Zobrazeno 1 - 7
of 7
pro vyhledávání: '"Dexter J Robichaux"'
Autor:
Jia Song, Jiao Wu, Dexter J. Robichaux, Tingting Li, Shuyue Wang, Maria J. Arredondo Sancristobal, Bingning Dong, Dobromir Dobrev, Jason Karch, Sandhya S. Thomas, Na Li
Publikováno v:
Cells, Vol 13, Iss 2, p 108 (2024)
High-protein diets (HPDs) offer health benefits, such as weight management and improved metabolic profiles. The effects of HPD on cardiac arrhythmogenesis remain unclear. Atrial fibrillation (AF), the most common arrhythmia, is associated with inflam
Externí odkaz:
https://doaj.org/article/93cccce91b474c99ac1b1a842161780d
Autor:
Pooja Patel, Arielys Mendoza, Dexter J. Robichaux, Meng C. Wang, Xander H. T. Wehrens, Jason Karch
Publikováno v:
Frontiers in Cell and Developmental Biology, Vol 9 (2021)
Mitochondrial permeability transition pore (MPTP)-dependent necrosis contributes to numerous pathologies in the heart, brain, and skeletal muscle. The MPTP is a non-selective pore in the inner mitochondrial membrane that is triggered by high levels o
Externí odkaz:
https://doaj.org/article/d0aa832a997846169e462d49c336ea7a
Publikováno v:
Journal of Molecular and Cellular Cardiology. 174:47-55
Mitochondrial permeability transition pore (mPTP)-dependent cell death is a form of necrotic cell death that is driven by mitochondrial dysfunction by the opening of the mPTP and is triggered by increases in matrix levels of Ca
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::cb0eec64c53cc1ba9ddfa5d074ace4fc
https://doi.org/10.1016/j.yjmcc.2022.11.003
https://doi.org/10.1016/j.yjmcc.2022.11.003
Autor:
Dharaniya Sakthivel, Alexandra N. Brown-Suedel, Francesca Keane, Shixia Huang, Kenneth Mc Sherry, Chloé I Charendoff, Kevin P. Dunne, Dexter J Robichaux, BaoChau Le, Crystal S. Shin, Alexandre F Carisey, Jonathan M. Flanagan, Lisa Bouchier-Hayes
Publikováno v:
bioRxiv
Mutation in nucleophosmin (NPM1) causes relocalization of this normally nucleolar protein to the cytoplasm (NPM1c+). Despite NPM1 mutation being the most common driver mutation in cytogenetically normal adult acute myeloid leukemia (AML), the mechani
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::068057070548de56646af1a6eb36ab5b
https://doi.org/10.1101/2023.05.29.542723
https://doi.org/10.1101/2023.05.29.542723
Autor:
Song, Jia1 (AUTHOR) majoarredondo@outlook.com, Wu, Jiao2 (AUTHOR), Robichaux, Dexter J.3 (AUTHOR) dobromir.dobrev@uk-essen.de, Li, Tingting1 (AUTHOR), Wang, Shuyue4 (AUTHOR), Arredondo Sancristobal, Maria J.1 (AUTHOR), Dong, Bingning4 (AUTHOR), Dobrev, Dobromir3,5,6 (AUTHOR), Karch, Jason3 (AUTHOR), Thomas, Sandhya S.2,7 (AUTHOR), Li, Na1 (AUTHOR) nal@bcm.edu
Publikováno v:
Cells (2073-4409). Jan2024, Vol. 13 Issue 2, p108. 17p.
Publikováno v:
Hematology Week; 8/22/2024, p1309-1309, 1p
Publikováno v:
Cardiovascular Week; 1/22/2024, p268-268, 1p