Genomewide search in familial Paget disease of bone shows evidence of genetic heterogeneity with candidate loci on chromosomes 2q36, 10p13, and 5q35
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Genetic association study of UCMA/GRP and OPTN genes (PDB6 locus) with Paget's disease of boneTwo siblings with Paget's disease of boneSHIP1 regulates MSC numbers and their osteolineage commitment by limiting induction of the PI3K/Akt/β-catenin/Id2 axis.Paget's disease of bone and genetic disorders of RANKL/OPG/RANK/NF-kappaB signaling.Emerging strategies and therapies for treatment of Paget's disease of bone.Genome-wide association study identifies variants at CSF1, OPTN and TNFRSF11A as genetic risk factors for Paget's disease of bone.Paget disease of bone.Paget's Disease of Bone: A Review of Epidemiology, Pathophysiology and ManagementFine mapping of bone structure and strength QTLs in heterogeneous stock rat.The role of immune cells and inflammatory cytokines in Paget's disease and multiple myeloma.Mechanisms of disease: genetics of Paget's disease of bone and related disorders.Contribution of genetic factors to the pathogenesis of Paget's disease of bone and related disorders.Comparison of genome screens for two independent cohorts provides replication of suggestive linkage of bone mineral density to 3p21 and 1p36.Recurrent mutation of the gene encoding sequestosome 1 (SQSTM1/p62) in Paget disease of boneClinical and Genetic Advances in Paget's Disease of Bone: a Review.Genetic determinants of Paget's disease of bone.Pathogenesis of Paget disease of bone.Characteristics and familial aggregation of Paget's disease of bone in Italy.Targeted sequencing of the Paget's disease associated 14q32 locus identifies several missense coding variants in RIN3 that predispose to Paget's disease of bone.Sequestosome 1: mutation frequencies, haplotypes, and phenotypes in familial Paget's disease of bone.Update on the epidemiology of Paget's disease of bone.Genetic variation in the TNFRSF11A gene encoding RANK is associated with susceptibility to Paget's disease of bone.Molecular effect of an OPTN common variant associated to Paget's disease of bone.Rab GTPases in Osteoclastic Endomembrane SystemsCan zebrafish be a valid model to study Paget's disease of bone?
P2860
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P2860
Genomewide search in familial Paget disease of bone shows evidence of genetic heterogeneity with candidate loci on chromosomes 2q36, 10p13, and 5q35
description
2001 nî lūn-bûn
@nan
2001 թուականի Սեպտեմբերին հրատարակուած գիտական յօդուած
@hyw
2001 թվականի սեպտեմբերին հրատարակված գիտական հոդված
@hy
2001年の論文
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2001年論文
@yue
2001年論文
@zh-hant
2001年論文
@zh-hk
2001年論文
@zh-mo
2001年論文
@zh-tw
2001年论文
@wuu
name
Genomewide search in familial ...... omosomes 2q36, 10p13, and 5q35
@ast
Genomewide search in familial ...... omosomes 2q36, 10p13, and 5q35
@en
Genomewide search in familial ...... omosomes 2q36, 10p13, and 5q35
@nl
type
label
Genomewide search in familial ...... omosomes 2q36, 10p13, and 5q35
@ast
Genomewide search in familial ...... omosomes 2q36, 10p13, and 5q35
@en
Genomewide search in familial ...... omosomes 2q36, 10p13, and 5q35
@nl
prefLabel
Genomewide search in familial ...... omosomes 2q36, 10p13, and 5q35
@ast
Genomewide search in familial ...... omosomes 2q36, 10p13, and 5q35
@en
Genomewide search in familial ...... omosomes 2q36, 10p13, and 5q35
@nl
P2093
P2860
P356
P1476
Genomewide search in familial ...... omosomes 2q36, 10p13, and 5q35
@en
P2093
Bennett ST
Herbert CA
Hocking LJ
Nicholls RK
Nicholson GC
Ralston SH
P2860
P304
P356
10.1086/323798
P407
P577
2001-09-05T00:00:00Z