Variations in the progranulin gene affect global gene expression in frontotemporal lobar degeneration (Q33978879)

30 July 2017

Variations in the progranulin gene affect global gene expression in frontotemporal lobar degeneration (English)

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frontotemporal lobar degeneration

30 July 2017

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9

John Q Trojanowski

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30 July 2017

7

Murray Grossman

1 reference

30 July 2017

3

Joshua B Plotkin

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30 July 2017

Alice S Chen-Plotkin

1

1 reference

30 July 2017

Felix Geser

2

1 reference

30 July 2017

Chris M Clark

4

1 reference

30 July 2017

Linda K Kwong

5

1 reference

30 July 2017

Wuxing Yuan

6

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30 July 2017

Vivianna M Van Deerlin

8

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30 July 2017

Virginia M-Y Lee

10

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30 July 2017

25 January 2008

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30 July 2017

Human Molecular Genetics

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30 July 2017

17

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30 July 2017

10

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30 July 2017

1349-1362

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describes a project that uses

30 July 2017

limma

1 reference

22 June 2022

https://europepmc.org/article/PMC/2900863

inferred from PubMed Central ID database lookup

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TDP-43 in familial and sporadic frontotemporal lobar degeneration with ubiquitin inclusions

5 July 2018

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Neuropathologic diagnostic and nosologic criteria for frontotemporal lobar degeneration: consensus of the Consortium for Frontotemporal Lobar Degeneration

5 July 2018

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Progranulin and frontotemporal lobar degeneration

5 July 2018

1 reference

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Gene expression analysis of frontotemporal lobar degeneration of the motor neuron disease type with ubiquitinated inclusions.

5 July 2018

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TDP-43 proteinopathy: the neuropathology underlying major forms of sporadic and familial frontotemporal lobar degeneration and motor neuron disease

5 July 2018

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5 July 2018

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

5 July 2018

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5 July 2018

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A century-old debate on protein aggregation and neurodegeneration enters the clinic

5 July 2018

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

5 July 2018

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5 July 2018

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

5 July 2018

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

5 July 2018

1 reference

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Characteristics of frontotemporal dementia patients with a Progranulin mutation

5 July 2018

1 reference

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The MicroArray Quality Control (MAQC) project shows inter- and intraplatform reproducibility of gene expression measurements

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2900863

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

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2900863

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

5 July 2018

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

5 July 2018

1 reference

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5 July 2018

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A protein-protein interaction network for human inherited ataxias and disorders of Purkinje cell degeneration

5 July 2018

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Linear models and empirical bayes methods for assessing differential expression in microarray experiments

5 July 2018

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Regional and cellular gene expression changes in human Huntington's disease brain

5 July 2018

1 reference

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5 July 2018

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From genomics to chemical genomics: new developments in KEGG

5 July 2018

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Depletion of TDP 43 overrides the need for exonic and intronic splicing enhancers in the human apoA-II gene.

5 July 2018

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TDP-43 binds heterogeneous nuclear ribonucleoprotein A/B through its C-terminal tail: an important region for the inhibition of cystic fibrosis transmembrane conductance regulator exon 9 splicing

5 July 2018

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Experimental design and low-level analysis of microarray data

5 July 2018

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5 July 2018

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Oxidative stress in neurodegeneration: cause or consequence?

5 July 2018

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Molecular pathways to neurodegeneration

5 July 2018

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5 July 2018

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Incipient Alzheimer's disease: microarray correlation analyses reveal major transcriptional and tumor suppressor responses

5 July 2018

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Structural diversity and functional implications of the eukaryotic TDP gene family

5 July 2018

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5 July 2018

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Summaries of Affymetrix GeneChip probe level data

5 July 2018

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MAPK signaling in neurodegeneration: influences of flavonoids and of nitric oxide

5 July 2018

1 reference

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The prevalence of frontotemporal dementia

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2900863

Analysis of Relative Gene Expression Data Using Real-Time Quantitative PCR and the 2−ΔΔCT Method

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2900863

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

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2900863

Characterization and functional implications of the RNA binding properties of nuclear factor TDP-43, a novel splicing regulator of CFTR exon 9

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2900863

Nuclear factor TDP-43 and SR proteins promote in vitro and in vivo CFTR exon 9 skipping

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2900863

Gene ontology: tool for the unification of biology

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2900863

Frontotemporal lobar degeneration: a consensus on clinical diagnostic criteria

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2900863

A mutant neurofilament subunit causes massive, selective motor neuron death: implications for the pathogenesis of human motor neuron disease

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2900863

Cloning and characterization of a novel cellular protein, TDP-43, that binds to human immunodeficiency virus type 1 TAR DNA sequence motifs

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2900863

Fine structural observations of neurofilamentous changes in amyotrophic lateral sclerosis

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2900863

Frontotemporal lobar degeneration with motor neuron disease-type inclusions predominates in 76 cases of frontotemporal degeneration.

5 July 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDN023

Pathological TDP-43 distinguishes sporadic amyotrophic lateral sclerosis from amyotrophic lateral sclerosis with SOD1 mutations.

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDN023

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.

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDN023

Human, Drosophila, and C.elegans TDP43: nucleic acid binding properties and splicing regulatory function

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDN023

Cerebral gene expression profiles in sporadic Creutzfeldt-Jakob disease.

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDN023

The commonality of protein interaction networks determined in neurodegenerative disorders (NDDs).

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDN023

Evidence of multisystem disorder in whole-brain map of pathological TDP-43 in amyotrophic lateral sclerosis

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDN023

The neuropathology of frontotemporal lobar degeneration caused by mutations in the progranulin gene.

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDN023

TDP-43 immunoreactivity in neuronal inclusions in familial amyotrophic lateral sclerosis with or without SOD1 gene mutation.

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDN023

A novel progranulin mutation associated with variable clinical presentation and tau, TDP43 and alpha-synuclein pathology.

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDN023

Clinical, genetic, and pathologic characteristics of patients with frontotemporal dementia and progranulin mutations.

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDN023

Increased expression of neurofilament subunit NF-L produces morphological alterations that resemble the pathology of human motor neuron disease

21 January 2018

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/18223198

12 December 2020

inferred from PubMed ID database lookup

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

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/18223198

12 December 2020

inferred from PubMed ID database lookup

TDP-43 gene analysis in frontotemporal lobar degeneration

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/18223198

12 December 2020

inferred from PubMed ID database lookup

Identifiers

DOI

10.1093/HMG/DDN023

1 reference

30 July 2017

1 reference

30 July 2017

1 reference