(Q79573361)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:17228326%20AND%20SRC:MED&resulttype=core&format=json

24 December 2019

title

Progranulin mutations in Dutch familial frontotemporal lobar degeneration (English)

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:17228326%20AND%20SRC:MED&resulttype=core&format=json

frontotemporal lobar degeneration

24 December 2019

main subject

1 reference

10

1 reference

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24 December 2019

author name string

Iraad F Bronner

1

1 reference

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24 December 2019

Patrizia Rizzu

2

1 reference

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24 December 2019

Harro Seelaar

3

1 reference

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24 December 2019

Saskia E van Mil

4

1 reference

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24 December 2019

Burcu Anar

5

1 reference

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24 December 2019

Asma Azmani

6

1 reference

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24 December 2019

Laura Donker Kaat

7

1 reference

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24 December 2019

Sonia Rosso

8

1 reference

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24 December 2019

Peter Heutink

9

1 reference

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24 December 2019

publication date

17 January 2007

1 reference

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European Journal of Human Genetics

24 December 2019

published in

1 reference

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24 December 2019

volume

15

1 reference

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24 December 2019

issue

3

1 reference

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24 December 2019

page(s)

369-374

1 reference

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https://scigraph.springernature.com/pub.10.1038/sj.ejhg.5201772

24 December 2019

exact match

0 references

cites work

Frontotemporal lobar degeneration: a consensus on clinical diagnostic criteria

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201772

7 January 2021

Frontotemporal dementia: clinicopathological correlations

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201772

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201772

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201772

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201772

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201772

7 January 2021

Linkage of familial amyotrophic lateral sclerosis with frontotemporal dementia to chromosome 9q21-q22

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201772

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/10.1038%2FSJ.EJHG.5201772

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201772

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201772

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/10.1038%2FSJ.EJHG.5201772

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201772

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201772

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201772

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201772

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201772

7 January 2021

Granulin and granulin repeats interact with the Tat.P-TEFb complex and inhibit Tat transactivation.

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201772

7 January 2021

A 30-residue fragment of the carp granulin-1 protein folds into a stack of two beta-hairpins similar to that found in the native protein

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201772

7 January 2021

Design and solution structure of a well-folded stack of two beta-hairpins based on the amino-terminal fragment of human granulin A

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201772

7 January 2021

Solution structures of a 30-residue amino-terminal domain of the carp granulin-1 protein and its amino-terminally truncated 3-30 subfragment: implications for the conformational stability of the stack of two beta-hairpins

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201772

7 January 2021

Frontotemporal dementia

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201772

7 January 2021

Identifiers

DOI

10.1038/SJ.EJHG.5201772

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:17228326%20AND%20SRC:MED&resulttype=core&format=json

24 December 2019

1 reference