PMID-sentid Pub_year Sent_text comp_official_name comp_offsetprotein_name organism prot_offset 20128812-6 2010 Further, the selective 5-HT reuptake inhibitor fluvoxamine increased WAY 100635 induced head twitches in SERT +/+ and +/- mice. Fluvoxamine 47-58 solute carrier family 6 (neurotransmitter transporter, serotonin), member 4 Mus musculus 105-109 16079297-9 2005 Furthermore, the time-dependent change of SERT mRNA expression and uptake activity in the midbrain is suggested to be the mechanism underlying the 24-h rhythm of anti-immobility effect of fluvoxamine. Fluvoxamine 188-199 solute carrier family 6 (neurotransmitter transporter, serotonin), member 4 Mus musculus 42-46 18655786-13 2008 Furthermore, differences in 5-HT transporter binding may cause variations in responses to fluvoxamine. Fluvoxamine 90-101 solute carrier family 6 (neurotransmitter transporter, serotonin), member 4 Mus musculus 28-44 15678084-3 2005 Oral administration of fluvoxamine, fluoxetine, paroxetine and sertraline at pharmacologically relevant doses exerted dose- and time-dependent binding activity of brain SERT as revealed by significant increases in KD for specific [3H]paroxetine binding, and the in vivo SERT-binding potency was in the order of paroxetine>>fluoxetine, sertraline>fluvoxamine. Fluvoxamine 23-34 solute carrier family 6 (neurotransmitter transporter, serotonin), member 4 Mus musculus 169-173 15678084-3 2005 Oral administration of fluvoxamine, fluoxetine, paroxetine and sertraline at pharmacologically relevant doses exerted dose- and time-dependent binding activity of brain SERT as revealed by significant increases in KD for specific [3H]paroxetine binding, and the in vivo SERT-binding potency was in the order of paroxetine>>fluoxetine, sertraline>fluvoxamine. Fluvoxamine 23-34 solute carrier family 6 (neurotransmitter transporter, serotonin), member 4 Mus musculus 270-274 15678084-3 2005 Oral administration of fluvoxamine, fluoxetine, paroxetine and sertraline at pharmacologically relevant doses exerted dose- and time-dependent binding activity of brain SERT as revealed by significant increases in KD for specific [3H]paroxetine binding, and the in vivo SERT-binding potency was in the order of paroxetine>>fluoxetine, sertraline>fluvoxamine. Fluvoxamine 355-366 solute carrier family 6 (neurotransmitter transporter, serotonin), member 4 Mus musculus 169-173 15678084-11 2005 In conclusion, the present study has provided the first in vivo evidences to support that fluvoxamine, fluoxetine, paroxetine and sertraline orally administered bind to the pharmacologically relevant brain SERT in mice and that their SERT-binding characteristics is closely associated with the pharmacokinetics and inhibition of marble-burying behaviour. Fluvoxamine 90-101 solute carrier family 6 (neurotransmitter transporter, serotonin), member 4 Mus musculus 206-210 15678084-11 2005 In conclusion, the present study has provided the first in vivo evidences to support that fluvoxamine, fluoxetine, paroxetine and sertraline orally administered bind to the pharmacologically relevant brain SERT in mice and that their SERT-binding characteristics is closely associated with the pharmacokinetics and inhibition of marble-burying behaviour. Fluvoxamine 90-101 solute carrier family 6 (neurotransmitter transporter, serotonin), member 4 Mus musculus 234-238 14501158-4 2003 The compound was as effective as SERT inhibitors such as fluoxetine and fluvoxamine in a 5-hydroxytryptophan-enhancing test in mice. Fluvoxamine 72-83 solute carrier family 6 (neurotransmitter transporter, serotonin), member 4 Mus musculus 33-37