SubjectsSubjects(version: 945)
Course, academic year 2018/2019
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Cytogenetics – View from Laboratory Praxis - EA0104030
Title: Cytogenetika - pohled z laboratorní praxe
Guaranteed by: Ústav biologie (14-30)
Faculty: Faculty of Medicine in Pilsen
Actual: from 2018
Semester: summer
Points: 2
E-Credits: 2
Examination process: summer s.:
Hours per week, examination: summer s.:4/0, C [HS]
Extent per academic year: 4 [hours]
Capacity: unknown / unknown (unknown)
Min. number of students: 3
4EU+: no
Virtual mobility / capacity: no
Key competences:  
State of the course: cancelled
Language: Czech
Teaching methods: full-time
Teaching methods: full-time
Level:  
For type:  
Guarantor: doc. RNDr. Pavel Dvořák, Ph.D.
Incompatibility : EAV030X01
Interchangeability : EAV030X01
Is incompatible with: EAV030X01
Is interchangeable with: EAV030X01
Annotation
Last update: Zdenka Křížková (03.11.2017)
This seminar extends the basic information about cytogenetics taught during the compulsory biology seminar in the first year. After a brief summary of the historical milestones in the cytogenetic field and an overview of the use of cytogenetic methods in present medicine, relevant examples from the areas of prenatal, postnatal and cancer cytogenetics are discussed.
Literature
Last update: Zdenka Křížková (03.11.2017)

I. D. Young: Medical genetics, Oxford University Press, 2010.

D. E. Rooney: Human Cytogenetics - Constitutional Analysis - Malignancy and Acquired Abnormalities, Oxford University Press, 2001.

J. L. Huret et al.: Atlas of Genetics and Cytogenetics in Oncology and Haematology [online]. http://atlasgeneticsoncology.org/

Syllabus
Last update: Zdenka Křížková (03.11.2017)

Morgan's fly room; Tjio and Levan – the correct number of chromosomes in humans; Lejeune and Jacobs - supernumerary copy of chromosome 21 in Down syndrome patients; Nowell and Hungerford – Philadelphia chromosome and leukemia; methodology of chromosome karyotyping; G and R banding; FISH and CGH methods; Denver and Paris cytogenetic nomenclature; ISCN and common chromosomal abnormalities; amniocentesis and prenatal screening of chromosomal abnormalities; chorionic villi sampling; microdeletion and microduplication syndromes; oncocytogenetics; the story of Gleevec; biological therapy in cancer.

 
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