Telomerase mutations in families with idiopathic pulmonary fibrosis (Q29615671)

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idiopathic pulmonary fibrosis

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12

Greider CW

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Armanios MY

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Chen JJ

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Cogan JD

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Alder JK

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Ingersoll RG

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Markin C

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Lawson WE

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Xie M

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Vulto I

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Phillips JA 3rd

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Lansdorp PM

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Loyd JE

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language of work or name

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publication date

29 March 2007

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The New England Journal of Medicine

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published in

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volume

356

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issue

13

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page(s)

1317-26

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Clinical and pathologic features of familial interstitial pneumonia

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

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

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Disease anticipation is associated with progressive telomere shortening in families with dyskeratosis congenita due to mutations in TERC.

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

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Telomeres shorten during ageing of human fibroblasts

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Essential role of mouse telomerase in highly proliferative organs

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Obesity, cigarette smoking, and telomere length in women

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Dyskeratosis congenita in all its forms

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Secondary structure of vertebrate telomerase RNA

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Short telomeres, even in the presence of telomerase, limit tissue renewal capacity

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The structure and function of telomerase reverse transcriptase

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Telomerase catalytic subunit homologs from fission yeast and human

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Reverse transcriptase motifs in the catalytic subunit of telomerase

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Template boundary definition in mammalian telomerase

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Dyskeratosis Congenita (DC) Registry: identification of new features of DC.

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The genetic approach in pulmonary fibrosis: can it provide clues to this complex disease?

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Longevity, Stress Response, and Cancer in Aging Telomerase-Deficient Mice

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Identification of a specific telomere terminal transferase activity in Tetrahymena extracts

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11 October 2022

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Crystal structure of the essential N-terminal domain of telomerase reverse transcriptase

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Dyskeratosis congenita: its link to telomerase and aplastic anaemia

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Adult familial cryptogenic fibrosing alveolitis in the United Kingdom

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

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11 October 2022

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

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11 October 2022

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Telomere shortening and tumor formation by mouse cells lacking telomerase RNA

1 reference

11 October 2022

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

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11 October 2022

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Human telomerase RNA template sequence is a determinant of telomere repeat extension rate

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11 October 2022

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Evidence for a mitotic clock in human hematopoietic stem cells: loss of telomeric DNA with age.

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11 October 2022

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Alveolar cell senescence in patients with pulmonary emphysema

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11 October 2022

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A DNA damage checkpoint response in telomere-initiated senescence

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11 October 2022

https://opencitations.net/index/coci/api/v1/references/10.1056/NEJMOA066157

The Shortest Telomere, Not Average Telomere Length, Is Critical for Cell Viability and Chromosome Stability

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11 October 2022

https://opencitations.net/index/coci/api/v1/references/10.1056/NEJMOA066157

A telomeric sequence in the RNA of Tetrahymena telomerase required for telomere repeat synthesis

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11 October 2022

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Heterozygosity for a surfactant protein C gene mutation associated with usual interstitial pneumonitis and cellular nonspecific interstitial pneumonitis in one kindred

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11 October 2022

https://opencitations.net/index/coci/api/v1/references/10.1056/NEJMOA066157

Identifiers

2 references

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/esummary.fcgi?db=pubmed&retmode=json&id=17392301

30 April 2017

Consolidated OpenCitations Corpus – April 2017

OpenCitations bibliographic resource ID

357894

OpenCitations bibliographic resource ID

357894

1 reference