Publications 2011

  • Castorino JJ, Gallagher-Colombo SM, Levin AV, Fitzgerald PG, Polishook J, Kloeckener-Gruissem B, Ostertag E, Philp NJ (2011) Juvenile cataract-associated mutation of solute carrier SLC16A12 impairs trafficking of the protein to the plasma membrane. Invest Ophthalmol Vis Sci 52:6774-6784
  • Curjuric I, Zemp E, Dratva J, Ackermann-Liebrich U, Bridevaux PO, Bettschart RW, Brutsche M, Frey M, Gerbase MW, Knöpfli B, Künzli N, Pons M, Schwartz J, Schindler C, Rochat T; SAPALDIA team (2011) Determinants of change in airway reactivity over 11 years in the SAPALDIA population study. Eur Respir J 37:492-500
  • Gerbase MW, Keidel D, Imboden M, Gemperli A, Bircher A, Schmid-Grendelmeier P, Bridevaux PO, Berger W, Schindler C, Rochat T, Probst-Hensch N (2011) Effect modification of IgE-mediated atopy and rhinitis by GST genotypes in passive smokers. Clin Exp Allergy 41:1579-1586
  • Glaus E, Schmid F, Da Costa R, Berger W, Neidhardt J (2011) Gene therapeutic approach using mutation-adapted U1 snRNA to correct a RPGR splice defect in patient-derived cells. Mol Ther 19:936-941
  • Kloeckener-Gruissem B, Barthelmes D, Labs S, Schindler C, Kurz-Levin M, Michels S, Fleischhauer J, Berger W, Sutter F, Menghini M (2011) Genetic association with response to intravitreal ranibizumab in patients with neovascular AMD. Invest Ophthalmol Vis Sci 52:4694-4702
  • Schmid F, Glaus E, Barthelmes D, Fliegauf M, Gaspar H, Nürnberg G, Nürnberg P, Omran H, Berger W, Neidhardt J (2011) U1 snRNA-mediated gene therapeutic correction of splice defects caused by an exceptionally mild BBS mutation. Hum Mutat 32:815-824
  • Schoenhoff FS, Cameron DE, Matyas G, Carrel TP (2011)  Cardiovascular surgery in Marfan syndrome: implications of new molecular concepts in thoracic aortic disease. Future Cardiol 7:557-569