• 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
Early B cell defects.早期B细胞缺陷。
Clin Exp Immunol. 2000 Mar;119(3):383-9. doi: 10.1046/j.1365-2249.2000.01192.x.
2
Immune-cell lineage commitment: translation from mice to humans.免疫细胞谱系定向分化：从小鼠到人类的转化
Immunity. 2007 Jun;26(6):674-7. doi: 10.1016/j.immuni.2007.05.011.
3
Clonal B-cell lymphocytosis: a new member?克隆性B细胞淋巴细胞增多症：一个新成员？
Blood. 2014 Feb 20;123(8):1118-9. doi: 10.1182/blood-2013-12-543330.
4
B cell lineages: documented at last!B细胞谱系：终于有记录了！
Nat Immunol. 2006 Mar;7(3):225-6. doi: 10.1038/ni0306-225.
5
Flow cytometric diagnosis of the cell lineage and developmental stage of acute lymphoblastic leukemia by novel monoclonal antibodies specific to human pre-B-cell receptor.利用针对人前B细胞受体的新型单克隆抗体通过流式细胞术诊断急性淋巴细胞白血病的细胞谱系和发育阶段。
Blood. 1998 Dec 1;92(11):4317-24.
6
The early history of B cells.B 细胞的早期历史。
Nat Rev Immunol. 2015 Mar;15(3):191-7. doi: 10.1038/nri3801. Epub 2015 Feb 6.
7
Instructing B cell fates on the fringe.引导边缘区B细胞的命运
Immunity. 2009 Feb 20;30(2):175-7. doi: 10.1016/j.immuni.2009.01.003.
8
Autoimmune neutropenia in multiple myeloma and the role of clonal T-cell expansion: evidence of cross-talk between B-cell and T-cell lineages?多发性骨髓瘤中的自身免疫性中性粒细胞减少症及克隆性T细胞扩增的作用：B细胞和T细胞谱系间存在相互作用的证据？
Clin Lymphoma Myeloma Leuk. 2014 Feb;14(1):e19-23. doi: 10.1016/j.clml.2013.08.002. Epub 2013 Oct 30.
9
Two lymphoid roads diverge--but does antigen bade B cells to take the road less traveled?
Immunity. 2005 Sep;23(3):242-4. doi: 10.1016/j.immuni.2005.09.001.
10
Transcription control of early B cell differentiation.早期 B 细胞分化的转录调控。
Curr Opin Immunol. 2010 Apr;22(2):161-7. doi: 10.1016/j.coi.2010.01.010. Epub 2010 Feb 9.

引用本文的文献

1
Patients and mice with deficiency in the SNARE protein SYNTAXIN-11 have a secondary B cell defect.患有 SNARE 蛋白 SYNTAXIN-11 缺乏症的患者和老鼠存在次级 B 细胞缺陷。
J Exp Med. 2024 Jul 1;221(7). doi: 10.1084/jem.20221122. Epub 2024 May 9.
2
B-cells absence in patients diagnosed as inborn errors of immunity: a registry-based study.B 细胞缺失症患者的诊断：基于登记的研究。
Immunogenetics. 2024 Jun;76(3):189-202. doi: 10.1007/s00251-024-01342-y. Epub 2024 Apr 29.
3
Selective IgM Deficiency: Evidence, Controversies, and Gaps.选择性IgM缺乏症：证据、争议与空白
Diagnostics (Basel). 2023 Sep 4;13(17):2861. doi: 10.3390/diagnostics13172861.
4
Response to mRNA COVID-19 vaccination in three XLA patients.三位 XLA 患者对 mRNA COVID-19 疫苗的反应。
Vaccine. 2022 Aug 26;40(36):5299-5301. doi: 10.1016/j.vaccine.2022.07.046. Epub 2022 Aug 3.
5
Dynamic regulation of hypoxia-inducible factor-1α activity is essential for normal B cell development.缺氧诱导因子-1α 活性的动态调节对正常 B 细胞发育至关重要。
Nat Immunol. 2020 Nov;21(11):1408-1420. doi: 10.1038/s41590-020-0772-8. Epub 2020 Aug 31.
6
X-linked Agammaglobulinemia Presenting with Multiviral Pneumonia.表现为多病毒肺炎的X连锁无丙种球蛋白血症
Cureus. 2020 Apr 29;12(4):e7884. doi: 10.7759/cureus.7884.
7
B-cell activating factor receptor deficiency is associated with an adult-onset antibody deficiency syndrome in humans.B细胞活化因子受体缺陷与人类成人期抗体缺陷综合征相关。
Proc Natl Acad Sci U S A. 2009 Aug 18;106(33):13945-50. doi: 10.1073/pnas.0903543106. Epub 2009 Aug 6.
8
Optimization of immunoglobulin substitution therapy by a stochastic immune response model.通过随机免疫反应模型优化免疫球蛋白替代疗法
PLoS One. 2009 May 28;4(5):e5685. doi: 10.1371/journal.pone.0005685.
9
Naturally occurring Bruton's tyrosine kinase mutations have no dominant negative effect in an X-linked agammaglobulinaemia cellular model.在X连锁无丙种球蛋白血症细胞模型中，自然发生的布鲁顿酪氨酸激酶突变无显性负效应。
Clin Exp Immunol. 2008 Apr;152(1):33-8. doi: 10.1111/j.1365-2249.2008.03589.x. Epub 2008 Jan 28.
10
[Classification and diagnosis of immunodeficiency syndromes].[免疫缺陷综合征的分类与诊断]
Internist (Berl). 2004 Aug;45(8):868-81. doi: 10.1007/s00108-004-1239-y.

本文引用的文献

1
Agammaglobulinemia.无丙种球蛋白血症
Trans Assoc Am Physicians. 1953;66:200-2.
2
Mutations in Igalpha (CD79a) result in a complete block in B-cell development.免疫球蛋白α（CD79a）的突变会导致B细胞发育完全受阻。
J Clin Invest. 1999 Oct;104(8):1115-21. doi: 10.1172/JCI7696.
3
Atypical X-linked agammaglobulinemia diagnosed in three adults.三名成年人被诊断为非典型X连锁无丙种球蛋白血症。
Intern Med. 1999 Sep;38(9):722-5. doi: 10.2169/internalmedicine.38.722.
4
Activity of pleconaril against enteroviruses.普来可那立对肠道病毒的活性。
Antimicrob Agents Chemother. 1999 Sep;43(9):2109-15. doi: 10.1128/AAC.43.9.2109.
5
Regulation of nuclear localization and transcriptional activity of TFII-I by Bruton's tyrosine kinase.布鲁顿酪氨酸激酶对TFII-I核定位和转录活性的调控
Mol Cell Biol. 1999 Jul;19(7):5014-24. doi: 10.1128/MCB.19.7.5014.
6
Mutations of the human BTK gene coding for bruton tyrosine kinase in X-linked agammaglobulinemia.X连锁无丙种球蛋白血症中编码布鲁顿酪氨酸激酶的人类BTK基因突变。
Hum Mutat. 1999;13(4):280-5. doi: 10.1002/(SICI)1098-1004(1999)13:4<280::AID-HUMU3>3.0.CO;2-L.
7
Unusual mutations in Btk: an insertion, a duplication, an inversion, and four large deletions.布鲁顿酪氨酸激酶（Btk）的罕见突变：一个插入突变、一个重复突变、一个倒位突变和四个大片段缺失。
Clin Immunol. 1999 Jan;90(1):28-37. doi: 10.1006/clim.1998.4629.
8
Host defense molecule polymorphisms influence the risk for immune-mediated complications in chronic granulomatous disease.宿主防御分子多态性影响慢性肉芽肿病免疫介导并发症的风险。
J Clin Invest. 1998 Dec 15;102(12):2146-55. doi: 10.1172/JCI5084.
9
Functional analysis of peripheral blood B cells in patients with X-linked agammaglobulinemia.X连锁无丙种球蛋白血症患者外周血B细胞的功能分析
J Immunol. 1998 Oct 15;161(8):3925-9.
10
Immunoglobulin replacement treatment by rapid subcutaneous infusion.通过快速皮下输注进行免疫球蛋白替代治疗。
Arch Dis Child. 1998 Jul;79(1):48-51. doi: 10.1136/adc.79.1.48.

Early B cell defects.

作者信息

Gaspar H B, Conley M E

机构信息

Molecular Immunology Unit, Institute of Child Health, University College London, London, UK.

出版信息

Clin Exp Immunol. 2000 Mar;119(3):383-9. doi: 10.1046/j.1365-2249.2000.01192.x.

DOI:10.1046/j.1365-2249.2000.01192.x
PMID:10691907
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC1905597/
Abstract
摘要