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Disease-Associated Human Telomerase RNA Variants Show Loss of Function for Telomere Synthesis without Dominant-Negative Interference

Telomerase adds simple-sequence repeats to chromosome ends to offset the terminal sequence loss inherent in each cycle of genome replication. Inherited mutations in genes encoding subunits of the human telomerase holoenzyme give rise to disease phenotypes including hematopoietic failure and pulmonar...

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Hlavní autoři: Errington, Timothy M., Fu, Dragony, Wong, Judy M. Y., Collins, Kathleen
Médium: Artigo
Jazyk:Inglês
Vydáno: American Society for Microbiology (ASM) 2008
Témata:
On-line přístup:https://ncbi.nlm.nih.gov/pmc/articles/PMC2577424/
https://ncbi.nlm.nih.gov/pubmed/18710936
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1128/MCB.00777-08
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