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of 5
pro vyhledávání: '"Jan B. Koenderink"'
Autor:
Frans G. M. Russel, Azza A.K. El-Sheikh, Jan B. Koenderink, Jeroen J. M. W. van den Heuvel, Elmar Krieger
Publikováno v:
Molecular Pharmacology, 74, 4, pp. 964-971
Molecular Pharmacology, 74, 964-971
Molecular Pharmacology, 74, 964-971
Contains fulltext : 70256.pdf (Publisher’s version ) (Open Access) Multidrug resistance protein (MRP) 4 transports a variety of endogenous and xenobiotic organic anions. MRP4 is widely expressed in the body and specifically localized to the renal a
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4ed1449c4f4e293b0951807a13d993ae
https://hdl.handle.net/2066/70256
https://hdl.handle.net/2066/70256
Publikováno v:
Trends in Pharmacological Sciences, 29, 200-207
Trends in Pharmacological Sciences, 29, 4, pp. 200-207
Trends in Pharmacological Sciences, 29, 4, pp. 200-207
Contains fulltext : 70675.pdf (Publisher’s version ) (Closed access) Multidrug resistance protein (MRP) 4 is a member of the MRP/ABCC subfamily of ATP-binding cassette transporters, which are capable of pumping a wide variety of endogenous and xeno
Autor:
Jan B. Koenderink, Herman G.P. Swarts, Nine V A M Knoers, Edinio R. Cairo, Leo A. H. Monnens, Peter H.G.M. Willems, Thomas Friedrich, Jan Joep H.H.M. De Pont, René J. M. Bindels
Publikováno v:
Biochimica et Biophysica Acta. Biomembranes, 1778, 2, pp. 398-404
Biochimica et Biophysica Acta. Biomembranes, 1778, 398-404
Biochimica et Biophysica Acta. Biomembranes, 1778, 398-404
Contains fulltext : 69840.pdf (Publisher’s version ) (Closed access) Autosomal dominant renal hypomagnesemia, associated with hypocalciurea, has been linked to a G to A mutation at nucleotide position 121 in the FXYD2 gene, resulting in the substit
Publikováno v:
Journal of Pharmacology and Experimental Therapeutics, 320, 1, pp. 229-35
Journal of Pharmacology and Experimental Therapeutics, 320, 229-35
Journal of Pharmacology and Experimental Therapeutics, 320, 229-35
Contains fulltext : 34599.pdf (Publisher’s version ) (Open Access) Methotrexate (MTX) has been used in combination with nonsteroidal anti-inflammatory drugs (NSAIDs) in the treatment of inflammatory diseases as well as malignancies. Especially at h
Autor:
Antoon J.M. Janssen, Henk J. Blom, Jan B. Koenderink, Adriana de Graaf-Hess, Leo A. H. Monnens, Lambertus P. van den Heuvel, Martijn J. Wilmer, Henk-Jan Visch, Elena Levtchenko, Peter H.G.M. Willems
Publikováno v:
Pediatric Research, 59, 287-92
Pediatric Research, 59, 2, pp. 287-92
Pediatric Research, 59, 2, pp. 287-92
Contains fulltext : 49755.pdf (Publisher’s version ) (Closed access) Cystinosis is an autosomal recessive lysosomal storage disorder caused by a defect in the lysosomal cystine carrier cystinosin. Cystinosis is the most common cause of inherited Fa