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scopus: 7402865204

Jansen, J.

(Jurgen Jansen)


patient thyroid mct 8 hormone transporter mutation protein uptake hmct 8 thyroid hormone expression transfected t 3 uptake transport figure level visser jeg 3 cells serum metabolism control fibroblast monocarboxylate result psychomotor retardation friesema brain activity monocarboxylate transporter 8 family chapter mct 8 patients pcdna function membrane psychomotor retardation endocrinol development study efflux cos 1 cells transfection thyroid hormone transporter deiodinase visser tj plasma membrane increase mct 8 mutations plasma friesema ec incubation patient p 4 intracellular hmct 10 cells transfected mutant jansen j jansen 1/1 iodothyronine medium tissue neuron serum t 3 wild-type x-linked psychomotor retardation mct 8 gene t 4 uptake domain effect iodothyronines thyroid hormone action concentration kester mh splice syndrome 3 activity liver thyroid hormone transporters




4 Most Recent Publications

Evidence for a homodimeric structure of human monocarboxylate transporter 8 (Article)
Visser, W.E. Philp, N.J. Dijk, T.B. van Klootwijk, W. Friesema, E.C.H. Jansen, J. Beesley, P.W. Ianculescu, A.G.
2009-11-01
Novel pathogenic mechanism suggested by ex vivo analysis of MCT8 (SLC16A2) mutations (Article)
Visser, W.E. Jansen, J. Friesema, E.C.H. Kester, M.H.A. Mancilla, E. Lundgren, J. Knaap, M.S. van der Lunsing, R.J. Brouwer, O.F. Visser, T.J.
2009-01-01
Mutations in Thyroid Hormone Transporter MCT8: genotype, function and phenotype (Doctoral Thesis)
Jansen, J.
2008-05-28
Thyroid hormone transport by the human monocarboxylate transporter 8 and its rate-limiting role in intracellular metabolism. (Article)
Friesema, E.C.H. Kuiper, G.G.J.M. Jansen, J. Visser, T.J. Kester, M.H.A.
2006-11-01