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Telomere Lengths, Pulmonary Fibrosis and Telomerase (TERT) Mutations

Overview of attention for article published in PLOS ONE, May 2010
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Title
Telomere Lengths, Pulmonary Fibrosis and Telomerase (TERT) Mutations
Published in
PLOS ONE, May 2010
DOI 10.1371/journal.pone.0010680
Pubmed ID
Authors

Alberto Diaz de Leon, Jennifer T. Cronkhite, Anna-Luise A. Katzenstein, J. David Godwin, Ganesh Raghu, Craig S. Glazer, Randall L. Rosenblatt, Carlos E. Girod, Edward R. Garrity, Chao Xing, Christine Kim Garcia

Abstract

Telomerase is an enzyme that catalyzes the addition of nucleotides on the ends of chromosomes. Rare loss of function mutations in the gene that encodes the protein component of telomerase (TERT) have been described in patients with idiopathic pulmonary fibrosis (IPF). Here we examine the telomere lengths and pulmonary fibrosis phenotype seen in multiple kindreds with heterozygous TERT mutations.

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Mendeley readers

Mendeley readers

The data shown below were compiled from readership statistics for 183 Mendeley readers of this research output. Click here to see the associated Mendeley record.

Geographical breakdown

Country Count As %
United States 5 3%
South Africa 1 <1%
Brazil 1 <1%
United Kingdom 1 <1%
India 1 <1%
Unknown 174 95%

Demographic breakdown

Readers by professional status Count As %
Student > Ph. D. Student 29 16%
Researcher 27 15%
Other 17 9%
Student > Bachelor 16 9%
Student > Master 13 7%
Other 45 25%
Unknown 36 20%
Readers by discipline Count As %
Medicine and Dentistry 61 33%
Agricultural and Biological Sciences 32 17%
Biochemistry, Genetics and Molecular Biology 20 11%
Immunology and Microbiology 5 3%
Pharmacology, Toxicology and Pharmaceutical Science 5 3%
Other 17 9%
Unknown 43 23%