Nature genetics

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  Año 2006, Vol. 38, Número 3

  • Syndromes run together in the RAS pathway

    pág. 267

    

  • Molecular gaze for the sci guy

    M. Axton

    pág. 269

    

  • An earlier formulation of the genetic conflict hypothesis of genomic imprinting

    D. Haig, M. Westoby

    pág. 271

    

  • Upending the hair follicle

    B. A. Morgan

    págs. 273-274

    

  • Genetics and epigenetics of hydatidiform moles

    D. Bourc'his, T. H. Bestor

    págs. 274-276

    

  • Marking time

    J. C. Eissenberg

    págs. 276-277

    

  • Hedgehogs on the road to polarity

    P. L. Beales

    págs. 277-279

    

  • Touching base

    pág. 281

    

  • Research Highlights

    pág. 283

    

  • Analysis of the human protein interactome and comparison with yeast, worm and fly interaction datasets

    T. K. Gandhi

    págs. 285-293

    

  • Germline KRAS and BRAF mutations in cardio-facio-cutaneous syndrome

    T. Niihori

    págs. 294-296

    

  • Dominance relationships between self-incompatibility alleles controlled by DNA methylation

    T. Kakizaki, H. Shiba

    págs. 297-299

    

  • Mutations in NALP7 cause recurrent hydatidiform moles and reproductive wastage in humans

    B. Mazhar, Sharlene Murdoch, U. Djuric

    págs. 300-302

    

  • Ciliogenesis defects in embryos lacking inturned or fuzzy function are associated with failure of planar cell polarity and Hedgehog signaling

    J. B. Wallingford, S. L. Haigo, T. J. Park

    págs. 303-311

    

  • Feedback repression is required for mammalian circadian clock function

    R. G. Yamada, T. K. Sato

    págs. 312-319

    

  • Variant of transcription factor 7-like 2 (TCF7L2) gene confers risk of type 2 diabetes

    G. Thorleifsson, S. F. Grant, I. Reynisdottir, R. Benediktsson

    págs. 320-323

    

  • A SNP in the ABCC11 gene is the determinant of human earwax type

    K. i. Yoshiura

    págs. 324-330

    

  • Germline KRAS mutations cause Noonan syndrome

    S. Schubbert

    págs. 331-336

    

  • Loss-of-function mutations in the gene encoding filaggrin cause ichthyosis vulgaris

    A. D. Irvine, F. J. Smith, A. Terron-Kwiatkowski

    págs. 337-342

    

  • Mutations in myosin heavy chain 11 cause a syndrome associating thoracic aortic aneurysm/aortic dissection and patent ductus arteriosus

    L. Zhu, P. K. Van Kien, R. Vranckx

    págs. 343-349

    

  • Identification of an imprinting control region affecting the expression of all transcripts in the Gnas cluster

    C. M. Williamson

    págs. 350-355

    

  • Morphogenesis in skin is governed by discrete sets of differentially expressed microRNAs

    D. O'Carroll, R. Yi, H. A. Pasolli

    págs. 356-362

    

  • Polygenic control of Caenorhabditis elegans fat storage

    H. Y. Mak, L. S. Nelson

    págs. 363-368

    

  • Rhythmic CLOCK-BMAL1 binding to multiple E-box motifs drives circadian Dbp transcription and chromatin transitions

    J. A. Ripperger

    págs. 369-374

    

  • Automating sequence-based detection and genotyping of SNPs from diploid samples

    M. Stephens, J. S. Sloan, P. D. Robertson

    págs. 375-381

    

  • Long-range polony haplotyping of individual human chromosome molecules

    K. Zhang

    págs. 382-387

    

  • Corrigendum: Trak1 mutation disrupts GABAA receptor homeostasis in hypertonic mice

    S. L. Gilbert

    pág. 389

    

  • Corrigendum: Probing tumor phenotypes using stable and regulated synthetic microRNA precursors

    D. R. Simpson, R. A. Dickins, J. T. Zilfou, M. T. Hemann

    pág. 389

    

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

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

    pág. 389

    

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

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

    pág. 390