Чему вы научитесь
- The course is devoted to particular questions of enzymology. The cause of hereditary enzymopathies is a genetically determined deficiency or complete absence of enzyme synthesis. We tried to make this course as modern as possible. Find out how in hereditary enzymopathies, certain metabolic pathways are disrupted, their end products are deficient and intermediates accumulate, which leads to clinical manifestations. We will acquaint you with the features of the course of hereditary enzymopathies and the presence of a latent period when the disease is not clinically manifested, but can be suspected or established on the basis of biochemical studies
О курсе
We have developed this course in such a mannerthat you can learn and understand how metabolic processes in the human body are connected and regulated, what role enzymes play in this, and what metabolic changes and consequences are caused by defects in specific enzymes, and what the successes of modern medicine in the treatment of such genetic defects are.
Для кого этот курс
First of all, this course is intended for students of medical specialties (master's or graduate students) interested in new knowledge about enzymes and pathologies associated with their defects, for practitioners, researchers in the field of biology (cell biology, molecular biology). We also recommend this course for students and researchers in all related fields.
Начальные требования
You will need a basic knowledge of inorganic and organic chemistry, biology, physiology, and biochemistry. Don't let that scare you! We have tried to make the course as accessible as possible for students. The information in the course is presented in a consistent and simple manner. We will help you understand complex topics and understand everything to the end.
Преподаватели курса
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