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Search for publications relevant for "anion transporters"
anion transporters
Publication
Class
Person
Publication
Programmes
publication
New insights in bilirubin metabolism and their clinical implications
2013 |
Third Faculty of Medicine
publication
Massive excretion of calcium oxalate from late prepupal salivary glands of Drosophila melanogaster demonstrates active nephridial-like anion transport
2016 |
First Faculty of Medicine
publication
Genome-wide association study to characterize serum bilirubin elevations in patients with HCV treated with GS-9256, an HCV NS3 serine protease inhibitor
2014 |
First Faculty of Medicine
publication
Down-regulation of OATP1B proteins correlates with hyperbilirubinemia in advanced cholestasis
2015 |
Third Faculty of Medicine, Second Faculty of Medicine
publication
A Transgenic Approach to Identify Thyroxine Transporter-Expressing Structures in Brain Development
2011 |
First Faculty of Medicine
publication
Honey flavonoids inhibit hOATP2B1 and hOATP1A2 transporters and hOATP-mediated rosuvastatin cell uptake in vitro
2018 |
Faculty of Pharmacy in Hradec Králové
publication
Autosomal dominant distal renal tubular acidosis is associated in three families with heterozygosity for the R589H mutation in the AE1 (band 3) Cl-/HCO3- exchanger
1998 |
Second Faculty of Medicine
publication
The in vivo disposition and in vitro transmembrane transport of two model radiometabolites of DOTA-conjugated receptor-specific peptides labelled with Lu-177
2015 |
Faculty of Pharmacy in Hradec Králové
publication
The involvement of selected membrane transport mechanisms in the cellular uptake of Lu-177-labeled bombesin, somatostatin and gastrin analogues
2015 |
Faculty of Pharmacy in Hradec Králové
publication
Renal handling of amphotericin B and amphotericin B-deoxycholate and potential renal drug-drug interactions with selected antivirals
2014 |
Faculty of Pharmacy in Hradec Králové
publication
Genetic and biochemical study of dual hereditary jaundice: Dubin-Johnson and Gilbert's syndromes. Haplotyping and founder effect of deletion in ABCC2
2016 |
First Faculty of Medicine
publication
Pendred syndrome in patients with hypothyroidism: genetic diagnosis, phenotypic variability and occurence of phenocopies
2008 |
Third Faculty of Medicine, Second Faculty of Medicine, Faculty of Medicine in Hradec Králové
publication
Transport of Anions across the Dialytic Membrane Induced by Complexation toward Dendritic Receptors
2021 |
Faculty of Science, Central Library of Charles University
publication
Pendrin and its role in the pathogenesis of congenital hypothyroidism and other diseases
2006 |
Third Faculty of Medicine, Second Faculty of Medicine
publication
Dubin-Johnson syndrome coinciding with colon cancer and atherosclerosis
2013 |
First Faculty of Medicine, Third Faculty of Medicine
publication
Interaction of soy isoflavones and their main metabolites with hOATP2B1 transporter
2018 |
Faculty of Pharmacy in Hradec Králové
publication
SLCO1B1 Polymorphism is not associated with Risk of Statin-Induced Myalgia/Myopathy in a Czech Population
2015 |
First Faculty of Medicine
publication
SLCO5A1 and synaptic assembly genes contribute to impulsivity in juvenile myoclonic epilepsy
2023 |
Second Faculty of Medicine
publication
Complete OATP1B1 and OATP1B3 deficiency causes human Rotor syndrome by interrupting conjugated bilirubin reuptake into the liver
2012 |
First Faculty of Medicine, Third Faculty of Medicine
publication
Functional reconstruction of human AML reveals stem cell origin and vulnerability of treatment-resistant MLL-rearranged leukemia
2021 |
Second Faculty of Medicine
publication
Pendred syndrome in the Czech Republic
2011 |
First Faculty of Medicine, Second Faculty of Medicine