Izzi B - Search Results

1

Allele-specific DNA methylation reinforces PEAR1 enhancer activity.

Izzi B, Pistoni M, Cludts K, Akkor P, Lambrechts D, Verfaillie C, Verhamme P, Freson K, Hoylaerts MF. Izzi B, et al. Blood. 2016 Aug 18;128(7):1003-12. doi: 10.1182/blood-2015-11-682153. Epub 2016 Jun 16. Blood. 2016. PMID: 27313330 Free article.

2

Compound heterozygous mutations in the GNAS gene of a boy with morbid obesity, thyroid-stimulating hormone resistance, pseudohypoparathyroidism, and a prothrombotic state.

Freson K, Izzi B, Jaeken J, Van Helvoirt M, Thys C, Wittevrongel C, de Zegher F, Van Geet C. Freson K, et al. Among authors: izzi b. J Clin Endocrinol Metab. 2008 Dec;93(12):4844-9. doi: 10.1210/jc.2008-0233. Epub 2008 Sep 16. J Clin Endocrinol Metab. 2008. PMID: 18796523

3

GNAS defects identified by stimulatory G protein alpha-subunit signalling studies in platelets.

Freson K, Izzi B, Labarque V, Van Helvoirt M, Thys C, Wittevrongel C, Bex M, Bouillon R, Godefroid N, Proesmans W, de Zegher F, Jaeken J, Van Geet C. Freson K, et al. Among authors: izzi b. J Clin Endocrinol Metab. 2008 Dec;93(12):4851-9. doi: 10.1210/jc.2008-0883. Epub 2008 Sep 23. J Clin Endocrinol Metab. 2008. PMID: 18812479

4

Human platelet pathology related to defects in the G-protein signaling cascade.

Van Geet C, Izzi B, Labarque V, Freson K. Van Geet C, et al. Among authors: izzi b. J Thromb Haemost. 2009 Jul;7 Suppl 1:282-6. doi: 10.1111/j.1538-7836.2009.03399.x. J Thromb Haemost. 2009. PMID: 19630817 Free article. Review.

5

A new approach to imprinting mutation detection in GNAS by Sequenom EpiTYPER system.

Izzi B, Decallonne B, Devriendt K, Bouillon R, Vanderschueren D, Levtchenko E, de Zegher F, Van den Bruel A, Lambrechts D, Van Geet C, Freson K. Izzi B, et al. Clin Chim Acta. 2010 Dec 14;411(23-24):2033-9. doi: 10.1016/j.cca.2010.08.034. Epub 2010 Aug 31. Clin Chim Acta. 2010. PMID: 20807523

6

Regulators of platelet cAMP levels: clinical and therapeutic implications.

Noé L, Peeters K, Izzi B, Van Geet C, Freson K. Noé L, et al. Among authors: izzi b. Curr Med Chem. 2010;17(26):2897-905. doi: 10.2174/092986710792065018. Curr Med Chem. 2010. PMID: 20858171 Review.

7

From genetics to epigenetics in platelet research.

Freson K, Izzi B, Van Geet C. Freson K, et al. Among authors: izzi b. Thromb Res. 2012 Mar;129(3):325-9. doi: 10.1016/j.thromres.2011.11.050. Epub 2011 Dec 20. Thromb Res. 2012. PMID: 22192152 Review.

8

No evidence for GNAS copy number variants in patients with features of Albright's hereditary osteodystrophy and abnormal platelet Gs activity.

Izzi B, de Zegher F, Francois I, del Favero J, Goossens D, Wittevrongel C, Thys C, Van Geet C, Freson K. Izzi B, et al. J Hum Genet. 2012 Apr;57(4):277-9. doi: 10.1038/jhg.2012.1. Epub 2012 Jan 26. J Hum Genet. 2012. PMID: 22277900

9

Recent advances in GNAS epigenetic research of pseudohypoparathyroidism.

Izzi B, Van Geet C, Freson K. Izzi B, et al. Curr Mol Med. 2012 Jun;12(5):566-73. doi: 10.2174/156652412800619969. Curr Mol Med. 2012. PMID: 22300135 Review.

10

Methylation defect in imprinted genes detected in patients with an Albright's hereditary osteodystrophy like phenotype and platelet Gs hypofunction.

Izzi B, Francois I, Labarque V, Thys C, Wittevrongel C, Devriendt K, Legius E, Van den Bruel A, D'Hooghe M, Lambrechts D, de Zegher F, Van Geet C, Freson K. Izzi B, et al. PLoS One. 2012;7(6):e38579. doi: 10.1371/journal.pone.0038579. Epub 2012 Jun 5. PLoS One. 2012. PMID: 22679513 Free PMC article.

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