n-acetylneuraminyl-(2-6)-galactose has been researched along with galactose in 1 studies
*Galactose: An aldohexose that occurs naturally in the D-form in lactose, cerebrosides, gangliosides, and mucoproteins. Deficiency of galactosyl-1-phosphate uridyltransferase (GALACTOSE-1-PHOSPHATE URIDYL-TRANSFERASE DEFICIENCY DISEASE) causes an error in galactose metabolism called GALACTOSEMIA, resulting in elevations of galactose in the blood. [MeSH]
*Galactose: An aldohexose that occurs naturally in the D-form in lactose, cerebrosides, gangliosides, and mucoproteins. Deficiency of galactosyl-1-phosphate uridyltransferase (GALACTOSE-1-PHOSPHATE URIDYL-TRANSFERASE DEFICIENCY DISEASE) causes an error in galactose metabolism called GALACTOSEMIA, resulting in elevations of galactose in the blood. [MeSH]
| Studies (n-acetylneuraminyl-(2-6)-galactose) | Trials (n-acetylneuraminyl-(2-6)-galactose) | Recent Studies (post-2010) (n-acetylneuraminyl-(2-6)-galactose) | Studies (galactose) | Trials (galactose) | Recent Studies (post-2010) (galactose) |
|---|---|---|---|---|---|
| 7 | 0 | 3 | 18,988 | 193 | 4,605 |
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 1 (100.00) | 18.7374 |
| 1990's | 0 (0.00) | 18.2507 |
| 2000's | 0 (0.00) | 29.6817 |
| 2010's | 0 (0.00) | 24.3611 |
| 2020's | 0 (0.00) | 2.80 |
| Authors | Studies |
|---|---|
| Hasegawa, A; Kartha, KP; Kiso, M; Murase, T | 1 |
1 other study(ies) available for n-acetylneuraminyl-(2-6)-galactose and galactose
| Article | Year |
|---|---|
Synthesis of the alpha-Neu5Ac-(2----6)-Gal structure. Facile 6-O-sialylation following stannylene activation of an unprotected D-galactopyranoside.
Topics: Carbohydrate Sequence; Disaccharides; Galactose; Molecular Sequence Data; Organotin Compounds; Trimethylsilyl Compounds | 1989 |