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Person
Dr. M.H.A. Kester
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Completed research (1)
Publications (8)
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activity
disease
gene
liver
mutations
patients
uptake
Digital Author ID
info:eu-repo/dai/nl/227239962
Grants/prizes
NWO-Veni 2005
Active as
Researcher
Organisation
Department of General Internal Medicine (EUR)
Email
m. kester -at- erasmusmc. nl
Publications
(the most recent at the top)
Effective cellular uptake and efflux of thyroid hormone by human monocarboxylate transporter 10
Genotype-phenotype relationship in patients with mutations in thyroid hormone transporter MCT8
Characterization of iodothyronine sulfatase activities in human and rat liver and placenta
Potent inhibition of estrogen sulfotransferase by hydroxylated metabolites of polyhalogenated aromatic hydrocarbons reveals alternative mechanism for estrogenic activity of endocrine disrupters
The importance of thyroid hormone sulfation during fetal development
All publications..
Completed research projects
(the most recent research is at the top)
Project leader
Regulation of the imprinted gene type III iodothyronine deiodinase: its role in human fetal development and in disease
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