Milenkovic, Uros; Duponselle, Jolien; Bivalacqua, Trinity J; Albersen, Maarten; 64231;
Peyronie's disease (PD) is an idiopathic chronic fibrotic disease that causes a penile curvature (PC), subsequent erectile dysfunction (ED) and impaired sexual intercourse in patients. As of yet, there are no reliable non-surgical treatment options available. Intralesional injection with collagenase Clostridum Histolyticum has been FDA approved sin...
Schipper, Tom Peelman, Luc Smets, Pascale Broeckx, Bart
Hypertrophic cardiomyopathy (HCM) is a common and potentially lethal heart disease in cats. To reduce its prevalence, breeding cats are frequently screened on the basis of their phenotype or genotype. Although echocardiography is the most reliable phenotypical method, its efficacy is limited by the incomplete penetrance of HCM and by difficulties i...
Schipper, Tom Van Poucke, Mario Sonck, Laurien Smets, Pascale Ducatelle, Richard Broeckx, Bart J. G. Peelman, Luc J.
Published in
European Journal of Human Genetics
Hypertrophic cardiomyopathy (HCM) is the most common inherited human heart disease. The same disease has a high prevalence in cats, where it is also suspected to be inherited. More than 1500 variants in MYBPC3, MYH7 and other sarcomeric genes are associated with human HCM, while in cats, only two causative variants in MYBPC3 are currently known. He...
Van Weehaeghe, Donatienne; 110770; Koole, Michel; 54596; Schmidt, Mark E; Deman, Stephanie; Jacobs, Andreas H; Souche, Erika; 48057; Serdons, Kim; Sunaert, Stefan; 15289; Bormans, Guy; 9552; Vandenberghe, Wim; 5312;
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PURPOSE: The P2X7 receptor (P2X7R) is an ATP-gated ion channel predominantly expressed on activated microglia and is important in neurodegenerative diseases including Parkinson's disease (PD). In this first-in-human study, we investigated [11C]JNJ54173717 ([11C]JNJ717), a selective P2X7R tracer, in healthy volunteers (HV) and PD patients. Biodistri...
Thonnard, David; 92785; Dreesen, Eline; Callaerts-Vegh, Zsuzsanna; 48902; D'Hooge, Rudi; 43549;
Cognitive flexibility helps organisms to respond adaptively to environmental changes. Deficits in this executive function have been associated with a variety of brain disorders, and it has been shown to rely on various concomitant neurobiological mechanisms. However, the involvement of the glutamatergic system in general, and NMDA receptors in part...
Ahmad, F. Soe, S. White, N. Johnston, R. Khan, I. Liao, J. Jones, M. Prabhu, R. Maconochie, I. Theobald, Peter
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Published in
Annals of Biomedical Engineering
The neonate transitions from placenta-derived oxygen, to supply from the pulmonary system, moments after birth. This requires a series of structural developments to divert more blood through the right heart and onto the lungs, with the tissue quickly remodelling to the changing ventricular workload. In some cases, however, the heart structure does ...
Vanvelk, N; Morgenstern, M; Moriarty, TF; Richards, RG; Nijs, S; 39354; Metsemakers, WJ; 85073;
A fracture-related infection (FRI) is an important complication that can lead to an increase in morbidity, mortality and economic costs. Preclinical in vivo models are critical in the evaluation of novel prevention and treatment strategies, yet it is important that these studies recapitulate the features of an FRI that make it such a clinical chall...
Crum, William R Sawiak, Stephen J Chege, Winfred Cooper, Jonathan D Williams, Steven C R Vernon, Anthony C
Published in
Brain, behavior, and immunity
Genetic and environmental risk factors for psychiatric disorders are suggested to disrupt the trajectory of brain maturation during adolescence, leading to the development of psychopathology in adulthood. Rodent models are powerful tools to dissect the specific effects of such risk factors on brain maturational profiles, particularly when combined ...
Messer, AE Chan, WS Daley, A Copeland, O Marston, SB Connolly, D
Hypertrophic cardiomyopathy (HCM) is the most common single gene inherited cardiomyopathy. In cats (Felix catus) HCM is even more prevalent and affects 16% of the outbred population and up to 26% in pedigree breeds such as Maine Coon and Ragdoll. Homozygous MYBPC3 mutations have been identified in these breeds but the mutations in other cats are un...
Garcia Diaz, Ana Isabel Moyon, Ben Coan, Philip M Alfazema, Neza Venda, Lara Woollard, Kevin Aitman, Tim
Published in
Disease models & mechanisms
The Wistar Kyoto (WKY) rat and the spontaneously hypertensive (SHR) rat inbred strains are well-established models for human crescentic glomerulonephritis (CRGN) and metabolic syndrome, respectively. Novel transgenic (Tg) strains add research opportunities and increase scientific value to well-established rat models. We have created two novel Tg st...