| Kabaeva, Zhyldyz: Genetic analysis in hypertrophic cardiomyopathy: missense mutations in the ventricular myosin regulatory light chain gene |
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Name: |
Zhyldyz Temirzhanovna Kabaeva |
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Date and place of birth: |
21.10.1972, Djany-Alysh (Kyrgyzstan) |
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Marital status |
single |
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Nationality: |
Kyrgyz |
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Education |
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09.1979 - 06.1989 |
Certificate of Secondary School Education. |
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Seconary School #7. Tokmok. Kyrgyzstan. |
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08.1989 - 06.1995 |
Medical Diploma of General Practitioner in Medicine. |
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09.1995 - 07.1997 |
Post-graduate clinical training course in Internal Medicine and Cardiology. |
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National Centre of Cardiology and Internal Medicine. Bishkek. Kyrgyzstan. |
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10.1999 - 2002 |
MD-PhD student Thesis title: Genetic analysis in hypertrophic cardiomyopathy: missense mutations in the ventriuclar myosin regulatory light chain gene. |
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Charité/Franz-Volhard-Klinik at Max-Delbrück-Centrum für molekülare Medizin Humboldt-Universität zu Berlin. Berlin. Germany. |
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Supervisors: Prof. Dr. med. K. J. Osterziel and Dipl.-Ing. A. Perrot |
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Work experience |
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09.1997 - 03.1999 |
Medical Doctor at Cardiology Intensive Care Department |
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National Centre of Cardiology and Internal Medicine. |
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Bishkek. Kyrgyzstan. |
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Research experience |
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09.1997 - 06.1999 |
Research duties at Department of non-invasive diagnostic methods: Clinical and Echo evaluation of patients with caridomyopathies |
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National Centre of Cardiology and Internal Medicine. Bishkek. Kyrgyzstan |
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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. |
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CardioGenetic Laboratory. Charitè/Franz-Volhrad-Klinik. Berlin. Germany |
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Awards and honours |
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06.1999 - 07.2000 |
Awarded the DAAD fellowship for research in molecular aspects of Familial Cardiomyopathies in Germany. |
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Publications |
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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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