• 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

A novel index to evaluate ineffective erythropoiesis in hematological diseases offers insights into sickle cell disease.

作者信息

Brewin John, El Hoss Sara, Strouboulis John, Rees David

机构信息

Molecular Haematology, Comprehensive Cancer Centre, School of Cancer and Pharmaceutical Sciences, King's College London, United Kingdom; Department of Haematological Medicine, King's College Hospital, London, United Kingdom.

Molecular Haematology, Comprehensive Cancer Centre, School of Cancer and Pharmaceutical Sciences, King's College London, United Kingdom.

出版信息

Haematologica. 2022 Jan 1;107(1):338-341. doi: 10.3324/haematol.2021.279623.

DOI:10.3324/haematol.2021.279623
PMID:34670360
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC8719095/
Abstract
摘要
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b7b7/8719095/1e6e26f4bc1c/107338.fig1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b7b7/8719095/1e6e26f4bc1c/107338.fig1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b7b7/8719095/1e6e26f4bc1c/107338.fig1.jpg

相似文献

1
A novel index to evaluate ineffective erythropoiesis in hematological diseases offers insights into sickle cell disease.一种评估血液系统疾病中无效红细胞生成的新指标为镰状细胞病提供了新见解。
Haematologica. 2022 Jan 1;107(1):338-341. doi: 10.3324/haematol.2021.279623.
2
Fetal hemoglobin rescues ineffective erythropoiesis in sickle cell disease.胎儿血红蛋白可挽救镰状细胞病无效的红细胞生成。
Haematologica. 2021 Oct 1;106(10):2707-2719. doi: 10.3324/haematol.2020.265462.
3
Comparison of mechanisms of anemia in mice with sickle cell disease and beta-thalassemia: peripheral destruction, ineffective erythropoiesis, and phospholipid scramblase-mediated phosphatidylserine exposure.镰状细胞病和β地中海贫血小鼠贫血机制的比较:外周破坏、无效红细胞生成以及磷脂翻转酶介导的磷脂酰丝氨酸暴露
Exp Hematol. 2002 May;30(5):394-402. doi: 10.1016/s0301-472x(02)00780-4.
4
[ON THE BEHAVIOR OF THE LIFE-SPAN OF THE ERYTHROCYTES AND SOME INDEXES OF ERYTHROPOIESIS MEASURED WITH CR-51 IN SUBJECTS WITH THALASSEMIA MAJOR AND THALASSO-DREPANOCYTIC ANEMIA, BEFORE AND AFTER SPLENECTOMY].[关于重型地中海贫血和地中海贫血-镰状细胞贫血患者脾切除前后红细胞寿命及用铬-51测定的一些红细胞生成指标的变化]
Pediatria (Napoli). 1964 Apr 30;72:266-82.
5
SIMULTANEOUS RADIOACTIVE TRACER STUDIES OF ERYTHROPOIESIS AND RED-CELL DESTRUCTION IN SICKLE-CELL DISEASE AND SICKLE-CELL HAEMOGLOBIN/THALASSAEMIA.镰状细胞病和镰状细胞血红蛋白/地中海贫血中红细胞生成与红细胞破坏的同步放射性示踪研究
Br J Haematol. 1963 Oct;9:487-98. doi: 10.1111/j.1365-2141.1963.tb05473.x.
6
Ineffective erythropoiesis in sickle cell disease: new insights and future implications.镰状细胞病中无效的红细胞生成:新的见解和未来的影响。
Curr Opin Hematol. 2021 May 1;28(3):171-176. doi: 10.1097/MOH.0000000000000642.
7
Megaloblastic erythropoiesis associated with sickle-cell anaemia.与镰状细胞贫血相关的巨幼红细胞生成
Br Med J. 1961 Mar 4;1(5226):640-1. doi: 10.1136/bmj.1.5226.640.
8
RETICULOCYTOPENIA IN SICKLE CELL DISEASE. APLASTIC EPISODES IN THE COURSE OF SICKLE CELL DISEASE IN CHILDREN.镰状细胞病中的网织红细胞减少症。儿童镰状细胞病病程中的再生障碍性发作。
Am J Dis Child. 1964 May;107:450-5. doi: 10.1001/archpedi.1964.02080060452004.
9
Effects of oxygen inhalation on endogenous erythropoietin kinetics, erythropoiesis, and properties of blood cells in sickle-cell anemia.吸氧对镰状细胞贫血患者内源性促红细胞生成素动力学、红细胞生成及血细胞特性的影响。
N Engl J Med. 1984 Aug 2;311(5):291-5. doi: 10.1056/NEJM198408023110504.
10
Hemolysis impairs sickle cell erythropoiesis.溶血会损害镰状细胞的红细胞生成。
Blood. 2024 Mar 14;143(11):947-949. doi: 10.1182/blood.2023023298.

引用本文的文献

1
Cellular and biochemical heterogeneity contributes to the phenotypic diversity of transfusion-dependent β-thalassemia.细胞和生化异质性导致了输血依赖型β地中海贫血的表型多样性。
Blood Adv. 2025 May 13;9(9):2091-2107. doi: 10.1182/bloodadvances.2024015232.
2
Reduced GATA1 levels are associated with ineffective erythropoiesis in sickle cell anemia.GATA1水平降低与镰状细胞贫血中无效的红细胞生成有关。
Haematologica. 2025 May 1;110(5):1150-1163. doi: 10.3324/haematol.2024.286010. Epub 2024 Dec 5.
3
Gene-environmental influence of space and microgravity on red blood cells with sickle cell disease.

本文引用的文献

1
Genome wide association study of silent cerebral infarction in sickle cell disease (HbSS and HbSC).全基因组关联研究镰状细胞病(HbSS 和 HbSC)中的无症状性脑梗死。
Haematologica. 2021 Jun 1;106(6):1770-1773. doi: 10.3324/haematol.2020.265827.
2
Fetal hemoglobin rescues ineffective erythropoiesis in sickle cell disease.胎儿血红蛋白可挽救镰状细胞病无效的红细胞生成。
Haematologica. 2021 Oct 1;106(10):2707-2719. doi: 10.3324/haematol.2020.265462.
3
Pathologic angiogenesis in the bone marrow of humanized sickle cell mice is reversed by blood transfusion.
太空和微重力对镰状细胞病红细胞的基因-环境影响。
NPJ Genom Med. 2024 Sep 30;9(1):44. doi: 10.1038/s41525-024-00427-7.
4
Does Hepcidin Tuning Have a Role among Emerging Treatments for Thalassemia?铁调素调节在新兴的地中海贫血治疗方法中起作用吗?
J Clin Med. 2022 Aug 30;11(17):5119. doi: 10.3390/jcm11175119.
5
Precision Medicine and Sickle Cell Disease.精准医学与镰状细胞病
Hemasphere. 2022 Aug 18;6(9):e762. doi: 10.1097/HS9.0000000000000762. eCollection 2022 Sep.
6
Extramedullary haematopoiesis in patients with transfusion dependent β-thalassaemia (TDT): a systematic review.输血依赖型β地中海贫血(TDT)患者的骨髓外造血:系统评价。
Ann Med. 2022 Dec;54(1):764-774. doi: 10.1080/07853890.2022.2048065.
人源化镰状细胞小鼠骨髓中的病理性血管生成可通过输血逆转。
Blood. 2020 Jun 4;135(23):2071-2084. doi: 10.1182/blood.2019002227.
4
The Evolving Pharmacotherapeutic Landscape for the Treatment of Sickle Cell Disease.镰状细胞病治疗中不断演变的药物治疗格局。
Mediterr J Hematol Infect Dis. 2020 Jan 1;12(1):e2020010. doi: 10.4084/MJHID.2020.010. eCollection 2020.
5
Hydroxyurea use in young infants with sickle cell disease.羟基脲在镰状细胞病婴幼儿中的应用。
Pediatr Blood Cancer. 2019 Jul;66(7):e27650. doi: 10.1002/pbc.27650. Epub 2019 Feb 7.
6
A systematic review of known mechanisms of hydroxyurea-induced fetal hemoglobin for treatment of sickle cell disease.对羟基脲诱导胎儿血红蛋白治疗镰状细胞病已知机制的系统评价。
Expert Rev Hematol. 2015 Oct;8(5):669-79. doi: 10.1586/17474086.2015.1078235. Epub 2015 Sep 1.
7
Hydroxyurea and growth in young children with sickle cell disease.羟基脲治疗镰状细胞病幼年患者的生长情况。
Pediatrics. 2014 Sep;134(3):465-72. doi: 10.1542/peds.2014-0917.
8
Ineffective erythropoiesis in β -thalassemia.β地中海贫血中的无效红细胞生成
ScientificWorldJournal. 2013 Mar 28;2013:394295. doi: 10.1155/2013/394295. Print 2013.
9
Utility of plasma transferrin receptor, ferritin and inflammatory markers in children with sickle cell disease.血浆转铁蛋白受体、铁蛋白及炎症标志物在镰状细胞病患儿中的应用
Paediatr Int Child Health. 2012 Feb;32(1):27-34. doi: 10.1179/2046905511Y.0000000009.
10
Reconstructing sickle cell disease: a data-based analysis of the "hyperhemolysis paradigm" for pulmonary hypertension from the perspective of evidence-based medicine.重构镰状细胞病:从循证医学的角度对肺动脉高压的“高溶血范例”进行基于数据的分析。
Am J Hematol. 2011 Feb;86(2):123-54. doi: 10.1002/ajh.21952.