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COG5-CDG: expanding the clinical spectrum.
Rymen D, Keldermans L, Race V, Régal L, Deconinck N, Dionisi-Vici C, Fung CW, Sturiale L, Rosnoblet C, Foulquier F, Matthijs G, Jaeken J. Rymen D, et al. Among authors: rosnoblet c. Orphanet J Rare Dis. 2012 Dec 10;7:94. doi: 10.1186/1750-1172-7-94. Orphanet J Rare Dis. 2012. PMID: 23228021 Free PMC article.
TMEM165 deficiency causes a congenital disorder of glycosylation.
Foulquier F, Amyere M, Jaeken J, Zeevaert R, Schollen E, Race V, Bammens R, Morelle W, Rosnoblet C, Legrand D, Demaegd D, Buist N, Cheillan D, Guffon N, Morsomme P, Annaert W, Freeze HH, Van Schaftingen E, Vikkula M, Matthijs G. Foulquier F, et al. Among authors: rosnoblet c. Am J Hum Genet. 2012 Jul 13;91(1):15-26. doi: 10.1016/j.ajhg.2012.05.002. Epub 2012 Jun 7. Am J Hum Genet. 2012. PMID: 22683087 Free PMC article.
Glycosylation disorders of membrane trafficking.
Rosnoblet C, Peanne R, Legrand D, Foulquier F. Rosnoblet C, et al. Glycoconj J. 2013 Jan;30(1):23-31. doi: 10.1007/s10719-012-9389-y. Epub 2012 May 15. Glycoconj J. 2013. PMID: 22584409 Review.
Protein S-nitrosylation: specificity and identification strategies in plants.
Lamotte O, Bertoldo JB, Besson-Bard A, Rosnoblet C, Aimé S, Hichami S, Terenzi H, Wendehenne D. Lamotte O, et al. Among authors: rosnoblet c. Front Chem. 2015 Jan 7;2:114. doi: 10.3389/fchem.2014.00114. eCollection 2014. Front Chem. 2015. PMID: 25750911 Free PMC article. Review.
32 results