Usage of "hypophosphatemic rickets x-linked dominant"

Human disease.

Términos relacionados

rare disease

Sinónimos

Examples for "hyp"

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 

The osteogenic sarcoma-derived bone-inducing substance was implanted in Hyp mice or control mice. 
 Pubmed 

These results will facilitate attempts further to localize and clone the HYP gene. 
 Pubmed 

The 3' end of this gene is deleted in Hyp mice. 
 Pubmed 

This study demonstrates that complement is an important mediator in early xenograft HYP injury. 
 Pubmed 

XLH patients are more likely to have elevated intact FGF23 than C-terminal FGF23. 
 Pubmed 

In this study, we sequenced the PHEX gene in subjects from 26 kindreds who were clinically diagnosed with XLH. 
 Pubmed 

Our data, in accord with those of others, indicate that there is no single predominant PHEX mutation responsible for XLH. 
 Pubmed 

Normal serum klotho levels were associated with normal FGF23 biologic activity in all XLH patients and a minority of ADPKD patients. 
 Pubmed 

Using a conceptual approach, we suggest that a defect in the skeletal response to parathyroid hormone contributes to hyperparathyroidism in XLH. 
 Pubmed 

X-linked hypophosphatemic rickets and autosomal dominant hypophosphatemic rickets are inherited phosphate wasting disorders. 
 Pubmed 

X-linked hypophosphatemic rickets in humans is caused by mutations in the PEX gene which codes for a protein homologous to neutral endopeptidases. 
 Pubmed 

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 

Lengua de interfaz

Significados de hypophosphatemic rickets x-linked dominant en inglés