Professor Info
Group leader: Effat Farrokhi
 
Group Name: undefined
Affiliation: School of Advanced Technology
 

Research Activities:
 

Osteonectin

bone sialoprotein

vascular smooth muscle cell

hearing loss, sensorineural

genetic linkage


Selected Publications:
 

1.       Sahebi, R., Hassanian, S.M., Ghayour-Mobarhan, M., (...), Ferns, G.A., Avan, A. Scavenger receptor Class B type I as a potential risk stratification biomarker and therapeutic target in cardiovascular disease. Journal of Cellular Physiology 2019, 234(10), pp. 16925-16932.

2.       Chaleshtori, M.H., Simpson, M.A., Farrokhi, E., (...), Geshnigani, S.A., Crosby, A.H. Novel mutations in the pejvakin gene are associated with autosomal recessive non-syndromic hearing loss in Iranian families. Clinical Genetics 2007, 72(3), pp. 261-263.

3.       Omrani, S.-M., Moosavi, S.-F., Farrokhi, E. Parathelohania iranica sp. nov. (Microsporidia: Amblyosporidae) infecting malaria mosquito Anopheles superpictus (Diptera: Culicidae): Ultrastructure and molecular characterization. Journal of Invertebrate Pathology 2017, 146, pp. 1-6.

4.       Tabatabaiefar, M.A., Alasti, F., Shariati, L., (...), Chaleshtori, M.H., Van Camp, G. DFNB93, a novel locus for autosomal recessive moderate-to-severe hearing impairment. Clinical Genetics 2011, 79(6), pp. 594-598.

5.       Tabatabaiefar, M.A., Alasti, F., Zohour, M.M., (...), Noori-Daloii, M.R., Chaleshtori, M.H. Genetic linkage analysis of 15 DFNB loci in a group of Iranian families with autosomal recessive hearing loss. Iranian Journal of Public Health 2011, 40(2), pp. 34-48.


Contact:
 

Address: Department of Molecular Medicine, School of Advanced Technologies, Shahrekord University of Medical Sciences, Shahrekord, Iran

Tel: +98-38-33335651-4

Email: farrokhi@skums.ac.ir -  e_farrokhi_k@yahoo.com

internationalaffairs@skums.ac.ir
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Last Update 07/01/2023
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