Bejelentkezés
 Fórum
 
 
Témakiírás
 
Málnási Csizmadia András
Motor Pharmacology: motor fehérje inhibitor hatóanyagok fejlesztése stroke utáni regeneráció elősegítésére

TÉMAKIÍRÁS

Intézmény: Eötvös Loránd Tudományegyetem
biológiai tudományok
Biológia Doktori Iskola

témavezető: Málnási Csizmadia András
helyszín (magyar oldal): ELTE TTK Biokémiai Tanszék
helyszín rövidítés: ELTE


A kutatási téma leírása:

"Recently we discovered the first in vivo applicable inhibitor specific to the myosin 2 motor protein. In our body there are several different myosin 2 enzymes responsible for series of physiological functions including skeletal, smooth and cardiac muscle contraction, as well as cell division, motility and neurite outgrowth, which is related to neural plasticity and regeneration. By targeting these motor proteins with specific drugs we will be capable of alleviating symptoms of stroke or helping people suffering from spasms, scarring or fibrocyte related disorders. Given its significant functions, non-muscle myosin 2 (NM2) is becoming an important therapeutic target in various diseases, including stroke, a leading cause of disability and mortality. Currently no effective therapy is available. Our laboratory has developed a biologically safe myosin 2 specific motor protein inhibitor, to repair the damaged brain tissue through the formation of vascular and neuronal networks. See more: http://www.motorpharmacology.com and http://www.malnalab.hu
The PhD candidate will characterize the pharmacological and biochemical activities of this inhibitor by in vivo, in vitro and biochemical methods. He/she will also contribute in the development of further drug candidates. "

előírt nyelvtudás: angol
további elvárások: 
"We expect high motivation and good knowledge in biochemistry and/or neuronal physiology.
"

felvehető hallgatók száma: 1

Jelentkezési határidő: 2019-05-31

 
Minden jog fenntartva © 2007, Országos Doktori Tanács - a doktori adatbázis nyilvántartási száma az adatvédelmi biztosnál: 02003/0001. Program verzió: 2.2358 ( 2017. X. 31. )