Phenotypic dissection of bone mineral density reveals skeletal site specificity and facilitates the identification of novel loci in the genetic regulation of bone mass attainment.
about
A new WNT on the bone: WNT16, cortical bone thickness, porosity and fracturesNovel genetic loci underlying human intracranial volume identified through genome-wide associationDifferential Recognition Preferences of the Three Src Homology 3 (SH3) Domains from the Adaptor CD2-associated Protein (CD2AP) and Direct Association with Ras and Rab Interactor 3 (RIN3).Integrating GWAS and Co-expression Network Data Identifies Bone Mineral Density Genes SPTBN1 and MARK3 and an Osteoblast Functional Module.Network Analysis Implicates Alpha-Synuclein (Snca) in the Regulation of Ovariectomy-Induced Bone LossIntegrative Analysis of Genomics and Transcriptome Data to Identify Potential Functional Genes of BMDs in Females.Genetic factors influencing the risk of multiple myeloma bone diseaseQuantitative imaging methods in osteoporosis.Challenges in conducting genome-wide association studies in highly admixed multi-ethnic populations: the Generation R Study.Genetic variants in adult bone mineral density and fracture risk genes are associated with the rate of bone mineral density acquisition in adolescenceUsing whole-genome sequences of the LG/J and SM/J inbred mouse strains to prioritize quantitative trait genes and nucleotides.A trans-ethnic genome-wide association study identifies gender-specific loci influencing pediatric aBMD and BMC at the distal radius.A genome-wide association study of body mass index across early life and childhoodGenetic Risk Scores Implicated in Adult Bone Fragility Associate With Pediatric Bone Density.Osteoblast-Specific Overexpression of Human WNT16 Increases Both Cortical and Trabecular Bone Mass and Structure in MiceBone Mass and Strength in School-Age Children Exhibit Sexual Dimorphism Related to Differences in Lean Mass: The Generation R Study.SNP- and haplotype-based genome-wide association studies for growth, carcass, and meat quality traits in a Duroc multigenerational population.Bone Mass and Strength are Significantly Improved in Mice Overexpressing Human WNT16 in Osteocytes.Using Genetic Variation to Explore the Causal Effect of Maternal Pregnancy Adiposity on Future Offspring Adiposity: A Mendelian Randomisation Study.BMD Loci Contribute to Ethnic and Developmental Differences in Skeletal Fragility across Populations: Assessment of Evolutionary Selection Pressures.Sixteen new lung function signals identified through 1000 Genomes Project reference panel imputationThe case for genome-wide association studies of bone acquisition in paediatric and adolescent populationsGenetics of pediatric bone strengthA genetic factor associated with low final bone mineral density in children after a long-term glucocorticoids treatment.Using Mendelian randomization to investigate a possible causal relationship between adiposity and increased bone mineral density at different skeletal sites in childrenRSPO3-LGR4 Regulates Osteogenic Differentiation Of Human Adipose-Derived Stem Cells Via ERK/FGF Signalling.Identification of IDUA and WNT16 Phosphorylation-Related Non-Synonymous Polymorphisms for Bone Mineral Density in Meta-Analyses of Genome-Wide Association Studies.The WNT system: background and its role in bone.Osteocyte-specific WNT1 regulates osteoblast function during bone homeostasisHow rare bone diseases have informed our knowledge of complex diseases.An Emerging Regulatory Landscape for Skeletal Development.Genetic Associations with Gestational Duration and Spontaneous Preterm Birth.Identification of 153 new loci associated with heel bone mineral density and functional involvement of GPC6 in osteoporosis.Bivariate genome-wide association meta-analysis of pediatric musculoskeletal traits reveals pleiotropic effects at the SREBF1/TOM1L2 locus.The Generation R Study: Biobank update 2015.A Genomewide Association Study Identifies Two Sex-Specific Loci, at SPTB and IZUMO3, Influencing Pediatric Bone Mineral Density at Multiple Skeletal Sites.Genetically Determined Later Puberty Impacts Lowered Bone Mineral Density in Childhood and Adulthood.A molecular roadmap of the AGM region reveals BMPER as a novel regulator of HSC maturation.Life-Course Genome-wide Association Study Meta-analysis of Total Body BMD and Assessment of Age-Specific Effects.Increased Ca2+ signaling through CaV1.2 promotes bone formation and prevents estrogen deficiency-induced bone loss.
P2860
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P2860
Phenotypic dissection of bone mineral density reveals skeletal site specificity and facilitates the identification of novel loci in the genetic regulation of bone mass attainment.
description
2014 nî lūn-bûn
@nan
2014 թուականի Յունիսին հրատարակուած գիտական յօդուած
@hyw
2014 թվականի հունիսին հրատարակված գիտական հոդված
@hy
2014年の論文
@ja
2014年論文
@yue
2014年論文
@zh-hant
2014年論文
@zh-hk
2014年論文
@zh-mo
2014年論文
@zh-tw
2014年论文
@wuu
name
Phenotypic dissection of bone ...... ation of bone mass attainment.
@ast
Phenotypic dissection of bone ...... ation of bone mass attainment.
@en
type
label
Phenotypic dissection of bone ...... ation of bone mass attainment.
@ast
Phenotypic dissection of bone ...... ation of bone mass attainment.
@en
prefLabel
Phenotypic dissection of bone ...... ation of bone mass attainment.
@ast
Phenotypic dissection of bone ...... ation of bone mass attainment.
@en
P2093
P2860
P50
P1433
P1476
Phenotypic dissection of bone ...... ation of bone mass attainment.
@en
P2093
Claudia J Kruithof
Daniel L Koller
Denise H M Heppe
Elin Grundberg
Jeroen van de Peppel
Jonathan H Tobias
Kaare Gautvik
Karol Estrada
P2860
P304
P356
10.1371/JOURNAL.PGEN.1004423
P50
P577
2014-06-19T00:00:00Z