Works matching IS 10614036 AND DT 2008 AND VI 40 AND IP 2
Results: 32
Role of retrotransposon-derived imprinted gene, Rtl1, in the feto-maternal interface of mouse placenta.
- Published in:
- Nature Genetics, 2008, v. 40, n. 2, p. 243, doi. 10.1038/ng.2007.51
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- Article
Ultraconservation identifies a small subset of extremely constrained developmental enhancers.
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- Nature Genetics, 2008, v. 40, n. 2, p. 158, doi. 10.1038/ng.2007.55
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- Article
Deletions and epimutations affecting the human 14q32.2 imprinted region in individuals with paternal and maternal upd(14)-like phenotypes.
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- Nature Genetics, 2008, v. 40, n. 2, p. 237, doi. 10.1038/ng.2007.56
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- Article
Genome-wide analysis of transcript isoform variation in humans.
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- Nature Genetics, 2008, v. 40, n. 2, p. 225, doi. 10.1038/ng.2007.57
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- Article
Epigenetic regulation and the variability of gene expression.
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- Nature Genetics, 2008, v. 40, n. 2, p. 141, doi. 10.1038/ng.2007.58
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- Article
Genome-wide scan identifies variation in MLXIPL associated with plasma triglycerides.
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- Nature Genetics, 2008, v. 40, n. 2, p. 149, doi. 10.1038/ng.2007.61
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- Article
Deficiency or inhibition of oxygen sensor Phd1 induces hypoxia tolerance by reprogramming basal metabolism.
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- Nature Genetics, 2008, v. 40, n. 2, p. 170, doi. 10.1038/ng.2007.62
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- Article
A reduction of mitochondrial DNA molecules during embryogenesis explains the rapid segregation of genotypes.
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- Nature Genetics, 2008, v. 40, n. 2, p. 249, doi. 10.1038/ng.2007.63
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- Article
Mutations in mRNA export mediator GLE1 result in a fetal motoneuron disease.
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- Nature Genetics, 2008, v. 40, n. 2, p. 155, doi. 10.1038/ng.2007.65
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- Article
A single gene network accurately predicts phenotypic effects of gene perturbation in Caenorhabditis elegans.
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- Nature Genetics, 2008, v. 40, n. 2, p. 181, doi. 10.1038/ng.2007.70
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- Article
Mutations in pericentrin cause Seckel syndrome with defective ATR-dependent DNA damage signaling.
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- Nature Genetics, 2008, v. 40, n. 2, p. 232, doi. 10.1038/ng.2007.80
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- Publication type:
- Article
A nonsynonymous functional variant in integrin-α<sub>M</sub> (encoded by ITGAM) is associated with systemic lupus erythematosus.
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- Nature Genetics, 2008, v. 40, n. 2, p. 152, doi. 10.1038/ng.71
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- Article
The same sequence variant on 9p21 associates with myocardial infarction, abdominal aortic aneurysm and intracranial aneurysm.
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- Nature Genetics, 2008, v. 40, n. 2, p. 217, doi. 10.1038/ng.72
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- Article
Common variants in the GDF5-UQCC region are associated with variation in human height.
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- Nature Genetics, 2008, v. 40, n. 2, p. 198, doi. 10.1038/ng.74
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- Publication type:
- Article
Six new loci associated with blood low-density lipoprotein cholesterol, high-density lipoprotein cholesterol or triglycerides in humans.
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- Nature Genetics, 2008, v. 40, n. 2, p. 189, doi. 10.1038/ng.75
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- Article
Newly identified loci that influence lipid concentrations and risk of coronary artery disease.
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- Nature Genetics, 2008, v. 40, n. 2, p. 161, doi. 10.1038/ng.76
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- Publication type:
- Article
Functional variants in the B-cell gene BANK1 are associated with systemic lupus erythematosus.
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- Nature Genetics, 2008, v. 40, n. 2, p. 211, doi. 10.1038/ng.79
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- Publication type:
- Article
Genome-wide association scan in women with systemic lupus erythematosus identifies susceptibility variants in ITGAM, PXK, KIAA1542 and other loci.
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- Nature Genetics, 2008, v. 40, n. 2, p. 204, doi. 10.1038/ng.81
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- Article
Positively disruptive.
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- Nature Genetics, 2008, v. 40, n. 2, p. 119, doi. 10.1038/ng0208-119
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- Article
Seymour Benzer 1921–2007.
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- 2008
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- Obituary
Islamic principles and decision making in bioethics.
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- 2008
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- Letter
A navigator for human genome epidemiology.
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- 2008
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- Letter
A genetic view of Jewish history.
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- 2008
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- Book Review
A treasure trove for lipoprotein biology.
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- Nature Genetics, 2008, v. 40, n. 2, p. 129, doi. 10.1038/ng0208-129
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- Article
The developing mosaic of autoimmune disease risk.
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- Nature Genetics, 2008, v. 40, n. 2, p. 131, doi. 10.1038/ng0208-131
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- Article
Hypoxic reprogramming.
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- Nature Genetics, 2008, v. 40, n. 2, p. 132, doi. 10.1038/ng0208-132
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- Article
Two ways to make an mtDNA bottleneck.
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- Nature Genetics, 2008, v. 40, n. 2, p. 134, doi. 10.1038/ng0208-134
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- Article
Touching base.
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- Nature Genetics, 2008, v. 40, n. 2, p. 137, doi. 10.1038/ng0208-137
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- Article
Research highlights.
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- Nature Genetics, 2008, v. 40, n. 2, p. 139, doi. 10.1038/ng0208-139
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- Article
Erratum: PU.1 is a major downstream target of AML1 (RUNX1) in adult mouse hematopoiesis.
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- 2008
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- Correction Notice
Erratum: Mutations in TTBK2, encoding a kinase implicated in tau phosphorylation, segregate with spinocerebellar ataxia type 11.
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- 2008
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- Correction Notice
Corrigendum: Mutations in smooth muscle α-actin (ACTA2) lead to thoracic aortic aneurysms and dissections.
- Published in:
- 2008
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- Correction Notice