Maksymilian Prondzynski
Overview
Explore the profile of Maksymilian Prondzynski including associated specialties, affiliations and a list of published articles.
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Citations
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Recent Articles
1.
Hilal N, An Z, Prondzynski M, Matsui E, Sahu D, Mao S, et al.
Res Sq
. 2025 Feb;
PMID: 39975917
Heart failure is a multifaceted syndrome contributing significantly to mortality and hospitalization rates among the global population. One of the prevalent causes of heart failure is ischemic heart disease (IHD),...
2.
Lu F, Liou C, Ma Q, Wu Z, Xue B, Xia Y, et al.
Nat Biomed Eng
. 2024 Sep;
PMID: 39237710
Cardiomyocytes derived from human induced pluripotent stem cells (hiPSC-CMs) lack nanoscale structures essential for efficient excitation-contraction coupling. Such nanostructures, known as dyads, are frequently disrupted in heart failure. Here we...
3.
Sweat M, Cao Y, Zhang X, Burnicka-Turek O, Perez-Cervantes C, Kulandaisamy A, et al.
Nat Cardiovasc Res
. 2024 Aug;
2(11):1095.
PMID: 39196102
No abstract available.
4.
Bortolin R, Nawar F, Park C, Trembley M, Prondzynski M, Sweat M, et al.
Circulation
. 2024 Aug;
150(15):1199-1210.
PMID: 39155863
Background: Calmodulinopathies are rare inherited arrhythmia syndromes caused by dominant heterozygous variants in , , or , which each encode the identical CaM (calmodulin) protein. We hypothesized that antisense oligonucleotide...
5.
Bezzerides V, Yoshinaga D, Feng R, Prondzynski M, Shani K, Tharani Y, et al.
Res Sq
. 2024 Jul;
PMID: 39070617
N-terminal-acetyltransferases including NAA10 catalyze N-terminal acetylation (Nt-acetylation), an evolutionarily conserved co-translational modification. Little is known about the role of Nt-acetylation in cardiac homeostasis. To gain insights, we studied a novel...
6.
Prondzynski M, Berkson P, Trembley M, Tharani Y, Shani K, Bortolin R, et al.
Nat Commun
. 2024 Jul;
15(1):5929.
PMID: 39009604
Human iPSC-derived cardiomyocytes (hiPSC-CMs) have proven invaluable for cardiac disease modeling and regeneration. Challenges with quality, inter-batch consistency, cryopreservation and scale remain, reducing experimental reproducibility and clinical translation. Here, we...
7.
Douvdevany G, Erlich I, Haimovich-Caspi L, Mashiah T, Prondzynski M, Pricolo M, et al.
Circ Res
. 2024 Jul;
135(4):474-487.
PMID: 38962864
Background: How the sarcomeric complex is continuously turned over in long-living cardiomyocytes is unclear. According to the prevailing model of sarcomere maintenance, sarcomeres are maintained by cytoplasmic soluble protein pools...
8.
Prondzynski M, Bortolin R, Berkson P, Trembley M, Shani K, Sweat M, et al.
bioRxiv
. 2024 Mar;
PMID: 38464269
In the last decade human iPSC-derived cardiomyocytes (hiPSC-CMs) proved to be valuable for cardiac disease modeling and cardiac regeneration, yet challenges with scale, quality, inter-batch consistency, and cryopreservation remain, reducing...
9.
Prondzynski M, Pioner J, Sala L, Bellin M, Meraviglia V
Front Physiol
. 2024 Mar;
15:1378495.
PMID: 38440346
No abstract available.
10.
Sweat M, Cao Y, Zhang X, Burnicka-Turek O, Perez-Cervantes C, Arulsamy K, et al.
Nat Cardiovasc Res
. 2024 Feb;
2(10):881-898.
PMID: 38344303
Understanding how the atrial and ventricular heart chambers maintain distinct identities is a prerequisite for treating chamber-specific diseases. Here, we selectively knocked out (KO) the transcription factor in the atrial...