The short and long telomere syndromes: Paired paradigms for molecular medicine

Susan E. Stanley, Mary Armanios

Research output: Contribution to journalReview articlepeer-review

Abstract

Recent advances have defined a role for abnormally short telomeres in a broad spectrum of genetic disorders. They include rare conditions such as dyskeratosis congenita as well pulmonary fibrosis and emphysema. Now, there is new evidence that some familial cancers, such as melanoma, are caused by mutations that lengthen telomeres. Here, we examine the significance of these short and long telomere length extremes for understanding the molecular basis of age-related disease and cancer.

Original languageEnglish (US)
Pages (from-to)1-9
Number of pages9
JournalCurrent Opinion in Genetics and Development
Volume33
DOIs
StatePublished - Aug 1 2015

ASJC Scopus subject areas

  • Genetics
  • Developmental Biology

Fingerprint Dive into the research topics of 'The short and long telomere syndromes: Paired paradigms for molecular medicine'. Together they form a unique fingerprint.

Cite this