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Article

Evidence for a Novel Osteosarcoma Tumor-Suppressor Gene in the Chromosome 18 Region Genetically Linked with Paget Disease of Bone

1 Sept 1998

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Source

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Identifiers

PMID: 9718349
DOI: 10.1086/302019

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Related research

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Research trail→

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Evidence for a Novel Osteosarcoma Tumor-Suppressor Gene in the Chromosome 18 Region Genetically Linked with Paget Disease of BonePMID 9718349Read ↗

Inheritance of osteosarcoma and Paget's disease of bone: a familial loss of heterozygosity study.Semantic proximity Read ↗

Familial Paget's disease of bone: nonlinkage to the PDB1 and PDB2 loci on chromosomes 6p and 18q in a large pedigree.Semantic proximity Read ↗

Common mechanisms of osteosarcoma and paget's diseaseSemantic proximity Read ↗

Familial Paget’s disease of bone: patterns of inheritance and frequency of linkage to chromosome 18qSemantic proximity Read ↗

Genomewide Search in Familial Paget Disease of Bone Shows Evidence of Genetic Heterogeneity with Candidate Loci on Chromosomes 2q36, 10p13, and 5q35Semantic proximity Read ↗

Paget's disease of bone: evidence for a susceptibility locus on chromosome 18q and for genetic heterogeneity.Semantic proximity Read ↗

Comparative genomic hybridization analysis identifies gains of 1p35∼p36 and chromosome 19 in osteosarcomaSemantic proximity Read ↗

Linkage of Paget disease of bone to a novel region on human chromosome 18q23.Semantic proximity Read ↗

Genetic linkage of Paget disease of the bone to chromosome 18q.Semantic proximity Read ↗

Genetic linkage of familial expansile osteolysis to chromosome 18qSemantic proximity Read ↗

The der(17)t(X;17)(p11;q25) of human alveolar soft part sarcoma fuses the TFE3 transcription factor gene to ASPL, a novel gene at 17q25Semantic proximity Read ↗

Mutation screening of the TNFRSF11A gene encoding receptor activator of NF kappa B (RANK) in familial and sporadic Paget's disease of bone and osteosarcoma.Semantic proximity Read ↗

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