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2015年6月26日《自然.遺傳學(xué)》第7期文章

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  • 創(chuàng)建時(shí)間:2015-06-26 20:43
  • 修改時(shí)間:2015-06-29 15:42
  • 介紹:2015年6月26號(hào)，《自然.遺傳學(xué)》在官網(wǎng)發(fā)布2015年7月最新一期文章，共19篇文章。
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Spatial genomic heterogeneity within localized, multifocal prostate cancer14 p
pdf Spatial genomic heterogeneity within localized, multifocal..
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Statistical colocalization of genetic risk variants for related autoimmune diseases in the context of common controls9 p
pdf Statistical colocalization of genetic risk variants for re..
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Mutations in the unfolded protein response regulator ATF6 cause the cone dysfunction disorder achromatopsia12 p
pdf Mutations in the unfolded protein response regulator ATF..
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Genome-wide maps of recombination and chromosome segregation in human oocytes and embryos show selection for maternal recombination rates11 p
pdf Genome-wide maps of recombination and chromosome segregati..
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A cascade of arabinosyltransferases controls shoot meristem size in tomato12 p
pdf A cascade of arabinosyltransferases controls shoot meriste..
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An allelic series of miR-17~92–mutant mice uncovers functional specialization and cooperation among members of a microRNA polycistron12 p
pdf An allelic series of miR-17~92–mutant mice uncovers func..
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Recurrent somatic mutations in regulatory regions of human cancer genomes9 p
pdf Recurrent somatic mutations in regulatory regions of human..
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Common variants at 10p12.31, 10q21.1 and 13q12.13 are associated with sporadic pituitary adenoma6 p
pdf Common variants at 10p12.31, 10q21.1 and 13q12.13 are asso..
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Factors influencing success of clinical genome sequencing across a broad spectrum of disorders13 p
pdf Factors influencing success of clinical genome sequencing ..
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Construction of a population-specific HLA imputation reference panel and its application to Graves’ disease risk in Japanese7 p
pdf Construction of a population-specific HLA imputation ref..
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Natural alleles of a proteasome α2 subunit gene contribute to thermotolerance and adaptation of African rice10 p
pdf Natural alleles of a proteasome α2 subunit gene contribut..
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A partially inactivating mutation in the sodium-dependent lysophosphatidylcholine transporter MFSD2A causes a non-lethal microcephaly syndrome5 p
pdf A partially inactivating mutation in the sodium-dependent ..
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Genome-wide patterns and properties of de novo mutations in humans8 p
pdf Genome-wide patterns and properties of de novo mutations i..
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Inactivating mutations in MFSD2A, required for omega-3 fatty acid transport in brain, cause a lethal microcephaly syndrome7 p
pdf Inactivating mutations in MFSD2A, required for omega-3 ..
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The European Genome-phenome Archive of human data consented for biomedical research4 p
pdf The European Genome-phenome Archive of human data consen..
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