Krstevski, Farrugia, Hsu, Dona, Gaynor, Cohen, Harper, Harrison, Raffaut, Claridge, Drack, Lelliott, Brown, McMullen, Donner, Lal, Greening, & Pinto (2026). Conserved Transcriptional Circuits Regulate Cardiac Fibroblast-Mediated Fibrosis.. Circulation research.
Krstevski, Farrugia, Hsu, Dona, Gaynor, Cohen, et al. Conserved Transcriptional Circuits Regulate Cardiac Fibroblast-Mediated Fibrosis.. Circulation research. 2026; PMID: 42125800
Krstevski, Farrugia, Hsu, et al. Conserved Transcriptional Circuits Regulate Cardiac Fibroblast-Mediated Fibrosis.[J]. Circulation research. 2026.
@article{krstevski2026,
author = {Krstevski and Farrugia and Hsu and Dona and Gaynor and Cohen and Harper and Harrison and Raffaut and Claridge and Drack and Lelliott and Brown and McMullen and Donner and Lal and Greening and Pinto},
title = {Conserved Transcriptional Circuits Regulate Cardiac Fibroblast-Mediated Fibrosis.},
journal = {Circulation research},
year = {2026},
note = {PMID: 42125800},
}
TY - JOUR AU - Krstevski AU - Farrugia AU - Hsu AU - Dona AU - Gaynor AU - Cohen AU - Harper AU - Harrison AU - Raffaut AU - Claridge AU - Drack AU - Lelliott AU - Brown AU - McMullen AU - Donner AU - Lal AU - Greening AU - Pinto TI - Conserved Transcriptional Circuits Regulate Cardiac Fibroblast-Mediated Fibrosis. T2 - Circulation research PY - 2026 AN - PMID:42125800 ER -
Cardiac fibrosis is a major cause of cardiac dysfunction and is associated with virtually all forms of heart disease. Recently, single-cell genomic approaches have revealed in unprecedented resolution the orchestrated cellular responses driving cardiac fibrosis. Yet, the fibrosis-inducing phenotypes that emerge in the heart after nonischemic cardiac stress and the transcriptional circuits that govern fibrogenic cellular phenotypes are not well understood.