• 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

Second spectroscopically abnormal methemoglobin associated with hereditary cyanosis.

作者信息

GERALD P S, GEORGE P

出版信息

Science. 1959 Feb 13;129(3346):393-4. doi: 10.1126/science.129.3346.393.

DOI:10.1126/science.129.3346.393
PMID:13634986
Abstract

Isolation of an abnormal methemoglobin from two families exhibiting dominantly transmitted cyanosis have permitted the recognition of two different pigments of the hemoglobin M type. It is possible that the abnormal properties which characterize the acidic methemoglobin derivatives result from a crevice configuration of the heme, with two Feprotein bonds.

摘要

相似文献

1
Second spectroscopically abnormal methemoglobin associated with hereditary cyanosis.
Science. 1959 Feb 13;129(3346):393-4. doi: 10.1126/science.129.3346.393.
2
The First Korean Family with Hemoglobin-M Milwaukee-2 Leading to Hereditary Methemoglobinemia.首例血红蛋白-M 密尔沃基-2 导致遗传性高铁血红蛋白血症的韩国家族。
Yonsei Med J. 2020 Dec;61(12):1064-1067. doi: 10.3349/ymj.2020.61.12.1064.
3
Congenital methemoglobinemia: a rare cause of cyanosis in the newborn--a case report.先天性高铁血红蛋白血症:新生儿发绀的罕见原因——病例报告
Pediatrics. 2003 Aug;112(2):e158-61. doi: 10.1542/peds.112.2.e158.
4
Interpreting sulfhemoglobin and methemoglobin in patients with cyanosis: An overview of patients with M-hemoglobin variants.解读发绀患者中的硫化血红蛋白和高铁血红蛋白:M 血红蛋白变异患者概述。
Int J Lab Hematol. 2021 Aug;43(4):837-844. doi: 10.1111/ijlh.13581. Epub 2021 Jun 6.
5
[CONGENITAL METHEMOGLOBINEMIA].[先天性高铁血红蛋白血症]
Coeur Med Interne. 1964 Jan;59:3-9.
6
Concise review: methemoglobinemia.简明综述:高铁血红蛋白血症
Am J Hematol. 1993 Jan;42(1):7-12. doi: 10.1002/ajh.2830420104.
7
Congenital methemoglobinemia due to NADH-methemoglobin reductase deficiency in three Indian families.三个印度家庭中因NADH-高铁血红蛋白还原酶缺乏导致的先天性高铁血红蛋白血症。
Haematologia (Budap). 2002;32(4):543-9.
8
[Cyanosis in children caused by inherited methemoglobinemia due to deficiency of NADH-dependent methemoglobin reductase in erythrocytes].[红细胞中依赖烟酰胺腺嘌呤二核苷酸(NADH)的高铁血红蛋白还原酶缺乏所致遗传性高铁血红蛋白血症引起的儿童发绀]
Pediatr Pol. 1989 Jan;64(1):53-9.
9
[Hereditary methemoglobin cyanosis].[遗传性高铁血红蛋白血症]
Mars Med. 1956;93(1):67-8.
10
A 5-hour-old male neonate with cyanosis.一名出生5小时、患有发绀的男婴。
Lab Med. 2015 Winter;46(1):60-3; quiz e14. doi: 10.1309/LMBQIZ5DRS4K9IMD.

引用本文的文献

1
A human hemoglobin with lowered oxygen affinity and impaired heme-heme interactions.一种氧亲和力降低且血红素-血红素相互作用受损的人血红蛋白。
J Clin Invest. 1961 Oct;40(10):1826-33. doi: 10.1172/JCI104406.
2
HUMAN HAEMOGLOBINS.人类血红蛋白
J Med Genet. 1965 Mar;2(1):48-90. doi: 10.1136/jmg.2.1.48.
3
[On methemoglobin reversal by ascorbic acid].[关于抗坏血酸对高铁血红蛋白的逆转作用]
Klin Wochenschr. 1961 Oct 1;39:1022-4. doi: 10.1007/BF02343817.
4
Chemical studies of several varieties of Hb M.几种血红蛋白M变种的化学研究。
Proc Natl Acad Sci U S A. 1961 Nov 15;47(11):1758-67. doi: 10.1073/pnas.47.11.1758.
5
[Hemoglobin anomalies].[血红蛋白异常]
Blut. 1961;7:443-51. doi: 10.1007/BF01636098.
6
A critical review of human haemoglobin variants. II. Individual haemoglobins.人类血红蛋白变体的批判性综述。II. 个体血红蛋白
J Clin Pathol. 1959 Mar;12(2):101-15. doi: 10.1136/jcp.12.2.101.
7
[HbM Hamburg, a beta chain anomaly: alpha-2-beta-2-63Tyr (equals HbM Saskatoon)].[血红蛋白M汉堡,一种β链异常:α-2-β-2-63酪氨酸(等同于血红蛋白M萨斯卡通)]
Klin Wochenschr. 1966 Aug 15;44(16):961-6. doi: 10.1007/BF01711469.
8
Polycythemia associated with a hemoglobinopathy.与血红蛋白病相关的红细胞增多症。
J Clin Invest. 1966 Jun;45(6):813-22. doi: 10.1172/JCI105397.