(Q34555400)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:21178100%20AND%20SRC:MED&resulttype=core&format=json

18 January 2020

title

TMEM106B regulates progranulin levels and the penetrance of FTLD in GRN mutation carriers (English)

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:21178100%20AND%20SRC:MED&resulttype=core&format=json

18 January 2020

35

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:21178100%20AND%20SRC:MED&resulttype=core&format=json

18 January 2020

Roberta Ghidoni

9

1 reference

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18 January 2020

Luisa Benussi

10

1 reference

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18 January 2020

Elizabeth Finger

12

1 reference

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18 January 2020

25

C L White 3rd

1 reference

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18 January 2020

Giuliano Binetti

30

1 reference

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18 January 2020

23

D S Knopman

1 reference

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18 January 2020

36

R C Petersen

1 reference

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18 January 2020

33

B F Boeve

1 reference

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18 January 2020

19

T G Beach

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:21178100%20AND%20SRC:MED&resulttype=core&format=json

18 January 2020

29

Z K Wszolek

1 reference

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18 January 2020

Minerva M Carrasquillo

2

object named as

M M Carrasquillo

1 reference

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18 January 2020

20

M Mesulam

1 reference

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18 January 2020

28

E H Bigio

1 reference

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18 January 2020

author name string

N Finch

1

1 reference

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18 January 2020

M Baker

3

1 reference

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18 January 2020

N J Rutherford

4

1 reference

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18 January 2020

G Coppola

5

1 reference

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18 January 2020

M Dejesus-Hernandez

6

1 reference

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18 January 2020

R Crook

7

1 reference

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18 January 2020

T Hunter

8

1 reference

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18 January 2020

J Crook

11

1 reference

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18 January 2020

K J Hantanpaa

13

1 reference

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18 January 2020

A M Karydas

14

1 reference

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18 January 2020

P Sengdy

15

1 reference

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18 January 2020

J Gonzalez

16

1 reference

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18 January 2020

W W Seeley

17

1 reference

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18 January 2020

N Johnson

18

1 reference

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18 January 2020

G Forloni

21

1 reference

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18 January 2020

A Kertesz

22

1 reference

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18 January 2020

R Uitti

24

1 reference

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18 January 2020

R Caselli

26

1 reference

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18 January 2020

C Lippa

27

1 reference

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18 January 2020

I R Mackenzie

31

1 reference

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18 January 2020

B L Miller

32

1 reference

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18 January 2020

S G Younkin

34

1 reference

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18 January 2020

N R Graff-Radford

37

1 reference

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18 January 2020

D H Geschwind

38

1 reference

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18 January 2020

R Rademakers

39

1 reference

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18 January 2020

language of work or name

English

0 references

publication date

22 December 2010

1 reference

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18 January 2020

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:21178100%20AND%20SRC:MED&resulttype=core&format=json

18 January 2020

volume

76

1 reference

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18 January 2020

issue

5

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:21178100%20AND%20SRC:MED&resulttype=core&format=json

18 January 2020

page(s)

467-474

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:21178100%20AND%20SRC:MED&resulttype=core&format=json

Accelerated lipofuscinosis and ubiquitination in granulin knockout mice suggest a role for progranulin in successful aging

18 January 2020

cites work

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3034409

Common variants at 7p21 are associated with frontotemporal lobar degeneration with TDP-43 inclusions

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3034409

Prediction of pathology in primary progressive language and speech disorders.

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3034409

Plasma progranulin levels predict progranulin mutation status in frontotemporal dementia patients and asymptomatic family members

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3034409

Genetic variation in PCDH11X is associated with susceptibility to late-onset Alzheimer's disease

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3034409

Low plasma progranulin levels predict progranulin mutations in frontotemporal lobar degeneration.

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3034409

Common variation in the miR-659 binding-site of GRN is a major risk factor for TDP43-positive frontotemporal dementia

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3034409

Gene expression study on peripheral blood identifies progranulin mutations

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3034409

Progranulin functions as a neurotrophic factor to regulate neurite outgrowth and enhance neuronal survival

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3034409

Loss of progranulin function in frontotemporal lobar degeneration

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3034409

The molecular genetics and neuropathology of frontotemporal lobar degeneration: recent developments

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3034409

The genetics of frontotemporal lobar degeneration

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3034409

PLINK: a tool set for whole-genome association and population-based linkage analyses

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3034409

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

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3034409

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

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3034409

Frontotemporal dementia: clinicopathological correlations

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3034409

Clinical and pathological characterization of progressive aphasia

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3034409

Clinicopathological correlates in frontotemporal dementia

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3034409

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

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3034409

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

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3034409

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

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3034409

Frontotemporal lobar degeneration: a consensus on clinical diagnostic criteria

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3034409

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

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3034409

Familial multiple system tauopathy with presenile dementia: a disease with abundant neuronal and glial tau filaments

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3034409

Missense mutations in the progranulin gene linked to frontotemporal lobar degeneration with ubiquitin-immunoreactive inclusions reduce progranulin production and secretion.

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3034409

Tau is a candidate gene for chromosome 17 frontotemporal dementia

27 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3034409

10.1212/WNL.0B013E31820A0E3B

27 October 2018

Identifiers

DOI

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:21178100%20AND%20SRC:MED&resulttype=core&format=json

18 January 2020

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:21178100%20AND%20SRC:MED&resulttype=core&format=json

18 January 2020

PubMed publication ID

21178100

1 reference