Sherilyn Grill, Jayakrishnan Nandakumar. J Biol Chem 2021
Times Cited: 10
Times Cited: 10
Times Cited
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40
An update on the biology and management of dyskeratosis congenita and related telomere biology disorders.
Marena R Niewisch, Sharon A Savage. Expert Rev Hematol 2019
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Molecular mechanisms of telomere biology disorders.
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Structural insights into POT1-TPP1 interaction and POT1 C-terminal mutations in human cancer.
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Structural and functional analysis of the human POT1-TPP1 telomeric complex.
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The TEL patch of telomere protein TPP1 mediates telomerase recruitment and processivity.
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A dynamic molecular link between the telomere length regulator TRF1 and the chromosome end protector TRF2.
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Combining conservation and species-specific differences to determine how human telomerase binds telomeres.
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TPP1 OB-fold domain controls telomere maintenance by recruiting telomerase to chromosome ends.
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The N Terminus of the OB Domain of Telomere Protein TPP1 Is Critical for Telomerase Action.
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Short telomeres are a risk factor for idiopathic pulmonary fibrosis.
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A novel dyskerin (DKC1) mutation is associated with familial interstitial pneumonia.
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The MUC5B promoter polymorphism and telomere length in patients with chronic hypersensitivity pneumonitis: an observational cohort-control study.
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20
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