Emran Esmaeilzadeh

I completed my Ph.D. course at the University of Social Welfare and rehabilitation science, Tehran, Iran (June 28, 2019) with a specialization in medical genetics. Currently, I am an assistant professor at the Fetal Health Center of Hope Generation Foundation in Iran. I am also the director and supervisor of a Medical genetics lab in Tehran, Iran. My MSc thesis was conducted in consultation with Dr. Mossa Gardaneh, Associate Professor in Molecular Genetics at the National Institute of Genetic Engineering and Biotechnology of Tehran, Iran, examines the use of recombinant lentiviral vectors for gene transferring in multiple cell lines for evaluating the changes in various genes expression. My doctoral dissertation was conducted in consultation with Prof. Hamid Reza Khorram Khorshid at the University of Social welfare and rehabilitation science and examines the properties and genetic effects of a new compound in a mouse model of Multiple sclerosis. In the MSc and Ph.D. courses, I have participated in various research programs that led to multiple publications. (https://scholar.google.com/scholar?hl=en&as_sdt=2007&q=emran+esmaeilzadeh&oq=emran)

Living in : Iran

Gender : MaleRace : White

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Academic Profile

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Educations

Laboratory SciencesPhDUniversity of Social Welfare and Rehabilitation Sciences Tehran2019-05-01 Iran

Supervisor's name :Prof. Hamid Reza Khorram Khorshid

Title :

Using Curcumin for evaluating the gene expression in Multiple sclerosis models.

Work Experiences

Laboratory Supervisor

at Hope generation foundatio

I am currently working in this role

research assistant

at Fetal health research cen

I am currently working in this role

English Scores

IELTS01-Mar-2022

6/9Total

Reading :

6.5/9

Speaking :

5.5/9

Listening :

6/9

Writing :

6/9

Journal Publications

Publication Title :

Protective effects of Herbal Compound (IM253) on the inflammatory responses and oxidative stress in a mouse model of multiple sclerosisFirst author

Journal :

Multiple Sclerosis and Related Disorders

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Publication Title :

Whole-exome sequencing revealed a novel homozygous missense variant in OSGEP gene: a case report of Galloway–Mowat syndrome in IranFirst author

Journal :

CEN Case Reports

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Publication Title :

Strong association of common variants in the miRNA-binding site of NOD2 gene with clinicopathological characteristics and disease activity of systemic lupus erythematosusFirst author

Journal :

Clinical Rheumatology

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Publication Title :

miRNA-binding site polymorphism in IL-15RA gene in rheumatoid arthritis and systemic lupus erythematosus: correlation with disease risk and clinical characteristicsFourth author

Journal :

Clinical Rheumatology

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Publication Title :

Whole exome sequencing identified a novel homozygous ARV1 mutation in an Iranian family with developmental and epileptic encephalopathy-38First author

Journal :

Meta Gene

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Publication Title :

Curcumin ameliorates experimental autoimmune encephalomyelitis in a C57BL/6 mouse modelFirst author

Journal :

Drug Development Research

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Publication Title :

Shikonin Protects Dopaminergic Cell Line PC12 Against 6-Hydroxydopamine-Mediated Neurotoxicity Via Both Glutathione-Dependent and Independent Pathways and by Inhibiting ApoptosisFirst author

Journal :

Neurochemical Research

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Research Keywords

Gene expression

whole exome sequencing