Nature genetics

• 

  Año 2006, Vol. 38, Número 9

  • Structural variants deconstruct the genome

    pág. 959

    

  • Structural variants deconstruct the genome

    pág. 959

    

  • The ciliary proteome database: an integrated community resource for the genetic and functional dissection of cilia

    Adrian Gherman, Erica E. Davis, Nicholas Katsanis

    págs. 961-962

    

  • Testing for association between MeCP2 and the brahma-associated SWI/SNF chromatin-remodeling complex

    Keping Hu, Xinsheng Nan, Adrian Bird, Weidong Wang

    págs. 962-964

    

  • Reply to “Testing for association between MeCP2 and the brahma-associated SWI/SNF chromatin-remodeling complex”

    K. N. Harikrishnan, Sharmistha Pal, Michael Yarski, Emma K. Baker, Maggie Z. Chow, Michelle G. de Silva, Jun Okabe, Peter L. Jones, Saïd Sif, Assam El-Osta

    págs. 964-967

    

  • Iron homeostasis in the brain: complete iron regulatory protein 2 deficiency without symptomatic neurodegeneration in the mouse

    Bruno Galy, Sabine M. Hölter, Thomas Klopstock, Dunja Ferring, Lore Becker, Sylvia Kaden, Wolfgang Wurst, Hermann-Josef Gröne, Matthias W. Hentze

    págs. 967-969

    

  • Reply to “Iron homeostasis in the brain: complete iron regulatory protein 2 deficiency without symptomatic neurodegeneration in the mouse”

    Manik C. Ghosh, Hayden Ollivierre-Wilson, Sharon Cooperman, Tracey A. Rouault

    págs. 969-970

    

  • Genetic testing: care, consent and liability

    Neil F. Sharpe

    pág. 970

    

  • Genetic testing: care, consent and liability

    N. F. Sharpe

    pág. 970

    

  • The magnum opus of a tough scientist

    Nori Satoh

    Es reseña de:

    • The Regulatory Genome: Gene Regulatory Networks in Development and Evolution

      Eric H Davidson

      Academic Press, 2006

    pág. 971

    

  • Chromosome instability leaves its mark

    Jonathan R. Pollack

    • Resumen

    págs. 973-974

    

  • Genome structural variation and sporadic disease traits

    James R. Lupski

    • Resumen

    págs. 974-976

    

  • Reversal of fortune

    Lubov Timchenko

    págs. 976-977

    

  • Reversal of fortune

    L. Timchenko

    págs. 976-977

    

  • A Hopscotch-chromatin connection

    Aurel Betz, James E. Darnell

    • Resumen

    págs. 977-979

    

  • Protein expression tells only half the story

    Susanna K. Remold

    • Resumen

    págs. 979-980

    

  • Touching base

    pág. 981

    

  • Touching base

    pág. 981

    

  • Research highlights

    pág. 983

    

  • Research highlights

    pág. 983

    

  • How genetic analysis tests theories of animal aging

    Siegfried Hekimi

    • Resumen

    págs. 985-991

    

  • Multiple knockout analysis of genetic robustness in the yeast metabolic network

    David Deutscher, Isaac Meilijson, Martin Kupiec, Eytan Ruppin

    • Resumen

    págs. 993-998

    

  • A new chromosome 17q21.31 microdeletion syndrome associated with a common inversion polymorphism

    Corrado Romano, Nicole de Leeuw, Joris A. Veltman, Albert Schinzel, Lisenka E. L. M. Vissers, Erik A. Sistermans, Ad Geurts van Kessel, Alessandra Baumer, Marco Fichera, Bert B. A. de Vries, Han G. Brunner, Jacqueline Schoumans, Britt-Marie Anderlid, Edwin Reyniers, R. Frank Kooy, Regina Regan, Samantha J. L. Knight, Rolph Pfundt, Nine V. Knoers, David A. Koolen

    págs. 999-1001

    

  • A new chromosome 17q21.31 microdeletion syndrome associated with a common inversion polymorphism

    D. A. Koolen, L. E. Vissers

    págs. 999-1001

    

  • In silico method for inferring genotypes in pedigrees

    Joshua T. Burdick, Gonçalo R. Abecasis, Vivian G. Cheung

    • Resumen

    págs. 1002-1004

    

  • Characterization of the Drosophila melanogaster genome at the nuclear lamina

    Bas van Steensel, Wendy Talhout, Helen Pickersgill, Maarten Fornerod, Bernike Kalverda, Elzo de Wit

    págs. 1005-1014

    

  • Characterization of the Drosophila melanogaster genome at the nuclear lamina

    H. Pickersgill

    págs. 1005-1014

    

  • Unraveling adaptive evolution: how a single point mutation affects the protein coregulation network

    Christopher G. Knight, Nicole Zitzmann, Sripadi Prabhakar, Robin Antrobus, Raymond Dwek, Holger Hebestreit, Paul B. Rainey

    • Resumen

    págs. 1015-1022

    

  • Molecular analysis of flies selected for aggressive behavior

    Herman A. Dierick, Ralph J. Greenspan

    • Resumen

    págs. 1023-1031

    

  • Microdeletion encompassing MAPT at chromosome 17q21.3 is associated with developmental delay and learning disability

    Nigel P. Carter, Carla Rosenberg, Elena Prigmore, Carolyn Dunn, Lisa Rickman, Dimitrios Kalaitzopoulos, Howard Martin, Alan M Pittman, Charles Shaw-Smith, Andrew J. Lees, Monica C. Varela, Keith Porter, Rebecca Curley, Celia P. Koiffmann, Sally Cumming, Susan Gribble, Lionel Willatt, Rohan de Silva, Ana C. V. Krepischi-Santos, Helen V. Firth

    págs. 1032-1037