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Journal Abstract Search

303 related items for PubMed ID: 30756140

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  • 3. Juvenile Paget's disease, familial expansile osteolysis and other genetic osteolytic disorders.
    Ralston SH.
    Best Pract Res Clin Rheumatol; 2008 Mar; 22(1):101-11. PubMed ID: 18328984
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  • 7. Familial Paget's disease of bone with ocular manifestations and a novel TNFRSF11A duplication variant (72dup27).
    Saito-Hakoda A, Kikuchi A, Takahashi T, Yokoyama Y, Himori N, Adachi M, Ikeda R, Nomura Y, Takayama J, Kawashima J, Katsuoka F, Fujishima F, Yamaguchi T, Ito A, Hanita T, Kanno J, Aizawa T, Nakazawa T, Kawase T, Tamiya G, Yamamoto M, Fujiwara I, Kure S.
    J Bone Miner Metab; 2023 Mar; 41(2):193-202. PubMed ID: 36520195
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  • 11. Genetics and aetiology of Pagetic disorders of bone.
    Helfrich MH, Hocking LJ.
    Arch Biochem Biophys; 2008 May 15; 473(2):172-82. PubMed ID: 18359282
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  • 12. Paget's disease of bone and genetic disorders of RANKL/OPG/RANK/NF-kappaB signaling.
    Whyte MP.
    Ann N Y Acad Sci; 2006 Apr 15; 1068():143-64. PubMed ID: 16831914
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  • 13. Mutation screening of the TNFRSF11A gene encoding receptor activator of NF kappa B (RANK) in familial and sporadic Paget's disease of bone and osteosarcoma.
    Sparks AB, Peterson SN, Bell C, Loftus BJ, Hocking L, Cahill DP, Frassica FJ, Streeten EA, Levine MA, Fraser CM, Adams MD, Broder S, Venter JC, Kinzler KW, Vogelstein B, Ralston SH.
    Calcif Tissue Int; 2001 Mar 15; 68(3):151-5. PubMed ID: 11351498
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  • 14. Genetics of Paget's disease of bone.
    Ralston SH, Albagha OM.
    Curr Osteoporos Rep; 2014 Sep 15; 12(3):263-71. PubMed ID: 24988994
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  • 16. New knowledge on critical osteoclast formation and activation pathways from study of rare genetic diseases of osteoclasts: focus on the RANK/RANKL axis.
    Crockett JC, Mellis DJ, Scott DI, Helfrich MH.
    Osteoporos Int; 2011 Jan 15; 22(1):1-20. PubMed ID: 20458572
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  • 17. Evaluation of the role of RANK and OPG genes in Paget's disease of bone.
    Wuyts W, Van Wesenbeeck L, Morales-Piga A, Ralston S, Hocking L, Vanhoenacker F, Westhovens R, Verbruggen L, Anderson D, Hughes A, Van Hul W.
    Bone; 2001 Jan 15; 28(1):104-7. PubMed ID: 11165949
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  • 18. Early-onset Paget's disease of bone in a Mexican family caused by a novel tandem duplication (77dup27) in TNFRSF11A that encodes RANK.
    Iwamoto SJ, Rothman MS, Duan S, Baker JC, Mumm S, Whyte MP.
    Bone; 2020 Apr 15; 133():115224. PubMed ID: 31923705
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  • 19. Genetic variation in the TNFRSF11A gene encoding RANK is associated with susceptibility to Paget's disease of bone.
    Chung PY, Beyens G, Riches PL, Van Wesenbeeck L, de Freitas F, Jennes K, Daroszewska A, Fransen E, Boonen S, Geusens P, Vanhoenacker F, Verbruggen L, Van Offel J, Goemaere S, Zmierczak HG, Westhovens R, Karperien M, Papapoulos S, Ralston SH, Devogelaer JP, Van Hul W.
    J Bone Miner Res; 2010 Dec 15; 25(12):2592-605. PubMed ID: 20564239
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  • 20. Genetic disorders associated with the RANKL/OPG/RANK pathway.
    Xue JY, Ikegawa S, Guo L.
    J Bone Miner Metab; 2021 Jan 15; 39(1):45-53. PubMed ID: 32940787
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