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Magda Wolna

Researcher at University of Oxford

Publications -  18
Citations -  636

Magda Wolna is an academic researcher from University of Oxford. The author has contributed to research in topics: Ferroportin & Hepcidin. The author has an hindex of 6, co-authored 14 publications receiving 335 citations.

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Cardiac ferroportin regulates cellular iron homeostasis and is important for cardiac function

TL;DR: It is shown that ferroportin expression in cardiomyocytes is essential to intracellular iron homeostasis and to normal cardiac function, and that the site of deposition of iron within the heart determines the severity with which it affects cardiac function.
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An essential cell-autonomous role for hepcidin in cardiac iron homeostasis.

TL;DR: These findings are the first demonstration of a cell-autonomous role for hepcidin in iron homeostasis and raise the possibility that such function may also be important in other tissues that express both hePCidin and ferroportin, such as the kidney and the brain.
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Antibody responses and correlates of protection in the general population after two doses of the ChAdOx1 or BNT162b2 vaccines

TL;DR: In this article , the authors investigated anti-spike IgG antibody responses and correlates of protection after second doses of ChAdOx1 or BNT162b2 vaccines for severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2).
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Dependency of the spindle assembly checkpoint on Cdk1 renders the anaphase transition irreversible.

TL;DR: Cyclin B is the only APC/CCdc20 substrate whose degradation at the onset of anaphase is necessary to prevent SAC reactivation, and the mutual activation of tension sensitive SAC and Cdk1 creates a bistable system that ensures complete activation of separase and total downregulation of Cdk2 when all chromosomes have bioriented.
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Sgol2 provides a regulatory platform that coordinates essential cell cycle processes during meiosis I in oocytes

TL;DR: In mammalian oocytes Shugoshin-like protein 2 (Sgol2) in addition to protecting cohesin, plays an important role in turning off the SAC, in promoting the congression and bi-orientation of bivalents on meiosis I spindles, in facilitating formation of K-fibers and in limiting bivalent stretching.