G-protein coupled receptor 88 knockdown in the associative striatum reduces psychiatric symptoms in a translational male rat model of Parkinson diseaseJOURNAL OF PSYCHIATRY & NEUROSCIENCEIF3.32021-01-014OAAI
Knock-down of G protein-coupled receptor 88 in the striatum reduces psychiatric symptoms in a rat non-motor model of Parkinson's diseaseEUROPEAN NEUROPSYCHOPHARMACOLOGYIF6.72018-03-010PREAI
No association between bipolar disorder and alleles at a functional polymorphism in the COMT gene - Biomed European Bipolar Collaborative GroupBRITISH JOURNAL OF PSYCHIATRYIF7.62018-01-0347PREAI
Inactivation of the orphan G protein-coupled receptor Gpr88 in the dorsal striatum reverses the effects of dopamine depletion in a rat model of Parkinson's diseaseEUROPEAN NEUROPSYCHOPHARMACOLOGYIF6.72017-10-010PREAI
Local inactivation of G protein-coupled receptor 88 restores motor and cognitive functions impaired in a rat model of schizophreniaEUROPEAN NEUROPSYCHOPHARMACOLOGYIF6.72014-10-010PREAI
Local inactivation of Gpr88 in the nucleus accumbens attenuates behavioral deficits elicited by the neonatal administration of phencyclidine in ratsMOLECULAR PSYCHIATRYIF10.12014-08-2622OAAI
Local inactivation of the G protein-coupled receptor 88 attenuates behavioural deficits elicited by neonatal administration of phencyclidine in ratsEUROPEAN NEUROPSYCHOPHARMACOLOGYIF6.72014-03-010PREAI
Zinc Finger Protein 191 (ZNF191/Zfp191) Is Necessary to Maintain Neural Cells As Cycling ProgenitorsStem CellsIF3.62009-04-0936OAAI
A model for in vivo studies of human tyrosine hydroxylase geneSCHIZOPHRENIA RESEARCHIF3.52003-03-010PREAI
Paradoxical Methylation of the tyrosine hydroxylase Gene in Mouse Preimplantation EmbryosGENOMICSIF32002-12-017PRE
A tetranucleotide polymorphic microsatellite, located in the first intron of the tyrosine hydroxylase gene, acts as a transcription regulatory element in vitroHUMAN MOLECULAR GENETICSIF3.21998-03-01156OAAI
A rare allele of a tetranucleotide polymorphic microsatellite, located in the first intron of the tyrosine hydroxylase gene, is associated with schizophrenia and shows transcription regulatory activity in vitroSCHIZOPHRENIA RESEARCHIF3.51998-01-010PREAI
Germline mutations of the CDKN2 gene in UK melanoma familiesHUMAN MOLECULAR GENETICSIF3.21997-11-01128OAAI
Association of DNA polymorphism in the first intron of the tyrosine hydroxylase gene with disturbances of the catecholaminergic system in schizophreniaSCHIZOPHRENIA RESEARCHIF3.51997-02-0142PREAI
ASSOCIATION OF MANIC-DEPRESSIVE ILLNESS WITH TYROSINE-HYDROXYLASE MICROSATELLITE MARKERLANCETIF88.51995-04-0175PREAI
COCAINE-INDUCED TURNING BEHAVIOR IN RATS WITH 6-HYDROXYDOPAMINE LESIONS - EFFECT OF TRANSPLANTS OF FETAL SUBSTANTIA-NIGRAEUROPEAN JOURNAL OF PHARMACOLOGYIF4.71991-12-014PREAI
SUPPRESSION BY PROGABIDE OF ETHANOL WITHDRAWAL SYNDROME IN RATSEUROPEAN JOURNAL OF PHARMACOLOGYIF4.71985-03-0126PREAI
个人简介
教育背景
工作经历
荣誉奖项
未登录.png){kind=icon}
未登录个人简介教育背景工作经历荣誉奖项
研究方向