• 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

相似文献

1
Ocular congenital cranial dysinnervation disorders (CCDDs): insights into axon growth and guidance.眼部先天性颅神经支配障碍(CCDDs):对轴突生长和导向的见解
Hum Mol Genet. 2017 Aug 1;26(R1):R37-R44. doi: 10.1093/hmg/ddx168.
2
An inherited TUBB2B mutation alters a kinesin-binding site and causes polymicrogyria, CFEOM and axon dysinnervation.一个遗传性 TUBB2B 突变改变了一个驱动蛋白结合位点,导致多小脑回畸形、CFEOM 和轴突去神经支配。
Hum Mol Genet. 2012 Dec 15;21(26):5484-99. doi: 10.1093/hmg/dds393. Epub 2012 Sep 21.
3
Clinical and genetic characteristics of Chinese patients with congenital cranial dysinnervation disorders.中国先天性颅神经发育障碍患者的临床和遗传特征。
Orphanet J Rare Dis. 2022 Dec 9;17(1):431. doi: 10.1186/s13023-022-02582-5.
4
Optic Nerve Head and Retinal Abnormalities Associated with Congenital Fibrosis of the Extraocular Muscles.与先天性眼外肌纤维化相关的视神经头和视网膜异常。
Int J Mol Sci. 2021 Mar 4;22(5):2575. doi: 10.3390/ijms22052575.
5
Magnetic resonance imaging evidence for widespread orbital dysinnervation in congenital fibrosis of extraocular muscles due to mutations in KIF21A.磁共振成像证据表明,由于KIF21A基因突变导致的先天性眼外肌纤维化存在广泛的眼眶去神经支配。
Invest Ophthalmol Vis Sci. 2005 Feb;46(2):530-9. doi: 10.1167/iovs.04-1125.
6
Mutant α2-chimaerin signals via bidirectional ephrin pathways in Duane retraction syndrome.突变型α2-嵌合蛋白通过双向 Ephrin 信号通路在杜安退缩综合征中发挥作用。
J Clin Invest. 2017 May 1;127(5):1664-1682. doi: 10.1172/JCI88502. Epub 2017 Mar 27.
7
The Rac-GAP alpha2-Chimaerin Signals via CRMP2 and Stathmins in the Development of the Ocular Motor System.α2- Rac GAP 衔接蛋白通过 CRMP2 和 Stathmin 信号通路在眼运动系统发育中发挥作用。
J Neurosci. 2021 Aug 4;41(31):6652-6672. doi: 10.1523/JNEUROSCI.0983-19.2021. Epub 2021 Jun 24.
8
MRI evaluation of cranial nerve abnormalities and extraocular muscle fibrosis in duane retraction syndrome and congenital extraocular muscle fibrosis.MRI 评估神经源性眼球后退综合征和先天性眼外肌纤维化中外展神经异常和眼外肌纤维化
Graefes Arch Clin Exp Ophthalmol. 2024 Aug;262(8):2633-2642. doi: 10.1007/s00417-024-06454-5. Epub 2024 Mar 26.
9
Evidence of an asymmetrical endophenotype in congenital fibrosis of extraocular muscles type 3 resulting from TUBB3 mutations.先天性眼外肌纤维化症 3 型 TUBB3 突变导致的非对称表型证据。
Invest Ophthalmol Vis Sci. 2010 Sep;51(9):4600-11. doi: 10.1167/iovs.10-5438. Epub 2010 Apr 14.
10
Congenital fibrosis of extraocular muscle type 1A due to KIF21A mutation: first case report from Hong Kong.先天性眼外肌纤维化 1A 型:KIF21A 突变所致:来自香港的首例病例报告。
Hong Kong Med J. 2013 Apr;19(2):182-5.

引用本文的文献

1
Loss of Shapes the Transcriptomic and Epigenetic Landscapes Across Multiple Muscle Types in Cattle.缺失塑造了牛多种肌肉类型的转录组和表观遗传景观。
Curr Issues Mol Biol. 2025 Jun 7;47(6):431. doi: 10.3390/cimb47060431.
2
Oculomotor axons use external and autocrine Slit signals for fasciculation, navigation, branching, and connectivity in mouse embryos.动眼神经轴突在小鼠胚胎中利用外部和自分泌的Slit信号进行成束、导航、分支和连接。
Res Sq. 2025 May 13:rs.3.rs-5718241. doi: 10.21203/rs.3.rs-5718241/v1.
3
Gene Identification for Ocular Congenital Cranial Motor Neuron Disorders Using Human Sequencing, Zebrafish Screening, and Protein Binding Microarrays.利用人类测序、斑马鱼筛选和蛋白质结合微阵列技术鉴定眼部先天性颅神经运动神经元疾病的相关基因
Invest Ophthalmol Vis Sci. 2025 Mar 3;66(3):62. doi: 10.1167/iovs.66.3.62.
4
Zebrafish as a model to understand extraocular motor neuron diversity.斑马鱼作为理解眼外运动神经元多样性的模型。
Curr Opin Neurobiol. 2025 Feb;90:102964. doi: 10.1016/j.conb.2024.102964. Epub 2024 Dec 30.
5
Duane retraction syndrome associated with variant of Rubinstein-Taybi syndrome.与鲁宾斯坦-泰比综合征变异型相关的杜安眼球后退综合征
Am J Ophthalmol Case Rep. 2024 Nov 28;36:102226. doi: 10.1016/j.ajoc.2024.102226. eCollection 2024 Dec.
6
A cell type-aware framework for nominating non-coding variants in Mendelian regulatory disorders.一种基于细胞类型的孟德尔调控疾病中非编码变异提名框架。
Nat Commun. 2024 Sep 27;15(1):8268. doi: 10.1038/s41467-024-52463-7.
7
Gene identification for ocular congenital cranial motor neuron disorders using human sequencing, zebrafish screening, and protein binding microarrays.利用人类测序、斑马鱼筛选和蛋白质结合微阵列技术对眼部先天性颅神经运动神经元疾病进行基因鉴定。
bioRxiv. 2024 Sep 15:2024.09.12.612713. doi: 10.1101/2024.09.12.612713.
8
Clinical and genetic characteristics of Chinese patients with congenital fibrosis of the extraocular muscles.中国先天性眼外肌纤维化患者的临床和遗传特征。
Orphanet J Rare Dis. 2024 Aug 15;19(1):300. doi: 10.1186/s13023-024-03206-w.
9
Expanding the genetics and phenotypes of ocular congenital cranial dysinnervation disorders.扩展眼部先天性颅神经支配障碍的遗传学和表型。
Genet Med. 2025 Apr;27(4):101216. doi: 10.1016/j.gim.2024.101216. Epub 2024 Jul 18.
10
Expanding the genetics and phenotypes of ocular congenital cranial dysinnervation disorders.拓展眼部先天性颅神经支配障碍的遗传学及表型研究
medRxiv. 2024 Mar 26:2024.03.22.24304594. doi: 10.1101/2024.03.22.24304594.

本文引用的文献

1
Ocular Motor Nerve Development in the Presence and Absence of Extraocular Muscle.眼外肌存在与缺失情况下的动眼神经发育
Invest Ophthalmol Vis Sci. 2017 Apr 1;58(4):2388-2396. doi: 10.1167/iovs.16-21268.
2
Mutant α2-chimaerin signals via bidirectional ephrin pathways in Duane retraction syndrome.突变型α2-嵌合蛋白通过双向 Ephrin 信号通路在杜安退缩综合征中发挥作用。
J Clin Invest. 2017 May 1;127(5):1664-1682. doi: 10.1172/JCI88502. Epub 2017 Mar 27.
3
Axons get ahead: Insights into axon guidance and congenital cranial dysinnervation disorders.轴突先行:对轴突导向和先天性颅神经支配障碍的见解。
Dev Neurobiol. 2017 Jul;77(7):861-875. doi: 10.1002/dneu.22477. Epub 2017 May 22.
4
Contralateral migration of oculomotor neurons is regulated by Slit/Robo signaling.动眼神经神经元的对侧迁移受Slit/Robo信号通路调控。
Neural Dev. 2016 Oct 22;11(1):18. doi: 10.1186/s13064-016-0073-y.
5
Loss of MAFB Function in Humans and Mice Causes Duane Syndrome, Aberrant Extraocular Muscle Innervation, and Inner-Ear Defects.人类和小鼠中MAFB功能丧失会导致杜安综合征、异常的眼外肌神经支配和内耳缺陷。
Am J Hum Genet. 2016 Jun 2;98(6):1220-1227. doi: 10.1016/j.ajhg.2016.03.023. Epub 2016 May 12.
6
Mutations in Human Tubulin Proximal to the Kinesin-Binding Site Alter Dynamic Instability at Microtubule Plus- and Minus-Ends.驱动蛋白结合位点附近的人类微管蛋白突变改变微管正端和负端的动态不稳定性。
Dev Cell. 2016 Apr 4;37(1):72-84. doi: 10.1016/j.devcel.2016.03.003.
7
Reversal of axonal growth defects in an extraocular fibrosis model by engineering the kinesin-microtubule interface.通过改造驱动蛋白-微管界面逆转眼外肌纤维化模型中的轴突生长缺陷
Nat Commun. 2016 Jan 18;7:10058. doi: 10.1038/ncomms10058.
8
Two unique TUBB3 mutations cause both CFEOM3 and malformations of cortical development.两种独特的TUBB3突变导致CFEOM3和皮质发育畸形。
Am J Med Genet A. 2016 Feb;170A(2):297-305. doi: 10.1002/ajmg.a.37362. Epub 2015 Dec 6.
9
Prevalence of amblyopia and strabismus in Eastern China: results from screening of preschool children aged 36-72 months.中国东部弱视和斜视的患病率:36至72个月学龄前儿童筛查结果
Br J Ophthalmol. 2016 Apr;100(4):515-9. doi: 10.1136/bjophthalmol-2015-306999. Epub 2015 Aug 10.
10
Recognizable cerebellar dysplasia associated with mutations in multiple tubulin genes.与多种微管蛋白基因突变相关的可识别的小脑发育异常。
Hum Mol Genet. 2015 Sep 15;24(18):5313-25. doi: 10.1093/hmg/ddv250. Epub 2015 Jun 30.

眼部先天性颅神经支配障碍(CCDDs):对轴突生长和导向的见解

Ocular congenital cranial dysinnervation disorders (CCDDs): insights into axon growth and guidance.

作者信息

Whitman Mary C, Engle Elizabeth C

机构信息

F.M. Kirby Neurobiology Center, Boston Children's Hospital, Boston, MA 02115, USA.

Department of Ophthalmology, Boston Children's Hospital, Boston, MA 02115, USA.

出版信息

Hum Mol Genet. 2017 Aug 1;26(R1):R37-R44. doi: 10.1093/hmg/ddx168.

DOI:10.1093/hmg/ddx168
PMID:28459979
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC5886468/
Abstract

Unraveling the genetics of the paralytic strabismus syndromes known as congenital cranial dysinnervation disorders (CCDDs) is both informing physicians and their patients and broadening our understanding of development of the ocular motor system. Genetic mutations underlying ocular CCDDs alter either motor neuron specification or motor nerve development, and highlight the importance of modulations of cell signaling, cytoskeletal transport, and microtubule dynamics for axon growth and guidance. Here we review recent advances in our understanding of two CCDDs, congenital fibrosis of the extraocular muscles (CFEOM) and Duane retraction syndrome (DRS), and discuss what they have taught us about mechanisms of axon guidance and selective vulnerability. CFEOM presents with congenital ptosis and restricted eye movements, and can be caused by heterozygous missense mutations in the kinesin motor protein KIF21A or in the β-tubulin isotypes TUBB3 or TUBB2B. CFEOM-causing mutations in these genes alter protein function and result in axon growth and guidance defects. DRS presents with inability to abduct one or both eyes. It can be caused by decreased function of several transcription factors critical for abducens motor neuron identity, including MAFB, or by heterozygous missense mutations in CHN1, which encodes α2-chimaerin, a Rac-GAP GTPase that affects cytoskeletal dynamics. Examination of the orbital innervation in mice lacking Mafb has established that the stereotypical misinnervation of the lateral rectus by fibers of the oculomotor nerve in DRS is secondary to absence of the abducens nerve. Studies of a CHN1 mouse model have begun to elucidate mechanisms of selective vulnerability in the nervous system.

摘要

揭示被称为先天性颅神经支配障碍(CCDDs)的麻痹性斜视综合征的遗传学,既能为医生及其患者提供信息,又能拓宽我们对眼球运动系统发育的理解。导致眼部CCDDs的基因突变会改变运动神经元的特化或运动神经的发育,并突出了细胞信号传导、细胞骨架运输和微管动力学调节对轴突生长和导向的重要性。在这里,我们回顾了我们对两种CCDDs,即先天性眼外肌纤维化(CFEOM)和杜安退缩综合征(DRS)的理解的最新进展,并讨论它们教会了我们哪些关于轴突导向和选择性易损性的机制。CFEOM表现为先天性上睑下垂和眼球运动受限,可由驱动蛋白运动蛋白KIF21A或β-微管蛋白亚型TUBB3或TUBB2B中的杂合错义突变引起。这些基因中导致CFEOM的突变会改变蛋白质功能,并导致轴突生长和导向缺陷。DRS表现为一只或两只眼睛外展无力。它可能由对展神经运动神经元身份至关重要的几种转录因子功能下降引起,包括MAFB,或由CHN1中的杂合错义突变引起,CHN1编码α2-嵌合蛋白,一种影响细胞骨架动力学的Rac-GAP GTP酶。对缺乏Mafb的小鼠的眼眶神经支配进行检查后发现,DRS中动眼神经纤维对外直肌的典型错误支配是展神经缺失的继发结果。对CHN1小鼠模型的研究已经开始阐明神经系统中选择性易损性的机制。