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Article

An intermediate form of juvenile Paget's disease caused by a truncating TNFRSF11B mutation

1 Mar 2005

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Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Identifiers

PMID: 15777670
DOI: 10.1016/j.bone.2004.12.004

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Related research

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An intermediate form of juvenile Paget's disease caused by a truncating TNFRSF11B mutationPMID 15777670Read ↗

Juvenile Paget disease with unique compound heterozygous sequence variants in the TNFRSF11B geneSemantic proximity Read ↗

Juvenile Paget's disease with heterozygous duplication within TNFRSF11A encoding RANK.Semantic proximity Read ↗

Genotype-phenotype correlation in juvenile Paget disease: role of molecular alterations of the TNFRSF11B gene.Semantic proximity Read ↗

Juvenile Paget's disease in an Iranian kindred with vitamin D deficiency and novel homozygous TNFRSF11B mutationSemantic proximity Read ↗

A new low-penetrance TNFRSF1A mutation causing atypical periodic fever.Semantic proximity Read ↗

Rare Inherited forms of Paget’s Disease and Related SyndromesSemantic proximity Read ↗

Juvenile Paget's Disease: The Second Reported, Oldest Patient Is Homozygous for the <i>TNFRSF11B</i> “Balkan” Mutation (966_969delTGACinsCTT), Which Elevates Circulating Immunoreactive Osteoprotegerin LevelsSemantic proximity Read ↗

Insertion Mutation in Tnfrsf11a Causes a Paget's Disease-Like Phenotype in Heterozygous Mice and Osteopetrosis in Homozygous Mice.Semantic proximity Read ↗

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Functional consequences of disease-associated mutations in TNFR1 elucidated by transcriptome analysis.Semantic proximity Read ↗

Genetic variation in the TNFRSF11A gene encoding RANK is associated with susceptibility to Paget's disease of bone.Semantic proximity Read ↗

Paget's disease of bone and genetic disorders of RANKL/OPG/RANK/NF-kappaB signaling.Semantic proximity Read ↗

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