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2
Published in 2020 at "Protein & Cell"
DOI: 10.1007/s13238-020-00753-3
Abstract: Sterol-regulatory element binding proteins (SREBPs) are the key transcriptional regulators of lipid metabolism. The activation of SREBP requires translocation of the SREBP precursor from the endoplasmic reticulum to the Golgi, where it is sequentially cleaved…
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Keywords:
protease;
srebp;
site protease;
c12orf49 ... See more keywords
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0
Published in 2021 at "Cell death and differentiation"
DOI: 10.1038/s41418-020-00731-6
Abstract: Site-1 protease (S1P) is a Golgi-located protein that activates unique membrane-bound latent transcription factors, and it plays an indispensable role in endoplasmic reticulum stress, lipid metabolism, inflammatory response and lysosome function. A patient with S1P…
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Keywords:
s1p;
transcription;
site protease;
osteoclastogenesis ... See more keywords
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Published in 2018 at "Scientific Reports"
DOI: 10.1038/s41598-018-32705-7
Abstract: The unfolded protein response (UPR) and activation of XBP1 is necessary for high secretory efficiency and functional differentiation of antibody secreting cells (ASCs). The UPR additionally includes a branch in which membrane-bound transcription factors, exemplified…
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Keywords:
secreting cells;
antibody secreting;
secretory;
site ... See more keywords
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Published in 2018 at "Biology Open"
DOI: 10.1242/bio.032094
Abstract: ABSTRACT Site-1 protease (S1P) is a proprotein convertase with essential functions in the conversion of precursor proteins to their active form. In earlier studies, we demonstrated that S1P ablation in the chondrocyte lineage results in…
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Keywords:
bone;
site protease;
differentiation;
mice ... See more keywords
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2
Published in 2023 at "Frontiers in Immunology"
DOI: 10.3389/fimmu.2023.1009973
Abstract: Sterol regulatory element-binding proteins (SREBPs) are key transcription factors that control fatty acid and cholesterol metabolism. As the major SREBP isoform in macrophages, SREBP1a is also required for inflammatory and phagocytotic functions. However, it is…
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Keywords:
response macrophages;
caspase;
site protease;
activation ... See more keywords