Improvements in haemolysis and indicators of erythrocyte survival do not correlate with acute vaso-occlusive crises in patients with sickle cell disease: a phase III randomized, placebo-controlled, double-blind study of the Gardos channel blocker se
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Biologic complexity in sickle cell disease: implications for developing targeted therapeuticsDrugs for preventing red blood cell dehydration in people with sickle cell diseaseDrugs for preventing red blood cell dehydration in people with sickle cell diseaseGenomic approaches to identifying targets for treating β hemoglobinopathiesIon channels and transporters in tumour cell migration and invasionGBT440 increases haemoglobin oxygen affinity, reduces sickling and prolongs RBC half-life in a murine model of sickle cell diseaseNew insights on hereditary erythrocyte membrane defects2015 Clinical trials update in sickle cell anemiaEpigenetic dysregulation of KCa 3.1 channels induces poor prognosis in lung cancer.Stroke in patients with sickle cell disease.Ca(2+)-activated K(+) channel-3.1 blocker TRAM-34 attenuates airway remodeling and eosinophilia in a murine asthma model.Treating sickle cell disease by targeting HbS polymerizationNS6180, a new K(Ca) 3.1 channel inhibitor prevents T-cell activation and inflammation in a rat model of inflammatory bowel disease.A GCH1 haplotype confers sex-specific susceptibility to pain crises and altered endothelial function in adults with sickle cell anemia.Echocardiographic markers of elevated pulmonary pressure and left ventricular diastolic dysfunction are associated with exercise intolerance in adults and adolescents with homozygous sickle cell anemia in the United States and United Kingdom.Anti-haemolytic effect of senicapoc and decrease in NT-proBNP in adults with sickle cell anaemia.The Lymphocyte Potassium Channels Kv1.3 and KCa3.1 as Targets for Immunosuppression.Mutations in the Gardos channel (KCNN4) are associated with hereditary xerocytosis.Structural Insights into the Atomistic Mechanisms of Action of Small Molecule Inhibitors Targeting the KCa3.1 Channel Pore.'Gardos Channelopathy': a variant of hereditary Stomatocytosis with complex molecular regulationThe Clinically Tested Gardos Channel Inhibitor Senicapoc Exhibits Antimalarial Activity.Cation Homeostasis in Red Cells From Patients With Sickle Cell Disease Heterologous for HbS and HbC (HbSC Genotype).Beyond hydroxyurea: new and old drugs in the pipeline for sickle cell disease.A non-electrolyte haemolysis assay for diagnosis and prognosis of sickle cell disease.N-ethylmaleimide activates a Cl(-)-independent component of K(+) flux in mouse erythrocytesThe relationship between the severity of hemolysis, clinical manifestations and risk of death in 415 patients with sickle cell anemia in the US and EuropeCurrent management of sickle cell anemia.IMPROVE trial: a randomized controlled trial of patient-controlled analgesia for sickle cell painful episodes: rationale, design challenges, initial experience, and recommendations for future studiesKCa3.1 channel inhibition sensitizes malignant gliomas to temozolomide treatment.Development of a QPatch automated electrophysiology assay for identifying KCa3.1 inhibitors and activators.Tissue resident memory T cells in the human conjunctiva and immune signatures in human dry eye disease.Ion channel drug discovery: challenges and future directions.Endothelial small-conductance and intermediate-conductance KCa channels: an update on their pharmacology and usefulness as cardiovascular targets.The CNS under pathophysiologic attack--examining the role of K₂p channels.The trials and hopes for drug development in sickle cell disease.Anti-steatotic and anti-fibrotic effects of the KCa3.1 channel inhibitor, Senicapoc, in non-alcoholic liver disease.Minireview: Genetic basis of heterogeneity and severity in sickle cell disease.Emerging point-of-care technologies for sickle cell disease screening and monitoring.KCa 3.1-a microglial target ready for drug repurposing?Advances in understanding the pathogenesis of the red cell volume disorders.
P2860
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P2860
Improvements in haemolysis and indicators of erythrocyte survival do not correlate with acute vaso-occlusive crises in patients with sickle cell disease: a phase III randomized, placebo-controlled, double-blind study of the Gardos channel blocker se
description
2011 nî lūn-bûn
@nan
2011年の論文
@ja
2011年学术文章
@wuu
2011年学术文章
@zh-cn
2011年学术文章
@zh-hans
2011年学术文章
@zh-my
2011年学术文章
@zh-sg
2011年學術文章
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2011年學術文章
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2011年學術文章
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name
Improvements in haemolysis and ...... the Gardos channel blocker se
@en
Improvements in haemolysis and ...... the Gardos channel blocker se
@nl
type
label
Improvements in haemolysis and ...... the Gardos channel blocker se
@en
Improvements in haemolysis and ...... the Gardos channel blocker se
@nl
prefLabel
Improvements in haemolysis and ...... the Gardos channel blocker se
@en
Improvements in haemolysis and ...... the Gardos channel blocker se
@nl
P2093
P2860
P921
P1476
Improvements in haemolysis and ...... the Gardos channel blocker se
@en
P2093
Abdullah Kutlar
Carolyn Bigelow
Frederic Galacteros
ICA-17043-10 Study Investigators
James H Hull
Jonathan W Stocker
Kenneth I Ataga
Luther St James
Marvin Reid
Samir K Ballas
P2860
P304
P356
10.1111/J.1365-2141.2010.08520.X
P407
P577
2011-02-17T00:00:00Z