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Update of spectrum c.35delG and c.‐23+1G>A mutations on the GJB2 gene in individuals with autosomal recessive nonsyndromic hearing loss

Annals of human genetics, 2019-01, Vol.83 (1), p.1-10

2019

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A Mutation in CABP2, Expressed in Cochlear Hair Cells, Causes Autosomal-Recessive Hearing Impairment

American journal of human genetics, 2012-10, Vol.91 (4), p.636-645

2012

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Silencing of α‐N‐acetylgalactosaminidase in the gastric cancer cells amplified cell death and attenuated migration, while the multidrug resistance remained unchanged

Cell biology international, 2022-02, Vol.46 (2), p.255-264

2022

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Plasma Level Of miR-21 And miR-451 In Primary And Recurrent Breast Cancer Patients

Breast cancer targets and therapy, 2019-10, Vol.11, p.293-301

2019

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In silico and in vitro effects of the I30T mutation on myelin protein zero instability in the cell membrane

Cell biology international, 2020-02, Vol.44 (2), p.671-683

2020

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A Simple, Rapid, and Efficient Method for Isolating Mesenchymal Stem Cells from the Entire Umbilical Cord

Cell transplantation, 2016-07, Vol.25 (7), p.1287-1297

2016

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Molecular Mechanisms behind Free Radical Scavengers Function against Oxidative Stress

Antioxidants, 2017-07, Vol.6 (3), p.51

2017

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Screening of Myo7A Mutations in Iranian Patients with Autosomal Recessive Hearing Loss from West of Iran

Iranian journal of public health, 2017-01, Vol.46 (1), p.76-82

2017

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An update of spectrum and frequency of GJB2 mutations causing hearing loss in the south of Iran: A literature review

International journal of pediatric otorhinolaryngology, 2019-04, Vol.119, p.136-140

2019

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Lack of Association between ESR1 and CYP1A1 Gene Polymorphisms and Susceptibility to Uterine Leiomyoma in Female Patients of Iranian Descent

Cell journal (Yakhteh), 2014, Vol.16 (2), p.225-230

2014

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Mesenchymal stem cells versus their conditioned medium in the treatment of ischemia/reperfusion injury: Evaluation of efficacy and hepatic specific gene expression in mice

Iranian journal of basic medical sciences, 2022-07, Vol.25 (7), p.799-807

2022

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The association of VEGF rs833061 and rs2010963 polymorphisms with susceptibility to colorectal cancer in an Iranian population

Cancer epidemiology, 2021-12, Vol.75, p.102041-102041, Article 102041

2021

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Novel MYO15A variants are associated with hearing loss in the two Iranian pedigrees

BMC medical genetics, 2020-11, Vol.21 (1), p.226-226, Article 226

2020

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MIR96 Has Good Potential to Differentiate Human Bone Marrow-Derived Mesenchymal Stem Cells into Photoreceptor-Like Cells

Experimental and clinical transplantation : official journal of the Middle East Society for Organ Transplantation, 2024-02, Vol.22 (2), p.148

2024

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GJB2 mutations causing autosomal recessive non-syndromic hearing loss (ARNSHL) in two Iranian populations: Report of two novel variants

International journal of pediatric otorhinolaryngology, 2018-04, Vol.107, p.121-126

2018

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Identification and Clinical Implications of a Novel MYO15A Variant in a Consanguineous Iranian Family by Targeted Exome Sequencing

Audiology & neurotology, 2019-01, Vol.24 (1), p.25-31

2019

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Next-generation sequencing reveals a novel pathological mutation in the TMC1 gene causing autosomal recessive non-syndromic hearing loss in an Iranian kindred

International journal of pediatric otorhinolaryngology, 2019-09, Vol.124, p.99-105

2019

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Virulence factors of Helicobacter pylori vacA increase markedly gastric mucosal TGF-β1 mRNA expression in gastritis patients

Microbial pathogenesis, 2014-02, Vol.67-68, p.1-7

2014

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A Novel Cadherin 23 Variant for Hereditary Hearing Loss Reveals Additional Support for a DFNB12 Nonsyndromic Phenotype of CDH23

Audiology & neurotology, 2020, Vol.25 (5), p.258-262

2020

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A Novel Pathogenic Variant in the CABP2 Gene Causes Severe Nonsyndromic Hearing Loss in a Consanguineous Iranian Family

Audiology & neurotology, 2019, Vol.24 (5), p.258-263

2019

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Genetics of Hearing Loss in North Iran Population: An Update of Spectrum and Frequency of GJB2 Mutations

Journal of Audiology & Otology, 2019, 23(4), , pp.175-180

2019

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A Novel Pathologic Variant in OTOF in an Iranian Family Segregating Hereditary Hearing Loss

Otolaryngology-head and neck surgery, 2018-06, Vol.158 (6), p.1084-1092

2018

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A preliminary study of inherited thrombophilic risk factors in different clinical manifestations of venous thromboembolism in central Iran

Indian journal of medical research (New Delhi, India : 1994), 2015-07, Vol.142 (1), p.46-52

2015

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A pathogenic variant in SLC26A4 is associated with Pendred syndrome in a consanguineous Iranian family

International journal of audiology, 2019-10, Vol.58 (10), p.628-634

2019

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Mutations in GJB2 as Major Causes of Autosomal Recessive Non-Syndromic Hearing Loss: First Report of c.299-300delAT Mutation in Kurdish Population of Iran

Journal of Audiology & Otology, 2019, 23(1), , pp.20-26

2019

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Update of spectrum c.35delG and c.‐23+1G>A mutations on the GJB2 gene in individuals with autosomal recessive nonsyndromic hearing loss

A Mutation in CABP2, Expressed in Cochlear Hair Cells, Causes Autosomal-Recessive Hearing Impairment

Silencing of α‐N‐acetylgalactosaminidase in the gastric cancer cells amplified cell death and attenuated migration, while the multidrug resistance remained unchanged

Plasma Level Of miR-21 And miR-451 In Primary And Recurrent Breast Cancer Patients

In silico and in vitro effects of the I30T mutation on myelin protein zero instability in the cell membrane

A Simple, Rapid, and Efficient Method for Isolating Mesenchymal Stem Cells from the Entire Umbilical Cord

Molecular Mechanisms behind Free Radical Scavengers Function against Oxidative Stress

Screening of Myo7A Mutations in Iranian Patients with Autosomal Recessive Hearing Loss from West of Iran

An update of spectrum and frequency of GJB2 mutations causing hearing loss in the south of Iran: A literature review

Lack of Association between ESR1 and CYP1A1 Gene Polymorphisms and Susceptibility to Uterine Leiomyoma in Female Patients of Iranian Descent

Mesenchymal stem cells versus their conditioned medium in the treatment of ischemia/reperfusion injury: Evaluation of efficacy and hepatic specific gene expression in mice

The association of VEGF rs833061 and rs2010963 polymorphisms with susceptibility to colorectal cancer in an Iranian population

Novel MYO15A variants are associated with hearing loss in the two Iranian pedigrees

MIR96 Has Good Potential to Differentiate Human Bone Marrow-Derived Mesenchymal Stem Cells into Photoreceptor-Like Cells

GJB2 mutations causing autosomal recessive non-syndromic hearing loss (ARNSHL) in two Iranian populations: Report of two novel variants

Identification and Clinical Implications of a Novel MYO15A Variant in a Consanguineous Iranian Family by Targeted Exome Sequencing

Next-generation sequencing reveals a novel pathological mutation in the TMC1 gene causing autosomal recessive non-syndromic hearing loss in an Iranian kindred

Virulence factors of Helicobacter pylori vacA increase markedly gastric mucosal TGF-β1 mRNA expression in gastritis patients

A Novel Cadherin 23 Variant for Hereditary Hearing Loss Reveals Additional Support for a DFNB12 Nonsyndromic Phenotype of CDH23

A Novel Pathogenic Variant in the CABP2 Gene Causes Severe Nonsyndromic Hearing Loss in a Consanguineous Iranian Family

Genetics of Hearing Loss in North Iran Population: An Update of Spectrum and Frequency of GJB2 Mutations

A Novel Pathologic Variant in OTOF in an Iranian Family Segregating Hereditary Hearing Loss

A preliminary study of inherited thrombophilic risk factors in different clinical manifestations of venous thromboembolism in central Iran

A pathogenic variant in SLC26A4 is associated with Pendred syndrome in a consanguineous Iranian family

Mutations in GJB2 as Major Causes of Autosomal Recessive Non-Syndromic Hearing Loss: First Report of c.299-300delAT Mutation in Kurdish Population of Iran

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