glucagon has been researched along with Ataxias, Hereditary in 1 studies
Timeframe | Studies, this research(%) | All Research% |
---|---|---|
pre-1990 | 0 (0.00) | 18.7374 |
1990's | 0 (0.00) | 18.2507 |
2000's | 1 (100.00) | 29.6817 |
2010's | 0 (0.00) | 24.3611 |
2020's | 0 (0.00) | 2.80 |
Authors | Studies |
---|---|
Alb, JG; Albin, RL; Bankaitis, VA; Cortese, JD; Hamilton, BA; Nagy, TR; Phillips, SE | 1 |
1 other study(ies) available for glucagon and Ataxias, Hereditary
Article | Year |
---|---|
Mice lacking phosphatidylinositol transfer protein-alpha exhibit spinocerebellar degeneration, intestinal and hepatic steatosis, and hypoglycemia.
Topics: Adenosine Triphosphate; Animals; Brain; Carrier Proteins; Cerebellum; Dose-Response Relationship, Drug; Endoplasmic Reticulum; Fatty Acids; Genetic Vectors; Genotype; Glucagon; Glycogen; Hypoglycemia; In Situ Nick-End Labeling; Intestinal Diseases; Lipid Metabolism; Liver; Liver Diseases; Membrane Proteins; Mice; Mice, Inbred C57BL; Mice, Transgenic; Microscopy, Electron; Models, Genetic; Phenotype; Phospholipid Transfer Proteins; Proglucagon; Protein Precursors; Saccharomyces cerevisiae Proteins; Spinocerebellar Degenerations; Time Factors | 2003 |