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Telomerase and idiopathic pulmonary fibrosis
scientific article
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instance of
scholarly article
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stated in
PubMed
title
Telomerase and idiopathic pulmonary fibrosis
(English)
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stated in
PubMed
main subject
idiopathy
0 references
pulmonary fibrosis
1 reference
based on heuristic
inferred from title
idiopathic pulmonary fibrosis
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based on heuristic
inferred from title
author
Mary Armanios
series ordinal
1
object named as
Mary Armanios
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stated in
Crossref
language of work or name
English
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stated in
PubMed
publication date
1 February 2012
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stated in
PubMed
published in
Mutation Research
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stated in
PubMed
volume
730
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PubMed
issue
1-2
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PubMed
page(s)
52-8
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PubMed
cites work
It all comes together at the ends: telomerase structure, function, and biogenesis
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=3292861
retrieved
7 April 2017
TINF2 mutations result in very short telomeres: analysis of a large cohort of patients with dyskeratosis congenita and related bone marrow failure syndromes
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=3292861
retrieved
7 April 2017
TINF2, a component of the shelterin telomere protection complex, is mutated in dyskeratosis congenita
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=3292861
retrieved
7 April 2017
Haploinsufficiency of telomerase reverse transcriptase leads to anticipation in autosomal dominant dyskeratosis congenita
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=3292861
retrieved
7 April 2017
A telomerase component is defective in the human disease dyskeratosis congenita
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=3292861
retrieved
7 April 2017
X-linked dyskeratosis congenita is caused by mutations in a highly conserved gene with putative nucleolar functions
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=3292861
retrieved
7 April 2017
Q28215495
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=3292861
retrieved
7 April 2017
The RNA component of telomerase is mutated in autosomal dominant dyskeratosis congenita
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=3292861
retrieved
7 April 2017
Secondary structure of vertebrate telomerase RNA
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=3292861
retrieved
7 April 2017
Identification of a specific telomere terminal transferase activity in Tetrahymena extracts
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=3292861
retrieved
7 April 2017
Telomerase mutations in families with idiopathic pulmonary fibrosis
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=3292861
retrieved
7 April 2017
A box H/ACA small nucleolar RNA-like domain at the human telomerase RNA 3' end
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=3292861
retrieved
7 April 2017
Essential role of mouse telomerase in highly proliferative organs
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=3292861
retrieved
7 April 2017
Telomere shortening and tumor formation by mouse cells lacking telomerase RNA
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=3292861
retrieved
7 April 2017
A telomeric sequence in the RNA of Tetrahymena telomerase required for telomere repeat synthesis
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=3292861
retrieved
7 April 2017
Telomere length is a determinant of emphysema susceptibility.
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=3292861
retrieved
28 September 2017
Dyskeratosis congenita as a disorder of telomere maintenance
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=3292861
retrieved
28 September 2017
Genetics of leukocyte telomere length and its role in atherosclerosis
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=3292861
retrieved
28 September 2017
Ancestral mutation in telomerase causes defects in repeat addition processivity and manifests as familial pulmonary fibrosis.
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=3292861
retrieved
28 September 2017
Phenotypes in mTERT⁺/⁻ and mTERT⁻/⁻ mice are due to short telomeres, not telomere-independent functions of telomerase reverse transcriptase
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=3292861
retrieved
28 September 2017
Syndrome complex of bone marrow failure and pulmonary fibrosis predicts germline defects in telomerase
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=3292861
retrieved
28 September 2017
Short telomeres compromise β-cell signaling and survival
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=3292861
retrieved
28 September 2017
Decreased dyskerin levels as a mechanism of telomere shortening in X-linked dyskeratosis congenita
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=3292861
retrieved
28 September 2017
Lung volumes and emphysema in smokers with interstitial lung abnormalities
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=3292861
retrieved
28 September 2017
Mechanisms of trinucleotide repeat instability during human development
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=3292861
retrieved
28 September 2017
Telomere lengths, pulmonary fibrosis and telomerase (TERT) mutations
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=3292861
retrieved
28 September 2017
Short telomeres are sufficient to cause the degenerative defects associated with aging
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=3292861
retrieved
28 September 2017
A spectrum of severe familial liver disorders associate with telomerase mutations
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=3292861
retrieved
28 September 2017
Defining the pathogenic role of telomerase mutations in myelodysplastic syndrome and acute myeloid leukemia.
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=3292861
retrieved
28 September 2017
Dyskeratosis congenita: the first NIH clinical research workshop
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=3292861
retrieved
28 September 2017
Syndromes of telomere shortening
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=3292861
retrieved
28 September 2017
TERC and TERT gene mutations in patients with bone marrow failure and the significance of telomere length measurements.
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=3292861
retrieved
28 September 2017
Short telomeres are a risk factor for idiopathic pulmonary fibrosis
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=3292861
retrieved
28 September 2017
Telomere shortening in familial and sporadic pulmonary fibrosis
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=3292861
retrieved
28 September 2017
Dyskeratosis congenita: a genetic disorder of many faces
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=3292861
retrieved
28 September 2017
Adult-onset pulmonary fibrosis caused by mutations in telomerase
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=3292861
retrieved
28 September 2017
State of the art. Cellular and molecular mechanisms of alveolar destruction in emphysema: an evolutionary perspective
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=3292861
retrieved
28 September 2017
Incidence and prevalence of idiopathic pulmonary fibrosis
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=3292861
retrieved
28 September 2017
Short telomeres, even in the presence of telomerase, limit tissue renewal capacity
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=3292861
retrieved
28 September 2017
Combined pulmonary fibrosis and emphysema: a distinct underrecognised entity.
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=3292861
retrieved
28 September 2017
Clinical and pathologic features of familial interstitial pneumonia
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=3292861
retrieved
28 September 2017
Mutations in TERT, the gene for telomerase reverse transcriptase, in aplastic anemia
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=3292861
retrieved
28 September 2017
Telomerase RNA structure and function: implications for dyskeratosis congenita.
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=3292861
retrieved
28 September 2017
Low-intensity hematopoietic stem-cell transplantation across human leucocyte antigen barriers in dyskeratosis congenita
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=3292861
retrieved
28 September 2017
The telomerase reverse transcriptase is limiting and necessary for telomerase function in vivo.
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=3292861
retrieved
28 September 2017
Dyskeratosis congenita in all its forms
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=3292861
retrieved
28 September 2017
The telomere terminal transferase of Tetrahymena is a ribonucleoprotein enzyme with two kinds of primer specificity
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=3292861
retrieved
28 September 2017
Disease-specific hematopoietic cell transplantation: nonmyeloablative conditioning regimen for dyskeratosis congenita.
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=3292861
retrieved
28 November 2018
Role of diabetes mellitus and gastro-oesophageal reflux in the aetiology of idiopathic pulmonary fibrosis
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=3292861
retrieved
28 November 2018
Disease anticipation is associated with progressive telomere shortening in families with dyskeratosis congenita due to mutations in TERC.
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=3292861
retrieved
28 November 2018
Mutations of the human telomerase RNA gene (TERC) in aplastic anemia and myelodysplastic syndrome
1 reference
stated in
PubMed
reference URL
https://pubmed.ncbi.nlm.nih.gov/22079513
retrieved
12 December 2020
based on heuristic
inferred from PubMed ID database lookup
Pulmonary fibrosis in families
1 reference
stated in
PubMed
reference URL
https://pubmed.ncbi.nlm.nih.gov/22079513
retrieved
12 December 2020
based on heuristic
inferred from PubMed ID database lookup
Longevity, Stress Response, and Cancer in Aging Telomerase-Deficient Mice
1 reference
stated in
PubMed
reference URL
https://pubmed.ncbi.nlm.nih.gov/22079513
retrieved
12 December 2020
based on heuristic
inferred from PubMed ID database lookup
Dyskeratosis congenita: Advances in the understanding of the telomerase defect and the role of stem cell transplantation
1 reference
stated in
PubMed
reference URL
https://pubmed.ncbi.nlm.nih.gov/22079513
retrieved
12 December 2020
based on heuristic
inferred from PubMed ID database lookup
Update in lung transplantation 2008
1 reference
stated in
PubMed
reference URL
https://pubmed.ncbi.nlm.nih.gov/22079513
retrieved
12 December 2020
based on heuristic
inferred from PubMed ID database lookup
Risk factors for idiopathic pulmonary fibrosis in a Mexican population. A case-control study
1 reference
stated in
PubMed
reference URL
https://pubmed.ncbi.nlm.nih.gov/22079513
retrieved
12 December 2020
based on heuristic
inferred from PubMed ID database lookup
Identifiers
DOI
10.1016/J.MRFMMM.2011.10.013
1 reference
stated in
Consolidated OpenCitations Corpus – April 2017
OpenCitations bibliographic resource ID
490422
OpenCitations bibliographic resource ID
490422
1 reference
stated in
Consolidated OpenCitations Corpus – April 2017
OpenCitations bibliographic resource ID
490422
PMC publication ID
3292861
1 reference
stated in
Consolidated OpenCitations Corpus – April 2017
OpenCitations bibliographic resource ID
490422
PubMed publication ID
22079513
1 reference
stated in
Consolidated OpenCitations Corpus – April 2017
OpenCitations bibliographic resource ID
490422
ResearchGate publication ID
51795099
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