(Q31047627)

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Zebrafish models for dyskeratosis congenita reveal critical roles of p53 activation contributing to hematopoietic defects through RNA processing

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scholarly article

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Europe PubMed Central

PMC publication ID

23 September 2017

Zebrafish models for dyskeratosis congenita reveal critical roles of p53 activation contributing to hematopoietic defects through RNA processing (English)

1 reference

Europe PubMed Central

PMC publication ID

23 September 2017

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Tumor protein p53

1 reference

GOA release 2020-03-11

dyskeratosis congenita

1 reference

based on heuristic

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author name string

Ying Zhang

1

1 reference

Europe PubMed Central

PMC publication ID

23 September 2017

Kenji Morimoto

2

1 reference

Europe PubMed Central

PMC publication ID

23 September 2017

Nadia Danilova

3

1 reference

Europe PubMed Central

PMC publication ID

23 September 2017

Bo Zhang

4

1 reference

Europe PubMed Central

PMC publication ID

23 September 2017

Shuo Lin

5

1 reference

Europe PubMed Central

PMC publication ID

23 September 2017

language of work or name

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publication date

27 January 2012

1 reference

Europe PubMed Central

PMC publication ID

23 September 2017

1 reference

Europe PubMed Central

PMC publication ID

23 September 2017

7

1 reference

Europe PubMed Central

PMC publication ID

23 September 2017

1

1 reference

Europe PubMed Central

PMC publication ID

23 September 2017

e30188

1 reference

Europe PubMed Central

PMC publication ID

23 September 2017

copyright license

Creative Commons Attribution 4.0 International

27 January 2012

1 reference

April 2022 Public Data File from Crossref

copyright status

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describes a project that uses

1 reference

Europe PubMed Central

11 June 2022

https://www.ebi.ac.uk/europepmc/webservices/rest/PMC3267717/fullTextXML

based on heuristic

inferred from PubMed Central ID database lookup

Differences in disease severity but similar telomere lengths in genetic subgroups of patients with telomerase and shelterin mutations

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3267717

21 June 2018

Dyskeratosis congenita as a disorder of telomere maintenance

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3267717

21 June 2018

Dyskerin is required for tumor cell growth through mechanisms that are independent of its role in telomerase and only partially related to its function in precursor rRNA processing

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3267717

21 June 2018

Disruption of telomerase trafficking by TCAB1 mutation causes dyskeratosis congenita

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3267717

21 June 2018

Mutations in C16orf57 and normal-length telomeres unify a subset of patients with dyskeratosis congenita, poikiloderma with neutropenia and Rothmund–Thomson syndrome

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3267717

21 June 2018

Telomere length and risk of incident cancer and cancer mortality

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3267717

21 June 2018

Box H/ACA small ribonucleoproteins

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3267717

21 June 2018

Dyskerin ablation in mouse liver inhibits rRNA processing and cell division

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3267717

21 June 2018

Association of telomere length with type 2 diabetes, oxidative stress and UCP2 gene variation

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3267717

21 June 2018

Dyskeratosis congenita, stem cells and telomeres

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3267717

21 June 2018

Cancer in dyskeratosis congenita

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3267717

21 June 2018

A non-canonical function of zebrafish telomerase reverse transcriptase is required for developmental hematopoiesis

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3267717

21 June 2018

The identification of zebrafish mutants showing alterations in senescence-associated biomarkers

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3267717

21 June 2018

Mutations in the telomerase component NHP2 cause the premature ageing syndrome dyskeratosis congenita

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3267717

21 June 2018

TINF2, a component of the shelterin telomere protection complex, is mutated in dyskeratosis congenita

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3267717

21 June 2018

Efficient genome-wide mutagenesis of zebrafish genes by retroviral insertions

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3267717

21 June 2018

Telomerase mutations in families with idiopathic pulmonary fibrosis

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3267717

21 June 2018

Perturbation of rRNA synthesis in the bap28 mutation leads to apoptosis mediated by p53 in the zebrafish central nervous system

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3267717

21 June 2018

The many facets of H/ACA ribonucleoproteins

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3267717

21 June 2018

tp53 mutant zebrafish develop malignant peripheral nerve sheath tumors

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3267717

21 June 2018

Zebrafish as a model organism for the identification and characterization of drugs and genes affecting p53 signaling

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3267717

21 June 2018

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3267717

21 June 2018

A telomerase component is defective in the human disease dyskeratosis congenita

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3267717

21 June 2018

minifly, a Drosophila gene required for ribosome biogenesis

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3267717

21 June 2018

Nhp2p and Nop10p are essential for the function of H/ACA snoRNPs

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3267717

21 June 2018

X-linked dyskeratosis congenita is caused by mutations in a highly conserved gene with putative nucleolar functions

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3267717

21 June 2018

A small nucleolar RNP protein is required for pseudouridylation of eukaryotic ribosomal RNAs

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3267717

21 June 2018

Structure of the zebrafish snail1 gene and its expression in wild-type, spadetail and no tail mutant embryos

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3267717

21 June 2018

GAR1 is an essential small nucleolar RNP protein required for pre-rRNA processing in yeast

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3267717

21 June 2018

Telomere shortening and mood disorders: preliminary support for a chronic stress model of accelerated aging

1 reference

https://api.crossref.org/works/10.1371%2FJOURNAL.PONE.0030188

21 January 2018

TCAB1: driving telomerase to Cajal bodies.

1 reference

https://api.crossref.org/works/10.1371%2FJOURNAL.PONE.0030188

21 January 2018

Ribosomal protein S19 deficiency in zebrafish leads to developmental abnormalities and defective erythropoiesis through activation of p53 protein family

1 reference

https://api.crossref.org/works/10.1371%2FJOURNAL.PONE.0030188

21 January 2018

Dyskeratosis congenita and cancer in mice deficient in ribosomal RNA modification

1 reference

https://api.crossref.org/works/10.1371%2FJOURNAL.PONE.0030188

21 January 2018

Birth of the snoRNPs: the evolution of the modification-guide snoRNAs.

1 reference

https://api.crossref.org/works/10.1371%2FJOURNAL.PONE.0030188

21 January 2018

Differential effects of genotoxic stress on both concurrent body growth and gradual senescence in the adult zebrafish

1 reference

https://api.crossref.org/works/10.1371%2FJOURNAL.PONE.0030188

21 January 2018

Ribosomal protein L11 mutation in zebrafish leads to haematopoietic and metabolic defects

1 reference

https://api.crossref.org/works/10.1371%2FJOURNAL.PONE.0030188

21 January 2018

A zebrafish model of dyskeratosis congenita reveals hematopoietic stem cell formation failure resulting from ribosomal protein-mediated p53 stabilization.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3267717

25 November 2018

Lower endothelial progenitor cell number, family history of cardiovascular disease and reduced HDL-cholesterol levels are associated with shorter leukocyte telomere length in healthy young adults

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3267717

25 November 2018

Identifiers

10.1371/JOURNAL.PONE.0030188

1 reference

Europe PubMed Central

PMC publication ID

23 September 2017

2012PLoSO...730188Z

0 references

PMC publication ID

1 reference

Europe PubMed Central

PMC publication ID

23 September 2017

PubMed publication ID

1 reference

Europe PubMed Central

PMC publication ID

23 September 2017

ResearchGate publication ID

0 references

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