Journal Club

Genetisches Literaturseminar und Diskussion wissenschaftlicher Arbeiten
(Vierzehntägig, Dienstag, 9.15 Uhr, Raum D1, Schorenstrasse 16, 8603 Schwerzenbach)

Herbstsemester 2012

  • 18.09.2012, André Halbach:
    Burga A, Casanueva MO, Lehner B (2011) Predicting mutation outcome from early stochastic variation in genetic interaction partners. Nature 480:250-253
  • 02.10.2012, Barbara Kloeckener:
    Veltman JA, Brunner HG (2012) De novo mutations in human genetic disease. Nat Rev Genet 13:565-575
  • 16.10.2012, no Journal Club
  • 31.10.2012 (Mittwoch), Amit Tiwari:
    Chaki M et al. (2012) Exome capture reveals ZNF423 and CEP164 mutations, linking renal ciliopathies to DNA damage response signaling. Cell 150:533-548
  • 14.11.2012 (Mittwoch), Pascal Joset:
    Rivière JB et al. (2012) De novo mutations in the actin genes ACTB and ACTG1 cause Baraitser-Winter syndrome. Nat Genet 44:440-444
  • 27.11.2012 (Room B91, not D1), Reza Asadollahi:
    Antonica F et al. (2012) Generation of functional thyroid from embryonic stem cells. Nature 491:66-71
  • 08.01.2013, István Magyar -> postponed to 15.01.2013:
    Kordasiewicz HB et al. (2012) Sustained therapeutic reversal of Huntington's disease by transient repression of huntingtin synthesis. Neuron 74:1031-1044
  • 22.01.2013, Wolfgang Berger:
    Jonsson T et al. (2012) A mutation in APP protects against Alzheimer's disease and age-related cognitive decline. Nature 488:96-99