Turnitin
降AI改写
早检测系统
早降重系统
Turnitin-UK版
万方检测-期刊版
维普编辑部版
Grammarly检测
Paperpass检测
checkpass检测
PaperYY检测
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 …
[HTML][HTML] Beyond HIV infection: neglected and varied impacts of CCR5 and CCR5Δ32 on viral diseases
The interactions between chemokine receptors and their ligands may affect susceptibility to
infectious diseases as well as their clinical manifestations. These interactions mediate both …
infectious diseases as well as their clinical manifestations. These interactions mediate both …
Hemopexin therapy reverts heme-induced proinflammatory phenotypic switching of macrophages in a mouse model of sickle cell disease
F Vinchi, M Costa da Silva, G Ingoglia… - Blood, The Journal …, 2016 - ashpublications.org
Hemolytic diseases, such as sickle cell anemia and thalassemia, are characterized by
enhanced release of hemoglobin and heme into the circulation, heme-iron loading of …
enhanced release of hemoglobin and heme into the circulation, heme-iron loading of …
Recipient inflammation affects the frequency and magnitude of immunization to transfused red blood cells
JE Hendrickson, M Desmarets, SS Deshpande… - …, 2006 - Wiley Online Library
BACKGROUND: Most alloantigens on transfused red blood cells (RBCs) are weakly
immunogenic, with only a 2 to 6 percent overall immunization rate even in patients receiving …
immunogenic, with only a 2 to 6 percent overall immunization rate even in patients receiving …
Energy expenditure, inflammation, and oxidative stress in steady-state adolescents with sickle cell anemia
SA Akohoue, S Shankar, GL Milne, J Morrow… - Pediatric …, 2007 - nature.com
Sickle cell anemia (HbSS) is characterized by hypermetabolism, chronic inflammation, and
increased oxidative stress, but the relationship between these factors is undefined. In this …
increased oxidative stress, but the relationship between these factors is undefined. In this …
Biologically active CD40 ligand is elevated in sickle cell anemia: potential role for platelet-mediated inflammation
SP Lee, KI Ataga, EP Orringer, DR Phillips… - … , and vascular biology, 2006 - ahajournals.org
Objective—After activation, platelets expose CD40 ligand (CD40L) on their surface, then
subsequently release the inflammatory mediator as a soluble fragment (sCD40L). Because …
subsequently release the inflammatory mediator as a soluble fragment (sCD40L). Because …
[PDF][PDF] Asthma is associated with increased mortality in individuals with sickle cell anemia
JH Boyd, EA Macklin, RC Strunk, MR DeBaun - 2007 - digitalcommons.wustl.edu
An analysis of a prospective cohort of individuals with sickle cell anemia (SCA), enrolled
from birth through adulthood, was conducted to determine if asthma is a risk factor for death …
from birth through adulthood, was conducted to determine if asthma is a risk factor for death …
Infections in thalassemia and hemoglobinopathies: focus on therapy-related complications
BM Ricerca, A Di Girolamo… - Mediterranean journal of …, 2009 - pmc.ncbi.nlm.nih.gov
The clinical approach to thalassemia and hemoglobinopathies, specifically Sickle Cell
Disease (SCD), based on transfusions, iron chelation and bone marrow transplantation has …
Disease (SCD), based on transfusions, iron chelation and bone marrow transplantation has …
Red blood cell alloimmunization in patients with sickle cell disease: correlation with HLA and cytokine gene polymorphisms
BACKGROUND The reason for the difference in susceptibility to red blood cell (RBC)
alloimmunization among patients with sickle cell disease (SCD) is not clearly understood …
alloimmunization among patients with sickle cell disease (SCD) is not clearly understood …
Heme oxygenase-1 gene promoter polymorphism is associated with reduced incidence of acute chest syndrome among children with sickle cell disease
CJ Bean, SL Boulet, D Ellingsen… - Blood, The Journal …, 2012 - ashpublications.org
Sickle cell disease is a common hemolytic disorder with a broad range of complications,
including vaso-occlusive episodes, acute chest syndrome (ACS), pain, and stroke. Heme …
including vaso-occlusive episodes, acute chest syndrome (ACS), pain, and stroke. Heme …