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Journal Abstract Search

457 related items for PubMed ID: 27117614

  • 21. Palovarotene Inhibits Heterotopic Ossification and Maintains Limb Mobility and Growth in Mice With the Human ACVR1(R206H) Fibrodysplasia Ossificans Progressiva (FOP) Mutation.
    Chakkalakal SA, Uchibe K, Convente MR, Zhang D, Economides AN, Kaplan FS, Pacifici M, Iwamoto M, Shore EM.
    J Bone Miner Res; 2016 Sep; 31(9):1666-75. PubMed ID: 26896819
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  • 22. ACVR1R206H receptor mutation causes fibrodysplasia ossificans progressiva by imparting responsiveness to activin A.
    Hatsell SJ, Idone V, Wolken DM, Huang L, Kim HJ, Wang L, Wen X, Nannuru KC, Jimenez J, Xie L, Das N, Makhoul G, Chernomorsky R, D'Ambrosio D, Corpina RA, Schoenherr CJ, Feeley K, Yu PB, Yancopoulos GD, Murphy AJ, Economides AN.
    Sci Transl Med; 2015 Sep 02; 7(303):303ra137. PubMed ID: 26333933
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  • 26. Fibrodysplasia ossificans progressiva.
    Kaplan FS, Le Merrer M, Glaser DL, Pignolo RJ, Goldsby RE, Kitterman JA, Groppe J, Shore EM.
    Best Pract Res Clin Rheumatol; 2008 Mar 02; 22(1):191-205. PubMed ID: 18328989
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  • 32. Role of altered signal transduction in heterotopic ossification and fibrodysplasia ossificans progressiva.
    Shore EM, Kaplan FS.
    Curr Osteoporos Rep; 2011 Jun 02; 9(2):83-8. PubMed ID: 21340697
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  • 34. Skeletal malformations and developmental arthropathy in individuals who have fibrodysplasia ossificans progressiva.
    Towler OW, Shore EM, Kaplan FS.
    Bone; 2020 Jan 02; 130():115116. PubMed ID: 31655222
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  • 35. The HIF-1α and mTOR Pathways Amplify Heterotopic Ossification.
    Wang H, Kaplan FS, Pignolo RJ.
    Biomolecules; 2024 Jan 24; 14(2):. PubMed ID: 38397384
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  • 36. Neofunction of ACVR1 in fibrodysplasia ossificans progressiva.
    Hino K, Ikeya M, Horigome K, Matsumoto Y, Ebise H, Nishio M, Sekiguchi K, Shibata M, Nagata S, Matsuda S, Toguchida J.
    Proc Natl Acad Sci U S A; 2015 Dec 15; 112(50):15438-43. PubMed ID: 26621707
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  • 37. Effects of FKBP12 and type II BMP receptors on signal transduction by ALK2 activating mutations associated with genetic disorders.
    Machiya A, Tsukamoto S, Ohte S, Kuratani M, Fujimoto M, Kumagai K, Osawa K, Suda N, Bullock AN, Katagiri T.
    Bone; 2018 Jun 15; 111():101-108. PubMed ID: 29551750
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  • 38. A novel mutation of ALK2, L196P, found in the most benign case of fibrodysplasia ossificans progressiva activates BMP-specific intracellular signaling equivalent to a typical mutation, R206H.
    Ohte S, Shin M, Sasanuma H, Yoneyama K, Akita M, Ikebuchi K, Jimi E, Maruki Y, Matsuoka M, Namba A, Tomoda H, Okazaki Y, Ohtake A, Oda H, Owan I, Yoda T, Furuya H, Kamizono J, Kitoh H, Nakashima Y, Susami T, Haga N, Komori T, Katagiri T.
    Biochem Biophys Res Commun; 2011 Apr 01; 407(1):213-8. PubMed ID: 21377447
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  • 39. TGF-Beta Induces Activin A Production in Dermal Fibroblasts Derived from Patients with Fibrodysplasia Ossificans Progressiva.
    de Ruiter RD, Wisse LE, Schoenmaker T, Yaqub M, Sánchez-Duffhues G, Eekhoff EMW, Micha D.
    Int J Mol Sci; 2023 Jan 24; 24(3):. PubMed ID: 36768622
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