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Items: 3

1.

GWAS for serum galactose-deficient IgA1 implicates critical genes of the O-glycosylation pathway.

Kiryluk K, Li Y, Moldoveanu Z, Suzuki H, Reily C, Hou P, Xie J, Mladkova N, Prakash S, Fischman C, Shapiro S, LeDesma RA, Bradbury D, Ionita-Laza I, Eitner F, Rauen T, Maillard N, Berthoux F, Floege J, Chen N, Zhang H, Scolari F, Wyatt RJ, Julian BA, Gharavi AG, Novak J.

PLoS Genet. 2017 Feb 10;13(2):e1006609. doi: 10.1371/journal.pgen.1006609. eCollection 2017 Feb.

2.

Dysregulation of follicle development in a mouse model of premature ovarian insufficiency.

Grasa P, Sheikh S, Krzys N, Millar K, Janjua S, Nawaggi P, Williams SA.

Reproduction. 2016 Nov;152(5):591-601. Epub 2016 Aug 31.

3.

Protein glycosylation: chaperone mutation in Tn syndrome.

Ju T, Cummings RD.

Nature. 2005 Oct 27;437(7063):1252.

PMID:
16251947

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