(Q36931728)

17 August 2017

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title

The molecular genetics and neuropathology of frontotemporal lobar degeneration: recent developments (English)

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frontotemporal lobar degeneration

17 August 2017

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2

Rosa Rademakers

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17 August 2017

Ian R A Mackenzie

1

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17 August 2017

6 September 2007

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17 August 2017

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17 August 2017

8

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17 August 2017

237-248

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17 August 2017

4

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https://scigraph.springernature.com/pub.10.1007/s10048-007-0102-4

17 August 2017

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Update on the neuropathological diagnosis of frontotemporal dementias

21 January 2018

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Dementia lacking distinctive histologic features: a common non-Alzheimer degenerative dementia

21 January 2018

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Chromosome 17 and hereditary dementia: linkage studies in three non-Alzheimer families and kindreds with late-onset FAD.

21 January 2018

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

21 January 2018

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Cellular localization of gene expression for progranulin

21 January 2018

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Neuronal ubiquitinated intranuclear inclusions in familial and non-familial frontotemporal dementia of the motor neuron disease type associated with amyotrophic lateral sclerosis.

21 January 2018

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21 January 2018

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Clinical delineation and localization to chromosome 9p13.3-p12 of a unique dominant disorder in four families: hereditary inclusion body myopathy, Paget disease of bone, and frontotemporal dementia

21 January 2018

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12 December 2020

Analysis of IFT74 as a candidate gene for chromosome 9p-linked ALS-FTD

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12 December 2020

Familial frontotemporal dementia with ubiquitin-positive inclusions is linked to chromosome 17q21-22.

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12 December 2020

The overlap of amyotrophic lateral sclerosis and frontotemporal dementia

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12 December 2020

Hippocampal and neocortical ubiquitin-immunoreactive inclusions in amyotrophic lateral sclerosis with dementia

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12 December 2020

Dementia lacking distinctive histology (DLDH) revisited

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12 December 2020

A novel deletion in progranulin gene is associated with FTDP-17 and CBS.

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12 December 2020

TDP-43 immunoreactivity in hippocampal sclerosis and Alzheimer's disease

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12 December 2020

Progranulin (granulin-epithelin precursor, PC-cell-derived growth factor, acrogranin) mediates tissue repair and tumorigenesis

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12 December 2020

Neuropathologic features of frontotemporal lobar degeneration with ubiquitin-positive inclusions with progranulin gene (PGRN) mutations

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12 December 2020

Novel ubiquitin neuropathology in frontotemporal dementia with valosin-containing protein gene mutations

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12 December 2020

Frontotemporal lobar degeneration: demographic characteristics of 353 patients

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12 December 2020

Familial amyotrophic lateral sclerosis with frontotemporal dementia is linked to a locus on chromosome 9p13.2-21.3.

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12 December 2020

Pathological TDP-43 distinguishes sporadic amyotrophic lateral sclerosis from amyotrophic lateral sclerosis with SOD1 mutations.

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12 December 2020

A novel progranulin mutation associated with variable clinical presentation and tau, TDP43 and alpha-synuclein pathology.

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12 December 2020

Frontotemporal lobar degeneration and ubiquitin immunohistochemistry

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12 December 2020

Nuclear factor TDP-43 and SR proteins promote in vitro and in vivo CFTR exon 9 skipping

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12 December 2020

Familial frontotemporal dementia with ubiquitin-positive, tau-negative inclusions

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12 December 2020

Progranulin gene mutations associated with frontotemporal dementia and progressive non-fluent aphasia

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12 December 2020

Null mutations in progranulin cause ubiquitin-positive frontotemporal dementia linked to chromosome 17q21

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12 December 2020

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

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12 December 2020

Molecular perspectives on p97-VCP: progress in understanding its structure and diverse biological functions

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12 December 2020

Pathological heterogeneity of frontotemporal lobar degeneration with ubiquitin-positive inclusions delineated by ubiquitin immunohistochemistry and novel monoclonal antibodies

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12 December 2020

Inclusion body myopathy associated with Paget disease of bone and frontotemporal dementia is caused by mutant valosin-containing protein

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12 December 2020

Mutations in the endosomal ESCRTIII-complex subunit CHMP2B in frontotemporal dementia

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12 December 2020

Nonsense-mediated mRNA decay: splicing, translation and mRNP dynamics

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12 December 2020

Mutant valosin-containing protein causes a novel type of frontotemporal dementia

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12 December 2020

TDP-43 gene analysis in frontotemporal lobar degeneration

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12 December 2020

The road less traveled: emerging principles of kinesin motor utilization

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12 December 2020

The neuropathology of frontotemporal lobar degeneration caused by mutations in the progranulin gene.

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12 December 2020

Novel splicing mutation in the progranulin gene causing familial corticobasal syndrome.

1 reference

12 December 2020

Ubiquitinated TDP-43 in frontotemporal lobar degeneration and amyotrophic lateral sclerosis

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12 December 2020

Three families with amyotrophic lateral sclerosis and frontotemporal dementia with evidence of linkage to chromosome 9p.

1 reference

12 December 2020

Linkage of familial amyotrophic lateral sclerosis with frontotemporal dementia to chromosome 9q21-q22

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12 December 2020

Ubiquitin immunohistochemistry suggests classic motor neuron disease, motor neuron disease with dementia, and frontotemporal dementia of the motor neuron disease type represent a clinicopathologic spectrum.

1 reference

12 December 2020

Characteristics of frontotemporal dementia patients with a Progranulin mutation

1 reference

12 December 2020

Heterogeneity of ubiquitin pathology in frontotemporal lobar degeneration: classification and relation to clinical phenotype

1 reference

12 December 2020

Mutations other than null mutations producing a pathogenic loss of progranulin in frontotemporal dementia.

1 reference

12 December 2020

Comparative biochemistry of tau in progressive supranuclear palsy, corticobasal degeneration, FTDP-17 and Pick's disease

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12 December 2020

Frequency of tau gene mutations in familial and sporadic cases of non-Alzheimer dementia

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12 December 2020

Progranulin mutations in primary progressive aphasia: the PPA1 and PPA3 families.

1 reference

12 December 2020

Mapping of a disease locus for familial rapidly progressive frontotemporal dementia to chromosome 17q12-21.

1 reference

12 December 2020

Progranulin mutations and amyotrophic lateral sclerosis or amyotrophic lateral sclerosis-frontotemporal dementia phenotypes

1 reference

12 December 2020

Mutations in progranulin are a major cause of ubiquitin-positive frontotemporal lobar degeneration

1 reference

12 December 2020

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

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12 December 2020

Progranulin in frontotemporal lobar degeneration and neuroinflammation

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12 December 2020

Clinicopathologic features of frontotemporal dementia with progranulin sequence variation.

1 reference

12 December 2020

Cloning and characterization of a novel cellular protein, TDP-43, that binds to human immunodeficiency virus type 1 TAR DNA sequence motifs

1 reference

12 December 2020

Progranulin mutations in Dutch familial frontotemporal lobar degeneration

1 reference

12 December 2020

TDP-43-positive white matter pathology in frontotemporal lobar degeneration with ubiquitin-positive inclusions.

1 reference

12 December 2020

Motor neurone disease-inclusion dementia.

1 reference

12 December 2020

TDP-43 in familial and sporadic frontotemporal lobar degeneration with ubiquitin inclusions

1 reference

12 December 2020

Progranulin null mutations in both sporadic and familial frontotemporal dementia

1 reference

12 December 2020

Mutation of Vps54 causes motor neuron disease and defective spermiogenesis in the wobbler mouse

1 reference

12 December 2020

A Canadian Cohort Study of Cognitive Impairment and Related Dementias (ACCORD): Study Methods and Baseline Results

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12 December 2020

A Reassessment of the Neuropathology of Frontotemporal Dementia Linked to Chromosome 3

1 reference

12 December 2020

A mutation in the vesicle-trafficking protein VAPB causes late-onset spinal muscular atrophy and amyotrophic lateral sclerosis

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12 December 2020

Frontotemporal dementia with ubiquitinated cytoplasmic and intranuclear inclusions.

1 reference

12 December 2020

Mutations in progranulin cause tau-negative frontotemporal dementia linked to chromosome 17

1 reference

12 December 2020

TDP-43 is a component of ubiquitin-positive tau-negative inclusions in frontotemporal lobar degeneration and amyotrophic lateral sclerosis

1 reference

12 December 2020

Depletion of TDP 43 overrides the need for exonic and intronic splicing enhancers in the human apoA-II gene.

1 reference

12 December 2020

No association of TDP-43 with sporadic frontotemporal dementia

1 reference

12 December 2020

A family with tau-negative frontotemporal dementia and neuronal intranuclear inclusions linked to chromosome 17

1 reference

12 December 2020

Inheritance of frontotemporal dementia

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12 December 2020

Neuronal intranuclear inclusions distinguish familial FTD-MND type from sporadic cases

1 reference

12 December 2020

Tau negative frontal lobe dementia at 17q21: significant finemapping of the candidate region to a 4.8 cM interval.

1 reference

12 December 2020

Epidemiology and genetics of frontotemporal dementia/Pick's disease.

1 reference

12 December 2020

Ubiquitinated pathological lesions in frontotemporal lobar degeneration contain the TAR DNA-binding protein, TDP-43.

1 reference

12 December 2020

Ubiquitin-positive intraneuronal inclusions in the extramotor cortices of presenile dementia patients with motor neuron disease

1 reference

12 December 2020

The role of tau (MAPT) in frontotemporal dementia and related tauopathies

1 reference

12 December 2020

Structural diversity and functional implications of the eukaryotic TDP gene family

1 reference

12 December 2020

Tau is a candidate gene for chromosome 17 frontotemporal dementia

1 reference

12 December 2020

HDDD2 is a familial frontotemporal lobar degeneration with ubiquitin-positive, tau-negative inclusions caused by a missense mutation in the signal peptide of progranulin

1 reference

12 December 2020

A locus on chromosome 9p confers susceptibility to ALS and frontotemporal dementia

1 reference

12 December 2020

Frontotemporal dementia in The Netherlands: patient characteristics and prevalence estimates from a population-based study.

1 reference

12 December 2020

10.1007/S10048-007-0102-4

Identifiers

DOI

1 reference

17 August 2017

1 reference

PubMed ID

17805587