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Year Number of Results
1997 1
1998 11
1999 13
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2001 40
2002 56
2003 65
2004 67
2005 59
2006 51
2007 17
2008 27
2009 25
2010 37
2011 38
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1,031 results

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Page 1
TNFRSF11B gene polymorphisms, bone mineral density, and fractures in Slovak postmenopausal women.
Boroňová I, Bernasovská J, Mačeková S, Petrejčíková E, Tomková Z, Kľoc J, Poráčová J, Blaščáková MM, Litavcová E. Boroňová I, et al. J Appl Genet. 2015 Feb;56(1):57-63. doi: 10.1007/s13353-014-0247-4. Epub 2014 Oct 17. J Appl Genet. 2015. PMID: 25323794
The polymorphism T245G (rs3134069) in the TNFRSF11B gene could be used together with other genetic markers to identify individuals at high risk of osteoporotic fractures. The results from the present study provided more evidence to reveal the role of TNFRSF11B
The polymorphism T245G (rs3134069) in the TNFRSF11B gene could be used together with other genetic markers to identify individ …
Pathogenesis of osteoporosis: concepts, conflicts, and prospects.
Raisz LG. Raisz LG. J Clin Invest. 2005 Dec;115(12):3318-25. doi: 10.1172/JCI27071. J Clin Invest. 2005. PMID: 16322775 Free PMC article. Review.
There are multiple mechanisms underlying the regulation of bone remodeling, and these involve not only the osteoblastic and osteoclastic cell lineages but also other marrow cells, in addition to the interaction of systemic hormones, local cytokines, growth factors, and transcript …
There are multiple mechanisms underlying the regulation of bone remodeling, and these involve not only the osteoblastic and osteoclastic cel …
Genotype-phenotype correlation in juvenile Paget disease: role of molecular alterations of the TNFRSF11B gene.
Brunetti G, Marzano F, Colucci S, Ventura A, Cavallo L, Grano M, Faienza MF. Brunetti G, et al. Endocrine. 2012 Oct;42(2):266-71. doi: 10.1007/s12020-012-9705-0. Epub 2012 May 26. Endocrine. 2012. PMID: 22638612 Review.
The patients affected with JPD present an altered bone turnover, therefore, show a phenotype characterized by progressive bone deformities, fractures, and short stature. Deletions or missense mutations of the TNFRSN11B gene are common in these children. This gene en …
The patients affected with JPD present an altered bone turnover, therefore, show a phenotype characterized by progressive bone deformities, …
TNFRSF11B gene polymorphisms 1181G > C and 245T > G as well as haplotype CT influence bone mineral density in postmenopausal women.
Mencej-Bedrač S, Preželj J, Marc J. Mencej-Bedrač S, et al. Maturitas. 2011 Jul;69(3):263-7. doi: 10.1016/j.maturitas.2011.02.010. Epub 2011 Mar 15. Maturitas. 2011. PMID: 21411255
As variations in the TNFRSF11B gene could alter the susceptibility to osteoporosis, the aim of study was to investigate association of two TNFRSF11B gene polymorphisms with BMD and serum OPG concentration in postmenopausal women. STUDY DESIGN: 478 post …
As variations in the TNFRSF11B gene could alter the susceptibility to osteoporosis, the aim of study was to investigate associ …
Exclusion of TNFRSF11B as Candidate Gene for Otosclerosis in Campania Population.
Iossa S, Morello G, Esposito T, Corvino V, Giannini P, Salvato R, Cavaliere M, Panetti M, Panetti G, Piantedosi B, Gianfrancesco F, Marciano E, Franzè A. Iossa S, et al. Indian J Otolaryngol Head Neck Surg. 2014 Sep;66(3):297-301. doi: 10.1007/s12070-014-0706-6. Epub 2014 Jan 30. Indian J Otolaryngol Head Neck Surg. 2014. PMID: 25032118 Free PMC article.
The etiopathogenesis of otosclerosis seems similar to that occurring in Paget's disease of bone, for which mutations or polymorphisms in several genes have been identified. Among these, TNFRSF11B gene encoding the osteoprotegerin is produced at high levels in …
The etiopathogenesis of otosclerosis seems similar to that occurring in Paget's disease of bone, for which mutations or polymorphisms in sev …
Juvenile Paget disease.
Polyzos SA, Cundy T, Mantzoros CS. Polyzos SA, et al. Metabolism. 2018 Mar;80:15-26. doi: 10.1016/j.metabol.2017.10.007. Epub 2017 Nov 22. Metabolism. 2018. PMID: 29080812 Review.
Juvenile Paget disease (JPD) is a rare disorder, mainly caused by mutations in the gene TNFRSF11B that encodes osteoprotegerin (OPG). Loss of OPG action causes generalized, extremely rapid bone turnover. ...The severity of the phenotype seems to be related to the se …
Juvenile Paget disease (JPD) is a rare disorder, mainly caused by mutations in the gene TNFRSF11B that encodes osteoprotegerin …
TNFRSF11B activates Wnt/beta-catenin signaling and promotes gastric cancer progression.
Luan F, Li X, Cheng X, Huangfu L, Han J, Guo T, Du H, Wen X, Ji J. Luan F, et al. Int J Biol Sci. 2020 Apr 25;16(11):1956-1971. doi: 10.7150/ijbs.43630. eCollection 2020. Int J Biol Sci. 2020. PMID: 32398963 Free PMC article.
However, little is unveiled regarding the complex mechanisms of TNFRSF11B in human gastric cancer (GC). The clinical significance of TNFRSF11B was assessed in 70 and 160 GC tissues using immunohistochemistry method and gene microarray analysis, respectively. …
However, little is unveiled regarding the complex mechanisms of TNFRSF11B in human gastric cancer (GC). The clinical significance of …
TNFRSF11B gene variants and bone mineral density in postmenopausal women in Malta.
Vidal C, Brincat M, Xuereb Anastasi A. Vidal C, et al. Maturitas. 2006 Mar 20;53(4):386-95. doi: 10.1016/j.maturitas.2005.11.003. Epub 2005 Dec 15. Maturitas. 2006. PMID: 16343827
OBJECTIVE: In this study, three single nucleotide polymorphisms (SNPs) within the TNFRSF11B gene were studied for association with an increased risk of osteoporosis in postmenopausal Maltese women (n=126). ...Statistical significance was reached when constructing ha …
OBJECTIVE: In this study, three single nucleotide polymorphisms (SNPs) within the TNFRSF11B gene were studied for association …
The role of TNFRSF11B in development of osteoarthritic cartilage.
Rodríguez Ruiz A, Tuerlings M, Das A, Coutinho de Almeida R, Suchiman HED, Nelissen RGHH, Ramos YFM, Meulenbelt I. Rodríguez Ruiz A, et al. Rheumatology (Oxford). 2022 Feb 2;61(2):856-864. doi: 10.1093/rheumatology/keab440. Rheumatology (Oxford). 2022. PMID: 33989379 Free PMC article.
OBJECTIVES: OA is a complex genetic disease with different risk factors contributing to its development. One of the genes, TNFRSF11B, previously identified with gain-of-function mutation in a family with early-onset OA with chondrocalcinosis, is among the highest up …
OBJECTIVES: OA is a complex genetic disease with different risk factors contributing to its development. One of the genes, TNFRSF1
TNFRSF11B gene haplotype and its association with bone mineral density variations in postmenopausal Mexican-Mestizo women.
Rojano-Mejía D, Coral-Vázquez RM, Espinosa LC, Romero-Hidalgo S, López-Medina G, García Mdel C, Coronel A, Ibarra R, Canto P. Rojano-Mejía D, et al. Maturitas. 2012 Jan;71(1):49-54. doi: 10.1016/j.maturitas.2011.10.009. Epub 2011 Nov 10. Maturitas. 2012. PMID: 22079369
The tumor necrosis factor receptor superfamily, member 11b (TNFRSF11B) gene, has been investigated in relation to BMD. Three polymorphisms in/nearby TNFRSF11B have been associated with BMD variations in some populations. ...DNA was obtained from blood leukocy …
The tumor necrosis factor receptor superfamily, member 11b (TNFRSF11B) gene, has been investigated in relation to BMD. Three p …
1,031 results