Works matching IS 10614036 AND DT 2014 AND VI 46 AND IP 6
Results: 34
Dystrophin is a tumor suppressor in human cancers with myogenic programs.
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- Nature Genetics, 2014, v. 46, n. 6, p. 601, doi. 10.1038/ng.2974
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Turtle ghrelin.
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- Nature Genetics, 2014, v. 46, n. 6, p. 526, doi. 10.1038/ng.2988
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An atlas of genetic influences on human blood metabolites.
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- Nature Genetics, 2014, v. 46, n. 6, p. 543, doi. 10.1038/ng.2982
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Mosaic loss of chromosome Y in peripheral blood is associated with shorter survival and higher risk of cancer.
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- Nature Genetics, 2014, v. 46, n. 6, p. 624, doi. 10.1038/ng.2966
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Cross-talk between imprinted loci in Prader-Willi syndrome.
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- Nature Genetics, 2014, v. 46, n. 6, p. 528, doi. 10.1038/ng.2994
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Corrigendum: The draft genomes of soft-shell turtle and green sea turtle yield insights into the development and evolution of the turtle-specific body plan.
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- Nature Genetics, 2014, v. 46, n. 6, p. 657, doi. 10.1038/ng0614-657a
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PARK2 orchestrates cyclins to avoid cancer.
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- Nature Genetics, 2014, v. 46, n. 6, p. 527, doi. 10.1038/ng.2992
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Mutations in CCNO result in congenital mucociliary clearance disorder with reduced generation of multiple motile cilia.
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- Nature Genetics, 2014, v. 46, n. 6, p. 646, doi. 10.1038/ng.2961
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iPSC models of ALS.
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- Nature Genetics, 2014, v. 46, n. 6, p. 532, doi. 10.1038/ng.2999
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Whole-genome sequencing and comprehensive molecular profiling identify new driver mutations in gastric cancer.
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- Nature Genetics, 2014, v. 46, n. 6, p. 573, doi. 10.1038/ng.2983
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A recurrent neomorphic mutation in MYOD1 defines a clinically aggressive subset of embryonal rhabdomyosarcoma associated with PI3K-AKT pathway mutations.
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- Nature Genetics, 2014, v. 46, n. 6, p. 595, doi. 10.1038/ng.2969
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Turtle ghrelin.
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- Nature Genetics, 2014, v. 46, n. 6, p. 525, doi. 10.1038/ng.2964
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Exploring new models of easiRNA biogenesis.
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- Nature Genetics, 2014, v. 46, n. 6, p. 530, doi. 10.1038/ng.2993
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Corrigendum: Mutations in the DNA methyltransferase gene DNMT3A cause an overgrowth syndrome with intellectual disability.
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- Nature Genetics, 2014, v. 46, n. 6, p. 657, doi. 10.1038/ng0614-657c
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RPGRIP1L, FTO and obesity.
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- Nature Genetics, 2014, v. 46, n. 6, p. 532, doi. 10.1038/ng.2997
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Triplication of a 21q22 region contributes to B cell transformation through HMGN1 overexpression and loss of histone H3 Lys27 trimethylation.
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- Nature Genetics, 2014, v. 46, n. 6, p. 618, doi. 10.1038/ng.2949
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Polar bear genomics.
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- Nature Genetics, 2014, v. 46, n. 6, p. 532, doi. 10.1038/ng.3001
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Large-scale genetic study in East Asians identifies six new loci associated with colorectal cancer risk.
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- Nature Genetics, 2014, v. 46, n. 6, p. 533, doi. 10.1038/ng.2985
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RAF1 mutations in childhood-onset dilated cardiomyopathy.
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- Nature Genetics, 2014, v. 46, n. 6, p. 635, doi. 10.1038/ng.2963
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Pan-cancer genetic analysis identifies PARK2 as a master regulator of G1/S cyclins.
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- Nature Genetics, 2014, v. 46, n. 6, p. 588, doi. 10.1038/ng.2981
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RGS2 rescues LRRK2 pathogenicity.
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- Nature Genetics, 2014, v. 46, n. 6, p. 532, doi. 10.1038/ng.2998
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Nature Plants.
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- Nature Genetics, 2014, v. 46, n. 6, p. 523, doi. 10.1038/ng.3005
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Erratum: Chalk5 encodes a vacuolar H<sup>+</sup>-translocating pyrophosphatase influencing grain chalkiness in rice.
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- Nature Genetics, 2014, v. 46, n. 6, p. 657, doi. 10.1038/ng0614-657b
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Immune cell-specific eQTLs.
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- Nature Genetics, 2014, v. 46, n. 6, p. 532, doi. 10.1038/ng.3000
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De novo mutations in HCN1 cause early infantile epileptic encephalopathy.
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- Nature Genetics, 2014, v. 46, n. 6, p. 640, doi. 10.1038/ng.2952
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Recurrent activating mutation in PRKACA in cortisol-producing adrenal tumors.
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- Nature Genetics, 2014, v. 46, n. 6, p. 613, doi. 10.1038/ng.2956
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Heterotrimeric G proteins regulate nitrogen-use efficiency in rice.
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- Nature Genetics, 2014, v. 46, n. 6, p. 652, doi. 10.1038/ng.2958
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Deep transcriptome profiling of mammalian stem cells supports a regulatory role for retrotransposons in pluripotency maintenance.
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- Nature Genetics, 2014, v. 46, n. 6, p. 558, doi. 10.1038/ng.2965
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The noncoding RNA IPW regulates the imprinted DLK1-DIO3 locus in an induced pluripotent stem cell model of Prader-Willi syndrome.
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- Nature Genetics, 2014, v. 46, n. 6, p. 551, doi. 10.1038/ng.2968
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Integrated genomic characterization of adrenocortical carcinoma.
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- Nature Genetics, 2014, v. 46, n. 6, p. 607, doi. 10.1038/ng.2953
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Turtle ghrelin.
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- Nature Genetics, 2014, v. 46, n. 6, p. 524, doi. 10.1038/ng.2960
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Genome sequence of the cultivated cotton Gossypium arboreum.
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- Nature Genetics, 2014, v. 46, n. 6, p. 567, doi. 10.1038/ng.2987
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Rare and low-frequency coding variants in CXCR2 and other genes are associated with hematological traits.
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- Nature Genetics, 2014, v. 46, n. 6, p. 629, doi. 10.1038/ng.2962
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Recurrent gain-of-function mutations of RHOA in diffuse-type gastric carcinoma.
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- Nature Genetics, 2014, v. 46, n. 6, p. 583, doi. 10.1038/ng.2984
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