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Marcus Conrad (1970-)

Name	Marcus Conrad
Time	1970- (Date of birth and death)
Place	Deutschland
Academic degree	Dr.
Further information	Diss. Fakultät für Biologie, LMU, München, 2001; Direktor des Instituts für Metabolismus und Zelltod München (2023)
Source	https://www.helmholtz-munich.de/mcd/pi/pi-marcus-conrad (Stand: 25.07.2023)
Record type	Person
GND-Identifier	124109284
Record ID	124109284
Involved in show all Author Correction: Mechanisms controlling cellular and systemic iron homeostasis Exploiting ferroptosis vulnerabilities in cancer PGE2 inhibits TIL expansion by disrupting IL-2 signalling and mitochondrial function Inhibition of 7-dehydrocholesterol reductase prevents hepatic ferroptosis under an active state of sterol synthesis Integrated chemical and genetic screens unveil FSP1 mechanisms of ferroptosis regulation Mechanisms controlling cellular and systemic iron homeostasis LRP8‐mediated selenocysteine uptake is a targetable vulnerability in MYCN‐amplified neuroblastoma A non-canonical vitamin K cycle is a potent ferroptosis suppressor Apolipoprotein E potently inhibits ferroptosis by blocking ferritinophagy A cozy niche in an iron world Ferroptosis: the Good, the Bad and the Ugly Mouse brain proteomics establishes MDGA1 and CACHD1 as in vivo substrates of the Alzheimer protease BACE1 Ferroptosis at the crossroads of cancer-acquired drug resistance and immune evasion Etablierung von Mausstämmen defizient für die Selenoproteine mitochondriale Thioredoxin-Reduktase und Phospholipid-Hydroperoxid-Glutathion-Peroxidase (PHGPx) und Charakterisierung einer Spermienkern-spezifischen Form der PHGPx Etablierung von Mausstämmen defizient für die Selenoproteine mitochondriale Thioredoxin-Reduktase und Phospholipid-Hydroperoxid-Glutathion-Peroxidase (PHGPx) und Charakterisierung einer Spermienkern-spezifischen Form der PHGPx

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Marcus Conrad (1970-)

Author Correction: Mechanisms controlling cellular and systemic iron homeostasis

Exploiting ferroptosis vulnerabilities in cancer

PGE2 inhibits TIL expansion by disrupting IL-2 signalling and mitochondrial function

Inhibition of 7-dehydrocholesterol reductase prevents hepatic ferroptosis under an active state of sterol synthesis

Integrated chemical and genetic screens unveil FSP1 mechanisms of ferroptosis regulation

Mechanisms controlling cellular and systemic iron homeostasis

LRP8‐mediated selenocysteine uptake is a targetable vulnerability in MYCN‐amplified neuroblastoma

A non-canonical vitamin K cycle is a potent ferroptosis suppressor

Apolipoprotein E potently inhibits ferroptosis by blocking ferritinophagy

A cozy niche in an iron world

Ferroptosis: the Good, the Bad and the Ugly

Mouse brain proteomics establishes MDGA1 and CACHD1 as in vivo substrates of the Alzheimer protease BACE1

Ferroptosis at the crossroads of cancer-acquired drug resistance and immune evasion

Etablierung von Mausstämmen defizient für die Selenoproteine mitochondriale Thioredoxin-Reduktase und Phospholipid-Hydroperoxid-Glutathion-Peroxidase (PHGPx) und Charakterisierung einer Spermienkern-spezifischen Form der PHGPx

Etablierung von Mausstämmen defizient für die Selenoproteine mitochondriale Thioredoxin-Reduktase und Phospholipid-Hydroperoxid-Glutathion-Peroxidase (PHGPx) und Charakterisierung einer Spermienkern-spezifischen Form der PHGPx