Access the full text.
Sign up today, get DeepDyve free for 14 days.
B. Sarkar, U. Chauhan (1967)
A new method for determining micro quantities of calcium in biological materials.Analytical biochemistry, 20 1
G. Kiebzak, B. Roos, R. Meyer (1982)
Secondary hyperparathyroidism in X-linked hypophosphatemic mice.Endocrinology, 111 2
Brown Brown, Wilkie Wilkie, Meyer Meyer, Meyer Meyer (1985)
Response of tissue phosphate content to acute dietary phosphate deprivation in the X ‐linked hypophosphatemic mouseCalcif Tissue Int, 37
Meyer Meyer, Jowsey Jowsey, Meyer Meyer (1979)
Osteomalacia and altered magnesium metabolism in the X ‐linked hypophosphatemic mouseCalcif Tissue Int, 27
Meyers Mh, Meyer Ra, Pollard Bd, Theys Rd (1984)
Abnormal trace mineral metabolism in adult X-linked hypophosphatemic mice: a possible role of increased food intakeMineral and Electrolyte Metabolism, 10
T. Reinhardt, R. Horst, J. Orf, B. Hollis (1984)
A microassay for 1,25-dihydroxyvitamin D not requiring high performance liquid chromatography: application to clinical studies.The Journal of clinical endocrinology and metabolism, 58 1
D. Walker (1973)
Osteopetrosis cured by temporary parabiosis.Science, 180 4088
J. Finerty (1952)
Parabiosis in physiological studies.Physiological reviews, 32 3
R. Meyer, M. Meyer, H. Tenenhouse, A. Klugerman (1989)
The renal phosphate transport defect in normal mice parabiosed to X‐linked hypophosphatemic mice persists after parathyroidectomyJournal of Bone and Mineral Research, 4
Raymond Mcbeide, N. Nisbet, Anna SKOWEON-CENDHZAK (1967)
RATE OF CROSS‐CIRCULATION IN PARABIOSIS: ITS SIGNIFICANCE, RELATIONSHIP TO GENETIC DISPARITY, AND EXPERIMENTAL MODIFICATIONTransplantation, 5
R. Meyer, R. Gray, B. Roos, G. Kiebzak (1982)
Increased plasma 1,25-dihydroxyvitamin D after low calcium challenge in X-linked hypophosphatemic mice.Endocrinology, 111 1
R. Sabina, M. Drezner, E. Holmes (1982)
Reduced renal cortical ribonucleoside triphosphate pools in three different hypophosphatemic animal models.Biochemical and biophysical research communications, 109 3
T. Nesbitt, B. Lobaugh, M. Drezner (1987)
Calcitonin stimulation of renal 25-hydroxyvitamin D-1 alpha-hydroxylase activity in hypophosphatemic mice. Evidence that the regulation of calcitriol production is not universally abnormal in X-linked hypophosphatemia.The Journal of clinical investigation, 79 1
M. Kay, M. Meyer, P. Delzer, R. Meyer (1985)
Changing patterns of femoral and skeletal mineralization during growth in juvenile X-linked hypophosphatemic mice.Mineral and electrolyte metabolism, 11 6
R. Rosenbaum, K. Hruska, A. Korkor, C. Anderson, E. Slatopolsky (1981)
Decreased phosphate reabsorption after renal transplantation: Evidence for a mechanism independent of calcium and parathyroid hormone.Kidney international, 19 4
G. Cotton, P. Puffelen (1986)
Hypophosphatemic osteomalacia secondary to neoplasia.The Journal of bone and joint surgery. American volume, 68 1
Delzer Delzer, Meyer Meyer (1983)
Normal milk composition in lactating X ‐linked hypophosphatemic mice despite continued hypophosphatemiaCalcif Tissue Int, 35
H. Tenenhouse, C. Scriver, R. Mcinnes, F. Glorieux (1978)
Renal handling of phosphate in vivo and in vitro by the X-linked hypophosphatemic male mouse: evidence for a defect in the brush border membrane.Kidney international, 14 3
C. Sloane, J. Bramis, D. Racelis, L. Burrows, R. Taub (1976)
Hematologic and immunologic aspects of parabiosis.The Mount Sinai journal of medicine, New York, 43 4
P. Chen, T. Toribara, H. Warner (1956)
Microdetermination of PhosphorusAnalytical Chemistry, 28
(1961)
Free skin grafting in mammals
Nesbitt Nesbitt, Lobaugh Lobaugh, Drezner Drezner (1987)
Calcitonin stimulation of renal 25‐hydroxyvitamin D‐lα‐hydroxylase activity in hypophosphatemic miceJ Clin Invest, 79
J. Morgan, W. Hawley, A. Chenoweth, W. Retan, A. Diethelm (1974)
Renal transplantation in hypophosphatemia with vitamin D-resistant rickets.Archives of internal medicine, 134 3
Martha Meyer, Ralph Meyer, Richard Gray, Richard Irwin (1985)
Picric acid methods greatly overestimate serum creatinine in mice: more accurate results with high-performance liquid chromatography.Analytical biochemistry, 144 1
E. Eicher, J. Southard, C. Scriver, F. Glorieux (1976)
Hypophosphatemia: mouse model for human familial hypophosphatemic (vitamin D-resistant) rickets.Proceedings of the National Academy of Sciences of the United States of America, 73 12
A. Nowotny (1979)
Microdetermination of Phosphorus
P. Delzer, R. Meyer (1984)
Normal handling of phosphate in the salivary glands of X-linked hypophosphataemic mice.Archives of oral biology, 29 12
(1981)
Mineral and skeletal changes in parabiotic normal and hypophosphatemic mice ( ah - stract )
R. Meyer, R. Gray, M. Meyer (1980)
Abnormal vitamin D metabolism in the X-linked hypophosphatemic mouse.Endocrinology, 107 5
Reduced renal tubular reabsorption of phosphate of unknown etiology is characteristic of X‐linked hypophosphatemia in both humans and mice. To test whether a humoral abnormality is involved in the renal effect, parabiosis was performed between Hyp and normal mice at 4 weeks of age. The normal mice joined to Hyp mice showed a progressive diminution of plasma phosphate over the next 3 weeks to approach the level of the Hyp mice. These normal mice had a greater renal phosphate excretion index (urine P/plasma P/urine creatinine) than normal‐normal pairs, thus suggesting a reduced renal tubular reabsorption of phosphate. At the same time the expected rises in plasma calcium and plasma 1,25‐dihydroxyvitamin D did not occur. There was a significant reduction in their femoral mineral content but not in their femoral length or body growth relative to normal‐normal pairs. This change in renal handling of phosphate was specific since the urinary losses of potassium and magnesium were not significantly changed. Separation of normal‐Hyp pairs 3 or 6 weeks after parabiosis caused the normal mice to achieve normal plasma phosphate levels within 24 h. At 48 h and 7 days after separation these normal mice had plasma phosphate levels higher than normal mice separated from normal‐normal pairs. In summary, the data suggest the presence of a phosphaturic factor in the Hyp mice that can cross a parabiotic union into normal mice and induce many of the symptoms of X‐linked hypophosphatemia.
Journal of Bone and Mineral Research – Oxford University Press
Published: Aug 1, 1989
Read and print from thousands of top scholarly journals.
Already have an account? Log in
Bookmark this article. You can see your Bookmarks on your DeepDyve Library.
To save an article, log in first, or sign up for a DeepDyve account if you don’t already have one.
Copy and paste the desired citation format or use the link below to download a file formatted for EndNote
Access the full text.
Sign up today, get DeepDyve free for 14 days.
All DeepDyve websites use cookies to improve your online experience. They were placed on your computer when you launched this website. You can change your cookie settings through your browser.