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Quoted phrase not found in phrase index: "Abnormal isoelectric focusing of serum transferrin"
Page 1
Carbohydrate-deficient transferrin in serum: a new marker of potentially harmful alcohol consumption reviewed.
Stibler H. Stibler H. Clin Chem. 1991 Dec;37(12):2029-37. Clin Chem. 1991. PMID: 1764777 Review.
Such isoforms have so far been detected by methods based on charge, i.e., isoelectric focusing, chromatofocusing, and anion-exchange chromatography of various designs combined with immunological detection techniques. ...The mechanism behind the transferrin …
Such isoforms have so far been detected by methods based on charge, i.e., isoelectric focusing, chromatofocusing, and anion-ex …
Separation of different forms of transferrin by isoelectric focusing to detect effects on the liver caused by xenobiotics.
Petrén S, Vesterberg O. Petrén S, et al. Electrophoresis. 1989 Aug-Sep;10(8-9):600-4. doi: 10.1002/elps.1150100812. Electrophoresis. 1989. PMID: 2806210
Several genetic variants and also isoforms of transferrin differing in carbohydrate structure can be separated by polyacrylamide or agarose gel isoelectric focusing. Numerous blood plasma or serum samples can be analyzed in parallel in each gel. Studie …
Several genetic variants and also isoforms of transferrin differing in carbohydrate structure can be separated by polyacrylamide or a …
Genetic and metabolic analysis of the first adult with congenital disorder of glycosylation type Ib: long-term outcome and effects of mannose supplementation.
Westphal V, Kjaergaard S, Davis JA, Peterson SM, Skovby F, Freeze HH. Westphal V, et al. Mol Genet Metab. 2001 May;73(1):77-85. doi: 10.1006/mgme.2001.3161. Mol Genet Metab. 2001. PMID: 11350186
The combination of symptoms was suggestive of the recently characterized congenital disorder of glycosylation type Ib (CDG-Ib), which is caused by a deficiency of the enzyme phosphomannose isomerase (PMI). An abnormal serum transferrin isoelectric …
The combination of symptoms was suggestive of the recently characterized congenital disorder of glycosylation type Ib (CDG-Ib), which …
Oral mannose therapy persistently corrects the severe clinical symptoms and biochemical abnormalities of phosphomannose isomerase deficiency.
Harms HK, Zimmer KP, Kurnik K, Bertele-Harms RM, Weidinger S, Reiter K. Harms HK, et al. Acta Paediatr. 2002;91(10):1065-72. doi: 10.1080/080352502760311566. Acta Paediatr. 2002. PMID: 12434892
Exogenous oral mannose supply bypasses the enzymatic block and leads to the disappearance of all symptoms in the patient. The striking ultrastructural abnormalities of the rough endoplasmatic reticulum of the duodenal epithelial cells completely normalize and the hypoglyco …
Exogenous oral mannose supply bypasses the enzymatic block and leads to the disappearance of all symptoms in the patient. The striking ultra …