Endometriotic Mesenchymal Stem Cells Epigenetic Pathogenesis: Deregulation Of MiR-200b, MiR-145, And Let7b In A Functional Imbalanced Epigenetic Disease

by Parisa Mashayekhi, Mehrdad Noruzinia, Sirous Zeinali, Sepideh Khodaverdi
Published 2019-02-01

A Study of Intron 22 Inversion Type I and II of Coagulation Factor 8 Gene in Patients with Severe Hemophilia A Using IS-PCR Technique

by Narges Rouzafzay, Leila Kokabi, Sirous Zeinali, Morteza Karimipour
Published 2013-11-01

A Study of Intron 22 Inversion Type I and II of Coagulation Factor 8 Gene in Patients with Severe Hemophilia A Using IS-PCR Technique

by Narges Rouzafzay, Leila Kokabi, Sirous Zeinali, Morteza Karimipour
Published 2008-01-01

A Large Cohort Study of Genotype and Phenotype Correlations of Beta-Thalassemia in Iranian Population

by Fereshteh Maryami, Azita Azarkeivan, Mohammad Sadegh Fallah, Sirous Zeinali
Published 2016-02-01

Mutational spectrum of autosomal recessive limb-girdle muscular dystrophies in a cohort of 112 Iranian patients and reporting of a possible founder effect

by Marzieh Mojbafan, Reza Bahmani, Samira Dabbagh Bagheri, Zohreh Sharifi, Sirous Zeinali
Published 2020-01-01

Genetic Assessment of Mucopolysaccharidosis Type IV and the First Pathological Mutation of c.313A>G in the Iranian Population

by Seyed Mehdi Shafaat, Mehrdad Hashemi, Ahmad Majd, Maryam Abiri, Sirous Zeinali
Published 2020-03-01

TuMV as an efficient transient vector for expressing heterologous proteins in Nicotiana tabacum and N. benthamiana

by Mostafa Modarresi, Mokhtar Jalali-Javaran, Masoud Shams-Bakhsh, Sirous Zeinali, Maliheh Mirzaee
Published 2019-02-01

In silico design, construction and cloning of Trastuzumab humanized monoclonal antibody: A possible biosimilar for Herceptin

by Soudabeh Akbarzadeh-Sharbaf, Bagher Yakhchali, Zarrin Minuchehr, Mohammad Ali Shokrgozar, Sirous Zeinali
Published 2012-01-01

Biosimilar Gene Therapy: Investigational Assessment of Secukinumab Gene Therapy

by Ali Fallah, Hajar Estiri, Elizabeth Parrish, Mansoureh Soleimani, Sirous Zeinali, Azita Zadeh-Vakili
Published 2019-08-01

Genetic variability in Iranian limb‐girdle muscular dystrophy type 2B patients: An evidence of a founder effect

by Marzieh Mojbafan, Shirzadeh Tina, Fatemeh Zafarghandi Motlagh, Andrei Surguchov, Yalda Nilipour, Sirous Zeinali
Published 2019-12-01

Studying the Activity of Fibroblast Growth Factor 18 and Urokinase Plasminogen Activator Receptor Promoters in Two Colon Cancer Cell Lines

by Ladan Teimoori-Toolabi, Kayhan Azadmanesh, Somayeh Jamali, Amir Amanzadeh, Morteza Karimipoor, Sirous Zeinali
Published 2009-01-01

Molecular Analysis of HS-111 and 3`HS1 Variations in β-Thalassemia Intermedia Patients with High Levels of HbF

by Mohammad Hamid, Morteza Karimipoor, Sirous Zeinali, Mohammad taghi Akbari, Leila Kokabi, Frouzandeh Mahjoubi
Published 2010-01-01

Improvement of K562 Cell Line Transduction by FBS Mediated Attachment to the Cell Culture Plate

by Maryam Abbasalipour, Mohammad Ali Khosravi, Sirous Zeinali, Hossein Khanahmad, Morteza Karimipoor, Kayhan Azadmanesh
Published 2019-01-01

Microsatellite Marker Analysis for Laboratory Mice Profiling

by Reza Ahangari Cohan, Davoud Nouri Inanlou, Mohammad Hasan Samiee Aref, Sirous Zeinali, Ramin Farhoudi
Published 2019-01-01

The Evaluation of miR-21 Level in Lung Tissue and Plasma of Nsclc Patients

by Ayda Arab, Morteza Karimipoor, Shiva Irani, Arda Kiani, Sirous Zeinali, Elham Tafsiri, Kambiz Sheikhy
Published 2018-04-01

Reporting a rare form of myopathy, myopathy with extrapyramidal signs, in an Iranian family using next generation sequencing: a case report

by Marzieh Mojbafan, Somayeh Takrim Nojehdeh, Faezeh Rahiminejad, Yalda Nilipour, Seyed Hasan Tonekaboni, Sirous Zeinali
Published 2020-04-01

Autozygosity Mapping by Genome-wide Single Nucleotide Polymorphism Array Identifies a Novel Homozygous HR Mutation in a Consanguineous Family with Universal Hereditary Hair Loss

by Sirous Zeinali, Leila Youssefian, Hassan Vahidnezhad, Amir Hossein Saeidian, Soheila Sotoudeh, Hamideh Bagherian, Jouni Uitto
Published 2021-06-01

Hypotrichosis with juvenile macular dystrophy: Combination of whole‐genome sequencing and genome‐wide homozygosity mapping identifies a large deletion in CDH3 initially undetected...

by Amir Hossein Saeidian, Hassan Vahidnezhad, Leila Youssefian, Soheila Sotudeh, Meisam Sargazi, Sirous Zeinali, Jouni Uitto
Published 2019-11-01

A novel mutation in ST14 at a functionally significant amino acid residue expands the spectrum of ichthyosis-hypotrichosis syndrome

by Leila Youssefian, Andrew Touati, Amir Hossein Saeidian, Omid Zargari, Sirous Zeinali, Hassan Vahidnezhad, Jouni Uitto
Published 2017-12-01

Transfection of Human Hematopoietic Stem Cells by a Gene Targeting Construct Containing the β-Globin Gene

by Sirous Zeinali, Bahman Zainali, Mohamadali Shokrgozar, Hossein Khanahmad, Seyedeh Soghra Moosavi, Esmat Kamali, Masood Soleimani, Mojhgan Shaikhpoor
Published 2010-01-01