aspartic acid has been researched along with Arthropathies in 5 studies
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 2 (40.00) | 18.7374 |
| 1990's | 1 (20.00) | 18.2507 |
| 2000's | 1 (20.00) | 29.6817 |
| 2010's | 1 (20.00) | 24.3611 |
| 2020's | 0 (0.00) | 2.80 |
| Authors | Studies |
|---|---|
| Catterall, JB; Dillon, JP; Gallagher, JA; Hsueh, MF; Huebner, JL; Kraus, VB; Ranganath, LR; Taylor, AM | 1 |
| Ala-Kokko, L; Haataja, L; Kääriäinen, H; Kivirikko, KI; Körkkö, J; Prockop, DJ; Ritvaniemi, P | 1 |
| Lawand, N; Lisse, J; McNearney, T; Speegle, D; Westlund, KN | 1 |
| Isenberg, JN; Sharp, HL | 1 |
| Lee, TY; Onisawa, J | 1 |
5 other study(ies) available for aspartic acid and Arthropathies
| Article | Year |
|---|---|
Cartilage biomarkers in the osteoarthropathy of alkaptonuria reveal low turnover and accelerated ageing.
Topics: Adult; Aged; Aged, 80 and over; Aging; Alkaptonuria; Aspartic Acid; Biomarkers; Cartilage Oligomeric Matrix Protein; Cartilage, Articular; Case-Control Studies; Female; Glycosaminoglycans; Hip Joint; Humans; Joint Diseases; Knee Joint; Male; Middle Aged; Ochronosis; Osteoarthritis, Hip; Osteoarthritis, Knee; Young Adult | 2017 |
Mutation in type II procollagen (COL2A1) that substitutes aspartate for glycine alpha 1-67 and that causes cataracts and retinal detachment: evidence for molecular heterogeneity in the Wagner syndrome and the Stickler syndrome (arthro-ophthalmopathy)
Topics: Adolescent; Adult; Amino Acid Sequence; Aspartic Acid; Base Sequence; Cataract; Child; Child, Preschool; DNA; DNA Mutational Analysis; Female; Glycine; Humans; Joint Diseases; Male; Molecular Sequence Data; Mutation; Polymerase Chain Reaction; Procollagen; Retinal Detachment; Syndrome | 1993 |
Excitatory amino acid profiles of synovial fluid from patients with arthritis.
Topics: Adolescent; Adult; Aged; Arthritis; Arthritis, Reactive; Aspartic Acid; Child; Child, Preschool; Chromatography, High Pressure Liquid; Cohort Studies; Excitatory Amino Acids; Glutamic Acid; Humans; Joint Diseases; Lupus Erythematosus, Systemic; Middle Aged; Reference Values; Synovial Fluid; Synovitis | 2000 |
Aspartylglucosaminuria: psychomotor retardation masquerading as a mucopolysaccharidosis.
Topics: Amidohydrolases; Aminoglycosides; Aspartic Acid; Child, Preschool; Chromatography, Thin Layer; Cleidocranial Dysplasia; Diagnosis, Differential; Facial Expression; Female; Glucosamine; Hepatomegaly; Humans; Joint Diseases; Leukocytes; Lymphocytes; Mass Screening; Metabolism, Inborn Errors; Mucopolysaccharidoses; Psychomotor Disorders; Splenomegaly; Vacuoles | 1975 |
Biochemical studies of urinary acid mucopolysaccharide--peptide complexes in Hurler's syndrome.
Topics: Amino Acids; Aspartic Acid; Bone and Bones; Carbohydrate Metabolism, Inborn Errors; Child; Child, Preschool; Chondroitin; Chromatography, Ion Exchange; Female; Galactosamine; Glucosamine; Glutamates; Glycine; Glycosaminoglycans; Humans; Hypertrichosis; Joint Diseases; Male; Mucopolysaccharidosis I; Retinitis Pigmentosa; Serine; Uronic Acids | 1970 |