University of Technology, Sydney

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91345 Biochemistry, Genes and Disease

6cp; 6hpw
Requisite(s): 91320 Metabolic Biochemistry
These requisites may not apply to students in certain courses. See access conditions.

Description

This subject covers biochemical and genetic aspects of human diseases for students planning careers in medical science, diagnostic biochemistry, molecular biology and biotechnology. In this subject, students learn about some of the more common heritable genetic defects and their medical and biochemical consequences. In addition, students further develop knowledge and practical skills in the biomedical applications of biochemical and molecular analysis. The lecture series covers three main areas: heritable metabolic defects, e.g. hypothyroidism, cystic fibrosis, familial hyperlipidemia, Down's syndrome; biochemical physiology and pathology, e.g. human biochemistry as expressed by lipid metabolism, detection of disease states resulting from altered biochemical systems; and current trends in biochemical/molecular research including cancer and gene therapy for diabetes. The practical component enables students to gain experience in test procedures used to detect and monitor disease, including techniques of radioimmunoassay, electrophoresis and PCR screening.

Typical availability

Spring session, City campus

Footnote(s)

This subject was formerly called Clinical Biochemistry 2.


Detailed subject description.

Fee information

Information to assist with determining the applicable fee type can be found at Understanding fees.

Access conditions

Note: The requisite information presented in this subject description covers only academic requisites. Full details of all enforced rules, covering both academic and admission requisites, are available at access conditions and My Student Admin.