Publications by authors named "C W Mandl"

Solid-state electrolytes with high ionic conductivity will be crucial for future energy storage systems. Among many possible materials, thiophosphates offer both favourable mechanical properties and fast ionic transport. β-LiPS, as a member of the thiophosphate family, has gained recent attention, due to its remarkable increase in Li ionic conductivity when prepared solvent-assisted synthesis.

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  • * MDM2-p53 antagonists can restore p53 activity but have dose-limiting toxicities such as thrombocytopenia and neutropenia; to reduce these side effects, less frequent dosing is being explored with drugs like brigimadlin.
  • * Brigimadlin, a new MDM2-p53 antagonist, has shown promise in preclinical models by effectively restoring p53 function and inhibiting tumor growth in cancers with TP53 mutations, supporting its further testing in cancer
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We recently reported that growth/differentiation factor 15 (GDF15) and its receptor GDNF family receptor alpha-like (GFRAL) are expressed in the periventricular germinal epithelium thereby regulating apical progenitor proliferation. However, the mechanisms are unknown. We now found GFRAL in primary cilia and altered cilia morphology upon GDF15 ablation.

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The expression of growth/differentiation factor (GDF) 15 increases in the ganglionic eminence (GE) late in neural development, especially in neural stem cells (NSCs). However, GDF15 function in this region remains unknown. We report that GDF15 receptor is expressed apically in the GE and that GDF15 ablation promotes proliferation and cell division in the embryonic GE and in the adult ventricular-subventricular zone (V-SVZ).

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Selective covalent labelling of enzymes using small molecule probes has advanced the scopes of protein profiling. The covalent bond formation to a specific target is the key step of activity-based protein profiling (ABPP), a method which has become an indispensable tool for measuring enzyme activity in complex matrices. With respect to carbohydrate processing enzymes, strategies for ABPP so far involve labelling the active site of the enzyme, which results in permanent loss of activity.

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