• 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

Causal association between major histocompatibility complex and myocardial infarction in NZW x BXSB F1 mice.

作者信息

Kawano H, Kawano Y, Shirai T, Okada R

机构信息

Research Laboratory for Cardiovascular Pathology, Juntendo University School of Medicine, Tokyo, Japan.

出版信息

Jpn Circ J. 1995 Feb;59(2):98-102. doi: 10.1253/jcj.59.98.

DOI:10.1253/jcj.59.98
PMID:7596028
Abstract

The NZW x BXSB F1 male mice that a model for systemic lupus erythematosus (SLE) develop myocardial infarction. To determine whether the gene(s) linked to the major histocompatibility complex (MHC) of NZW mice are involved in myocardial infarction, we developed an H-2-congenic NZW.H-2d strain and compared the incidence of myocardial infarction in NZW x BXSB F1 (H-2z/b) male mice to that in NZW. H-2d x BXSB F1 male mice (H-2d/b). H-2z/b heterozygous F1 male mice showed a higher incidence of myocardial infarction than H-2d/b F1 male mice. This observation suggests that the myocardial infarction seen in SLE may be related to MHC.

摘要

相似文献

1
Causal association between major histocompatibility complex and myocardial infarction in NZW x BXSB F1 mice.
Jpn Circ J. 1995 Feb;59(2):98-102. doi: 10.1253/jcj.59.98.
2
Heterozygosity of the major histocompatibility complex controls the autoimmune disease in (NZW x BXSB) F1 mice.主要组织相容性复合体的杂合性控制着(新西兰白兔×BXSB)F1代小鼠的自身免疫性疾病。
Clin Immunol Immunopathol. 1992 Dec;65(3):308-14. doi: 10.1016/0090-1229(92)90162-h.
3
(NZW x BXSB)F1 hybrid. A model of acute lupus and coronary vascular disease with myocardial infarction.(新西兰白兔×BXSB)F1杂交种。一种伴有心肌梗死的急性狼疮和冠状血管疾病模型。
J Exp Med. 1981 Jul 1;154(1):216-21. doi: 10.1084/jem.154.1.216.
4
Monoclonal anticardiolipin autoantibodies established from the (New Zealand white x BXSB)F1 mouse model of antiphospholipid syndrome cross-react with oxidized low-density lipoprotein.从抗磷脂综合征的(新西兰白兔×BXSB)F1小鼠模型中建立的单克隆抗心磷脂自身抗体与氧化型低密度脂蛋白发生交叉反应。
Arthritis Rheum. 1995 Oct;38(10):1382-8. doi: 10.1002/art.1780381005.
5
Dissection of the effects of tumor necrosis factor-alpha and class II gene polymorphisms within the MHC on murine systemic lupus erythematosus (SLE).剖析肿瘤坏死因子-α及主要组织相容性复合体(MHC)内II类基因多态性对小鼠系统性红斑狼疮(SLE)的影响。
Int Immunol. 1998 Oct;10(10):1467-72. doi: 10.1093/intimm/10.10.1467.
6
Multigenic control of lupus-associated antiphospholipid syndrome in a model of (NZW x BXSB) F1 mice.
Eur J Immunol. 1998 Sep;28(9):2694-703. doi: 10.1002/(SICI)1521-4141(199809)28:09<2694::AID-IMMU2694>3.0.CO;2-#.
7
Treatment with high doses of anti-IgM prevents, but with lower doses accelerates autoimmune disease in (NZW x BXSB)F1 hybrid mice.用高剂量抗IgM治疗可预防(新西兰黑鼠×BXSB)F1杂交小鼠的自身免疫性疾病,但低剂量治疗会加速该疾病的发展。
J Immunol. 1987 Jun 15;138(12):4222-8.
8
The Yaa gene abrogates the major histocompatibility complex association of murine lupus in (NZB x BXSB)F1 hybrid mice.Yaa基因消除了(NZB×BXSB)F1杂交小鼠中鼠狼疮与主要组织相容性复合体的关联。
J Clin Invest. 1994 Aug;94(2):521-5. doi: 10.1172/JCI117364.
9
Genetic complementation in female (BXSB x NZW)F2 mice.雌性(BXSB×NZW)F2小鼠中的基因互补。
J Immunol. 2003 Dec 15;171(12):6442-7. doi: 10.4049/jimmunol.171.12.6442.
10
IL-4Ralpha polymorphism in regulation of IL-4 synthesis by T cells: implication in susceptibility to a subset of murine lupus.白细胞介素-4受体α多态性对T细胞合成白细胞介素-4的调控:与小鼠狼疮一个亚群易感性的关系
Int Immunol. 2007 Feb;19(2):175-83. doi: 10.1093/intimm/dxl134. Epub 2006 Dec 22.