1992
DOI: 10.1016/0960-9822(92)90024-5
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Cloners quick on the uptake

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Cited by 15 publications
(11 citation statements)
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“…Besides, sodium: neurotransmitter symporter (SNF) family genes (such as SLC6A1 , SLC6A6 , SLC6A8 , SLC6A11 , SLC6A12, and SLC6A13 ) were also expanded in yellow drum in contrast to large yellow croaker. Those genes are essential for the release, re‐uptaking, and recycling of neurotransmitters at synapses (Attwell & Bouvier, ). SLC6A1 , SLC6A11, and SLC6A13 , widely distributed in brain, encode sodium‐dependent transporters that uptake gamma‐aminobutyric acid (GABA) (Zhou et al, ).…”
Section: Resultsmentioning
confidence: 99%
“…Besides, sodium: neurotransmitter symporter (SNF) family genes (such as SLC6A1 , SLC6A6 , SLC6A8 , SLC6A11 , SLC6A12, and SLC6A13 ) were also expanded in yellow drum in contrast to large yellow croaker. Those genes are essential for the release, re‐uptaking, and recycling of neurotransmitters at synapses (Attwell & Bouvier, ). SLC6A1 , SLC6A11, and SLC6A13 , widely distributed in brain, encode sodium‐dependent transporters that uptake gamma‐aminobutyric acid (GABA) (Zhou et al, ).…”
Section: Resultsmentioning
confidence: 99%
“…It is possible that proline oxidase plays a significant role in the formation of some neural glutamate pools (34). The possible role ofproline as a neurotransmitter has recently become the focus of considerable attention, with the cloning of a proline transporter molecule (35,36). This is expressed in or near glutamatergic neurons, whereas the relevant enzymes for synthesis of glutamate from proline are found in glial cells, not neurons (reviewed in ref.…”
Section: Discussionmentioning
confidence: 99%
“…This uncertainty has led to the assumption that the glycine concentration in the synaptic cleft is close to the values (1-10 M) measured in the CSF (Westergren et al, 1994), which corresponds to a saturating level for the glycine site of most NMDARs. In contrast, based on the thermodynamics of the transporter, which predicts a limiting external glycine concentration in the 100 nM range, it has been suggested that an active uptake of glycine by transporters might be sufficient to reduce below saturation the glycine concentration in the synaptic cleft (Ascher, 1990;Attwell and Bouvier, 1992;Attwell et al, 1993), thereby allowing the variations in the local glycine concentration to become a signal acting on NMDARs. This hypothesis has two major kinetic limitations.…”
Section: Abstract: Glutamate Receptor; Nmda; Coagonist; D-serine; Samentioning
confidence: 99%
“…The theoretical limit for the decrease of the external glycine concentration is imposed by the thermodynamics of the transport, as defined by the relation (Attwell and Bouvier, 1992;Attwell et al, 1993): noted that under our experimental condition, the equilibrium is never obtained, because a steady-state inward flux is present between the bath and the oocyte cytoplasm.…”
Section: Control Of the [Gly] M By Glyt1bmentioning
confidence: 99%