A spectrum of severe familial liver disorders associate with telomerase mutations (Q30913791)

20 August 2017

A spectrum of severe familial liver disorders associate with telomerase mutations (English)

1 reference

20 August 2017

Rodrigo T Calado

1

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David E. Kleiner

object named as

David E Kleiner

3

0 references

Stephen Chanock

7

object named as

Stephen J Chanock

1 reference

20 August 2017

Joshua A Regal

2

1 reference

20 August 2017

David S Schrump

4

1 reference

20 August 2017

Nathan R Peterson

5

1 reference

20 August 2017

Veronica Pons

6

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20 August 2017

Peter M Lansdorp

8

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20 August 2017

Neal S Young

9

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20 August 2017

language of work or name

English

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publication date

20 November 2009

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20 August 2017

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20 August 2017

4

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20 August 2017

e7926

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20 August 2017

11

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Creative Commons CC0 License

20 August 2017

start time

20 November 2009

1 reference

April 2022 Public Data File from Crossref

copyright status

copyrighted, dedicated to the public domain by copyright holder

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cites work

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1 reference

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Cancer in dyskeratosis congenita

21 June 2018

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Sequence variants at the TERT-CLPTM1L locus associate with many cancer types

21 June 2018

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Constitutional hypomorphic telomerase mutations in patients with acute myeloid leukemia

21 June 2018

1 reference

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Lung cancer susceptibility locus at 5p15.33

21 June 2018

1 reference

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Common 5p15.33 and 6p21.33 variants influence lung cancer risk

21 June 2018

1 reference

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Short telomeres are a risk factor for idiopathic pulmonary fibrosis

21 June 2018

1 reference

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21 June 2018

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Telomere maintenance and human bone marrow failure

21 June 2018

1 reference

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Telomere length, stem cells and aging

21 June 2018

1 reference

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Adult-onset pulmonary fibrosis caused by mutations in telomerase

21 June 2018

1 reference

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Flow cytometry and FISH to measure the average length of telomeres (flow FISH).

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2775683

Telomerase mutations in families with idiopathic pulmonary fibrosis

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2775683

Common and unique mechanisms regulate fibrosis in various fibroproliferative diseases

21 June 2018

1 reference

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Nodular regenerative hyperplasia associated to aplastic anemia: a case report and literature review.

21 June 2018

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Hepatocytes with extensive telomere deprotection and fusion remain viable and regenerate liver mass through endoreduplication

21 June 2018

1 reference

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Haploinsufficiency of telomerase reverse transcriptase leads to anticipation in autosomal dominant dyskeratosis congenita

21 June 2018

1 reference

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Mutations in TERT, the gene for telomerase reverse transcriptase, in aplastic anemia

21 June 2018

1 reference

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SNP500Cancer: a public resource for sequence validation and assay development for genetic variation in candidate genes

21 June 2018

1 reference

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The RNA component of telomerase is mutated in autosomal dominant dyskeratosis congenita

21 June 2018

1 reference

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Switching and signaling at the telomere

21 June 2018

1 reference

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Dyskeratosis congenita in all its forms

21 June 2018

1 reference

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

21 June 2018

1 reference

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Principle of marginotomy in template synthesis of polynucleotides

21 June 2018

1 reference

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Recognition and elongation of telomeres by telomerase

21 June 2018

1 reference

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Micronodular transformation (nodular regenerative hyperplasia) of the liver: a report of 64 cases among 2,500 autopsies and a new classification of benign hepatocellular nodules

21 June 2018

1 reference

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Familial idiopathic pulmonary fibrosis in association with bone marrow hypoplasia and hepatic nodular regenerative hyperplasia: a new "trimorphic" syndrome

21 June 2018

1 reference

12 December 2020

Inhibition of experimental liver cirrhosis in mice by telomerase gene delivery

1 reference

12 December 2020

Mutations of the human telomerase RNA gene (TERC) in aplastic anemia and myelodysplastic syndrome

1 reference

12 December 2020

Late presentation of dyskeratosis congenita as apparently acquired aplastic anaemia due to mutations in telomerase RNA

1 reference

12 December 2020

A new syndrome of familial aplastic anemia and chronic liver disease

1 reference

12 December 2020

Unusual complications after bone marrow transplantation for dyskeratosis congenita

1 reference

12 December 2020

Cooperative interactions of p53 mutation, telomere dysfunction, and chronic liver damage in hepatocellular carcinoma progression

1 reference

12 December 2020

Functional characterization of natural telomerase mutations found in patients with hematologic disorders

1 reference

12 December 2020

10.1371/JOURNAL.PONE.0007926

Identifiers

DOI

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20 August 2017

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20 August 2017

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