Profil bibliographique

K. Campbell

Informations fournies par OpenAlex. Research Africa ne déduit ni nationalité, ni poste, ni coordonnées personnelles.

4Publications signalées
0Citations signalées
1Affiliations récentes

Les institutions déclarées

University of Kentucky

Les domaines associés

Cardiomyopathy and Myosin StudiesMicrotubule and mitosis dynamicsCardiac electrophysiology and arrhythmiasCellular Mechanics and InteractionsMuscle Physiology and Disorders

Les publications récentes

Accès ouvert 2026 preprint OpenAlex

Biomolecular condensation of cMLCK enables myosin motor phosphorylation in the heart

Kyler J Carl, Austin G Welette-Hunsucker, Ivanka Sevrieva, K. Campbell et autres

The heart needs to adapt its output to the metabolic demands of the organism. Phosphorylation of the myosin motors by cardiac myosin light chain kinase (cMLCK) increases heart muscle contractile function, yet its regulation and mechanism of action have remained unclear. Here, …

us, gb (code pays fourni par la source)

0 citations bioRxiv (Cold Spring Harbor Laboratory)
Accès ouvert 2026 preprint OpenAlex

Hearts may grow concentrically to balance ATP supply and demand and eccentrically to stabilize titin-based stress

John Kotter, Steve Leung, Thomas Kampourakis, Lik-Chuan Lee et autres

Abstract Hearts change their wall thickness (concentric growth) and chamber size (eccentric growth) as they adapt to circulatory demands and the intrinsic function of their contractile cells. Factors associated with wall thickening include variants of sarcomeric proteins that enhance contractility, mitochondrial dysfunction, …

us (code pays fourni par la source)

0 citations bioRxiv (Cold Spring Harbor Laboratory)
Accès ouvert 2026 preprint OpenAlex

Single-molecule analysis sheds light on cardiac myosin dysfunction due to hypertrophic cardiomyopathy mutation A57D in ventricular myosin light chain-1 (MLC1v)

Tianbang Wang, Emrulla Spahiu, Tim Holler, K. Campbell et autres

Abstract Ventricular myosin light chain-1 (MLC1v) is a key structural and function-modulating component of the β-cardiac myosin (βM-II) motor complex. Single-point mutations in MLC1v are linked to severe forms of hypertrophic cardiomyopathy (HCM) and sudden cardiac death (SCD) at a young age. …

de, us, au (code pays fourni par la source)

0 citations bioRxiv (Cold Spring Harbor Laboratory)
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