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Kristina Lorenz (1972-)

Pharmakologin

Name	Kristina Lorenz
Time	1972- (Date of birth and death)
Place	Kassel (Geburtsort) Deutschland
Gender	weiblich
Academic degree	Prof. Dr. rer. nat.
Profession	Pharmakologin (characteristic profession) Herzforscherin Hochschullehrerin
Related	Julius-Maximilians-Universität Würzburg. Institut für Toxikologie und Pharmakologie Leibniz-Institut für Analytische Wissenschaften (Direktorin Biomedizinische Forschung) (2016-) Universität Duisburg-Essen (Professorin) Universitätsklinikum Essen Mechanismen kardiovaskulärer Erkrankungen (Thema) Biomedizin (Thema) Vorbeugungs- und Therapiestrategien gegen Herzinsuffizienz (Thema)
Further information	Diss. Naturwissenschaftliche Fakultät (Pharmazie), Würzburg, 2004; Apothekerin; Professorin an der Uni Würzburg
Source	Homepage: http://www.sfb688.uni-wuerzburg.de/fileadmin/88100000/user_upload/CV/Lorenz0509.pdf (02.10.2018) Homepage: https://www.uk-essen.de/aktuelles/detailanzeige0/?tx_ttnews%5Btt_news%5D=2126&cHash=21b1e87cf859ccef4131eacddee29a9f (02.10.2018) Homepage: https://www.isas.de/node/3749 (02.10.2018)
Record type	Person
GND-Identifier	130422347
Record ID	130422347
Involved in show all “Cardiac glycosides”—quo vaditis?—past, present, and future? “Photo‐Adrenalines”: Photoswitchable β 2 ‐Adrenergic Receptor Agonists as Molecular Probes for the Study of Spatiotemporal Adrenergic Signaling “Cardiac glycosides”-quo vaditis? - past, present, and future? “Photo‐Adrenalines”: Photoswitchable β2‐Adrenergic Receptor Agonists as Molecular Probes for the Study of Spatiotemporal Adrenergic Signaling Cardiac multiscale bioimaging: from nano- through micro- to mesoscales Kardiotoxische Effekte von Chemotherapeutika – Evaluierung eines impedanzbasierten in vitro Testsystems und Bestimmung der Kardiotoxizität niedermolekularer Kinaseinhibitoren Mutations in DNAJC19 cause altered mitochondrial structure and increased mitochondrial respiration in human iPSC-derived cardiomyocytes Targeting cardiomyocyte ADAM10 ectodomain shedding promotes survival early after myocardial infarction Visible‐Light Photoswitchable Benzimidazole Azo‐Arenes as β‐Arrestin2‐Biased Selective Cannabinoid 2 Receptor Agonists Mit sichtbarem Licht schaltbare Benzimidazol‐Azo‐Arene wirken als β‐Arrestin2 funktionell selektive Cannabinoid‐Rezeptor 2 Agonisten Frontispiz: Mit sichtbarem Licht schaltbare Benzimidazol‐Azo‐Arene wirken als β‐Arrestin2 funktionell selektive Cannabinoid‐Rezeptor 2 Agonisten Frontispiece: Visible‐Light Photoswitchable Benzimidazole Azo‐Arenes as β‐Arrestin2‐Biased Selective Cannabinoid 2 Receptor Agonists Cellular mechanisms of the anti-arrhythmic effect of cardiac PDE2 overexpression ERK1/2 activity is critical for the outcome of ischemic stroke Targeting cardiomyocyte ADAM10 ectodomain shedding promotes survival early after myocardial infarction The potential of remdesivir to affect function, metabolism and proliferation of cardiac and kidney cells in vitro beta-Adrenoceptor-mediated Relaxation of Urinary Bladder Muscle in beta 2-Adrenoceptor Knockout Mice Interference with ERK-dimerization at the nucleocytosolic interface targets pathological ERK1/2 signaling without cardiotoxic side-effects Modeling atrial fibrosis in vitro - generation and characterization of a novel human atrial fibroblast cell line Biochemical and pathological changes result from mutated Caveolin-3 in muscle Ectopic expression of S28A-mutated Histone H3 modulates longevity, stress resistance and cardiac function in Drosophila Biochemical and pathological changes result from mutated Caveolin-3 in muscle Sex-difference in expression and function of beta-adrenoceptors in macrovessels: role of the endothelium Beta-adrenoceptor-mediated relaxation of urinary bladder muscle in beta 2-adrenoceptor knockout mice β-adrenoceptor-mediated relaxation of urinary bladder muscle in β2-adrenoceptor knockout mice Wechselwirkungen zwischen G-Protein- und MAP-Kinase-Signalwegen

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Katalog der Deutschen Nationalbibliothek

Kristina Lorenz (1972-)

“Cardiac glycosides”—quo vaditis?—past, present, and future?

“Photo‐Adrenalines”: Photoswitchable β 2 ‐Adrenergic Receptor Agonists as Molecular Probes for the Study of Spatiotemporal Adrenergic Signaling

“Cardiac glycosides”-quo vaditis? - past, present, and future?

“Photo‐Adrenalines”: Photoswitchable β2‐Adrenergic Receptor Agonists as Molecular Probes for the Study of Spatiotemporal Adrenergic Signaling

Cardiac multiscale bioimaging: from nano- through micro- to mesoscales

Kardiotoxische Effekte von Chemotherapeutika – Evaluierung eines impedanzbasierten in vitro Testsystems und Bestimmung der Kardiotoxizität niedermolekularer Kinaseinhibitoren

Mutations in DNAJC19 cause altered mitochondrial structure and increased mitochondrial respiration in human iPSC-derived cardiomyocytes

Targeting cardiomyocyte ADAM10 ectodomain shedding promotes survival early after myocardial infarction

Visible‐Light Photoswitchable Benzimidazole Azo‐Arenes as β‐Arrestin2‐Biased Selective Cannabinoid 2 Receptor Agonists

Mit sichtbarem Licht schaltbare Benzimidazol‐Azo‐Arene wirken als β‐Arrestin2 funktionell selektive Cannabinoid‐Rezeptor 2 Agonisten

Frontispiz: Mit sichtbarem Licht schaltbare Benzimidazol‐Azo‐Arene wirken als β‐Arrestin2 funktionell selektive Cannabinoid‐Rezeptor 2 Agonisten

Frontispiece: Visible‐Light Photoswitchable Benzimidazole Azo‐Arenes as β‐Arrestin2‐Biased Selective Cannabinoid 2 Receptor Agonists

Cellular mechanisms of the anti-arrhythmic effect of cardiac PDE2 overexpression

ERK1/2 activity is critical for the outcome of ischemic stroke

Targeting cardiomyocyte ADAM10 ectodomain shedding promotes survival early after myocardial infarction

The potential of remdesivir to affect function, metabolism and proliferation of cardiac and kidney cells in vitro

beta-Adrenoceptor-mediated Relaxation of Urinary Bladder Muscle in beta 2-Adrenoceptor Knockout Mice

Interference with ERK-dimerization at the nucleocytosolic interface targets pathological ERK1/2 signaling without cardiotoxic side-effects

Modeling atrial fibrosis in vitro - generation and characterization of a novel human atrial fibroblast cell line

Biochemical and pathological changes result from mutated Caveolin-3 in muscle

Ectopic expression of S28A-mutated Histone H3 modulates longevity, stress resistance and cardiac function in Drosophila

Biochemical and pathological changes result from mutated Caveolin-3 in muscle

Sex-difference in expression and function of beta-adrenoceptors in macrovessels: role of the endothelium

Beta-adrenoceptor-mediated relaxation of urinary bladder muscle in beta 2-adrenoceptor knockout mice

β-adrenoceptor-mediated relaxation of urinary bladder muscle in β2-adrenoceptor knockout mice

Wechselwirkungen zwischen G-Protein- und MAP-Kinase-Signalwegen