trehalose has been researched along with Astrocytosis in 4 studies
Timeframe | Studies, this research(%) | All Research% |
---|---|---|
pre-1990 | 0 (0.00) | 18.7374 |
1990's | 0 (0.00) | 18.2507 |
2000's | 0 (0.00) | 29.6817 |
2010's | 3 (75.00) | 24.3611 |
2020's | 1 (25.00) | 2.80 |
Authors | Studies |
---|---|
Ganesh, S; Sinha, P; Verma, B | 1 |
Ballester, MI; Berthier, A; García-Cabrero, AM; Heredia, M; Payá, M; Sánchez, MP; Sanz, P; Serratosa, JM | 1 |
Chen, ZZ; Hsieh-Li, HM; Hsu, HC; Huang, HJ; Lee, GC; Lee-Chen, GJ; Lin, CW; Ma, CK; Wang, CM; Wu, TL | 1 |
Casarejos, MJ; de Yébenes, JG; Gómez, A; Mena, MÁ; Muñoz, MP; Perucho, J | 1 |
4 other study(ies) available for trehalose and Astrocytosis
Article | Year |
---|---|
Trehalose Ameliorates Seizure Susceptibility in Lafora Disease Mouse Models by Suppressing Neuroinflammation and Endoplasmic Reticulum Stress.
Topics: Animals; Autophagy; Brain; Calcium-Binding Proteins; Disease Models, Animal; Disease Susceptibility; Endoplasmic Reticulum Stress; Gene Expression Regulation; Glial Fibrillary Acidic Protein; Gliosis; Glucans; Inflammation; Lafora Disease; Membrane Proteins; Mice, Knockout; Microfilament Proteins; Nerve Tissue Proteins; Pentylenetetrazole; Protein Tyrosine Phosphatases, Non-Receptor; Seizures; Trehalose; Ubiquitin-Protein Ligases | 2021 |
Pharmacological Interventions to Ameliorate Neuropathological Symptoms in a Mouse Model of Lafora Disease.
Topics: Animals; Brain; Disease Models, Animal; Fluorescent Antibody Technique; Gliosis; Glucans; Hippocampus; Inclusion Bodies; Lafora Disease; Metformin; Mice, Inbred C57BL; Mice, Knockout; Nerve Degeneration; Neuropsychological Tests; Phenylbutyrates; Protein Aggregates; Trehalose; Ubiquitin-Protein Ligases; Ubiquitinated Proteins | 2016 |
Trehalose attenuates the gait ataxia and gliosis of spinocerebellar ataxia type 17 mice.
Topics: Animals; Blood Glucose; Body Weight; Gait Ataxia; Gliosis; Male; Mice; Mice, Transgenic; Purkinje Cells; Spinocerebellar Ataxias; Trehalose | 2015 |
Trehalose rescues glial cell dysfunction in striatal cultures from HD R6/1 mice at early postnatal development.
Topics: alpha-Synuclein; Animals; Brain-Derived Neurotrophic Factor; Cells, Cultured; Corpus Striatum; Cytoskeleton; Female; Glial Cell Line-Derived Neurotrophic Factor; Gliosis; Humans; Huntingtin Protein; Huntington Disease; Male; Mice; Mice, Inbred C57BL; Neuroglia; Neuroprotective Agents; Protein Transport; Trehalose | 2016 |