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Martha Hanschkow

Researcher at Leipzig University

Publications -  5
Citations -  25

Martha Hanschkow is an academic researcher from Leipzig University. The author has contributed to research in topics: Adipogenesis & Adipose tissue. The author has an hindex of 1, co-authored 4 publications receiving 2 citations.

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In Depth Quantitative Proteomic and Transcriptomic Characterization of Human Adipocyte Differentiation using the SGBS Cell Line

TL;DR: A comprehensive analysis of combined transcriptomic and proteomic alterations during adipocyte differentiation in Simpson–Golabi–Behmel Syndrome (SGBS) cells is provided and provides a deep molecular profile of adipogenesis that will support future studies to understand adipocyte function.
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PTEN regulates adipose progenitor cell growth, differentiation, and replicative aging.

TL;DR: In this article, the role of PTEN in adipose tissue development was investigated and RNA-Seq of control and PTEN knockdown APCs was performed. And the results provided evidence that PTEN is involved in the regulation of APC proliferation, differentiation, and senescence.
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Expression of the adipocyte progenitor markers MSCA1 and CD36 is associated with adipose tissue function in children.

TL;DR: In this paper, MSCA1 and cluster of differentiation 36 (CD36) were found to be associated with obesity-related alterations in adipose tissue (AT) development in children.
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Aberrant expression of agouti signaling protein (ASIP) as a cause of monogenic severe childhood obesity

TL;DR: In this article , a heterozygous tandem duplication at the ASIP (agouti signaling protein) gene locus causing ubiquitous, ectopic ASIP expression in a female patient with extreme childhood obesity was reported.
Posted ContentDOI

PTEN regulates adipocyte progenitor growth, differentiation and replicative aging

TL;DR: In this article, the role of PTEN in adipose tissue development was investigated and RNA sequencing of control and PTEN knockdown APCs was performed and it was shown that reducing PTEN levels using siRNA or CRISPR leads to an enhanced proliferation and differentiation of APCs.