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6. Osteoblast-specific expression of the fibrous dysplasia (FD)-causing mutation Gsα(R201C) produces a high bone mass phenotype but does not reproduce FD in the mouse. Remoli C; Michienzi S; Sacchetti B; Consiglio AD; Cersosimo S; Spica E; Robey PG; Holmbeck K; Cumano A; Boyde A; Davis G; Saggio I; Riminucci M; Bianco P J Bone Miner Res; 2015 Jun; 30(6):1030-43. PubMed ID: 25487351 [TBL] [Abstract][Full Text] [Related]
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9. Expression of FGF23 is correlated with serum phosphate level in isolated fibrous dysplasia. Kobayashi K; Imanishi Y; Koshiyama H; Miyauchi A; Wakasa K; Kawata T; Goto H; Ohashi H; Koyano HM; Mochizuki R; Miki T; Inaba M; Nishizawa Y Life Sci; 2006 Apr; 78(20):2295-301. PubMed ID: 16337659 [TBL] [Abstract][Full Text] [Related]
10. Direct evidence for the age-dependent demise of GNAS-mutated cells in oral fibrous dysplasia. Isobe Y; Takahashi K; Kiso H; Nakao K; Ikeno M; Koyama N; Sugai M; Shimizu A; Haga H; Bessho K Arch Oral Biol; 2018 Sep; 93():133-140. PubMed ID: 29909118 [TBL] [Abstract][Full Text] [Related]
11. Changes in gene expression in human skeletal stem cells transduced with constitutively active Gsα correlates with hallmark histopathological changes seen in fibrous dysplastic bone. Raimondo D; Remoli C; Astrologo L; Burla R; La Torre M; Vernì F; Tagliafico E; Corsi A; Del Giudice S; Persichetti A; Giannicola G; Robey PG; Riminucci M; Saggio I PLoS One; 2020; 15(1):e0227279. PubMed ID: 31999703 [TBL] [Abstract][Full Text] [Related]
12. Glucocorticoids decrease interleukin-6 levels and induce mineralization of cultured osteogenic cells from children with fibrous dysplasia. Stanton RP; Hobson GM; Montgomery BE; Moses PA; Smith-Kirwin SM; Funanage VL J Bone Miner Res; 1999 Jul; 14(7):1104-14. PubMed ID: 10404010 [TBL] [Abstract][Full Text] [Related]
13. GNAS mutation detection is related to disease severity in girls with McCune-Albright syndrome and precocious puberty. Wagoner HA; Steinmetz R; Bethin KE; Eugster EA; Pescovitz OH; Hannon TS Pediatr Endocrinol Rev; 2007 Aug; 4 Suppl 4():395-400. PubMed ID: 17982386 [TBL] [Abstract][Full Text] [Related]
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16. A disruptive mutation in exon 3 of the GNAS gene with albright hereditary osteodystrophy, normocalcemic pseudohypoparathyroidism, and selective long transcript variant Gsalpha-L deficiency. Thiele S; Werner R; Ahrens W; Hoppe U; Marschke C; Staedt P; Hiort O J Clin Endocrinol Metab; 2007 May; 92(5):1764-8. PubMed ID: 17299070 [TBL] [Abstract][Full Text] [Related]
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18. A highly sensitive polymerase chain reaction method detects activating mutations of the GNAS gene in peripheral blood cells in McCune-Albright syndrome or isolated fibrous dysplasia. Lietman SA; Ding C; Levine MA J Bone Joint Surg Am; 2005 Nov; 87(11):2489-94. PubMed ID: 16264125 [TBL] [Abstract][Full Text] [Related]
19. Identification of GNAS Variants in Circulating Cell-Free DNA from Patients with Fibrous Dysplasia/McCune Albright Syndrome. Roszko KL; Guthrie L; Li X; Collins MT; de Castro LF; Boyce AM J Bone Miner Res; 2023 Mar; 38(3):443-450. PubMed ID: 36593655 [TBL] [Abstract][Full Text] [Related]
20. The CREB-Smad6-Runx2 axis contributes to the impaired osteogenesis potential of bone marrow stromal cells in fibrous dysplasia of bone. Fan QM; Yue B; Bian ZY; Xu WT; Tu B; Dai KR; Li G; Tang TT J Pathol; 2012 Sep; 228(1):45-55. PubMed ID: 22450860 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]