André Terzic

ORCID: 0000-0001-9210-009X
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About
Contact & Profiles
Research Areas
  • Cardiac Ischemia and Reperfusion
  • Pluripotent Stem Cells Research
  • Tissue Engineering and Regenerative Medicine
  • Ion channel regulation and function
  • Cardiac electrophysiology and arrhythmias
  • Mitochondrial Function and Pathology
  • Congenital heart defects research
  • Biomedical Ethics and Regulation
  • Mesenchymal stem cell research
  • CRISPR and Genetic Engineering
  • Cardiac Arrest and Resuscitation
  • Fuel Cells and Related Materials
  • Cardiac Fibrosis and Remodeling
  • 3D Printing in Biomedical Research
  • Cardiomyopathy and Myosin Studies
  • Biomedical and Engineering Education
  • Neuroscience and Neuropharmacology Research
  • Cardiac Structural Anomalies and Repair
  • Health and Medical Research Impacts
  • Mechanical Circulatory Support Devices
  • Cardiovascular Function and Risk Factors
  • Electrospun Nanofibers in Biomedical Applications
  • Pharmacogenetics and Drug Metabolism
  • Computational Drug Discovery Methods
  • Pancreatic function and diabetes

Mayo Clinic
2016-2025

Mayo Clinic in Florida
2015-2025

WinnMed
2014-2024

Mayo Clinic in Arizona
2015-2024

Center for Neuroscience and Regenerative Medicine
2011-2023

Io Therapeutics (United States)
2005-2021

University of Minnesota Rochester
1994-2021

Onze Lieve Vrouwziekenhuis Hospital
2013-2020

Clinical Orthopaedics and Related Research
2018-2019

Weatherford College
2018

Atrial fibrillation is a rhythm disorder characterized by chaotic electrical activity of cardiac atria. Predisposing to stroke and heart failure, this common condition increasingly recognized as heritable disorder. To identify genetic defects conferring disease susceptibility, patients with idiopathic atrial fibrillation, lacking traditional risk factors, were evaluated. Genomic DNA scanning revealed nonsense mutation in KCNA5 that encodes Kv1.5, voltage-gated potassium channel expressed...

10.1093/hmg/ddl143 article EN Human Molecular Genetics 2006-06-13

ABSTRACT Members of the transforming growth factor pβ (TGF‐β) superfamily‐namely, TGF‐β and BMP2—applied to undifferentiated murine embryonic stem cells up‐regulated mRNA mesodermal (Brachyury) cardiac specific transcription factors (Nkx2.5, MEF2C). Embryoid bodies generated from primed with these demonstrated an increased potential for differentiation a significant increase in beating areas enhanced myofibrillogenesis. In environment postmitotic cardiomyocytes, engineered express...

10.1096/fj.02-0072com article EN The FASEB Journal 2002-10-01

Nuclear reprogramming provides an emerging strategy to produce embryo-independent pluripotent stem cells from somatic tissue. Induced (iPS) demonstrate aptitude for de novo cardiac differentiation, yet their potential heart disease therapy has not been tested.In this study, fibroblasts transduced with human stemness factors OCT3/4, SOX2, KLF4, and c-MYC converted into embryonic cell-like phenotype demonstrated the ability spontaneously assimilate preimplantation host morula via diploid...

10.1161/circulationaha.109.865154 article EN Circulation 2009-07-21

Nerve regeneration after injury is a critical medical issue. In previous work, we have developed an oligo(poly(ethylene glycol) fumarate) (OPF) hydrogel incorporated with positive charges as promising nerve conduit. this study, introduced cross-linkable bonds to graphene oxide and carbon nanotube obtain the functionalized acrylate (GOa) poly(ethylene (CNTpega). An electrically conductive was then fabricated by covalently embedding GOa CNTpega within OPF through chemical cross-linking...

10.1021/acsami.7b02072 article EN ACS Applied Materials & Interfaces 2017-04-13

Muscle weakness and myopathy are observed in vitamin D deficiency chronic renal failure, where concentrations of the active D3 metabolite, 1α,25-dihydroxyvitamin (1α,25(OH)2D3), low. To evaluate mechanism action 1α,25(OH)2D3 skeletal muscle, we examined mitochondrial oxygen consumption, dynamics, biogenesis changes expression nuclear genes encoding proteins human muscle cells following treatment with 1α,25(OH)2D3. The consumption rate (OCR) increased 1α,25(OH)2D3-treated cells. Vitamin...

10.1074/jbc.m115.684399 article EN cc-by Journal of Biological Chemistry 2015-11-25

1. Mitochondrial dysfunction, secondary to excessive accumulation of Ca2+, has been implicated in cardiac injury. We here examined the action potassium channel openers on mitochondrial Ca2+ homeostasis, as these cardioprotective ion modulators have recently shown target a ATP-sensitive K+ channel. 2. In isolated mitochondria, diazoxide and pinacidil decreased rate magnitude uptake into matrix with an IC50 65 128 microM, respectively. At all stages uptake, depolarized membrane thereby...

10.1111/j.1469-7793.1999.0347m.x article EN The Journal of Physiology 1999-09-01

Discovered in the cardiac sarcolemma, ATP-sensitive K + (K ATP ) channels have more recently also been identified within inner mitochondrial membrane. Yet consequences of channel activation on function remain partially documented. Therefore, we isolated mitochondria from rat hearts and used openers to examine effect opening membrane potential, respiration, generation, Ca 2+ transport, matrix volume. From a potential −180 ± 15 mV, openers, pinacidil (100 μM), cromakalim (25 levcromakalim (20...

10.1152/ajpheart.1998.275.5.h1567 article EN AJP Heart and Circulatory Physiology 1998-11-01

Reaction to stress requires feedback adaptation of cellular functions secure a response without distress, but the molecular order this process is only partially understood. Here, we report previously unrecognized regulatory element in general syndrome. Kir6.2, ion-conducting subunit metabolically responsive ATP-sensitive potassium (K ATP ) channel, was mandatory for optimal capacity under stress. Genetic deletion Kir6.2 disrupted K channel-dependent adjustment membrane excitability and...

10.1073/pnas.212315199 article EN Proceedings of the National Academy of Sciences 2002-09-23
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