(Q28254281)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:17953663%20AND%20SRC:MED&resulttype=core&format=json

9 January 2020

review article

1 reference

title

Progranulin: normal function and role in neurodegeneration (English)

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:17953663%20AND%20SRC:MED&resulttype=core&format=json

9 January 2020

1 reference

1

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:17953663%20AND%20SRC:MED&resulttype=core&format=json

9 January 2020

author name string

Ian R A Mackenzie

series ordinal

2

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:17953663%20AND%20SRC:MED&resulttype=core&format=json

9 January 2020

language of work or name

English

0 references

publication date

22 October 2007

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:17953663%20AND%20SRC:MED&resulttype=core&format=json

Journal of Neurochemistry

9 January 2020

published in

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:17953663%20AND%20SRC:MED&resulttype=core&format=json

9 January 2020

volume

104

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:17953663%20AND%20SRC:MED&resulttype=core&format=json

9 January 2020

issue

2

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:17953663%20AND%20SRC:MED&resulttype=core&format=json

9 January 2020

page(s)

287-297

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:17953663%20AND%20SRC:MED&resulttype=core&format=json

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

9 January 2020

cites work

1 reference

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Granulins, a novel class of peptide from leukocytes

21 April 2017

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

21 April 2017

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

21 April 2017

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

21 April 2017

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

21 April 2017

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

21 April 2017

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Localization of a highly active pool of type II phosphatidylinositol 4-kinase in a p97/valosin-containing-protein-rich fraction of the endoplasmic reticulum

21 April 2017

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

21 April 2017

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

21 April 2017

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Structural and functional analysis of a promoter of the human granulin/epithelin gene

21 April 2017

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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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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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Frontotemporal dementia and parkinsonism associated with the IVS1+1G->A mutation in progranulin: a clinicopathologic study.

21 January 2018

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Inheritance of frontotemporal dementia

21 January 2018

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Cellular localization of gene expression for progranulin

21 January 2018

1 reference

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

21 January 2018

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Neurodegenerative diseases: a decade of discoveries paves the way for therapeutic breakthroughs

21 January 2018

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

21 January 2018

1 reference

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

21 January 2018

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

21 January 2018

1 reference

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1471-4159.2007.04968.X

Progranulin is a mediator of the wound response

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1471-4159.2007.04968.X

The hairpin stack fold, a novel protein architecture for a new family of protein growth factors

21 January 2018

1 reference

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Characteristics of frontotemporal dementia patients with a Progranulin mutation

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1471-4159.2007.04968.X

Identification of genes involved in the host response to neurovirulent alphavirus infection

21 January 2018

1 reference

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Microglia: a sensor for pathological events in the CNS

21 January 2018

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Bone marrow derived elements and resident microglia in brain inflammation.

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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Frontotemporal lobar degeneration with motor neuron disease-type inclusions predominates in 76 cases of frontotemporal degeneration.

21 January 2018

1 reference

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The role of hypothermia in the management of severe brain injury: a meta-analysis.

21 January 2018

1 reference

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Inhibition of PC cell-derived growth factor (PCDGF, epithelin/granulin precursor) expression by antisense PCDGF cDNA transfection inhibits tumorigenicity of the human breast carcinoma cell line MDA-MB-468.

21 January 2018

1 reference

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1471-4159.2007.04968.X

Clinical and pathological diagnosis of frontotemporal dementia: report of the Work Group on Frontotemporal Dementia and Pick's Disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1471-4159.2007.04968.X

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1471-4159.2007.04968.X

Frontotemporal lobar degeneration: a consensus on clinical diagnostic criteria

21 January 2018

1 reference

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Activated microglia in cortex of mouse models of mucopolysaccharidoses I and IIIB

21 January 2018

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Mutations in progranulin explain atypical phenotypes with variants in MAPT.

21 January 2018

1 reference

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Tau is a candidate gene for chromosome 17 frontotemporal dementia

21 January 2018

1 reference

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

21 January 2018

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

21 January 2018

1 reference

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

21 January 2018

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

21 January 2018

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

21 January 2018

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

21 January 2018

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Familial aggregation in frontotemporal dementia

21 January 2018

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Identification of a sex steroid-inducible gene in the neonatal rat hypothalamus.

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1471-4159.2007.04968.X

Update on the neuropathological diagnosis of frontotemporal dementias

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1471-4159.2007.04968.X

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1471-4159.2007.04968.X

Microglial activation precedes acute neurodegeneration in Sandhoff disease and is suppressed by bone marrow transplantation

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1471-4159.2007.04968.X

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1471-4159.2007.04968.X

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1471-4159.2007.04968.X

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1471-4159.2007.04968.X

10.1111/J.1471-4159.2007.04968.X

21 January 2018

Identifiers

DOI

2 references

Consolidated OpenCitations Corpus – April 2017

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:17953663%20AND%20SRC:MED&resulttype=core&format=json

9 January 2020

1 reference

Consolidated OpenCitations Corpus – April 2017

2 references

Consolidated OpenCitations Corpus – April 2017