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Erratum: Carboxylated N-glycans on RAGE promote S100A12 binding and signaling, in Journal of Cellular Biochemistry, by Srikrishna et al.
- Published in:
- Journal of Cellular Biochemistry, 2010, v. 111, n. 1, p. 248, doi. 10.1002/jcb.22746
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- Publication type:
- Article
Carboxylated N-glycans on RAGE promote S100A12 binding and signaling.
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- Journal of Cellular Biochemistry, 2010, v. 110, n. 3, p. 645, doi. 10.1002/jcb.22575
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- Publication type:
- Article
Three unreported cases of TMEM199-CDG, a rare genetic liver disease with abnormal glycosylation.
- Published in:
- 2018
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- Publication type:
- journal article
Mannose supplements induce embryonic lethality and blindness in phosphomannose isomerase hypomorphic mice.
- Published in:
- FASEB Journal, 2014, v. 28, n. 4, p. 1854, doi. 10.1096/fj.13-245514
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- Publication type:
- Article
A sensitive green fluorescent protein biomarker of N-glycosylation site occupancy.
- Published in:
- FASEB Journal, 2012, v. 26, n. 10, p. 4210, doi. 10.1096/fj.12-211656
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- Publication type:
- Article
Genetic defects in the human glycome.
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- 2006
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- Publication type:
- Correction notice
Genetic defects in the human glycome.
- Published in:
- Nature Reviews Genetics, 2006, v. 7, n. 7, p. 537, doi. 10.1038/nrg1894
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- Publication type:
- Article
Sweet solution: sugars to the rescue.
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- Journal of Cell Biology, 2002, v. 158, n. 4, p. 615, doi. 10.1083/jcb.200207155
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- Publication type:
- Article
RAGE, carboxylated glycans and S100A8/A9 play essential roles in colitis-associated carcinogenesis.
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- Carcinogenesis, 2008, v. 29, n. 10, p. 2035, doi. 10.1093/carcin/bgn188
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- Publication type:
- Article
A new congenital disorder of glycosylation caused by a mutation in SSR4, the signal sequence receptor 4 protein of the TRAP complex.
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- Human Molecular Genetics, 2014, v. 23, n. 6, p. 1602
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- Publication type:
- Article
Mutations in STT3A and STT3B cause two congenital disorders of glycosylation.
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- Human Molecular Genetics, 2013, v. 22, n. 22, p. 4638, doi. 10.1093/hmg/ddt312
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- Publication type:
- Article
COG8 deficiency causes new congenital disorder of glycosylation type IIh.
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- Human Molecular Genetics, 2007, v. 16, n. 7, p. 731, doi. 10.1093/hmg/ddm028
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- Publication type:
- Article
Dissecting the molecular organization of the translocon-associated protein complex.
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- Nature Communications, 2017, v. 8, n. 2, p. 14516, doi. 10.1038/ncomms14516
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- Publication type:
- Article
Insufficient ER-stress response causes selective mouse cerebellar granule cell degeneration resembling that seen in congenital disorders of glycosylation.
- Published in:
- Molecular Brain, 2013, v. 6, n. 1, p. 2, doi. 10.1186/1756-6606-6-52
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- Publication type:
- Article
A mutation map for human glycoside hydrolase genes.
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- Glycobiology, 2020, v. 30, n. 8, p. 500, doi. 10.1093/glycob/cwaa010
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- Publication type:
- Article
Glycosyltransferase genes that cause monogenic congenital disorders of glycosylation are distinct from glycosyltransferase genes associated with complex diseases.
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- Glycobiology, 2018, v. 28, n. 5, p. 284, doi. 10.1093/glycob/cwy015
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- Publication type:
- Article
Variant in human POFUT1 reduces enzymatic activity and likely causes a recessive microcephaly, global developmental delay with cardiac and vascular features.
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- Glycobiology, 2018, v. 28, n. 5, p. 276, doi. 10.1093/glycob/cwy014
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- Publication type:
- Article
A "Glyconutrient Sham" and the Jenner Glycobiology and Medicine Symposium.
- Published in:
- 2017
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- Publication type:
- Proceeding
Symbol Nomenclature for Graphical Representations of Glycans.
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- Glycobiology, 2015, v. 25, n. 12, p. 1323, doi. 10.1093/glycob/cwv091
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- Publication type:
- Article
A congenital disorder of deglycosylation: Biochemical characterization of N-glycanase 1 deficiency in patient fibroblasts.
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- Glycobiology, 2015, v. 25, n. 8, p. 836, doi. 10.1093/glycob/cwv024
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- Publication type:
- Article
A glycogene mutation map for discovery of diseases of glycosylation.
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- Glycobiology, 2015, v. 25, n. 2, p. 211, doi. 10.1093/glycob/cwu104
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- Publication type:
- Article
N-glycosylation deficiency reduces ICAM-1 induction and impairs inflammatory response.
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- Glycobiology, 2014, v. 24, n. 4, p. 392, doi. 10.1093/glycob/cwu006
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- Publication type:
- Article
A "Glyconutrient Sham".
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- Glycobiology, 2008, v. 18, n. 9, p. 652, doi. 10.1093/glycob/cwm098
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- Publication type:
- Article
Hydrophobic Man-1-P derivatives correct abnormal glycosylation in Type I congenital disorder of glycosylation fibroblasts.
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- Glycobiology, 2005, v. 15, n. 11, p. 1084, doi. 10.1093/glycob/cwj006
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- Publication type:
- Article
Molecular cloning, gene organization, and expression of mouse Mpi encoding phosphomannose isomerase.
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- Glycobiology, 2002, v. 12, n. 7, p. 435, doi. 10.1093/glycob/cwf060
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- Publication type:
- Article
Update and perspectives on congenitaldisorders of glycosylation.
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- Glycobiology, 2001, v. 11, n. 12, p. 129r, doi. 10.1093/glycob/11.12.129R
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- Publication type:
- Article
Mannose supplementation corrects GDP-mannose deficiency in cultured fibroblasts from some patients with Congenital Disorders of Glycosylation (CDG).
- Published in:
- Glycobiology, 2000, v. 10, n. 8, p. 829, doi. 10.1093/glycob/10.8.829
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- Publication type:
- Article
Characterization of mammalian UDP‐GalNAc:glucuronide α1-4‐N‐acetylgalactosaminyltransferase.
- Published in:
- Glycobiology, 1999, v. 9, n. 10, p. 1053, doi. 10.1093/glycob/9.10.1053
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- Publication type:
- Article
Corrigendum: ALG1-CDG Caused by Non-Functional Alternative Splicing Involving a Novel Pathogenic Complex Allele.
- Published in:
- 2021
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- Publication type:
- Correction Notice
ALG1-CDG Caused by Non-functional Alternative Splicing Involving a Novel Pathogenic Complex Allele.
- Published in:
- Frontiers in Genetics, 2021, v. 12, p. 1, doi. 10.3389/fgene.2021.744884
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- Publication type:
- Article
Proteomics reveals signal peptide features determining the client specificity in human TRAP-dependent ER protein import.
- Published in:
- Nature Communications, 2018, v. 9, n. 1, p. 1, doi. 10.1038/s41467-018-06188-z
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- Publication type:
- Article
A recurrent homozygous missense DPM3 variant leads to muscle and brain disease.
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- Clinical Genetics, 2022, v. 102, n. 6, p. 530, doi. 10.1111/cge.14208
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- Publication type:
- Article
Cell-free N-glycosylation in Dictyostelium discoideum: Analysis of wild-type and mutants defective in lipid-linked oligosaccharide biosynthesis.
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- Journal of Cellular Biochemistry, 1990, v. 43, n. 1, p. 27, doi. 10.1002/jcb.240430104
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- Publication type:
- Article
An immunological assessment of lysosomal enzymes and other macromolecules sulfated during vegetative growth of Dictyostelium discoideum.
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- Journal of Cellular Biochemistry, 1988, v. 38, n. 2, p. 113, doi. 10.1002/jcb.240380205
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- Publication type:
- Article
Congenital Disorder of Glycosylation Id Presenting with Hyperinsulinemic Hypoglycemia and Islet Cell Hyperplasia.
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- Journal of Clinical Endocrinology & Metabolism, 2005, v. 90, n. 7, p. 4371, doi. 10.1210/jc.2005-0250
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- Publication type:
- Article
Symbol nomenclature for glycan representation.
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- Proteomics, 2009, v. 9, n. 24, p. 5398, doi. 10.1002/pmic.200900708
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- Publication type:
- Article
Dissecting Functions of the Conserved Oligomeric Golgi Tethering Complex Using a Cell-Free Assay.
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- Traffic, 2014, v. 15, n. 1, p. 12, doi. 10.1111/tra.12128
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- Publication type:
- Article
Deficiency of the Cog8 Subunit in Normal and CDG-Derived Cells Impairs the Assembly of the COG and Golgi SNARE Complexes.
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- Traffic, 2013, v. 14, n. 10, p. 1065, doi. 10.1111/tra.12093
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- Publication type:
- Article
Spatial Regulation of Golgi Phosphatidylinositol-4-Phosphate is Required for Enzyme Localization and Glycosylation Fidelity.
- Published in:
- Traffic, 2010, v. 11, n. 9, p. 1180, doi. 10.1111/j.1600-0854.2010.01092.x
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- Publication type:
- Article
Congenital nephrotic syndrome in an infant with ALG1-congenital disorder of glycosylation.
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- Pediatrics International, 2016, v. 58, n. 8, p. 785, doi. 10.1111/ped.12988
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- Publication type:
- Article
The relative contribution of mannose salvage pathways to glycosylation in PMI-deficient mouse embryonic fibroblast cells.
- Published in:
- FEBS Journal, 2008, v. 275, n. 4, p. 788, doi. 10.1111/j.1742-4658.2008.06246.x
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- Publication type:
- Article
Evolutionary conservation of human ketodeoxynonulosonic acid production is independent of sialoglycan biosynthesis.
- Published in:
- 2021
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- Publication type:
- journal article
XMEN: welcome to the glycosphere.
- Published in:
- 2020
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- Publication type:
- journal article
XMEN: welcome to the glycosphere.
- Published in:
- Journal of Clinical Investigation, 2020, v. 130, n. 1, p. 80, doi. 10.1172/JCI134240
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- Publication type:
- Article
Heparan sulfate and syndecan-1 are essential in maintaining murine and human intestinal epithelial barrier function.
- Published in:
- 2008
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- Publication type:
- journal article
Deficient glycan extension and endoplasmic reticulum stresses in ALG3‐CDG.
- Published in:
- Journal of Inherited Metabolic Disease, 2024, v. 47, n. 4, p. 766, doi. 10.1002/jimd.12739
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- Publication type:
- Article
Beyond genetics: Deciphering the impact of missense variants in CAD deficiency.
- Published in:
- Journal of Inherited Metabolic Disease, 2023, v. 46, n. 6, p. 1170, doi. 10.1002/jimd.12667
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- Publication type:
- Article
Elevated oxysterol and N‐palmitoyl‐O‐phosphocholineserine levels in congenital disorders of glycosylation.
- Published in:
- Journal of Inherited Metabolic Disease, 2023, v. 46, n. 2, p. 326, doi. 10.1002/jimd.12595
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- Publication type:
- Article
DDOST‐CDG: Clinical and molecular characterization of a third patient with a milder and a predominantly movement disorder phenotype.
- Published in:
- Journal of Inherited Metabolic Disease, 2023, v. 46, n. 1, p. 92, doi. 10.1002/jimd.12565
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- Publication type:
- Article
ALG8‐CDG: Molecular and phenotypic expansion suggests clinical management guidelines.
- Published in:
- Journal of Inherited Metabolic Disease, 2022, v. 45, n. 5, p. 969, doi. 10.1002/jimd.12527
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- Publication type:
- Article