PDF) Rapid Determination of Transferrin Isoforms by Immunoaffinity Liquid Chromatography and Electrospray Mass Spectrometry | Stephen Naylor - Academia.edu
Value of Determining Carbohydrate-Deficient Transferrin Isoforms in the Diagnosis of Alcoholic Liver Disease - Mayo Clinic Proceedings
Detection of Hypo‐N‐Glycosylation Using Mass Spectrometry of Transferrin - O'Brien - 2007 - Current Protocols in Human Genetics - Wiley Online Library
Carbohydrate Deficient Transferrin
Reference intervals of seven steroids in Korean subjects in comparison... | Download Table
The impact of mass spectrometry in the diagnosis of congenital disorders of glycosylation - Sturiale - 2011 - Journal of Inherited Metabolic Disease - Wiley Online Library
Oral D-galactose supplementation in PGM1-CDG - Genetics in Medicine
Value of Determining Carbohydrate-Deficient Transferrin Isoforms in the Diagnosis of Alcoholic Liver Disease - Mayo Clinic Proceedings
Abstracts - 2021 - Journal of Inherited Metabolic Disease - Wiley Online Library
Frontiers | Pediatric Liver Disease Patients and Secondary Glycosylation Abnormalities
The Functional Versatility of Transferrin Receptor 2 and Its Therapeutic Value. - Abstract - Europe PMC
TMT-Based Multiplexed Quantitation of N-Glycopeptides Reveals Glycoproteome Remodeling Induced by Oncogenic Mutations | ACS Omega
Transferrin isoelectric focusing profiles before and after... | Download Scientific Diagram
Ferritin levels in the cerebrospinal fluid predict Alzheimer's disease outcomes and are regulated by APOE | Nature Communications
Congenital disorder of glycosylation caused by starting site-specific variant in syntaxin-5 | Nature Communications
IJMS | Free Full-Text | Therapeutic Advances in Diabetes, Autoimmune, and Neurological Diseases | HTML
Value of Determining Carbohydrate-Deficient Transferrin Isoforms in the Diagnosis of Alcoholic Liver Disease - Mayo Clinic Proceedings
PDF) Multicentre evaluation of a new assay for determination of carbohydrate-deficient transferrin
Intact transferrin and total plasma glycoprofiling for diagnosis and therapy monitoring in phosphoglucomutase-I deficiency. - Abstract - Europe PMC
Oral D-galactose supplementation in PGM1-CDG. - Abstract - Europe PMC
IJMS | Free Full-Text | Transferrin Saturation/Hepcidin Ratio Discriminates TMPRSS6-Related Iron Refractory Iron Deficiency Anemia from Patients with Multi-Causal Iron Deficiency Anemia | HTML
Statistical analysis of serum/plasma %CDT reference values in the... | Download Scientific Diagram
Statistical analysis of serum/plasma %CDT reference values in the... | Download Scientific Diagram
Transgelin: a new gene involved in LDL endocytosis identified by a genome-wide CRISPR-Cas9 screen - Journal of Lipid Research
Oral D-galactose supplementation in PGM1-CDG - Genetics in Medicine
Serum 1-AT isoform profiles from CDG patients and controls. Lane 1:... | Download Scientific Diagram
