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Table representation of search results timeline featuring number of search results per year.

Year Number of Results
1994 1
1995 2
1996 1
1997 4
1999 5
2000 2
2001 2
2003 1
2004 1
2005 4
2008 5
2009 4
2010 3
2011 3
2012 1
2013 2
2014 1
2015 1
2016 1
2018 1
2019 1
2020 3
2021 1
2022 1
2023 1
2024 0

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48 results

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Page 1
Cardiomyoblast caveolin expression: Effects of simulated diabetes, α-linolenic acid and cell signaling pathways.
Russell JS, Griffith TA, Peart JN, Headrick JP. Russell JS, et al. Am J Physiol Cell Physiol. 2020 Apr 29. doi: 10.1152/ajpcell.00499.2019. Online ahead of print. Am J Physiol Cell Physiol. 2020. PMID: 32348174
Cells were exposed to glucose (25 vs. 5 mM), insulin (100 nM) or palmitate (0.1 mM), individually or combined, and effects of adenylate cyclase (AC) activation (50 muM forskolin), focal adhesion kinase (FAK) or protein kinase C b(2) (PKCbeta(2)) inhibition (1 muM FAK Inhibitor 14 …
Cells were exposed to glucose (25 vs. 5 mM), insulin (100 nM) or palmitate (0.1 mM), individually or combined, and effects of adenylate cycl …
Bioinformatics exploration of potential common therapeutic targets for systemic and pulmonary arterial hypertension-induced myocardial hypertrophy.
Chen L, Li M, Shen M, Zhu Y, Chen K, Huang X, Zheng C, Wang Q, Lin H, Liao W, Bin J, Ma S, Liao Y. Chen L, et al. Acta Biochim Biophys Sin (Shanghai). 2023 May 25;55(5):831-841. doi: 10.3724/abbs.2023071. Acta Biochim Biophys Sin (Shanghai). 2023. PMID: 37232575 Free PMC article.
Furthermore, we identify dehydroisoandrosterone (DHEA), iloprost and 4,5-dianilinophthalimide (DAPH) as potential therapeutic drugs targeting both left and right ventricular hypertrophy and validate the effect of DHEA. ...
Furthermore, we identify dehydroisoandrosterone (DHEA), iloprost and 4,5-dianilinophthalimide (DAPH) as potential thera …
Zymosan suppresses leukotriene C₄ synthase activity in differentiating monocytes: antagonism by aspirin and protein kinase inhibitors.
Esser J, Gehrmann U, Salvado MD, Wetterholm A, Haeggström JZ, Samuelsson B, Gabrielsson S, Scheynius A, Rådmark O. Esser J, et al. FASEB J. 2011 Apr;25(4):1417-27. doi: 10.1096/fj.10-175828. Epub 2011 Jan 12. FASEB J. 2011. PMID: 21228223
Several findings indicate phosphoregulation of LTC(4)S: increased activity during MM6 cell differentiation correlated with reduced phosphorylation of 70-kDa ribosomal protein S6 kinase (p70S6K), which could phosphorylate purified LTC(4)S; the p70S6K inhibitor rapamycin (20 nM) do …
Several findings indicate phosphoregulation of LTC(4)S: increased activity during MM6 cell differentiation correlated with reduced phosphory …
Protein kinase CbetaI interacts with the beta1-adrenergic signaling pathway to attenuate lipolysis in rat adipocytes.
Nakamura J. Nakamura J. Biochim Biophys Acta. 2008 May;1781(5):277-81. doi: 10.1016/j.bbalip.2008.03.007. Epub 2008 Apr 8. Biochim Biophys Acta. 2008. PMID: 18440322
The lipolysis-attenuating effect of PMA was blocked by the PKCbetaI/betaII inhibitor LY 333531, but not by the PKCbetaII inhibitor CGP 53353 or the PKCdelta inhibitor rottlerin. These data suggest that PKCbetaI interacts with beta1-AR signaling and attenuates lipoly …
The lipolysis-attenuating effect of PMA was blocked by the PKCbetaI/betaII inhibitor LY 333531, but not by the PKCbetaII inhibitor CGP …
Acute glucose-induced downregulation of PKC-betaII accelerates cultured VSMC proliferation.
Yamamoto M, Acevedo-Duncan M, Chalfant CE, Patel NA, Watson JE, Cooper DR. Yamamoto M, et al. Am J Physiol Cell Physiol. 2000 Sep;279(3):C587-95. doi: 10.1152/ajpcell.2000.279.3.C587. Am J Physiol Cell Physiol. 2000. PMID: 10942708 Free article.
High glucose (25 mM) increased DNA synthesis and accelerated cell proliferation compared with normal glucose (5.5 mM) in AoSMC and A10 cells, but not in betaI-A10 and betaII-A10 cells. The PKC-betaII specific inhibitor CGP-53353 inhibited glucose-induced cell prolif …
High glucose (25 mM) increased DNA synthesis and accelerated cell proliferation compared with normal glucose (5.5 mM) in AoSMC and A10 cells …
Real-Time Translocation and Function of PKCβII Isoform in Response to Nociceptive Signaling via the TRPV1 Pain Receptor.
Mandadi S, Armati PJ, Roufogalis BD. Mandadi S, et al. Pharmaceuticals (Basel). 2011 Nov 11;4(11):1503-1517. doi: 10.3390/ph4111503. Pharmaceuticals (Basel). 2011. PMID: 27721335 Free PMC article.
In addition PMA-induced sensitization of TRPV1 to capsaicin response in DRG neurons was attenuated by PKCbetaII blocker CGP 53353. Capsaicin response via TRPV1 in the DRG neurons was confirmed by TRPV1 antagonist AMG 9810. ...
In addition PMA-induced sensitization of TRPV1 to capsaicin response in DRG neurons was attenuated by PKCbetaII blocker CGP 53353 …
Phorbol 12-myristate 13-acetate inhibits the antilipolytic action of insulin, probably via the activity of protein kinase Cε.
Nakamura J. Nakamura J. Eur J Pharmacol. 2010 Dec 1;648(1-3):188-94. doi: 10.1016/j.ejphar.2010.08.048. Epub 2010 Sep 15. Eur J Pharmacol. 2010. PMID: 20826143
The pan-PKC inhibitors GF 109203X and chelerythrine inhibited the PMA effect, but the PKCalpha/beta inhibitors Go 6976 and CGP 53353 did not. Exposure of cells to PMA downregulated PKCs alpha, betaI, and delta within 3 h and PKCepsilon within 12 h. ...
The pan-PKC inhibitors GF 109203X and chelerythrine inhibited the PMA effect, but the PKCalpha/beta inhibitors Go 6976 and CGP 533 …
48 results