Glutamate receptor, ionotropic, N-methyl D-aspartate 2A (GRIN2A) gene as a positional candidate for attention-deficit/hyperactivity disorder in the 16p13 region.
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MicroRNA-219 modulates NMDA receptor-mediated neurobehavioral dysfunctionCandidate genes and neuropsychological phenotypes in children with ADHD: review of association studiesAssociation of the glutamate receptor subunit gene GRIN2B with attention-deficit/hyperactivity disorderGenetic polymorphisms affecting susceptibility to mercury neurotoxicity in children: summary findings from the Casa Pia Children's Amalgam clinical trialAttention-deficit hyperactivity disorder (ADHD).Positive selection, relaxation, and acceleration in the evolution of the human and chimp genome.Molecular genetics of attention deficit hyperactivity disorder.Investigation of post-transcriptional gene regulatory networks associated with autism spectrum disorders by microRNA expression profiling of lymphoblastoid cell lines.Association between the GRM7 rs3792452 polymorphism and attention deficit hyperacitiveity disorder in a Korean sample.Are endophenotypes based on measures of executive functions useful for molecular genetic studies of ADHD?The uncompetitive NMDA receptor antagonists ketamine and memantine preferentially increase the choice for a small, immediate reward in low-impulsive ratsCommon and specific liability to addiction: approaches to association studies of opioid addictionHeroin addiction in African Americans: a hypothesis-driven association studyAttention-deficit hyperactivity disorder (ADHD) and tuberous sclerosis complex.Molecular genetics of attention-deficit/hyperactivity disorder: an overviewNeuropsychological endophenotypes in attention-deficit/hyperactivity disorder: a review of genetic association studies.The role of memantine in the treatment of psychiatric disorders other than the dementias: a review of current preclinical and clinical evidence.Memantine versus Methylphenidate in Children and Adolescents with Attention Deficit Hyperactivity Disorder: A Double-Blind, Randomized Clinical Trial.The effects of GRIN2B and DRD4 gene variants on local functional connectivity in attention-deficit/hyperactivity disorder.The GRIN2B and GRIN2A Gene Variants Are Associated With Continuous Performance Test Variables in ADHD.Genetic Insights Into ADHD Biology.Genetic polymorphisms of GRIN2A and GRIN2B modify the neurobehavioral effects of low-level lead exposure in children
P2860
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P2860
Glutamate receptor, ionotropic, N-methyl D-aspartate 2A (GRIN2A) gene as a positional candidate for attention-deficit/hyperactivity disorder in the 16p13 region.
description
2004 nî lūn-bûn
@nan
2004年の論文
@ja
2004年学术文章
@wuu
2004年学术文章
@zh-cn
2004年学术文章
@zh-hans
2004年学术文章
@zh-my
2004年学术文章
@zh-sg
2004年學術文章
@yue
2004年學術文章
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2004年學術文章
@zh-hant
name
Glutamate receptor, ionotropic ...... disorder in the 16p13 region.
@en
Glutamate receptor, ionotropic ...... disorder in the 16p13 region.
@nl
type
label
Glutamate receptor, ionotropic ...... disorder in the 16p13 region.
@en
Glutamate receptor, ionotropic ...... disorder in the 16p13 region.
@nl
prefLabel
Glutamate receptor, ionotropic ...... disorder in the 16p13 region.
@en
Glutamate receptor, ionotropic ...... disorder in the 16p13 region.
@nl
P2093
P2860
P356
P1433
P1476
Glutamate receptor, ionotropic ...... disorder in the 16p13 region.
@en
P2093
Ickowicz A
Kennedy JL
P2860
P2888
P304
P356
10.1038/SJ.MP.4001455
P407
P577
2004-05-01T00:00:00Z