Universität Wien FIND
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301585 VO Molecular Medicine 1 (2018S)

Monogenetic Diseases

2.00 ECTS (2.00 SWS), SPL 30 - Biologie

Details


Information

Aims, contents and method of the course

Introduction - Methods in Molecular Medicine ;- Laminopathies: mutations in nuclear lamina ;- Hämoglobin/Sickle cell anaemia and Thalassemia ;- The Presenelins/Alzheimer Disease ;- Opsine/Colour blindness ;- LDL Receptor/Familial Hypercholesterolemia ;- ApoE/Dysbetalipoproteinemia ;- Abetalipoproteinemia ;- ER Storage Diseases ;- Lysosomal Storage Diseases ; Alpha1-Antitrypsin-Mutations ;- Defects in ABC Transporters ;- CFTR/Cystic Fibrosis ;- Monogenic Heart(muscle) defects ;- Defects in Chromatin-proteins and DNA Repair ;- RNA Processing - Relevance to Diseases ;- Viral and nonviral Gene transfer in Gene therapie; Transscriptionfactors in Diseases and in Tumors ;- pRB, p53, und Tumor Suppression ;- DNA-Tumorviruses, e.g., Papilloma und Hepatitis B.

Assessment and permitted materials

Written exam.
Dates: End of June, end of October, middle of January, end of March.

Minimum requirements and assessment criteria

For a positive grade: min 50%

Examination topics

The lectures of the course

Reading list


Association in the course directory

MMB IV-1, MMB W-2, MMEI III

Last modified: Fr 15.02.2019 16:08