PMID-sentid Pub_year Sent_text comp_official_name comp_offsetprotein_name organism prot_offset 11682442-13 2001 Long term exposure (48 and 72 h) of villus strips to anti-sense oligonucleotides (5 microM) directed against transcription of OCT1 and OCT3 reduced the release of acetylcholine, whereas OCT2 anti-sense oliogonucleotides were ineffective. Acetylcholine 163-176 solute carrier family 22 member 1 Homo sapiens 126-130 11682442-15 2001 It is concluded that the release of non-neuronal acetylcholine from the human placenta is mediated via organic cation transporters of the OCT1 and OCT3 subtype. Acetylcholine 49-62 solute carrier family 22 member 1 Homo sapiens 138-142 33967805-1 2021 Organic Cation Transporter 1 (OCT1, gene symbol: SLC22A1) is predominately expressed in human liver, localized in the basolateral membrane of hepatocytes and facilitates the uptake of endogenous compounds (e.g. serotonin, acetylcholine, thiamine), and widely prescribed drugs (e.g. metformin, fenoterol, morphine). Acetylcholine 222-235 solute carrier family 22 member 1 Homo sapiens 0-28 33967805-1 2021 Organic Cation Transporter 1 (OCT1, gene symbol: SLC22A1) is predominately expressed in human liver, localized in the basolateral membrane of hepatocytes and facilitates the uptake of endogenous compounds (e.g. serotonin, acetylcholine, thiamine), and widely prescribed drugs (e.g. metformin, fenoterol, morphine). Acetylcholine 222-235 solute carrier family 22 member 1 Homo sapiens 30-34 33967805-1 2021 Organic Cation Transporter 1 (OCT1, gene symbol: SLC22A1) is predominately expressed in human liver, localized in the basolateral membrane of hepatocytes and facilitates the uptake of endogenous compounds (e.g. serotonin, acetylcholine, thiamine), and widely prescribed drugs (e.g. metformin, fenoterol, morphine). Acetylcholine 222-235 solute carrier family 22 member 1 Homo sapiens 49-56 19702534-1 2009 The polyspecific organic cation transporters OCT1 (SLC22A1), OCT2 (SLC22A2) and OCT3 (SLC22A3) mediate facilitated and bidirectional diffusion of small (< or = 500Da) organic cations with broad specificities for endogenous substrates such as choline, acetylcholine and monoamine neurotransmitters, as well as a variety of xenobiotics. Acetylcholine 254-267 solute carrier family 22 member 1 Homo sapiens 45-49 19702534-1 2009 The polyspecific organic cation transporters OCT1 (SLC22A1), OCT2 (SLC22A2) and OCT3 (SLC22A3) mediate facilitated and bidirectional diffusion of small (< or = 500Da) organic cations with broad specificities for endogenous substrates such as choline, acetylcholine and monoamine neurotransmitters, as well as a variety of xenobiotics. Acetylcholine 254-267 solute carrier family 22 member 1 Homo sapiens 51-58 15817714-6 2005 Tracer flux measurements showed that ACh is transported by OCT1 and OCT2 but not by OCT3. Acetylcholine 37-40 solute carrier family 22 member 1 Homo sapiens 59-63 15817714-10 2005 The data show that OCT1 and OCT2 mediate luminal ACh release in human airways and suggest that ACh release is blocked after inhalation of budesonide. Acetylcholine 49-52 solute carrier family 22 member 1 Homo sapiens 19-23 15817714-10 2005 The data show that OCT1 and OCT2 mediate luminal ACh release in human airways and suggest that ACh release is blocked after inhalation of budesonide. Acetylcholine 95-98 solute carrier family 22 member 1 Homo sapiens 19-23