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Journal Abstract Search


167 related items for PubMed ID: 20426955

  • 1. [Clinical diagnosis and WISP3 gene mutation analysis for progressive pseudorheumatoid dysplasia].
    Ye J, Zhang HW, Wang T, Cao LF, Qiu WJ, Han LS, Zhang YF, Gu XF.
    Zhonghua Er Ke Za Zhi; 2010 Mar; 48(3):194-8. PubMed ID: 20426955
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  • 3. Identification of novel mutations in WISP3 gene in two unrelated Chinese families with progressive pseudorheumatoid dysplasia.
    Yue H, Zhang ZL, He JW.
    Bone; 2009 Apr; 44(4):547-54. PubMed ID: 19064006
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  • 4. Novel and recurrent mutations of WISP3 in two Chinese families with progressive pseudorheumatoid dysplasia.
    Sun J, Xia W, He S, Zhao Z, Nie M, Li M, Jiang Y, Xing X, Wang O, Meng X, Zhou X.
    PLoS One; 2012 Apr; 7(6):e38643. PubMed ID: 22685593
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  • 5. Analysis of the WISP3 gene in Indian families with progressive pseudorheumatoid dysplasia.
    Dalal A, Bhavani G SL, Togarrati PP, Bierhals T, Nandineni MR, Danda S, Danda D, Shah H, Vijayan S, Gowrishankar K, Phadke SR, Bidchol AM, Rao AP, Nampoothiri S, Kutsche K, Girisha KM.
    Am J Med Genet A; 2012 Nov; 158A(11):2820-8. PubMed ID: 22987568
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  • 13. Progressive pseudorheumatoid dysplasia with new-found gene mutation of Wntl inducible signaling pathway protein 3.
    Chen W, Mo S, Luo G, Wang Y, Deng X, Zhu J, Zhao W.
    Pediatr Rheumatol Online J; 2018 Sep 10; 16(1):55. PubMed ID: 30200995
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  • 14. Molecular study of WISP3 in nine families originating from the Middle-East and presenting with progressive pseudorheumatoid dysplasia: identification of two novel mutations, and description of a founder effect.
    Delague V, Chouery E, Corbani S, Ghanem I, Aamar S, Fischer J, Levy-Lahad E, Urtizberea JA, Mégarbané A.
    Am J Med Genet A; 2005 Oct 01; 138A(2):118-26. PubMed ID: 16152649
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  • 15. WISP3, the gene responsible for the human skeletal disease progressive pseudorheumatoid dysplasia, is not essential for skeletal function in mice.
    Kutz WE, Gong Y, Warman ML.
    Mol Cell Biol; 2005 Jan 01; 25(1):414-21. PubMed ID: 15601861
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  • 16. Skeletal phenotype/genotype in progressive pseudorheumatoid chondrodysplasia.
    Al Kaissi A, Kenis V, Jemaa LB, Sassi H, Shboul M, Grill F, Ganger R, Kircher SG.
    Clin Rheumatol; 2020 Feb 01; 39(2):553-560. PubMed ID: 31628567
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  • 18. Mutations in the CCN gene family member WISP3 cause progressive pseudorheumatoid dysplasia.
    Hurvitz JR, Suwairi WM, Van Hul W, El-Shanti H, Superti-Furga A, Roudier J, Holderbaum D, Pauli RM, Herd JK, Van Hul EV, Rezai-Delui H, Legius E, Le Merrer M, Al-Alami J, Bahabri SA, Warman ML.
    Nat Genet; 1999 Sep 01; 23(1):94-8. PubMed ID: 10471507
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  • 20. WISP3 mutational analysis in Indian patients diagnosed with progressive pseudorheumatoid dysplasia and report of a novel mutation at p.Y198.
    Madhuri V, Santhanam M, Rajagopal K, Sugumar LK, Balaji V.
    Bone Joint Res; 2016 Jul 01; 5(7):301-6. PubMed ID: 27436824
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