proline and Hypophosphatemia, Familial

proline has been researched along with Hypophosphatemia, Familial in 2 studies

Research

Studies (2)

TimeframeStudies, this research(%)All Research%
pre-19901 (50.00)18.7374
1990's0 (0.00)18.2507
2000's1 (50.00)29.6817
2010's0 (0.00)24.3611
2020's0 (0.00)2.80

Authors

AuthorsStudies
Abu-Zahra, H; Banerjee, S; Bergwitz, C; Jüppner, H; Kaji, H; Miyauchi, A; Sugimoto, T1
Ecarot-Charrier, B; Glorieux, FH1

Other Studies

2 other study(ies) available for proline and Hypophosphatemia, Familial

ArticleYear
Defective O-glycosylation due to a novel homozygous S129P mutation is associated with lack of fibroblast growth factor 23 secretion and tumoral calcinosis.
    The Journal of clinical endocrinology and metabolism, 2009, Volume: 94, Issue:11

    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.
    Calcified tissue international, 1983, Volume: 35, Issue:3

    Topics: Animals; Bone and Bones; Calcitriol; Cells, Cultured; Collagen; Dose-Response Relationship, Drug; Hydroxyproline; Hypophosphatemia, Familial; Male; Mice; Mice, Inbred C57BL; Phosphates; Proline

1983