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.
2
The osteogenic sarcoma-derived bone-inducing substance was implanted in Hyp mice or control mice.
3
These results will facilitate attempts further to localize and clone the HYP gene.
4
The 3' end of this gene is deleted in Hyp mice.
5
This study demonstrates that complement is an important mediator in early xenograft HYP injury.
1
X-linkedhypophosphatemicrickets and autosomal dominant hypophosphatemic rickets are inherited phosphate wasting disorders.
2
X-linkedhypophosphatemicrickets in humans is caused by mutations in the PEX gene which codes for a protein homologous to neutral endopeptidases.
3
X-linkedhypophosphatemicrickets results from mutations in the PHEX gene, which codes for a protein that is a member of the neutral endopeptidase family.
Uso de xlh en inglés
1
XLH patients are more likely to have elevated intact FGF23 than C-terminal FGF23.
2
In this study, we sequenced the PHEX gene in subjects from 26 kindreds who were clinically diagnosed with XLH.
3
Our data, in accord with those of others, indicate that there is no single predominant PHEX mutation responsible for XLH.
4
Normal serum klotho levels were associated with normal FGF23 biologic activity in all XLH patients and a minority of ADPKD patients.
5
Using a conceptual approach, we suggest that a defect in the skeletal response to parathyroid hormone contributes to hyperparathyroidism in XLH.
6
Methods: Subjects included 25 untreated outpatients with XLH at a tertiary medical center and 158 healthy adult controls.
7
These lines of evidence suggested that the pathogenesis of osteomalacia in HHRH was different from XLH in terms of the utility of phosphate in osteoblasts.
8
The relationships of iron to FGF23 in XLH suggest that altered regulation of FGF23 cleaving may contribute to maintaining hypophosphatemia around an abnormal set-point.
9
We hypothesized that in XLH serum iron would inversely correlate to C-terminal FGF23, but not to intact FGF23, mirroring the relationships in normal controls.