These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

302 related articles for article (PubMed ID: 30756140)

  • 1. Rare Inherited forms of Paget's Disease and Related Syndromes.
    Ralston SH; Taylor JP
    Calcif Tissue Int; 2019 May; 104(5):501-516. PubMed ID: 30756140
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Mechanisms of disease: genetics of Paget's disease of bone and related disorders.
    Daroszewska A; Ralston SH
    Nat Clin Pract Rheumatol; 2006 May; 2(5):270-7. PubMed ID: 16932700
    [TBL] [Abstract][Full Text] [Related]  

  • 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
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Genetics of Paget's disease of bone.
    Daroszewska A; Ralston SH
    Clin Sci (Lond); 2005 Sep; 109(3):257-63. PubMed ID: 16104845
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Pathogenesis of Paget's disease of bone.
    Ralston SH
    Bone; 2008 Nov; 43(5):819-25. PubMed ID: 18672105
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Juvenile Paget's disease with heterozygous duplication within TNFRSF11A encoding RANK.
    Whyte MP; Tau C; McAlister WH; Zhang X; Novack DV; Preliasco V; Santini-Araujo E; Mumm S
    Bone; 2014 Nov; 68():153-61. PubMed ID: 25063546
    [TBL] [Abstract][Full Text] [Related]  

  • 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
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Contribution of genetic factors to the pathogenesis of Paget's disease of bone and related disorders.
    Lucas GJ; Daroszewska A; Ralston SH
    J Bone Miner Res; 2006 Dec; 21 Suppl 2():P31-7. PubMed ID: 17229006
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Insertion Mutation in Tnfrsf11a Causes a Paget's Disease-Like Phenotype in Heterozygous Mice and Osteopetrosis in Homozygous Mice.
    Alonso N; Wani S; Rose L; Van't Hof RJ; Ralston SH; Albagha OME
    J Bone Miner Res; 2021 Jul; 36(7):1376-1386. PubMed ID: 33724536
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Sporadic hyperphosphatasia syndrome featuring periostitis and accelerated skeletal turnover without receptor activator of nuclear factor-kappaB, osteoprotegerin, or sequestosome-1 gene defects.
    Simsek S; Basoski NM; Bravenboer N; Zhang X; Mumm S; Whyte MP; Netelenbos JC
    J Clin Endocrinol Metab; 2007 May; 92(5):1897-901. PubMed ID: 17284635
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Genetics and aetiology of Pagetic disorders of bone.
    Helfrich MH; Hocking LJ
    Arch Biochem Biophys; 2008 May; 473(2):172-82. PubMed ID: 18359282
    [TBL] [Abstract][Full Text] [Related]  

  • 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; 1068():143-64. PubMed ID: 16831914
    [TBL] [Abstract][Full Text] [Related]  

  • 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; 68(3):151-5. PubMed ID: 11351498
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Genetics of Paget's disease of bone.
    Ralston SH; Albagha OM
    Curr Osteoporos Rep; 2014 Sep; 12(3):263-71. PubMed ID: 24988994
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Familial Early-Onset Paget's Disease of Bone Associated with a Novel hnRNPA2B1 Mutation.
    Qi X; Pang Q; Wang J; Zhao Z; Wang O; Xu L; Mao J; Jiang Y; Li M; Xing X; Yu W; Asan ; Xia W
    Calcif Tissue Int; 2017 Aug; 101(2):159-169. PubMed ID: 28389692
    [TBL] [Abstract][Full Text] [Related]  

  • 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; 22(1):1-20. PubMed ID: 20458572
    [TBL] [Abstract][Full Text] [Related]  

  • 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; 28(1):104-7. PubMed ID: 11165949
    [TBL] [Abstract][Full Text] [Related]  

  • 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; 133():115224. PubMed ID: 31923705
    [TBL] [Abstract][Full Text] [Related]  

  • 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; 25(12):2592-605. PubMed ID: 20564239
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Genetic disorders associated with the RANKL/OPG/RANK pathway.
    Xue JY; Ikegawa S; Guo L
    J Bone Miner Metab; 2021 Jan; 39(1):45-53. PubMed ID: 32940787
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 16.