Abteilungen

Abteilung Humangenetik

• Batsukh T, Pieper L, Koszucka AM, von Velsen N, Hoyer-Fender S, Elbracht M, Bergman JEH, Hoefsloot LH, Pauli S (2010):
  CHD8 interacts with CHD7, a protein which is mutated in CHARGE syndrome. HUM MOL GENET, 19(14): 2858-66.
  
• Bonn F, Pantakani K, Shoukier M, Langer T, Mannan AU (2010):
  Functional evaluation of paraplegin mutations by a yeast complementation assay. HUM MUTAT, 31(5): 617-21.
  
• Dressel R, Nolte J, Elsner L, Novota P, Guan K, Streckfuss-Bömeke K, Hasenfuss G, Jaenisch R, Engel W (2010):
  Pluripotent stem cells are highly susceptible targets for syngeneic, allogeneic, and xenogeneic natural killer cells. FASEB J, [Epub ahead of print].
  
• Ecke I, Petry F, Rosenberger A, Tauber S, Mönkemeyer S, Hess I, Dullin C, Kimmina S, Pirngruber J, Johnsen Steven A, Uhmann A, Nitzki F, Wojnowski L, Schulz-Schaeffer W, Witt O, Hahn H (2009):
  Antitumor effects of a combined 5-aza-2'deoxycytidine and valproic acid treatment on rhabdomyosarcoma and medulloblastoma in Ptch mutant mice. CANCER RES, 69(3): 887-95.
  
• Unger S, Böhm D, Kaiser FJ, Kaulfuss S, Borozdin W, Buiting K, Burfeind P, Böhm J, Barrionuevo F, Craig A, Borowski K, Keppler-Noreuil K, Schmitt-Mechelke T, Steiner B, Bartholdi D, Lemke J, Mortier G, Sandford R, Zabel B, Superti-Furga A, Kohlhase J (2008):
  Mutations in the cyclin family member FAM58A cause an X-linked dominant disorder characterized by syndactyly, telecanthus and anogenital and renal malformations. NAT GENET, 40(3): 287-9.

Suchworte: Chromosomendiagnostik, DNA-Diagnostik, Entwicklungsgenetik, Erblich bedingte Erkrankungen, Erbkrankheiten, Genetische Beratungsstelle, Gentests, männliche Infertilität, Unfruchtbarkeit des Mannes, Stammzellen, Tumorgenetik