A genome-wide perspective of genetic variation in human metabolism. - Wikidata - awgldk - TriplyDB

A genome-wide perspective of genetic variation in human metabolism.

A genome-wide perspective of genetic variation in human metabolism.

http://www.wikidata.org/entity/Q34090221

about

A genome-wide metabolic QTL analysis in Europeans implicates two loci shaped by recent positive selection Discovery of sexual dimorphisms in metabolic and genetic biomarkers GWAS of 126,559 individuals identifies genetic variants associated with educational attainment Cohort Profile: TwinsUK and healthy ageing twin study Metabolomics and Type 2 Diabetes: Translating Basic Research into Clinical Application Neuroinflammation and comorbidities are frequently ignored factors in CNS pathology Metabolomics and cardiovascular biomarker discovery Genetics of human metabolism: an update Obesity and psychotic disorders: uncovering common mechanisms through metabolomics Guidelines for the design, analysis and interpretation of 'omics' data: focus on human endometrium Metabolomics in the studies of islet autoimmunity and type 1 diabetes Inflammatory-induced hibernation in the fetus: priming of fetal sheep metabolism correlates with developmental brain injury Metabolic and Phenotypic Differences between Mice Producing a Werner Syndrome Helicase Mutant Protein and Wrn Null Mice Preservation of metabolic flexibility in skeletal muscle by a combined use of n-3 PUFA and rosiglitazone in dietary obese mice Genome-wide association study identifies novel genetic variants contributing to variation in blood metabolite levels Plasma Acylcarnitines and Amino Acid Levels As an Early Complex Biomarker of Propensity to High-Fat Diet-Induced Obesity in Mice Genetic variation in lipid desaturases and its impact on the development of human disease ASXL1 exon 12 mutations are frequent in AML with intermediate risk karyotype and are independently associated with an adverse outcome.Metabolomics in epidemiology: from metabolite concentrations to integrative reaction networks Human metabolic individuality in biomedical and pharmaceutical research Structuring research methods and data with the research object model: genomics workflows as a case study Genome-wide association study identifies multiple loci influencing human serum metabolite levels Long-chain acyl-CoA dehydrogenase deficiency as a cause of pulmonary surfactant dysfunction Addressing human variability in next-generation human health risk assessments of environmental chemicals Unmasking differential effects of rosiglitazone and pioglitazone in the combination treatment with n-3 fatty acids in mice fed a high-fat diet Mining the unknown: a systems approach to metabolite identification combining genetic and metabolic information.Automated workflow-based exploitation of pathway databases provides new insights into genetic associations of metabolite profiles Genome-wide association study of metabolic traits reveals novel gene-metabolite-disease links Accurate, fully-automated NMR spectral profiling for metabolomics Genetic Influences on Metabolite Levels: A Comparison across Metabolomic Platforms ELOVL2 controls the level of n-6 28:5 and 30:5 fatty acids in testis, a prerequisite for male fertility and sperm maturation in mice Genome-wide screen for metabolic syndrome susceptibility Loci reveals strong lipid gene contribution but no evidence for common genetic basis for clustering of metabolic syndrome traits Two new ArrayTrack libraries for personalized biomedical research Mixing omics: combining genetics and metabolomics to study rheumatic diseases.New quantitative trait loci for carotid atherosclerosis identified in an intercross derived from apolipoprotein E-deficient mouse strains.Genetic analysis of atherosclerosis and glucose homeostasis in an intercross between C57BL/6 and BALB/cJ apolipoprotein E-deficient mice.Juvenile cataract-associated mutation of solute carrier SLC16A12 impairs trafficking of the protein to the plasma membrane.A systems biology approach using metabolomic data reveals genes and pathways interacting to modulate divergent growth in cattle.Validated and predictive processing of gas chromatography-mass spectrometry based metabolomics data for large scale screening studies, diagnostics and metabolite pattern verification.PATZ1 down-regulates FADS1 by binding to rs174557 and is opposed by SP1/SREBP1c.

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A genome-wide perspective of genetic variation in human metabolism.

http://www.wikidata.org/entity/Q34090221

description

2009 nî lūn-bûn

@nan

2009 թուականի Դեկտեմբերին հրատարակուած գիտական յօդուած

@hyw

2009 թվականի դեկտեմբերին հրատարակված գիտական հոդված

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2009年の論文

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2009年論文

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2009年論文

@zh-hant

2009年論文

@zh-hk

2009年論文

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2009年論文

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2009年论文

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name

A genome-wide perspective of genetic variation in human metabolism.

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A genome-wide perspective of genetic variation in human metabolism.

@en

A genome-wide perspective of genetic variation in human metabolism.

@nl

type

label

A genome-wide perspective of genetic variation in human metabolism.

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A genome-wide perspective of genetic variation in human metabolism.

@en

A genome-wide perspective of genetic variation in human metabolism.

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prefLabel

A genome-wide perspective of genetic variation in human metabolism.

@ast

A genome-wide perspective of genetic variation in human metabolism.

@en

A genome-wide perspective of genetic variation in human metabolism.

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Nature Genetics

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A genome-wide perspective of genetic variation in human metabolism.

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Bernet S Kato

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Elisabeth Altmaier

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Guangju Zhai

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H-Erich Wichmann

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Jerzy Adamski

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Tim D Spector

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Genetics meets metabolomics: a genome-wide association study of metabolite profiles in human serum

Novel associations of CPS1, MUT, NOX4, and DPEP1 with plasma homocysteine in a healthy population: a genome-wide evaluation of 13 974 participants in the Women's Genome Health Study

Common variants at 30 loci contribute to polygenic dyslipidemia

Variants in MTNR1B influence fasting glucose levels.

Six new loci associated with blood low-density lipoprotein cholesterol, high-density lipoprotein cholesterol or triglycerides in humans

Identification of a lipokine, a lipid hormone linking adipose tissue to systemic metabolism

Genome-wide association analysis of metabolic traits in a birth cohort from a founder population

Moderation of breastfeeding effects on the IQ by genetic variation in fatty acid metabolism

Functional variants of OCTN cation transporter genes are associated with Crohn disease

Newly identified loci that influence lipid concentrations and risk of coronary artery disease

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137-141

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10.1038/NG.507

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2

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42

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Thomas Meitinger

Christian Gieger

Florian Kronenberg

Martin Hrabě de Angelis

Hans-Werner Mewes

Rui Wang-Sattler

Gabi Kastenmüller

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2009-12-27T00:00:00Z

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40786335

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20037589

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3773904

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