Zobrazeno 1 - 10
of 25
pro vyhledávání: '"Jessica K. Nelson"'
Autor:
Jessica K. Nelson, May Zaw Thin, Theodore Evan, Steven Howell, Mary Wu, Bruna Almeida, Nathalie Legrave, Duco S. Koenis, Gabriela Koifman, Yoichiro Sugimoto, Miriam Llorian Sopena, James MacRae, Emma Nye, Michael Howell, Ambrosius P. Snijders, Andreas Prachalias, Yoh Zen, Debashis Sarker, Axel Behrens
Publikováno v:
Nature Communications, Vol 13, Iss 1, Pp 1-18 (2022)
The biological roles of deubiquitinating enzymes (DUBs) in pancreatic ductal adenocarcinoma (PDAC) are not fully explored. Here the authors perform activity based proteomics with a loss of function genetic screen and identify that USP25 promotes PDAC
Externí odkaz:
https://doaj.org/article/cd8dab384b2a46bf9a9f3d5ce3b2663f
Autor:
Omar M. Khan, Jorge Almagro, Jessica K. Nelson, Stuart Horswell, Vesela Encheva, Kripa S. Keyan, Bruce E. Clurman, Ambrosius P. Snijders, Axel Behrens
Publikováno v:
Nature Communications, Vol 12, Iss 1, Pp 1-14 (2021)
The tumor suppressor FBW7 is a substrate adaptor for the E3 ubiquitin ligase complex SKP1-CUL1-F-box (SCF) and itself a target for ubiquitylation. Here, the authors show that TRIP12 mediates branched K11-linked ubiquitylation of FBW7, to regulate its
Externí odkaz:
https://doaj.org/article/6e27448b8929476da30da600acc41eb2
Autor:
Vincenzo Sorrentino, Jessica K. Nelson, Elena Maspero, André R.A. Marques, Lilith Scheer, Simona Polo, Noam Zelcer
Publikováno v:
Journal of Lipid Research, Vol 54, Iss 8, Pp 2174-2184 (2013)
Low density lipoprotein (LDL) cholesterol is taken up into cells via clathrin-mediated endocytosis of the LDL receptor (LDLR). Following dissociation of the LDLR-LDL complex, LDL is directed to lysosomes whereas the LDLR recycles to the plasma membra
Externí odkaz:
https://doaj.org/article/695bff5da0664a00b1b31b5753bab0ed
Autor:
Emma C L Cook, Jessica K Nelson, Vincenzo Sorrentino, Duco Koenis, Martina Moeton, Saskia Scheij, Roelof Ottenhoff, Boris Bleijlevens, Anke Loregger, Noam Zelcer
Publikováno v:
PLoS ONE, Vol 12, Iss 2, p e0172721 (2017)
Cellular cholesterol metabolism is subject to tight regulation to maintain adequate levels of this central lipid molecule. Herein, the sterol-responsive Liver X Receptors (LXRs) play an important role owing to their ability to reduce cellular cholest
Externí odkaz:
https://doaj.org/article/ace271f92020402192c273dfc41da462
Autor:
Kripa S. Keyan, Jorge Almagro, Bruce E. Clurman, Ambrosius P. Snijders, Stuart Horswell, Vesela Encheva, Jessica K. Nelson, Axel Behrens, Omar M. Khan
Publikováno v:
Nature Communications, Vol 12, Iss 1, Pp 1-14 (2021)
Nature Communications
Nature Communications
The tumour suppressor FBW7 is a substrate adaptor for the E3 ubiquitin ligase complex SKP1-CUL1-F-box (SCF), that targets several oncoproteins for proteasomal degradation. FBW7 is widely mutated and FBW7 protein levels are commonly downregulated in c
Autor:
Jessica K. Nelson, May Zaw Thin, Theodore Evan, Steven Howell, Mary Wu, Bruna Almeida, Nathalie Legrave, Duco S. Koenis, Gabriela Koifman, Yoichiro Sugimoto, Miriam Llorian Sopena, James MacRae, Emma Nye, Michael Howell, Ambrosius P. Snijders, Andreas Prachalias, Yoh Zen, Debashis Sarker, Axel Behrens
Publikováno v:
Nature communications. 13(1)
Deubiquitylating enzymes (DUBs) play an essential role in targeted protein degradation and represent an emerging therapeutic paradigm in cancer. However, their therapeutic potential in pancreatic ductal adenocarcinoma (PDAC) has not been explored. He
Autor:
Jessica K. Nelson, Nienke M. van Loon, Noam Zelcer, Martina Moeton, Suzanne A.E. van Wouw, Roelof Ottenhoff, Saskia Scheij, Jenina Kingma
Publikováno v:
Atherosclerosis, 315, 1-9. Elsevier Ireland Ltd
Background and aims Cholesterol metabolism is tightly regulated by transcriptional and post-transcriptional mechanisms. Accordingly, dysregulation of cholesterol metabolism is a major risk factor for the development of coronary artery disease and ass
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::aadca31bfc399e7a7a2573f7b82e1a09
https://pure.amc.nl/en/publications/regulation-of-intestinal-ldlr-by-the-lxridol-axis(6a64ee1d-17dd-474a-a545-fbf6e6d967c8).html
https://pure.amc.nl/en/publications/regulation-of-intestinal-ldlr-by-the-lxridol-axis(6a64ee1d-17dd-474a-a545-fbf6e6d967c8).html
Autor:
Ambrosius P. Snijders, Atanu Chakraborty, Vesela Encheva, Alessandro Annibaldi, Mathias Rosenfeldt, Paula Moreno, Marco A. Calzado, Rocio Sancho, Jessica K. Nelson, Axel Behrens, Richard Mitter, E. Josue Ruiz, Markus E. Diefenbacher, Gianmaria Liccardi, Pascal Meier, Fabio Pucci
Publikováno v:
The Journal of Experimental Medicine
Ruiz, E J, Diefenbacher, M E, Nelson, J K, Sancho, R, Pucci, F, Chakraborty, A, Moreno, P, Annibaldi, A, Liccardi, G, Encheva, V, Mitter, R, Rosenfeldt, M, Snijders, A P, Meier, P, Calzado, M A & Behrens, A 2019, ' LUBAC determines chemotherapy resistance in squamous cell lung cancer ', The Journal of experimental medicine, vol. 216, no. 2, pp. 450-465 . https://doi.org/10.1084/jem.20180742
Ruiz, E J, Diefenbacher, M E, Nelson, J K, Sancho, R, Pucci, F, Chakraborty, A, Moreno, P, Annibaldi, A, Liccardi, G, Encheva, V, Mitter, R, Rosenfeldt, M, Snijders, A P, Meier, P, Calzado, M A & Behrens, A 2019, ' LUBAC determines chemotherapy resistance in squamous cell lung cancer ', The Journal of experimental medicine, vol. 216, no. 2, pp. 450-465 . https://doi.org/10.1084/jem.20180742
This study identifies a novel therapeutic strategy against cisplatin-resistant lung squamous cell carcinoma (LSCC) using mouse models and patient samples. LSCC chemoresistance depends on LUBAC and high NF-κB activity, mechanisms that can be targeted
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::938586481f7b5e9f80a52af1980992d2
https://nbn-resolving.org/urn:nbn:de:bvb:20-opus-227146
https://nbn-resolving.org/urn:nbn:de:bvb:20-opus-227146
Autor:
Peter L. Hordijk, Igor Kovacevic, Saskia Scheij, Emma C. L. Cook, Noam Zelcer, Jessica K. Nelson, Anke Loregger, Huib Ovaa, Marten A. Hoeksema
Publikováno v:
Journal of biological chemistry, 291(9), 4813-4825. American Society for Biochemistry and Molecular Biology Inc.
Journal of Biological Chemistry, 291(9), 4813-4825. American Society for Biochemistry and Molecular Biology Inc.
Nelson, J K, Cook, E C L, Loregger, A, Hoeksema, M A, Scheij, S, Kovacevic, I, Hordijk, P L, Ovaa, H & Zelcer, N 2016, ' Deubiquitylase Inhibition Reveals Liver X Receptor-independent Transcriptional Regulation of the E3 Ubiquitin Ligase IDOL and Lipoprotein Uptake ', Journal of Biological Chemistry, vol. 291, no. 9, pp. 4813-4825 . https://doi.org/10.1074/jbc.M115.698688
Journal of Biological Chemistry, 291(9), 4813-4825. American Society for Biochemistry and Molecular Biology Inc.
Nelson, J K, Cook, E C L, Loregger, A, Hoeksema, M A, Scheij, S, Kovacevic, I, Hordijk, P L, Ovaa, H & Zelcer, N 2016, ' Deubiquitylase Inhibition Reveals Liver X Receptor-independent Transcriptional Regulation of the E3 Ubiquitin Ligase IDOL and Lipoprotein Uptake ', Journal of Biological Chemistry, vol. 291, no. 9, pp. 4813-4825 . https://doi.org/10.1074/jbc.M115.698688
Cholesterol metabolism is subject to complex transcriptional and nontranscriptional regulation. Herein, the role of ubiquitylation is emerging as an important post-translational modification that regulates cholesterol synthesis and uptake. Similar to
Autor:
Rossella Avagliano Trezza, Claire Heride, Vincenzo Sorrentino, Sylvie Urbé, Jessica K. Nelson, Ben Distel, Noam Zelcer
Publikováno v:
Circulation research, 118(3), 410-419. Lippincott Williams and Wilkins
Rationale: The low-density lipoprotein (LDL) receptor (LDLR) is a central determinant of circulating LDL-cholesterol and as such subject to tight regulation. Recent studies and genetic evidence implicate the inducible degrader of the LDLR (IDOL) as a