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Regulators of G protein signaling: role in hematopoiesis, megakaryopoiesis and platelet function.
J Thromb Haemost. 2012 Nov;10(11):2215-22. doi: 10.1111/j.1538-7836.2012.04903.x.
J Thromb Haemost. 2012.
PMID: 22908964
Free article.
Review.
Regulator of G-protein signaling 18 controls megakaryopoiesis and the cilia-mediated vertebrate mechanosensory system.
Louwette S, Labarque V, Wittevrongel C, Thys C, Metz J, Gijsbers R, Debyser Z, Arnout J, Van Geet C, Freson K.
Louwette S, et al.
FASEB J. 2012 May;26(5):2125-36. doi: 10.1096/fj.11-198739. Epub 2012 Feb 3.
FASEB J. 2012.
PMID: 22308195
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NPC1 defect results in abnormal platelet formation and function: studies in Niemann-Pick disease type C1 patients and zebrafish.
Louwette S, Régal L, Wittevrongel C, Thys C, Vandeweeghde G, Decuyper E, Leemans P, De Vos R, Van Geet C, Jaeken J, Freson K.
Louwette S, et al.
Hum Mol Genet. 2013 Jan 1;22(1):61-73. doi: 10.1093/hmg/dds401. Epub 2012 Sep 24.
Hum Mol Genet. 2013.
PMID: 23010472
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PEAR1 attenuates megakaryopoiesis via control of the PI3K/PTEN pathway.
Kauskot A, Vandenbriele C, Louwette S, Gijsbers R, Tousseyn T, Freson K, Verhamme P, Hoylaerts MF.
Kauskot A, et al. Among authors: louwette s.
Blood. 2013 Jun 27;121(26):5208-17. doi: 10.1182/blood-2012-10-462887. Epub 2013 May 10.
Blood. 2013.
PMID: 23667054
Free article.
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Severe gastrointestinal bleeding and thrombocytopenia in a child with an anti-GATA1 autoantibody.
de Waele L, Freson K, Louwette S, Thys C, Wittevrongel C, de Vos R, Debeer A, van Geet C.
de Waele L, et al. Among authors: louwette s.
Pediatr Res. 2010 Mar;67(3):314-9. doi: 10.1203/PDR.0b013e3181caafd2.
Pediatr Res. 2010.
PMID: 19924028
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DNA methylation analysis of Homeobox genes implicates HOXB7 hypomethylation as risk factor for neural tube defects.
Rochtus A, Izzi B, Vangeel E, Louwette S, Wittevrongel C, Lambrechts D, Moreau Y, Winand R, Verpoorten C, Jansen K, Van Geet C, Freson K.
Rochtus A, et al. Among authors: louwette s.
Epigenetics. 2015;10(1):92-101. doi: 10.1080/15592294.2014.998531. Epub 2015 Jan 29.
Epigenetics. 2015.
PMID: 25565354
Free PMC article.
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Unravelling the disease mechanism for TSPYL1 deficiency.
Buyse G, Di Michele M, Wijgaerts A, Louwette S, Wittevrongel C, Thys C, Downes K, Ceulemans B, Van Esch H, Van Geet C, Freson K.
Buyse G, et al. Among authors: louwette s.
Hum Mol Genet. 2020 Dec 18;29(20):3431-3442. doi: 10.1093/hmg/ddaa233.
Hum Mol Genet. 2020.
PMID: 33075815
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