Nature genetics

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  Año 2006, Vol. 38, Número 2

  • Organ, organelle, organism

    pág. 131

    

  • Robustness from top to bottom

    H. Kitano

    pág. 133

    

  • Ciliary proteins and exencephaly

    N. Katsanis

    págs. 135-136

    

  • Anthrax target in macrophages unveiled

    S. H. Leppla, T. H. Bugge

    págs. 137-138

    

  • Defense and counterdefense in the plant world

    P. M. Waterhouse

    págs. 138-139

    

  • Expressing physiology

    N. Hubner

    págs. 140-141

    

  • The rise and fall of the ape Y chromosome?

    C. Tyler-Smith

    págs. 141-143

    

  • Touching base

    pág. 145

    

  • Research Highlights

    pág. 147

    

  • Evidence for an instructive mechanism of de novo methylation in cancer cells

    Y. Schlesinger, I. Keshet

    págs. 149-153

    

  • MKS1, encoding a component of the flagellar apparatus basal body proteome, is mutated in Meckel syndrome

    J. Tallila, R. Salonen, M. Kyttala

    págs. 155-157

    

  • Comparative analysis of chimpanzee and human Y chromosomes unveils complex evolutionary pathway

    H. Noguchi, Y. Kuroki, T. D. Taylor, A. Toyoda

    págs. 158-167

    

  • Evolution of new protein topologies through multistep gene rearrangements

    S. G. Peisajovich

    págs. 168-174

    

  • Cooperative and antagonistic interactions between Sall4 and Tbx5 pattern the mouse limb and heart

    K. Koshiba-Takeuchi

    págs. 175-183

    

  • Spectrin mutations cause spinocerebellar ataxia type 5

    M. R. Weatherspoon, Y. Ikeda, K. A. Dick

    págs. 184-190

    

  • The transmembrane protein meckelin (MKS3) is mutated in Meckel-Gruber syndrome and the wpk rat

    M. Consugar, U. M. Smith

    págs. 191-196

    

  • Disrupted function and axonal distribution of mutant tyrosyl-tRNA synthetase in dominant intermediate Charcot-Marie-Tooth neuropathy

    A. Jordanova

    págs. 197-202

    

  • A unified mixed-model method for association mapping that accounts for multiple levels of relatedness

    G. Pressoir, J. Yu, W. H. Briggs

    págs. 203-208

    

  • Joint analysis is more efficient than replication-based analysis for two-stage genome-wide association studies

    Gonçalo R. Abecasis, A. D. Skol, L. J. Scott

    págs. 209-213

    

  • Evaluating potential for whole-genome studies in Kosrae, an isolated population in Micronesia

    P. E. Bonnen

    págs. 214-217

    

  • The sex-specific genetic architecture of quantitative traits in humans

    L. A. Weiss

    págs. 218-222

    

  • Conserved noncoding sequences are selectively constrained and not mutation cold spots

    J. A. Drake

    págs. 223-227

    

  • The role of microRNA-1 and microRNA-133 in skeletal muscle proliferation and differentiation

    J. F. Chen, E. M. Mandel, J. M. Thomson

    págs. 228-233

    

  • Physiogenomic resources for rat models of heart, lung and blood disorders

    A. E. Kwitek, H. y. Wang, N. Bhagabati, R. L. Malek, A. S. Greene, G. Borchardt

    págs. 234-239

    

  • Nalp1b controls mouse macrophage susceptibility to anthrax lethal toxin

    E. D. Boyden, W. F. Dietrich

    págs. 240-244

    

  • Trak1 mutation disrupts GABAA receptor homeostasis in hypertonic mice

    S. L. Gilbert

    págs. 245-250

    

  • Identification of direct DAF-16 targets controlling longevity, metabolism and diapause by chromatin immunoprecipitation

    S. Wook Oh, A. Mukhopadhyay

    págs. 251-257

    

  • Induction, suppression and requirement of RNA silencing pathways in virulent Agrobacterium tumefaciens infections

    P. Dunoyer, C. Himber, O. Voinnet

    págs. 258-263

    

  • Corrigendum: Deficiency of UBR1, a ubiquitin ligase of the N-end rule pathway, causes pancreatic dysfunction, malformations and mental retardation (Johanson-Blizzard syndrome)

    M. M. Lerch, J. Mayerle, M. Zenker, A. Tagariello

    pág. 265