• 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

Mutational analysis in familial and sporadic patients with white sponge naevus.

作者信息

Liu X, Li Q, Gao Y, Song S, Hua H

出版信息

Br J Dermatol. 2011 Aug;165(2):448-51. doi: 10.1111/j.1365-2133.2011.10404.x.

DOI:10.1111/j.1365-2133.2011.10404.x
PMID:21561439
Abstract
摘要

相似文献

1
Mutational analysis in familial and sporadic patients with white sponge naevus.
Br J Dermatol. 2011 Aug;165(2):448-51. doi: 10.1111/j.1365-2133.2011.10404.x.
2
[A boy with white sponge naevus of the buccal mucosa].[一名患有颊黏膜白色海绵状痣的男孩]
Ned Tijdschr Geneeskd. 2020 Sep 15;164:D4895.
3
Mutations in the genes for keratin-4 and keratin-13 in Swedish patients with white sponge nevus.瑞典白海绵状痣患者角蛋白-4 和角蛋白-13 基因突变。
J Oral Pathol Med. 2018 Feb;47(2):152-157. doi: 10.1111/jop.12652. Epub 2017 Nov 1.
4
Mutation of keratin 4 gene causing white sponge nevus in a Japanese family.基因突变导致日本一家庭出现白海绵状痣。
Int J Oral Maxillofac Surg. 2013 May;42(5):615-8. doi: 10.1016/j.ijom.2012.10.030. Epub 2012 Nov 24.
5
White sponge nevus: presentation of a new family.
Pediatr Dermatol. 2008 Jan-Feb;25(1):116-7. doi: 10.1111/j.1525-1470.2007.00599.x.
6
Two new mutations in the keratin 4 gene causing oral white sponge nevus in Chinese family.
Oral Dis. 2009 Jan;15(1):100-5. doi: 10.1111/j.1601-0825.2008.01498.x. Epub 2008 Oct 25.
7
White sponge nevus - a rare autosomal dominant keratinopathy.
Klin Padiatr. 2014 Nov;226(6-7):375-6. doi: 10.1055/s-0034-1371843. Epub 2014 May 8.
8
Clinical features and molecular genetic analysis in a Turkish family with oral white sponge nevus.一个患有口腔白色海绵状痣的土耳其家族的临床特征及分子遗传学分析
Med Oral Patol Oral Cir Bucal. 2018 Mar 1;23(2):e144-e150. doi: 10.4317/medoral.21437.
9
Oral medicine case book 25. White sponge naevus.口腔医学案例集25. 白色海绵状痣。
SADJ. 2010 Apr;65(3):130-1.
10
A de novo missense mutation in the keratin 13 gene in oral white sponge naevus.
Br J Dermatol. 2008 Sep;159(4):974-5. doi: 10.1111/j.1365-2133.2008.08716.x. Epub 2008 Jul 4.

引用本文的文献

1
A Rare Clinical Case of Oral White Sponge Nevus and the Associated Challenges in Its Differential Diagnosis.一例罕见的口腔白色海绵状痣临床病例及其鉴别诊断中的相关挑战。
Case Rep Dent. 2024 Mar 18;2024:2251450. doi: 10.1155/2024/2251450. eCollection 2024.
2
Non-familial White Sponge Nevus, an Innocuous yet Clinically Significant Entity: Report of a Case with Review of the Literature.非家族性白色海绵状痣,一种无害但具有临床意义的病症:病例报告并文献复习
Indian J Otolaryngol Head Neck Surg. 2023 Dec;75(4):4012-4015. doi: 10.1007/s12070-023-04050-3. Epub 2023 Jul 1.
3
Exfoliative Cytology and Genetic Analysis for a Non-Invasive Approach to the Diagnosis of White Sponge Nevus: Case Series.
用于白色海绵状痣诊断的非侵入性方法:病例系列的脱落细胞学和基因分析
Bioengineering (Basel). 2023 Jan 23;10(2):154. doi: 10.3390/bioengineering10020154.
4
White Sponge Nevus Caused by Keratin 4 Gene Mutation: A Case Report.角化蛋白 4 基因突变致白色海绵状斑痣 1 例报告
Genes (Basel). 2022 Nov 22;13(12):2184. doi: 10.3390/genes13122184.
5
Oral White Sponge Nevus: An Exceptional Differential Diagnosis in Childhood.口腔白色海绵状痣:儿童期一种特殊的鉴别诊断。
Case Rep Dermatol Med. 2020 Aug 26;2020:9296768. doi: 10.1155/2020/9296768. eCollection 2020.
6
A2ML1 and otitis media: novel variants, differential expression, and relevant pathways.A2ML1 与中耳炎:新型变异体、差异表达及相关通路。
Hum Mutat. 2019 Aug;40(8):1156-1171. doi: 10.1002/humu.23769. Epub 2019 May 21.
7
Clinical features and molecular genetic analysis in a Turkish family with oral white sponge nevus.一个患有口腔白色海绵状痣的土耳其家族的临床特征及分子遗传学分析
Med Oral Patol Oral Cir Bucal. 2018 Mar 1;23(2):e144-e150. doi: 10.4317/medoral.21437.
8
Keratin 13 mutations associated with oral white sponge nevus in two Chinese families.两个中国家庭中与口腔白色海绵状痣相关的角蛋白13突变
Meta Gene. 2014 May 17;2:374-83. doi: 10.1016/j.mgene.2014.04.008. eCollection 2014 Dec.