Progranulin: normal function and role in neurodegeneration (Q28254281)

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9 January 2020

review article

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title

Progranulin: normal function and role in neurodegeneration (English)

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9 January 2020

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1

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9 January 2020

author name string

Ian R A Mackenzie

series ordinal

2

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9 January 2020

language of work or name

English

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publication date

22 October 2007

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Journal of Neurochemistry

9 January 2020

published in

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9 January 2020

volume

104

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9 January 2020

issue

2

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9 January 2020

page(s)

287-297

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

9 January 2020

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Cellular localization of gene expression for progranulin

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

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

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

21 January 2018

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

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

21 January 2018

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

21 January 2018

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Progranulin is a mediator of the wound response

21 January 2018

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

21 January 2018

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Characteristics of frontotemporal dementia patients with a Progranulin mutation

21 January 2018

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

21 January 2018

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Microglia: a sensor for pathological events in the CNS

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21 January 2018

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21 January 2018

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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

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21 January 2018

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21 January 2018

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21 January 2018

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

21 January 2018

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21 January 2018

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

21 January 2018

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

21 January 2018

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10.1111/J.1471-4159.2007.04968.X

21 January 2018

Identifiers

DOI

2 references

Consolidated OpenCitations Corpus – April 2017

3510475

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

9 January 2020

3510475

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Consolidated OpenCitations Corpus – April 2017

Consolidated OpenCitations Corpus – April 2017

2 references

3510475