Detail Nature Genetics vol. 44 no. 01 (Jan. 2012) Bibliografi Bahasa: (EN )    ISSN: 1061-4036    Year:: 2012    Bulan: 01    Edisi: Jan 2012     Penerbit: Nature Publishing Group Jenis: Journal - ilmiah internasional [Lihat daftar eksemplar jurnal Nature Genetics] Ketersediaan Perpustakaan FK Nomor Panggil: N12.K.2012.01 Non-tandon: 1 (dapat dipinjam: 0) Tandon: tidak ada     Lihat Detail Induk Artikel dalam koleksi ini Rare and functional SIAE variants are not associated with autoimmune disease risk in up to 66,924 individuals of European ancestry, halaman 3–5 Improved imputation of common and uncommon SNPs with a new reference set, halaman 6–7 Spliceosome mutations in hematopoietic malignancies, halaman 9–10 Following evolution of bacterial antibiotic resistance in real time, halaman 11–13 Dnmt3a silences hematopoietic stem cell self-renewal, halaman 13–14 Frequent mutations of genes encoding ubiquitin-mediated proteolysis pathway components in clear cell renal cell carcinoma, halaman 17–19 GATA6 haploinsufficiency causes pancreatic agenesis in humans, halaman 20–22 Dnmt3a is essential for hematopoietic stem cell differentiation, halaman 23–31 Genome-wide association study of flowering time and grain yield traits in a worldwide collection of rice germplasm, halaman 32–39 Regions of focal DNA hypermethylation and long-range hypomethylation in colorectal cancer coincide with nuclear lamina–associated domains, halaman 40–46 Exome sequencing identifies recurrent mutations of the splicing factor SF3B1 gene in chronic lymphocytic leukemia, halaman 47–52 Recurrent mutations in the U2AF1 splicing factor in myelodysplastic syndromes, halaman 53–57 Common variation at 3p22.1 and 7p15.3 influences multiple myeloma risk, halaman 58–61 Genome-wide association study identifies five loci associated with susceptibility to pancreatic cancer in Chinese populations, halaman 62–66 Meta-analysis of genome-wide association studies identifies eight new loci for type 2 diabetes in east Asians, halaman 67–72 A genome-wide association study in Han Chinese identifies new susceptibility loci for ankylosing spondylitis, halaman 73–77 Genome-wide copy number variation study associates metabotropic glutamate receptor gene networks with attention deficit hyperactivity disorder, halaman 78–84 Mutations at a single codon in Mad homology 2 domain of SMAD4 cause Myhre syndrome, halaman 85–88 Large-scale discovery of enhancers from human heart tissue, halaman 89–93 A chromatin-modifying function of JNK during stem cell differentiation, halaman 94–100 Evolutionary paths to antibiotic resistance under dynamically sustained drug selection, halaman 101–105 Whole-genome sequencing of rifampicin-resistant Mycobacterium tuberculosis strains identifies compensatory mutations in RNA polymerase genes, halaman 106–110  Edit Artikel Lihat Sejarah Pengadaan  Konversi Metadata   Kembali

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