Nonsense mutation in the LGR4 gene is associated with several human diseases and other traits. - Wikidata - wikimedia - TriplyDB

Nonsense mutation in the LGR4 gene is associated with several human diseases and other traits.

Nonsense mutation in the LGR4 gene is associated with several human diseases and other traits.

http://www.wikidata.org/entity/Q44274525

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RANK-RANKL signalling in cancer Gene-Lifestyle Interactions in Complex Diseases: Design and Description of the GLACIER and VIKING Studies LGR4 Is a Direct Target of MicroRNA-34a and Modulates the Proliferation and Migration of Retinal Pigment Epithelial ARPE-19 Cells Genome of The Netherlands population-specific imputations identify an ABCA6 variant associated with cholesterol levels Gene-based rare allele analysis identified a risk gene of Alzheimer's disease Genomic view of bipolar disorder revealed by whole genome sequencing in a genetic isolate Rare variants of large effect in BRCA2 and CHEK2 affect risk of lung cancer Dissecting the genetics of complex traits using summary association statistics Using GWAS to identify novel therapeutic targets for osteoporosis.Whole-genome sequencing identifies EN1 as a determinant of bone density and fracture.Mutations in eIF4ENIF1 are associated with primary ovarian insufficiency.Wnt-responsive cancer stem cells are located close to distorted blood vessels and not in hypoxic regions in a p53-null mouse model of human breast cancer.Efficient Bayesian mixed-model analysis increases association power in large cohorts.The impact of rare and low-frequency genetic variants in common disease Local control of intestinal stem cell homeostasis by enteroendocrine cells in the adult Drosophila midgut 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.Genome-wide Association Studies for Osteoporosis: A 2013 Update.Genomic variability in Mexican chicken population using copy number variants.The association between the baseline bone resorption marker CTX and incident dysglycemia after 4 years Distribution and medical impact of loss-of-function variants in the Finnish founder population.Sequencing an Ashkenazi reference panel supports population-targeted personal genomics and illuminates Jewish and European origins.The revolution in human monogenic disease mapping.Variants in ELL2 influencing immunoglobulin levels associate with multiple myeloma.Analysis of LGR4 receptor distribution in human and mouse tissues Targeted deletion of the murine Lgr4 gene decreases lens epithelial cell resistance to oxidative stress and induces age-related cataract formation.A Splice Region Variant in LDLR Lowers Non-high Density Lipoprotein Cholesterol and Protects against Coronary Artery Disease.Common and rare variants associated with kidney stones and biochemical traits.A rare IL33 loss-of-function mutation reduces blood eosinophil counts and protects from asthma.Interactions within the MHC contribute to the genetic architecture of celiac disease Two-Variance-Component Model Improves Genetic Prediction in Family Datasets.Bivariate Genome-Wide Association Study Implicates ATP6V1G1 as a Novel Pleiotropic Locus Underlying Osteoporosis and Age at Menarche Sequence variants in the PTCH1 gene associate with spine bone mineral density and osteoporotic fractures.A Common Variant in CLDN14 is Associated with Primary Biliary Cirrhosis and Bone Mineral Density Common and rare variants associating with serum levels of creatine kinase and lactate dehydrogenase.A large genome-wide association study of age-related macular degeneration highlights contributions of rare and common variants.Identification of Common Genetic Variants Influencing Spontaneous Dizygotic Twinning and Female Fertility.The Tohoku Medical Megabank Project: Design and Mission.Pubertal timing and bone phenotype in early old age: findings from a British birth cohort study.HLA class II sequence variants influence tuberculosis risk in populations of European ancestry.Epigenetic and genetic components of height regulation.

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P2860

Nonsense mutation in the LGR4 gene is associated with several human diseases and other traits.

http://www.wikidata.org/entity/Q44274525

description

2013 nî lūn-bûn

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2013年の論文

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2013年学术文章

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2013年学术文章

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2013年学术文章

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2013年学术文章

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2013年学术文章

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2013年學術文章

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2013年學術文章

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2013年學術文章

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name

Nonsense mutation in the LGR4 ...... man diseases and other traits.

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Nonsense mutation in the LGR4 ...... man diseases and other traits.

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Nonsense mutation in the LGR4 ...... man diseases and other traits.

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Nonsense mutation in the LGR4 ...... man diseases and other traits.

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Nonsense mutation in the LGR4 ...... man diseases and other traits.

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Nonsense mutation in the LGR4 ...... man diseases and other traits.

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Nonsense mutation in the LGR4 ...... man diseases and other traits.

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Adalbjorg Jonasdottir

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Agnar Helgason

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Asgeir Sigurdsson

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Asgeir Theodors

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Aslaug Jonasdottir

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Claus Christiansen

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Erikur Steingrimsson

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G Bragi Walters

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Gisli Masson

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Gudmundur I Eyjolfsson

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P2860

Twenty bone-mineral-density loci identified by large-scale meta-analysis of genome-wide association studies

R-spondins function as ligands of the orphan receptors LGR4 and LGR5 to regulate Wnt/beta-catenin signaling

Lgr5 homologues associate with Wnt receptors and mediate R-spondin signalling

Cellular signaling and biological functions of R-spondins

New sequence variants associated with bone mineral density

Regulation of bone formation and remodeling by G-protein-coupled receptor 48

Defective postnatal development of the male reproductive tract in LGR4 knockout mice

Gene inactivation and its implications for annotation in the era of personal genomics

Association of JAG1 with bone mineral density and osteoporotic fractures: a genome-wide association study and follow-up replication studies.

Genome-wide association study using extreme truncate selection identifies novel genes affecting bone mineral density and fracture risk

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Gudmar Thorleifsson

Unnur Þorsteinsdóttir

Daniel F Gudbjartsson

Unnur Styrkarsdottir

Laufey Tryggvadottir

Asmundur Oddsson

Jacqueline R. Center

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2013-05-05T00:00:00Z

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