(Q80162804)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:17436289%20AND%20SRC:MED&resulttype=core&format=json

29 December 2019

title

Progranulin null mutations in both sporadic and familial frontotemporal dementia (English)

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:17436289%20AND%20SRC:MED&resulttype=core&format=json

29 December 2019

main subject

frontotemporal dementia

1 reference

3

Didier Hannequin

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:17436289%20AND%20SRC:MED&resulttype=core&format=json

29 December 2019

5

Dominique Campion

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:17436289%20AND%20SRC:MED&resulttype=core&format=json

Christine Van Broeckhoven

29 December 2019

23

object named as

Christine Van Broeckhoven

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:17436289%20AND%20SRC:MED&resulttype=core&format=json

29 December 2019

12

François Sellal

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:17436289%20AND%20SRC:MED&resulttype=core&format=json

29 December 2019

20

Charles Duyckaerts

1 reference

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29 December 2019

author name string

Isabelle Le Ber

1

1 reference

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29 December 2019

Julie van der Zee

2

1 reference

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29 December 2019

Ilse Gijselinck

4

1 reference

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29 December 2019

Michèle Puel

6

1 reference

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29 December 2019

Annie Laquerrière

7

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:17436289%20AND%20SRC:MED&resulttype=core&format=json

29 December 2019

Tim De Pooter

8

1 reference

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29 December 2019

Agnès Camuzat

9

1 reference

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29 December 2019

Marleen Van den Broeck

10

1 reference

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29 December 2019

Bruno Dubois

11

1 reference

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29 December 2019

Lucette Lacomblez

13

1 reference

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29 December 2019

Martine Vercelletto

14

1 reference

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29 December 2019

Catherine Thomas-Antérion

15

1 reference

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29 December 2019

Bernard-François Michel

16

1 reference

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29 December 2019

Véronique Golfier

17

1 reference

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29 December 2019

Mira Didic

18

1 reference

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29 December 2019

François Salachas

19

1 reference

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29 December 2019

Marc Cruts

21

1 reference

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29 December 2019

Patrice Verpillat

22

1 reference

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29 December 2019

Alexis Brice

24

1 reference

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29 December 2019

French Research Network on FTD/FTD-MND

25

1 reference

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29 December 2019

publication date

1 September 2007

1 reference

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29 December 2019

1 reference

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29 December 2019

volume

28

1 reference

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29 December 2019

issue

9

1 reference

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29 December 2019

page(s)

846-855

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:17436289%20AND%20SRC:MED&resulttype=core&format=json

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

29 December 2019

cites work

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20520

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20520

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20520

7 January 2021

Tandem repeats finder: a program to analyze DNA sequences

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20520

7 January 2021

Progranulin mutations in Dutch familial frontotemporal lobar degeneration

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20520

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20520

7 January 2021

Cellular localization of gene expression for progranulin

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20520

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20520

7 January 2021

Segregation of a missense mutation in the microtubule-associated protein tau gene with familial frontotemporal dementia and parkinsonism.

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20520

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20520

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20520

7 January 2021

Progranulin is a mediator of the wound response

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20520

7 January 2021

Characteristics of frontotemporal dementia patients with a Progranulin mutation

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20520

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20520

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20520

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20520

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20520

7 January 2021

The U1 snRNP base pairs with the 5' splice site within a penta-snRNP complex

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20520

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20520

7 January 2021

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

https://api.crossref.org/works/10.1002%2FHUMU.20520

7 January 2021

Frontotemporal lobar degeneration: a consensus on clinical diagnostic criteria

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20520

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20520

7 January 2021

Tau is a candidate gene for chromosome 17 frontotemporal dementia

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20520

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20520

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20520

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20520

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20520

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20520

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20520

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20520

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20520

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20520

7 January 2021

novoSNP, a novel computational tool for sequence variation discovery

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20520

7 January 2021

Identifiers

DOI

10.1002/HUMU.20520

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:17436289%20AND%20SRC:MED&resulttype=core&format=json

29 December 2019

1 reference