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Publikationen
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Weber, Stefanie; Thiele, Holger; Mir, Sevgi et al.

Muscarinic acetylcholine receptor M3 (CHRM3) mutation causes congenital bladder disease and a prune-belly-like syndrome

PEDIATRIC 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 Trial

HUMAN 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 metabolism

NATURE 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 class

EUROPEAN 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 Therapy

JOURNAL 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 dysgenesis

EUROPEAN 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 inhibitors

CELL 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 Inhibitors

EUROPEAN 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 disease

ACTA NEUROPATHOLOGICA. Bd. 123. H. 3. 2012 S. 419-432