Markus Mandl

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Johannes Kepler University Linz

Austria

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Recent Grants

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Alterations of the Molecular Clock by Modulating ARNTL2 Expression in Human Adipose Stem/Progenitor Cells Aiming to Treat Obesity and Ameliorate Aging

Open Date: 2020-09-01

Close Date:

Grant: Close

Role of Sprouty1 in Adipogenesis

Open Date: 2018-01-01

Close Date: 2018-06-01

Articles (7)

Year:

2022

Year:

2022

Year:

2022

Year:

2021

Year:

2021

Year:

2020

Year:

2020

Collaborators (1)

Alexander Weiss

European Research Institute for the Biology of Ageing, University of Groningen, UMC Groningen: Groningen, Netherlands

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Markus Mandl

Research Interests

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Recent Grants

Articles (7)

An organoid model derived from human adipose stem/progenitor cells to study adipose tissue physiology.

Dipeptidyl peptidase-4 cell surface expression marks an abundant adipose stem/progenitor cell population with high stemness in human white adipose tissue.

The circadian transcription factor ARNTL2 is regulated by weight-loss interventions in human white adipose tissue and inhibits adipogenesis

Selinexor decreases HIF-1α via inhibition of CRM1 in human osteosarcoma and hepatoma cells associated with an increased radiosensitivity.

Quiescence, Stemness and Adipogenic Differentiation Capacity in Human DLK1<sup>-</sup>/CD34<sup>+</sup>/CD24<sup>+</sup> Adipose Stem/Progenitor Cells.

CRISPR/Cas9-mediated gene knockout in human adipose stem/progenitor cells.

Sprouty1 Prevents Cellular Senescence Maintaining Proliferation and Differentiation Capacity of Human Adipose Stem/Progenitor Cells.

Collaborators (1)

Alexander Weiss

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