112 related articles for article (PubMed ID: 3720010)
21. Constitutive stimulatory G protein activity in limb mesenchyme impairs bone growth.
Karaca A; Malladi VR; Zhu Y; Tafaj O; Paltrinieri E; Wu JY; He Q; Bastepe M
Bone; 2018 May; 110():230-237. PubMed ID: 29471062
[TBL] [Abstract][Full Text] [Related]
22. A case of gradually manifesting McCune-Albright syndrome with a 10-year follow-up.
Honda T; Itoh F; Nakamura K; Ohba T; Katabuchi H
Reprod Med Biol; 2016 Oct; 15(4):261-265. PubMed ID: 29259443
[TBL] [Abstract][Full Text] [Related]
23. Induced
Khan SK; Yadav PS; Elliott G; Hu DZ; Xu R; Yang Y
Proc Natl Acad Sci U S A; 2018 Jan; 115(3):E418-E427. PubMed ID: 29158412
[TBL] [Abstract][Full Text] [Related]
24. Natural history of cranial fibrous dysplasia revealed during long-term follow-up: Case report and literature review.
Penn DL; Tartarini RJ; Glass CH; De Girolami U; Zamani AA; Dunn IF
Surg Neurol Int; 2017; 8():209. PubMed ID: 28966816
[TBL] [Abstract][Full Text] [Related]
25. Heterotrimeric G proteins in the control of parathyroid hormone actions.
Bastepe M; Turan S; He Q
J Mol Endocrinol; 2017 May; 58(4):R203-R224. PubMed ID: 28363951
[TBL] [Abstract][Full Text] [Related]
26. Knockin mouse with mutant G
Roszko KL; Bi R; Gorvin CM; Bräuner-Osborne H; Xiong XF; Inoue A; Thakker RV; Strømgaard K; Gardella T; Mannstadt M
JCI Insight; 2017 Feb; 2(3):e91079. PubMed ID: 28194446
[TBL] [Abstract][Full Text] [Related]
27. CDC73 gene mutations in sporadic ossifying fibroma of the jaws.
Chen Y; Hu DY; Wang TT; Zhang R; Dong Q; Xu ZX; Wang L; Li TJ
Diagn Pathol; 2016 Sep; 11(1):91. PubMed ID: 27658992
[TBL] [Abstract][Full Text] [Related]
28. The Role of gsp Mutations on the Development of Adrenocortical Tumors and Adrenal Hyperplasia.
Villares Fragoso MC; Wanichi IQ; Cavalcante IP; Mariani BM
Front Endocrinol (Lausanne); 2016; 7():104. PubMed ID: 27512387
[TBL] [Abstract][Full Text] [Related]
29. Fibrous dysplasia of bone: craniofacial and dental implications.
Burke AB; Collins MT; Boyce AM
Oral Dis; 2017 Sep; 23(6):697-708. PubMed ID: 27493082
[TBL] [Abstract][Full Text] [Related]
30. Fibrous Dysplasia/McCune-Albright Syndrome: Clinical and Translational Perspectives.
Robinson C; Collins MT; Boyce AM
Curr Osteoporos Rep; 2016 Oct; 14(5):178-86. PubMed ID: 27492469
[TBL] [Abstract][Full Text] [Related]
31. GNAS Mutations in Fibrous Dysplasia: A Comparative Study of Standard Sequencing and Locked Nucleic Acid PCR Sequencing on Decalcified and Nondecalcified Formalin-fixed Paraffin-embedded Tissues.
Jour G; Oultache A; Sadowska J; Mitchell T; Healey J; Nafa K; Hameed M
Appl Immunohistochem Mol Morphol; 2016 Oct; 24(9):660-667. PubMed ID: 26574629
[TBL] [Abstract][Full Text] [Related]
32. Neonatal McCune-Albright syndrome with systemic involvement: a case report.
Lourenço R; Dias P; Gouveia R; Sousa AB; Oliveira G
J Med Case Rep; 2015 Sep; 9():189. PubMed ID: 26341786
[TBL] [Abstract][Full Text] [Related]
33. GNAS Spectrum of Disorders.
Turan S; Bastepe M
Curr Osteoporos Rep; 2015 Jun; 13(3):146-58. PubMed ID: 25851935
[TBL] [Abstract][Full Text] [Related]
34. Detection of SQSTM1/P392L post-zygotic mutations in Paget's disease of bone.
Guay-Bélanger S; Picard S; Gagnon E; Morissette J; Siris ES; Orcel P; Brown JP; Michou L
Hum Genet; 2015 Jan; 134(1):53-65. PubMed ID: 25241215
[TBL] [Abstract][Full Text] [Related]
35. A randomized, double blind, placebo-controlled trial of alendronate treatment for fibrous dysplasia of bone.
Boyce AM; Kelly MH; Brillante BA; Kushner H; Wientroub S; Riminucci M; Bianco P; Robey PG; Collins MT
J Clin Endocrinol Metab; 2014 Nov; 99(11):4133-40. PubMed ID: 25033066
[TBL] [Abstract][Full Text] [Related]
36. Constitutive expression of Gsα(R201C) in mice produces a heritable, direct replica of human fibrous dysplasia bone pathology and demonstrates its natural history.
Saggio I; Remoli C; Spica E; Cersosimo S; Sacchetti B; Robey PG; Holmbeck K; Cumano A; Boyde A; Bianco P; Riminucci M
J Bone Miner Res; 2014 Nov; 29(11):2357-68. PubMed ID: 24764158
[TBL] [Abstract][Full Text] [Related]
37. A high throughput screening assay system for the identification of small molecule inhibitors of gsp.
Bhattacharyya N; Hu X; Chen CZ; Mathews Griner LA; Zheng W; Inglese J; Austin CP; Marugan JJ; Southall N; Neumann S; Northup JK; Ferrer M; Collins MT
PLoS One; 2014; 9(3):e90766. PubMed ID: 24667240
[TBL] [Abstract][Full Text] [Related]
38. Detectable clonal mosaicism in the human genome.
Machiela MJ; Chanock SJ
Semin Hematol; 2013 Oct; 50(4):348-59. PubMed ID: 24246702
[TBL] [Abstract][Full Text] [Related]
39. Multilineage somatic activating mutations in HRAS and NRAS cause mosaic cutaneous and skeletal lesions, elevated FGF23 and hypophosphatemia.
Lim YH; Ovejero D; Sugarman JS; Deklotz CM; Maruri A; Eichenfield LF; Kelley PK; Jüppner H; Gottschalk M; Tifft CJ; Gafni RI; Boyce AM; Cowen EW; Bhattacharyya N; Guthrie LC; Gahl WA; Golas G; Loring EC; Overton JD; Mane SM; Lifton RP; Levy ML; Collins MT; Choate KA
Hum Mol Genet; 2014 Jan; 23(2):397-407. PubMed ID: 24006476
[TBL] [Abstract][Full Text] [Related]
40. A genomic view of mosaicism and human disease.
Biesecker LG; Spinner NB
Nat Rev Genet; 2013 May; 14(5):307-20. PubMed ID: 23594909
[TBL] [Abstract][Full Text] [Related]
[Previous] [Next] [New Search]