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Postdoctoral Profiles

kabaeva

Zhyldyz Kabaeva , M.D., Ph.D.

M.D., Kyrgyz State Medical Academy, Kyrgyzstan

Ph.D., Charité-Humboldt University, Germany

 

7757 Med Sci. II
(734)764-5742

kabaeva@umich.edu

 


Current Research: 
After completing my PhD on molecular genetics of hypertrophic cardiomyopathy, I was looking for a postdoctoral position in a laboratory, which, firstly, focuses on cardiovascular research and, secondly, offers multidisciplinary approaches. Although it has been quite a bit of a transition from one field to another, Dr. Michele’s laboratory has been an ideal place. My current research is focused on molecular mechanisms of cardiomyopathy associated with muscular dystrophies.

 

 

Selected Publications:

Kabaeva Z, Zhao M, and Michele DE.   Blebbistatin extends culture life of adult mouse cardiac myocytes and allows efficient and stable transgene expression.   American journal of physiology 294: H1667-1674, 2008.

Kabaeva Z, Perrot A, Pilz B, Schulz-Menger J, Mohr FW, Dietz R, and Osterziel KJ. Returning hypertrophy after surgery in a patient with hypertrophic cardiomyopathy caused by a myosin-binding protein C mutation.   International journal of cardiology 100: 343-345, 2005.

Perrot A, Schmidt-Traub H, Hoffmann B, Prager M, Bit-Avragim N, Rudenko RI, Usupbaeva DA, Kabaeva Z, Imanov B, Mirrakhimov MM, Dietz R, Wycisk A, Tendera M, Gessner R, and Osterziel KJ.   Prevalence of cardiac beta-myosin heavy chain gene mutations in patients with hypertrophic cardiomyopathy.   Journal of molecular medicine (Berlin, Germany) 83: 468-477, 2005.

Perrot A, Kabaeva Z, Wenzel K, and Osterziel KJ.   Gene expression analysis of human tissue from patients with cardiomyopathies: a new tool for guiding therapies in the future?   Journal of cardiac surgery 20: S17-19, 2005.

Kabaeva ZT, Perrot A, Wolter B, Dietz R, Cardim N, Correia JM, Schulte HD, Aldashev AA, Mirrakhimov MM, and Osterziel KJ.   Systematic analysis of the regulatory and essential myosin light chain genes: genetic variants and mutations in hypertrophic cardiomyopathy.   Eur J Hum Genet 10: 741-748, 2002.

 

 


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