cysteine has been researched along with Hypophosphatasia in 2 studies
Timeframe | Studies, this research(%) | All Research% |
---|---|---|
pre-1990 | 0 (0.00) | 18.7374 |
1990's | 0 (0.00) | 18.2507 |
2000's | 2 (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-IriƩ, M; Ikehara, Y; Ito, M; Oda, K; Omura, S; Ozawa, H | 1 |
1 review(s) available for cysteine 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 |
1 other study(ies) available for cysteine 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 |