• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

A novel in-frame deletion in ARX is associated with lissencephaly with absent corpus callosum and hypoplastic genitalia.

作者信息

Bhat Shambhu S, Rogers R Curtis, Holden Kenton R, Srivastava Anand K

出版信息

Am J Med Genet A. 2005 Sep 15;138(1):70-2. doi: 10.1002/ajmg.a.30892.

DOI:10.1002/ajmg.a.30892
PMID:16097002
Abstract
摘要

相似文献

1
A novel in-frame deletion in ARX is associated with lissencephaly with absent corpus callosum and hypoplastic genitalia.ARX基因中的一种新型框内缺失与无脑胼胝体和生殖器发育不全的无脑回畸形相关。
Am J Med Genet A. 2005 Sep 15;138(1):70-2. doi: 10.1002/ajmg.a.30892.
2
Mutations of ARX are associated with striking pleiotropy and consistent genotype-phenotype correlation.ARX基因的突变与显著的多效性和一致的基因型-表型相关性有关。
Hum Mutat. 2004 Feb;23(2):147-159. doi: 10.1002/humu.10310.
3
ARX mutations in X-linked lissencephaly with abnormal genitalia.伴有生殖器异常的X连锁无脑回畸形中的ARX突变
Neurology. 2003 Jul 22;61(2):232-5. doi: 10.1212/01.wnl.0000079371.19562.ba.
4
Lissencephaly, abnormal genitalia and refractory epilepsy: case report of XLAG syndrome.无脑回畸形、生殖器异常与难治性癫痫:XLAG综合征病例报告
Arq Neuropsiquiatr. 2006 Dec;64(4):1023-6. doi: 10.1590/s0004-282x2006000600027.
5
X-linked lissencephaly with absent corpus callosum and ambiguous genitalia (XLAG): clinical, magnetic resonance imaging, and neuropathological findings.伴有胼胝体缺失及生殖器模糊的X连锁无脑回畸形(XLAG):临床、磁共振成像及神经病理学发现
Ann Neurol. 2002 Mar;51(3):340-9. doi: 10.1002/ana.10119.
6
[X-linked lissencephaly with absent corpus callosum and abnormal genitalia: a report of siblings followed from the prenatal period].[伴有胼胝体缺失和生殖器异常的X连锁无脑回畸形:一对同胞从孕期起的随访报告]
No To Hattatsu. 2007 May;39(3):206-9.
7
X-linked lissencephaly with abnormal genitalia as a tangential migration disorder causing intractable epilepsy: proposal for a new term, "interneuronopathy".伴有生殖器异常的X连锁无脑回畸形作为一种导致难治性癫痫的切线迁移障碍:关于一个新术语“中间神经元病”的提议
J Child Neurol. 2005 Apr;20(4):392-7. doi: 10.1177/08830738050200042001.
8
Humero-radial synostosis, microcephaly, short corpus callosum, and abnormal genitalia in sibs.同胞兄弟姐妹出现肱桡关节融合、小头畸形、胼胝体短小及生殖器异常。
Am J Med Genet A. 2008 Jul 15;146A(14):1775-80. doi: 10.1002/ajmg.a.32380.
9
Agenesis of the corpus callosum, abnormal genitalia and intractable epilepsy due to a novel familial mutation in the Aristaless-related homeobox gene.由于无尾相关同源框基因的一种新型家族突变导致的胼胝体发育不全、生殖器异常和难治性癫痫。
Neuropediatrics. 2004 Jun;35(3):157-60. doi: 10.1055/s-2004-817919.
10
[ARX--one gene--many phenotypes].[ARX——一个基因——多种表型]
Neurol Neurochir Pol. 2008 Jul-Aug;42(4):338-44.

引用本文的文献

1
X-Linked Lissencephaly With Absent Corpus Callosum and Abnormal Genitalia: An Evolving Multisystem Syndrome With Severe Congenital Intestinal Diarrhea Disease.伴有胼胝体缺失和生殖器异常的X连锁无脑回畸形:一种伴有严重先天性肠道腹泻病的不断演变的多系统综合征。
Child Neurol Open. 2017 Nov 7;4:2329048X17738625. doi: 10.1177/2329048X17738625. eCollection 2017 Jan-Dec.
2
Reinitiation of mRNA translation in a patient with X-linked infantile spasms with a protein-truncating variant in ARX.一名患有X连锁婴儿痉挛症且ARX基因存在蛋白截短变异的患者中mRNA翻译的重新起始
Eur J Hum Genet. 2016 May;24(5):681-9. doi: 10.1038/ejhg.2015.176. Epub 2015 Aug 26.
3
The c.429_452 duplication of the ARX gene: a unique developmental-model of limb kinetic apraxia.
ARX基因的c.429_452重复:肢体运动性失用症的独特发育模型。
Orphanet J Rare Dis. 2014 Feb 14;9:25. doi: 10.1186/1750-1172-9-25.
4
Genetics, molecular biology, and phenotypes of x-linked epilepsy.X连锁癫痫的遗传学、分子生物学及表型
Mol Neurobiol. 2014 Jun;49(3):1166-80. doi: 10.1007/s12035-013-8589-1. Epub 2013 Nov 22.
5
Mutations in the nuclear localization sequence of the Aristaless related homeobox; sequestration of mutant ARX with IPO13 disrupts normal subcellular distribution of the transcription factor and retards cell division.无翅相关同源框基因核定位序列中的突变;突变型ARX与IPO13的隔离破坏了转录因子的正常亚细胞分布并延缓细胞分裂。
Pathogenetics. 2010 Jan 5;3:1. doi: 10.1186/1755-8417-3-1.
6
Ohtahara syndrome in a family with an ARX protein truncation mutation (c.81C>G/p.Y27X).ARX 蛋白截断突变(c.81C>G/p.Y27X)致家族性大田原综合征
Eur J Hum Genet. 2010 Feb;18(2):157-62. doi: 10.1038/ejhg.2009.139. Epub 2009 Sep 9.
7
Identification of Arx transcriptional targets in the developing basal forebrain.发育中的基底前脑内Arx转录靶点的鉴定
Hum Mol Genet. 2008 Dec 1;17(23):3740-60. doi: 10.1093/hmg/ddn271. Epub 2008 Sep 16.