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《Nature Genetics》杂志2017年发表文章

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《Nature Genetics》杂志2017年发表文章

Science创建于2017-01-03 最后编辑: 2018-02-26 21:16 6,761阅读 5人收藏
Journal:Nature Genetics<br/>Year:2017
共 229 个文档
ng.3771-A somatic-mutational process recurrently duplicates germline susceptibility loci and tissue-specific super-enhancers in breast cancers 11p
pdf ng.3771-A somatic-mutational process recurrently duplicate..
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  • 作者: Science
  • 2017-01-24
  • 格式: PDF
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ng.3772-Pediatric non–Down syndrome acute megakaryoblastic leukemia is characterized by distinct genomic subsets with varying outcomes 8p
pdf ng.3772-Pediatric non–Down syndrome acute megakaryoblast..
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  • 作者: Science
  • 2017-01-24
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ng.3773-Acquired CYP19A1 amplification is an early specific mechanism of aromatase inhibitor resistance in ERα metastatic breast cancer 9p
pdf ng.3773-Acquired CYP19A1 amplification is an early speci..
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  • 作者: Science
  • 2017-01-24
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ng.3753-Epigenomic reprogramming during pancreatic cancer progression links anabolic glucose metabolism to distant metastasis 12p
pdf ng.3753-Epigenomic reprogramming during pancreatic cancer ..
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  • 作者: Science
  • 2017-01-17
  • 格式: PDF
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ng.3756-Precision oncology for acute myeloid leukemia using a knowledge bank approach 10p
pdf ng.3756-Precision oncology for acute myeloid leukemia usin..
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  • 作者: Science
  • 2017-01-17
  • 格式: PDF
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ng.3762-Biallelic mutations in the 3′ exonuclease TOE1 cause pontocerebellar hypoplasia and uncover a role in snRNA processing 10p
pdf ng.3762-Biallelic mutations in the 3′ exonuclease TOE1 ..
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  • 作者: Science
  • 2017-01-17
  • 格式: PDF
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ng.3764-Limited heterogeneity of known driver gene mutations among the metastases of individual patients with pancreatic cancer 11p
pdf ng.3764-Limited heterogeneity of known driver gene mutatio..
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  • 作者: Science
  • 2017-01-17
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ng.3766-Case–control association mapping by proxy using family history of disease 9p
pdf ng.3766-Case–control association mapping by proxy using f..
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  • 作者: Science
  • 2017-01-17
  • 格式: PDF
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ng.3761-Exploring the genetic architecture of inflammatory bowel disease by whole-genome sequencing identifies association at ADCY7 9p
pdf ng.3761-Exploring the genetic architecture of inflammatory..
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  • 作者: Science
  • 2017-01-10
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ng.3765-De novo mutations in SMCHD1 cause Bosma arhinia microphthalmia syndrome and abrogate nasal development 9p
pdf ng.3765-De novo mutations in SMCHD1 cause Bosma arhinia..
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  • 作者: Science
  • 2017-01-10
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ng.3760-Genome-wide association study implicates immune activation of multiple integrin genes in inflammatory bowel disease 8p
pdf ng.3760-Genome-wide association study implicates immune ac..
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  • 作者: Science
  • 2017-01-10
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ng.3755-Genome-wide association study identifies distinct genetic contributions to prognosis and susceptibility in Crohn´s disease 9p
pdf ng.3755-Genome-wide association study identifies distinct ..
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  • 作者: Science
  • 2017-01-10
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ng.3743-SMCHD1 mutations associated with a rare muscular dystrophy can also cause isolated arhinia and Bosma arhinia microphthalmia syndrome 14p
pdf ng.3743-SMCHD1 mutations associated with a rare muscular..
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  • 作者: Science
  • 2017-01-10
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ng.3757-Impaired H3K36 methylation defines a subset of head and neck squamous cell carcinomas 8p
pdf ng.3757-Impaired H3K36 methylation defines a subset of he..
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  • 作者: Science
  • 2017-01-10
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ng.3711-Qki deficiency maintains stemness of glioma stem cells in suboptimal environment by downregulating endolysosomal degradation 15p
pdf ng.3711-Qki deficiency maintains stemness of glioma stem c..
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  • 作者: Science
  • 2016-11-15
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