Paget's disease of bone: evidence for a susceptibility locus on chromosome 18q and for genetic heterogeneity
about
Paget disease of bone: mapping of two loci at 5q35-qter and 5q31.Mutations in TNFRSF11A, affecting the signal peptide of RANK, cause familial expansile osteolysisProtocol for stage 1 of the GaP study (Genetic testing acceptability for Paget's disease of bone): an interview study about genetic testing and preventive treatment: would relatives of people with Paget's disease want testing and treatment if they wThe role of osteogenic cells in the pathophysiology of Paget's disease.Common mechanisms of osteosarcoma and Paget's disease.Receptor activator of nuclear factor-kappaB ligand and osteoprotegerin: potential implications for the pathogenesis and treatment of malignant bone diseases.Genomewide search in familial Paget disease of bone shows evidence of genetic heterogeneity with candidate loci on chromosomes 2q36, 10p13, and 5q35Paget's disease of bone and genetic disorders of RANKL/OPG/RANK/NF-kappaB signaling.The genetics of osteosarcoma.Principles of management of osteometabolic disorders affecting the aging spine.Paget disease of bone.Paget's Disease of Bone: A Review of Epidemiology, Pathophysiology and ManagementThe spine in Paget's diseaseRecurrent mutation of the gene encoding sequestosome 1 (SQSTM1/p62) in Paget disease of boneLinkage of Paget disease of bone to a novel region on human chromosome 18q23.Runx2, p53, and pRB status as diagnostic parameters for deregulation of osteoblast growth and differentiation in a new pre-chemotherapeutic osteosarcoma cell line (OS1).Clinical and Genetic Advances in Paget's Disease of Bone: a Review.c-FMS inhibitors: a patent review.Pathogenesis of Paget disease of bone.A nonsynonymous TNFRSF11A variation increases NFκB activity and the severity of Paget's disease.Inheritance of osteosarcoma and Paget's disease of bone: a familial loss of heterozygosity studyGenetic variation in the TNFRSF11A gene encoding RANK is associated with susceptibility to Paget's disease of bone.Paget's disease with craniofacial and skeletal bone involvement.A putative role for c-Fos in the pathophysiology of Paget's disease.Molecular effect of an OPTN common variant associated to Paget's disease of bone.Lack of mutations in the RANK gene in Spanish patients with Paget disease of bone
P2860
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P2860
Paget's disease of bone: evidence for a susceptibility locus on chromosome 18q and for genetic heterogeneity
description
1998 nî lūn-bûn
@nan
1998 թուականի Յունիսին հրատարակուած գիտական յօդուած
@hyw
1998 թվականի հունիսին հրատարակված գիտական հոդված
@hy
1998年の論文
@ja
1998年論文
@yue
1998年論文
@zh-hant
1998年論文
@zh-hk
1998年論文
@zh-mo
1998年論文
@zh-tw
1998年论文
@wuu
name
Paget's disease of bone: evide ...... and for genetic heterogeneity
@ast
Paget's disease of bone: evide ...... and for genetic heterogeneity
@en
Paget's disease of bone: evide ...... and for genetic heterogeneity
@nl
type
label
Paget's disease of bone: evide ...... and for genetic heterogeneity
@ast
Paget's disease of bone: evide ...... and for genetic heterogeneity
@en
Paget's disease of bone: evide ...... and for genetic heterogeneity
@nl
prefLabel
Paget's disease of bone: evide ...... and for genetic heterogeneity
@ast
Paget's disease of bone: evide ...... and for genetic heterogeneity
@en
Paget's disease of bone: evide ...... and for genetic heterogeneity
@nl
P2093
P1476
Paget's disease of bone: evide ...... and for genetic heterogeneity
@en
P2093
A Morales-Piga
J L San-Millan
K Nakatsuka
N E Haites
S H Ralston
S I Haslam
W Balemans
P356
10.1359/JBMR.1998.13.6.911
P407
P577
1998-06-01T00:00:00Z