arginine has been researched along with Hypophosphatasia in 3 studies
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 0 (0.00) | 18.7374 |
| 1990's | 0 (0.00) | 18.2507 |
| 2000's | 3 (100.00) | 29.6817 |
| 2010's | 0 (0.00) | 24.3611 |
| 2020's | 0 (0.00) | 2.80 |
| Authors | Studies |
|---|---|
| Essmyer, K; Geimer, M; Mumm, S; Whyte, MP | 1 |
| Amaya, Y; Amizuka, N; Fukushi-Irié, M; Ikehara, Y; Ito, M; Oda, K; Omura, S; Ozawa, H | 1 |
| Arnon, S; Dolfin, T; Grinshpan, G; Ozono, K; Regev, R; Reish, O; Yamazaki, M | 1 |
1 review(s) available for arginine and Hypophosphatasia
| Article | Year |
|---|---|
Homozygosity for TNSALP mutation 1348c>T (Arg433Cys) causes infantile hypophosphatasia manifesting transient disease correction and variably lethal outcome in a kindred of black ancestry.
Topics: Alkaline Phosphatase; Arginine; Black or African American; Child, Preschool; Cysteine; Electrophoresis, Gel, Two-Dimensional; Homozygote; Humans; Hypophosphatasia; Infant, Newborn; Isoenzymes; Male; Mutation, Missense; Pedigree; Prevalence; RNA Splice Sites | 2006 |
2 other study(ies) available for arginine and Hypophosphatasia
| Article | Year |
|---|---|
Possible interference between tissue-non-specific alkaline phosphatase with an Arg54-->Cys substitution and acounterpart with an Asp277-->Ala substitution found in a compound heterozygote associated with severe hypophosphatasia.
Topics: Alanine; Alkaline Phosphatase; Amino Acid Substitution; Animals; Arginine; Aspartic Acid; COS Cells; Cysteine; DNA, Complementary; Heterozygote; Hypophosphatasia; Mutation, Missense; Transfection | 2000 |
Glu274Lys/Gly309Arg mutation of the tissue-nonspecific alkaline phosphatase gene in neonatal hypophosphatasia associated with convulsions.
Topics: Alkaline Phosphatase; Arginine; Female; Glutamic Acid; Humans; Hypophosphatasia; Infant, Newborn; Lysine; Mutation, Missense; Seizures | 2002 |