SubjectsSubjects(version: 945)
Course, academic year 2023/2024
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. - CSVA3PDN
Title: Genetická predispozice k diabetické nefropatii
Guaranteed by: Department of Medical Genetics 3FM CU (12-GEN)
Faculty: Third Faculty of Medicine
Actual: from 2011
Semester: both
Points: 4
E-Credits: 4
Examination process:
Hours per week, examination: 0/0, C [HT]
Capacity: winter:unknown / unknown (unknown)
summer:unknown / unknown (unknown)
Min. number of students: unlimited
4EU+: no
Virtual mobility / capacity: no
Key competences:  
State of the course: not taught
Language: Czech
Teaching methods: full-time
Teaching methods: full-time
Level:  
Note: you can enroll for the course in winter and in summer semester
Guarantor: prof. MUDr. Marie Černá, DrSc.
prof. MUDr. Romana Šlamberová, Ph.D.
Examination dates   Schedule   
Annotation -
Last update: DEMOVA (24.11.2008)
Molecular-biologic analysis of predisposition genes connected with diabetic nephropathy. The comparision of genotype and phenotype. The subject is addressed to students of the 3rd and 4th years of General Medicine.
Aim of the course -
Last update: DEMOVA (24.11.2008)

Students will be introduced to basic methods of molecular biology research and predisposition to polygennic diseases.

Literature -
Last update: DEMOVA (24.11.2008)

Basic textbooks:

Thompson & Thompson: Genetics in Medicine, 6th edition, Elsevier 2004

Complementary and facultative textbooks:

Mueller RF, Young ID: Emery?s Elements of Medical Genetics, 11th edit., Churchill Livingstone 2002

Gelehrter TD, Collins FS, Ginsburg D: Principles of Medical Genetics, 2nd edit., Williams & Wilkins 1998

Sack Jr GH: Medical Genetics, McGraw-Hill 1999

Teaching methods -
Last update: DEMOVA (24.11.2008)

practice

Requirements to the exam -
Last update: DEMOVA (24.11.2008)

genotyping and phenotyping of 20 selected patients - requierement for credit

Syllabus -
Last update: RNDr. Zdeňka Polívková (16.03.2009)

The subject runs in intervale of one week, always 4 hours per week, it is a practise in laboratory containing DNA and RNA isolation and subsequenly PCR procedure.

 
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