about
MEPE, a new gene expressed in bone marrow and tumors causing osteomalaciaTreatment of X-linked hypophosphatemia with calcitriol and phosphate increases circulating fibroblast growth factor 23 concentrationsGenome-wide association study of bone mineral density in premenopausal European-American women and replication in African-American womenMolecular cloning of a novel human UDP-GalNAc:polypeptide N-acetylgalactosaminyltransferase, GalNAc-T8, and analysis as a candidate autosomal dominant hypophosphatemic rickets (ADHR) geneThe autosomal dominant hypophosphatemic rickets (ADHR) gene is a secreted polypeptide overexpressed by tumors that cause phosphate wastingChloride channel 7 (ClCN7) gene mutations and autosomal dominant osteopetrosis, type IITumoral calcinosis presenting with eyelid calcifications due to novel missense mutations in the glycosyl transferase domain of the GALNT3 geneFibroblast growth factor 23: roles in health and diseaseBone loss at the femoral neck in premenopausal white women: effects of weight change and sex-hormone levels.Identification of genes influencing skeletal phenotypes in congenic P/NP rats.Heritability of changes in bone size and bone mass with age in premenopausal white sisters.Meta-analysis of genome-wide scans provides evidence for sex- and site-specific regulation of bone mass.Association of adenylate cyclase 10 (ADCY10) polymorphisms and bone mineral density in healthy adults.New insights into the pathogenesis of inherited phosphate wasting disorders.Mosaicism in osteopathia striata with cranial sclerosisHigh-resolution genome screen for bone mineral density in heterogeneous stock rat.SIBLING family genes and bone mineral density: association and allele-specific expression in humansConfirmation of linkage to chromosome 1q for peak vertebral bone mineral density in premenopausal white women.Mutations that cause osteoglophonic dysplasia define novel roles for FGFR1 in bone elongationEstablishment of sandwich ELISA for soluble alpha-Klotho measurement: Age-dependent change of soluble alpha-Klotho levels in healthy subjectsDisorders of phosphate metabolism.Hypophosphatemic rickets: revealing novel control points for phosphate homeostasis.Replication of previous genome-wide association studies of bone mineral density in premenopausal American women.Genetic rescue of glycosylation-deficient Fgf23 in the Galnt3 knockout mouse.FGF-23 in fibrous dysplasia of bone and its relationship to renal phosphate wastingEfficient and stable gene expression into human osteoclasts using an HIV-1-based lentiviral vectorSex-specific quantitative trait loci contribute to normal variation in bone structure at the proximal femur in menHeterogeneous stock rat: a unique animal model for mapping genes influencing bone fragility.Iron modifies plasma FGF23 differently in autosomal dominant hypophosphatemic rickets and healthy humans.Dietary phosphate restriction normalizes biochemical and skeletal abnormalities in a murine model of tumoral calcinosisMost osteomalacia-associated mesenchymal tumors are a single histopathologic entity: an analysis of 32 cases and a comprehensive review of the literature.Renal phosphate wasting disorders: clinical features and pathogenesis.A Phex mutation in a murine model of X-linked hypophosphatemia alters phosphate responsiveness of bone cells.Osteoblast-Specific Overexpression of Human WNT16 Increases Both Cortical and Trabecular Bone Mass and Structure in MiceApproach to the hypophosphatemic patientA homozygous missense mutation in human KLOTHO causes severe tumoral calcinosis.Polymorphisms in the estrogen receptor beta (ESR2) gene are associated with bone mineral density in Caucasian men and women.regSNPs: a strategy for prioritizing regulatory single nucleotide substitutions.Conventional Therapy in Adults With XLH Improves Dental Manifestations, But Not EnthesopathyPersistent tumor-induced osteomalacia confirmed by elevated postoperative levels of serum fibroblast growth factor-23 and 5-year follow-up of bone density changes.
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Michael J Econs
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Michael J Econs
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P21
P31
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0000-0003-0940-1911