fucose has been researched along with Carbohydrate-Deficient Glycoprotein Syndrome in 7 studies
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 0 (0.00) | 18.7374 |
| 1990's | 1 (14.29) | 18.2507 |
| 2000's | 0 (0.00) | 29.6817 |
| 2010's | 3 (42.86) | 24.3611 |
| 2020's | 3 (42.86) | 2.80 |
| Authors | Studies |
|---|---|
| Abraham, R; Barnes, S; Boyer, S; Jacob, E; Kumanovics, A; League, S; Menon, P; Morava, E; Quade, M; Raymond, K; Tahata, S | 1 |
| Brimble, E; Dastsooz, H; Faghihi, MA; Fard, MAF; Freeze, HH; Habibzadeh, P; Halliday, BJ; Jahan, SB; Ng, BG; Raymond, K; Robertson, SP; Ruzhnikov, MRZ; Silawi, M; Tabatabaei, Z; Taghipour-Sheshdeh, A | 1 |
| Falkenstein, K; Feichtinger, RG; Frenz, S; Herget, T; Huidekoper, H; Hüllen, A; Khoshnevisan, R; Kotlarz, D; Lefeber, DJ; Mayr, JA; Momen, T; Naumann-Bartsch, N; Rennings, A; Riedhammer, KM; Santer, R; Schaefers, J; Spenger, J; Thiel, C; Weigel, C; Wortmann, SB | 1 |
| Andreotti, G; Brasil, S; Dos Reis Ferreira, V; Francisco, R; Jaeken, J; Marques-da-Silva, D; Morava, E; Pascoal, C; Videira, PA | 1 |
| Haltiwanger, RS; Takeuchi, H | 1 |
| Lühn, K; Wild, MK | 1 |
| Ferens-Sieczkowska, M; Katnik-Prastowska, I; Midro, A; Mierzejewska-Iwanowska, B; Zwierz, K | 1 |
4 review(s) available for fucose and Carbohydrate-Deficient Glycoprotein Syndrome
| Article | Year |
|---|---|
Defining the mild variant of leukocyte adhesion deficiency type II (SLC35C1-congenital disorder of glycosylation) and response to l-fucose therapy: Insights from two new families and review of the literature.
Topics: Congenital Disorders of Glycosylation; Fucose; Glycosylation; Humans; Leukocyte-Adhesion Deficiency Syndrome; Leukocytes; Monosaccharide Transport Proteins | 2022 |
CDG Therapies: From Bench to Bedside.
Topics: Animals; Biomarkers; Clinical Trials as Topic; Congenital Disorders of Glycosylation; Dietary Supplements; Disease Models, Animal; Fucose; Galactose; Genetic Therapy; Glycosylation; Humans; Mannose; Organ Transplantation | 2018 |
Significance of glycosylation in Notch signaling.
Topics: Animals; Congenital Disorders of Glycosylation; Fucose; Glucose; Glycosylation; Glycosyltransferases; Humans; Models, Molecular; Polysaccharides; Protein Interaction Domains and Motifs; Protein Processing, Post-Translational; Receptors, Notch; Repetitive Sequences, Amino Acid; Signal Transduction | 2014 |
Human deficiencies of fucosylation and sialylation affecting selectin ligands.
Topics: Aged; Animals; Cell Adhesion; Cell Adhesion Molecules; Congenital Disorders of Glycosylation; Fucose; Fucosyltransferases; Glycosylation; Humans; Infant; Leukocytes; Ligands; Male; Mice; Selectins | 2012 |
3 other study(ies) available for fucose and Carbohydrate-Deficient Glycoprotein Syndrome
| Article | Year |
|---|---|
Expanding the molecular and clinical phenotypes of FUT8-CDG.
Topics: Congenital Disorders of Glycosylation; Exome Sequencing; Female; Fucose; Fucosyltransferases; Humans; Male; Mass Spectrometry; Phenotype; Polysaccharides | 2020 |
Congenital disorders of glycosylation with defective fucosylation.
Topics: Adolescent; Adult; Child; Child, Preschool; Congenital Disorders of Glycosylation; Female; Fibroblasts; Fucose; Glycoproteins; Glycosylation; Humans; Infant; Male; Monosaccharide Transport Proteins; Treatment Outcome; Young Adult | 2021 |
Haptoglobin glycoforms in a case of carbohydrate-deficient glycoprotein syndrome.
Topics: Adolescent; Amidohydrolases; Blotting, Western; Child; Congenital Disorders of Glycosylation; Electrophoresis, Polyacrylamide Gel; Female; Fucose; Glycosylation; Haptoglobins; Humans; Infant; Lectins; Molecular Weight; N-Acetylneuraminic Acid; Neuraminidase; Peptide-N4-(N-acetyl-beta-glucosaminyl) Asparagine Amidase; Poland; Polysaccharides; Protein Binding; Protein Isoforms | 1999 |