Works matching IS 10614036 AND DT 2009 AND VI 41 AND IP 1
Results: 25
Somatic mutations in angiopoietin receptor gene TEK cause solitary and multiple sporadic venous malformations.
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- Nature Genetics, 2009, v. 41, n. 1, p. 118, doi. 10.1038/ng.272
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- Article
The lysine demethylase LSD1 (KDM1) is required for maintenance of global DNA methylation.
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- Nature Genetics, 2009, v. 41, n. 1, p. 125, doi. 10.1038/ng.268
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- Article
Reticular dysgenesis (aleukocytosis) is caused by mutations in the gene encoding mitochondrial adenylate kinase 2.
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- Nature Genetics, 2009, v. 41, n. 1, p. 101, doi. 10.1038/ng.265
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- Article
Human adenylate kinase 2 deficiency causes a profound hematopoietic defect associated with sensorineural deafness.
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- Nature Genetics, 2009, v. 41, n. 1, p. 106, doi. 10.1038/ng.278
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- Article
Genome-wide association yields new sequence variants at seven loci that associate with measures of obesity.
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- Nature Genetics, 2009, v. 41, n. 1, p. 18, doi. 10.1038/ng.274
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- Article
New sequence variants associated with bone mineral density.
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- Nature Genetics, 2009, v. 41, n. 1, p. 15, doi. 10.1038/ng.284
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- Article
Six new loci associated with body mass index highlight a neuronal influence on body weight regulation.
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- Nature Genetics, 2009, v. 41, n. 1, p. 25, doi. 10.1038/ng.287
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- Article
Heritable somatic methylation and inactivation of MSH2 in families with Lynch syndrome due to deletion of the 3′ exons of TACSTD1.
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- Nature Genetics, 2009, v. 41, n. 1, p. 112, doi. 10.1038/ng.283
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- Article
Genome-wide association analysis of metabolic traits in a birth cohort from a founder population.
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- Nature Genetics, 2009, v. 41, n. 1, p. 35, doi. 10.1038/ng.271
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- Article
Loci influencing lipid levels and coronary heart disease risk in 16 European population cohorts.
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- Nature Genetics, 2009, v. 41, n. 1, p. 47, doi. 10.1038/ng.269
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- Article
Common variants at 30 loci contribute to polygenic dyslipidemia.
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- Nature Genetics, 2009, v. 41, n. 1, p. 56, doi. 10.1038/ng.291
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- Article
Accelerated genetic drift on chromosome X during the human dispersal out of Africa.
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- Nature Genetics, 2009, v. 41, n. 1, p. 66, doi. 10.1038/ng.303
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- Article
Common variants in the NLRP3 region contribute to Crohn's disease susceptibility.
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- Nature Genetics, 2009, v. 41, n. 1, p. 71, doi. 10.1038/ng.285
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- Article
Variants in MTNR1B influence fasting glucose levels.
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- Nature Genetics, 2009, v. 41, n. 1, p. 77, doi. 10.1038/ng.290
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- Article
Common variant in MTNR1B associated with increased risk of type 2 diabetes and impaired early insulin secretion.
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- Nature Genetics, 2009, v. 41, n. 1, p. 82, doi. 10.1038/ng.288
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- Article
A variant near MTNR1B is associated with increased fasting plasma glucose levels and type 2 diabetes risk.
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- Nature Genetics, 2009, v. 41, n. 1, p. 89, doi. 10.1038/ng.277
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- Article
Germline mutations in WTX cause a sclerosing skeletal dysplasia but do not predispose to tumorigenesis.
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- Nature Genetics, 2009, v. 41, n. 1, p. 95, doi. 10.1038/ng.270
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- Article
Tandem array–based expression screens identify host mRNA targets of virus-encoded microRNAs.
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- Nature Genetics, 2009, v. 41, n. 1, p. 130, doi. 10.1038/ng.266
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- Article
Teamwork.
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- Nature Genetics, 2009, v. 41, n. 1, p. 1, doi. 10.1038/ng0109-1
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- Article
Protein demethylation required for DNA methylation.
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- Nature Genetics, 2009, v. 41, n. 1, p. 10, doi. 10.1038/ng0109-10
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- Article
Research Highlights.
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- Nature Genetics, 2009, v. 41, n. 1, p. 13, doi. 10.1038/ng0109-13
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- Article
Cohort studies and the genetics of complex disease.
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- Nature Genetics, 2009, v. 41, n. 1, p. 5, doi. 10.1038/ng0109-5
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- Article
Searching for targets of viral microRNAs.
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- Nature Genetics, 2009, v. 41, n. 1, p. 7, doi. 10.1038/ng0109-7
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- Article
Evaluating signatures of sex-specific processes in the human genome.
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- Nature Genetics, 2009, v. 41, n. 1, p. 8, doi. 10.1038/ng0109-8
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- Article
Without apology.
- Published in:
- 2009
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- Publication type:
- Book Review