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Page 1
Developmental defects and rescue from glucose intolerance of a catalytically-inactive novel Ship2 mutant mouse.
Cell Signal. 2012 Nov;24(11):1971-80. doi: 10.1016/j.cellsig.2012.06.012. Epub 2012 Jun 30.
Cell Signal. 2012.
PMID: 22750293
INPP5E mutations cause primary cilium signaling defects, ciliary instability and ciliopathies in human and mouse.
Jacoby M, Cox JJ, Gayral S, Hampshire DJ, Ayub M, Blockmans M, Pernot E, Kisseleva MV, Compère P, Schiffmann SN, Gergely F, Riley JH, Pérez-Morga D, Woods CG, Schurmans S.
Jacoby M, et al. Among authors: blockmans m.
Nat Genet. 2009 Sep;41(9):1027-31. doi: 10.1038/ng.427. Epub 2009 Aug 9.
Nat Genet. 2009.
PMID: 19668215
Free article.
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The inositol Inpp5k 5-phosphatase affects osmoregulation through the vasopressin-aquaporin 2 pathway in the collecting system.
Pernot E, Terryn S, Cheong SC, Markadieu N, Janas S, Blockmans M, Jacoby M, Pouillon V, Gayral S, Rossier BC, Beauwens R, Erneux C, Devuyst O, Schurmans S.
Pernot E, et al. Among authors: blockmans m.
Pflugers Arch. 2011 Dec;462(6):871-83. doi: 10.1007/s00424-011-1028-0. Epub 2011 Sep 22.
Pflugers Arch. 2011.
PMID: 21938401
Free article.
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The association between the SH2-containing inositol polyphosphate 5-Phosphatase 2 (SHIP2) and the adaptor protein APS has an impact on biochemical properties of both partners.
Onnockx S, De Schutter J, Blockmans M, Xie J, Jacobs C, Vanderwinden JM, Erneux C, Pirson I.
Onnockx S, et al. Among authors: blockmans m.
J Cell Physiol. 2008 Jan;214(1):260-72. doi: 10.1002/jcp.21193.
J Cell Physiol. 2008.
PMID: 17620296
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