Mutations in progranulin cause tau-negative frontotemporal dementia linked to chromosome 17 (Q28253651)

Julie Snowden

7

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Howard Feldman

Howard Feldman

26

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Stuart Pickering-Brown

Stuart M Pickering-Brown

3

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Dennis W. Dickson

Dennis Dickson

16

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Rosa Rademakers

5

Rosa Rademakers

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Bradley F Boeve

25

Bradley Boeve

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David Neary

13

David Neary

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author name string

Matt Baker

1

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Ian R Mackenzie

2

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Jennifer Gass

4

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Caroline Lindholm

6

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Jennifer Adamson

8

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A Dessa Sadovnick

9

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Sara Rollinson

10

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Ashley Cannon

11

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Emily Dwosh

12

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Stacey Melquist

14

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Anna Richardson

15

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Zdenek Berger

17

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Todd Robinson

19

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Cynthia Zehr

20

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Chad A Dickey

21

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Richard Crook

22

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Eileen McGowan

23

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David Mann

24

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Mike Hutton

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

27

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language of work or name

English

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publication date

24 August 2006

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published in

Nature

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volume

442

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page(s)

916-9

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issue

7105

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cites work

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Inheritance of frontotemporal dementia

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

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

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

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

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

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

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

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

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A Belgian ancestral haplotype harbours a highly prevalent mutation for 17q21-linked tau-negative FTLD.

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

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

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Differential expression of 14 genes in amyotrophic lateral sclerosis spinal cord detected using gridded cDNA arrays

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Unique inflammatory RNA profiles of microglia in Creutzfeldt-Jakob disease

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Classification and description of frontotemporal dementias.

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Update on the neuropathological diagnosis of frontotemporal dementias

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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.

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

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

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

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

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

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Cellular localization of gene expression for progranulin

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Alzheimer-like neurodegeneration in aged antinerve growth factor transgenic mice

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Alzheimer's disease and NGF signaling

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PC cell-derived growth factor (PCDGF/GP88, progranulin) stimulates migration, invasiveness and VEGF expression in breast cancer cells

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ANG mutations segregate with familial and 'sporadic' amyotrophic lateral sclerosis.

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Progranulin is a mediator of the wound response

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7 January 2021

Identifiers

DOI

10.1038/NATURE05016

1 reference

Consolidated OpenCitations Corpus – April 2017

Dimensions Publication ID

39036

1038649717

0 references

39036

1 reference

Consolidated OpenCitations Corpus – April 2017

Consolidated OpenCitations Corpus – April 2017

1 reference