Detail Nature Genetics vol. 47 no. 06 (Jun. 2015) Bibliografi Bahasa: (EN )    ISSN: 1061-4036    Year:: 2015    Bulan: 06    Edisi: Jun 2015     Penerbit: Nature Publishing Group Jenis: Journal - ilmiah internasional [Lihat daftar eksemplar jurnal Nature Genetics] Ketersediaan Perpustakaan FK Nomor Panggil: N12.K Non-tandon: 1 (dapat dipinjam: 0) Tandon: tidak ada     Lihat Detail Induk Artikel dalam koleksi ini Understanding multicellular function and disease with human tissue-specific networks, halaman 569–576 Fine mapping in the MHC region accounts for 18% additional genetic risk for celiac disease, halaman 577–578 Mutations in XPR1 cause primary familial brain calcification associated with altered phosphate export, halaman 579–581 Excess of rare, inherited truncating mutations in autism, halaman 582–588 The impact of low-frequency and rare variants on lipid levels, halaman 589–597 Mapping long-range promoter contacts in human cells with high-resolution capture Hi-C, halaman 598–606 NALP3 inflammasome upregulation and CASP1 cleavage of the glucocorticoid receptor cause glucocorticoid resistance in leukemia cells, halaman 607–614 A Sleeping Beauty forward genetic screen identifies new genes and pathways driving osteosarcoma development and metastasis, halaman 615–624 The draft genome of the grass carp (Ctenopharyngodon idellus) provides insights into its evolution and vegetarian adaptation, halaman 625–631 Phylogeographical analysis of the dominant multidrug-resistant H58 clade of Salmonella Typhi identifies inter- and intracontinental transmission events, halaman 632–639 Analysis of loss-of-function variants and 20 risk factor phenotypes in 8,554 individuals identifies loci influencing chronic disease, halaman 640–642 Germline RECQL mutations are associated with breast cancer susceptibility, halaman 643–646 PDE3A mutations cause autosomal dominant hypertension with brachydactyly, halaman 647–653 COPA mutations impair ER-Golgi transport and cause hereditary autoimmune-mediated lung disease and arthritis, halaman 654–660 Mutations in KCNH1 and ATP6V1B2 cause Zimmermann-Laband syndrome, halaman 661–667 A germline homozygous mutation in the base-excision repair gene NTHL1 causes adenomatous polyposis and colorectal cancer, halaman 668–671 The genomic landscape of high hyperdiploid childhood acute lymphoblastic leukemia, halaman 672–676 DNA replication fidelity in Mycobacterium tuberculosis is mediated by an ancestral prokaryotic proofreader, halaman 677–681 Improved genome inference in the MHC using a population reference graph, halaman 682–688  Edit Artikel Lihat Sejarah Pengadaan  Konversi Metadata   Kembali

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