Results 161 to 170 of about 68,210 (242)

Viability and Longevity of Human Miniaturized Living Myocardial Slices. [PDF]

J Cardiovasc Dev Dis
Zhou Z, van Steenis YP, Henry S, van Doorn ECH, Amesz JH, van de Woestijne PC, de Groot NMS, Manintveld OC, Bartelds B, Taverne YJHJ.   +9 more
europepmc   +1 more source

Vascular dysfunction in women with recurrent pregnancy loss: Possible association with antiphospholipid antibodies

International Journal of Gynecology &Obstetrics, Volume 169, Issue 1, Page 206-214, April 2025.
Abstract Objective Antiphospholipid antibodies (aPL) are recognized to have a pivotal role in recurrent pregnancy loss (RPL) and cardiovascular disease. Therefore, we assessed the vascular function of women with RPL and examined the association with each type of aPL.
Titi Yang, Emi Okada, Maho Todoroki, Siyu Liu, Rukmali Athurupana, Kumie Kataoka, Chiaki Kashino, Takashi Mitsui, Toru Hasegawa, Yasuhiko Kamada, Hisashi Masuyama, Mikiya Nakatsuka   +11 more
wiley   +1 more source

Contraction-induced endocardial id2b plays a dual role in regulating myocardial contractility and valve formation

Shuo Chen, Jie Yin, Jinxiu Liang, Weijia Zhang, Peijun Jiang, Wenyuan Wang, Xiaoying Chen, Yuanhong Zhou, Peng Xia, Fan Yang, Ying Gu, Ruilin Zhang, Peidong Han   +12 more
openalex   +2 more sources

NEXN deficiency leads to dilated cardiomyopathy in human pluripotent stem cell-derived cardiomyocytes. [PDF]

Stem Cell Res Ther
Jiang M, Chen X, Song Y, Wei M, Cao J, Lu W, Lan F, Bai Y, Cui M.   +8 more
europepmc   +1 more source

Mitochondrial dysfunction: Related diseases, influencing factors, and detection

Interdisciplinary Medicine, EarlyView.
Mitochondrial dysfunction is implicated in the pathogenesis of numerous diseases, including neurological disorders, cancers, and cardiovascular conditions, through mechanisms such as mitochondrial DNA mutations, dysregulation of mitochondrial network dynamics, and impaired mitophagy.
Zhaojin Li, Shiyu Li, Wanying Chen, Ziyu Zhang, Chun Pan, Peng Lei, Cheng Cheng, Junyou Zhu, Hanxiao Sun, Zhenning Dai   +9 more
wiley   +1 more source

Unraveling septal perfusion abnormalities in Ebstein's anomaly: A case report contrasting PET MPI with myocardial reality. [PDF]

Radiol Case Rep
Alibazoglu H, Khalil AM, Alibazoglu D, Sherif A, Bafadel A, Hillis A, Ansari HA, Sabbour H, Alibazoglu B, Hussein RA, Khalil ME.   +10 more
europepmc   +1 more source

New insights into applications of base editor in hereditary disorders

Interdisciplinary Medicine, EarlyView.
Abstract Hereditary disorders are a group of diseases caused by genetic mutations or chromosomal variations. Although the incidence of each genetic disorder is relatively low, patients affected by the disease generally experience a range of severe symptoms, including blindness, disability, and even premature death. In addition, the available treatments
Maoping Cai, Linhui Zhang, Liqing Li, Yue Liu, Canbin Lv, Yan Shi, Jianyuan Zhao, Dingwei Ye, Yuanyuan Qu   +8 more
wiley   +1 more source

Reviving the Failing Heart: Contractile Reserve and Remodeling Reversal. [PDF]

Int J Heart Fail
Chung H.
europepmc   +1 more source

Targeting dipeptidyl peptidase 3 (DPP3) in extreme‐critically ill patients with refractory shock: First‐in‐human report on the safety and efficacy of an anti‐DPP3 antibody

European Journal of Heart Failure, EarlyView.
Dominik Jarczak, Axel Nierhaus, Alexandre Mebazaa, Antoine Herpain, Peter Pickkers, Sanchir Anar, Stefan Kluge   +6 more
wiley   +1 more source