Related references
Note: Only part of the references are listed.Oxidative stress and phosphatidylserine exposure in red cells from patients with sickle cell anaemia
Anke Hannemann et al.
BRITISH JOURNAL OF HAEMATOLOGY (2018)
Genetic modifiers of severity in sickle cell disease
Alicia K. Chang et al.
CLINICAL HEMORHEOLOGY AND MICROCIRCULATION (2018)
Rapid Fire: Sickle Cell Disease
Michael Porter
EMERGENCY MEDICINE CLINICS OF NORTH AMERICA (2018)
Association between Oxidative Stress, Genetic Factors, and Clinical Severity in Children with Sickle Cell Anemia
Celine Renoux et al.
JOURNAL OF PEDIATRICS (2018)
Sickle Cell Disease: Bone, Joint, Muscle, and Motor Complications
Irina Benenson et al.
ORTHOPAEDIC NURSING (2018)
A common molecular signature of patients with sickle cell disease revealed by microarray meta-analysis and a genome-wide association study
Cherif Ben Hamda et al.
PLOS ONE (2018)
Pb(II) Induces Scramblase Activation and Ceramide-Domain Generation in Red Blood Cells
Hasna Ahyayauch et al.
SCIENTIFIC REPORTS (2018)
Measuring success: utility of biomarkers in sickle cell disease clinical trials and care
Ram Kalpatthi et al.
HEMATOLOGY-AMERICAN SOCIETY OF HEMATOLOGY EDUCATION PROGRAM (2018)
Sickle Cell Disease A Brief Update
Shari Azar et al.
MEDICAL CLINICS OF NORTH AMERICA (2017)
GeneHancer: genome-wide integration of enhancers and target genes in GeneCards
Simon Fishilevich et al.
DATABASE-THE JOURNAL OF BIOLOGICAL DATABASES AND CURATION (2017)
Role of innate immunity-triggered pathways in the pathogenesis of Sickle Cell Disease: a meta-analysis of gene expression studies
Bidossessi Wilfried Hounkpe et al.
SCIENTIFIC REPORTS (2015)
Clinical biomarkers in sickle cell disease
Ghazi A. Damanhouri et al.
SAUDI JOURNAL OF BIOLOGICAL SCIENCES (2015)
The Co-Inheritance of Alpha-Thalassemia and Sickle Cell Anemia Is Associated with Better Hematological Indices and Lower Consultations Rate in Cameroonian Patients and Could Improve Their Survival
Maryam Bibi Rumaney et al.
PLOS ONE (2014)
Genomic architecture of sickle cell disease in West African children
Jacklyn Quinlan et al.
FRONTIERS IN GENETICS (2014)
The broad-spectrum antiviral functions of IFIT and IFITM proteins
Michael S. Diamond et al.
NATURE REVIEWS IMMUNOLOGY (2013)
Genetic modifiers of sickle cell disease
Martin H. Steinberg et al.
AMERICAN JOURNAL OF HEMATOLOGY (2012)
Biochemical and functional characterization of human phospholipid scramblase 4 (hPLSCR4)
Vincent Gerard Francis et al.
BIOLOGICAL CHEMISTRY (2012)
Biomarkers in sickle cell disease
David C. Rees et al.
BRITISH JOURNAL OF HAEMATOLOGY (2012)
Killing me softly - Suicidal erythrocyte death
Elisabeth Lang et al.
INTERNATIONAL JOURNAL OF BIOCHEMISTRY & CELL BIOLOGY (2012)
GENETIC MODIFIERS OF SICKLE CELL DISEASE
Swee Lay Thein
HEMOGLOBIN (2011)
Microvascular endothelial cells express a phosphatidylserine receptor: a functionally active receptor for phosphatidylserine-positive erythrocytes
B. N. Yamaja Setty et al.
BLOOD (2008)
Red Cell Membrane Lipids in Hemoglobinopathies
Frans A. Kuypers
CURRENT MOLECULAR MEDICINE (2008)
Mechanisms and significance of eryptosis
Florian Lang et al.
ANTIOXIDANTS & REDOX SIGNALING (2006)
Hydrolysis of phosphatidylserine-exposing red blood cells by secretory phospholipase A2 generates lysophosphatidic acid and results in vascular dysfunction
NA Neidlinger et al.
JOURNAL OF BIOLOGICAL CHEMISTRY (2006)
Predicting clinical severity in sickle cell anaemia
MH Steinberg
BRITISH JOURNAL OF HAEMATOLOGY (2005)
Blood mononuclear cell gene expression profiles characterize the oxidant, hemolytic, and inflammatory stress of sickle cell disease
ML Jison et al.
BLOOD (2004)
Comparison of mechanisms of anemia in mice with sickle cell disease and β-thalassemia:: Peripheral destruction, ineffective erythropoiesis, and phospholipid scramblase-mediated phosphatidylserine exposure
LS Kean et al.
EXPERIMENTAL HEMATOLOGY (2002)
Share Paper
