n-acetylneuraminic acid has been researched along with Autosomal Chromosome Disorders in 2 studies
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 1 (50.00) | 18.7374 |
| 1990's | 0 (0.00) | 18.2507 |
| 2000's | 1 (50.00) | 29.6817 |
| 2010's | 0 (0.00) | 24.3611 |
| 2020's | 0 (0.00) | 2.80 |
| Authors | Studies |
|---|---|
| Broccolini, A; De Cristofaro, R; Gidaro, T; Gliubizzi, C; Mirabella, M; Morosetti, R; Ricci, E; Tonali, PA | 1 |
| Dube, S; Sethi, BB; Sharma, M | 1 |
1 review(s) available for n-acetylneuraminic acid and Autosomal Chromosome Disorders
| Article | Year |
|---|---|
Markers in psychoses: studies from India.
Topics: Adrenal Cortex Hormones; Affective Disorders, Psychotic; Blood Platelets; Body Constitution; Chromosome Aberrations; Chromosome Disorders; Creatine Kinase; Dermatoglyphics; Genetic Markers; Genotype; Humans; Hydroxyindoleacetic Acid; India; Kinetics; Monoamine Oxidase; N-Acetylneuraminic Acid; Phenotype; Psychotic Disorders; Schizophrenia; Sialic Acids | 1984 |
1 other study(ies) available for n-acetylneuraminic acid and Autosomal Chromosome Disorders
| Article | Year |
|---|---|
Hyposialylation of neprilysin possibly affects its expression and enzymatic activity in hereditary inclusion-body myopathy muscle.
Topics: Adult; Amyloid beta-Peptides; Cells, Cultured; Chromosome Disorders; Down-Regulation; Female; Genes, Recessive; Glycosylation; Humans; Male; Muscle Fibers, Skeletal; Muscle, Skeletal; Myositis, Inclusion Body; N-Acetylneuraminic Acid; Neprilysin; Neuraminidase | 2008 |