Schizophrenia
|
0.400 |
GeneticVariation
|
disease |
BEFREE |
Association study of the excitatory amino acid transporter 2 (EAAT2) and glycine transporter 1 (GlyT1) gene polymorphism with schizophrenia in a Polish population.
|
31118638 |
2019 |
Schizophrenia
|
0.400 |
Biomarker
|
disease |
BEFREE |
The glycine transporter 1 (GlyT1) has emerged as a key novel target for the treatment of schizophrenia.
|
30080045 |
2018 |
Schizophrenia
|
0.400 |
Biomarker
|
disease |
BEFREE |
Numerous research groups have developed GlyT-1 inhibitors in the pursuit of providing a novel antipsychotic treatment for schizophrenia.
|
29338548 |
2018 |
Schizophrenia
|
0.400 |
Biomarker
|
disease |
BEFREE |
The development of glycine transporter 1 (GlyT1) inhibitors may offer putative treatments for schizophrenia and other disorders associated with hypofunction of the glutaminergic N-methyl-d-aspartate (NMDA) receptor.
|
29969029 |
2018 |
Schizophrenia
|
0.400 |
GeneticVariation
|
disease |
BEFREE |
PF-03463275 increased long-term potentiation only in SZs with peak effects at 40 mg twice a day (∼75% GlyT1 occupancy) and with a profile suggestive of an inverted U dose response.PF-03463275 was well-tolerated.
|
29499855 |
2018 |
Schizophrenia
|
0.400 |
Biomarker
|
disease |
BEFREE |
We proposed simultaneously inhibiting DAAO and GlyT-1 may be more effective than inhibition of either in improving the cognitive and global functioning of schizophrenia patients.
|
26691576 |
2017 |
Schizophrenia
|
0.400 |
Biomarker
|
disease |
BEFREE |
These results replicate previous reports of an inverted-U dose response curve and suggest further evaluation of GlyT1 inhibitors in schizophrenia negative symptoms is warranted.
|
27789188 |
2017 |
Schizophrenia
|
0.400 |
Biomarker
|
disease |
BEFREE |
These findings are of translational value since GlyT1 inhibitors are already in clinical development to treat cognitive symptoms in schizophrenia.
|
26302655 |
2015 |
Schizophrenia
|
0.400 |
Biomarker
|
disease |
PSYGENET |
Inhibition of glycine transporter 1 (GlyT1) augments N-methyl-D-aspartate receptor (NMDAR)-mediated transmission and represents a potential antipsychotic drug target according to the NMDAR hypofunction hypothesis of schizophrenia.
|
20647165 |
2011 |
Schizophrenia
|
0.400 |
Biomarker
|
disease |
PSYGENET |
This may be relevant for the suggested clinical application of GlyT1 inhibitors in the treatment of cognitive deficits, including schizophrenia, which is characterized by cognitive inflexibility in addition to the positive symptoms of the disease.
|
19824767 |
2009 |
Schizophrenia
|
0.400 |
Biomarker
|
disease |
PSYGENET |
We concluded that at least one susceptibility locus for schizophrenia may be located within or nearby SLC6A5, whereas SLC1A4, SLC1A5 and SLC6A9 are unlikely to be major susceptibility genes for schizophrenia in the Japanese population.
|
18638388 |
2008 |
Schizophrenia
|
0.400 |
Biomarker
|
disease |
LHGDN |
We concluded that at least one susceptibility locus for schizophrenia may be located within or nearby SLC6A5, whereas SLC1A4, SLC1A5 and SLC6A9 are unlikely to be major susceptibility genes for schizophrenia in the Japanese population.
|
18638388 |
2008 |
Schizophrenia
|
0.400 |
Biomarker
|
disease |
BEFREE |
We concluded that at least one susceptibility locus for schizophrenia may be located within or nearby SLC6A5, whereas SLC1A4, SLC1A5 and SLC6A9 are unlikely to be major susceptibility genes for schizophrenia in the Japanese population.
|
18638388 |
2008 |
Schizophrenia
|
0.400 |
Biomarker
|
disease |
PSYGENET |
Unchanged GlyT1 suggests that glycine transport is not markedly affected in schizophrenia, and therefore that increased synaptic removal is not the basis for the putative deficit in glycine modulation of NMDA receptors in the disorder.
|
18400471 |
2008 |
Schizophrenia
|
0.400 |
Biomarker
|
disease |
BEFREE |
Unchanged GlyT1 suggests that glycine transport is not markedly affected in schizophrenia, and therefore that increased synaptic removal is not the basis for the putative deficit in glycine modulation of NMDA receptors in the disorder.
|
18400471 |
2008 |
Schizophrenia
|
0.400 |
Biomarker
|
disease |
BEFREE |
The new generation of GlyT1 inhibitors may represent a novel treatment of patients suffering from schizophrenia and/or other neuropathological conditions.
|
16611082 |
2006 |
Schizophrenia
|
0.400 |
GeneticVariation
|
disease |
BEFREE |
Further studies with other GlyT1 variants, relating either to schizophrenia, psychotic symptoms or to therapeutic response in schizophrenia, are suggested.
|
16604304 |
2006 |