methylglucoside has been researched along with Malabsorption Syndromes in 2 studies
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 0 (0.00) | 18.7374 |
| 1990's | 2 (100.00) | 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 |
|---|---|
| Kerner, C; Lostao, MP; Martín, MG; Turk, E; Wright, EM | 1 |
| Kreman, M; Lam, J; Lostao, MP; Martín, MG; Turk, E; Wright, EM | 1 |
2 other study(ies) available for methylglucoside and Malabsorption Syndromes
| Article | Year |
|---|---|
Defects in Na+/glucose cotransporter (SGLT1) trafficking and function cause glucose-galactose malabsorption.
Topics: Amino Acid Sequence; Animals; Base Sequence; Biological Transport; Cell Membrane; Galactose; Genetic Carrier Screening; Glucose; Homozygote; Humans; Malabsorption Syndromes; Membrane Glycoproteins; Membrane Potentials; Methylglucosides; Molecular Sequence Data; Monosaccharide Transport Proteins; Mutation; Oocytes; Polymorphism, Single-Stranded Conformational; Protein Structure, Secondary; Sodium-Glucose Transporter 1; Xenopus laevis | 1996 |
Compound missense mutations in the sodium/D-glucose cotransporter result in trafficking defects.
Topics: Amino Acid Sequence; Animals; Biological Transport; Cell Membrane; Electrophysiology; Endoplasmic Reticulum; Female; Humans; Infant, Newborn; Malabsorption Syndromes; Membrane Glycoproteins; Methylglucosides; Molecular Sequence Data; Monosaccharide Transport Proteins; Mutation; Oocytes; Pedigree; Sodium-Glucose Transporter 1; Xenopus laevis | 1997 |