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Significados de familial hypophosphatemic rickets en inglés

Human disease.

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      Examples for "hyp"
      Examples for "hyp"
      1
      But everything depended upon getting off-hyp-getting to Drammen-hyp, hyp-intime to catch the train which left for Modum at two o'clock.
      Norse Tales and Sketches
      2
      The osteogenic sarcoma-derived bone-inducing substance was implanted in Hyp mice or control mice.
      Pubmed
      3
      These results will facilitate attempts further to localize and clone the HYP gene.
      Pubmed
      4
      The 3' end of this gene is deleted in Hyp mice.
      Pubmed
      5
      This study demonstrates that complement is an important mediator in early xenograft HYP injury.
      Pubmed
      1
      XLH patients are more likely to have elevated intact FGF23 than C-terminal FGF23.
      Pubmed
      2
      In this study, we sequenced the PHEX gene in subjects from 26 kindreds who were clinically diagnosed with XLH.
      Pubmed
      3
      Our data, in accord with those of others, indicate that there is no single predominant PHEX mutation responsible for XLH.
      Pubmed
      4
      Normal serum klotho levels were associated with normal FGF23 biologic activity in all XLH patients and a minority of ADPKD patients.
      Pubmed
      5
      Using a conceptual approach, we suggest that a defect in the skeletal response to parathyroid hormone contributes to hyperparathyroidism in XLH.
      Pubmed
      1
      X-linked hypophosphatemic rickets and autosomal dominant hypophosphatemic rickets are inherited phosphate wasting disorders.
      Pubmed
      2
      X-linked hypophosphatemic rickets in humans is caused by mutations in the PEX gene which codes for a protein homologous to neutral endopeptidases.
      Pubmed
      3
      X-linked hypophosphatemic rickets results from mutations in the PHEX gene, which codes for a protein that is a member of the neutral endopeptidase family.
      Pubmed