PMID-sentid Pub_year Sent_text comp_official_name comp_offsetprotein_name organism prot_offset 27551099-7 2016 We also found that intracellular infusion of a selective PKCalpha inhibitor (Go6976) blocked LTD induction in the mutants, as in WT, suggesting that functional compensation occurred downstream of PKCalpha. Go 6976 77-83 protein kinase C, alpha Mus musculus 57-65 27770660-6 2016 Selective inhibition of PKC alpha/beta II using Go6976 or siRNA abolished the CA-induced Nrf-2/HO-1 signaling, and consequently suppressed the cytoprotective activity of CA on the LPS-induced cell death. Go 6976 48-54 protein kinase C, alpha Mus musculus 24-41 27551099-7 2016 We also found that intracellular infusion of a selective PKCalpha inhibitor (Go6976) blocked LTD induction in the mutants, as in WT, suggesting that functional compensation occurred downstream of PKCalpha. Go 6976 77-83 protein kinase C, alpha Mus musculus 196-204 27142955-3 2016 We used 2 different approaches: blockade of biological activity of PKCalpha by intraperitoneal application of the conventional PKC inhibitor Go6976 in C57BL/6 wild-type mice and PKCalpha-deficient mice on a 129/Sv genetic background. Go 6976 141-147 protein kinase C, alpha Mus musculus 67-75 27131602-7 2016 Additionally, treatment with Go6976 blocked the effect of t10-c12CLA on perilipin-1 phosphorylation, implicating PKCalpha in perilipin-1 phosphorylation, and thus a regulator of triglyceride catabolism. Go 6976 29-35 protein kinase C, alpha Mus musculus 113-121 20973912-6 2011 Pre-treatment of pancreatic acinar cells with Go6976 (1-10 nM) and rottlerin (1-10 muM) inhibited PKC-alpha and PKC-delta phosphorylation, respectively, but not the other way round. Go 6976 46-52 protein kinase C, alpha Mus musculus 98-107 26190181-7 2015 Treatment of cells with 1 muM Go 6976, a Ca(2+)-specific PKC inhibitor reduced Ca(2+) mobilization and membrane-associated PKCalpha and p-PKCalpha in both cell types. Go 6976 30-37 protein kinase C, alpha Mus musculus 57-60 26190181-7 2015 Treatment of cells with 1 muM Go 6976, a Ca(2+)-specific PKC inhibitor reduced Ca(2+) mobilization and membrane-associated PKCalpha and p-PKCalpha in both cell types. Go 6976 30-37 protein kinase C, alpha Mus musculus 123-131 26190181-7 2015 Treatment of cells with 1 muM Go 6976, a Ca(2+)-specific PKC inhibitor reduced Ca(2+) mobilization and membrane-associated PKCalpha and p-PKCalpha in both cell types. Go 6976 30-37 protein kinase C, alpha Mus musculus 138-146 23977428-12 2013 Go6976 (100 nM), a PKCalpha inhibitor, abolished the effect of CCPA to inhibit BK current (99+-3% of control). Go 6976 0-6 protein kinase C, alpha Mus musculus 19-27 23402219-7 2014 However, in the presence of a selective classical PKC isoform inhibitor, Go6976, proplatelet formation was conversely enhanced. Go 6976 73-79 protein kinase C, alpha Mus musculus 50-53 23220724-9 2013 To determine if PKC is involved in aldosterone-induced O(2)(-) production, we exposed the O(2)(-) cells to a nonselective PKC inhibitor chelerythrine chloride, a specific PKCalpha inhibitor Go6976, or a PKCalpha siRNA, and the aldosterone-induced increase in O(2)(-) production was blocked. Go 6976 190-196 protein kinase C, alpha Mus musculus 171-179 23028752-5 2012 However, the induced effect of FSH was dose-dependently inhibited by the specific PKC alpha and betaI inhibitor Go6976, and 100 nM Go6976 completely blocked FSH function in oocyte meiotic resumption. Go 6976 112-118 protein kinase C, alpha Mus musculus 82-91 23028752-5 2012 However, the induced effect of FSH was dose-dependently inhibited by the specific PKC alpha and betaI inhibitor Go6976, and 100 nM Go6976 completely blocked FSH function in oocyte meiotic resumption. Go 6976 131-137 protein kinase C, alpha Mus musculus 82-91 21705673-8 2011 Finally, we found that ACh-induced vasodilation was inhibited by the PKCalpha inhibitor Go-6976 in small mesenteric arteries from wild-type mice, but not in TRPV4 null mice. Go 6976 88-95 protein kinase C, alpha Mus musculus 69-77 20951242-5 2011 Treatment with Go6976, an inhibitor of PKCalpha and PKCbetaI, increased alkaline phosphatase (ALP) activity as well as gene expression of ALP and Osteocalcin (OCN), and enhanced calcification of the extracellular matrix. Go 6976 15-21 protein kinase C, alpha Mus musculus 39-47 21473788-12 2011 Inhibition of conventional PKC by Go6976 mitigated the TNF-alpha-induced p115RhoGEF phosphorylation and RhoA activation. Go 6976 34-40 protein kinase C, alpha Mus musculus 27-30 20053794-10 2010 The PKC-alpha- and betaI-selective inhibitor Go 6976 (100 nM) decreased flow-stimulated net O(2)(-) production from 54 +/- 15 to 2 +/- 1 AU/s (P < 0.04; n = 5). Go 6976 45-52 protein kinase C, alpha Mus musculus 4-13 20417251-6 2010 Intrathecal pretreatment with inhibitors (Go6976, PKCepsilonV1-2 or PKC zetapseudosubstrate) of the PKCalpha, epsilon or zeta isoforms significantly reduced the PRE-induced pain facilitatory effect. Go 6976 42-48 protein kinase C, alpha Mus musculus 100-108 19592614-9 2009 These effects of ENBA were blocked by Go-6976 (PKC-alpha inhibitor) and PD-98059 (p42/p44 MAPK inhibitor). Go 6976 38-45 protein kinase C, alpha Mus musculus 47-56 16740968-3 2006 After a 3-d treatment with 3 nm Go6976, a specific inhibitor of classical PKC isoforms, cells were characterized by the presence of one elongated process similar to that observed after treatment with Ang II or with CGP42112, a selective AT2 receptor agonist. Go 6976 32-38 protein kinase C, alpha Mus musculus 74-77 19403597-6 2009 Inhibition of PKCalpha and PKCbeta with Go6976 had no effect. Go 6976 40-46 protein kinase C, alpha Mus musculus 14-22 18367332-7 2008 We found that knocking out PS1 or PS2 alone resulted in increased Erk activity and that this effect could be reversed by the PKCalpha inhibitor Go6976. Go 6976 144-150 protein kinase C, alpha Mus musculus 125-133 16740968-8 2006 Incubation of NG108-15 cells with Go6976 (3 nm) inhibited basal p42/p44(mapk) phosphorylation, but failed to interfere with its activation by the AT(2) receptor, indicating that inhibition of PKC alpha is not directly involved in the Rap1-MEK-p42/p44(mapk) cascade. Go 6976 34-40 protein kinase C, alpha Mus musculus 192-201 11841365-8 2002 Go 6976, an inhibitor of calcium-dependent (conventional) PKC, proved to promote hair epithelial cell growth. Go 6976 0-7 protein kinase C, alpha Mus musculus 58-61 15161371-6 2004 In addition, Go6976, a classical PKC (cPKC) inhibitor, which specifically inhibits PKC (alpha and betaI), also promoted apoptosis. Go 6976 13-19 protein kinase C, alpha Mus musculus 33-36 15161371-6 2004 In addition, Go6976, a classical PKC (cPKC) inhibitor, which specifically inhibits PKC (alpha and betaI), also promoted apoptosis. Go 6976 13-19 protein kinase C, alpha Mus musculus 39-42 12093473-5 2002 The zymosan-induced increase in iPLA2 activity was suppressed by pretreatment with 4beta-phorbol 12-myristate 13-acetate for 10 hr, by which PKCalpha and PKCdelta, but not PKCbeta and PKCepsilon, were depleted, and by Go6976, a PKCalpha inhibitor, but not rottlerin, a PKCdelta inhibitor. Go 6976 218-224 protein kinase C, alpha Mus musculus 141-149 15198639-7 2004 Inhibition of PKC-alpha with Go6976 had no effect on cell number in the zinc-deficient group. Go 6976 29-35 protein kinase C, alpha Mus musculus 14-23 15262987-4 2004 The PKC inhibitors bisindolymaleimide I and Go6976, blocked CREB phosphorylation. Go 6976 44-50 protein kinase C, alpha Mus musculus 4-7 15150589-3 2004 Proteasome expression induced by PIF was attenuated by 4alpha-phorbol 12-myristate 13-acetate (100 nM) and by the PKC inhibitors Ro31-8220 (10 microM), staurosporine (300 nM), calphostin C (300 nM) and Go 6976 (200 microM). Go 6976 202-209 protein kinase C, alpha Mus musculus 114-117 34078525-7 2021 Similar results were obtained from the mouse embryonic fibroblasts exposed to a PKCalpha inhibitor, Go6976. Go 6976 100-106 protein kinase C, alpha Mus musculus 80-88 11483412-4 2001 In addition, the effect of PKCalpha inhibitor Go6976 on the SPP-induced PLD activation in myoblasts, where RhoA function was inactivated, was consistent with a dual regulation of the enzyme through RhoA and PKCalpha. Go 6976 46-52 protein kinase C, alpha Mus musculus 27-35 11488451-9 2001 A significant reduction of the euxanthone-induced neuritogenic effect was also observed when the PKC isoform-specific inhibitor Go6976 was included in the culture. Go 6976 128-134 protein kinase C, alpha Mus musculus 97-100 11278470-4 2001 Here, we report that treatment of Swiss 3T3 cells with Go6976, a selective inhibitor of PKC alpha, caused a sustained elevation of IGF-I-stimulated nuclear PLC activity. Go 6976 55-61 protein kinase C, alpha Mus musculus 88-97 32783140-6 2020 Similar to Calphostin C, PKC alpha and betaI inhibitor Go6976 exposure also reduced ASIC1a protein expression. Go 6976 55-61 protein kinase C, alpha Mus musculus 11-44