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机译:典型WNT-信号传导受体LRP5和LRP6基因变异与ADHD和性二剖形的参与:关联研究和荟萃分析
Univ Zurich Univ Hosp Psychiat Zurich Dept Child &
Adolescent Psychiat &
Psychotherapy Zurich;
Semmelweis Univ Inst Med Chem Mol Biol &
Pathobiochem Budapest Hungary;
Univ Zurich Univ Hosp Psychiat Zurich Dept Child &
Adolescent Psychiat &
Psychotherapy Zurich;
Univ Zurich Univ Hosp Psychiat Zurich Dept Child &
Adolescent Psychiat &
Psychotherapy Zurich;
Semmelweis Univ Inst Med Chem Mol Biol &
Pathobiochem Budapest Hungary;
Vadaskert Child &
Adolescent Psychiat Hosp Budapest Hungary;
German Canc Res Ctr Div Mol Genet Epidemiol C050 Heidelberg Germany;
Univ Duisburg Essen Univ Hosp Essen Dept Child &
Adolescent Psychiat Psychosomat &
Psychotherapy;
Univ Duisburg Essen Univ Hosp Essen Dept Child &
Adolescent Psychiat Psychosomat &
Psychotherapy;
Univ Duisburg Essen Univ Hosp Essen Dept Child &
Adolescent Psychiat Psychosomat &
Psychotherapy;
Univ Wuezburg Div Mol Psychiat Ctr Mental Hlth Wurzburg Germany;
Univ Hosp Wuerzburg Dept Child &
Adolescent Psychiat Psychosomat &
Psychotherapy Ctr Mental Hlth;
Univ Zurich Univ Hosp Psychiat Zurich Dept Child &
Adolescent Psychiat &
Psychotherapy Zurich;
attention-deficit hyperactivity disorder; gender; genetics; polymorphism; SNP;
机译:典型WNT-信号传导受体LRP5和LRP6基因变异与ADHD和性二剖形的参与:关联研究和荟萃分析
机译:Cripto-1通过与LRP5和LRP6协同受体结合来增强经典Wnt /β-catenin信号通路
机译:混杂的“规范” WNT3a-以及特定的“非规范” WNT4-和WNT5a-FZD受体组合均具有β-连环蛋白依赖性途径激活,在LRP5和LRP6依赖性上有很大差异
机译:PS1基因多态性与中国人群阿尔茨海默氏病的关联:病例对照研究的荟萃分析
机译:维生素D受体基因变体的反族荟萃分析在多基因风险背景下,与族群中血管介导的脑出血发生率的差异相关
机译:典型的Wnt信号受体LRP5和LRP6基因变异与ADHD和性二态性的关系:关联研究和荟萃分析
机译:Wnt受体,骨量和骨折:LRP5和LRP6多态性与复制的全基因关联分析