Nature genetics

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  Año 2005, Vol. 37, Número 8

  • Microdeletion and IGF2 loss of imprinting in a cascade causing Beckwith-Wiedemann syndrome with Wilms' tumor

    págs. 785-788

    

  • Are we making progress in the debate over racial and ethnic categories in biomedical research?

    S. M. Wolf

    págs. 789-790

    

  • Endless Forms Most Beautiful: The New Science of Evo-Devo By Sean B Carroll

    A. S. Wilkins

    págs. 791-792

    

  • Unraveling TACIt functions

    F. Martin, V. M. Dixit

    pág. 793

    

  • Pharmacogenetics goes 3D

    Howard Lewis McLeod

    págs. 794-795

    

  • Splicing on the brain

    B. J. Blencowe

    págs. 796-798

    

  • A deletion in the gene encoding sphingomyelin phosphodiesterase 3 (Smpd3) results in osteogenesis and dentinogenesis imperfecta in the mouse

    I. Aubin, C. P. Adams

    págs. 803-805

    

  • Mutations in the endosomal ESCRTIII-complex subunit CHMP2B in frontotemporal dementia

    G. Skibinski, N. J. Parkinson

    págs. 806-808

    

  • Comprehensive analysis of heterochromatin- and RNAi-mediated epigenetic control of the fission yeast genome

    H. P. Cam, T. Sugiyama

    págs. 809-819

    

  • Mutations in TNFRSF13B encoding TACI are associated with common variable immunodeficiency in humans

    H. M. Chapel, Q. Pan-Hammarstrom, A. D. B. Webster, U. Salzer

    págs. 820-828

    

  • TACI is mutant in common variable immunodeficiency and IgA deficiency

    E. Castigli, S. A. Wilson

    págs. 829-834

    

  • Complement factor 5 is a quantitative trait gene that modifies liver fibrogenesis in mice and humans

    H. E. Wasmuth, R. Weiskirchen, S. Hillebrandt, C. Hellerbrand

    págs. 835-843

    

  • Nova regulates brain-specific splicing to shape the synapse

    A. Williams, J. Spencer, J. Ule, A. Ule

    págs. 844-852

    

  • Chromosome-wide and promoter-specific analyses identify sites of differential DNA methylation in normal and transformed human cells

    M. I. Weber, J. J. Davies

    págs. 853-862

    

  • Variants of ENPP1 are associated with childhood and adult obesity and increase the risk of glucose intolerance and type 2 diabetes

    N. Bouatia-Naji, D. Meyre

    págs. 863-867

    

  • Demonstrating stratification in a European American population

    C. D. Campbell

    págs. 868-872

    

  • Recombination of mitochondrial DNA in skeletal muscle of individuals with multiple mitochondrial DNA heteroplasmy

    G. Zsurka, Y. Kraytsberg

    págs. 873-877

    

  • Karyotypic abnormalities create discordance of germline genotype and cancer cell phenotypes

    W. J. Yang, S. C. Raimondi, Q. Cheng

    págs. 878-882

    

  • Plk4 haploinsufficiency causes mitotic infidelity and carcinogenesis

    M. A. Ko, C. O. Rosario

    págs. 883-888

    

  • Inversion-induced disruption of the Hoxd cluster leads to the partition of regulatory landscapes

    F. Spitz, C. Herkenne, M. A. Morris

    págs. 889-893

    

  • A stress-sensitive reporter predicts longevity in isogenic populations of Caenorhabditis elegans

    S. L. Rea

    págs. 894-898

    

  • Distinct epigenetic changes in the stromal cells of breast cancers

    J. Yao, L. Cai, M. Hu, K. E. Bachman, F. van den Brule

    págs. 899-905

    

  • Short double-stranded RNA induces transcriptional gene silencing in human cancer cells in the absence of DNA methylation

    A. H. Ting, K. E. Schuebel

    págs. 906-909