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Genetics of frontotemporal lobar degeneration
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scholarly article
1 reference
stated in
Europe PubMed Central
PMC publication ID
3039162
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:21369419%20AND%20SRC:MED&resulttype=core&format=json
retrieved
24 January 2020
review article
1 reference
stated in
Europe PubMed Central
title
Genetics of frontotemporal lobar degeneration
(English)
1 reference
stated in
Europe PubMed Central
PMC publication ID
3039162
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:21369419%20AND%20SRC:MED&resulttype=core&format=json
retrieved
24 January 2020
main subject
frontotemporal lobar degeneration
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based on heuristic
inferred from title
author
P S Mathuranath
series ordinal
3
1 reference
stated in
Europe PubMed Central
PMC publication ID
3039162
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:21369419%20AND%20SRC:MED&resulttype=core&format=json
retrieved
24 January 2020
author name string
P M Aswathy
series ordinal
1
1 reference
stated in
Europe PubMed Central
PMC publication ID
3039162
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:21369419%20AND%20SRC:MED&resulttype=core&format=json
retrieved
24 January 2020
P S Jairani
series ordinal
2
1 reference
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Europe PubMed Central
PMC publication ID
3039162
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:21369419%20AND%20SRC:MED&resulttype=core&format=json
retrieved
24 January 2020
publication date
1 December 2010
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PMC publication ID
3039162
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:21369419%20AND%20SRC:MED&resulttype=core&format=json
retrieved
24 January 2020
published in
Annals of Indian Academy of Neurology
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stated in
Europe PubMed Central
PMC publication ID
3039162
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:21369419%20AND%20SRC:MED&resulttype=core&format=json
retrieved
24 January 2020
volume
13
1 reference
stated in
Europe PubMed Central
PMC publication ID
3039162
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:21369419%20AND%20SRC:MED&resulttype=core&format=json
retrieved
24 January 2020
issue
Suppl 2
1 reference
stated in
Europe PubMed Central
PMC publication ID
3039162
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:21369419%20AND%20SRC:MED&resulttype=core&format=json
retrieved
24 January 2020
page(s)
S55-62
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Europe PubMed Central
PMC publication ID
3039162
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:21369419%20AND%20SRC:MED&resulttype=core&format=json
retrieved
24 January 2020
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7 July 2018
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7 July 2018
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7 July 2018
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7 July 2018
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7 July 2018
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7 July 2018
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7 July 2018
Localization of disinhibition-dementia-parkinsonism-amyotrophy complex to 17q21-22.
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7 July 2018
Fetal-type phosphorylation of the tau in paired helical filaments
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7 July 2018
Isolation and sequence of the granulin precursor cDNA from human bone marrow reveals tandem cysteine-rich granulin domains
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7 July 2018
Structure and novel exons of the human tau gene
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7 July 2018
Purification of tau, a microtubule-associated protein that induces assembly of microtubules from purified tubulin
1 reference
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7 July 2018
The CST3 B haplotype is associated with frontotemporal lobar degeneration.
1 reference
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PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3039162
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27 October 2018
The NOS3 G894T (Glu298Asp) polymorphism is a risk factor for frontotemporal lobar degeneration
1 reference
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PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3039162
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27 October 2018
Atypical frontotemporal lobar degeneration with ubiquitin-positive, TDP-43-negative neuronal inclusions
1 reference
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PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3039162
retrieved
27 October 2018
Phenotype variability in progranulin mutation carriers: a clinical, neuropsychological, imaging and genetic study.
1 reference
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PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3039162
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27 October 2018
Phenotypic variability associated with progranulin haploinsufficiency in patients with the common 1477C-->T (Arg493X) mutation: an international initiative.
1 reference
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PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3039162
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27 October 2018
TDP-43 in the ubiquitin pathology of frontotemporal dementia with VCP gene mutations
1 reference
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PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3039162
retrieved
27 October 2018
The role of tau phosphorylation and cleavage in neuronal cell death
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PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3039162
retrieved
27 October 2018
The neuropathology of frontotemporal lobar degeneration caused by mutations in the progranulin gene
1 reference
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PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3039162
retrieved
27 October 2018
An R5L tau mutation in a subject with a progressive supranuclear palsy phenotype
1 reference
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PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3039162
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27 October 2018
Frontotemporal dementia with ubiquitinated cytoplasmic and intranuclear inclusions.
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3039162
retrieved
27 October 2018
5' splice site mutations in tau associated with the inherited dementia FTDP-17 affect a stem-loop structure that regulates alternative splicing of exon 10.
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3039162
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27 October 2018
Genetic Variability in CHMP2B and Frontotemporal Dementia
1 reference
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PubMed Central
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https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3039162
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9 December 2018
Frontotemporal lobar degeneration and ubiquitin immunohistochemistry
1 reference
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PubMed
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https://pubmed.ncbi.nlm.nih.gov/21369419
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12 December 2020
based on heuristic
inferred from PubMed ID database lookup
LRRK2 mutations and Parkinsonism
1 reference
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PubMed
reference URL
https://pubmed.ncbi.nlm.nih.gov/21369419
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12 December 2020
based on heuristic
inferred from PubMed ID database lookup
Novel ubiquitin neuropathology in frontotemporal dementia with valosin-containing protein gene mutations
1 reference
stated in
PubMed
reference URL
https://pubmed.ncbi.nlm.nih.gov/21369419
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12 December 2020
based on heuristic
inferred from PubMed ID database lookup
Dementia lacking distinctive histology (DLDH) revisited
1 reference
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PubMed
reference URL
https://pubmed.ncbi.nlm.nih.gov/21369419
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12 December 2020
based on heuristic
inferred from PubMed ID database lookup
Progranulin null mutations in both sporadic and familial frontotemporal dementia
1 reference
stated in
PubMed
reference URL
https://pubmed.ncbi.nlm.nih.gov/21369419
retrieved
12 December 2020
based on heuristic
inferred from PubMed ID database lookup
A Reassessment of the Neuropathology of Frontotemporal Dementia Linked to Chromosome 3
1 reference
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PubMed
reference URL
https://pubmed.ncbi.nlm.nih.gov/21369419
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12 December 2020
based on heuristic
inferred from PubMed ID database lookup
Neuronal nitric oxide synthase C276T polymorphism increases the risk for frontotemporal lobar degeneration
1 reference
stated in
PubMed
reference URL
https://pubmed.ncbi.nlm.nih.gov/21369419
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12 December 2020
based on heuristic
inferred from PubMed ID database lookup
Frontotemporal lobar degeneration: toward the end of conFUSion
1 reference
stated in
PubMed
reference URL
https://pubmed.ncbi.nlm.nih.gov/21369419
retrieved
12 December 2020
based on heuristic
inferred from PubMed ID database lookup
Clinical and neuropathological criteria for frontotemporal dementia. The Lund and Manchester Groups
1 reference
stated in
PubMed
reference URL
https://pubmed.ncbi.nlm.nih.gov/21369419
retrieved
12 December 2020
based on heuristic
inferred from PubMed ID database lookup
Granulin mutations associated with frontotemporal lobar degeneration and related disorders: an update
1 reference
stated in
PubMed
reference URL
https://pubmed.ncbi.nlm.nih.gov/21369419
retrieved
12 December 2020
based on heuristic
inferred from PubMed ID database lookup
Identifiers
DOI
10.4103/0972-2327.74246
1 reference
stated in
Europe PubMed Central
PMC publication ID
3039162
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:21369419%20AND%20SRC:MED&resulttype=core&format=json
retrieved
24 January 2020
PMC publication ID
3039162
1 reference
stated in
Europe PubMed Central
PMC publication ID
3039162
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:21369419%20AND%20SRC:MED&resulttype=core&format=json
retrieved
24 January 2020
PubMed publication ID
21369419
1 reference
stated in
Europe PubMed Central
PMC publication ID
3039162
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:21369419%20AND%20SRC:MED&resulttype=core&format=json
retrieved
24 January 2020
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