Works matching IS 10614036 AND DT 2014 AND VI 46 AND IP 1
Results: 24
Inactivating CUX1 mutations promote tumorigenesis.
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- Nature Genetics, 2014, v. 46, n. 1, p. 33, doi. 10.1038/ng.2846
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A developmental program drives aggressive embryonal brain tumors.
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- Nature Genetics, 2014, v. 46, n. 1, p. 2, doi. 10.1038/ng.2857
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ARMC5 and adrenal hyperplasia.
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- Nature Genetics, 2014, v. 46, n. 1, p. 7, doi. 10.1038/ng.2867
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Gain-of-function mutations in the phosphatidylserine synthase 1 (PTDSS1) gene cause Lenz-Majewski syndrome.
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- Nature Genetics, 2014, v. 46, n. 1, p. 70, doi. 10.1038/ng.2829
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Common and low-frequency variants associated with genome-wide recombination rate.
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- Nature Genetics, 2014, v. 46, n. 1, p. 11, doi. 10.1038/ng.2833
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ELABELA, a peptide hormone for heart development.
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- Nature Genetics, 2014, v. 46, n. 1, p. 7, doi. 10.1038/ng.2866
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EIF2AK4 mutations cause pulmonary veno-occlusive disease, a recessive form of pulmonary hypertension.
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- Nature Genetics, 2014, v. 46, n. 1, p. 65, doi. 10.1038/ng.2844
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Recessive mutations in a distal PTF1A enhancer cause isolated pancreatic agenesis.
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- Nature Genetics, 2014, v. 46, n. 1, p. 61, doi. 10.1038/ng.2826
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High prevalence of MAP2K1 mutations in variant and IGHV4-34-expressing hairy-cell leukemias.
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- Nature Genetics, 2014, v. 46, n. 1, p. 8, doi. 10.1038/ng.2828
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The cancer epigenome of mice and men.
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- Nature Genetics, 2014, v. 46, n. 1, p. 7, doi. 10.1038/ng.2863
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OXA resistance from QTL to crystal structure.
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- Nature Genetics, 2014, v. 46, n. 1, p. 7, doi. 10.1038/ng.2865
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Minke whale genome and aquatic adaptation in cetaceans.
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- Nature Genetics, 2014, v. 46, n. 1, p. 88, doi. 10.1038/ng.2835
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Genetic variation of a bacterial pathogen within individuals with cystic fibrosis provides a record of selective pressures.
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- Nature Genetics, 2014, v. 46, n. 1, p. 82, doi. 10.1038/ng.2848
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Fusion of TTYH1 with the C19MC microRNA cluster drives expression of a brain-specific DNMT3B isoform in the embryonal brain tumor ETMR.
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- Nature Genetics, 2014, v. 46, n. 1, p. 39, doi. 10.1038/ng.2849
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Large conserved domains of low DNA methylation maintained by Dnmt3a.
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- Nature Genetics, 2014, v. 46, n. 1, p. 17, doi. 10.1038/ng.2836
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A genome-wide association study identifies multiple susceptibility loci for chronic lymphocytic leukemia.
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- Nature Genetics, 2014, v. 46, n. 1, p. 56, doi. 10.1038/ng.2843
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Genetic signature of bacterial pathogen adaptation during chronic pulmonary infections.
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- Nature Genetics, 2014, v. 46, n. 1, p. 5, doi. 10.1038/ng.2859
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Transposon mutagenesis identifies genes driving hepatocellular carcinoma in a chronic hepatitis B mouse model.
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- Nature Genetics, 2014, v. 46, n. 1, p. 24, doi. 10.1038/ng.2847
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A large-scale screen for coding variants predisposing to psoriasis.
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- Nature Genetics, 2014, v. 46, n. 1, p. 45, doi. 10.1038/ng.2827
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Credit for code.
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- Nature Genetics, 2014, v. 46, n. 1, p. 1, doi. 10.1038/ng.2869
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A genome-wide association study identifies CDHR3 as a susceptibility locus for early childhood asthma with severe exacerbations.
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- Nature Genetics, 2014, v. 46, n. 1, p. 51, doi. 10.1038/ng.2830
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Genome-wide association study using cellular traits identifies a new regulator of root development in Arabidopsis.
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- Nature Genetics, 2014, v. 46, n. 1, p. 77, doi. 10.1038/ng.2824
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Isogenic iPSC-derived models of disease.
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- Nature Genetics, 2014, v. 46, n. 1, p. 7, doi. 10.1038/ng.2864
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Enhancer mutations and phenotype modularity.
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- Nature Genetics, 2014, v. 46, n. 1, p. 3, doi. 10.1038/ng.2861
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