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Detail
JurnalNature Genetics vol. 44 no. 02 (Feb. 2012)
Bibliografi
Bahasa: (EN )    ISSN: 1061-4036    Year:: 2012    Bulan: 02    Edisi: Feb 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
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Artikel dalam koleksi ini
  1. Exome sequencing identifies recurrent somatic MAP2K1 and MAP2K2 mutations in melanoma, halaman 133–139
  2. PNPLA1 mutations cause autosomal recessive congenital ichthyosis in golden retriever dogs and humans, halaman 140–147
  3. Tissue-specific analysis of chromatin state identifies temporal signatures of enhancer activity during embryonic development, halaman 148–156
  4. Amplification of siRNA in Caenorhabditis elegans generates a transgenerational sequence-targeted histone H3 lysine 9 methylation footprint, halaman 157–164
  5. Frequent somatic mutations in MAP3K5 and MAP3K9 in metastatic melanoma identified by exome sequencing, halaman 165–169
  6. ABCB6 is dispensable for erythropoiesis and specifies the new blood group system Langereis, halaman 170–173
  7. Null alleles of ABCG2 encoding the breast cancer resistance protein define the new blood group system Junior, halaman 174–177
  8. A genome-wide association study in Han Chinese identifies multiple susceptibility loci for IgA nephropathy, halaman 178–182
  9. A genome-wide association study in Chinese men identifies three risk loci for non-obstructive azoospermia, halaman 183–186
  10. Meta-analysis of genome-wide association studies identifies three new risk loci for atopic dermatitis, halaman 187–192
  11. CEP41 is mutated in Joubert syndrome and is required for tubulin glutamylation at the cilium, halaman 193–199
  12. Mutations in the colony stimulating factor 1 receptor (CSF1R) gene cause hereditary diffuse leukoencephalopathy with spheroids, halaman 200–205
  13. Crh and Oprm1 mediate anxiety-related behavior and social approach in a mouse model of MECP2 duplication syndrome, halaman 206–211
  14. Genome-wide patterns of genetic variation in worldwide Arabidopsis thaliana accessions from the RegMap panel, halaman 212–216
  15. Genomic and metabolic prediction of complex heterotic traits in hybrid maize, halaman 217–220
  16. De novo assembly and genotyping of variants using colored de Bruijn graphs, halaman 226–232

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