The genetics of frontotemporal lobar degeneration (Q36926070)

17 August 2017

1 reference

title

The genetics of frontotemporal lobar degeneration (English)

1 reference

17 August 2017

1

Rosa Rademakers

1 reference

17 August 2017

Mike Hutton

2

1 reference

17 August 2017

1 September 2007

1 reference

Current Neurology and Neuroscience Reports

17 August 2017

1 reference

17 August 2017

7

1 reference

17 August 2017

5

1 reference

17 August 2017

434-442

1 reference

https://scigraph.springernature.com/pub.10.1007/s11910-007-0067-6

17 August 2017

0 references

cites work

Frontotemporal lobar degeneration: a consensus on clinical diagnostic criteria

1 reference

https://api.crossref.org/works/10.1007%2FS11910-007-0067-6

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS11910-007-0067-6

Missense and splice site mutations in tau associated with FTDP-17: multiple pathogenic mechanisms

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS11910-007-0067-6

Cellular localization of gene expression for progranulin

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS11910-007-0067-6

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

1 reference

12 December 2020

Microtubule organization and dynamics dependent on microtubule-associated proteins

1 reference

12 December 2020

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

1 reference

12 December 2020

The overlap of amyotrophic lateral sclerosis and frontotemporal dementia

1 reference

12 December 2020

Familial non-specific dementia maps to chromosome 3

1 reference

12 December 2020

Cloning and sequencing of the cDNA encoding an isoform of microtubule-associated protein tau containing four tandem repeats: differential expression of tau protein mRNAs in human brain

1 reference

12 December 2020

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

1 reference

12 December 2020

Granulins: the structure and function of an emerging family of growth factors

1 reference

12 December 2020

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

1 reference

12 December 2020

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

1 reference

12 December 2020

The MAPT H1c risk haplotype is associated with increased expression of tau and especially of 4 repeat containing transcripts

1 reference

12 December 2020

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

1 reference

12 December 2020

Frontotemporal lobar degeneration and ubiquitin immunohistochemistry

1 reference

12 December 2020

Microtubule-associated proteins regulate microtubule function as the track for intracellular membrane organelle transports

1 reference

12 December 2020

Genomic architecture of human 17q21 linked to frontotemporal dementia uncovers a highly homologous family of low-copy repeats in the tau region

1 reference

12 December 2020

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

1 reference

12 December 2020

Developmentally regulated expression of specific tau sequences

1 reference

12 December 2020

Conversion of proepithelin to epithelins: roles of SLPI and elastase in host defense and wound repair

1 reference

12 December 2020

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

1 reference

12 December 2020

Genetic Variability in CHMP2B and Frontotemporal Dementia

1 reference

12 December 2020

Inclusion body myopathy and Paget disease is linked to a novel mutation in the VCP gene

1 reference

12 December 2020

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

1 reference

12 December 2020

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

1 reference

12 December 2020

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

1 reference

12 December 2020

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

1 reference

12 December 2020

ALS phenotypes with mutations in CHMP2B (charged multivesicular body protein 2B)

1 reference

12 December 2020

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

1 reference

12 December 2020

Domains of tau protein and interactions with microtubules

1 reference

12 December 2020

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

1 reference

12 December 2020

p97, a protein coping with multiple identities

1 reference

12 December 2020

TDP-43 in the ubiquitin pathology of frontotemporal dementia with VCP gene mutations.

1 reference

12 December 2020

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

1 reference

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

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

1 reference

12 December 2020

Valosin-containing protein gene mutations: clinical and neuropathologic features.

1 reference

12 December 2020

Differential assembly of human tau isoforms in the presence of arachidonic acid

1 reference

12 December 2020

The genetic and pathological classification of familial frontotemporal dementia.

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

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

1 reference

12 December 2020

Frontotemporal dementia and parkinsonism linked to chromosome 17 (FTDP-17)

1 reference

12 December 2020

Multiple-motor based transport and its regulation by Tau.

1 reference

12 December 2020

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

1 reference

12 December 2020

Tau gene mutations: dissecting the pathogenesis of FTDP-17.

1 reference

12 December 2020

Clinicopathologic features of frontotemporal dementia with progranulin sequence variation.

1 reference

12 December 2020

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

1 reference

12 December 2020

Progranulin mutations in Dutch familial frontotemporal lobar degeneration

1 reference

12 December 2020

TDP-43 pathology in familial frontotemporal dementia and motor neuron disease without Progranulin mutations

1 reference

12 December 2020

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

1 reference

12 December 2020

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

1 reference

12 December 2020

Progranulin null mutations in both sporadic and familial frontotemporal dementia

1 reference

12 December 2020

CHMP2B mutations are not a common cause of frontotemporal lobar degeneration

1 reference

12 December 2020

A protein's final ESCRT.

1 reference

12 December 2020

Progranulin is a mediator of the wound response

1 reference

12 December 2020

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

1 reference

12 December 2020

Apolipoprotein E gene in frontotemporal dementia: an association study and meta-analysis

1 reference

12 December 2020

Untangling tau-related dementia

1 reference

12 December 2020

CHMP2B mutations are not a cause of dementia in Dutch patients with familial and sporadic frontotemporal dementia

1 reference

12 December 2020

Localization of disinhibition-dementia-parkinsonism-amyotrophy complex to 17q21-22.

1 reference

12 December 2020

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

1 reference

12 December 2020

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

Mutations in progranulin explain atypical phenotypes with variants in MAPT.

1 reference

12 December 2020

Haplotype-specific expression of exon 10 at the human MAPT locus

1 reference

12 December 2020

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

1 reference

12 December 2020

Expression of separate isoforms of human tau protein: correlation with the tau pattern in brain and effects on tubulin polymerization

1 reference

12 December 2020

10.1007/S11910-007-0067-6

Identifiers

DOI

1 reference

release_rthhslnaz5eaxmgee34d3t7wni

17 August 2017

1 reference

Fatcat

https://api.fatcat.wiki/v0/release/rthhslnaz5eaxmgee34d3t7wni

24 November 2022

mapped directly with Wikidata item

PubMed ID

17764635

1 reference

PubMed ID

17764635