Works matching IS 10614036 AND DT 2012 AND VI 44 AND IP 7
Results: 29
Asking for more.
- Published in:
- Nature Genetics, 2012, v. 44, n. 7, p. 733, doi. 10.1038/ng.2345
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- Article
Mutations in the PCNA-binding domain of CDKN1C cause IMAGe syndrome.
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- Nature Genetics, 2012, v. 44, n. 7, p. 788, doi. 10.1038/ng.2275
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Targeting cancer stem cells.
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- Nature Genetics, 2012, v. 44, n. 7, p. 739, doi. 10.1038/ng.2339
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Maize HapMap2 identifies extant variation from a genome in flux.
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- Nature Genetics, 2012, v. 44, n. 7, p. 803, doi. 10.1038/ng.2313
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Genome-wide association analysis identifies susceptibility loci for migraine without aura.
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- Nature Genetics, 2012, v. 44, n. 7, p. 777, doi. 10.1038/ng.2307
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Gain of function in CDKN1C.
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- Nature Genetics, 2012, v. 44, n. 7, p. 737, doi. 10.1038/ng.2336
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A genome-wide association study identifies susceptibility loci for Wilms tumor.
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- Nature Genetics, 2012, v. 44, n. 7, p. 831, doi. 10.1038/ng0712-831c
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- Article
Postzygotic HRAS and KRAS mutations cause nevus sebaceous and Schimmelpenning syndrome.
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- Nature Genetics, 2012, v. 44, n. 7, p. 783, doi. 10.1038/ng.2316
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Rare variation in human populations.
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- Nature Genetics, 2012, v. 44, n. 7, p. 739, doi. 10.1038/ng.2342
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Dominant missense mutations in ABCC9 cause Cantú syndrome.
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- Nature Genetics, 2012, v. 44, n. 7, p. 793, doi. 10.1038/ng.2324
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- Article
BAP1 loss defines a new class of renal cell carcinoma.
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- Nature Genetics, 2012, v. 44, n. 7, p. 751, doi. 10.1038/ng.2323
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Comparative population genomics of maize domestication and improvement.
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- Nature Genetics, 2012, v. 44, n. 7, p. 808, doi. 10.1038/ng.2309
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Hypermutation in breast cancer.
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- Nature Genetics, 2012, v. 44, n. 7, p. 739, doi. 10.1038/ng.2338
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STAT3 activation in rare T-cell leukemia.
- Published in:
- Nature Genetics, 2012, v. 44, n. 7, p. 739, doi. 10.1038/ng.2340
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Manipulating nucleosome disfavoring sequences allows fine-tune regulation of gene expression in yeast.
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- Nature Genetics, 2012, v. 44, n. 7, p. 743, doi. 10.1038/ng.2305
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- Article
Genome-wide genetic changes during modern breeding of maize.
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- Nature Genetics, 2012, v. 44, n. 7, p. 812, doi. 10.1038/ng.2312
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Mapping 5-hydroxylmethylcytosine.
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- Nature Genetics, 2012, v. 44, n. 7, p. 739, doi. 10.1038/ng.2341
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Mutations in NNT encoding nicotinamide nucleotide transhydrogenase cause familial glucocorticoid deficiency.
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- Nature Genetics, 2012, v. 44, n. 7, p. 740, doi. 10.1038/ng.2299
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- Article
Genome-wide survey of recurrent HBV integration in hepatocellular carcinoma.
- Published in:
- Nature Genetics, 2012, v. 44, n. 7, p. 765, doi. 10.1038/ng.2295
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Genome-wide efficient mixed-model analysis for association studies.
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- Nature Genetics, 2012, v. 44, n. 7, p. 821, doi. 10.1038/ng.2310
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Tuning gene expression with nucleosome-disfavoring sequences.
- Published in:
- Nature Genetics, 2012, v. 44, n. 7, p. 735, doi. 10.1038/ng.2328
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- Article
The beet R locus encodes a new cytochrome P450 required for red betalain production.
- Published in:
- Nature Genetics, 2012, v. 44, n. 7, p. 816, doi. 10.1038/ng.2297
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- Article
Common variation near CDKN1A, POLD3 and SHROOM2 influences colorectal cancer risk.
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- Nature Genetics, 2012, v. 44, n. 7, p. 770, doi. 10.1038/ng.2293
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Estimating the proportion of variation in susceptibility to schizophrenia captured by common SNPs.
- Published in:
- Nature Genetics, 2012, v. 44, n. 7, p. 831, doi. 10.1038/ng0712-831a
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An efficient multi-locus mixed-model approach for genome-wide association studies in structured populations.
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- Nature Genetics, 2012, v. 44, n. 7, p. 825, doi. 10.1038/ng.2314
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Mutations in the phospholipid remodeling gene SERAC1 impair mitochondrial function and intracellular cholesterol trafficking and cause dystonia and deafness.
- Published in:
- Nature Genetics, 2012, v. 44, n. 7, p. 797, doi. 10.1038/ng.2325
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- Publication type:
- Article
Ascorbic acid prevents loss of Dlk1-Dio3 imprinting and facilitates generation of all-iPS cell mice from terminally differentiated B cells.
- Published in:
- Nature Genetics, 2012, v. 44, n. 7, p. 831, doi. 10.1038/ng0712-831b
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A crop of maize variants.
- Published in:
- Nature Genetics, 2012, v. 44, n. 7, p. 734, doi. 10.1038/ng.2326
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- Article
Whole-genome sequencing of liver cancers identifies etiological influences on mutation patterns and recurrent mutations in chromatin regulators.
- Published in:
- Nature Genetics, 2012, v. 44, n. 7, p. 760, doi. 10.1038/ng.2291
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- Article