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.
96 related articles for article (PubMed ID: 22789636)
1. Rare variations in WNT3A and DKK1 may predispose carriers to primary osteoporosis. Korvala J; Löija M; Mäkitie O; Sochett E; Jüppner H; Schnabel D; Mora S; Cole WG; Ala-Kokko L; Männikkö M Eur J Med Genet; 2012 Oct; 55(10):515-9. PubMed ID: 22789636 [TBL] [Abstract][Full Text] [Related]
2. More severe phenotype of early-onset osteoporosis associated with recessive form of LRP5 and combination with DKK1 or WNT3A. Caetano da Silva C; Ricquebourg M; Orcel P; Fabre S; Funck-Brentano T; Cohen-Solal M; Collet C Mol Genet Genomic Med; 2021 Jun; 9(6):e1681. PubMed ID: 33939331 [TBL] [Abstract][Full Text] [Related]
3. Mutations in LRP5 cause primary osteoporosis without features of OI by reducing Wnt signaling activity. Korvala J; Jüppner H; Mäkitie O; Sochett E; Schnabel D; Mora S; Bartels CF; Warman ML; Deraska D; Cole WG; Hartikka H; Ala-Kokko L; Männikkö M BMC Med Genet; 2012 Apr; 13():26. PubMed ID: 22487062 [TBL] [Abstract][Full Text] [Related]
4. Analysis of association of LRP5, LRP6, SOST, DKK1, and CTNNB1 genes with bone mineral density in a Slovenian population. Mencej-Bedrac S; Prezelj J; Kocjan T; Komadina R; Marc J Calcif Tissue Int; 2009 Dec; 85(6):501-6. PubMed ID: 19898734 [TBL] [Abstract][Full Text] [Related]
5. Downregulation of ErbB3 by Wnt3a contributes to wnt-induced osteoblast differentiation in mesenchymal cells. Jullien N; Maudinet A; Leloutre B; Ringe J; Häupl T; Marie PJ J Cell Biochem; 2012 Jun; 113(6):2047-56. PubMed ID: 22274864 [TBL] [Abstract][Full Text] [Related]
6. Structure-based mutation analysis shows the importance of LRP5 beta-propeller 1 in modulating Dkk1-mediated inhibition of Wnt signaling. Bhat BM; Allen KM; Liu W; Graham J; Morales A; Anisowicz A; Lam HS; McCauley C; Coleburn V; Cain M; Fortier E; Bhat RA; Bex FJ; Yaworsky PJ Gene; 2007 Apr; 391(1-2):103-12. PubMed ID: 17276019 [TBL] [Abstract][Full Text] [Related]
7. Dkk1-induced inhibition of Wnt signaling in osteoblast differentiation is an underlying mechanism of bone loss in multiple myeloma. Qiang YW; Barlogie B; Rudikoff S; Shaughnessy JD Bone; 2008 Apr; 42(4):669-80. PubMed ID: 18294945 [TBL] [Abstract][Full Text] [Related]
8. Common genetic variation in the DKK1 gene is associated with hip axis length but not with bone mineral density and bone turnover markers in young adult men: results from the Odense Androgen Study. Piters E; Balemans W; Nielsen TL; Andersen M; Boudin E; Brixen K; Van Hul W Calcif Tissue Int; 2010 Apr; 86(4):271-81. PubMed ID: 20101398 [TBL] [Abstract][Full Text] [Related]
9. Genetic association study of Dickkopf-1 and sclerostin genes with paget disease of bone. Beauregard M; Gagnon E; Guay-Bélanger S; Siris ES; Morissette J; Brown JP; Michou L Calcif Tissue Int; 2013 Nov; 93(5):405-12. PubMed ID: 23836157 [TBL] [Abstract][Full Text] [Related]
10. [Wnt signaling molecules related to osteoporosis]. Kubota T; Ozono K Clin Calcium; 2013 Jun; 23(6):855-60. PubMed ID: 23719498 [TBL] [Abstract][Full Text] [Related]
11. Genetic analyses in a sample of individuals with high or low BMD shows association with multiple Wnt pathway genes. Sims AM; Shephard N; Carter K; Doan T; Dowling A; Duncan EL; Eisman J; Jones G; Nicholson G; Prince R; Seeman E; Thomas G; Wass JA; Brown MA J Bone Miner Res; 2008 Apr; 23(4):499-506. PubMed ID: 18021006 [TBL] [Abstract][Full Text] [Related]
12. Reduced affinity to and inhibition by DKK1 form a common mechanism by which high bone mass-associated missense mutations in LRP5 affect canonical Wnt signaling. Ai M; Holmen SL; Van Hul W; Williams BO; Warman ML Mol Cell Biol; 2005 Jun; 25(12):4946-55. PubMed ID: 15923613 [TBL] [Abstract][Full Text] [Related]
13. Common and rare variants of WNT16, DKK1 and SOST and their relationship with bone mineral density. Martínez-Gil N; Roca-Ayats N; Monistrol-Mula A; García-Giralt N; Díez-Pérez A; Nogués X; Mellibovsky L; Grinberg D; Balcells S Sci Rep; 2018 Jul; 8(1):10951. PubMed ID: 30026596 [TBL] [Abstract][Full Text] [Related]
14. Wnt3a stimulates Mepe, matrix extracellular phosphoglycoprotein, expression directly by the activation of the canonical Wnt signaling pathway and indirectly through the stimulation of autocrine Bmp-2 expression. Cho YD; Kim WJ; Yoon WJ; Woo KM; Baek JH; Lee G; Kim GS; Ryoo HM J Cell Physiol; 2012 Jun; 227(6):2287-96. PubMed ID: 22213482 [TBL] [Abstract][Full Text] [Related]
15. Clinical relevance of genetic polymorphisms in WNT signaling pathway ( Huang Q; Wang CC; Liu YG; Zhao CM; Zhang TP; Liu Y; Wang H Front Immunol; 2022; 13():1011700. PubMed ID: 36569862 [TBL] [Abstract][Full Text] [Related]
16. Expression, purification and functional characterization of Wnt signaling co-receptors LRP5 and LRP6. Fleury D; Vayssiere B; Touitou R; Gillard C; Lebhar H; Rawadi G; Mollat P Protein Expr Purif; 2010 Mar; 70(1):39-47. PubMed ID: 19716419 [TBL] [Abstract][Full Text] [Related]
17. A rate-limiting role for Dickkopf-1 in bone formation and the remediation of bone loss in mouse and primate models of postmenopausal osteoporosis by an experimental therapeutic antibody. Glantschnig H; Scott K; Hampton R; Wei N; McCracken P; Nantermet P; Zhao JZ; Vitelli S; Huang L; Haytko P; Lu P; Fisher JE; Sandhu P; Cook J; Williams D; Strohl W; Flores O; Kimmel D; Wang F; An Z J Pharmacol Exp Ther; 2011 Aug; 338(2):568-78. PubMed ID: 21531794 [TBL] [Abstract][Full Text] [Related]
18. LRP5 gene polymorphisms and idiopathic osteoporosis in men. Ferrari SL; Deutsch S; Baudoin C; Cohen-Solal M; Ostertag A; Antonarakis SE; Rizzoli R; de Vernejoul MC Bone; 2005 Dec; 37(6):770-5. PubMed ID: 16168727 [TBL] [Abstract][Full Text] [Related]
19. Osteoporotic fractures are associated with an 86-base pair repeat polymorphism in the interleukin-1--receptor antagonist gene but not with polymorphisms in the interleukin-1beta gene. Langdahl BL; Løkke E; Carstens M; Stenkjaer LL; Eriksen EF J Bone Miner Res; 2000 Mar; 15(3):402-14. PubMed ID: 10750554 [TBL] [Abstract][Full Text] [Related]
20. Deletion of a single allele of the Dkk1 gene leads to an increase in bone formation and bone mass. Morvan F; Boulukos K; Clément-Lacroix P; Roman Roman S; Suc-Royer I; Vayssière B; Ammann P; Martin P; Pinho S; Pognonec P; Mollat P; Niehrs C; Baron R; Rawadi G J Bone Miner Res; 2006 Jun; 21(6):934-45. PubMed ID: 16753024 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]