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This book focuses on the emerging role of ferroptosis in human
diseases. It gives a detailed perspective on how to induce or
suppress ferroptosis to treat challenging conditions such as
infectious diseases, including COVID-19, tuberculosis, parasitic
diseases and cancer. The book serves as a practical guide by
providing a valuable collection of all currently known activators
or inhibitors of ferroptosis. It will enable readers to choose
molecules for experimental design for in vitro and in vivo studies
of ferroptosis. Furthermore, this volume highlights the aspects of
iron metabolism and its connection to ferritinophagy, a ferritin
selective autophagy, with profound implications in
neurodegenerative diseases such as Alzheimer, Parkinson, Huntington
and ALS. Lastly, it describes necroptosis, another important form
of cell death, along with its connections to human disorders and
potential crosstalk with ferroptosis. While covering basic
concepts, the book delves into mechanisms and modulation of
ferroptosis for treating a wide variety of human diseases thus
offering a valuable and informative resource for both, scientists
and clinical researchers.
Hamed Alborzinia uses the biosensor chip to monitor the metabolic
and morphological changes in cancer cell lines in real time,
particularly: (i) real-time measurements of basic cancer cell
metabolism of different cancer cell lines; (ii) a detailed timeline
of the metabolic response to cisplatin treatment and clear
detection of the time span between start of cisplatin treatment and
onset of cell death, which reflects the time required for the
underlying molecular mechanisms of cell fate decision; (iii) direct
functional measurement of the biological activity of a key
regulatory protein of cellular metabolism following the kinetic
change in respiration upon SIRT3 overexpression; and (iv) the
time-resolved impact of several organometallic compounds on cell
metabolism and cell morphology, including unexpected and not yet
understood highly significant and specific effects on cell-cell
interaction and adhesion.
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