An unusual presentation of pheochromocytoma accompanied by catecholamineāinduced cardiomyopathy
ESC Heart Failure, EarlyView.
Hugh O.J. Roberts+2 more
wiley +1 more source
Mitochondrial dysfunction: Related diseases, influencing factors, and detection
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+9 more
wiley +1 more source
Research into the physiology of myosins - a personal odyssey. [PDF]
Hoh JFY.
europepmc +1 more source
New insights into applications of base editor in hereditary disorders
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+8 more
wiley +1 more source
Update on left ventricular outflow tract obstruction. [PDF]
Song JK, Sun BJ, Kim DH, Jung SH.
europepmc +1 more source
Omecamtiv Mecarbil in Systolic Heart Failure: Clinical Efficacy and Future Directions of a Novel Myosin-Activating Inotropic Agent. [PDF]
Ramadan MM+4 more
europepmc +1 more source
Wnt-dependent mechanism of the apical constriction of roof plate cells in developing mouse spinal cord. [PDF]
Shinozuka T, Okubo T, Sasai N, Takada S.
europepmc +1 more source
Integrated single-cell functional-proteomic profiling reveals a shift in myofibre specificity in human nemaline myopathy: A proof-of-principle study. [PDF]
Seaborne RAE+9 more
europepmc +1 more source
Cardiac myosin inhibitors: a silver lining for an old disease. [PDF]
Yadav S, Agstam S, Singh S.
europepmc +1 more source