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Impact of the Oscillating Bead Size and Shape on Induced Mechanical Stress on Red Blood Cells and Associated Hemolysis in Bead Milling 振荡珠的大小和形状对磨珠过程中红细胞机械应力和溶血的影响
Pub Date : 2019-06-27 DOI: 10.23937/2469-5696/1410041
M. Tarasev, M. Muchnik, S. Chakraborty
Citation: Tarasev M, Muchnik M, Chakraborty S (2019) Impact of the Oscillating Bead Size and Shape on Induced Mechanical Stress on Red Blood Cells and Associated Hemolysis in Bead Milling. Int J Blood Res Disord 6:041. doi.org/10.23937/2469-5696/1410041 Accepted: June 25, 2019: Published: June 27, 2019 Copyright: © 2019 Tarasev M, et al. This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
引用本文:Tarasev M, Muchnik M, Chakraborty S(2019)振荡珠粒大小和形状对铣削过程中诱导红细胞机械应力和相关溶血的影响。中华血液病杂志(英文版)6:41。doi.org/10.23937/2469-5696/1410041录用日期:2019年6月25日发布日期:2019年6月27日版权所有:©2019 Tarasev M, et al.。这是一篇根据知识共享署名许可协议发布的开放获取文章,该协议允许在任何媒体上不受限制地使用、分发和复制,前提是要注明原作者和来源。
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引用次数: 2
Fatal Systemic Mucormycosis after Rabbit Anti-Thymocyte Globulin Therapy in a Severe Aplastic Anemia Patient 兔抗胸腺细胞球蛋白治疗严重再生障碍性贫血致死性全身毛霉病
Pub Date : 2019-05-16 DOI: 10.23937/2469-5696/1410039
Tashiro Haruko, Oshima Yasutoshi, Sumiyoshi Ritsu, Matsuo Takuji, Y. Tadashi, M. Kensuke, Ooi Jun, Matsunaga Naohisa, Kikuchi Yoshinao, Shirafuji Naoki
Citation: Tashiro H, Oshima Y, Sumiyoshi R, Matsuo T, Yamamoto T, et al. (2019) Fatal Systemic Mucormycosis after Rabbit Anti-Thymocyte Globulin Therapy in a Severe Aplastic Anemia Patient. Int J Blood Res Disord 6:039. doi.org/10.23937/2469-5696/1410039 Accepted: May 14, 2019: Published: May 16, 2019 Copyright: © 2019 Tashiro H, et al. This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
引用本文:Tashiro H, Oshima Y, Sumiyoshi R, Matsuo T, Yamamoto T等。(2019)兔抗胸腺细胞球蛋白治疗后致死性全身毛霉病。中华血液病杂志6:39。doi.org/10.23937/2469-5696/1410039接收日期:2019年5月14日发布日期:2019年5月16日版权所有:©2019 Tashiro H, et al.。这是一篇根据知识共享署名许可协议发布的开放获取文章,该协议允许在任何媒体上不受限制地使用、分发和复制,前提是要注明原作者和来源。
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引用次数: 0
MEK1/2 as a Therapeutic Target in Sickle Cell Disease MEK1/2作为镰状细胞病的治疗靶点
Pub Date : 2019-04-04 DOI: 10.23937/2469-5696/1410038
R. Zennadi
Identification of novel therapeutic targets has improved diagnostics and treatment of many diseases. Many innovative treatment strategies have been developed based on the newly identified biomarkers and key molecules. Most of the research focused on ways to manipulate signaling pathways by activating or suppressing them, validate new therapeutic targets for treatment, and epigenetic treatment of diseases. With the identification of aberrations in multiple growth pathways, the focus then shifted to the small molecules involved in these pathways for targeted therapy. In this communication/short review, we highlight the importance of identification of abnormal activation of the mitogen-activated protein kinase (MAPK), ERK1/2, and its upstream mediator MEK1/2, in erythrocytes in patients with sickle cell disease (SCD) critical for the adhesive interactions of these cells with the endothelium, and leukocytes promoting circulatory obstruction leading to tissue ischemia and infraction. We also discuss how targeting this signaling cascade with MEK1/2 inhibitors can reverse acute vasoocclusive crises in SCD.
新的治疗靶点的发现改善了许多疾病的诊断和治疗。基于新发现的生物标志物和关键分子,开发了许多创新的治疗策略。大多数研究集中在通过激活或抑制信号通路来操纵信号通路的方法,验证新的治疗靶点,以及疾病的表观遗传治疗。随着多种生长途径的畸变的识别,重点转移到这些途径中涉及的靶向治疗的小分子。在这篇简短的综述中,我们强调了鉴定镰状细胞病(SCD)患者红细胞中丝裂原活化蛋白激酶(MAPK) ERK1/2及其上游介质MEK1/2异常激活的重要性,这些异常激活对于这些细胞与内皮的粘附相互作用至关重要,并且白细胞促进循环阻塞导致组织缺血和梗死。我们还讨论了用MEK1/2抑制剂靶向这种信号级联如何逆转SCD的急性血管闭合性危像。
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引用次数: 9
Lenalidomide Plus Dexamethasone is an Active Rescue Treatment for Myeloma with Severe Renal Impairment Failing to Bortezomib-Based Induction Therapy 来那度胺加地塞米松是一种积极的挽救治疗骨髓瘤严重肾功能损害失败硼替佐米为基础的诱导治疗
Pub Date : 2018-12-31 DOI: 10.23937/2469-5696/1410031
M. Giuseppe, P. Domenico
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引用次数: 0
The Results of the Single Center Pilot Randomized Russian Clinical Trial of Mesenchymal Stromal Cells in Severe Neutropenic Patients with Septic Shock (RUMCESS) 俄罗斯间充质基质细胞在严重中性粒细胞性败血症休克(RUMCESS)患者中的单中心试点随机临床试验结果
Pub Date : 2018-12-31 DOI: 10.23937/2469-5696/1410033
Galstyan Gennadiy, M. Polina, Parovichnikova Elena, Kuzmina Larisa, T. Vera, Gemdzhian Eduard, S. Valeriy
Citation: Galstyan G, Makarova P, Parovichnikova E, Kuzmina L, Troitskaya V, et al. (2018) The Results of the Single Center Pilot Randomized Russian Clinical Trial of Mesenchymal Stromal Cells in Severe Neutropenic Patients with Septic Shock (RUMCESS). Int J Blood Res Disord 5:033. doi. org/10.23937/2469-5696/1410033 Accepted: October 10, 2018: Published: October 12, 2018 Copyright: © 2018 Galstyan G, et al. This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
引用本文:Galstyan G, Makarova P, Parovichnikova E, Kuzmina L, Troitskaya V,等。(2018)重型中性粒细胞减少合并感染性休克患者间充质基质细胞单中心随机试验结果。中华血液病杂志5:033。doi。收稿日期:2018年10月10日发布日期:2018年10月12日版权所有:©2018 Galstyan G, et al.。这是一篇根据知识共享署名许可协议发布的开放获取文章,该协议允许在任何媒体上不受限制地使用、分发和复制,前提是要注明原作者和来源。
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引用次数: 14
Bioinformatics Analysis of Altered lncRNAs in Peripheral Blood Molecular Cells from Major Depressive Disorder (MDD) Patients 抑郁症患者外周血分子细胞lncRNA改变的生物信息学分析
Pub Date : 2018-12-31 DOI: 10.23937/2469-5696/1410034
He Mingjun, Zhu Xiaoli, Niu Wei, K. Ling-ming, Yao Gaofeng, Zhang Li-yi
Citation: He M, Zhu X, Niu W, Kong L, Yao G, et al. (2018) Bioinformatics Analysis of Altered lncRNAs in Peripheral Blood Molecular Cells from Major Depressive Disorder (MDD) Patients. Int J Blood Res Disord 5:034. doi.org/10.23937/2469-5696/1410034 Accepted: December 10, 2018: Published: December 12, 2018 Copyright: © 2018 He M, et al. This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
引用本文:何敏,朱鑫,牛伟,孔磊,姚刚,等。(2018)重度抑郁症患者外周血分子细胞lncrna改变的生物信息学分析。中华血液病杂志5:034。doi.org/10.23937/2469-5696/1410034录用日期:2018年12月10日发布日期:2018年12月12日版权所有:©2018何m等。这是一篇根据知识共享署名许可协议发布的开放获取文章,该协议允许在任何媒体上不受限制地使用、分发和复制,前提是要注明原作者和来源。
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引用次数: 3
Multiple Myeloma Associated with Dermatomyositis: A Short Report and Mini-Review 多发性骨髓瘤与皮肌炎:一个简短的报告和小型回顾
Pub Date : 2018-12-31 DOI: 10.23937/2469-5696/1410029
I. M. Serajul, K. Pavel
Citation: Islam MS, Kotoucek P (2018) Multiple Myeloma Associated with Dermatomyositis: A Short Report and Mini-Review. Int J Blood Res Disord 5:029. doi.org/10.23937/2469-5696/1410029 Accepted: June 18, 2018: Published: June 20, 2018 Copyright: © 2018 Islam MS, et al. This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
引用本文:Islam MS, Kotoucek P(2018)多发性骨髓瘤与皮肌炎相关:简短报告和迷你综述。中华血液病杂志5:29。doi.org/10.23937/2469-5696/1410029接收日期:2018年6月18日发布日期:2018年6月20日版权所有:©2018 Islam MS, et al。这是一篇根据知识共享署名许可协议发布的开放获取文章,该协议允许在任何媒体上不受限制地使用、分发和复制,前提是要注明原作者和来源。
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引用次数: 3
Benign Lymphadenopathy Presented in a Malignant Pathway - A Rare Case of Proteinaceous Lymphadenopathy 以恶性途径表现的良性淋巴结病——一例罕见的蛋白缺乏性淋巴结病
Pub Date : 2018-12-31 DOI: 10.23937/2469-5696/1410030
I. M. Serajul, K. Pavel
Citation: Islam MS, Kotoucek P (2018) Benign Lymphadenopathy Presented in a Malignant Pathway A Rare Case of Proteinaceous Lymphadenopathy. Int J Blood Res Disord 5:030. doi.org/10.23937/24695696/1410030 Accepted: June 28, 2018: Published: June 30, 2018 Copyright: © 2018 Islam MS, et al. This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
引文:Islam MS,Kotoucek P(2018)恶性途径中的良性淋巴结病——一种罕见的蛋白质性淋巴结病。国际血液研究杂志5:030。doi.org/10.23937/24695696/1410030接受时间:2018年6月28日:发布时间:2018月30日版权所有:©2018 Islam MS等人。这是一篇根据知识共享署名许可证条款分发的开放获取文章,该许可证允许在任何介质中不受限制地使用、分发和复制,前提是原作者和来源可信。
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引用次数: 1
期刊
International journal of blood research and disorders
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