Comparison of the effects of olsalazine and decitabine on the expression of CDH1 and uPA genes and cytotoxicity in MDA-MB-231 breast cancer cells

by Misagh Mohammadi Asl, Javad Mohammadi Asl, Mojgan Naghitorabi
Published 2021-01-01

Identification of a novel non-stop mutation in PDE6C gene in an Iranian family with Con-Rod Dystrophy

by Shahram Nasiri, Farah Talebi, Javad Mohammadi Asl, Farideh Ghanbari Mardasi
Published 2020-08-01

Evaluation of the effect of oral taurine supplementation on fasting levels of fibroblast growth factors, β-Klotho co-receptor, some biochemical indices and body composition in obes...

by Fatemeh Haidari, Maryam Asadi, Javad mohammadi-asl, Kambiz Ahmadi-Angali
Published 2019-05-01

Identification of a Novel Frameshift Mutation in the TECTA Gene in an Iranian Family With Autosomal Nonsyndromic Hearing Loss

by Javad Mohammadi-Asl, Nader Saki, Majid Karimi, Farideh Ghanbari Mardasi
Published 2021-03-01

An intelligent prenatal screening system for the prediction of Trisomy-21

by Amir Jamshidnezhad, Seyed Mohsen Hosseini, Javad Mohammadi-Asl, Mandana Mahmudi
Published 2021-01-01

Melatonin improves spermatogonial stem cells transplantation efficiency in azoospermic mice

by Mohammadreza Gholami, Ghasem Saki, Masoud Hemadi, Ali Khodadadi, Javad Mohammadi-asl
Published 2014-02-01

Identification of A Novel Missense Mutation in The Norrie Disease Gene: The First Molecular Genetic Analysis and Prenatal Diagnosis of Norrie Disease in An Iranian Family

by Farah Talebi, Farideh Ghanbari Mardasi, Javad Mohammadi Asl, Ali Lashgari, Freidoon Farhadi
Published 2018-04-01

بررسی پلی‌مورفیسم ژن سوپراکسید دیسموتاز 1 و ارتباط آن با رتینوپاتی و نفروپاتی در بیماران مبتلا به دیابت نوع 2 در اهواز...

by Javad Mohammadi-Asl, Arghavan Soleimanizadeh, Hajieh Bibi Shahbazian, Heshmatollah Shahbazian, Neda Golchin
Published 2014-06-01

Identification of a Novel WFS1 Mutation Using the Whole Exome Sequencing in an Iranian Pedigree with Autosomal Dominant Hearing Loss

by Javad Mohammadi Asl, Nader Saki, Masoud Dehdashtiyan, Mostafa Neissi, Farideh Ghanbari Mardasi
Published 2021-05-01

Identification of a novel mutation in ARSA gene in three patients of an Iranian family with metachromatic leukodystrophy disorder

by Neda Golchin, Mohammadreza Hajjari, Reza Azizi Malamiri, Majid Aminzadeh, Javad Mohammadi-asl
Published 2017-11-01

Identification of Novel PTPRQ and MYO1A Mutations in An Iranian Pedigree with Autosomal Recessive Hearing Loss

by Farah Talebi, Farideh Ghanbari Mardasi, Javad Mohammadi Asl, Saeed Tizno, Marziyeh Najafvand Zadeh
Published 2018-01-01

Molecular Aspects of Bone Resorption in β-Thalassemia Major

by Najmaldin Saki, Saeid Abroun, Fatemeh Salari, Fakher Rahim, Mohammad Shahjahani, Javad Mohammadi-Asl
Published 2016-07-01

Ginger in patients with active ulcerative colitis: a study protocol for a randomized controlled trial

by Forough Shayesteh, Fatemeh Haidari, Ali Akbar Shayesteh, Javad Mohammadi-Asl, Kambiz Ahmadi-Angali
Published 2020-03-01

Coexistence of P190 BCR/ABL transcript and CALR 52-bp deletion in chronic myeloid leukemia blast crisis: a case report

by najmaldin saki, Mohammad Seghatoleslami, Neda Ketabchi, Alireza Ordo, Javad Mohammadi-Asl, Neda Golchin
Published 2016-01-01

The Diagnostic Value of Gene Expression of FHL1 in the Differential Diagnosis of Papillary Thyroid Carcinoma and Benign Tumors

by Javad Mohammadi-Asl, Gholamabbas Dinarvand, Neda Golchin, Nader Saki, Nastran Ranjberi, Iran Rashidi
Published 2014-02-01

The pattern of gene copy number alteration (CNAs) in hepatocellular carcinoma: an in silico analysis

by Arman Shahrisa, Maryam Tahmasebi-Birgani, Hossein Ansari, Zahra Mohammadi, Vinicio Carloni, Javad Mohammadi Asl
Published 2021-07-01

Association of CYP3A4 and CYP3A5 polymorphisms with Iranian breast cancer patients

by Elham Badavi, Babak Safavi, Amir Jalali, Ghazaleh Mohammadzadeh Shahriary, Javad Mohammadi-Asl, Javad Babaei
Published 2015-07-01

Genetic Linkage Analysis of DFNB2 Locus with Autosomal Recessive Hearing Loss in Families Negative for GJB2 Mutations in Khuzestan Province

by Parisa Tahmasebi, Seyed Reza Kazemi Nezhad, Mohammad Amin Tabatabaiefar, Javad Mohammadi Asl, Nader Saki
Published 2016-09-01

Whole exome sequencing revealed a novel dystrophin-related protein-2 (DRP2) deletion in an Iranian family with symptoms of polyneuropathy

by Maryam Tahmasebi Birgani, Mohammadreza Hajjari, Neda Golchin, Bita Shalbafan, Javad Mohammadi-Asl, Forouzan Sadeghian
Published 2019-05-01

Genotype and allelic frequencies of CYP2E1*5B polymorphism in the southwest population of Iran

by Fatemeh Zanganeh, Amir Jalali, Hamid Galehdari, Ghazaleh Mohammadzadeh Shahriary, Mohamed Taha Jalali, Javad Mohammadi-Asl
Published 2014-10-01