PMID-sentid Pub_year Sent_text comp_official_name comp_offsetprotein_name organism prot_offset 34030609-5 2021 Overexpressed interleukin (IL)-6 induced the MEK5/ERK5, JAK2/STAT3, and MAPK signalling cascades in streptozotocin-induced diabetic rats. Streptozocin 100-114 Janus kinase 2 Rattus norvegicus 56-60 24802166-8 2014 Additionally, adenovirus-mediated upregulation of renal SOCS2 markedly inhibited STZ-induced phosphorylation increases of Janus kinase (JAK) 2, signal transducer and activator of transcription (STAT) 3, STAT5 and extracellular receptor-activated kinase (ERK) 1/2. Streptozocin 81-84 Janus kinase 2 Rattus norvegicus 122-142 15601754-8 2005 Treatment of streptozotocin-induced diabetic rats with ketanserin (5 mg.kg-1.day-1) reduced activation of JAK2 and STAT1 but not STAT3 in endothelium-denuded thoracic aorta in vivo. Streptozocin 13-27 Janus kinase 2 Rattus norvegicus 106-110 17526654-9 2007 These results demonstrate that JAK2 activation in vivo participates in the development of vascular complications associated with STZ-induced diabetes. Streptozocin 129-132 Janus kinase 2 Rattus norvegicus 31-35 16449352-4 2006 Consistent with these in vitro results, both albumin protein excretion and phosphorylation of JAK2, STAT1, and STAT3 were attenuated in renal glomeruli by administration of simvastatin in a streptozotocin-induced rat model of HG diabetes. Streptozocin 190-204 Janus kinase 2 Rattus norvegicus 94-98 16290054-7 2005 In vivo administration of apocynin (1.5 mM) resulted in a significant decrease ( 50%), while the ETA receptor antagonist ABT-627 completely inhibited phosphorylation of JAK2 in aortae from STZ-induced diabetic rats. Streptozocin 189-192 Janus kinase 2 Rattus norvegicus 169-173 14678947-8 2004 STZ stimulated glomerular phosphorylation of JAK2, STAT1, STAT3, and STAT5. Streptozocin 0-3 Janus kinase 2 Rattus norvegicus 45-49 35219163-16 2022 Besides, STZ-induced inflammatory response, oxidative stress, and phosphorylation levels of PI3K, AKT, JAK2, and STAT3 were reduced by CAD in the rats. Streptozocin 9-12 Janus kinase 2 Rattus norvegicus 103-107 12086960-4 2002 Our results demonstrate that JAK2, insulin receptor substrate (IRS)-1, Shc, ERKs, and Akt are widely distributed in the kidney, and after GH treatment, there is a significant increase in phosphorylation of these proteins in STZ-induced diabetic rats compared with controls. Streptozocin 224-227 Janus kinase 2 Rattus norvegicus 29-33 34178835-11 2021 Results: Oral administration of M. charantia nanoparticles (50 mg/kg) to STZ-induced diabetic untreated rats significantly ((p < 0.05) down-regulated the mRNA expression of Akt, PI3k, TGF-beta, JAK2, STAT3 and upregulated the mRNA expression of PTEN, SOCS3 and SOCS4, thus establishing the role of M. charantia nanoparticles in alleviating DN in diabetic rats. Streptozocin 73-76 Janus kinase 2 Rattus norvegicus 194-198