Articles with "ppp1cb" as a keyword



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Delineation of LZTR1 mutation-positive patients with Noonan syndrome and identification of LZTR1 binding to RAF1–PPP1CB complexes

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Published in 2018 at "Human Genetics"

DOI: 10.1007/s00439-018-1951-7

Abstract: RASopathies are a group of developmental disorders caused by mutations in genes that regulate the RAS/MAPK pathway and include Noonan syndrome (NS), Costello syndrome, cardiofaciocutaneous syndrome and other related disorders. Whole exome sequencing studies recently… read more here.

Keywords: raf1 ppp1cb; noonan syndrome; mutation positive; ppp1cb ... See more keywords
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Chebulinic Acid Suppresses Adipogenesis in 3T3-L1 Preadipocytes by Inhibiting PPP1CB Activity

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Published in 2022 at "International Journal of Molecular Sciences"

DOI: 10.3390/ijms23020865

Abstract: Depletion of protein phosphatase-1 catalytic subunit beta (PPP1CB), a serine/threonine protein phosphatase and potent adipogenic activator, suppresses the differentiation of 3T3-L1 preadipocytes into mature adipocytes. Therefore, PPP1CB is considered as a potential therapeutic target for… read more here.

Keywords: acid suppresses; 3t3 preadipocytes; ppp1cb; adipogenesis 3t3 ... See more keywords