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TMEM165 deficiency causes a congenital disorder of glycosylation.
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.
Impact of disease-causing mutations on TMEM165 subcellular localization, a recently identified protein involved in CDG-II.
Rosnoblet C, Legrand D, Demaegd D, Hacine-Gherbi H, de Bettignies G, Bammens R, Borrego C, Duvet S, Morsomme P, Matthijs G, Foulquier F.
Rosnoblet C, et al. Among authors: bammens r.
Hum Mol Genet. 2013 Jul 15;22(14):2914-28. doi: 10.1093/hmg/ddt146. Epub 2013 Apr 10.
Hum Mol Genet. 2013.
PMID: 23575229
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Abnormal cartilage development and altered N-glycosylation in Tmem165-deficient zebrafish mirrors the phenotypes associated with TMEM165-CDG.
Bammens R, Mehta N, Race V, Foulquier F, Jaeken J, Tiemeyer M, Steet R, Matthijs G, Flanagan-Steet H.
Bammens R, et al.
Glycobiology. 2015 Jun;25(6):669-82. doi: 10.1093/glycob/cwv009. Epub 2015 Jan 21.
Glycobiology. 2015.
PMID: 25609749
Free PMC article.
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Identification and characterisation of monoclonal antibodies that impair the activation of human thrombin activatable fibrinolysis inhibitor through different mechanisms.
Mishra N, Vercauteren E, Develter J, Bammens R, Declerck PJ, Gils A.
Mishra N, et al. Among authors: bammens r.
Thromb Haemost. 2011 Jul;106(1):90-101. doi: 10.1160/TH10-08-0546. Epub 2011 May 5.
Thromb Haemost. 2011.
PMID: 21544309
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