pyridoxal phosphate has been researched along with Glycogen Storage Disease Type V in 2 studies
Pyridoxal Phosphate: This is the active form of VITAMIN B 6 serving as a coenzyme for synthesis of amino acids, neurotransmitters (serotonin, norepinephrine), sphingolipids, aminolevulinic acid. During transamination of amino acids, pyridoxal phosphate is transiently converted into pyridoxamine phosphate (PYRIDOXAMINE).
pyridoxal 5'-phosphate : The monophosphate ester obtained by condensation of phosphoric acid with the primary hydroxy group of pyridoxal.
Glycogen Storage Disease Type V: Glycogenosis due to muscle phosphorylase deficiency. Characterized by painful cramps following sustained exercise.
| Excerpt | Relevance | Reference |
|---|---|---|
| "Pyridoxal phosphate is a covalently bound cofactor of glycogen phosphorylase." | 1.27 | Low muscle levels of pyridoxine in McArdle's syndrome. ( Cook, JD; Dempsey, WB; Feit, H; Haller, RG; Knochel, JP, 1983) |
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 1 (50.00) | 18.7374 |
| 1990's | 1 (50.00) | 18.2507 |
| 2000's | 0 (0.00) | 29.6817 |
| 2010's | 0 (0.00) | 24.3611 |
| 2020's | 0 (0.00) | 2.80 |
| Authors | Studies |
|---|---|
| Haller, RG | 1 |
| Dempsey, WB | 1 |
| Feit, H | 1 |
| Cook, JD | 1 |
| Knochel, JP | 1 |
| Beynon, RJ | 1 |
| Bartram, C | 1 |
| Flannery, A | 1 |
| Evershed, RP | 1 |
| Leyland, D | 1 |
| Hopkins, P | 1 |
| Toescu, V | 1 |
| Phoenix, J | 1 |
| Edwards, RH | 1 |
1 review available for pyridoxal phosphate and Glycogen Storage Disease Type V
| Article | Year |
|---|---|
Interrelationships between metabolism of glycogen phosphorylase and pyridoxal phosphate--implications in McArdle's disease.
Topics: Animals; Glycogen Storage Disease Type V; Humans; Isotope Labeling; Models, Biological; Muscles; Pho | 1996 |
1 other study available for pyridoxal phosphate and Glycogen Storage Disease Type V
| Article | Year |
|---|---|
Low muscle levels of pyridoxine in McArdle's syndrome.
Topics: Adolescent; Adult; Animals; Female; Glycogen Storage Disease; Glycogen Storage Disease Type V; Human | 1983 |