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1
A large replication study and meta-analysis in European samples provides further support for association of AHI1 markers with schizophrenia.一项在欧洲样本中进行的大型复制研究和荟萃分析为 AHI1 标记物与精神分裂症的关联提供了进一步的支持。
Hum Mol Genet. 2010 Apr 1;19(7):1379-86. doi: 10.1093/hmg/ddq009. Epub 2010 Jan 12.
2
Lymphoblast and brain expression of AHI1 and the novel primate-specific gene, C6orf217, in schizophrenia and bipolar disorder.精神分裂症和双相情感障碍中淋巴母细胞和大脑中 AHI1 和新型灵长类特异性基因 C6orf217 的表达。
Schizophr Res. 2010 Jul;120(1-3):159-66. doi: 10.1016/j.schres.2010.03.041. Epub 2010 May 8.
3
A cis-eQTL in AHI1 confers risk to schizophrenia in European populations.AHI1基因中的一个顺式表达数量性状基因座(cis-eQTL)在欧洲人群中增加了患精神分裂症的风险。
Neurosci Lett. 2016 Oct 6;632:130-5. doi: 10.1016/j.neulet.2016.08.050. Epub 2016 Aug 29.
4
Impact of the AHI1 gene on the vulnerability to schizophrenia: a case-control association study.AHI1 基因对精神分裂症易感性的影响:一项病例对照关联研究。
PLoS One. 2010 Aug 18;5(8):e12254. doi: 10.1371/journal.pone.0012254.
5
Fine mapping of AHI1 as a schizophrenia susceptibility gene: from association to evolutionary evidence.AHI1 作为精神分裂症易感基因的精细定位:从关联到进化证据。
FASEB J. 2010 Aug;24(8):3066-82. doi: 10.1096/fj.09-152611. Epub 2010 Apr 6.
6
AHI1, a pivotal neurodevelopmental gene, and C6orf217 are associated with susceptibility to schizophrenia.AHI1是一个关键的神经发育基因,C6orf217与精神分裂症易感性相关。
Eur J Hum Genet. 2006 Oct;14(10):1111-9. doi: 10.1038/sj.ejhg.5201675. Epub 2006 Jun 14.
7
Support for involvement of the AHI1 locus in schizophrenia.支持AHI1基因座与精神分裂症有关。
Eur J Hum Genet. 2007 Sep;15(9):988-91. doi: 10.1038/sj.ejhg.5201848. Epub 2007 May 2.
8
Association of common variants in the Joubert syndrome gene (AHI1) with autism.乔布综合征基因(AHI1)中的常见变异与自闭症的关联。
Hum Mol Genet. 2008 Dec 15;17(24):3887-96. doi: 10.1093/hmg/ddn291. Epub 2008 Sep 9.
9
Evidence for rare and common genetic risk variants for schizophrenia at protein kinase C, alpha.精神分裂症蛋白激酶 C,α 中罕见和常见遗传风险变异的证据。
Mol Psychiatry. 2010 Nov;15(11):1101-11. doi: 10.1038/mp.2009.96. Epub 2009 Sep 29.
10
Evidence for an interaction of schizophrenia susceptibility loci on chromosome 6q23.3 and 10q24.33-q26.13 in Arab Israeli families.阿拉伯裔以色列家庭中6号染色体q23.3和10号染色体q24.33 - q26.13上精神分裂症易感基因座相互作用的证据。
Am J Med Genet B Neuropsychiatr Genet. 2009 Oct 5;150B(7):914-25. doi: 10.1002/ajmg.b.30918.

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1
The mechanism of PDE7B inhibiting the development of hepatocellular carcinoma through oxidative stress.磷酸二酯酶7B(PDE7B)通过氧化应激抑制肝细胞癌发展的机制。
Front Immunol. 2024 Nov 21;15:1469740. doi: 10.3389/fimmu.2024.1469740. eCollection 2024.
2
Abelson Helper Integration Site 1 haplotypes and peripheral blood expression associates with lithium response and immunomodulation in bipolar patients.阿贝尔森辅助整合位点1单倍型与外周血表达与双相情感障碍患者的锂反应及免疫调节相关。
Psychopharmacology (Berl). 2024 Apr;241(4):727-738. doi: 10.1007/s00213-023-06505-5. Epub 2023 Dec 1.
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AHI1: linking depression and impaired antiviral immune response.AHI1:连接抑郁症与抗病毒免疫反应受损
Cell Res. 2022 Oct;32(10):869-870. doi: 10.1038/s41422-022-00702-1.
4
Ahi1 regulates the nuclear translocation of glucocorticoid receptor to modulate stress response.Ahi1 通过调控糖皮质激素受体的核转位来调节应激反应。
Transl Psychiatry. 2021 Mar 29;11(1):188. doi: 10.1038/s41398-021-01305-x.
5
Patterns of cilia gene dysregulations in major psychiatric disorders.主要精神疾病中线粒体基因失调的模式。
Prog Neuropsychopharmacol Biol Psychiatry. 2021 Jul 13;109:110255. doi: 10.1016/j.pnpbp.2021.110255. Epub 2021 Jan 27.
6
Ahi1 promotes Arl13b ciliary recruitment, regulates Arl13b stability and is required for normal cell migration.Ahi1 促进 Arl13b 纤毛募集,调节 Arl13b 的稳定性,并且是细胞正常迁移所必需的。
J Cell Sci. 2019 Sep 4;132(17):jcs230680. doi: 10.1242/jcs.230680.
7
Mutant Ahi1 Affects Retinal Axon Projection in Zebrafish Toxic Gain of Function.突变型Ahi1影响斑马鱼视网膜轴突投射 毒性功能获得。
Front Cell Neurosci. 2019 Mar 21;13:81. doi: 10.3389/fncel.2019.00081. eCollection 2019.
8
Primary Cilia-An Underexplored Topic in Major Mental Illness.原发性纤毛——主要精神疾病中一个未被充分探索的主题。
Front Psychiatry. 2019 Mar 4;10:104. doi: 10.3389/fpsyt.2019.00104. eCollection 2019.
9
AMPK signaling linked to the schizophrenia-associated 1q21.1 deletion is required for neuronal and sleep maintenance.AMPK 信号与精神分裂症相关的 1q21.1 缺失有关,对于神经元和睡眠维持是必需的。
PLoS Genet. 2018 Dec 19;14(12):e1007623. doi: 10.1371/journal.pgen.1007623. eCollection 2018 Dec.
10
Effect of chronic unpredictable stress on mice with developmental under-expression of the Ahi1 gene: behavioral manifestations and neurobiological correlates.慢性不可预测应激对 Ahi1 基因发育性低表达小鼠的影响:行为表现和神经生物学相关性。
Transl Psychiatry. 2018 Jul 2;8(1):124. doi: 10.1038/s41398-018-0171-1.

本文引用的文献

1
Expanding the range of ZNF804A variants conferring risk of psychosis.扩大 ZNF804A 变异体的范围,这些变异体赋予了患精神病的风险。
Mol Psychiatry. 2011 Jan;16(1):59-66. doi: 10.1038/mp.2009.149. Epub 2010 Jan 5.
2
Replication of association between schizophrenia and ZNF804A in the Irish Case-Control Study of Schizophrenia sample.爱尔兰精神分裂症病例对照研究样本中精神分裂症与 ZNF804A 关联性的复制。
Mol Psychiatry. 2010 Jan;15(1):29-37. doi: 10.1038/mp.2009.109. Epub 2009 Oct 20.
3
Common polygenic variation contributes to risk of schizophrenia and bipolar disorder.常见的多基因变异会增加患精神分裂症和双相情感障碍的风险。
Nature. 2009 Aug 6;460(7256):748-52. doi: 10.1038/nature08185. Epub 2009 Jul 1.
4
Common variants on chromosome 6p22.1 are associated with schizophrenia.6号染色体p22.1区域的常见变异与精神分裂症有关。
Nature. 2009 Aug 6;460(7256):753-7. doi: 10.1038/nature08192. Epub 2009 Jul 1.
5
Common variants conferring risk of schizophrenia.增加精神分裂症风险的常见变异
Nature. 2009 Aug 6;460(7256):744-7. doi: 10.1038/nature08186. Epub 2009 Jul 1.
6
Dissecting the many genetic faces of schizophrenia.
Epidemiol Psichiatr Soc. 2009 Apr-Jun;18(2):91-5.
7
Evidence for an interaction of schizophrenia susceptibility loci on chromosome 6q23.3 and 10q24.33-q26.13 in Arab Israeli families.阿拉伯裔以色列家庭中6号染色体q23.3和10号染色体q24.33 - q26.13上精神分裂症易感基因座相互作用的证据。
Am J Med Genet B Neuropsychiatr Genet. 2009 Oct 5;150B(7):914-25. doi: 10.1002/ajmg.b.30918.
8
Common genetic determinants of schizophrenia and bipolar disorder in Swedish families: a population-based study.瑞典家庭中精神分裂症和双相情感障碍的常见遗传决定因素:一项基于人群的研究。
Lancet. 2009 Jan 17;373(9659):234-9. doi: 10.1016/S0140-6736(09)60072-6.
9
Disruption of the neurexin 1 gene is associated with schizophrenia.神经连接蛋白1基因的破坏与精神分裂症有关。
Hum Mol Genet. 2009 Mar 1;18(5):988-96. doi: 10.1093/hmg/ddn351. Epub 2008 Oct 22.
10
'Fat mass and obesity associated' gene (FTO): no significant association of variant rs9939609 with weight loss in a lifestyle intervention and lipid metabolism markers in German obese children and adolescents.“肥胖相关”基因(FTO):在德国肥胖儿童和青少年的生活方式干预中,变异体rs9939609与体重减轻及脂质代谢标志物无显著关联。
BMC Med Genet. 2008 Sep 17;9:85. doi: 10.1186/1471-2350-9-85.

一项在欧洲样本中进行的大型复制研究和荟萃分析为 AHI1 标记物与精神分裂症的关联提供了进一步的支持。

A large replication study and meta-analysis in European samples provides further support for association of AHI1 markers with schizophrenia.

机构信息

Research Institute of Biological Psychiatry, Copenhagen University Hospital, Roskilde, Denmark.

出版信息

Hum Mol Genet. 2010 Apr 1;19(7):1379-86. doi: 10.1093/hmg/ddq009. Epub 2010 Jan 12.

DOI:10.1093/hmg/ddq009
PMID:20071346
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC2838541/
Abstract

The Abelson helper integration site 1 (AHI1) gene locus on chromosome 6q23 is among a group of candidate loci for schizophrenia susceptibility that were initially identified by linkage followed by linkage disequilibrium mapping, and subsequent replication of the association in an independent sample. Here, we present results of a replication study of AHI1 locus markers, previously implicated in schizophrenia, in a large European sample (in total 3907 affected and 7429 controls). Furthermore, we perform a meta-analysis of the implicated markers in 4496 affected and 18,920 controls. Both the replication study of new samples and the meta-analysis show evidence for significant overrepresentation of all tested alleles in patients compared with controls (meta-analysis; P = 8.2 x 10(-5)-1.7 x 10(-3), common OR = 1.09-1.11). The region contains two genes, AHI1 and C6orf217, and both genes-as well as the neighbouring phosphodiesterase 7B (PDE7B)-may be considered candidates for involvement in the genetic aetiology of schizophrenia.

摘要

6q23 染色体上的 Abelson 辅助整合位点 1(AHI1)基因座是一组最初通过连锁分析随后通过连锁不平衡映射以及在独立样本中对关联的后续复制确定的精神分裂症易感性候选基因座之一。在这里,我们报告了先前与精神分裂症相关的 AHI1 基因座标记在大型欧洲样本(总共 3907 名患者和 7429 名对照)中的复制研究结果。此外,我们对 4496 名患者和 18920 名对照中涉及的标记进行了荟萃分析。新样本的复制研究和荟萃分析均表明,与对照组相比,所有测试的等位基因在患者中明显过表达(荟萃分析;P = 8.2 x 10(-5)-1.7 x 10(-3),常见 OR = 1.09-1.11)。该区域包含两个基因,AHI1 和 C6orf217,以及两个基因-以及邻近的磷酸二酯酶 7B(PDE7B)-可能被认为是参与精神分裂症遗传病因的候选基因。