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Items: 19

1.

Identification of the first COG-CDG patient of Indian origin.

Ng BG, Sharma V, Sun L, Loh E, Hong W, Tay SK, Freeze HH.

Mol Genet Metab. 2011 Mar;102(3):364-7. doi: 10.1016/j.ymgme.2010.11.161. Epub 2010 Nov 24.

2.

How Golgi glycosylation meets and needs trafficking: the case of the COG complex.

Reynders E, Foulquier F, Annaert W, Matthijs G.

Glycobiology. 2011 Jul;21(7):853-63. doi: 10.1093/glycob/cwq179. Epub 2010 Nov 26. Review.

PMID:
21112967
3.

COG defects, birth and rise!

Foulquier F.

Biochim Biophys Acta. 2009 Sep;1792(9):896-902. doi: 10.1016/j.bbadis.2008.10.020. Epub 2008 Nov 6. Review.

4.

Deficiencies in subunits of the Conserved Oligomeric Golgi (COG) complex define a novel group of Congenital Disorders of Glycosylation.

Zeevaert R, Foulquier F, Jaeken J, Matthijs G.

Mol Genet Metab. 2008 Jan;93(1):15-21. Epub 2007 Sep 29. Review.

PMID:
17904886
5.

Glycosylation disorders of membrane trafficking.

Rosnoblet C, Peanne R, Legrand D, Foulquier F.

Glycoconj J. 2013 Jan;30(1):23-31. doi: 10.1007/s10719-012-9389-y. Epub 2012 May 15. Review.

PMID:
22584409
6.

TMEM165 deficiencies in Congenital Disorders of Glycosylation type II (CDG-II): Clues and evidences for roles of the protein in Golgi functions and ion homeostasis.

Dulary E, Potelle S, Legrand D, Foulquier F.

Tissue Cell. 2017 Apr;49(2 Pt A):150-156. doi: 10.1016/j.tice.2016.06.006. Epub 2016 Jun 16. Review.

PMID:
27401145
7.

Role of the conserved oligomeric Golgi (COG) complex in protein glycosylation.

Smith RD, Lupashin VV.

Carbohydr Res. 2008 Aug 11;343(12):2024-31. doi: 10.1016/j.carres.2008.01.034. Epub 2008 Feb 2. Review.

8.

Retrograde transport on the COG railway.

Ungar D, Oka T, Krieger M, Hughson FM.

Trends Cell Biol. 2006 Feb;16(2):113-20. Epub 2006 Jan 10. Review.

PMID:
16406524
9.

Congenital disorders of glycosylation: sweet news.

Theodore M, Morava E.

Curr Opin Pediatr. 2011 Dec;23(6):581-7. doi: 10.1097/MOP.0b013e32834cd693. Review.

PMID:
21970833
10.

Congenital disorders of glycosylation.

Jaeken J.

Ann N Y Acad Sci. 2010 Dec;1214:190-8. doi: 10.1111/j.1749-6632.2010.05840.x. Review.

PMID:
21175687
11.

Re'COG'nition at the Golgi.

Miller VJ, Ungar D.

Traffic. 2012 Jul;13(7):891-7. doi: 10.1111/j.1600-0854.2012.01338.x. Epub 2012 Feb 27. Review.

12.

Congenital disorders of glycosylation. Part I. Defects of protein N-glycosylation.

Cylwik B, Naklicki M, Chrostek L, Gruszewska E.

Acta Biochim Pol. 2013;60(2):151-61. Epub 2013 May 31. Review.

13.

Congenital disorders of glycosylation.

Jaeken J, Matthijs G.

Annu Rev Genomics Hum Genet. 2001;2:129-51. Review.

PMID:
11701646
14.

Congenital disorders of glycosylation. Part II. Defects of protein O-glycosylation.

Cylwik B, Lipartowska K, Chrostek L, Gruszewska E.

Acta Biochim Pol. 2013;60(3):361-8. Epub 2013 Sep 19. Review.

15.

Congenital disorders of glycosylation.

Jaeken J.

Handb Clin Neurol. 2013;113:1737-43. doi: 10.1016/B978-0-444-59565-2.00044-7. Review.

PMID:
23622397
16.

Congenital disorders of glycosylation with emphasis on cerebellar involvement.

Barone R, Fiumara A, Jaeken J.

Semin Neurol. 2014 Jul;34(3):357-66. doi: 10.1055/s-0034-1387197. Epub 2014 Sep 5. Review.

PMID:
25192513
17.

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.

18.

Congenital disorders involving defective N-glycosylation of proteins.

Schachter H.

Cell Mol Life Sci. 2001 Jul;58(8):1085-104. Review.

PMID:
11529501
19.

Neurological aspects of human glycosylation disorders.

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

Annu Rev Neurosci. 2015 Jul 8;38:105-25. doi: 10.1146/annurev-neuro-071714-034019. Epub 2015 Apr 2. Review.

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