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Excessive Osteocytic Fgf23 Secretion Contributes to Pyrophosphate Accumulation and Mineralization Defect in Hyp Mice.
- Published in:
- PLoS Biology, 2016, v. 14, n. 4, p. 1, doi. 10.1371/journal.pbio.1002427
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- Publication type:
- Article
Generation of two multipotent mesenchymal progenitor cell lines capable of osteogenic, mature osteocyte, adipogenic, and chondrogenic differentiation.
- Published in:
- Scientific Reports, 2021, v. 11, n. 1, p. 1, doi. 10.1038/s41598-021-02060-1
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- Publication type:
- Article
Circulating aKlotho influences phosphate handling by controlling FGF23 production.
- Published in:
- Journal of Clinical Investigation, 2012, v. 122, n. 12, p. 4710, doi. 10.1172/JCI64986
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- Article
A homozygous missense mutation in human KLOTHO causes severe tumoral calcinosis.
- Published in:
- 2007
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- Publication type:
- journal article
Segregating the effects of ferric citrate‐mediated iron utilization and FGF23 in a mouse model of CKD.
- Published in:
- Physiological Reports, 2022, v. 10, n. 11, p. 1, doi. 10.14814/phy2.15307
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- Publication type:
- Article
Erythropoietin and a hypoxia‐inducible factor prolyl hydroxylase inhibitor (HIF‐PHDi) lowers FGF23 in a model of chronic kidney disease (CKD).
- Published in:
- Physiological Reports, 2020, v. 8, n. 11, p. 1, doi. 10.14814/phy2.14434
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- Publication type:
- Article
Hyperphosphatemic familial tumoral calcinosis: Response to acetazolamide and postulated mechanisms.
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- American Journal of Medical Genetics. Part A, 2014, v. 164A, n. 6, p. 1545, doi. 10.1002/ajmg.a.36476
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- Publication type:
- Article
A case of Robin sequence, microgastria, radiohumeral synostosis, femoral deficiency, and other unusual findings: A newly recognized syndrome?
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- American Journal of Medical Genetics. Part A, 2014, v. 164A, n. 2, p. 287, doi. 10.1002/ajmg.a.36273
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- Publication type:
- Article
The pathophysiology of early-stage chronic kidney disease-mineral bone disorder (CKD-MBD) and response to phosphate binders in the rat.
- Published in:
- Journal of Bone & Mineral Research, 2011, v. 26, n. 11, p. 2672, doi. 10.1002/jbmr.485
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- Publication type:
- Article
Chloride Channel 7 (ClCN7) Gene Mutations and Autosomal Dominant Osteopetrosis, Type II.
- Published in:
- Journal of Bone & Mineral Research, 2003, v. 18, n. 8, p. 1513, doi. 10.1359/jbmr.2003.18.8.1513
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- Publication type:
- Article
Na<sup>+</sup>/Ca<sup>2+</sup> exchange in rat osteoblast-like UMR 106 cells.
- Published in:
- Journal of Bone & Mineral Research, 1996, v. 11, n. 11, p. 1666, doi. 10.1002/jbmr.5650111110
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- Publication type:
- Article
Loss of DMP1 causes rickets and osteomalacia and identifies a role for osteocytes in mineral metabolism.
- Published in:
- Nature Genetics, 2006, v. 38, n. 11, p. 1310, doi. 10.1038/ng1905
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- Publication type:
- Article
Autosomal dominant hypophosphataemic rickets is associated with mutations in FGF23.
- Published in:
- Nature Genetics, 2000, v. 26, n. 3, p. 345, doi. 10.1038/81664
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- Publication type:
- Article
Osteocyte Egln1/Phd2 links oxygen sensing and biomineralization via FGF23.
- Published in:
- Bone Research, 2023, v. 11, n. 1, p. 1, doi. 10.1038/s41413-022-00241-w
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- Publication type:
- Article
Osteocytic FGF23 and Its Kidney Function.
- Published in:
- Frontiers in Endocrinology, 2020, v. 11, p. N.PAG, doi. 10.3389/fendo.2020.00592
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- Publication type:
- Article
Hypophosphatemia with elevations in serum fibroblast growth factor 23 in a child with Jansen's metaphyseal chondrodysplasia.
- Published in:
- 2009
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- Publication type:
- journal article
The Role of Mutant UDP-N-Acetyl-α-D-Galactosamine-Polypeptide N-Acetylgalactosaminyltransferase 3 in Regulating Serum Intact Fibroblast Growth Factor 23 and Matrix Extracellular Phosphoglycoprotein in Heritable Tumoral Calcinosis.
- Published in:
- Journal of Clinical Endocrinology & Metabolism, 2006, v. 91, n. 10, p. 4037, doi. 10.1210/jc.2006-0305
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- Publication type:
- Article
A Novel Recessive Mutation in Fibroblast Growth Factor-23 Causes Familial Tumoral Calcinosis.
- Published in:
- Journal of Clinical Endocrinology & Metabolism, 2005, v. 90, n. 4, p. 2424, doi. 10.1210/jc.2004-2238
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- Publication type:
- Article
Measurement of Tartrate-Resistant Acid Phosphatase and the Brain Isoenzyme of Creatine Kinase Accurately Diagnoses Type II Autosomal Dominant Osteopetrosis but Does Not Identify Gene Carriers.
- Published in:
- Journal of Clinical Endocrinology & Metabolism, 2002, v. 87, n. 5, p. 2212, doi. 10.1210/jcem.87.5.8497
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- Publication type:
- Article
The autosomal dominant hypophosphatemic rickets (ADHR) gene Is a secreted olpypeptide overexpressed by Tumors that cause phosphate wasting.
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- Journal of Clinical Endocrinology & Metabolism, 2001, v. 86, n. 2, p. 497, doi. 10.1210/jcem.86.2.7408
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- Publication type:
- Article
Locus Heterogeneity of Autosomal Dominant Osteopetrosis (ADO).
- Published in:
- Journal of Clinical Endocrinology & Metabolism, 1999, v. 84, n. 3, p. 1047, doi. 10.1210/jcem.84.3.5578
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- Publication type:
- Article
Gabapentin Disrupts Binding of Perlecan to the α 2 δ 1 Voltage Sensitive Calcium Channel Subunit and Impairs Skeletal Mechanosensation.
- Published in:
- Biomolecules (2218-273X), 2022, v. 12, n. 12, p. 1857, doi. 10.3390/biom12121857
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- Publication type:
- Article
Pharmacological management of X‐linked hypophosphataemia.
- Published in:
- British Journal of Clinical Pharmacology, 2019, v. 85, n. 6, p. 1188, doi. 10.1111/bcp.13763
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- Publication type:
- Article
Hypophosphatemic Rickets in Opsismodysplasia.
- Published in:
- Journal of Pediatric Endocrinology & Metabolism, 2007, v. 20, n. 1, p. 79
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- Publication type:
- Article
The pathophysiology of the chronic kidney disease-mineral bone disorder: synopsis of a symposium at the Sun Valley Musculoskeletal Biology Workshop.
- Published in:
- IBMS BoneKEy, 2013, v. 10, n. 11, p. 444, doi. 10.1038/bonekey.2013.178
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- Publication type:
- Article
Single cell cortical bone transcriptomics define novel osteolineage gene sets altered in chronic kidney disease.
- Published in:
- Frontiers in Endocrinology, 2023, v. 14, p. 1, doi. 10.3389/fendo.2023.1063083
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- Publication type:
- Article
The HIF‐PHI BAY 85‐3934 (Molidustat) Improves Anemia and Is Associated With Reduced Levels of Circulating FGF23 in a CKD Mouse Model.
- Published in:
- Journal of Bone & Mineral Research, 2021, v. 36, n. 6, p. 1117, doi. 10.1002/jbmr.4272
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- Publication type:
- Article
Phenotypic and Genotypic Characterization and Treatment of a Cohort With Familial Tumoral Calcinosis/Hyperostosis-Hyperphosphatemia Syndrome.
- Published in:
- Journal of Bone & Mineral Research, 2016, v. 31, n. 10, p. 1845, doi. 10.1002/jbmr.2870
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- Publication type:
- Article
Conditional Deletion of Murine Fgf23: Interruption of the Normal Skeletal Responses to Phosphate Challenge and Rescue of Genetic Hypophosphatemia.
- Published in:
- Journal of Bone & Mineral Research, 2016, v. 31, n. 6, p. 1247, doi. 10.1002/jbmr.2792
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- Publication type:
- Article
Neonatal Iron Deficiency Causes Abnormal Phosphate Metabolism by Elevating FGF23 in Normal and ADHR Mice.
- Published in:
- Journal of Bone & Mineral Research, 2014, v. 29, n. 2, p. 361, doi. 10.1002/jbmr.2049
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- Publication type:
- Article
Fibroblast Growth Factor 23 and Its Receptors.
- Published in:
- Therapeutic Apheresis & Dialysis, 2005, v. 9, n. 4, p. 308, doi. 10.1111/j.1744-9987.2005.00287.x
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- Publication type:
- Article
Letters to the Editors: 1.
- Published in:
- Clinical Endocrinology, 2003, v. 58, n. 6, p. 795, doi. 10.1046/j.1365-2265.2003.18021.x
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- Publication type:
- Article
A rat model of chronic kidney disease-mineral bone disorder.
- Published in:
- Kidney International, 2009, v. 75, n. 2, p. 176, doi. 10.1038/ki.2008.456
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- Publication type:
- Article
Autosomal-dominant hypophosphatemic rickets (ADHR) mutations stabilize FGF-23.
- Published in:
- Kidney International, 2001, v. 60, n. 6, p. 2079, doi. 10.1046/j.1523-1755.2001.00064.x
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- Publication type:
- Article
NCX1 Na/Ca exchanger inhibition by antisense oligonucleotides in mouse distal convoluted tubule cells.
- Published in:
- Kidney International, 1998, v. 54, n. 3, p. 897, doi. 10.1046/j.1523-1755.1998.00056.x
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- Publication type:
- Article