uridine diphosphate galactose has been researched along with transferrin in 3 studies
Timeframe | Studies, this research(%) | All Research% |
---|---|---|
pre-1990 | 0 (0.00) | 18.7374 |
1990's | 0 (0.00) | 18.2507 |
2000's | 2 (66.67) | 29.6817 |
2010's | 1 (33.33) | 24.3611 |
2020's | 0 (0.00) | 2.80 |
Authors | Studies |
---|---|
Berger, EG; Hansske, B; Hasilik, M; Heidemann, PH; Hoffmann, GF; Höning, S; Körner, C; Lübke, T; Peters, V; Thiel, C; von Figura, K | 1 |
de Jong, JG; Hermus, AR; Lutterman, JA; Olthaar, AJ; Pouwels, MJ; Span, PN; Sweep, CG; Tack, CJ; van Engelen, BG | 1 |
Bamshad, MJ; Buckingham, KJ; Chong, JX; Eroshkin, A; Freeze, HH; Gilbert, RD; He, M; Kircher, M; Kozenko, M; Li, C; Losfeld, ME; Ng, BG; Nickerson, DA; Patterson, MC; Raymond, K; Shendure, J; Smith, JD; Szybowska, M; Turner, EH | 1 |
3 other study(ies) available for uridine diphosphate galactose and transferrin
Article | Year |
---|---|
Deficiency of UDP-galactose:N-acetylglucosamine beta-1,4-galactosyltransferase I causes the congenital disorder of glycosylation type IId.
Topics: beta-N-Acetylglucosaminylglycopeptide beta-1,4-Galactosyltransferase; Cells, Cultured; Child, Preschool; Chromatography, Affinity; Congenital Disorders of Glycosylation; Fibroblasts; Galactose; Glycoproteins; Golgi Apparatus; Humans; Immunohistochemistry; Infant; Leukocytes; Male; Protein Transport; Skin; Transferrin; Uridine Diphosphate Galactose | 2002 |
Muscle uridine diphosphate-hexosamines do not decrease despite correction of hyperglycemia-induced insulin resistance in type 2 diabetes.
Topics: Adult; Biopsy; Diabetes Mellitus; Diabetes Mellitus, Type 2; Female; Glucose Clamp Technique; Glycosaminoglycans; Humans; Hyperglycemia; Hyperinsulinism; Insulin; Insulin Resistance; Isoelectric Focusing; Male; Middle Aged; Muscle, Skeletal; Obesity; Transferrin; Uridine Diphosphate Galactose; Uridine Diphosphate Glucose; Uridine Diphosphate N-Acetylgalactosamine; Uridine Diphosphate N-Acetylglucosamine; Uridine Diphosphate Sugars | 2002 |
Mosaicism of the UDP-galactose transporter SLC35A2 causes a congenital disorder of glycosylation.
Topics: Biological Transport; Case-Control Studies; Child; Child, Preschool; Congenital Disorders of Glycosylation; Exome; Female; Glycosylation; Humans; Male; Monosaccharide Transport Proteins; Mosaicism; Mutation; Spectrometry, Mass, Electrospray Ionization; Transferrin; Uridine Diphosphate Galactose | 2013 |