换一批LRRTM1 on chromosome 2p12 is a maternally suppressed gene that is associated paternally with handedness and schizophrenia.
第一作者：
C,Francks
第一单位：
Wellcome Trust Centre for Human Genetics, University of Oxford, Oxford, UK. clyde.francks@well.ox.ac.uk
作者：
医学主题词
动物(Animals);脑(Brain);细胞系, 转化(Cell Line, Transformed);染色体, 人, 2对(Chromosomes, Human, Pair 2);家庭卫生(Family Health);女(雌)性(Female);功能偏侧化(Functional Laterality);基因表达调控, 发育期(Gene Expression Regulation, Developmental);疾病遗传易感性(Genetic Predisposition to Disease);基因型(Genotype);人类(Humans);原位杂交(In Situ Hybridization);核型分析(Karyotyping);男(雄)性(Male);膜蛋白质类(Membrane Proteins);小鼠(Mice);神经组织蛋白质类(Nerve Tissue Proteins);精神分裂症(Schizophrenia);亚细胞部分(Subcellular Fractions)
DOI
10.1038/sj.mp.4002053
PMID
17667961
发布时间
2025-05-29
基金项目
G9900837/MRC_/Medical Research Council/United Kingdom
G9826762/MRC_/Medical Research Council/United Kingdom
MH61399/MH/NIMH NIH HHS/United States
R01 MH061399/MH/NIMH NIH HHS/United States
R37 NS033020/NS/NINDS NIH HHS/United States
R01 NS039962-10/NS/NINDS NIH HHS/United States
R01 MH-44245/MH/NIMH NIH HHS/United States
R01 MH041953/MH/NIMH NIH HHS/United States
MH41953/MH/NIMH NIH HHS/United States
R01 NS039962/NS/NINDS NIH HHS/United States
WT_/Wellcome Trust/United Kingdom
R01 NS042304/NS/NINDS NIH HHS/United States
R37 NS033020-17/NS/NINDS NIH HHS/United States
R01 NS042304-08/NS/NINDS NIH HHS/United States
073141/WT_/Wellcome Trust/United Kingdom
- 浏览2
Molecular psychiatry
1129-39, 1057页
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