n-acetylneuraminic acid has been researched along with Muscular Dystrophy in 7 studies
Timeframe | Studies, this research(%) | All Research% |
---|---|---|
pre-1990 | 2 (28.57) | 18.7374 |
1990's | 1 (14.29) | 18.2507 |
2000's | 3 (42.86) | 29.6817 |
2010's | 1 (14.29) | 24.3611 |
2020's | 0 (0.00) | 2.80 |
Authors | Studies |
---|---|
Iwata, Y; Suzuki, O; Wakabayashi, S | 1 |
Freeze, HH; Martin, PT | 1 |
Fujita, M; Goto, Y; Hayashi, YK; Imazawa, M; Kawahara, G; Keira, Y; Murayama, K; Nishino, I; Noguchi, S; Nonaka, I; Ogawa, M; Oya, Y | 1 |
Arai, K; Kanda, T; Matsumura, K; Mizusawa, H; Nakai, S; Saito, F; Shimizu, T; Tomimitsu, H | 1 |
Stibler, H; Sydow, O | 1 |
Fagiolari, G; Gallanti, A; Moggio, M; Prelle, A; Scarlato, G; Sciacco, M | 1 |
Sydow, O | 1 |
1 review(s) available for n-acetylneuraminic acid and Muscular Dystrophy
Article | Year |
---|---|
Glycobiology of neuromuscular disorders.
Topics: Animals; Cytoskeletal Proteins; Glycoproteins; Humans; Inclusion Bodies; Muscular Dystrophies; N-Acetylneuraminic Acid; Neuromuscular Diseases | 2003 |
6 other study(ies) available for n-acetylneuraminic acid and Muscular Dystrophy
Article | Year |
---|---|
Decreased surface sialic acid content is a sensitive indicator of muscle damage.
Topics: Animals; Biomarkers; Biopsy; Cricetinae; Cytosol; Fluorescent Dyes; Humans; Laminin; Lectins; Mice; Mice, Inbred mdx; Muscular Dystrophies; Muscular Dystrophy, Animal; N-Acetylneuraminic Acid; Peanut Agglutinin; Sarcolemma | 2013 |
Reduction of UDP-N-acetylglucosamine 2-epimerase/N-acetylmannosamine kinase activity and sialylation in distal myopathy with rimmed vacuoles.
Topics: Animals; Biopolymers; Case-Control Studies; COS Cells; Humans; Multienzyme Complexes; Muscular Dystrophies; Mutation; N-Acetylneuraminic Acid; Vacuoles | 2004 |
A Japanese patient with distal myopathy with rimmed vacuoles: missense mutations in the epimerase domain of the UDP-N-acetylglucosamine 2-epimerase/N-acetylmannosamine kinase (GNE) gene accompanied by hyposialylation of skeletal muscle glycoproteins.
Topics: Adult; Carbohydrate Epimerases; Carrier Proteins; Cytoskeletal Proteins; Dystroglycans; Glycoproteins; Humans; Immunohistochemistry; Japan; Male; Membrane Glycoproteins; Muscle Fibers, Skeletal; Muscle Proteins; Muscle, Skeletal; Muscular Dystrophies; Mutation, Missense; N-Acetylneuraminic Acid; Phosphotransferases (Alcohol Group Acceptor); Protein Structure, Tertiary; Vacuoles | 2004 |
Carbohydrate composition of erythrocyte membranes and glycosidase activities in serum in patients with myotonic dystrophy, limb-girdle dystrophy and congenital myotonia.
Topics: Acetylglucosaminidase; Adolescent; Adult; beta-N-Acetyl-Galactosaminidase; Carbohydrates; Child; Erythrocyte Membrane; Female; Galactosemias; Glycoside Hydrolases; Hexosamines; Hexosaminidases; Humans; Kinetics; Male; Middle Aged; Muscular Dystrophies; Myotonia Congenita; N-Acetylneuraminic Acid; Neuraminidase; Sialic Acids | 1984 |
Lack of anionic phospholipid calcium binding sites in Duchenne muscular dystrophy.
Topics: Binding Sites; Calcium; Child; Child, Preschool; Humans; Immunohistochemistry; Male; Muscles; Muscular Dystrophies; N-Acetylneuraminic Acid; Phospholipids; Sialic Acids | 1992 |
Sialic acid content in serum IgG from patients with myotonic dystrophy compared with healthy controls.
Topics: Adult; Female; Humans; Immunoglobulin gamma-Chains; Immunoglobulin Heavy Chains; Male; Middle Aged; Muscular Dystrophies; N-Acetylneuraminic Acid; Sialic Acids | 1989 |