Author details

Full Name

Thomas Wieland

Affiliation

ORCID

Career Start Year

1988

Papers

263

H Index

Expertise

CM4AI Collaborator

PMID	Paper Title	Journal Title	Published Year
37172821	Contribution of the hexosamine biosynthetic pathway in the hyperglycemia-dependent and -independent breakdown of the retinal neurovascular unit.		2023
37124426	Spatial shopping behavior during the Corona pandemic: insights from a micro-econometric store choice model for consumer electronics and furniture retailing in Germany.		2023
37183567	Chemical Tools for Studying Phosphohistidine: Generation of Selective Ï¿-Phosphohistidine and Ï¿-Phosphohistidine Antibodies.	Chembiochem	2023
35286475	Chronic isoprenaline/phenylephrine vs. exclusive isoprenaline stimulation in mice: critical contribution of alpha-adrenoceptors to early cardiac stress responses.	Basic Research in Cardiology	2022
35963849	Functional antagonism between CagA and DLC1 in gastric cancer.	Cell Death Discov	2022
36333314	Lamin A/C-dependent chromatin architecture safeguards naÃ¯ve pluripotency to prevent aberrant cardiovascular cell fate and function.	Nature Communications	2022
35033869	The orphan receptor GPRC5B activates pro-inflammatory signaling in the vascular wall via Fyn and NFÎºB.	Biochemical and Biophysical Research Communications	2022
34506973	Glucosamine protects against neuronal but not vascular damage in experimental diabetic retinopathy.	Molecular Metabolism	2021
33801779	RhoGEF17-An Essential Regulator of Endothelial Cell Death and Growth.	Cells	2021
34282193	TRPV1 activation and internalization is part of the LPS-induced inflammation in human iPSC-derived cardiomyocytes.	Scientific Reports	2021
32834516	A phenomenological approach to assessing the effectiveness of COVID-19 related nonpharmaceutical interventions in Germany.	Safety Science	2020
32323889	Antitumor Activity of Larotrectinib in Esophageal Carcinoma with NTRK Gene Amplification.	Oncologist	2020
32244061	The WD40 repeat protein, WDR36, orchestrates sphingosine kinase-1 recruitment and phospholipase C-Î² activation by G-coupled receptors.	Biochimica et Biophysica Acta - Molecular and Cell Biology of Lipids	2020
32050722	Nucleoside Diphosphate Kinase B Contributes to Arrhythmogenesis in Human-Induced Pluripotent Stem Cell-Derived Cardiomyocytes from a Patient with Arrhythmogenic Right Ventricular Cardiomyopathy.	Journal of Clinical Medicine	2020
32384736	PA Delivers the Tumor Metastasis Suppressor Protein NDPK-A/NME1 into Breast Cancer Cells.	International Journal of Molecular Sciences	2020
32466219	Role of the Ang2-Tie2 Axis in Vascular Damage Driven by High Glucose or Nucleoside Diphosphate Kinase B Deficiency.	International Journal of Molecular Sciences	2020
33086728	Involvement of NDPK-B in Glucose Metabolism-Mediated Endothelial Damage via Activation of the Hexosamine Biosynthesis Pathway and Suppression of O-GlcNAcase Activity.	Cells	2020
33003441	Dissecting G-Mediated Plasma Membrane Translocation of Sphingosine Kinase-1.	Cells	2020
31101932	cAMP guided his way: a life for G protein-mediated signal transduction and molecular pharmacology-tribute to Karl H. Jakobs.	Naunyn-Schmiedeberg's Archives of Pharmacology	2019
31737628	Studying Brugada Syndrome With an SCN1B Variants in Human-Induced Pluripotent Stem Cell-Derived Cardiomyocytes.	Frontiers in Cell and Developmental Biology	2019
30948775	Serum of patients with acute myocardial infarction prevents inflammation in iPSC-cardiomyocytes.	Scientific Reports	2019
30947366	Drug Testing in Human-Induced Pluripotent Stem Cell-Derived Cardiomyocytes From a Patient With Short QT Syndrome Type 1.	Clinical Pharmacology and Therapeutics	2019
31106349	A cellular model of Brugada syndrome with SCN10A variants using human-induced pluripotent stem cell-derived cardiomyocytes.	Europace	2019
31104767	The orphan receptor GPRC5B modulates inflammatory and fibrotic pathways in cardiac fibroblasts and mice hearts.	Biochemical and Biophysical Research Communications	2019
30777893	Quantification and discovery of sequence determinants of protein-per-mRNA amount inÂ 29Â human tissues.	Mol Syst Biol	2019
30777892	A deep proteome and transcriptome abundance atlas of 29 healthy human tissues.	Mol Syst Biol	2019
29574456	Modeling Short QT Syndrome Using Human-Induced Pluripotent Stem Cell-Derived Cardiomyocytes.	Journal of the American Heart Association	2018
28911825	Paving the Rho in cancer metastasis: Rho GTPases and beyond.	Pharmacology and Therapeutics	2018
29035382	Regulation of heterotrimeric G-protein signaling by NDPK/NME proteins and caveolins: an update.	Laboratory Investigation	2018
30025539	Clinical, biochemical and genetic spectrum of 70 patients with ACAD9 deficiency: is riboflavin supplementation effective?	Orphanet J Rare Dis	2018
30167850	Genetic variants in components of the NALCN-UNC80-UNC79 ion channel complex cause a broad clinical phenotype (NALCN channelopathies).	Hum Genet	2018
30533531	TPP2 mutation associated with sterile brain inflammation mimicking MS.	Neurology: Genetics	2018
30002415	O-GlcNAcylation of FoxO1 mediates nucleoside diphosphate kinase B deficiency induced endothelial damage.	Scientific Reports	2018
29907596	Inflammation leads through PGE/EP signaling to HDAC5/MEF2-dependent transcription in cardiac myocytes.	EMBO Molecular Medicine	2018
29535773	Ion Channel Expression and Characterization in Human Induced Pluripotent Stem Cell-Derived Cardiomyocytes.		2018
29566126	Electrical dysfunctions in human-induced pluripotent stem cell-derived cardiomyocytes from a patient with an arrhythmogenic right ventricular cardiomyopathy.	Europace	2018
29654304	Defective immuno- and thymoproteasome assembly causes severe immunodeficiency.	Sci Rep	2018
29208700	Hypertension-evoked RhoA activity in vascular smooth muscle cells requires RGS5.	FASEB Journal	2018
29373579	An AKAP-Lbc-RhoA interaction inhibitor promotes the translocation of aquaporin-2 to the plasma membrane of renal collecting duct principal cells.	PLoS One	2018
29416708	Targeting altered Nme heterooligomerization in disease?	Oncotarget	2018
29545480	Ion Channel Dysfunctions in Dilated Cardiomyopathy in Limb-Girdle Muscular Dystrophy.	Circulation. Genomic and precision medicine	2018
29407091	Estradiol protection against toxic effects of catecholamine on electrical properties in human-induced pluripotent stem cell derived cardiomyocytes.	International Journal of Cardiology	2018
29360107	Erratum: Sequence data and association statistics from 12,940 type 2 diabetes cases and controls.	Sci Data	2018
27901041	Bainbridge-Ropers syndrome caused by loss-of-function variants in ASXL3: a recognizable condition.	Eur J Hum Genet	2017
28512254	Catecholamines facilitate VEGF-dependent angiogenesis via Î²2-adrenoceptor-induced Epac1 and PKA activation.	Oncotarget	2017
28393272	Heterozygous HNRNPU variants cause early onset epilepsy and severe intellectual disability.	Hum Genet	2017
28592841	Lipopolysaccharides induced inflammatory responses and electrophysiological dysfunctions in human-induced pluripotent stem cell derived cardiomyocytes.	Scientific Reports	2017
28422131	Variants in CPLX1 in two families with autosomal-recessive severe infantile myoclonic epilepsy and ID.	European Journal of Human Genetics	2017
28341696	A Low-Frequency Inactivating <i>AKT2</i> Variant Enriched in the Finnish Population Is Associated With Fasting Insulin Levels and Type 2 Diabetes Risk.	Diabetes	2017
28759639	G protein-coupled receptor kinase 2 promotes cardiac hypertrophy.	PLoS ONE	2017