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Analysis of TMIE gene mutations including the first large deletion of exon 1 with autosomal recessive non-syndromic deafness

BMC medical genomics, 2022-06, Vol.15 (1), p.1-133, Article 133

2022

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The genetic landscape and possible therapeutics of neurofibromatosis type 2

Cancer cell international, 2023-05, Vol.23 (1), p.99-99, Article 99

2023

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Association study between polymorphisms in MIA3, SELE, SMAD3 and CETP genes and coronary artery disease in an Iranian population

BMC cardiovascular disorders, 2022-06, Vol.22 (1), p.1-298, Article 298

2022

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Genetic insights into PHARC syndrome: identification of a novel frameshift mutation in ABHD12

BMC medical genomics, 2023-10, Vol.16 (1), p.1-235, Article 235

2023

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A novel nonsense mutation in TUSC3 is responsible for non‐syndromic autosomal recessive mental retardation in a consanguineous Iranian family

American journal of medical genetics. Part A, 2011-08, Vol.155 (8), p.1976-1980

2011

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Alginate/chitosan hydrogel containing olfactory ectomesenchymal stem cells for sciatic nerve tissue engineering

Journal of cellular physiology, 2019-09, Vol.234 (9), p.15357-15368

2019

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How Transmembrane Inner Ear (TMIE) plays role in the auditory system: A mystery to us

Journal of cellular and molecular medicine, 2021-07, Vol.25 (13), p.5869-5883

2021

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Deep sequencing reveals 50 novel genes for recessive cognitive disorders

Nature (London), 2011-10, Vol.478 (7367), p.57-63

2011

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Human olfactory stem cells: As a promising source of dopaminergic neuron-like cells for treatment of Parkinson's disease

Neuroscience letters, 2019-03, Vol.696, p.52-59

2019

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Differentiation of human mesenchymal stem cells (MSC) to dopaminergic neurons: A comparison between Wharton’s Jelly and olfactory mucosa as sources of MSCs

Journal of chemical neuroanatomy, 2019-03, Vol.96, p.126-133

2019

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Novel phenotype and genotype spectrum of NARS2 and literature review of previous mutations

Irish journal of medical science, 2022-08, Vol.191 (4), p.1877-1890

2022

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Transcranial sonography in neurodegeneration with brain iron accumulation disorders

Clinical neurology and neurosurgery, 2024-01, Vol.236, p.108074-108074, Article 108074

2024

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Differentiation of neural crest stem cells from nasal mucosa into motor neuron-like cells

Journal of chemical neuroanatomy, 2018-10, Vol.92, p.35-40

2018

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Role of GJB2 and GJB6 in Iranian Nonsyndromic Hearing Impairment: From Molecular Analysis to Literature Reviews

Fetal and pediatric pathology, 2020-01, Vol.39 (1), p.1-12

2020

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Expanding phenotype heterogeneity of NARS2 by presenting subdural hematoma and parenchymal hemorrhage

Journal of clinical laboratory analysis, 2023-11, Vol.37 (21-22), p.e24983-n/a

2023

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Association between TBXT rs2305089 polymorphism and chordoma in Iranian patients identified by a developed T‐ARMS‐PCR assay

Journal of clinical laboratory analysis, 2022-01, Vol.36 (1), p.e24150-n/a

2022

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Expression levels of the BAK1 and BCL2 genes highlight the role of apoptosis in age-related hearing impairment

Clinical interventions in aging, 2016-01, Vol.11, p.1003-1008

2016

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Expression levels of the BAKI and BCL2 genes highlight the role of apoptosis in age-related hearing impairment.(ORIGINAL RESEARCH)

Clinical interventions in aging, 2016-01, Vol.11

2016

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پیرگوشی: از دانش کنونی تا چشم‌اندازهای آینده‌ی درمان

Majallah-i dānishkadah-i pizishkī-i Iṣfahān. (Online), 2016-07, Vol.34 (382), p.526-535

2016

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Association of genetic variations in the mitochondrial DNA control region with presbycusis

Clinical interventions in aging, 2017-01, Vol.12, p.459-465

2017

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The potential role for use of mitochondrial DNA copy number as predictive biomarker in presbycusis

Therapeutics and clinical risk management, 2016-01, Vol.12, p.1573-1578

2016

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Association of nuclear and mitochondrial genes with audiological examinations in Iranian patients with nonaminoglycoside antibiotics-induced hearing loss

Therapeutics and clinical risk management, 2016-01, Vol.12 (Issue 1), p.117-128

2016

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The anticipation and inheritance pattern of c.487A>G mutation in the GJB2 gene

Archives of Iranian medicine, 2012-01, Vol.15 (1), p.49

2012

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Analysis of TMIE gene mutations including the first large deletion of exon 1 with autosomal recessive non-syndromic deafness

The genetic landscape and possible therapeutics of neurofibromatosis type 2

Association study between polymorphisms in MIA3, SELE, SMAD3 and CETP genes and coronary artery disease in an Iranian population

Genetic insights into PHARC syndrome: identification of a novel frameshift mutation in ABHD12

A novel nonsense mutation in TUSC3 is responsible for non‐syndromic autosomal recessive mental retardation in a consanguineous Iranian family

Alginate/chitosan hydrogel containing olfactory ectomesenchymal stem cells for sciatic nerve tissue engineering

How Transmembrane Inner Ear (TMIE) plays role in the auditory system: A mystery to us

Deep sequencing reveals 50 novel genes for recessive cognitive disorders

Human olfactory stem cells: As a promising source of dopaminergic neuron-like cells for treatment of Parkinson's disease

Differentiation of human mesenchymal stem cells (MSC) to dopaminergic neurons: A comparison between Wharton’s Jelly and olfactory mucosa as sources of MSCs

Novel phenotype and genotype spectrum of NARS2 and literature review of previous mutations

Transcranial sonography in neurodegeneration with brain iron accumulation disorders

Differentiation of neural crest stem cells from nasal mucosa into motor neuron-like cells

Role of GJB2 and GJB6 in Iranian Nonsyndromic Hearing Impairment: From Molecular Analysis to Literature Reviews

Expanding phenotype heterogeneity of NARS2 by presenting subdural hematoma and parenchymal hemorrhage

Association between TBXT rs2305089 polymorphism and chordoma in Iranian patients identified by a developed T‐ARMS‐PCR assay

Expression levels of the BAK1 and BCL2 genes highlight the role of apoptosis in age-related hearing impairment

Expression levels of the BAKI and BCL2 genes highlight the role of apoptosis in age-related hearing impairment.(ORIGINAL RESEARCH)

پیرگوشی: از دانش کنونی تا چشم‌اندازهای آینده‌ی درمان

Association of genetic variations in the mitochondrial DNA control region with presbycusis

Autosomal recessive mental retardation: homozygosity mapping identifies 27 single linkage intervals, at least 14 novel loci and several mutation hotspots

The potential role for use of mitochondrial DNA copy number as predictive biomarker in presbycusis

Homozygosity mapping in consanguineous families reveals extreme heterogeneity of non-syndromic autosomal recessive mental retardation and identifies 8 novel gene loci

Association of nuclear and mitochondrial genes with audiological examinations in Iranian patients with nonaminoglycoside antibiotics-induced hearing loss

The anticipation and inheritance pattern of c.487A>G mutation in the GJB2 gene

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