PMID-sentid Pub_year Sent_text comp_official_name comp_offsetprotein_name organism prot_offset 14583742-9 2004 CCK-8s injected into the dPAG induced Fos immunoreactivity in several brain areas related to defensive behavior, including the PAG, median, and dorsal raphe nuclei, superior colliculus, lateral septal nuclei, medial hypothalamus, and medial amygdala. dpag 25-29 Fos proto-oncogene, AP-1 transcription factor subunit Rattus norvegicus 38-41 12900043-2 2003 A previous Fos study also revealed a marked activation of the ventrolateral part of the periaqueductal gray (VLPAG) and a much smaller activation of its dorsal part (DPAG). dpag 166-170 Fos proto-oncogene, AP-1 transcription factor subunit Rattus norvegicus 11-14 12900043-4 2003 We now test the role of the DPAG to see if its small activation (as revealed by Fos) is of any functional significance in the contextual fear response. dpag 28-32 Fos proto-oncogene, AP-1 transcription factor subunit Rattus norvegicus 80-83 27856260-8 2017 Furthermore, Fos protein-labelled neurons were observed in the dPAG after the stimulation of the dmVMH with 9nmol of NMDA. dpag 63-67 Fos proto-oncogene, AP-1 transcription factor subunit Rattus norvegicus 13-16 9389166-4 1996 When both NRO and dPAG were stimulated, Fos- like immunoreactive (FLI) cells in the ventral periaqueductal grey (vPAG) and paragigantocellularis lateralis (PGL) were increased as compared with cases in which the stimulation was only delivered to dPAG, i.e., reaching a FLI cell count value of 66.5 +/- 8.3 and 10.8 +/- 1.5 respectively. dpag 18-22 Fos proto-oncogene, AP-1 transcription factor subunit Rattus norvegicus 40-43 9389166-4 1996 When both NRO and dPAG were stimulated, Fos- like immunoreactive (FLI) cells in the ventral periaqueductal grey (vPAG) and paragigantocellularis lateralis (PGL) were increased as compared with cases in which the stimulation was only delivered to dPAG, i.e., reaching a FLI cell count value of 66.5 +/- 8.3 and 10.8 +/- 1.5 respectively. dpag 246-250 Fos proto-oncogene, AP-1 transcription factor subunit Rattus norvegicus 40-43 20514481-7 2010 Ultrasound application increased c-Fos expression in the dorsal and dorsolateral PAG (dPAG, dlPAG) and amygdaloid subregions. dpag 86-90 Fos proto-oncogene, AP-1 transcription factor subunit Rattus norvegicus 33-38 24878577-4 2014 This LPS-induced hyperalgesia was accompanied by distinct recruitment of supra-spinal regions involved in analgesia as indicated by significantly attenuated Fos-protein induction in the rostral dorsal periaqueductal grey (DPAG) as well as rostral and caudal axes of the ventrolateral PAG (VLPAG). dpag 222-226 Fos proto-oncogene, AP-1 transcription factor subunit Rattus norvegicus 157-160 25567506-10 2015 Moreover, c-Fos study shows the optical stimulation activates restricted range in midbrain: the optical stimulation affected only dPAG and its downstreams but electric stimulation activates both the upstream and downstream circuits, in which the glutamatergic neurons are largely occupied and play important role in "Stop" and "Escape" behavior controls. dpag 130-134 Fos proto-oncogene, AP-1 transcription factor subunit Rattus norvegicus 10-15 24409327-9 2014 However, the immunohistochemical analysis revealed that LPA 18:1 increased c-Fos expression in the DPAG. dpag 99-103 Fos proto-oncogene, AP-1 transcription factor subunit Rattus norvegicus 75-80 23183042-11 2013 These data refute a cause-and-effect relationship between enhanced dPAG c-fos expression and a reduction in SR. dpag 67-71 Fos proto-oncogene, AP-1 transcription factor subunit Rattus norvegicus 72-77 17900567-3 2007 The present paper examines the Fos-protein distribution in the brain of rats submitted to a conditioned place aversion (CPA) paradigm using the dPAG chemical stimulation with semicarbazide (SMC), an inhibitor of the GABA synthesizing enzyme, as US and the quadrant of an arena where the drug was injected as the paired neutral stimulus. dpag 144-148 Fos proto-oncogene, AP-1 transcription factor subunit Rattus norvegicus 31-34 15649440-1 2005 Freezing and escape responses induced by gradual increases in the intensity of the electrical current applied to dorsal regions of the periaqueductal gray (dPAG) cause a distinct pattern of Fos distribution in the brain. dpag 156-160 Fos proto-oncogene, AP-1 transcription factor subunit Rattus norvegicus 190-193 15649440-4 2005 To examine further this issue we measured Fos protein expression in brain areas activated by stimulation of the dPAG with glutamate (5 nmol/0.2 microL) and N-methyl-D-aspartate (NMDA) at doses that provoke either freezing (4 nmol/0.2 microL) or escape (7 nmol/0.2 microL) responses, respectively. dpag 112-116 Fos proto-oncogene, AP-1 transcription factor subunit Rattus norvegicus 42-45 15265647-11 2004 Thus, the present results support the Fos data and indicate that the DPAG is involved in the expression of some but not all of the cardiovascular and behavioral components of the response to cat odor. dpag 69-73 Fos proto-oncogene, AP-1 transcription factor subunit Rattus norvegicus 38-41