• 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

勘误:与Wolf-Hirschhorn综合征相关的基因在运动性神经嵴细胞中富集,并影响……的颅面发育。

Corrigendum: Wolf-Hirschhorn Syndrome-Associated Genes Are Enriched in Motile Neural Crest Cells and Affect Craniofacial Development in .

作者信息

Mills Alexandra, Bearce Elizabeth, Cella Rachael, Kim Seung Woo, Selig Megan, Lee Sangmook, Lowery Laura Anne

机构信息

Biology Department, Boston College, Chestnut Hill, MA, United States.

出版信息

Front Physiol. 2021 Feb 16;11:644596. doi: 10.3389/fphys.2020.644596. eCollection 2020.

DOI:10.3389/fphys.2020.644596
PMID:33664672
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC7924074/
Abstract

[This corrects the article DOI: 10.3389/fphys.2019.00431.].

摘要

[本文更正了文章的数字对象标识符:10.3389/fphys.2019.00431。]

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/49bc/7924074/d37b57cf9697/fphys-11-644596-g0002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/49bc/7924074/fb3944dda236/fphys-11-644596-g0001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/49bc/7924074/d37b57cf9697/fphys-11-644596-g0002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/49bc/7924074/fb3944dda236/fphys-11-644596-g0001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/49bc/7924074/d37b57cf9697/fphys-11-644596-g0002.jpg

相似文献

1
Corrigendum: Wolf-Hirschhorn Syndrome-Associated Genes Are Enriched in Motile Neural Crest Cells and Affect Craniofacial Development in .勘误:与Wolf-Hirschhorn综合征相关的基因在运动性神经嵴细胞中富集,并影响……的颅面发育。
Front Physiol. 2021 Feb 16;11:644596. doi: 10.3389/fphys.2020.644596. eCollection 2020.
2
Wolf-Hirschhorn Syndrome-Associated Genes Are Enriched in Motile Neural Crest Cells and Affect Craniofacial Development in .与Wolf-Hirschhorn综合征相关的基因在运动性神经嵴细胞中富集,并影响……的颅面发育。
Front Physiol. 2019 Apr 12;10:431. doi: 10.3389/fphys.2019.00431. eCollection 2019.
3
The Many Faces of : as a Model System to Study Wolf-Hirschhorn Syndrome.《 的多面性:作为研究沃夫-贺许宏氏症候群的模型系统》 (注:原文标题不完整,翻译可能不太准确,需根据完整准确的原文标题进一步完善)
Front Physiol. 2019 Jun 26;10:817. doi: 10.3389/fphys.2019.00817. eCollection 2019.
4
Exploring the developmental mechanisms underlying Wolf-Hirschhorn Syndrome: Evidence for defects in neural crest cell migration.探索Wolf-Hirschhorn综合征潜在的发育机制:神经嵴细胞迁移缺陷的证据。
Dev Biol. 2016 Dec 1;420(1):1-10. doi: 10.1016/j.ydbio.2016.10.012. Epub 2016 Oct 21.
5
109 kb deletion of chromosome 4p16.3 in a patient with mild phenotype of Wolf-Hirschhorn syndrome.一名患有轻度表型的沃尔夫-赫希霍恩综合征患者的4号染色体p16.3区域发生109 kb缺失。
Am J Med Genet A. 2013 Jun;161A(6):1465-9. doi: 10.1002/ajmg.a.35910. Epub 2013 May 1.
6
Wolf-Hirschhorn Syndrome Candidate 1 (whsc1) Functions as a Tumor Suppressor by Governing Cell Differentiation.沃尔夫-赫希霍恩综合征候选基因1(whsc1)通过调控细胞分化发挥肿瘤抑制作用。
Neoplasia. 2017 Aug;19(8):606-616. doi: 10.1016/j.neo.2017.05.001. Epub 2017 Jun 24.
7
A novel 4p16.3 microduplication distal to WHSC1 and WHSC2 characterized by oligonucleotide array with new phenotypic features.一种新型的 4p16.3 微重复,位于 WHSC1 和 WHSC2 远端,具有寡核苷酸阵列的新表型特征。
Am J Med Genet A. 2011 Sep;155A(9):2224-8. doi: 10.1002/ajmg.a.34120. Epub 2011 Aug 3.
8
First known microdeletion within the Wolf-Hirschhorn syndrome critical region refines genotype-phenotype correlation.首次发现的位于Wolf-Hirschhorn综合征关键区域内的微缺失改善了基因型-表型相关性。
Am J Med Genet. 2001 Apr 1;99(4):338-42. doi: 10.1002/ajmg.1203.
9
Natural histories of patients with Wolf-Hirschhorn syndrome derived from variable chromosomal abnormalities.源于可变染色体异常的Wolf-Hirschhorn综合征患者的自然病史。
Congenit Anom (Kyoto). 2019 Sep;59(5):169-173. doi: 10.1111/cga.12318. Epub 2018 Nov 15.
10
Molecular and clinical characterization of a patient with a chromosome 4p deletion, Wolf-Hirschhorn syndrome, and congenital glaucoma.一名患有4号染色体短臂缺失、沃尔夫-赫希霍恩综合征和先天性青光眼患者的分子与临床特征
Ophthalmic Genet. 2001 Mar;22(1):35-41. doi: 10.1076/opge.22.1.35.2234.

引用本文的文献

1
Lymphocyte to High-density Lipoprotein Cholesterol Ratio is Positively Associated with Pre-diabetes, Metabolic Syndrome, and Non-traditional Cardiometabolic Risk Markers: A Cross-sectional Study at Secondary Health Care.淋巴细胞与高密度脂蛋白胆固醇比值与糖尿病前期、代谢综合征及非传统心脏代谢风险标志物呈正相关:一项二级医疗保健机构的横断面研究
Inflammation. 2025 Feb;48(1):276-287. doi: 10.1007/s10753-024-02063-w. Epub 2024 Jun 6.
2
Epigenetic regulation of craniofacial development and disease.颅面发育和疾病的表观遗传调控。
Birth Defects Res. 2024 Jan;116(1):e2271. doi: 10.1002/bdr2.2271. Epub 2023 Nov 14.
3
Virtual reality as a countermeasure for astronaut motion sickness during simulated post-flight water landings.
虚拟现实作为模拟飞行后水上着陆期间宇航员晕动病的对策。
Exp Brain Res. 2023 Dec;241(11-12):2669-2682. doi: 10.1007/s00221-023-06715-5. Epub 2023 Oct 5.