ENVIRONMENTAL FACTORS ASSOCIATED WITH PAGET'S DISEASE OF BONE OR WITH THE SQSTM1/P392L MUTATION CARRIAGE

被引:1
|
作者
Audet, M. -C. [1 ]
Beaudoin, C. [2 ]
Guay-Belanger, S. [2 ]
Dumont, J. [2 ]
Brown, J. P. [1 ]
Michou, L. [1 ]
机构
[1] CHU Quebec, Dept Rheumatol, Quebec City, PQ, Canada
[2] CHU Quebec, Res Ctr, Quebec City, PQ, Canada
关键词
D O I
10.1136/annrheumdis-2014-eular.4393
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
SAT0525
引用
收藏
页码:781 / 781
页数:1
相关论文
共 50 条
  • [21] The Implications of the Sequestosome 1 Mutation P392L in Patients with Paget's Disease in a United States Cohort
    Seton, Margaret
    Hansen, Marc
    Solomon, Daniel H.
    CALCIFIED TISSUE INTERNATIONAL, 2016, 98 (05) : 489 - 496
  • [22] Increased IκB levels in patients with Paget's disease of bone carrying the P392L sequestosome 1 gene mutation
    Daroszewska, A
    van't Hof, RJ
    Ralston, SH
    RHEUMATOLOGY, 2005, 44 : I7 - I7
  • [23] Mutation analysis of the SQSTM1 gene in Paget's disease of bone in a Hungarian family
    Donath, J.
    Gergely Jr, P.
    Blazsek, A.
    Poor, G.
    OSTEOPOROSIS INTERNATIONAL, 2006, 17 : S347 - S347
  • [24] Clinical phenotype of adult offspring carriers of the p.Pro392Leu mutation within the SQSTM1 gene in Paget's disease of bone
    Dessay, Mariam
    Gervais, Francois Jobin
    Simonyan, David
    Samson, Andreanne
    Gleeton, Guylaine
    Gagnon, Edith
    Albert, Caroline
    Brown, Jacques P.
    Michou, Laetitia
    BONE REPORTS, 2020, 13
  • [25] Large phenotypic variability of Paget disease of bone caused by the P392L sequestosome1/p62 mutation.
    Laurin, N
    Morissette, J
    Raymond, V
    Brown, JP
    JOURNAL OF BONE AND MINERAL RESEARCH, 2002, 17 : S380 - S381
  • [26] The p62 P392L Mutation Linked to Paget's Disease Induces Activation of Human Osteoclasts
    Chamoux, Estelle
    Couture, Julie
    Bisson, Martine
    Morissette, Jean
    Brown, Jacques P.
    Roux, Sophie
    MOLECULAR ENDOCRINOLOGY, 2009, 23 (10) : 1668 - 1680
  • [27] Absence of Somatic SQSTM1 Mutations in Paget's Disease of Bone
    Matthews, Brya G.
    Naot, Dorit
    Bava, Usha
    Callon, Karen E.
    Pitto, Rocco P.
    McCowan, Stuart A.
    Wattie, Diana
    Cundy, Tim
    Cornish, Jill
    Reid, Ian R.
    JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM, 2009, 94 (02): : 691 - 694
  • [28] A SQSTM1/p62 mutation linked to Paget's disease increases the osteoclastogenic potential of the bone microenvironment
    Hiruma, Yuko
    Kurihara, Noriyoshi
    Subler, Mark A.
    Zhou, Hua
    Boykin, Christina S.
    Zhang, Heju
    Ishizuka, Seiichi
    Dempster, David W.
    Roodman, G. David
    Windle, Jolene J.
    HUMAN MOLECULAR GENETICS, 2008, 17 (23) : 3708 - 3719
  • [29] Recurrent mutation of the gene encoding sequestosome 1 (SQSTM1/p62) in Paget disease of bone
    Laurin, N
    Brown, JP
    Morissette, J
    Raymond, V
    AMERICAN JOURNAL OF HUMAN GENETICS, 2002, 70 (06) : 1582 - 1588
  • [30] Mutations of SQSTM1 Are Associated With Severity and Clinical Outcome in Paget Disease of Bone
    Visconti, Micaela Rios
    Langston, Anne L.
    Alonso, Nerea
    Goodman, Kirsteen
    Selby, Peter L.
    Fraser, William D.
    Ralston, Stuart H.
    JOURNAL OF BONE AND MINERAL RESEARCH, 2010, 25 (11) : 2368 - 2373