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Red blood cell storage lesion: causes and potential clinical consequences
T Yoshida, M Prudent, A D'Alessandro - Blood Transfusion, 2019 - pmc.ncbi.nlm.nih.gov
Red blood cells (RBCs) are a specialised organ that enabled the evolution of multicellular
organisms by supplying a sufficient quantity of oxygen to cells that cannot obtain oxygen …
organisms by supplying a sufficient quantity of oxygen to cells that cannot obtain oxygen …
Carbon monoxide poisoning: pathogenesis, management, and future directions of therapy
Carbon monoxide (CO) poisoning affects 50,000 people a year in the United States. The
clinical presentation runs a spectrum, ranging from headache and dizziness to coma and …
clinical presentation runs a spectrum, ranging from headache and dizziness to coma and …
Neutrophils, platelets, and inflammatory pathways at the nexus of sickle cell disease pathophysiology
Sickle cell disease (SCD) is a severe genetic blood disorder characterized by hemolytic
anemia, episodic vaso-occlusion, and progressive organ damage. Current management of …
anemia, episodic vaso-occlusion, and progressive organ damage. Current management of …
Hemolysis and free hemoglobin revisited: exploring hemoglobin and hemin scavengers as a novel class of therapeutic proteins
Hemolysis occurs in many hematologic and nonhematologic diseases. Extracellular
hemoglobin (Hb) has been found to trigger specific pathophysiologies that are associated …
hemoglobin (Hb) has been found to trigger specific pathophysiologies that are associated …
The red blood cell—inflammation vicious circle in sickle cell disease
E Nader, M Romana, P Connes - Frontiers in immunology, 2020 - frontiersin.org
Sickle cell disease (SCD) is a genetic disease caused by a single mutation in the β-globin
gene, leading to the production of an abnormal hemoglobin called hemoglobin S (HbS) …
gene, leading to the production of an abnormal hemoglobin called hemoglobin S (HbS) …
Heme in pathophysiology: a matter of scavenging, metabolism and trafficking across cell membranes
Heme (iron-protoporphyrin IX) is an essential co-factor involved in multiple biological
processes: oxygen transport and storage, electron transfer, drug and steroid metabolism …
processes: oxygen transport and storage, electron transfer, drug and steroid metabolism …
[HTML][HTML] The macrophage heme-heme oxygenase-1 system and its role in inflammation
V Vijayan, FA Wagener, S Immenschuh - Biochemical pharmacology, 2018 - Elsevier
Abstract Heme oxygenase (HO)-1, the inducible isoform of the heme-degrading enzyme HO,
plays a critical role in inflammation and iron homeostasis. Regulatory functions of HO-1 are …
plays a critical role in inflammation and iron homeostasis. Regulatory functions of HO-1 are …
Mechanisms of haemolysis-induced kidney injury
K Van Avondt, E Nur, S Zeerleder - Nature Reviews Nephrology, 2019 - nature.com
Intravascular haemolysis is a fundamental feature of chronic hereditary and acquired
haemolytic anaemias, including those associated with haemoglobinopathies, complement …
haemolytic anaemias, including those associated with haemoglobinopathies, complement …
Heme on innate immunity and inflammation
Heme is an essential molecule expressed ubiquitously all through our tissues. Heme plays
major functions in cellular physiology and metabolism as the prosthetic group of diverse …
major functions in cellular physiology and metabolism as the prosthetic group of diverse …
The clinical sequelae of intravascular hemolysis and extracellular plasma hemoglobin: a novel mechanism of human disease
ContextThe efficient sequestration of hemoglobin by the red blood cell membrane and the
presence of multiple hemoglobin clearance mechanisms suggest a critical need to prevent …
presence of multiple hemoglobin clearance mechanisms suggest a critical need to prevent …