(Q34170826)

English

Progranulin transcripts with short and long 5' untranslated regions (UTRs) are differentially expressed via posttranscriptional and translational repression

scientific article

In more languages

Statements

scholarly article

1 reference

Europe PubMed Central

31 July 2017

Progranulin transcripts with short and long 5' untranslated regions (UTRs) are differentially expressed via posttranscriptional and translational repression (English)

1 reference

Europe PubMed Central

31 July 2017

Christian Haass

3

object named as

Christian Haass

0 references

1

object named as

Anja Capell

1 reference

Europe PubMed Central

31 July 2017

author name string

Katrin Fellerer

2

1 reference

Europe PubMed Central

31 July 2017

language of work or name

0 references

publication date

23 July 2014

1 reference

Europe PubMed Central

31 July 2017

Journal of Biological Chemistry

1 reference

Europe PubMed Central

31 July 2017

289

1 reference

Europe PubMed Central

31 July 2017

37

1 reference

Europe PubMed Central

31 July 2017

25879-25889

1 reference

Europe PubMed Central

31 July 2017

A mutation in the 5'-UTR of GRN gene associated with frontotemporal lobar degeneration: phenotypic variability and possible pathogenetic mechanisms

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4162188

28 July 2018

Gene expression regulation by upstream open reading frames and human disease

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4162188

28 July 2018

Mutations in prion-like domains in hnRNPA2B1 and hnRNPA1 cause multisystem proteinopathy and ALS

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4162188

28 July 2018

Mechanisms of granulin deficiency: lessons from cellular and animal models

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4162188

28 July 2018

Strikingly different clinicopathological phenotypes determined by progranulin-mutation dosage

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4162188

28 July 2018

Rescue of progranulin deficiency associated with frontotemporal lobar degeneration by alkalizing reagents and inhibition of vacuolar ATPase.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4162188

28 July 2018

Sortilin-mediated endocytosis determines levels of the frontotemporal dementia protein, progranulin.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4162188

28 July 2018

Expression of the anti-amyloidogenic secretase ADAM10 is suppressed by its 5'-untranslated region

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4162188

28 July 2018

The granulin gene family: from cancer to dementia

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4162188

28 July 2018

Upstream open reading frames cause widespread reduction of protein expression and are polymorphic among humans

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4162188

28 July 2018

Mutations in FUS, an RNA processing protein, cause familial amyotrophic lateral sclerosis type 6

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4162188

28 July 2018

TDP-43 mutations in familial and sporadic amyotrophic lateral sclerosis

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4162188

28 July 2018

Progranulin mutations and amyotrophic lateral sclerosis or amyotrophic lateral sclerosis-frontotemporal dementia phenotypes

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4162188

28 July 2018

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4162188

28 July 2018

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4162188

28 July 2018

Expression of the Alzheimer protease BACE1 is suppressed via its 5'-untranslated region

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4162188

28 July 2018

Frontotemporal dementia.

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M114.560128

21 January 2018

The prevalence of frontotemporal dementia

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M114.560128

21 January 2018

Klotho as a potential biomarker and therapy for acute kidney injury

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M114.560128

21 January 2018

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

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M114.560128

21 January 2018

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

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M114.560128

21 January 2018

Genetic variability in progranulin contributes to risk for clinically diagnosed Alzheimer disease

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M114.560128

21 January 2018

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

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M114.560128

21 January 2018

Molecular characterization of novel progranulin (GRN) mutations in frontotemporal dementia

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M114.560128

21 January 2018

Point mutations define a sequence flanking the AUG initiator codon that modulates translation by eukaryotic ribosomes

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M114.560128

21 January 2018

Mutation of the CDKN2A 5' UTR creates an aberrant initiation codon and predisposes to melanoma

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M114.560128

21 January 2018

An activating splice donor mutation in the thrombopoietin gene causes hereditary thrombocythaemia.

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M114.560128

21 January 2018

Loss-of-function mutations of an inhibitory upstream ORF in the human hairless transcript cause Marie Unna hereditary hypotrichosis

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M114.560128

21 January 2018

Phosphorylation of the translation initiation factor eIF2alpha increases BACE1 levels and promotes amyloidogenesis

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M114.560128

21 January 2018

Suberoylanilide hydroxamic acid (vorinostat) up-regulates progranulin transcription: rational therapeutic approach to frontotemporal dementia

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M114.560128

21 January 2018

The mechanism of eukaryotic translation initiation and principles of its regulation

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M114.560128

21 January 2018

Mutations in the FUS/TLS gene on chromosome 16 cause familial amyotrophic lateral sclerosis

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M114.560128

21 January 2018

Advances in understanding the molecular basis of frontotemporal dementia

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4162188

28 October 2018

Identifiers

10.1074/JBC.M114.560128

1 reference

Europe PubMed Central

31 July 2017

1 reference

Europe PubMed Central

31 July 2017

1 reference

Europe PubMed Central

31 July 2017

Sitelinks

Wikipedia(0 entries)

Wikibooks(0 entries)

Wikinews(0 entries)

Wikiquote(0 entries)

Wikisource(0 entries)

Wikiversity(0 entries)

Wikivoyage(0 entries)

Wiktionary(0 entries)

Multilingual sites(0 entries)

Retrieved from "https://www.wikidata.org/w/index.php?title=Q34170826&oldid=1541373110"