| scholarly article | Q13442814 |
| P2093 | author name string | R Griffiths | |
| M K Drezner | |||
| T M Coffman | |||
| T Nesbitt | |||
| P2860 | cites work | Arteriosclerosis in normal and von Willebrand pigs: long-term prospective study and aortic transplantation study | Q34270628 |
| 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 | Q34553262 | ||
| Functional role of thromboxane production by acutely rejecting renal allografts in rats | Q34625251 | ||
| Hypophosphatemia: mouse model for human familial hypophosphatemic (vitamin D-resistant) rickets | Q35044977 | ||
| Abnormal regulation of renal 25-hydroxyvitamin D-1 alpha-hydroxylase activity in the X-linked hypophosphatemic mouse | Q35203463 | ||
| Primary cultures of renal epithelial cells from X-linked hypophosphatemic (Hyp) mice express defects in phosphate transport and vitamin D metabolism | Q35246892 | ||
| Evidence for an Intrinsic Renal Tubular Defect in Mice with Genetic Hypophosphatemic Rickets | Q37038611 | ||
| A possible primary role for the kidney in essential hypertension | Q38605285 | ||
| Phosphate Transport by Isolated Renal and Intestinal Plasma Membranes | Q39162783 | ||
| Vitamin D-resistant rickets associated withepidermal nevus syndrome: Demonstration of a phosphaturic substance in the dermal lesions | Q40079451 | ||
| Micropuncture study of renal phosphorus transport in hypophosphatemic vitamin D resistant rickets mice | Q40119858 | ||
| 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 | Q40190899 | ||
| Defective bone formation by transplanted Hyp mouse bone cells into normal mice | Q41429487 | ||
| Abnormal regulation of 25-hydroxyvitamin D3-1 alpha-hydroxylase activity by calcium and calcitonin in renal cortex from hypophosphatemic (Hyp) mice | Q42461631 | ||
| Abnormal parathyroid function in the X-linked hypophosphatemic mouse | Q42528043 | ||
| Serum parathyroid hormone in X-linked hypophosphatemia | Q43620855 | ||
| Occurrence of hyperparathyroidism in children with X-linked hypophosphatemia under treatment with vitamin D and phsophate | Q50979549 | ||
| Incorporation in vivo of intracisternally injected 33 P i into phospholipids of rat brain. | Q51118572 | ||
| Uric acid metabolism in dalmatians and other dogs. Role of the liver. | Q54419228 | ||
| Renal transplantation in hypophosphatemia with vitamin D-resistant rickets. | Q54421161 | ||
| Serum parathyroid hormone concentrations in hypophosphataemic vitamin D resistant rickets. | Q54635818 | ||
| Renal function before and after unilateral ephrectomy in renal donors | Q67316649 | ||
| Enhanced renal leukotriene production in murine lupus: Role of lipoxygenase metabolites | Q67914077 | ||
| Abnormal parathyroid hormone-related peptide stimulation of renal 25-hydroxyvitamin D-1-hydroxylase in Hyp mice: evidence for a generalized defect of enzyme activity in the proximal convoluted tubule | Q68859111 | ||
| Abnormal adenosine 3'.5'-monophosphate stimulation of renal 1,25-dihydroxyvitamin D production in hyp mice: evidence that 25-hydroxyvitamin D-1 alpha-hydroxylase dysfunction results from aberrant intracellular function | Q69329673 | ||
| Parabiosis suggests a humoral factor is involved in X-linked hypophosphatemia in mice | Q69800704 | ||
| The renal phosphate transport defect in normal mice parabiosed to X-linked hypophosphatemic mice persists after parathyroidectomy | Q69800707 | ||
| Hemangiopericytoma-induced osteomalacia: tumor transplantation in nude mice causes hypophosphatemia and tumor extracts inhibit renal 25-hydroxyvitamin D 1-hydroxylase activity | Q69829169 | ||
| Defective adaptation to a low phosphate environment by cultured renal tubular cells from X-linked hypophosphatemic (Hyp) mice | Q70178075 | ||
| Normal handling of phosphate in the salivary glands of X-linked hypophosphataemic mice | Q70975971 | ||
| Normal milk composition in lactating X-linked hypophosphatemic mice despite continued hypophosphatemia | Q71247833 | ||
| Transplantation of extensor carpi radialis longus muscle in normal and dystrophic chicks | Q71258690 | ||
| Effect of 1,25-dihydroxyvitamin D3 on phosphate homeostasis in the X-linked hypophosphatemic (Hyp) mouse | Q71854444 | ||
| Decreased phosphate reabsorption after renal transplantation: Evidence for a mechanism independent of calcium and parathyroid hormone | Q72895780 | ||
| The determination of phosphorus and phosphatase with N-phenyl-p-phenylenediamine | Q74455851 | ||
| P433 | issue | 5 | |
| P407 | language of work or name | English | Q1860 |
| P921 | main subject | phenotype | Q104053 |
| P304 | page(s) | 1453-1459 | |
| P577 | publication date | 1992-05-01 | |
| P1433 | published in | Journal of Clinical Investigation | Q3186904 |
| P1476 | title | Crosstransplantation of kidneys in normal and Hyp mice. Evidence that the Hyp mouse phenotype is unrelated to an intrinsic renal defect | |
| P478 | volume | 89 |
| Q36308619 | "Phosphatonins" and the regulation of phosphorus homeostasis |
| Q24308202 | A gene (PEX) with homologies to endopeptidases is mutated in patients with X-linked hypophosphatemic rickets. The HYP Consortium |
| Q54236504 | A report of familial hyperphosphataemia in an Irish family. |
| Q36303697 | Aberrant Phex function in osteoblasts and osteocytes alone underlies murine X-linked hypophosphatemia |
| Q37604151 | Application of modified small bladder patch-to-bladder double-layer sutures to improve renal transplantation in mice |
| Q28077005 | Association between GRK4 and DRD1 gene polymorphisms and hypertension: a meta-analysis |
| Q49109372 | Chromosomal localization of the human renal sodium phosphate transporter to chromosome 5: implications for X-linked hypophosphatemia. |
| Q24623628 | Cloning and characterization of FGF23 as a causative factor of tumor-induced osteomalacia |
| Q24318022 | Cloning of human PEX cDNA. Expression, subcellular localization, and endopeptidase activity |
| Q35978987 | Correction of proximal tubule phosphate transport defect in Hyp mice in vivo and in vitro with indomethacin |
| Q28579664 | Differential regulation of PHEX expression in bone and parathyroid gland by chronic renal insufficiency and 1,25-dihydroxyvitamin D3 |
| Q71769763 | Direct demonstration of a humorally-mediated inhibition of renal phosphate transport in the Hyp mouse |
| Q35612256 | Disorders of phosphate metabolism--pathomechanisms and management of hypophosphataemic disorders |
| Q34061540 | Disorders of phosphate metabolism. |
| Q24309057 | Expression and cloning of the human X-linked hypophosphatemia gene cDNA |
| Q38123396 | FGF-23 and secondary hyperparathyroidism in chronic kidney disease |
| Q26851904 | FGF23 and Phosphate Wasting Disorders |
| Q28177435 | FGF23, PHEX, and MEPE regulation of phosphate homeostasis and skeletal mineralization |
| Q42067681 | Fibroblast Growth Factor 23 (FGF23) and Disorders of Phosphate Metabolism |
| Q37043623 | G protein-coupled receptor kinase 4: role in blood pressure regulation |
| Q27022049 | Genetic disorders of phosphate regulation |
| Q37086206 | Hearing loss and fluctuating hearing levels in X-linked hypophosphataemic osteomalacia |
| Q34436396 | Hypophosphatemic rickets |
| Q38103455 | Hypophosphatemic rickets due to perturbations in renal tubular function |
| Q73750227 | Hypophosphatemic rickets: easy to diagnose, difficult to treat |
| Q44130801 | Inhibition of MEPE cleavage by Phex. |
| Q73267379 | Inhibition of Prolyl-4-Hydroxylase Ameliorates Chronic Rejection of Mouse Kidney Allografts |
| Q35837766 | Inorganic phosphate homeostasis and the role of dietary phosphorus. |
| Q40590136 | MEPE has the properties of an osteoblastic phosphatonin and minhibin. |
| Q28569996 | MRNA expression of Phex in mice and rats: the effect of low phosphate diet |
| Q33910987 | McCune Albright syndrome and hypophosphatemic rickets |
| Q72802820 | Molecular biology of hypophosphataemic rickets and oncogenic osteomalacia |
| Q33927876 | Molecular mechanisms of mammalian inorganic phosphate homeostasis |
| Q33697498 | New insights into the pathogenesis of inherited phosphate wasting disorders. |
| Q28236776 | New perspectives on the biology and treatment of X-linked hypophosphatemic rickets |
| Q33585463 | Organ transplantation in mice: current status and future prospects |
| Q35059741 | Osteo-renal regulation of systemic phosphate metabolism |
| Q38081019 | Osteocyte regulation of phosphate homeostasis and bone mineralization underlies the pathophysiology of the heritable disorders of rickets and osteomalacia |
| Q73509264 | Osteomalacia |
| Q40768048 | Overexpression of Phex in osteoblasts fails to rescue the Hyp mouse phenotype. |
| Q70495937 | Parental origin of mutant allele does not explain absence of gene dose in X-linked Hyp mice |
| Q37364983 | Pex/PEX tissue distribution and evidence for a deletion in the 3' region of the Pex gene in X-linked hypophosphatemic mice |
| Q28580930 | Phex cDNA cloning from rat bone and studies on phex mRNA expression: tissue-specificity, age-dependency, and regulation by insulin-like growth factor (IGF) I in vivo |
| Q54203140 | Phosphate transport in osteoblasts from normal and X-linked hypophosphatemic mice. |
| Q34030128 | Phosphatonin washout in Hyp mice proximal tubules: evidence for posttranscriptional regulation |
| Q41022417 | Positional cloning of the HYP gene: a review |
| Q28275381 | Proteolytic processing of osteopontin by PHEX and accumulation of osteopontin fragments in Hyp mouse bone, the murine model of X-linked hypophosphatemia |
| Q28140211 | Proximal tubular phosphate reabsorption: molecular mechanisms |
| Q42762333 | RAS in FGF23: another piece in the puzzle |
| Q36739668 | Regulation of phosphate homeostasis by the phosphatonins and other novel mediators |
| Q34125548 | Renal Na(+)-phosphate cotransport in murine X-linked hypophosphatemic rickets. Molecular characterization |
| Q40920435 | Renal adaptation to phosphate deprivation: lessons from the X-linked Hyp mouse |
| Q33858669 | Renal physiology of the mouse |
| Q38362148 | Role of abnormal neutral endopeptidase-like activities in Hyp mouse bone cells in renal phosphate transport |
| Q36487782 | Role of prostaglandins in the pathogenesis of X-linked hypophosphatemia. |
| Q58759632 | Selective Deletion of Heparan Sulfotransferase Enzyme, Ndst1, in Donor Endothelial and Myeloid Precursor Cells Significantly Decreases Acute Allograft Rejection |
| Q49127184 | Sodium-phosphate transport in the kidney and intestine of the hypophosphatemic mouse |
| Q38115828 | Systematic review of mouse kidney transplantation |
| Q73783878 | Systemic autoimmune nephritogenic components induce CSF-1 and TNF-alpha in MRL kidneys |
| Q41607810 | The PEX gene: not a simple answer for X-linked hypophosphataemic rickets and oncogenic osteomalacia |
| Q71482742 | The gene for X-linked hypophosphataemic rickets maps to a 200-300kb region in Xp22.1, and is located on a single YAC containing a putative vitamin D response element (VDRE) |
| Q52553441 | The genomic response of the mouse kidney to low-phosphate diet is altered in X-linked hypophosphatemia. |
| Q83202578 | The phosphatonins and the regulation of phosphate homeostasis |
| Q38050402 | The skeleton as an endocrine organ |
| Q37403473 | The use of pre-operative imaging and intraoperative parathyroid hormone level to guide surgical management of tertiary hyperparathyroidism from X-linked hypophosphatemic rickets: a case report |
| Q35911345 | The wrickkened pathways of FGF23, MEPE and PHEX. |
| Q71437949 | Transplant approach establishes that kidneys are responsible for serum CSF-1 but require a stimulus in MRL-lpr mice |
| Q34178089 | Tumor-induced osteomalacia |
| Q34016470 | Tumor-induced osteomalacia and the regulation of phosphate homeostasis |
| Q28069314 | Tumour-induced osteomalacia: a literature review and a case report |
| Q73146517 | Urinary supersaturation of calcium oxalate and phosphate in patients with X-linked hypophosphatemic rickets and in healthy schoolchildren |
| Q37063367 | What's new in hypophosphataemic rickets? |
| Q35848808 | X-linked hypophosphataemia: a homologous phenotype in humans and mice with unusual organ-specific gene dosage |
| Q81857590 | [Genetic hypophosphatemia: recent advances in physiopathogenic concept] |
| Q73563089 | [Molecular mechanisms of familial rachitis] |
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