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Page 1
Interaction between hamartin and tuberin, the TSC1 and TSC2 gene products.
van Slegtenhorst M, Nellist M, Nagelkerken B, Cheadle J, Snell R, van den Ouweland A, Reuser A, Sampson J, Halley D, van der Sluijs P. van Slegtenhorst M, et al. Among authors: van der sluijs p, van den ouweland a. Hum Mol Genet. 1998 Jun;7(6):1053-7. doi: 10.1093/hmg/7.6.1053. Hum Mol Genet. 1998. PMID: 9580671 Free article.
Identification and characterization of the interaction between tuberin and 14-3-3zeta.
Nellist M, Goedbloed MA, de Winter C, Verhaaf B, Jankie A, Reuser AJ, van den Ouweland AM, van der Sluijs P, Halley DJ. Nellist M, et al. Among authors: van der sluijs p, van den ouweland am. J Biol Chem. 2002 Oct 18;277(42):39417-24. doi: 10.1074/jbc.M204802200. Epub 2002 Aug 9. J Biol Chem. 2002. PMID: 12176984 Free article.
A novel epitope tag for the detection of rabGTPases.
Nagelkerken B, Mohrmann K, Gerez L, van Raak M, Leijendekker R, van der Sluijs P. Nagelkerken B, et al. Among authors: van der sluijs p, van raak m. Electrophoresis. 1997 Dec;18(14):2694-8. doi: 10.1002/elps.1150181427. Electrophoresis. 1997. PMID: 9527500
Early endosome membrane dynamics characterized by flow cytometry.
Chavrier P, van der Sluijs P, Mishal Z, Nagelkerken B, Gorvel JP. Chavrier P, et al. Among authors: van der sluijs p. Cytometry. 1997 Sep 1;29(1):41-9. doi: 10.1002/(sici)1097-0320(19970901)29:1<41::aid-cyto4>3.0.co;2-g. Cytometry. 1997. PMID: 9298810 Free article.
A novel mechanism in recessive nephrogenic diabetes insipidus: wild-type aquaporin-2 rescues the apical membrane expression of intracellularly retained AQP2-P262L.
de Mattia F, Savelkoul PJ, Bichet DG, Kamsteeg EJ, Konings IB, Marr N, Arthus MF, Lonergan M, van Os CH, van der Sluijs P, Robertson G, Deen PM. de Mattia F, et al. Among authors: van os ch, van der sluijs p. Hum Mol Genet. 2004 Dec 15;13(24):3045-56. doi: 10.1093/hmg/ddh339. Epub 2004 Oct 27. Hum Mol Genet. 2004. PMID: 15509592
MYO5B, STX3, and STXBP2 mutations reveal a common disease mechanism that unifies a subset of congenital diarrheal disorders: A mutation update.
Dhekne HS, Pylypenko O, Overeem AW, Zibouche M, Ferreira RJ, van der Velde KJ, Rings EHHM, Posovszky C, van der Sluijs P, Swertz MA, Houdusse A, van IJzendoorn SCD. Dhekne HS, et al. Among authors: van der velde kj, van der sluijs p, van ijzendoorn scd. Hum Mutat. 2018 Mar;39(3):333-344. doi: 10.1002/humu.23386. Epub 2018 Jan 17. Hum Mutat. 2018. PMID: 29266534 Free PMC article. Review.
131 results