✦ LIBER ✦

Identification of Sex-Specific Associations Between Polymorphisms of the Osteoprotegerin Gene, TNFRSF11B, and Paget's Disease of Bone

✍ Scribed by Greet Beyens; Anna Daroszewska; Fenna de Freitas; Erik Fransen; Filip Vanhoenacker; Leon Verbruggen; Hans-Georg Zmierczak; René Westhovens; Jan Van Offel; Stuart H Ralston; Jean-Pierre Devogelaer; Wim Van Hul

Book ID: 111485501
Publisher: American Society for Bone and Mineral Research
Year: 2007
Tongue: English
Weight: 815 KB
Volume: 22
Category: Article
ISSN: 0884-0431
DOI: 10.1359/jbmr.070333

No coin nor oath required. For personal study only.

📜 SIMILAR VOLUMES

No association between variants of the T

No association between variants of the TNFRSF11B gene and Paget's disease of bone

✍ N. Alonso; O.M. Albagha; S.H. Ralston 📂 Article 📅 2011 🏛 Elsevier Science 🌐 English ⚖ 58 KB

Genetic variation in the TNFRSF11A gene

Genetic variation in the TNFRSF11A gene encoding RANK is associated with susceptibility to Paget's disease of bone

✍ Pui Yan Jenny Chung; Greet Beyens; Philip L Riches; Liesbeth Van Wesenbeeck; Fen 📂 Article 📅 2010 🏛 American Society for Bone and Mineral Research 🌐 English ⚖ 494 KB 👁 1 views

Identification of a novel mutation (78du

Identification of a novel mutation (78dup27) of the TNFRSF11A gene in a Chinese family with early onset Paget's disease of bone

✍ Zhenlin Zhang 📂 Article 📅 2008 🏛 Elsevier Science 🌐 English ⚖ 71 KB

Mutation Screening of the TNFRSF11A Gene

Mutation Screening of the TNFRSF11A Gene Encoding Receptor Activator of NFkB (RANK) in Familial and Sporadic Paget's Disease of Bone and Osteosarcoma

✍ A.B. Sparks; S.N. Peterson; C. Bell; B.J. Loftus; L. Hocking; D.P. Cahill; F.J. 📂 Article 📅 2001 🏛 Springer 🌐 English ⚖ 207 KB

Indications for a genetic association of

Indications for a genetic association of a VCP polymorphism with the pathogenesis of sporadic Paget's disease of bone, but not for TNFSF11 (RANKL) and IL-6 polymorphisms

✍ Pui Yan Jenny Chung; Greet Beyens; Fenna de Freitas; Steven Boonen; Piet Geusens 📂 Article 📅 2011 🏛 Elsevier Science 🌐 English ⚖ 236 KB

Familial Paget's disease in The Netherla

Familial Paget's disease in The Netherlands: Occurrence, identification of new mutations in the sequestosome 1 gene, and their clinical associations

✍ E. W. M. Eekhoff; M. Karperien; D. Houtsma; A. H. Zwinderman; C. Dragoiescu; A. 📂 Article 📅 2004 🏛 John Wiley and Sons 🌐 English ⚖ 103 KB 👁 2 views

## Abstract ## Objective To estimate the occurrence of familial Paget's disease of bone in The Netherlands, to examine the prevalence of mutations of the sequestosome 1 gene (__SQSTM1__) in identified families, and to assess potential genotype–phenotype associations. ## Methods We performed a ca