• 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
Loss of Function of Evc2 in Dental Mesenchyme Leads to Hypomorphic Enamel.牙间充质中Evc2功能丧失导致釉质发育不全。
J Dent Res. 2017 Apr;96(4):421-429. doi: 10.1177/0022034516683674. Epub 2017 Jan 12.
2
Elevated Fibroblast Growth Factor Signaling Is Critical for the Pathogenesis of the Dwarfism in Evc2/Limbin Mutant Mice.成纤维细胞生长因子信号升高对Evc2/Limbin突变小鼠侏儒症的发病机制至关重要。
PLoS Genet. 2016 Dec 27;12(12):e1006510. doi: 10.1371/journal.pgen.1006510. eCollection 2016 Dec.
3
Novel and recurrent EVC and EVC2 mutations in Ellis-van Creveld syndrome and Weyers acrofacial dyostosis.埃利斯-范克雷维尔德综合征和韦尔斯肢端面部发育不全中新型和复发性EVC及EVC2突变
Eur J Med Genet. 2013 Feb;56(2):80-7. doi: 10.1016/j.ejmg.2012.11.005. Epub 2012 Dec 7.
4
The Role of Ellis-Van Creveld 2(EVC2) in Mice During Cranial Bone Development.埃利斯-范克雷维尔德2(EVC2)在小鼠颅骨发育过程中的作用
Anat Rec (Hoboken). 2018 Jan;301(1):46-55. doi: 10.1002/ar.23692. Epub 2017 Oct 6.
5
Generation of Evc2/Limbin global and conditional KO mice and its roles during mineralized tissue formation.Evc2/Limbin 全身及条件性基因敲除小鼠的构建及其在矿化组织形成过程中的作用。
Genesis. 2015 Sep;53(9):612-626. doi: 10.1002/dvg.22879. Epub 2015 Aug 10.
6
[From gene to disease; EVC, EVC2, and Ellis-van Creveld syndrome].[从基因到疾病;EVC、EVC2与埃利斯-范克里弗德综合征]
Ned Tijdschr Geneeskd. 2005 Apr 23;149(17):929-31.
7
Ellis-van Creveld syndrome and Weyers acrodental dysostosis are caused by cilia-mediated diminished response to hedgehog ligands.Ellis-van Creveld 综合征和 Weyers 肢-齿发育不良是由纤毛介导的 Hedgehog 配体反应减弱引起的。
Am J Med Genet C Semin Med Genet. 2009 Nov 15;151C(4):341-51. doi: 10.1002/ajmg.c.30226.
8
Elevated WNT signaling and compromised Hedgehog signaling due to loss of function contribute to the abnormal molar patterning.由于功能丧失导致的WNT信号通路增强和Hedgehog信号通路受损,促成了磨牙模式异常。
Front Dent Med. 2022;3. doi: 10.3389/fdmed.2022.876015. Epub 2022 Aug 1.
9
Novel homozygous mutations in the EVC and EVC2 genes in two consanguineous families segregating autosomal recessive Ellis-van Creveld syndrome.两个患常染色体隐性埃利斯-范克里维德综合征的近亲家庭中,EVC和EVC2基因存在新的纯合突变。
Clin Dysmorphol. 2016 Jan;25(1):1-6. doi: 10.1097/MCD.0000000000000104.
10
Common atrium/atrioventricular canal defect and postaxial polydactyly: A mild clinical subtype of Ellis-van Creveld syndrome caused by hypomorphic mutations in the EVC gene.共同心房/房室管缺损与轴后多指畸形:由EVC基因低表达突变引起的埃利斯-范克里维尔德综合征的一种轻度临床亚型。
Hum Mutat. 2020 Dec;41(12):2087-2093. doi: 10.1002/humu.24112. Epub 2020 Oct 14.

引用本文的文献

1
Case Report: A novel compound heterozygosity of the 2 gene identified in a Chinese pedigree with congenital heart defect.病例报告:在中国一个患有先天性心脏病的家系中鉴定出该基因的一种新型复合杂合性。
Front Pediatr. 2025 Jul 14;13:1352571. doi: 10.3389/fped.2025.1352571. eCollection 2025.
2
The association between maternal smoking during pregnancy and dental development in offspring: a systematic review.孕期母亲吸烟与子代牙齿发育之间的关联:一项系统综述。
Evid Based Dent. 2025 May 29. doi: 10.1038/s41432-025-01168-x.
3
Elevated WNT signaling and compromised Hedgehog signaling due to loss of function contribute to the abnormal molar patterning.由于功能丧失导致的WNT信号通路增强和Hedgehog信号通路受损,促成了磨牙模式异常。
Front Dent Med. 2022;3. doi: 10.3389/fdmed.2022.876015. Epub 2022 Aug 1.
4
The oligodontia phenotype in a X-linked hypohidrotic ectodermal dysplasia patient with a novel variant.一名患有新型变异的X连锁少汗性外胚层发育不良患者的无牙畸形表型
Heliyon. 2023 Dec 6;10(1):e23056. doi: 10.1016/j.heliyon.2023.e23056. eCollection 2024 Jan 15.
5
Dental Anomalies in Ciliopathies: Lessons from Patients with , and Mutations.纤毛病相关的牙齿异常: 、 和 基因突变患者的启示。
Genes (Basel). 2022 Dec 27;14(1):84. doi: 10.3390/genes14010084.
6
Association between Smoking during Pregnancy and Short Root Anomaly in Offspring.妊娠期间吸烟与子女短根畸形的关联。
Int J Environ Res Public Health. 2021 Nov 6;18(21):11662. doi: 10.3390/ijerph182111662.
7
Molecular and Cellular Pathogenesis of Ellis-van Creveld Syndrome: Lessons from Targeted and Natural Mutations in Animal Models.埃-范二氏综合征的分子与细胞发病机制:来自动物模型中靶向突变和自然突变的启示
J Dev Biol. 2020 Oct 9;8(4):25. doi: 10.3390/jdb8040025.
8
A Ciliary Protein EVC2/LIMBIN Plays a Critical Role in the Skull Base for Mid-Facial Development.一种纤毛蛋白EVC2/LIMBIN在颅底中部面部发育中起关键作用。
Front Physiol. 2018 Oct 25;9:1484. doi: 10.3389/fphys.2018.01484. eCollection 2018.
9
Association between DNA methylation in cord blood and maternal smoking: The Hokkaido Study on Environment and Children's Health.脐带血中 DNA 甲基化与母亲吸烟的关联:北海道环境与儿童健康研究。
Sci Rep. 2018 Apr 4;8(1):5654. doi: 10.1038/s41598-018-23772-x.
10
The Role of Ellis-Van Creveld 2(EVC2) in Mice During Cranial Bone Development.埃利斯-范克雷维尔德2(EVC2)在小鼠颅骨发育过程中的作用
Anat Rec (Hoboken). 2018 Jan;301(1):46-55. doi: 10.1002/ar.23692. Epub 2017 Oct 6.

本文引用的文献

1
Expression of Evc2 in craniofacial tissues and craniofacial bone defects in Evc2 knockout mouse.Evc2在颅面组织中的表达以及Evc2基因敲除小鼠的颅面骨缺损
Arch Oral Biol. 2016 Aug;68:142-52. doi: 10.1016/j.archoralbio.2016.05.002. Epub 2016 May 3.
2
Ellis Van Creveld2 is Required for Postnatal Craniofacial Bone Development.埃利斯-范克里夫德综合征2对出生后颅面骨发育是必需的。
Anat Rec (Hoboken). 2016 Aug;299(8):1110-20. doi: 10.1002/ar.23353. Epub 2016 May 2.
3
Generation of Evc2/Limbin global and conditional KO mice and its roles during mineralized tissue formation.Evc2/Limbin 全身及条件性基因敲除小鼠的构建及其在矿化组织形成过程中的作用。
Genesis. 2015 Sep;53(9):612-626. doi: 10.1002/dvg.22879. Epub 2015 Aug 10.
4
Deletion in the EVC2 gene causes chondrodysplastic dwarfism in Tyrolean Grey cattle.EVC2基因的缺失导致蒂罗尔灰牛软骨发育不良性侏儒症。
PLoS One. 2014 Apr 14;9(4):e94861. doi: 10.1371/journal.pone.0094861. eCollection 2014.
5
Secretion of shh by a neurovascular bundle niche supports mesenchymal stem cell homeostasis in the adult mouse incisor.神经血管束龛分泌的 shh 支持成年小鼠切牙间充质干细胞的体内平衡。
Cell Stem Cell. 2014 Feb 6;14(2):160-73. doi: 10.1016/j.stem.2013.12.013.
6
Molecular patterning of the mammalian dentition.哺乳动物牙齿的分子模式。
Semin Cell Dev Biol. 2014 Jan-Feb;25-26:61-70. doi: 10.1016/j.semcdb.2013.12.003. Epub 2013 Dec 16.
7
Evc regulates a symmetrical response to Shh signaling in molar development.Evc 调控摩尔牙发育中 Shh 信号的对称反应。
J Dent Res. 2013 Mar;92(3):222-8. doi: 10.1177/0022034512471826. Epub 2013 Jan 11.
8
The ciliary Evc/Evc2 complex interacts with Smo and controls Hedgehog pathway activity in chondrocytes by regulating Sufu/Gli3 dissociation and Gli3 trafficking in primary cilia.纤毛中的 Evc/Evc2 复合物与 Smo 相互作用,并通过调节初级纤毛中 Sufu/Gli3 的解离和 Gli3 的运输来控制软骨细胞中的 Hedgehog 信号通路活性。
Hum Mol Genet. 2013 Jan 1;22(1):124-39. doi: 10.1093/hmg/dds409. Epub 2012 Oct 1.
9
A Smoothened-Evc2 complex transduces the Hedgehog signal at primary cilia.Smoothened-Evc2 复合物在初级纤毛中转导 Hedgehog 信号。
Dev Cell. 2012 Oct 16;23(4):823-35. doi: 10.1016/j.devcel.2012.07.004. Epub 2012 Sep 13.
10
Signaling networks regulating tooth organogenesis and regeneration, and the specification of dental mesenchymal and epithelial cell lineages.调控牙齿器官发生和再生的信号网络,以及牙齿间充质和上皮细胞谱系的特化。
Cold Spring Harb Perspect Biol. 2012 Apr 1;4(4):a008425. doi: 10.1101/cshperspect.a008425.

牙间充质中Evc2功能丧失导致釉质发育不全。

Loss of Function of Evc2 in Dental Mesenchyme Leads to Hypomorphic Enamel.

作者信息

Zhang H, Takeda H, Tsuji T, Kamiya N, Kunieda T, Mochida Y, Mishina Y

机构信息

1 Department of Biologic and Materials Sciences, School of Dentistry, University of Michigan, Ann Arbor, MI, USA.

2 Unit of Animal Genomics, GIGA Research Center and Faculty of Veterinary Medicine, University of Liège, 1 Avenue de l'Hôpital, Liège, Belgium.

出版信息

J Dent Res. 2017 Apr;96(4):421-429. doi: 10.1177/0022034516683674. Epub 2017 Jan 12.

DOI:10.1177/0022034516683674
PMID:28081373
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC5384488/
Abstract

Ellis-van Creveld (EvC) syndrome is an autosomal-recessive skeletal dysplasia, characterized by short stature and postaxial polydactyly. A series of dental abnormalities, including hypomorphic enamel formation, has been reported in patients with EvC. Despite previous studies that attempted to uncover the mechanism leading to abnormal tooth development, little is known regarding how hypomorphic enamel is formed in patients with EvC. In the current study, using Evc2/ Limbin mutant mice we recently generated, we analyzed enamel formation in the mouse incisor. Consistent with symptoms in human patients, we observed that Evc2 mutant mice had smaller incisors with enamel hypoplasia. Histologic observations coupled with ameloblast marker analyses suggested that Evc2 mutant preameloblasts were capable of differentiating to secretory ameloblasts; this process, however, was apparently delayed, due to delayed odontoblast differentiation, mediated by a limited number of dental mesenchymal stem cells in Evc2 mutant mice. This concept was further supported by the observation that dental mesenchymal-specific deletion of Evc2 phenocopied the tooth abnormalities in Evc2 mutants. Overall, our findings suggest that mutations in Evc2 affect dental mesenchymal stem cell homeostasis, which further leads to hypomorphic enamel formation.

摘要

埃利斯-范克里维尔德(EvC)综合征是一种常染色体隐性遗传的骨骼发育不良疾病,其特征为身材矮小和轴后多指畸形。已有报道称,EvC患者存在一系列牙齿异常,包括釉质形成不全。尽管此前有研究试图揭示导致牙齿发育异常的机制,但对于EvC患者釉质发育不全的形成过程仍知之甚少。在本研究中,我们利用最近培育出的Evc2/Limbin突变小鼠,对小鼠门齿的釉质形成进行了分析。与人类患者的症状一致,我们观察到Evc2突变小鼠的门齿较小,伴有釉质发育不全。组织学观察及成釉细胞标志物分析表明,Evc2突变的前成釉细胞能够分化为分泌型成釉细胞;然而,由于Evc2突变小鼠中数量有限的牙间充质干细胞介导的成牙本质细胞分化延迟,这一过程明显推迟。Evc2在牙间充质中的特异性缺失模拟了Evc2突变体中的牙齿异常,这一观察结果进一步支持了这一观点。总体而言,我们的研究结果表明,Evc2突变会影响牙间充质干细胞的稳态,进而导致釉质发育不全。