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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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          2015年6月26日《自然.遺傳學(xué)》第7期文章
          
        
          
            
                
                    Science創(chuàng)建于2015-06-26
            最后編輯: 2015-06-29 15:42
            6,462閱讀
            7人收藏
            
          
        
          
            
          
            
          
                2015年6月26號，《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。
          
        
          
        
          
            共 19 個文檔
        
          
        
          
            
          
                
          
                    
                        Spatial genomic heterogeneity within localized, multifocal prostate cancer
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                    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 controls
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                    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 achromatopsia
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                    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 rates
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                    Genome-wide maps of recombination and chromosome segregati..
                
          
                
          
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                        A cascade of arabinosyltransferases controls shoot meristem size in tomato
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                    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 polycistron
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                    An allelic series of miR-17~92–mutant mice uncovers func..
                
          
                
          
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                        Recurrent somatic mutations in regulatory regions of human cancer genomes
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                    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 adenoma
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                    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 disorders
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                    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 Japanese
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                    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 rice
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                    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 syndrome
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                    A partially inactivating mutation in the sodium-dependent ..
                
          
                
          
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                        Genome-wide patterns and properties of de novo mutations in humans
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                    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 syndrome
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                    Inactivating mutations in MFSD2A, required for omega-3 ..
                
          
                
          
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                        The European Genome-phenome Archive of human data consented for biomedical research
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                    The European Genome-phenome Archive of human data consen..
                
          
                
          
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