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Results: 4
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Cation Homeostasis in Red Cells From Patients With Sickle Cell Disease Heterologous for HbS and HbC (HbSC Genotype).
A Hannemann
,
DC Rees
,
S Tewari
,
JS Gibson
Sep 16, 2015
HbSC
KCl cotransport
Potassium permeability
Red cells
Sickle cell disease
Anemia
Sickle Cell
Biological Transport
cations
Erythrocytes
Erythrocytes
abnormal
Genotype
Hemoglobin C
Hemoglobin
Sickle
Homeostasis
Humans
Oxygen Consumption
Potassium
Symporters
Published by:
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The effect of the antisickling compound GBT1118 on the permeability of red blood cells from patients with sickle cell anemia.
Halima Al Balushi
,
Kobina Dufu
,
David C Rees
,
John N Brewin
,
Anke Hannemann
,
Donna Oksenberg
,
David C-Y Lu
,
John S Gibson
Feb 28, 2019
GBT1118
O2 affinity
sickle cell anemia
cell volume
Hemolysis
Potassium permeability
sickling
Anemia
Sickle Cell
Antisickling Agents
Benzaldehydes
Cell Size
Erythrocyte Membrane
Hemoglobin
Sickle
Hemolysis
Humans
Intermediate-Conductance Calcium-Activated Potassium Channels
Niacinamide
Oxygen
Permeability
Symporters
Published by:
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The pleiotropic effects of α-thalassemia on HbSS and HbSC sickle cell disease
John N Brewin
,
Amina Nardo-Marino
,
Sara Stuart-Smith
,
Sara El Hoss
,
Anke Hanneman
,
John Strouboulis
,
Stephan Menzel
,
John S Gibson
,
David C Rees
Jul 18, 2022
Anemia
Sickle Cell
cations
Erythrocytes
Erythropoietin
Hemoglobin SC Disease
Hemoglobin
Sickle
Humans
alpha-Thalassemia
Published by:
View Article
How benign is sickle cell trait?
John S Gibson
,
David C Rees
Oct 03, 2016
This is the final version of the article. It first appeared from Elsevier at http://dx.doi.org/10.1016/j.ebiom.2016.08.023.
Red cells
Sickle cell
Sickle cell trait
Animals
Blood Donors
Blood Safety
Erythrocytes
abnormal
Hemoglobin A
Hemoglobin
Sickle
Humans
Sickle Cell Trait
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