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Correction to: Golgi.
Wang Y, Lupashin VV, Graham TR. Wang Y, et al. Among authors: lupashin vv. Methods Mol Biol. 2023;2557:C1. doi: 10.1007/978-1-0716-2639-9_48. Methods Mol Biol. 2023. PMID: 36763332 No abstract available.
Molecular and clinical characterization of a Moroccan Cog7 deficient patient.
Ng BG, Kranz C, Hagebeuk EE, Duran M, Abeling NG, Wuyts B, Ungar D, Lupashin V, Hartdorff CM, Poll-The BT, Freeze HH. Ng BG, et al. Mol Genet Metab. 2007 Jun;91(2):201-4. doi: 10.1016/j.ymgme.2007.02.011. Epub 2007 Mar 28. Mol Genet Metab. 2007. PMID: 17395513 Free PMC article.
Role of tethering factors in secretory membrane traffic.
Sztul E, Lupashin V. Sztul E, et al. Am J Physiol Cell Physiol. 2006 Jan;290(1):C11-26. doi: 10.1152/ajpcell.00293.2005. Am J Physiol Cell Physiol. 2006. PMID: 16338975 Free article. Review.
COG8 deficiency causes new congenital disorder of glycosylation type IIh.
Kranz C, Ng BG, Sun L, Sharma V, Eklund EA, Miura Y, Ungar D, Lupashin V, Winkel RD, Cipollo JF, Costello CE, Loh E, Hong W, Freeze HH. Kranz C, et al. Hum Mol Genet. 2007 Apr 1;16(7):731-41. doi: 10.1093/hmg/ddm028. Epub 2007 Mar 1. Hum Mol Genet. 2007. PMID: 17331980
87 results