Kabaeva, Zhyldyz: Genetic analysis in hypertrophic cardiomyopathy: missense mutations in the ventricular myosin regulatory light chain gene

II

B. Curriculum Vitae

Name:

Zhyldyz Temirzhanovna Kabaeva

Date and place of birth:

21.10.1972, Djany-Alysh (Kyrgyzstan)

Marital status

single

Nationality:

Kyrgyz

 

 

 

 

Education

 

 

 

09.1979 - 06.1989

Certificate of Secondary School Education.

Seconary School #7. Tokmok. Kyrgyzstan.

 

 

08.1989 - 06.1995

Medical Diploma of General Practitioner in Medicine.
Kyrgyz State Medical Institute. Bishkek. Kyrgyzstan

 

 

09.1995 - 07.1997

Post-graduate clinical training course in Internal Medicine and Cardiology.

National Centre of Cardiology and Internal Medicine. Bishkek. Kyrgyzstan.

 

 

10.1999 - 2002

MD-PhD student Thesis title: Genetic analysis in hypertrophic cardiomyopathy: missense mutations in the ventriuclar myosin regulatory light chain gene.

Charité/Franz-Volhard-Klinik at Max-Delbrück-Centrum für molekülare Medizin Humboldt-Universität zu Berlin. Berlin. Germany.

Supervisors: Prof. Dr. med. K. J. Osterziel and Dipl.-Ing. A. Perrot

 

 

Work experience

 

 

 

09.1997 - 03.1999

Medical Doctor at Cardiology Intensive Care Department

National Centre of Cardiology and Internal Medicine.

Bishkek. Kyrgyzstan.

 

 

Research experience

 

 

 

09.1997 - 06.1999

Research duties at Department of non-invasive diagnostic methods: Clinical and Echo evaluation of patients with caridomyopathies

National Centre of Cardiology and Internal Medicine. Bishkek. Kyrgyzstan

 

 

10.1999 - 2002

Molecular genetics of cardiomyopathies: identification of causative genes and mutations in patients with Hypertrophic and Dilated Cardiomyopathies using PCR, single strand confromation polymorphism analysis, restriction fragment length polymorphism analysis, and direct automated DNA sequencing. Genotype-phenotype correlations.

CardioGenetic Laboratory. Charitè/Franz-Volhrad-Klinik. Berlin. Germany

 

 

Awards and honours

 

 

 

06.1999 - 07.2000

Awarded the DAAD fellowship for research in molecular aspects of Familial Cardiomyopathies in Germany.

 

 


III

Publications

 

 

 

Zhyldyz T Kabaeva, Andreas Perrot, Bastian Wolter, Rainer Dietz, Nuno Cardim, João Martins Correira, Hagen D. Schulte, Almaz A. Aldashev, Mirsaid M. Mirrakhimov , Karl Josef Osterziel. "Systematic analysis of the regulatory and essential light chain genes: genetic variants and mutations in hypertrophic cardiomyopathy“. European Journal of Human Genetics 2002; 10:741-748.

N. Bit-Avragim, A. Perrot, Z. Kabaeva, D. Usupbaeva, R. Rudenko, B. Imanov, B. Isalieva, H. Schmidt-Traub, B. Hoffmann, M.M. Mirrakhimov, R. Geßner, K.J. Osterziel. "Novel mutations in the ß-myosin heavy chain gene in Kyrgyz families with hypertrophic cardiomyopathy". 66. Jahrestagung der Deutschen Gesellschaft für Kardiologie-Herz- und Kreislaufforschung, April 2000, Mannheim.

A. Perrot, Z. Kabaeva, C. Geier, N. Bit-Avragim, R. Bergmann-Lips, E. von Hodenberg, P. Binner, T. Scheffold, K.J. Osterziel. "Die Mutation Arg58Gln für die Regulatorische Myosin Leichtkette ist assoziiert mit plötzlichen Herztod". 67. Jahrestagung der Deutschen Gesellschaft für Kardiologie-Herz- und Kreislaufforschung, April 2001, Mannheim.

Z. Kabaeva, A. Perrot, C. Geier, M. Fitschen, N. Bit-Avragim, P. Binner, T. Scheffold, N Cardim, K.J. Osterziel. "The mutation Arg58Gln in the regulatory myosin light chain gene is associated with sudden cardiac death". XXII Annual Congress of the European Society of Cardiology, September 2001, Stockholm.


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