Nature genetics

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  Año 2006, Vol. 38, Número 5

  • Animal research and the search for understanding

    págs. 497-498

    

  • PTPN22 and invasive bacterial disease

    S. J. Chapman

    págs. 499-500

    

  • GenePattern 2.0

    M. Reich, T. Liefeld

    págs. 500-501

    

  • Iron metabolism meets signal transduction

    G. J. Anderson

    págs. 503-504

    

  • A broad band of silence

    J. F. Costello, J. S. Smith

    págs. 504-506

    

  • An adaptive path through jungle DNA

    J. de Meaux

    págs. 506-507

    

  • mtDNA clock runs out for dopaminergic neurons

    G. Manfredi

    págs. 507-508

    

  • Touching base

    pág. 509

    

  • Research Highlights

    pág. 511

    

  • Integrating genomics against infectious disease

    H. Poland

    págs. 513-514

    

  • High levels of mitochondrial DNA deletions in substantia nigra neurons in aging and Parkinson disease

    A. Bender, K. J. Krishnan

    págs. 515-517

    

  • Mitochondrial DNA deletions are abundant and cause functional impairment in aged human substantia nigra neurons

    E. Kudryavtseva, Y. Kraytsberg

    págs. 518-520

    

  • BBS10 encodes a vertebrate-specific chaperonin-like protein and is a major BBS locus

    V. Laurier, E. E. Davis, C. Stoetzel

    págs. 521-524

    

  • A recurrent mutation in the BMP type I receptor ACVR1 causes inherited and sporadic fibrodysplasia ossificans progressiva

    E. M. Shore

    págs. 525-527

    

  • X-linked Cornelia de Lange syndrome owing to SMC1L1 mutations

    A. Musio, A. Selicorni, M. L. Focarelli

    págs. 528-530

    

  • Bone morphogenetic protein signaling by hemojuvelin regulates hepcidin expression

    F. W. Huang, J. L. Babitt, D. M. Wrighting

    págs. 531-539

    

  • Epigenetic remodeling in colorectal cancer results in coordinate gene suppression across an entire chromosome band

    J. Frigola

    págs. 540-549

    

  • A common haplotype of interferon regulatory factor 5 (IRF5) regulates splicing and expression and is associated with increased risk of systemic lupus erythematosus

    E. C. Baechler, S. V. Kozyrev, R. R. Graham

    págs. 550-555

    

  • Magnitude and distribution of linkage disequilibrium in population isolates and implications for genome-wide association studies

    M. Karayiorgou, S. Service, J. DeYoung

    págs. 556-560

    

  • Mutations in embryonic myosin heavy chain (MYH3) cause Freeman-Sheldon syndrome and Sheldon-Hall syndrome

    A. Rutherford, R. M. Toydemir

    págs. 561-565

    

  • A truncating mutation of HDAC2 in human cancers confers resistance to histone deacetylase inhibition

    M. F. Fraga, S. Ropero, E. Ballestar

    págs. 566-569

    

  • MPV17 encodes an inner mitochondrial membrane protein and is mutated in infantile hepatic mitochondrial DNA depletion

    A. Spinazzola

    págs. 570-575

    

  • Systematic identification of human mitochondrial disease genes through integrative genomics

    M. Jain, S. Calvo

    págs. 576-582

    

  • Total insulin and IGF-I resistance in pancreatic ß cells causes overt diabetes

    T. Okada, K. Ueki

    págs. 583-588

    

  • Ablation of PDK1 in pancreatic ß cells induces diabetes as a result of loss of ß cell mass

    N. Hashimoto

    págs. 589-593

    

  • A distant upstream enhancer at the maize domestication gene tb1 has pleiotropic effects on plant and inflorescent architecture

    T. N. Wagler, R. M. Clark

    págs. 594-597

    

  • Corrigendum: Germline KRAS mutations cause Noonan syndrome

    S. Schubbert

    pág. 598