Abstract
Keywords:
CRISPR-Cas Systems; DNA damage; cardiotoxicity; clonal hematopoiesis; heart failure; inflammasome; macrophages.
Publication types
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Research Support, N.I.H., Extramural
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Research Support, Non-U.S. Gov't
MeSH terms
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Angiotensin II / toxicity
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Animals
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Clonal Hematopoiesis / genetics*
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DNA Damage
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Gain of Function Mutation*
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Heart Failure / etiology
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Heart Failure / genetics*
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Heart Failure / metabolism
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Hematopoietic Stem Cells / metabolism
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Inflammasomes / metabolism*
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Interleukin-18 / metabolism
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Interleukin-1beta / metabolism
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Macrophages / metabolism
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Male
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Mice
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Mice, Inbred C57BL
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NLR Family, Pyrin Domain-Containing 3 Protein / metabolism
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Protein Phosphatase 2C / genetics*
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Protein Phosphatase 2C / metabolism
Substances
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Inflammasomes
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Interleukin-18
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Interleukin-1beta
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NLR Family, Pyrin Domain-Containing 3 Protein
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Nlrp3 protein, mouse
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Angiotensin II
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Ppm1d protein, mouse
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Protein Phosphatase 2C