Pages that link to "Q57534153"
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The following pages link to Mutation Screening of the TNFRSF11A Gene Encoding Receptor Activator of NFkB (RANK) in Familial and Sporadic Paget's Disease of Bone and Osteosarcoma (Q57534153):
Displaying 26 items.
- Paget disease of bone: mapping of two loci at 5q35-qter and 5q31. (Q24535825) (← links)
- Segregation of a M404V mutation of the p62/sequestosome 1 (p62/SQSTM1) gene with polyostotic Paget's disease of bone in an Italian family (Q24812895) (← links)
- Early onset Paget's disease of bone caused by a novel mutation (78dup27) of the TNFRSF11A gene in a Chinese family (Q33552815) (← links)
- Genomewide search in familial Paget disease of bone shows evidence of genetic heterogeneity with candidate loci on chromosomes 2q36, 10p13, and 5q35 (Q34113018) (← links)
- Paget's disease of bone and genetic disorders of RANKL/OPG/RANK/NF-kappaB signaling (Q34546256) (← links)
- Osteosarcoma in Paget's disease of bone (Q34574123) (← links)
- Pathogenesis and management of Paget's disease of bone. (Q34795095) (← links)
- Emerging strategies and therapies for treatment of Paget’s disease of bone (Q34987305) (← links)
- Updates on the cytogenetics and molecular genetics of bone and soft tissue tumors: osteosarcoma and related tumors (Q35186715) (← links)
- Panostotic expansile bone disease with massive jaw tumor formation and a novel mutation in the signal peptide of RANK. (Q35568480) (← links)
- Mechanisms of disease: genetics of Paget's disease of bone and related disorders (Q36577488) (← links)
- Contribution of genetic factors to the pathogenesis of Paget's disease of bone and related disorders (Q36710160) (← links)
- Osteosarcoma development and stem cell differentiation (Q36803600) (← links)
- RANKL inhibition for the management of patients with benign metabolic bone disorders. (Q37532561) (← links)
- Pathogenesis of Paget disease of bone. (Q38006389) (← links)
- A nonsynonymous TNFRSF11A variation increases NFκB activity and the severity of Paget's disease (Q39460310) (← links)
- Paget's disease of bone in Italy. (Q39782394) (← links)
- Inheritance of osteosarcoma and Paget's disease of bone: a familial loss of heterozygosity study (Q42040310) (← links)
- Update: Cytokine Dysregulation in Chronic Nonbacterial Osteomyelitis (CNO) (Q42182068) (← links)
- Familial expansive osteolysis otological and dental manifestations of genetic origin (Q45265379) (← links)
- Familial sarcoma: challenging pedigrees (Q47416952) (← links)
- Genetic variation in the TNFRSF11A gene encoding RANK is associated with susceptibility to Paget's disease of bone (Q51558602) (← links)
- Three Novel Mutations in SQSTM1 Identified in Familial Paget's Disease of Bone (Q52552380) (← links)
- RANK-Fc inhibits malignancy via inhibiting ERK activation and evoking caspase-3-mediated anoikis in human osteosarcoma cells. (Q54681646) (← links)
- Chronic recurrent multifocal osteomyelitis (CRMO): evidence for a susceptibility gene located on chromosome 18q21.3-18q22 (Q57251883) (← links)
- Guidelines for diagnosis and management of Paget's disease of bone in Japan (Q64046430) (← links)