BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

203 related articles for article (PubMed ID: 26991965)

  • 21. The diagnostic challenge of progressive pseudorheumatoid dysplasia (PPRD): a review of clinical features, radiographic features, and WISP3 mutations in 63 affected individuals.
    Garcia Segarra N; Mittaz L; Campos-Xavier AB; Bartels CF; Tuysuz B; Alanay Y; Cimaz R; Cormier-Daire V; Di Rocco M; Duba HC; Elcioglu NH; Forzano F; Hospach T; Kilic E; Kuemmerle-Deschner JB; Mortier G; Mrusek S; Nampoothiri S; Obersztyn E; Pauli RM; Selicorni A; Tenconi R; Unger S; Utine GE; Wright M; Zabel B; Warman ML; Superti-Furga A; Bonafé L
    Am J Med Genet C Semin Med Genet; 2012 Aug; 160C(3):217-29. PubMed ID: 22791401
    [TBL] [Abstract][Full Text] [Related]  

  • 22. 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; 5(7):301-6. PubMed ID: 27436824
    [TBL] [Abstract][Full Text] [Related]  

  • 23. Cellular and molecular responses in progressive pseudorheumatoid dysplasia articular cartilage associated with compound heterozygous WISP3 gene mutation.
    Zhou HD; Bu YH; Peng YQ; Xie H; Wang M; Yuan LQ; Jiang Y; Li D; Wei QY; He YL; Xiao T; Ni JD; Liao EY
    J Mol Med (Berl); 2007 Sep; 85(9):985-96. PubMed ID: 17483925
    [TBL] [Abstract][Full Text] [Related]  

  • 24. A homozygous recurring mutation in WISP3 causing progressive pseudorheumatoid arthropathy.
    Temiz F; Ozbek MN; Kotan D; Sangun O; Mungan NO; Yuksel B; Topaloglu AK
    J Pediatr Endocrinol Metab; 2011; 24(1-2):105-8. PubMed ID: 21528827
    [TBL] [Abstract][Full Text] [Related]  

  • 25. Clinical and molecular characterization in a cohort of patients with progressive pseudorheumatoid dysplasia.
    El Dessouki D; Amr K; Kholoussi N; Rady HM; Temtamy SA; Abdou MMS; Aglan M
    Am J Med Genet A; 2023 Sep; 191(9):2329-2336. PubMed ID: 37377052
    [TBL] [Abstract][Full Text] [Related]  

  • 26. An argument for early genomic sequencing in atypical cases: a WISP3 variant leads to diagnosis of progressive pseudorheumatoid arthropathy of childhood.
    Cassa CA; Smith SE; Docken W; Hoffman E; McLaughlin H; Chun S; Leshchiner I; Miraoui H; Raychaudhuri S; Frank NY; Wilson BJ; Sunyaev SR; Maas RL; ; Vuzman D
    Rheumatology (Oxford); 2016 Mar; 55(3):586-9. PubMed ID: 26493744
    [No Abstract]   [Full Text] [Related]  

  • 27. A homozygous deletion of exon 1 in WISP3 causes progressive pseudorheumatoid dysplasia in two siblings.
    Neerinckx B; Thues C; Wouters C; Lechner S; Westhovens R; Van Esch H
    Hum Genome Var; 2015; 2():15049. PubMed ID: 27081554
    [TBL] [Abstract][Full Text] [Related]  

  • 28. 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; 23(1):94-8. PubMed ID: 10471507
    [TBL] [Abstract][Full Text] [Related]  

  • 29. Novel COL2A1 variant (c.619G>A, p.Gly207Arg) manifesting as a phenotype similar to progressive pseudorheumatoid dysplasia and spondyloepiphyseal dysplasia, Stanescu type.
    Jurgens J; Sobreira N; Modaff P; Reiser CA; Seo SH; Seong MW; Park SS; Kim OH; Cho TJ; Pauli RM
    Hum Mutat; 2015 Oct; 36(10):1004-8. PubMed ID: 26183434
    [TBL] [Abstract][Full Text] [Related]  

  • 30. 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; 25(1):414-21. PubMed ID: 15601861
    [TBL] [Abstract][Full Text] [Related]  

  • 31. CCN6 mutation detection in Chinese patients with progressive pseudo-rheumatoid dysplasia and identification of four novel mutations.
    Wang Y; Xiao K; Yang Y; Wu Z; Jin J; Qiu G; Weng X; Zhao X
    Mol Genet Genomic Med; 2020 Jul; 8(7):e1261. PubMed ID: 32351055
    [TBL] [Abstract][Full Text] [Related]  

  • 32. The CCN family member Wisp3, mutant in progressive pseudorheumatoid dysplasia, modulates BMP and Wnt signaling.
    Nakamura Y; Weidinger G; Liang JO; Aquilina-Beck A; Tamai K; Moon RT; Warman ML
    J Clin Invest; 2007 Oct; 117(10):3075-86. PubMed ID: 17823661
    [TBL] [Abstract][Full Text] [Related]  

  • 33. Progressive pseudorheumatoid dysplasia misdiagnosed as juvenile idiopathic arthritis: a case report.
    Omar AA; Ahmed S; Rodrigues JC; Kayiza A; Owino L
    J Med Case Rep; 2021 Nov; 15(1):551. PubMed ID: 34749805
    [TBL] [Abstract][Full Text] [Related]  

  • 34. Association analysis on polymorphisms in WISP3 gene and developmental dysplasia of the hip in Han Chinese population: A case-control study.
    Zhang J; Yan M; Zhang Y; Yang H; Sun Y
    Gene; 2018 Jul; 664():192-195. PubMed ID: 29680248
    [TBL] [Abstract][Full Text] [Related]  

  • 35. Delayed-onset progressive pseudorheumatoid dysplasia with secondary synovial chondromatosis.
    Shahi P; Sehgal A; Sudan A; Sehgal S
    BMJ Case Rep; 2020 May; 13(5):. PubMed ID: 32430353
    [TBL] [Abstract][Full Text] [Related]  

  • 36. Ilizarov technique in an adolescent patient with progressive pseudorheumatoid dysplasia: A case report.
    Xiao K; Li T; Jiang Y; Li Z; Zhu Q; Wu Z; Weng X
    Medicine (Baltimore); 2018 Aug; 97(31):e11375. PubMed ID: 30075503
    [TBL] [Abstract][Full Text] [Related]  

  • 37. Specific early signs and long-term follow-up findings of progressive pseudorheumatoid dysplasia (PPRD) in the Turkish cohort.
    Uludağ Alkaya D; Kasapçopur Ö; Bursalı A; Adrovic A; Demir B; Aykut A; Tüysüz B
    Rheumatology (Oxford); 2022 Aug; 61(9):3693-3703. PubMed ID: 34919662
    [TBL] [Abstract][Full Text] [Related]  

  • 38. Novel and recurrent mutations in WISP3 and an atypical phenotype.
    Bhavani GS; Shah H; Dalal AB; Shukla A; Danda S; Aggarwal S; Phadke SR; Gupta N; Kabra M; Gowrishankar K; Gupta A; Bhat M; Puri RD; Bijarnia-Mahay S; Nampoothiri S; Mohanasundaram KM; Rajeswari S; Kulkarni AM; Kulkarni ML; Ranganath P; Ramadevi AR; Hariharan SV; Girisha KM
    Am J Med Genet A; 2015 Oct; 167A(10):2481-4. PubMed ID: 25988854
    [No Abstract]   [Full Text] [Related]  

  • 39. Case Report: Recurrent Variant c.298 TA in
    Sheth H; Shah J; Nair A; Naik P; Sheth J
    Front Genet; 2021; 12():724824. PubMed ID: 34650595
    [TBL] [Abstract][Full Text] [Related]  

  • 40.
    ; ; . PubMed ID:
    [No Abstract]   [Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 11.