Zobrazeno 1 - 2
of 2
pro vyhledávání: '"Herbert J. Zeh"'
Autor:
Jun Huang, Ke Liu, Guido Kroemer, Changfeng Li, Borong Zou, Daolin Tang, Rui Kang, Jiao Liu, Herbert J. Zeh
Publikováno v:
Cellular and Molecular Gastroenterology and Hepatology
Cellular and Molecular Gastroenterology and Hepatology, Philadelphia, PA : American Gastroenterological Association, [2015]-, 2022, 13 (2), pp.483-500. ⟨10.1016/j.jcmgh.2021.09.008⟩
Cellular and Molecular Gastroenterology and Hepatology, Vol 13, Iss 2, Pp 483-500 (2022)
Cellular and Molecular Gastroenterology and Hepatology, Philadelphia, PA : American Gastroenterological Association, [2015]-, 2022, 13 (2), pp.483-500. ⟨10.1016/j.jcmgh.2021.09.008⟩
Cellular and Molecular Gastroenterology and Hepatology, Vol 13, Iss 2, Pp 483-500 (2022)
Background & Aims Pancreatitis is characterized by acinar cell death and persistent inflammation. Ferroptosis is a type of lipid peroxidation-dependent necrosis, which is negatively regulated by glutathione peroxidase 4. We studied how trypsin, a ser
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2672294190e99060699bb76afc1e37a6
https://hal.sorbonne-universite.fr/hal-03549632/file/1-s2.0-S2352345X2100196X-main.pdf
https://hal.sorbonne-universite.fr/hal-03549632/file/1-s2.0-S2352345X2100196X-main.pdf
Autor:
Rui Kang, Guido Kroemer, Yangchun Xie, Lin Zhang, Xinxin Song, Timothy R. Billiar, Meizuo Zhong, Hua Yuan, Jinbao Liu, Shan Zhu, Xiaofang Sun, Herbert J. Zeh, Michael T. Lotze, Yong Fan, Daolin Tang
Publikováno v:
Cell Reports
Cell Reports, 2017, 20 (7), pp.1692-1704. ⟨10.1016/j.celrep.2017.07.055⟩
Cell Reports, Elsevier Inc, 2017, 20 (7), pp.1692-1704. 〈10.1016/j.celrep.2017.07.055〉
Cell Reports, Elsevier Inc, 2017, 20 (7), pp.1692-1704. ⟨10.1016/j.celrep.2017.07.055⟩
Cell Reports, Vol 20, Iss 7, Pp 1692-1704 (2017)
Cell Reports, 2017, 20 (7), pp.1692-1704. ⟨10.1016/j.celrep.2017.07.055⟩
Cell Reports, Elsevier Inc, 2017, 20 (7), pp.1692-1704. 〈10.1016/j.celrep.2017.07.055〉
Cell Reports, Elsevier Inc, 2017, 20 (7), pp.1692-1704. ⟨10.1016/j.celrep.2017.07.055⟩
Cell Reports, Vol 20, Iss 7, Pp 1692-1704 (2017)
International audience; Ferroptosis is a form of regulated cell death that may facilitate the selective elimination of tumor cells. The tumor suppressor p53 (TP53) has been demonstrated to promote ferroptosis via a transcription-dependent mechanism.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8bcd40efe94c05ae26a8725b052d94fc
https://hal.sorbonne-universite.fr/hal-01581142
https://hal.sorbonne-universite.fr/hal-01581142