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期刊名:Blood cells molecules and diseases

缩写:BLOOD CELL MOL DIS

ISSN:1079-9796

e-ISSN:1096-0961

IF/分区:1.7/Q3

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共收录本刊相关文章索引1521
Clinical Trial Case Reports Meta-Analysis RCT Review Systematic Review
Classical Article Case Reports Clinical Study Clinical Trial Clinical Trial Protocol Comment Comparative Study Editorial Guideline Letter Meta-Analysis Multicenter Study Observational Study Randomized Controlled Trial Review Systematic Review
Debashree Das,Souvik Sen,Santanu Bhakta et al. Debashree Das et al.
The drugs containing nitrates like isosorbide dinitrate, isosorbide mononitrate and glyceryl trinitrate, etc., trigger the oxidation of hemoglobin which is manifested in the pathological disorder named methemoglobinemia. It was considered i...
Marisa Silva,Andreia Coelho,Sofia Vargas et al. Marisa Silva et al.
Endothelial dysfunction plays a major role in sickle cell anemia (SCA) systemic vasculopathy, with upregulation of adhesion molecules (e.g., VCAM-1), decreased nitric oxide bioavailability, and oxidative stress. We aimed to assess the modul...
Revathi Raman,Ramanagouda Ramanagoudr-Bhojappa,Sanchi Dhinoja et al. Revathi Raman et al.
Progressive pancytopenia is a common feature observed in DNA crosslink repair deficiency disorder, Fanconi anemia (FA). However, this phenotype has not been recapitulated in single FA gene knockout animal models. In this study, we analyzed ...
Roy L Kao,Audrey A Jacobsen,Charles J Billington Jr et al. Roy L Kao et al.
Vacuoles, E1, X-linked, autoimmunity, somatic (VEXAS) syndrome is characterized by a pathogenic mutation in UBA1, which leads to protean complications including autoimmunity and myelodysplasia. A 56-year-old man with steroid-dependent, late...
Louis H Junker,Biaoru Li,Xingguo Zhu et al. Louis H Junker et al.
Induction of fetal hemoglobin (HbF) expression ameliorates the clinical severity and prolong survival in persons with sickle cell disease (SCD). Hydroxyurea (HU) is the only FDA-approved HbF inducer however, additional therapeutics that pro...
Nalan Yurtsever,Vijay Nandi,Yonah Ziemba et al. Nalan Yurtsever et al.
Background: Equipoise exists regarding sickle cell disease (SCD) as a risk factor for COVID-19 disease severity and variables that increase risk of COVID-19 severity in SCD. Given our health system's large SCD patient cat...
Ghada E M Abdallah,Wael A Abbas,Esam A S Elbeih et al. Ghada E M Abdallah et al.
Introduction: There are unmet answers about the effect of the different forms of corticosteroids in the treatment of the warm autoimmune hemolytic anemia (WAIHA). We aimed to describe the initial response rate and the saf...
Seema Bhatlekar,Shancy Jacob,Bhanu K Manne et al. Seema Bhatlekar et al.
The purpose of this research was to assess the effects of a microRNA (miRNA) cluster on platelet production. Human chromosome 19q13.41 harbors an evolutionarily conserved cluster of three miRNA genes (MIR99B, MIRLET7E, MIR125A) within 727 b...