Results 351 to 360 of about 13,330,610 (394)
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1988
Blood transfusion centres use cell separators to harvest granulocytes, platelets or plasma from donors. These machines can also be used to replace a patient’s plasma containing harmful components with crystalloid or colloid solutions (plasma exchange, therapeutic plasmapheresis) or to remove an excess of cells (therapeutic cytopheresis).
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Blood transfusion centres use cell separators to harvest granulocytes, platelets or plasma from donors. These machines can also be used to replace a patient’s plasma containing harmful components with crystalloid or colloid solutions (plasma exchange, therapeutic plasmapheresis) or to remove an excess of cells (therapeutic cytopheresis).
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Organelle Separation and Cell Signaling
2017Recent findings indicate that some signaling hubs coalesce at the surfaces of organelles through the accumulation of ubiquitylated components required for the signal transduction. For instance, ubiquitylated components of the NF-κB pathway accumulated at the endoplasmic reticulum while ubiquitylated components of the IRF3 pathway are found at the Golgi
Damien Arnoult, Leandro Silva da Costa
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1979
1 Computer Analysis of Lymphocyte Images.- I. Introduction.- A. Computable Image Information.- B. Chromatin Distribution Patterns.- II. Selection of Equipment.- A. The Microscope Photometer.- B. Interface.- C. Computer.- D. Photomicrography and Video-Recording.- III. Computer Programs.- A. Design Considerations.- B. Data Staging and File Handling.- IV.
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1 Computer Analysis of Lymphocyte Images.- I. Introduction.- A. Computable Image Information.- B. Chromatin Distribution Patterns.- II. Selection of Equipment.- A. The Microscope Photometer.- B. Interface.- C. Computer.- D. Photomicrography and Video-Recording.- III. Computer Programs.- A. Design Considerations.- B. Data Staging and File Handling.- IV.
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Separation of White Blood Cells
Nature, 1964A CONVENIENT way of obtaining white cells from whole blood is simply to allow EDTA-blood to settle in siliconized glasses and then pipette off the leucocyte-rich supernatant after 1.5 h or more. A more rapid separation occurs when agents which aggregate erythrocytes are added to the blood1. The effect of these agents may be utilized even without mixing
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Spiral Inertial Microfluidics for Cell Separation and Biomedical Applications
Bioanalysis, 2019Ning Liu +4 more
semanticscholar +1 more source
Automated Microfluidic Instrument for Label-Free and High-Throughput Cell Separation.
Analytical Chemistry, 2018Xinjie Zhang +4 more
semanticscholar +1 more source
Critical care management of chimeric antigen receptor T‐cell therapy recipients
Ca-A Cancer Journal for Clinicians, 2022Alexander Shimabukuro-Vornhagen +2 more
exaly

