• 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

STK4 Deficiency in a Patient with Immune Complex Glomerulonephritis, Salt-Losing Tubulopathy, and Castleman's-Like Disease.

作者信息

Al-Saud Bandar, Alajlan Huda, Sabar Haneen, Anwar Siddiq, Alruwaili Hibah, Al-Hussain Turki, Alamri Nada, Alazami Anas M

机构信息

Section of Pediatric Allergy/Immunology, Department of Pediatrics, King Faisal Specialist Hospital & Research Center, MBC-58, PO Box 3354, Riyadh, 11211, Saudi Arabia.

College of Medicine, Alfaisal University, Riyadh, Saudi Arabia.

出版信息

J Clin Immunol. 2019 Nov;39(8):823-826. doi: 10.1007/s10875-019-00682-9. Epub 2019 Aug 23.

DOI:10.1007/s10875-019-00682-9
PMID:31444685
Abstract
摘要

相似文献

1
STK4 Deficiency in a Patient with Immune Complex Glomerulonephritis, Salt-Losing Tubulopathy, and Castleman's-Like Disease.一名患有免疫复合物性肾小球肾炎、失盐性肾小管病和类卡斯特曼病患者的STK4缺陷
J Clin Immunol. 2019 Nov;39(8):823-826. doi: 10.1007/s10875-019-00682-9. Epub 2019 Aug 23.
2
Bartter Syndrome and Gitelman Syndrome.巴特综合征和吉特林综合征。
Pediatr Clin North Am. 2019 Feb;66(1):121-134. doi: 10.1016/j.pcl.2018.08.010.
3
Fibrillary glomerulonephritis in Castleman's disease.卡斯特尔曼病中的纤维性肾小球肾炎
Leuk Lymphoma. 1998 Jan;28(3-4):429-35. doi: 10.3109/10428199809092700.
4
Antineutrophil cytoplasmic antibody-associated necrotizing glomerulonephritis: Not always pauci-immune.抗中性粒细胞胞浆抗体相关性坏死性肾小球肾炎：并非总是少免疫性的。
Nephrology (Carlton). 2013 Aug;18(8):579. doi: 10.1111/nep.12098.
5
Massive asphyxiating pulmonary hemorrhage and glomerulonephritis in a 41-year-old woman.一名41岁女性的大量窒息性肺出血和肾小球肾炎
South Med J. 1983 Jun;76(6):775-81. doi: 10.1097/00007611-198306000-00024.
6
A transitional variant of Castleman's disease presenting as a chylous pleural effusion.表现为乳糜性胸腔积液的Castleman病过渡型变异。
Chest. 1999 Jan;115(1):285-8. doi: 10.1378/chest.115.1.285.
7
Bartter and Gitelman syndromes.巴特综合征和吉特曼综合征。
Cas Lek Cesk. 2022 Summer;161(3-4):131-134.
8
Interleukin-1 beta gene expression in experimental glomerulonephritis in the rat: an in-situ hybridization study.大鼠实验性肾小球肾炎中白细胞介素-1β基因表达：一项原位杂交研究
Int J Exp Pathol. 1994 Jun;75(3):157-63.
9
Clinical membranous nephropathy.临床膜性肾病
Nephron. 1983;34(4):209-19. doi: 10.1159/000183018.
10
Fulminant multicentric Castleman's disease in a patient with well-controlled human immunodeficiency virus infection-lessons from the patient.一名人类免疫缺陷病毒感染控制良好的患者发生暴发性多中心Castleman病——来自该患者的经验教训
J Formos Med Assoc. 2018 Mar;117(3):244-246. doi: 10.1016/j.jfma.2017.06.008. Epub 2017 Jun 27.

引用本文的文献

1
RNA-binding proteins regulate immune-related alternative splicing in inherited salt-losing tubulopathies.RNA结合蛋白在遗传性失盐性肾小管病中调节免疫相关的可变剪接。
Orphanet J Rare Dis. 2025 Aug 9;20(1):416. doi: 10.1186/s13023-025-03972-1.
2
Case Report of Two Independent Moroccan Families with Syndromic Epidermodysplasia Verruciformis and STK4 Deficiency.两例独立的综合征型疣状表皮发育不良伴 STK4 缺陷的摩洛哥家系病例报告
Viruses. 2024 Sep 5;16(9):1415. doi: 10.3390/v16091415.
3
Epidermodysplasia Verruciformis and Vδ2 γδ T-cell Expansion in STK4 Deficiency.

本文引用的文献

1
Digenetic inheritance of SLC12A3 and CLCNKB genes in a Chinese girl with Gitelman syndrome.SLC12A3 和 CLCNKB 基因在一名患 Gitelman 综合征中国女孩中的双基因遗传。
BMC Pediatr. 2019 Apr 18;19(1):114. doi: 10.1186/s12887-019-1498-3.
2
B cell-intrinsic requirement for STK4 in humoral immunity in mice and human subjects.小鼠和人类受试者体液免疫中STK4的B细胞内在需求。
J Allergy Clin Immunol. 2019 Jun;143(6):2302-2305. doi: 10.1016/j.jaci.2019.02.010. Epub 2019 Feb 20.
3
Gitelman syndrome: consensus and guidance from a Kidney Disease: Improving Global Outcomes (KDIGO) Controversies Conference.
STK4 缺乏症中的疣状表皮发育不良和 Vδ2 γδ T 细胞扩增
J Clin Immunol. 2024 Aug 7;44(8):172. doi: 10.1007/s10875-024-01780-z.
4
A unique STK4 mutation truncating only the C-terminal SARAH domain results in a mild clinical phenotype despite severe T cell lymphopenia: Case report.一个独特的 STK4 突变仅截断 C 末端 SARAH 结构域，导致严重 T 细胞淋巴细胞减少症的情况下仍表现出轻度临床表型：病例报告。
Front Immunol. 2024 Feb 1;15:1329610. doi: 10.3389/fimmu.2024.1329610. eCollection 2024.
5
Inborn Errors of the Immune System Associated With Atopy.与过敏相关的先天性免疫系统错误。
Front Immunol. 2022 Apr 27;13:860821. doi: 10.3389/fimmu.2022.860821. eCollection 2022.
6
Epstein-Barr Virus in Inborn Immunodeficiency-More Than Infection.先天性免疫缺陷中的爱泼斯坦-巴尔病毒——不仅仅是感染
Cancers (Basel). 2021 Sep 23;13(19):4752. doi: 10.3390/cancers13194752.
7
A Novel STK4 Mutation Impairs T Cell Immunity Through Dysregulation of Cytokine-Induced Adhesion and Chemotaxis Genes.一种新型 STK4 突变通过细胞因子诱导的黏附和趋化基因失调损害 T 细胞免疫。
J Clin Immunol. 2021 Nov;41(8):1839-1852. doi: 10.1007/s10875-021-01115-2. Epub 2021 Aug 24.
8
Human genetic dissection of papillomavirus-driven diseases: new insight into their pathogenesis.人类遗传剖析乳头瘤病毒驱动的疾病：对其发病机制的新认识。
Hum Genet. 2020 Jun;139(6-7):919-939. doi: 10.1007/s00439-020-02183-x. Epub 2020 May 20.
Gitelman 综合征：改善全球肾脏病预后组织（KDIGO）争议会议的共识和指导意见。
Kidney Int. 2017 Jan;91(1):24-33. doi: 10.1016/j.kint.2016.09.046.
4
Unbiased targeted next-generation sequencing molecular approach for primary immunodeficiency diseases.用于原发性免疫缺陷病的无偏靶向下一代测序分子方法。
J Allergy Clin Immunol. 2016 Jun;137(6):1780-1787. doi: 10.1016/j.jaci.2015.12.1310. Epub 2016 Feb 23.
5
Primary Immunodeficiency Diseases: an Update on the Classification from the International Union of Immunological Societies Expert Committee for Primary Immunodeficiency 2015.原发性免疫缺陷病：国际免疫学会联盟原发性免疫缺陷病专家委员会2015年分类更新
J Clin Immunol. 2015 Nov;35(8):696-726. doi: 10.1007/s10875-015-0201-1. Epub 2015 Oct 19.
6
STK4 (MST1) deficiency in two siblings with autoimmune cytopenias: A novel mutation.两名自身免疫性血细胞减少症同胞中STK4（MST1）缺乏症：一种新突变。
Clin Immunol. 2015 Dec;161(2):316-23. doi: 10.1016/j.clim.2015.06.010. Epub 2015 Jun 25.
7
Mst1/Mst2 regulate development and function of regulatory T cells through modulation of Foxo1/Foxo3 stability in autoimmune disease.Mst1/Mst2 通过调节自身免疫疾病中 Foxo1/Foxo3 的稳定性来调节调节性 T 细胞的发育和功能。
J Immunol. 2014 Feb 15;192(4):1525-35. doi: 10.4049/jimmunol.1301060. Epub 2014 Jan 22.
8
Inherited MST1 deficiency underlies susceptibility to EV-HPV infections.遗传性 MST1 缺乏导致易感染 EV-HPV。
PLoS One. 2012;7(8):e44010. doi: 10.1371/journal.pone.0044010. Epub 2012 Aug 27.
9
Defining combined immunodeficiency.定义联合免疫缺陷。
J Allergy Clin Immunol. 2012 Jul;130(1):177-83. doi: 10.1016/j.jaci.2012.04.029. Epub 2012 Jun 2.
10
The phenotype of human STK4 deficiency.人类 STK4 缺乏症的表型。
Blood. 2012 Apr 12;119(15):3450-7. doi: 10.1182/blood-2011-09-378158. Epub 2012 Jan 31.