK II.

1 reference

https://api.crossref.org/works/10.1016%2FS0891-0618%2800%2900100-9

7 January 2021

A mutation in the microtubule-associated protein tau in pallido-nigro-luysian degeneration

1 reference

https://api.crossref.org/works/10.1016%2FS0891-0618%2800%2900100-9

7 January 2021

A novel mutation at position +12 in the intron following exon 10 of the tau gene in familial frontotemporal dementia (FTD-Kumamoto)

1 reference

https://api.crossref.org/works/10.1016%2FS0891-0618%2800%2900100-9

7 January 2021

Tau in paired helical filaments is functionally distinct from fetal tau: assembly incompetence of paired helical filament-tau

1 reference

https://api.crossref.org/works/10.1016%2FS0891-0618%2800%2900100-9

7 January 2021

10.1016/S0891-0618(00)00100-9

Identifiers

DOI

1 reference

31 July 2017

1 reference