Works matching IS 10614036 AND DT 2013 AND VI 45 AND IP 9
Results: 29
The wheat powdery mildew genome shows the unique evolution of an obligate biotroph.
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- Nature Genetics, 2013, v. 45, n. 9, p. 1092, doi. 10.1038/ng.2704
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GRIN2A mutations cause epilepsy-aphasia spectrum disorders.
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- Nature Genetics, 2013, v. 45, n. 9, p. 1073, doi. 10.1038/ng.2727
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A suppressor screen in Mecp2 mutant mice implicates cholesterol metabolism in Rett syndrome.
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- Nature Genetics, 2013, v. 45, n. 9, p. 1013, doi. 10.1038/ng.2714
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Evidence for APOBEC3B mutagenesis in multiple human cancers.
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- Nature Genetics, 2013, v. 45, n. 9, p. 977, doi. 10.1038/ng.2701
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Hexokinase 2 required in tumors.
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- Nature Genetics, 2013, v. 45, n. 9, p. 969, doi. 10.1038/ng.2751
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Mutations in GRIN2A cause idiopathic focal epilepsy with rolandic spikes.
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- Nature Genetics, 2013, v. 45, n. 9, p. 1067, doi. 10.1038/ng.2728
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Passage through the mammalian gut triggers a phenotypic switch that promotes Candida albicans commensalism.
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- Nature Genetics, 2013, v. 45, n. 9, p. 1088, doi. 10.1038/ng.2710
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Somatic and germline CACNA1D calcium channel mutations in aldosterone-producing adenomas and primary aldosteronism.
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- Nature Genetics, 2013, v. 45, n. 9, p. 1050, doi. 10.1038/ng.2695
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Reconstructing de novo silencing of an active plant retrotransposon.
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- Nature Genetics, 2013, v. 45, n. 9, p. 1029, doi. 10.1038/ng.2703
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Control of root system architecture by DEEPER ROOTING 1 increases rice yield under drought conditions.
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- Nature Genetics, 2013, v. 45, n. 9, p. 1097, doi. 10.1038/ng.2725
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Nuclear reprogramming and the cancer genome.
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- Nature Genetics, 2013, v. 45, n. 9, p. 963, doi. 10.1038/ng.2755
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An APOBEC cytidine deaminase mutagenesis pattern is widespread in human cancers.
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- Nature Genetics, 2013, v. 45, n. 9, p. 970, doi. 10.1038/ng.2702
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Common variants at SCN5A-SCN10A and HEY2 are associated with Brugada syndrome, a rare disease with high risk of sudden cardiac death.
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- Nature Genetics, 2013, v. 45, n. 9, p. 1044, doi. 10.1038/ng.2712
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Mutations in the gene encoding PDGF-B cause brain calcifications in humans and mice.
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- Nature Genetics, 2013, v. 45, n. 9, p. 1077, doi. 10.1038/ng.2723
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A deeper look back at Y.
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- Nature Genetics, 2013, v. 45, n. 9, p. 969, doi. 10.1038/ng.2753
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Cholesterol metabolism and Rett syndrome pathogenesis.
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- Nature Genetics, 2013, v. 45, n. 9, p. 965, doi. 10.1038/ng.2738
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Independent specialization of the human and mouse X chromosomes for the male germ line.
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- Nature Genetics, 2013, v. 45, n. 9, p. 1083, doi. 10.1038/ng.2705
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APOBEC3B mutagenesis in cancer.
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- Nature Genetics, 2013, v. 45, n. 9, p. 964, doi. 10.1038/ng.2736
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Schizophrenia exomes.
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- Nature Genetics, 2013, v. 45, n. 9, p. 969, doi. 10.1038/ng.2750
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DYX1C1 is required for axonemal dynein assembly and ciliary motility.
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- Nature Genetics, 2013, v. 45, n. 9, p. 995, doi. 10.1038/ng.2707
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Loss of cilia suppresses cyst growth in genetic models of autosomal dominant polycystic kidney disease.
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- Nature Genetics, 2013, v. 45, n. 9, p. 1004, doi. 10.1038/ng.2715
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Association between large detectable clonal mosaicism and type 2 diabetes with vascular complications.
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- Nature Genetics, 2013, v. 45, n. 9, p. 1040, doi. 10.1038/ng.2700
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Massively parallel decoding of mammalian regulatory sequences supports a flexible organizational model.
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- Nature Genetics, 2013, v. 45, n. 9, p. 1021, doi. 10.1038/ng.2713
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Mutation signature of aristolochic acid.
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- Nature Genetics, 2013, v. 45, n. 9, p. 969, doi. 10.1038/ng.2749
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A developmental program for Candida commensalism.
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- Nature Genetics, 2013, v. 45, n. 9, p. 967, doi. 10.1038/ng.2737
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Transcription factors in combination.
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- Nature Genetics, 2013, v. 45, n. 9, p. 969, doi. 10.1038/ng.2752
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Somatic mutations in ATP1A1 and CACNA1D underlie a common subtype of adrenal hypertension.
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- Nature Genetics, 2013, v. 45, n. 9, p. 1055, doi. 10.1038/ng.2716
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GRIN2A mutations in acquired epileptic aphasia and related childhood focal epilepsies and encephalopathies with speech and language dysfunction.
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- Nature Genetics, 2013, v. 45, n. 9, p. 1061, doi. 10.1038/ng.2726
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Genetic relationship between five psychiatric disorders estimated from genome-wide SNPs.
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- Nature Genetics, 2013, v. 45, n. 9, p. 984, doi. 10.1038/ng.2711
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