Works matching IS 10614036 AND DT 2015 AND VI 47 AND IP 6
Results: 32
Mapping long-range promoter contacts in human cells with high-resolution capture Hi-C.
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- Nature Genetics, 2015, v. 47, n. 6, p. 598, doi. 10.1038/ng.3286
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Erratum: The genome and transcriptome of the zoonotic hookworm Ancylostoma ceylanicum identify infection-specific gene families.
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- Nature Genetics, 2015, v. 47, n. 6, p. 689, doi. 10.1038/ng0615-689a
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A Sleeping Beauty forward genetic screen identifies new genes and pathways driving osteosarcoma development and metastasis.
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- Nature Genetics, 2015, v. 47, n. 6, p. 615, doi. 10.1038/ng.3293
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A germline homozygous mutation in the base-excision repair gene NTHL1 causes adenomatous polyposis and colorectal cancer.
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- Nature Genetics, 2015, v. 47, n. 6, p. 668, doi. 10.1038/ng.3287
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Improved genome inference in the MHC using a population reference graph.
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- Nature Genetics, 2015, v. 47, n. 6, p. 682, doi. 10.1038/ng.3257
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Corrigendum: Analysis of the genetic phylogeny of multifocal prostate cancer identifies multiple independent clonal expansions in neoplastic and morphologically normal prostate tissue.
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- Nature Genetics, 2015, v. 47, n. 6, p. 689, doi. 10.1038/ng0615-689b
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- Article
Fine mapping in the MHC region accounts for 18% additional genetic risk for celiac disease.
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- Nature Genetics, 2015, v. 47, n. 6, p. 577, doi. 10.1038/ng.3268
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Hypertension linked to PDE3A activation.
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- Nature Genetics, 2015, v. 47, n. 6, p. 562, doi. 10.1038/ng.3316
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The genomic landscape of high hyperdiploid childhood acute lymphoblastic leukemia.
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- Nature Genetics, 2015, v. 47, n. 6, p. 672, doi. 10.1038/ng.3301
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Corrigendum: Analyses of allele-specific gene expression in highly divergent mouse crosses identifies pervasive allelic imbalance.
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- Nature Genetics, 2015, v. 47, n. 6, p. 690, doi. 10.1038/ng0615-690a
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- Article
Transposon mutagenesis disentangles osteosarcoma genetic drivers.
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- Nature Genetics, 2015, v. 47, n. 6, p. 564, doi. 10.1038/ng.3317
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Mutations in XPR1 cause primary familial brain calcification associated with altered phosphate export.
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- Nature Genetics, 2015, v. 47, n. 6, p. 579, doi. 10.1038/ng.3289
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Corrigendum: A common variant mapping to CACNA1A is associated with susceptibility to exfoliation syndrome.
- Published in:
- Nature Genetics, 2015, v. 47, n. 6, p. 689, doi. 10.1038/ng0615-689c
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Phylogeographical analysis of the dominant multidrug-resistant H58 clade of Salmonella Typhi identifies inter- and intracontinental transmission events.
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- Nature Genetics, 2015, v. 47, n. 6, p. 632, doi. 10.1038/ng.3281
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PDE3A mutations cause autosomal dominant hypertension with brachydactyly.
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- Nature Genetics, 2015, v. 47, n. 6, p. 647, doi. 10.1038/ng.3302
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Understanding multicellular function and disease with human tissue-specific networks.
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- Nature Genetics, 2015, v. 47, n. 6, p. 569, doi. 10.1038/ng.3259
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The draft genome of the grass carp (Ctenopharyngodon idellus) provides insights into its evolution and vegetarian adaptation.
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- Nature Genetics, 2015, v. 47, n. 6, p. 625, doi. 10.1038/ng.3280
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Regulatory rewiring.
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- Nature Genetics, 2015, v. 47, n. 6, p. 568, doi. 10.1038/ng.3329
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Analysis of loss-of-function variants and 20 risk factor phenotypes in 8,554 individuals identifies loci influencing chronic disease.
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- Nature Genetics, 2015, v. 47, n. 6, p. 640, doi. 10.1038/ng.3270
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COPA mutations impair ER-Golgi transport and cause hereditary autoimmune-mediated lung disease and arthritis.
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- Nature Genetics, 2015, v. 47, n. 6, p. 654, doi. 10.1038/ng.3279
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Mutations in KCNH1 and ATP6V1B2 cause Zimmermann-Laband syndrome.
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- Nature Genetics, 2015, v. 47, n. 6, p. 661, doi. 10.1038/ng.3282
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Fibrogenic lineage identified.
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- Nature Genetics, 2015, v. 47, n. 6, p. 568, doi. 10.1038/ng.3326
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Germline RECQL mutations are associated with breast cancer susceptibility.
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- Nature Genetics, 2015, v. 47, n. 6, p. 643, doi. 10.1038/ng.3284
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Call for crop improvement Analysis articles.
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- Nature Genetics, 2015, v. 47, n. 6, p. 561, doi. 10.1038/ng.3334
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- Article
Spermatogenic signaling through Rarg.
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- Nature Genetics, 2015, v. 47, n. 6, p. 568, doi. 10.1038/ng.3327
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NALP3 inflammasome upregulation and CASP1 cleavage of the glucocorticoid receptor cause glucocorticoid resistance in leukemia cells.
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- Nature Genetics, 2015, v. 47, n. 6, p. 607, doi. 10.1038/ng.3283
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The impact of low-frequency and rare variants on lipid levels.
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- Nature Genetics, 2015, v. 47, n. 6, p. 589, doi. 10.1038/ng.3300
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DNA replication fidelity in Mycobacterium tuberculosis is mediated by an ancestral prokaryotic proofreader.
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- Nature Genetics, 2015, v. 47, n. 6, p. 677, doi. 10.1038/ng.3269
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Heterochromatin and human aging.
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- Nature Genetics, 2015, v. 47, n. 6, p. 568, doi. 10.1038/ng.3325
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Modeling NOTCH1 haploinsufficiency.
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- Nature Genetics, 2015, v. 47, n. 6, p. 568, doi. 10.1038/ng.3328
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Excess of rare, inherited truncating mutations in autism.
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- Nature Genetics, 2015, v. 47, n. 6, p. 582, doi. 10.1038/ng.3303
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Massive lineage replacements and cryptic outbreaks of Salmonella Typhi in eastern and southern Africa.
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- Nature Genetics, 2015, v. 47, n. 6, p. 565, doi. 10.1038/ng.3318
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