The differences of hemogram, myelogram, and driver gene mutations in classic myeloproliferative neoplasms [0.03%]
经典骨髓增殖性肿瘤的血液学、骨髓和驱动基因突变特点分析
Jin Wang,Jin Zhang,Jinjin Huang et al.
Jin Wang et al.
The aim of this study was to explore and compare routine blood features and pathological characteristics of bone marrow tissues in essential thrombocythemia (ET), polycythemia vera (PV), primary myelofibrosis, prefibrotic stage (prePMF) and...
Danfeng Lin,Yongguang Zhang,Dongya Cui et al.
Danfeng Lin et al.
MicroRNAs are known to regulate cell proliferation, differentiation, and apoptosis. However, the immunological mechanism and role of microRNA9-3 (miR9-3) are unknown. This study used CRISPR/cas9 technology to knock out miR9-3 to modulate it...
Missense mutation in RPS7 causes Diamond-Blackfan anemia via alteration of erythrocyte metabolism, protein translation and induction of ribosomal stress [0.03%]
RPS7错义突变通过改变红细胞代谢、蛋白质翻译和诱导核糖体应激导致Diamond-Blackfan贫血症
Agata Kubickova,Zuzana Maceckova,Petr Vojta et al.
Agata Kubickova et al.
Diamond-Blackfan anemia (DBA) is predominantly underlined by mutations in genes encoding ribosomal proteins (RP); however, its etiology remains unexplained in approximately 25 % of patients. We previously reported a novel heterozygous RPS7 ...
Indices of iron homeostasis in asymptomatic subjects with HFE mutations and moderate ferritin elevation during iron removal treatment [0.03%]
HFE基因突变并中度铁蛋白升高的无症状患者中铁稳态指标的变化及去除治疗期间的反应
Laura Infanti,Gerda Leitner,Morten K Moe et al.
Laura Infanti et al.
We analysed iron biomarkers and their relationships in 30 subjects with HFE mutations and moderate hyperferritinaemia undergoing iron removal at our blood donation centre. Body mass index (BMI) and liver enzymes were assessed. Serum iron (S...
Retraction notice to "MZF1 regulates α-globin gene transcription via long-range interactions in erythroid differentiation" [Blood Cells, Mol. Dis., Volume 87, March 2021, 102533] [0.03%]
有关“MZF1通过长程相互作用在红细胞分化中调节α-珠蛋白基因转录”的撤稿声明[Blood Cells, Mol. Dis., Volume 87, March 2021, 102533]
Haoli Li,Jingjing Zeng,Yongzhong Zhao et al.
Haoli Li et al.
Retraction of Publication
Blood cells, molecules & diseases. 2022 Nov:97:102687. DOI:10.1016/j.bcmd.2022.102687 2022
Liver kinase B1 (LKB1) in murine erythroid progenitors modulates erythropoietin setpoint in association with maturation control [0.03%]
肝激酶B1(LKB1)通过与成熟度控制相关联调节小鼠红系祖细胞的促红细胞生成素定值点
Zollie White rd,Kamaleldin E Elagib,Alejandro A Gru et al.
Zollie White rd et al.
Erythropoiesis is a tightly regulated process. It is stimulated by decreased oxygen in circulation, which leads to the secretion of the hormone erythropoietin (Epo) by the kidneys. An additional layer of control involves the coordinated sen...
Identification of TCR repertoires in asymptomatic COVID-19 patients by single-cell T-cell receptor sequencing [0.03%]
通过单细胞T细胞受体测序鉴定无症状COVID-19患者TCR库
Han Bai,Junpeng Ma,Weikang Mao et al.
Han Bai et al.
The T cell-mediated immune responses associated with asymptomatic infection (AS) of SARS-CoV-2 remain largely unknown. The diversity of T-cell receptor (TCR) repertoire is essential for generating effective immunity against viral infections...
The significance of surface neutrophilic MPO expression level in NETosis and NETosis-associated coagulopathies in covid-19 infected patients [0.03%]
Covid-19感染患者的NETosis及NETosis相关凝血病中表面中性粒细胞MPO表达水平的意义
Elham Jamali,Mojdeh Abbasi,Akbar Hashemi Tayer et al.
Elham Jamali et al.
Introduction: Inflammatory response-induced coagulopathy is a common complication associated with severe form of covid-19 infection. Evidences suggest that neutrophil extracellular traps (NETs) play a significant role in ...
Investigation on abnormal gene loci of a Chinese pedigree with hereditary combined deficiency of blood coagulation factor XI, XII, and protein S [0.03%]
中国人联合缺乏凝血因子XI、XII和蛋白S遗传性缺陷家系的基因定位分析
Ze Wen Zhang,Da Ming Xu,Jin Feng Qiu et al.
Ze Wen Zhang et al.
Objective: In order to clarify the interaction mechanism, the phenotype and abnormal gene loci of FXI, FXII, and PS were investigated in this study. Metho...
Diagnostic challenges posed by a rare unstable hemoglobin variant Hb Southampton [HBB: c.320T → C] with pyrimidine 5' nucleotidase deficiency and the response to HU therapy [0.03%]
罕见不稳定血红蛋白变异体Hb Southampton[HBB：c.320T → C]合并嘧啶5'-核苷酸酶缺乏的诊断挑战及HU治疗反应
Manju Gorivale,Priya Hariharan,Neha Kargutkar et al.
Manju Gorivale et al.