{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2026,10,7]],"date-time":"2026-10-07T23:57:32Z","timestamp":1791417452404,"version":"4.3.3"},"reference-count":69,"publisher":"American Association for the Advancement of Science (AAAS)","issue":"5456","content-domain":{"domain":[],"crossmark-restriction":false},"short-container-title":["Science"],"published-print":{"date-parts":[[2000,2,18]]},"abstract":"<jats:p>\n            Accelerated telomere loss has been proposed to be a factor leading to end-stage organ failure in chronic diseases of high cellular turnover such as liver cirrhosis. To test this hypothesis directly, telomerase-deficient mice, null for the essential telomerase RNA (mTR) gene, were subjected to genetic, surgical, and chemical ablation of the liver. Telomere dysfunction was associated with defects in liver regeneration and accelerated the development of liver cirrhosis in response to chronic liver injury. Adenoviral delivery of mTR into the livers of mTR\n            <jats:sup>\u2212\/\u2212<\/jats:sup>\n            mice with short dysfunctional telomeres restored telomerase activity and telomere function, alleviated cirrhotic pathology, and improved liver function. These studies indicate that telomere dysfunction contributes to chronic diseases of continual cellular loss-replacement and encourage the evaluation of \u201ctelomerase therapy\u201d for such diseases.\n          <\/jats:p>","DOI":"10.1126\/science.287.5456.1253","type":"journal-article","created":{"date-parts":[[2002,7,27]],"date-time":"2002-07-27T09:48:21Z","timestamp":1027763301000},"page":"1253-1258","source":"Crossref","is-referenced-by-count":359,"title":["Inhibition of Experimental Liver Cirrhosis in Mice by Telomerase Gene Delivery"],"prefix":"10.1126","volume":"287","author":[{"given":"Karl Lenhard","family":"Rudolph","sequence":"first","affiliation":[{"name":"Department of Adult Oncology, Medicine and Genetics, Dana-Farber Cancer Institute, 44 Binney Street (M413), and Harvard Medical School, Boston, MA 02115, USA."}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Sandy","family":"Chang","sequence":"additional","affiliation":[{"name":"Department of Adult Oncology, Medicine and Genetics, Dana-Farber Cancer Institute, 44 Binney Street (M413), and Harvard Medical School, Boston, MA 02115, USA."},{"name":"Department of Pathology, Brigham and Women's Hospital and Harvard Medical School, Boston, MA 02115, USA."}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Melissa","family":"Millard","sequence":"additional","affiliation":[{"name":"Department of Adult Oncology, Medicine and Genetics, Dana-Farber Cancer Institute, 44 Binney Street (M413), and Harvard Medical School, Boston, MA 02115, USA."}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Nicole","family":"Schreiber-Agus","sequence":"additional","affiliation":[{"name":"Department of Molecular Genetics, Albert Einstein College of Medicine, Bronx, NY 10461, USA."}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Ronald A.","family":"DePinho","sequence":"additional","affiliation":[{"name":"Department of Adult Oncology, Medicine and Genetics, Dana-Farber Cancer Institute, 44 Binney Street (M413), and Harvard Medical School, Boston, MA 02115, USA."}],"role":[{"vocabulary":"crossref","role":"author"}]}],"member":"221","reference":[{"key":"e_1_3_1_2_2","doi-asserted-by":"crossref","first-page":"245","DOI":"10.15288\/jsa.1998.59.245","volume":"59","author":"Smart R. 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