proline has been researched along with Hypophosphatemia, Familial in 2 studies
Timeframe | Studies, this research(%) | All Research% |
---|---|---|
pre-1990 | 1 (50.00) | 18.7374 |
1990's | 0 (0.00) | 18.2507 |
2000's | 1 (50.00) | 29.6817 |
2010's | 0 (0.00) | 24.3611 |
2020's | 0 (0.00) | 2.80 |
Authors | Studies |
---|---|
Abu-Zahra, H; Banerjee, S; Bergwitz, C; Jüppner, H; Kaji, H; Miyauchi, A; Sugimoto, T | 1 |
Ecarot-Charrier, B; Glorieux, FH | 1 |
2 other study(ies) available for proline and Hypophosphatemia, Familial
Article | Year |
---|---|
Defective O-glycosylation due to a novel homozygous S129P mutation is associated with lack of fibroblast growth factor 23 secretion and tumoral calcinosis.
Topics: Amino Acid Sequence; Amino Acid Substitution; Animals; Base Sequence; Calcinosis; Carrier State; Chlorocebus aethiops; Codon; COS Cells; DNA Primers; Exons; Fibroblast Growth Factor-23; Fibroblast Growth Factors; Glycosylation; Homozygote; Humans; Hypophosphatemia, Familial; Molecular Sequence Data; Neoplasms; Polymorphism, Single Nucleotide; Proline; Serine | 2009 |
Effects of phosphate and 1,25(OH)2D3 on in vitro bone collagen synthesis in the hypophosphatemic mouse.
Topics: Animals; Bone and Bones; Calcitriol; Cells, Cultured; Collagen; Dose-Response Relationship, Drug; Hydroxyproline; Hypophosphatemia, Familial; Male; Mice; Mice, Inbred C57BL; Phosphates; Proline | 1983 |