alanine has been researched along with Hyperoxaluria in 8 studies
Alanine: A non-essential amino acid that occurs in high levels in its free state in plasma. It is produced from pyruvate by transamination. It is involved in sugar and acid metabolism, increases IMMUNITY, and provides energy for muscle tissue, BRAIN, and the CENTRAL NERVOUS SYSTEM.
alanine : An alpha-amino acid that consists of propionic acid bearing an amino substituent at position 2.
Hyperoxaluria: Excretion of an excessive amount of OXALATES in the urine.
| Excerpt | Relevance | Reference |
|---|---|---|
| "We have studied the characteristics of human liver alanine-glyoxylate aminotransferase, which is deficient in hyperoxaluria type I, an inherited disorder of glyoxylate metabolism." | 7.68 | Human liver L-alanine-glyoxylate aminotransferase: characteristics and activity in controls and hyperoxaluria type I patients using a simple spectrophotometric method. ( Jurriaans, S; Ofman, R; Ruiter, J; Schutgens, RB; Tager, JM; van Roermund, CW; Wanders, RJ, 1990) |
| "A case of primary hyperoxaluria type 1 with complete deficiency of alanine:glyoxalate aminotransferase that first manifested at the age of 59 with irreversible acute on chronic renal failure is reported." | 3.68 | Late presentation and development of nephrocalcinosis in primary hyperoxaluria. ( Doust, B; Irish, AB, 1992) |
| "We examined the effect of vitamin B6 deficiency on glyoxylate metabolism and hepatic alanine: glyoxylate aminotransferase (AGT) activity in rats with normal or high glyoxylate intake." | 1.33 | Effect of vitamin B6 deficiency on glyoxylate metabolism in rats with or without glyoxylate overload. ( Hokama, S; Morozumi, M; Nishijima, S; Ogawa, Y; Oshiro, Y; Sugaya, K; Uchida, A, 2006) |
| "We found that AGT activity in two hyperoxaluria type 1 patients was reduced as compared with controls." | 1.28 | High-performance liquid chromatographic microassay for L-alanine:glyoxylate aminotransferase activity in human liver. ( Cosseddu, D; Linari, F; Marangella, M; Pellegrino, S; Petrarulo, M, 1992) |
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 2 (25.00) | 18.7374 |
| 1990's | 4 (50.00) | 18.2507 |
| 2000's | 1 (12.50) | 29.6817 |
| 2010's | 1 (12.50) | 24.3611 |
| 2020's | 0 (0.00) | 2.80 |
| Authors | Studies |
|---|---|
| Assimos, DG | 1 |
| GABURRO, D | 1 |
| VOLPATO, S | 1 |
| SCARPA, P | 1 |
| Nishijima, S | 1 |
| Sugaya, K | 1 |
| Hokama, S | 1 |
| Oshiro, Y | 1 |
| Uchida, A | 1 |
| Morozumi, M | 1 |
| Ogawa, Y | 1 |
| Pirulli, D | 1 |
| Puzzer, D | 1 |
| Ferri, L | 1 |
| Crovella, S | 1 |
| Amoroso, A | 1 |
| Ferrettini, C | 1 |
| Marangella, M | 2 |
| Mazzola, G | 1 |
| Florian, F | 1 |
| Petrarulo, M | 1 |
| Pellegrino, S | 1 |
| Cosseddu, D | 1 |
| Linari, F | 1 |
| Irish, AB | 1 |
| Doust, B | 1 |
| Wanders, RJ | 1 |
| Ruiter, J | 1 |
| van Roermund, CW | 1 |
| Schutgens, RB | 1 |
| Ofman, R | 1 |
| Jurriaans, S | 1 |
| Tager, JM | 1 |
| Danpure, CJ | 1 |
| Jennings, PR | 1 |
| Watts, RW | 1 |
8 other studies available for alanine and Hyperoxaluria
| Article | Year |
|---|---|
Re: Pyridoxamine and Pyridoxal are More Effective than Pyridoxine in Rescuing Folding-Defective Variants of Human Alanine:Glyoxylate Aminotransferase Causing Primary Hyperoxaluria Type I.
Topics: Alanine; Humans; Hyperoxaluria; Hyperoxaluria, Primary; Pyridoxal; Pyridoxamine; Pyridoxine | 2016 |
[CONGENITAL DYSMETABOLIC CEREBROPATHY WITH HYPERGLYCEMIA, HYPERALANINURIA AND HYPEROXALURIA].
Topics: Alanine; Brain Diseases; Child; Humans; Hyperglycemia; Hyperoxaluria; Infant; Intellectual Disabilit | 1963 |
Effect of vitamin B6 deficiency on glyoxylate metabolism in rats with or without glyoxylate overload.
Topics: Alanine; Alanine Transaminase; Animals; Glyoxylates; Hyperoxaluria; Liver; Male; Rats; Rats, Wistar; | 2006 |
Molecular analysis of hyperoxaluria type 1 in Italian patients reveals eight new mutations in the alanine: glyoxylate aminotransferase gene.
Topics: Alanine; Base Sequence; Exons; Gene Deletion; Humans; Hyperoxaluria; Italy; Molecular Sequence Data; | 1999 |
High-performance liquid chromatographic microassay for L-alanine:glyoxylate aminotransferase activity in human liver.
Topics: Alanine; Alanine Transaminase; Chromatography, High Pressure Liquid; Colorimetry; Glyoxylates; Human | 1992 |
Late presentation and development of nephrocalcinosis in primary hyperoxaluria.
Topics: Alanine; Female; Humans; Hyperoxaluria; Middle Aged; Nephrocalcinosis; Radionuclide Imaging | 1992 |
Human liver L-alanine-glyoxylate aminotransferase: characteristics and activity in controls and hyperoxaluria type I patients using a simple spectrophotometric method.
Topics: Alanine; Alanine Transaminase; Biopsy; Glyoxylates; Humans; Hydrogen-Ion Concentration; Hyperoxaluri | 1990 |
Enzymological diagnosis of primary hyperoxaluria type 1 by measurement of hepatic alanine: glyoxylate aminotransferase activity.
Topics: Adolescent; Alanine; Child; Child, Preschool; Female; Humans; Hyperoxaluria; Liver; Male; Prognosis; | 1987 |