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      Role of Lysocardiolipin Acyltransferase in Cigarette Smoke-Induced Lung Epithelial Cell Mitochondrial ROS, Mitochondrial Dynamics, and Apoptosis

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          A RAPID METHOD OF TOTAL LIPID EXTRACTION AND PURIFICATION

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            Calcium, ATP, and ROS: a mitochondrial love-hate triangle.

            The mitochondrion is at the core of cellular energy metabolism, being the site of most ATP generation. Calcium is a key regulator of mitochondrial function and acts at several levels within the organelle to stimulate ATP synthesis. However, the dysregulation of mitochondrial Ca(2+) homeostasis is now recognized to play a key role in several pathologies. For example, mitochondrial matrix Ca(2+) overload can lead to enhanced generation of reactive oxygen species, triggering of the permeability transition pore, and cytochrome c release, leading to apoptosis. Despite progress regarding the independent roles of both Ca(2+) and mitochondrial dysfunction in disease, the molecular mechanisms by which Ca(2+) can elicit mitochondrial dysfunction remain elusive. This review highlights the delicate balance between the positive and negative effects of Ca(2+) and the signaling events that perturb this balance. Overall, a "two-hit" hypothesis is developed, in which Ca(2+) plus another pathological stimulus can bring about mitochondrial dysfunction.
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              Is Open Access

              THE COLORIMETRIC DETERMINATION OF PHOSPHORUS

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                Author and article information

                Contributors
                (View ORCID Profile)
                Journal
                Cell Biochemistry and Biophysics
                Cell Biochem Biophys
                Springer Science and Business Media LLC
                1085-9195
                1559-0283
                March 2022
                November 01 2021
                March 2022
                : 80
                : 1
                : 203-216
                Article
                10.1007/s12013-021-01043-3
                34724158
                1afa2a05-a620-4cee-b6b8-ce8a118132c4
                © 2022

                https://www.springer.com/tdm

                https://www.springer.com/tdm

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