Jürgen Hescheler - Nanotechnology

Author Information

Dr. Jürgen Hescheler is affiliated with the Center for Physiology and Pathophysiology, Institute for Neurophysiology, Medical Faculty, University of Cologne, located in Cologne, Germany. His research focuses primarily on neurophysiology, stem cell biology, and cardiovascular physiology, contributing significantly to the understanding of cellular mechanisms and therapeutic applications.

Research Contributions

Dr. Hescheler has made substantial contributions to the fields of neurophysiology and stem cell research. His recent works include studies on T-Type Voltage-Gated Ca2+ Channels in amyloidogenic environments, live-cell imaging of human stem cell-derived cardiomyocytes, and the effects of various compounds on pluripotent stem cell-derived cardiomyocytes. He has also explored the immunomodulatory potential of adipose-derived stem cells and the impact of surface modifications on stem cell differentiation. His research aims to advance the understanding of cellular mechanisms and develop new therapeutic strategies for cardiovascular and neurological diseases.

Aliases

Dr. Jürgen Hescheler is also known by several aliases including J Hescheler, Jurgen Hescheler, J Rgen Hescheler, J. Hescheler, and Jürgen Hescheler.

Publication and Citation Metrics

Publication Year	Title	DOI
2022	Cav3 T-Type Voltage-Gated Ca2+ Channels and the Amyloidogenic Environment: Pathophysiology and Implications on Pharmacotherapy and Pharmacovigilance	10.3390/ijms23073457
2022	Live-Cell Imaging of the Contractile Velocity and Transient Intracellular Ca2+ Fluctuations in Human Stem Cell-Derived Cardiomyocytes	10.3390/cells11081280
2021	QuinoMit Q10-Fluid attenuates hydrogen peroxide-induced irregular beating in mouse pluripotent stem cell-derived cardiomyocytes	10.1016/j.biopha.2021.112089
2021	Inflammatory Pre-conditioning of Adipose Derived Stem Cells (ADSCs) with Cerebrospinal Fluid (CSF) from Traumatic Brain Injury Patients Alters the Immunomodulatory Potential of ADSC Secretomes	10.1089/neu.2020.7017
2021	Impact of Poly(dimethylsiloxane) Surface Modification with Conventional and Amino Acid-Conjugated Self-Assembled Monolayers on the Differentiation of Induced Pluripotent Stem Cells into Cardiomyocytes	10.1021/acsbiomaterials.0c01434
2021	Assessment of the In Vitro Cytotoxicity Effects of the Leaf Methanol Extract of Crinum zeylanicum on Mouse Induced Pluripotent Stem Cells and Their Cardiomyocytes Derivatives	10.3390/ph14121208
2021	Salicylic diamines selectively eliminate residual undifferentiated cells from pluripotent stem cell-derived cardiomyocyte preparations	10.1038/s41598-021-81351-z
2021	Pharmacological Neuroenhancement: Current Aspects of Categorization, Epidemiology, Pharmacology, Drug Development, Ethics, and Future Perspectives	10.1155/2021/8823383
2021	Co-transplantation of Mesenchymal Stromal Cells and Induced Pluripotent Stem Cell-Derived Cardiomyocytes Improves Cardiac Function After Myocardial Damage	10.3389/fcvm.2021.794690
2021	Retinal Vessel Responses to Flicker Stimulation Are Impaired in Cav2.3-Deficient Mice—An in-vivo Evaluation Using Retinal Vessel Analysis (RVA)	10.3389/fneur.2021.659890