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Year | Number of Results |
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2012 | 2 |
2013 | 1 |
2016 | 1 |
2024 | 0 |
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A zebrafish model of congenital disorders of glycosylation with phosphomannose isomerase deficiency reveals an early opportunity for corrective mannose supplementation.
Dis Model Mech. 2013 Jan;6(1):95-105. doi: 10.1242/dmm.010116. Epub 2012 Aug 16.
Dis Model Mech. 2013.
PMID: 22899857
Free PMC article.
trappc11 is required for protein glycosylation in zebrafish and humans.
DeRossi C, Vacaru A, Rafiq R, Cinaroglu A, Imrie D, Nayar S, Baryshnikova A, Milev MP, Stanga D, Kadakia D, Gao N, Chu J, Freeze HH, Lehrman MA, Sacher M, Sadler KC.
DeRossi C, et al.
Mol Biol Cell. 2016 Apr 15;27(8):1220-34. doi: 10.1091/mbc.E15-08-0557. Epub 2016 Feb 24.
Mol Biol Cell. 2016.
PMID: 26912795
Free PMC article.
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The Cx43-like connexin protein Cx40.8 is differentially localized during fin ontogeny and fin regeneration.
Gerhart SV, Eble DM, Burger RM, Oline SN, Vacaru A, Sadler KC, Jefferis R, Iovine MK.
Gerhart SV, et al.
PLoS One. 2012;7(2):e31364. doi: 10.1371/journal.pone.0031364. Epub 2012 Feb 8.
PLoS One. 2012.
PMID: 22347467
Free PMC article.
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