Wittler, Lars; Hilger, Alina; Proske, Judith et al.
Murine expression and mutation analyses of the prostate androgen-regulated mucin-like protein 1 (Parm1) gene, a candidate for human epispadiasGENE. Bd. 506. H. 2. 2012 S. 392-395
Weber, Stefanie; Thiele, Holger; Mir, Sevgi et al.
Muscarinic acetylcholine receptor M3 (CHRM3) mutation causes congenital bladder disease and a prune-belly-like syndromePEDIATRIC NEPHROLOGY. Bd. 27. H. 9. 2012 S. 1624-1624
Kubuschok, Boris; Pfreundschuh, Michael; Breit, Rainer et al.
Mutated Ras-Transfected, EBV-Transformed Lymphoblastoid Cell Lines as a Model Tumor Vaccine for Boosting T-Cell Responses Against Pancreatic Cancer: A Pilot TrialHUMAN GENE THERAPY. Bd. 23. H. 12. 2012 S. 1224-1236
Coelho, David; Kim, Jaeseung C.; Miousse, Isabelle R. et al.
Mutations in ABCD4 cause a new inborn error of vitamin B-12 metabolismNATURE GENETICS. Bd. 44. H. 10. 2012 S. 1152-+
Buers, I; Coelho, D; Kim, JC et al.
Mutations in ABCD4 lead to a novel cobalamin complementation classEUROPEAN JOURNAL OF PEDIATRICS. Bd. 171. H. 9. 2012 S. 1427-1427
Stanger, C; Wulff, K; Hardt, J et al.
Mutations in the Factor XII Gene in Solitary Cases of Recurrent Angioedema with Normal C1 Inhibitor Induced or Worsened by Oral Contraceptives or Hormonal Replacement TherapyJOURNAL OF ALLERGY AND CLINICAL IMMUNOLOGY. Bd. 129. H. 2. 2012 S. AB226-AB226
Hermanns, P; Morlot, M; Haberland, H et al.
Mutations in the PAX8 promoter region cause thyroid dysgenesisEUROPEAN JOURNAL OF PEDIATRICS. Bd. 171. H. 9. 2012 S. 1425-1425
Labisso, WL; Wirth, M; Stojanovic, N et al.
MYC directs transcription of MCL1 and eIF4E genes to control sensitivity of gastric cancer cells toward HDAC inhibitorsCELL CYCLE. Bd. 11. H. 8. 2012 S. 1593-1602
Stojanovic, N.; Labisso, L.; Wirth, M. et al.
MYC Directs Transcription of MCL1 and EIF4E Genes to Control Sensitivity of Gastric Cancer Cells Towards HDAC InhibitorsEUROPEAN JOURNAL OF CANCER. Bd. 48. 2012 S. S42-S42
Wrede, Arne; Margraf, Nils G.; Goebel, Hans H. et al.
Myofibrillar disorganization characterizes myopathy of camptocormia in Parkinson's diseaseACTA NEUROPATHOLOGICA. Bd. 123. H. 3. 2012 S. 419-432