AHI1 gene mutation in a consanguineous Iranian family affected by Joubert syndrome: A case report

por Neissi, Mostafa, Mabudi, Hadideh, Mohammadi‐Asl, Javad
Publicado 2021

Identification of a Novel Stop Loss Mutation in P2RX2 Gene in an Iranian Family with Autosomal Nonsyndromic Hearing Loss

por Azizi Malamiri, Reza, Mohammadi Asl, Javad, Ghanbari, Farideh
Publicado 2021

Regression Modeling and Meta-Analysis of Diagnostic Accuracy of SNP-Based Pathogenicity Detection Tools for UGT1A1 Gene Mutation

por Rahim, Fakher, Galehdari, Hamid, Mohammadi-asl, Javad, Saki, Najmaldin
Publicado 2013

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...

por Haidari, Fatemeh, Asadi, Maryam, mohammadi-asl, Javad, Ahmadi-Angali, Kambiz
Publicado 2019

Do NGS‐based techniques represent a first‐line testing in suspected Duchenne muscular dystrophy?

por Hosseini, Seyed Mohammad, Alizadeh, Nosratollah, Amini, Abolfazl, Mohammadi‐Asl, Javad
Publicado 2022

Melatonin and Testicular Damage in Busulfan Treated Mice

por Mirhoseini, Mehri, Saki, Ghasem, Hemadi, Masoud, Khodadadi, Ali, Mohammadi Asl, Javad
Publicado 2014

Melatonin improves spermatogonial stem cells transplantation efficiency in azoospermic mice

por Gholami, Mohammadreza, Saki, Ghasem, Hemadi, Masoud, Khodadadi, Ali, Mohammadi-asl, Javad
Publicado 2014

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

por Golchin, Neda, Hajjari, Mohammadreza, Malamiri, Reza Azizi, Aminzadeh, Majid, Mohammadi-asl, Javad
Publicado 2017

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

por Talebi, Farah, Ghanbari Mardasi, Farideh, Mohammadi Asl, Javad, Lashgari, Ali, Farhadi, Freidoon
Publicado 2018

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

por Mohammadi-asl, Javad, Saki, Nader, Dehdashtiyan, Masoud, Neissi, Mostafa, Ghanbari Mardasi, Farideh
Publicado 2021

Digenic Mutations in Junctional Epidermolysis Bullosa in An Iranian Family

por Riahi, Kourosh, Ghanbari Mardasi, Farideh, Talebi, Farah, Jasemi, Farzad, Mohammadi Asl, Javad
Publicado 2021

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

por Talebi, Farah, Ghanbari Mardasi, Farideh, Mohammadi Asl, Javad, Tizno, Saeed, Najafvand Zadeh, Marziye
Publicado 2018

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

por Shayesteh, Forough, Haidari, Fatemeh, Shayesteh, Ali Akbar, Mohammadi-Asl, Javad, Ahmadi-Angali, Kambiz
Publicado 2020

Study of the Role of siRNA Mediated Promoter Methylation in DNMT3B Knockdown and Alteration of Promoter Methylation of CDH1, GSTP1 Genes in MDA-MB -453 Cell Line

por Naghitorabi, Mojgan, Mir Mohammad Sadeghi, Hamid, Mohammadi Asl, Javad, Rabbani, Mohammad, Jafarian-Dehkordi, Abbas
Publicado 2017

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

por Tahmasebi-Birgani, Maryam, Hajjari, Mohammadreza, Golchin, Neda, Shalbafan, Bita, Mohammadi-Asl, Javad, Sadeghian, Forouzan
Publicado 2019

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

por Shahrisa, Arman, Tahmasebi-Birgani, Maryam, Ansari, Hossein, Mohammadi, Zahra, Carloni, Vinicio, Mohammadi Asl, Javad
Publicado 2021

MicroRNA Expression in β-Thalassemia and Sickle Cell Disease: A Role in The Induction of Fetal Hemoglobin

por Saki, Najmaldin, Abroun, Saeid, Soleimani, Masoud, Kavianpour, Maria, Shahjahani, Mohammad, Mohammadi-Asl, Javad, Hajizamani, Saeideh
Publicado 2016

A Novel Splicesite Mutation in the EDAR Gene Causes Severe Autosomal Recessive Hypohydrotic (Anhidrotic) Ectodermal Dysplasia in an Iranian Family

por Torkamandi, Shahram, Gholami, Milad, Mohammadi-asl, Javad, Rezaie, Somaye, Zaimy, Mohammad Ali, Omrani, Mir Davood
Publicado 2016

Quantitation of CDH1 promoter methylation in formalin-fixed paraffin-embedded tissues of breast cancer patients using differential high resolution melting analysis

por Naghitorabi, Mojgan, Mohammadi-Asl, Javad, Sadeghi, Hamid Mir Mohammad, Rabbani, Mohammad, Jafarian-Dehkordi, Abbas, Javanmard, Shaghayegh Haghjooy
Publicado 2016

UGT1A1 Gene Mutation due to Crigler-Najjar Syndrome in Iranian Patients: Identification of a Novel Mutation

por Mohammadi Asl, Javad, Tabatabaiefar, Mohammad Amin, Galehdari, Hamid, Riahi, Kourosh, Masbi, Mohammad Hosein, Zargar Shoshtari, Zohre, Rahim, Fakher
Publicado 2013