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The interactome of the copper transporter ATP7A belongs to a network of neurodevelopmental and neurodegeneration factors.

Comstra HS, McArthy J, Rudin-Rush S, Hartwig C, Gokhale A, Zlatic SA, Blackburn JB, Werner E, Petris M, D'Souza P, Panuwet P, Barr DB, Lupashin V, Vrailas-Mortimer A, Faundez V.

Elife. 2017 Mar 29;6. pii: e24722. doi: 10.7554/eLife.24722.


Molecular architecture of the complete COG tethering complex.

Ha JY, Chou HT, Ungar D, Yip CK, Walz T, Hughson FM.

Nat Struct Mol Biol. 2016 Aug;23(8):758-60. doi: 10.1038/nsmb.3263. Epub 2016 Jul 18.


COG lobe B sub-complex engages v-SNARE GS15 and functions via regulated interaction with lobe A sub-complex.

Willett R, Blackburn JB, Climer L, Pokrovskaya I, Kudlyk T, Wang W, Lupashin V.

Sci Rep. 2016 Jul 7;6:29139. doi: 10.1038/srep29139.


COG Complex Complexities: Detailed Characterization of a Complete Set of HEK293T Cells Lacking Individual COG Subunits.

Bailey Blackburn J, Pokrovskaya I, Fisher P, Ungar D, Lupashin VV.

Front Cell Dev Biol. 2016 Mar 30;4:23. doi: 10.3389/fcell.2016.00023. eCollection 2016.


Emerging Insights into the Roles of Membrane Tethers from Analysis of Whole Organisms: The Tip of an Iceberg?

Toh WH, Gleeson PA.

Front Cell Dev Biol. 2016 Feb 29;4:12. doi: 10.3389/fcell.2016.00012. eCollection 2016. Review.


Glycosylation Quality Control by the Golgi Structure.

Zhang X, Wang Y.

J Mol Biol. 2016 Aug 14;428(16):3183-3193. doi: 10.1016/j.jmb.2016.02.030. Epub 2016 Mar 5. Review.


Defects in the COG complex and COG-related trafficking regulators affect neuronal Golgi function.

Climer LK, Dobretsov M, Lupashin V.

Front Neurosci. 2015 Oct 27;9:405. doi: 10.3389/fnins.2015.00405. eCollection 2015. Review.


Physiologic and pathophysiologic consequences of altered sialylation and glycosylation on ion channel function.

Baycin-Hizal D, Gottschalk A, Jacobson E, Mai S, Wolozny D, Zhang H, Krag SS, Betenbaugh MJ.

Biochem Biophys Res Commun. 2014 Oct 17;453(2):243-53. doi: 10.1016/j.bbrc.2014.06.067. Epub 2014 Jun 24. Review.


TMEM115 is an integral membrane protein of the Golgi complex involved in retrograde transport.

Ong YS, Tran TH, Gounko NV, Hong W.

J Cell Sci. 2014 Jul 1;127(Pt 13):2825-39. doi: 10.1242/jcs.136754. Epub 2014 May 7.


Mislocalization of phosphotransferase as a cause of mucolipidosis III αβ.

van Meel E, Qian Y, Kornfeld SA.

Proc Natl Acad Sci U S A. 2014 Mar 4;111(9):3532-7. doi: 10.1073/pnas.1401417111. Epub 2014 Feb 18.


Comparative genomic analysis of multi-subunit tethering complexes demonstrates an ancient pan-eukaryotic complement and sculpting in Apicomplexa.

Klinger CM, Klute MJ, Dacks JB.

PLoS One. 2013 Sep 27;8(9):e76278. doi: 10.1371/journal.pone.0076278. eCollection 2013.


Deficiency of the Cog8 subunit in normal and CDG-derived cells impairs the assembly of the COG and Golgi SNARE complexes.

Laufman O, Freeze HH, Hong W, Lev S.

Traffic. 2013 Oct;14(10):1065-77. doi: 10.1111/tra.12093. Epub 2013 Jul 31.


Congenital protein hypoglycosylation diseases.

Sparks SE.

Appl Clin Genet. 2012 Jul 5;5:43-54. doi: 10.2147/TACG.S18673. Print 2012.


Fluorescent microscopy as a tool to elucidate dysfunction and mislocalization of Golgi glycosyltransferases in COG complex depleted mammalian cells.

Willett RA, Pokrovskaya ID, Lupashin VV.

Methods Mol Biol. 2013;1022:61-72. doi: 10.1007/978-1-62703-465-4_6.


Newly characterized Golgi-localized family of proteins is involved in calcium and pH homeostasis in yeast and human cells.

Demaegd D, Foulquier F, Colinet AS, Gremillon L, Legrand D, Mariot P, Peiter E, Van Schaftingen E, Matthijs G, Morsomme P.

Proc Natl Acad Sci U S A. 2013 Apr 23;110(17):6859-64. doi: 10.1073/pnas.1219871110. Epub 2013 Apr 8.


Deficiency of Subunit 6 of the Conserved Oligomeric Golgi Complex (COG6-CDG): Second Patient, Different Phenotype.

Huybrechts S, De Laet C, Bontems P, Rooze S, Souayah H, Sznajer Y, Sturiale L, Garozzo D, Matthijs G, Ferster A, Jaeken J, Goyens P.

JIMD Rep. 2012;4:103-8. doi: 10.1007/8904_2011_79. Epub 2011 Nov 2.


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.

Orphanet J Rare Dis. 2012 Dec 10;7:94. doi: 10.1186/1750-1172-7-94. Erratum in: Orphanet J Rare Dis. 2013;8:120.


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.

Am J Hum Genet. 2012 Jul 13;91(1):15-26. doi: 10.1016/j.ajhg.2012.05.002. Epub 2012 Jun 7.


Neurology of inherited glycosylation disorders.

Freeze HH, Eklund EA, Ng BG, Patterson MC.

Lancet Neurol. 2012 May;11(5):453-66. doi: 10.1016/S1474-4422(12)70040-6.


The conserved oligomeric Golgi complex is required for fucosylation of N-glycans in Caenorhabditis elegans.

Struwe WB, Reinhold VN.

Glycobiology. 2012 Jun;22(6):863-75. doi: 10.1093/glycob/cws053. Epub 2012 Feb 28.

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