His primary areas of study are Neuroscience, Gene, Cell biology, Genetics and Midbrain. While the research belongs to areas of Neuroscience, Wolfgang Wurst spends his time largely on the problem of Stem cell, intersecting his research to questions surrounding Regulation of gene expression and Neurogenesis. Wolfgang Wurst has researched Cell biology in several fields, including GPX4, Neurodegeneration, Immunology, Molecular biology and Receptor.
His Midbrain study combines topics from a wide range of disciplines, such as FGF8, Hindbrain, Neural tube, Anatomy and WNT1. Wolfgang Wurst has included themes like Mutagenesis and Computational biology in his Genome study. His research on Forebrain is centered around Endocrinology and Internal medicine.
Wolfgang Wurst mainly focuses on Cell biology, Neuroscience, Internal medicine, Endocrinology and Genetics. His research investigates the link between Cell biology and topics such as Molecular biology that cross with problems in Gene expression and Gene knockdown. His Neuroscience study frequently draws connections between related disciplines such as GABAergic.
His Endocrinology study often links to related topics such as Receptor. His work in Gene, Mutant, Phenotype, Gene targeting and Allele is related to Genetics. The various areas that Wolfgang Wurst examines in his Midbrain study include Hindbrain and Anatomy.
His main research concerns Cell biology, Genetics, Neuroscience, Gene and Phenotype. Wolfgang Wurst interconnects Autophagy and Transcription factor in the investigation of issues within Cell biology. His research related to Mutant, Genome editing and Embryonic stem cell might be considered part of Genetics.
His study in Neuroscience is interdisciplinary in nature, drawing from both Genetic model, Schizophrenia and Anxiety. As part of the same scientific family, Wolfgang Wurst usually focuses on Gene, concentrating on Computational biology and intersecting with Gene knockout, CRISPR and Disease. The concepts of his Phenotype study are interwoven with issues in Human genetics and Autism spectrum disorder.
Wolfgang Wurst focuses on Cell biology, Neuroscience, Phenotype, Neurogenesis and Dopaminergic. His biological study spans a wide range of topics, including Autophagy, Neurodegeneration, Frameshift mutation, TREM2 and Skeletal muscle. His Neuroscience study combines topics in areas such as Schizophrenia, Green fluorescent protein, Anxiety, Cell type and Mitochondrion.
His Phenotype research is included under the broader classification of Gene. His work deals with themes such as Hippocampal formation, Molecular biology and Transcription factor, which intersect with Neurogenesis. His studies deal with areas such as Parkinson's disease, Optogenetics and Midbrain as well as Dopaminergic.
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ACSL4 dictates ferroptosis sensitivity by shaping cellular lipid composition
Sebastian Doll;Bettina Proneth;Yulia Y Tyurina;Elena Panzilius.
Nature Chemical Biology (2017)
Impaired stress response and reduced anxiety in mice lacking a functional corticotropin-releasing hormone receptor 1
Peter Timpl;Rainer Spanagel;Inge Sillaber;Adelheid Kresse.
Nature Genetics (1998)
Glutathione Peroxidase 4 Senses and Translates Oxidative Stress into 12/15-Lipoxygenase Dependent- and AIF-Mediated Cell Death
Alexander Seiler;Manuela Schneider;Heidi Förster;Stephan Roth.
Cell Metabolism (2008)
Arc/Arg3.1 Is Essential for the Consolidation of Synaptic Plasticity and Memories
Niels Plath;Ora Ohana;Ora Ohana;Björn Dammermann;Mick L. Errington.
The knockout mouse project
Christopher P. Austin;James F. Battey;Allan Bradley;Maja Bucan.
Nature Genetics (2004)
Neural plate patterning: Upstream and downstream of the isthmic organizer
Wolfgang Wurst;Laure Bally-Cuif.
Nature Reviews Neuroscience (2001)
Selenium Utilization by GPX4 Is Required to Prevent Hydroperoxide-Induced Ferroptosis
Irina Ingold;Carsten Berndt;Sabine Schmitt;Sebastian Doll.
A humanized version of Foxp2 affects cortico-basal ganglia circuits in mice
Wolfgang Enard;Sabine Gehre;Kurt Hammerschmidt;Sabine M. Hölter.
Rescue of the En-1 mutant phenotype by replacement of En-1 with En-2
Mark Hanks;Wolfgang Wurst;Lynn Anson-Cartwright;Anna B. Auerbach.
Essential role for mitochondrial thioredoxin reductase in hematopoiesis, heart development, and heart function.
Marcus Conrad;Cemile Jakupoglu;Stéphanie G. Moreno;Stefanie Lippl.
Molecular and Cellular Biology (2004)
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