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  1. Article

    Open Access

    Depression, anxiety, and quality of life as predictors of rehospitalization in patients with chronic heart failure

    Chronic heart failure (CHF) is a severe condition, often co-occurring with depression and anxiety, that strongly affects the quality of life (QoL) in some patients. Conversely, depressive and anxiety symptoms ...

    Jovan Veskovic, Mina Cvetkovic, Elvis Tahirovic in BMC Cardiovascular Disorders (2023)

  2. Article

    Open Access

    First-in-Human Study of the Safety, Pharmacokinetics, and Pharmacodynamics of MHV370, a Dual Inhibitor of Toll-Like Receptors 7 and 8, in Healthy Adults

    MHV370, a dual antagonist of human Toll-like receptors (TLR) 7 and 8, suppresses cytokines and interferon-stimulated genes in vitro and in vivo, and  has demonstrated efficacy in murine models of lupus. This f...

    Tamas Shisha, Maximilian G. Posch in European Journal of Drug Metabolism and Ph… (2023)

  3. No Access

    Article

    CCN1 Mutation is Associated with Atrial Septal Defect

    The genetic basis of congenital heart disease remains unknown in most of the cases. Recently, a novel mouse model shed new light on the role of CCN1/CYR61, a matricellular regulatory factor, in cardiac morphogene...

    Andreas Perrot, Katharina R. Schmitt, Eva-Maria G. Roth in Pediatric Cardiology (2015)

  4. Article

    Open Access

    Molecular genetics of congenital atrial septal defects

    Congenital heart defects (CHD) are the most common developmental errors in humans, affecting 8 out of 1,000 newborns. Clinical diagnosis and treatment of CHD has dramatically improved in the last decades. Henc...

    Maximilian G. Posch, Andreas Perrot, Felix Berger in Clinical Research in Cardiology (2010)

  5. No Access

    Article

    Identification of mutational hot spots in LMNA encoding lamin A/C in patients with familial dilated cardiomyopathy

    The familial form of dilated cardiomyopathy (DCM) occurs in about 20%–50% of DCM cases. It is a heterogenous genetic disease: mutations in more than 20 different genes have been shown to cause familial DCM. LMNA,...

    Andreas Perrot, Shwan Hussein, Volker Ruppert in Basic Research in Cardiology (2009)

  6. Article

    Variations in DSG2: V56M, V158G and V920G are not pathogenic for arrhythmogenic right ventricular dysplasia/cardiomyopathy

    Maximilian G Posch, Matthias J Posch in Nature Clinical Practice Cardiovascular Me… (2008)

  7. No Access

    Article

    Mutations in the EGF-CFC Gene Cryptic Are an Infrequent Cause of Congenital Heart Disease

    Cryptic (CFC1), a member of the epidermal growth factor–Cripto/FRL-1/Cryptic (EGF–CFC) gene family, is involved in the evolutionarily conserved establishment of left–right lateral asymmetry. Inac...

    Cemil Özcelik, Nana Bit-Avragim, Anna Panek, Ursula Gaio in Pediatric Cardiology (2006)

  8. No Access

    Article

    Ligands for PPARγ and RAR Cause Induction of Growth Inhibition and Apoptosis in Human Glioblastomas

    High-grade gliomas are characterized by a rapid proliferation rate, invasiveness and angiogenesis. Our previous data indicated that the combination of ligands for peroxisome proliferator-activated receptor γ (...

    Chuanbing Zang, Marlies Wächter, Hongyu Liu in Journal of Neuro-Oncology (2003)