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Christian Münch

Molekularbiologe

Name	Christian Münch
Zeit	2011- (Wirkungsdaten)
Ort	Frankfurt am Main (Wirkungsort) Boston, Mass. (Wirkungsort) Cambridge (Wirkungsort) Deutschland USA Großbritannien
Geschlecht	männlich
Akademischer Grad bzw. Titel	Dr. (University of Cambridge, Laboratory of Molecular Biology) (2011)
Beruf	Molekularbiologe (charakteristischer Beruf)
Variante	C. Münch Christian Munch
Beziehung	Goethe-Universität Frankfurt am Main. Institut für Biochemie (Gruppenleiter) (2016-) Harvard Medical School (Postdoktorand) (2012-2016)
Weitere Angaben	Seit 2018 zusätzlich als Forscher am Frankfurt Cancer Institute und Cardio-Pulmonary Institute in Frankfurt am Main tätig
Quelle	https://biochem2.com/people/muench-christian (Stand: 12.11.2024)
Datensatztyp	Person
GND-Nummer	1343225906
Datensatz-ID	1343225906
Beteiligt an alle anzeigen Mammalian target of rapamycin inhibition protects glioma cells from temozolomide-induced cell death A high-resolution map of functional miR-181 response elements in the thymus reveals the role of coding sequence targeting and an alternative seed match A high-resolution map of functional miR-181 response elements in the thymus reveals the role of coding sequence targeting and an alternative seed match Interaction proteomics display the spatio-temporal complexity of mitochondrial RNA granules Signalling the mammalian mitochondrial unfolded protein response Distinct and targetable role of calcium-sensing receptor in leukaemia Protein quality control: from molecular mechanisms to therapeutic intervention—EMBO workshop, May 21–26 2023, Srebreno, Croatia A high-resolution map of functional miR-181 response elements in the thymus reveals the role of coding sequence targeting and an alternative seed match An atypical GABARAP binding module drives the pro-autophagic potential of the AML-associated NPM1c variant Impact of mesenchymal stromal cell–derived vesicular cargo on B-cell acute lymphoblastic leukemia progression LUBAC assembles a ubiquitin signaling platform at mitochondria for signal amplification and transport of NF‐κB to the nucleus Correction: Translatome proteomics identifies autophagy as a resistance mechanism to on-target FLT3 inhibitors in acute myeloid leukemia Lipid and protein content profiling of isolated native autophagic vesicles Inhibition of mTOR signaling protects human glioma cells from hypoxia-induced cell death in an autophagy-independent manner Protein import motor complex reacts to mitochondrial misfolding by reducing protein import and activating mitophagy Translatome proteomics identifies autophagy as a resistance mechanism to on-target FLT3 inhibitors in acute myeloid leukemia The beginning of a new era: pioneering direct screens for RNA modulators Mitochondrial RNA modifications shape metabolic plasticity in metastasis Mitochondrial protein import motor PAM reacts on protein misfolding stress by protein import reduction and induction of PINK1-mitophagy SRSF3 and SRSF7 modulate 3′UTR length through suppression or activation of proximal polyadenylation sites and regulation of CFIm levels A chemical toolbox for labeling and degrading engineered Cas proteins DynaTMT: a user-friendly tool to process combined SILAC/TMT data SRSF3 and SRSF7 modulate 3′UTR length through suppression or activation of proximal polyadenylation sites and regulation of CFIm levels Loss of mitochondrial ClpP, Lonp1, and Tfam triggers transcriptional induction of Rnf213, a susceptibility factor for moyamoya disease Growth factor receptor signaling inhibition prevents SARS-CoV-2 replication Loss of mitochondrial ClpP, Lonp1, and Tfam triggers transcriptional induction of Rnf213, a susceptibility factor for moyamoya disease

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Christian Münch

Mammalian target of rapamycin inhibition protects glioma cells from temozolomide-induced cell death

A high-resolution map of functional miR-181 response elements in the thymus reveals the role of coding sequence targeting and an alternative seed match

A high-resolution map of functional miR-181 response elements in the thymus reveals the role of coding sequence targeting and an alternative seed match

Interaction proteomics display the spatio-temporal complexity of mitochondrial RNA granules

Signalling the mammalian mitochondrial unfolded protein response

Distinct and targetable role of calcium-sensing receptor in leukaemia

Protein quality control: from molecular mechanisms to therapeutic intervention—EMBO workshop, May 21–26 2023, Srebreno, Croatia

A high-resolution map of functional miR-181 response elements in the thymus reveals the role of coding sequence targeting and an alternative seed match

An atypical GABARAP binding module drives the pro-autophagic potential of the AML-associated NPM1c variant

Impact of mesenchymal stromal cell–derived vesicular cargo on B-cell acute lymphoblastic leukemia progression

LUBAC assembles a ubiquitin signaling platform at mitochondria for signal amplification and transport of NF‐κB to the nucleus

Correction: Translatome proteomics identifies autophagy as a resistance mechanism to on-target FLT3 inhibitors in acute myeloid leukemia

Lipid and protein content profiling of isolated native autophagic vesicles

Inhibition of mTOR signaling protects human glioma cells from hypoxia-induced cell death in an autophagy-independent manner

Protein import motor complex reacts to mitochondrial misfolding by reducing protein import and activating mitophagy

Translatome proteomics identifies autophagy as a resistance mechanism to on-target FLT3 inhibitors in acute myeloid leukemia

The beginning of a new era: pioneering direct screens for RNA modulators

Mitochondrial RNA modifications shape metabolic plasticity in metastasis

Mitochondrial protein import motor PAM reacts on protein misfolding stress by protein import reduction and induction of PINK1-mitophagy

SRSF3 and SRSF7 modulate 3′UTR length through suppression or activation of proximal polyadenylation sites and regulation of CFIm levels

A chemical toolbox for labeling and degrading engineered Cas proteins

DynaTMT: a user-friendly tool to process combined SILAC/TMT data

SRSF3 and SRSF7 modulate 3′UTR length through suppression or activation of proximal polyadenylation sites and regulation of CFIm levels

Loss of mitochondrial ClpP, Lonp1, and Tfam triggers transcriptional induction of Rnf213, a susceptibility factor for moyamoya disease

Growth factor receptor signaling inhibition prevents SARS-CoV-2 replication

Loss of mitochondrial ClpP, Lonp1, and Tfam triggers transcriptional induction of Rnf213, a susceptibility factor for moyamoya disease