Publications by authors named "Mohammad Amin Tabatabaiefar"

80Publications

Next generation sequencing reveals a novel pathogenic variant in the gene.

Int J Neurosci 2020 Sep 23:1-8. Epub 2020 Sep 23.

Department of Genetics and Molecular Biology, School of Medicine, Isfahan University of Medical Sciences, Isfahan, Iran.

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http://dx.doi.org/10.1080/00207454.2020.1826944DOI Listing
September 2020

Upregulation of MTOR, RPS6KB1, and EIF4EBP1 in the whole blood samples of Iranian patients with multiple sclerosis compared to healthy controls.

Metab Brain Dis 2020 12 18;35(8):1309-1316. Epub 2020 Aug 18.

Department of Medical Genetics, School of Medicine, Tehran University of Medical Sciences, Poursina St., Tehran, 14155-6447, Iran.

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http://dx.doi.org/10.1007/s11011-020-00590-7DOI Listing
December 2020

Whole exome sequencing identifies novel compound heterozygous pathogenic variants in the MYO15A gene leading to autosomal recessive non-syndromic hearing loss.

Mol Biol Rep 2020 Jul 4;47(7):5355-5364. Epub 2020 Jul 4.

Department of Genetics and Molecular Biology, School of Medicine, Isfahan University of Medical Sciences, Isfahan, Iran.

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http://dx.doi.org/10.1007/s11033-020-05618-wDOI Listing
July 2020

Genetic polymorphisms of Y-chromosome short tandem repeats (Y-STRs) in a male population from Golestan province, Iran.

Mol Biol Res Commun 2020 Apr;9(1):11-16

Iranian Legal Medicine Research Center, Legal Medicine Organization, Tehran, Iran.

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http://dx.doi.org/10.22099/mbrc.2020.35547.1462DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC7275825PMC
April 2020

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

Audiol Neurootol 2020 2;25(5):258-262. Epub 2020 Jun 2.

Department of Genetics and Molecular Biology, School of Medicine, Isfahan University of Medical Sciences, Isfahan, Iran,

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http://dx.doi.org/10.1159/000506500DOI Listing
June 2020

A Patient with Trisomy 4p and Monosomy 10q

Arch Iran Med 2019 07 1;22(7):414-417. Epub 2019 Jul 1.

Department of Genetics and Molecular Biology, School of Medicine, Isfahan University of Medical Sciences, Isfahan, Iran.

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July 2019

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

Audiol Neurootol 2019 29;24(5):258-263. Epub 2019 Oct 29.

Department of Genetics and Molecular Biology, School of Medicine, Isfahan University of Medical Sciences, Isfahan, Iran,

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http://dx.doi.org/10.1159/000502251DOI Listing
May 2020

Evidence for expression of promoterless GFP cassette: Is GFP an ideal reporter gene in biotechnology science?

Res Pharm Sci 2019 Aug;14(4):351-358

Isfahan Cardiovascular Research Center, Cardiovascular Research Institute, Isfahan University of Medical Sciences, Isfahan, I.R. Iran.

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http://dx.doi.org/10.4103/1735-5362.263559DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6714119PMC
August 2019

Epigenetics and Common Non Communicable Disease.

Adv Exp Med Biol 2019 ;1121:7-20

Genetics Department, Erythron Pathobiology and Genetics lab, Isfahan, Iran.

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http://dx.doi.org/10.1007/978-3-030-10616-4_2DOI Listing
August 2019

Clinical and molecular assessment of 13 Iranian families with Wolfram syndrome.

Endocrine 2019 11 16;66(2):185-191. Epub 2019 Jul 16.

Department of Medical Genetics, School of Medicine, Tehran University of Medical Sciences, Poursina Ave, 16 Azar St. Keshavarz BLVD, Tehran, 1417613151, Iran.

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http://dx.doi.org/10.1007/s12020-019-02004-wDOI Listing
November 2019

Homozygosity mapping and direct sequencing identify a novel pathogenic variant in the CISD2 gene in an Iranian Wolfram syndrome family.

Acta Diabetol 2020 Jan 15;57(1):81-87. Epub 2019 Jul 15.

Department of Genetics and Molecular Biology, School of Medicine, Isfahan University of Medical Sciences, Isfahan, 81746-73461, Iran.

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http://dx.doi.org/10.1007/s00592-019-01381-yDOI Listing
January 2020

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

Int J Audiol 2019 10 12;58(10):628-634. Epub 2019 Jun 12.

Cellular and Molecular Research Center, Basic Health Sciences Institute, Shahrekord University of Medical Sciences , Shahrekord , Iran.

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http://dx.doi.org/10.1080/14992027.2019.1619945DOI Listing
October 2019

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

Int J Pediatr Otorhinolaryngol 2019 Sep 21;124:99-105. Epub 2019 May 21.

Cellular and Molecular Research Center, Basic Health Sciences Institute, Shahrekord University of Medical Sciences, Shahrekord, Iran. Electronic address:

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http://dx.doi.org/10.1016/j.ijporl.2019.05.023DOI Listing
September 2019

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

Audiol Neurootol 2019 3;24(1):25-31. Epub 2019 Apr 3.

Cellular and Molecular Research Center, Basic Health Sciences Institute, Shahrekord University of Medical Sciences, Shahrekord, Iran,

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http://dx.doi.org/10.1159/000498843DOI Listing
February 2020

Engineered zinc-finger nuclease to generate site-directed modification in the KLF1 gene for fetal hemoglobin induction.

J Cell Biochem 2018 Dec 16. Epub 2018 Dec 16.

Department of Genetics and Molecular Biology, School of Medicine, Isfahan University of Medical Sciences, Isfahan, Iran.

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http://dx.doi.org/10.1002/jcb.28130DOI Listing
December 2018

Molecular genetic study of glutaric aciduria, type I: Identification of a novel mutation.

J Cell Biochem 2019 03 11;120(3):3367-3372. Epub 2018 Sep 11.

Department of Genetics and Molecular Biology, School of Medicine, Isfahan University of Medical Sciences, Isfahan, Iran.

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http://doi.wiley.com/10.1002/jcb.27607
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http://dx.doi.org/10.1002/jcb.27607DOI Listing
March 2019

A novel variant of SLC26A4 and first report of the c.716T>A variant in Iranian pedigrees with non-syndromic sensorineural hearing loss.

Am J Otolaryngol 2018 Nov - Dec;39(6):719-725. Epub 2018 Jul 27.

Cellular and Molecular Research Center, Basic Health Sciences Institute, Shahrekord University of Medical Sciences, Shahrekord, Iran. Electronic address:

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http://dx.doi.org/10.1016/j.amjoto.2018.07.022DOI Listing
February 2019

A novel pathogenic variant in the MARVELD2 gene causes autosomal recessive non-syndromic hearing loss in an Iranian family.

Genomics 2019 07 9;111(4):840-848. Epub 2018 May 9.

Cellular and Molecular Research Center, Basic Health Sciences Institute, Shahrekord University of Medical Sciences, Shahrekord, Iran. Electronic address:

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http://dx.doi.org/10.1016/j.ygeno.2018.05.008DOI Listing
July 2019

A novel missense mutation in GIPC3 causes sensorineural hearing loss in an Iranian family revealed by targeted next-generation sequencing.

Int J Pediatr Otorhinolaryngol 2018 May 31;108:8-11. Epub 2018 Jan 31.

Cellular and Molecular Research Center, Basic Health Sciences Institute, Shahrekord University of Medical Sciences, Shahrekord, Iran. Electronic address:

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https://linkinghub.elsevier.com/retrieve/pii/S01655876183002
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http://dx.doi.org/10.1016/j.ijporl.2018.01.006DOI Listing
May 2018

Novel Variants and Copy Number Variation in CDH1 Gene in Iranian Patients with Sporadic Diffuse Gastric Cancer.

J Gastrointest Cancer 2019 Sep;50(3):420-427

Department of Pathology, School of Medicine, Isfahan University of Medical Sciences, Isfahan, Iran.

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http://dx.doi.org/10.1007/s12029-018-0082-7DOI Listing
September 2019

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

Int J Pediatr Otorhinolaryngol 2018 Apr 31;107:121-126. Epub 2018 Jan 31.

Department of Genetics and Molecular Biology, School of Medicine, Isfahan University of Medical Sciences, Isfahan, Iran; Pediatric Inherited Diseases Research Center, Research Institute for Primordial Prevention of Noncommunicable Disease, Isfahan University of Medical Sciences, Isfahan, Iran. Electronic address:

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http://dx.doi.org/10.1016/j.ijporl.2018.01.012DOI Listing
April 2018

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

Otolaryngol Head Neck Surg 2018 06 27;158(6):1084-1092. Epub 2018 Feb 27.

6 Department of Medical Genetics, School of Medicine, Ahvaz Jundishapur University of Medical Sciences, Ahvaz, Iran.

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http://dx.doi.org/10.1177/0194599818759007DOI Listing
June 2018

The silencing effect of miR-30a on gene expression : an approach for gene therapy.

Res Pharm Sci 2017 Dec;12(6):456-464

Department of Genetics and Molecular Biology, School of Medicine, Isfahan University of Medical Sciences, Isfahan, I.R. Iran.

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http://dx.doi.org/10.4103/1735-5362.217426DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC5691572PMC
December 2017

Inducing indel mutation in the SOX6 gene by zinc finger nuclease for gamma reactivation: An approach towards gene therapy of beta thalassemia.

J Cell Biochem 2018 03 30;119(3):2512-2519. Epub 2017 Nov 30.

Department of Genetics and Molecular biology, School of Medicine, Isfahan University of Medical Sciences, Isfahan, Iran.

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http://dx.doi.org/10.1002/jcb.26412DOI Listing
March 2018

A novel pathogenic variant in an Iranian Ataxia telangiectasia family revealed by next-generation sequencing followed by in silico analysis.

J Neurol Sci 2017 Aug 12;379:212-216. Epub 2017 Jun 12.

Ahvaz Noor Genetics Laboratory, Ahvaz, Iran; Department of Medical Genetics, School of Medicine, Ahvaz Jundishapur University of Medical Sciences, Ahvaz, Iran. Electronic address:

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http://dx.doi.org/10.1016/j.jns.2017.06.012DOI Listing
August 2017

Genetic study of the BRAF gene reveals new variants and high frequency of the V600E mutation among Iranian ameloblastoma patients.

J Oral Pathol Med 2018 Jan 7;47(1):86-90. Epub 2017 Nov 7.

Department of Oral and Maxillofacial Pathology, School of Dentistry, Isfahan University of Medical Sciences, Isfahan, Iran.

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http://dx.doi.org/10.1111/jop.12610DOI Listing
January 2018

A novel pathogenic variant in the FZD6 gene causes recessive nail dysplasia in a large Iranian kindred.

J Dermatol Sci 2017 Oct 13;88(1):134-138. Epub 2017 May 13.

Department of Genetics and Molecular Biology, School of Medicine, Isfahan University of Medical Sciences, Isfahan, Iran; Pediatric Inherited Diseases Research Center, Research Institute for Primordial Prevention of Non-Communicable Disease, Isfahan University of Medical Sciences, Isfahan, Iran. Electronic address:

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http://dx.doi.org/10.1016/j.jdermsci.2017.04.017DOI Listing
October 2017

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

Iran J Public Health 2017 Jan;46(1):76-82

Cellular and Molecular Research Center, Shahrekord University of Medical Sciences, Shahrekord, Iran.

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http://www.ncbi.nlm.nih.gov/pmc/articles/PMC5401939PMC
January 2017

SOX10 mutation causes Waardenburg syndrome associated with distinctive phenotypic features in an Iranian family: A clue for phenotype-directed genetic analysis.

Int J Pediatr Otorhinolaryngol 2017 May 16;96:122-126. Epub 2017 Mar 16.

Department of Medical Genetics, School of Medicine, Tehran University of Medical Sciences, Tehran, Iran. Electronic address:

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http://dx.doi.org/10.1016/j.ijporl.2017.03.016DOI Listing
May 2017

A PCR-Based Molecular Detection of Strongyloides stercoralisin Human Stool Samples from Tabriz City, Iran.

Sci Pharm 2017 Mar 27;85(2). Epub 2017 Mar 27.

Departments of Parasitology and Mycology, School of Medicine, Tabriz University of Medical Sciences, Tabriz 3848176941, Iran.

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http://dx.doi.org/10.3390/scipharm85020017DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC5489921PMC
March 2017

A novel TECTA mutation causes ARNSHL.

Int J Pediatr Otorhinolaryngol 2017 Jan 15;92:88-93. Epub 2016 Nov 15.

Cellular and Molecular Research Center, Shahrekord University of Medical Sciences, Shahrekord, Iran. Electronic address:

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http://dx.doi.org/10.1016/j.ijporl.2016.11.010DOI Listing
January 2017

Genetic disruption of the KLF1 gene to overexpress the γ-globin gene using the CRISPR/Cas9 system.

J Gene Med 2016 Oct;18(10):294-301

Department of Medical Genetics, School of Medicine, Tehran University of Medical Sciences, Tehran, Iran.

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http://doi.wiley.com/10.1002/jgm.2928
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http://dx.doi.org/10.1002/jgm.2928DOI Listing
October 2016

Sequence-identification of species isolated from candidemia.

Adv Biomed Res 2016 26;5:150. Epub 2016 Sep 26.

Department of Biology, Ashkezar Branch, Islamic Azad University, Ashkezar, Yazd, Iran.

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http://dx.doi.org/10.4103/2277-9175.188485DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC5046752PMC
September 2016

Staphylococcus aureus Isolates Carrying Panton-Valentine Leucocidin Genes: Their Frequency, Antimicrobial Patterns, and Association With Infectious Disease in Shahrekord City, Southwest Iran.

Jundishapur J Microbiol 2016 Jan 2;9(1):e28291. Epub 2016 Jan 2.

Department of Genetics and Molecular Biology, School of Medicine, Isfahan University of Medical Sciences, Isfahan, IR Iran; Pediatric Inherited Diseases Research Center, Research Institute for Primordial Prevention of Non-Communicable Disease, Isfahan University of Medical Sciences, Isfahan, IR Iran.

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http://dx.doi.org/10.5812/jjm.28291DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4834141PMC
January 2016

Comparison of different methods for erythroid differentiation in the K562 cell line.

Biotechnol Lett 2016 Aug 13;38(8):1243-50. Epub 2016 Apr 13.

Department of Molecular Medicine, School of Advanced Technologies in Medicine, Tehran University of Medical Sciences, Tehran, Iran.

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http://dx.doi.org/10.1007/s10529-016-2101-8DOI Listing
August 2016

Association of interleukin-1 gene cluster polymorphisms and haplotypes with multiple sclerosis in an Iranian population.

J Neuroimmunol 2015 Nov 25;288:114-9. Epub 2015 Sep 25.

Medical Cellular & Molecular Research Center, Golestan University of Medical Sciences, Gorgan, Iran. Electronic address:

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http://dx.doi.org/10.1016/j.jneuroim.2015.09.009DOI Listing
November 2015

A novel mutation in the PAX3 gene causes Waardenburg syndrome type I in an Iranian family.

Int J Pediatr Otorhinolaryngol 2015 Oct 3;79(10):1736-40. Epub 2015 Aug 3.

Department of Medical Genetics, School of Medicine, Tehran University of Medical Sciences, Tehran, Iran. Electronic address:

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http://dx.doi.org/10.1016/j.ijporl.2015.07.039DOI Listing
October 2015

Molecular and clinical characterization of Waardenburg syndrome type I in an Iranian cohort with two novel PAX3 mutations.

Gene 2015 Dec 11;574(2):302-7. Epub 2015 Aug 11.

Department of Medical Genetics, School of Medicine, Tehran University of Medical Sciences, Tehran, Iran. Electronic address:

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https://linkinghub.elsevier.com/retrieve/pii/S03781119150099
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http://dx.doi.org/10.1016/j.gene.2015.08.023DOI Listing
December 2015

Effect of Oxidized Low Density Lipoprotein on the Expression of Runx2 and SPARC Genes in Vascular Smooth Muscle Cells.

Iran Biomed J 2015 30;19(3):160-4. Epub 2015 May 30.

Dept. of Genetics and Molecular Biology, School of Medicine, Isfahan University of Medical Sciences, Isfahan, Iran.

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http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4571011PMC
http://dx.doi.org/10.7508/ibj.2015.03.005DOI Listing
March 2016

Effect of Oxidized Low Density Lipoprotein on the Expression of Runx2 and SPARC Genes in Vascular Smooth Muscle Cells.

Iran Biomed J 2015 30;19(3):160-4. Epub 2015 May 30.

Dept. of Genetics and Molecular Biology, School of Medicine, Isfahan University of Medical Sciences, Isfahan, Iran.

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http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4571011PMC
http://dx.doi.org/10.7508/ibj.2015.03.005DOI Listing
March 2016

Detection of Metallo-Beta Lactamases Among Carbapenem-Resistant Pseudomonas aeruginosa.

Jundishapur J Microbiol 2014 Nov 1;7(11):e12289. Epub 2014 Nov 1.

Department of Microbiology, Ahvaz Jundishapur University of Medical Sciences, Ahvaz, IR Iran.

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http://jjmicrobiol.com/en/articles/18812.html
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http://dx.doi.org/10.5812/jjm.12289DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4332233PMC
November 2014

Post Neurosurgical Meningitis due to Colistin Heteroresistant Acinetobacter baumannii.

Jundishapur J Microbiol 2014 Oct 1;7(10):e12287. Epub 2014 Oct 1.

Microbiology Department, Qazvin University of Medical Sciences, Qazvin, IR Iran.

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http://jjmicrobiol.com/en/articles/56373.html
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http://dx.doi.org/10.5812/jjm.12287DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4295316PMC
October 2014

The role and spectrum of SLC26A4 mutations in Iranian patients with autosomal recessive hereditary deafness.

Int J Audiol 2015 Feb 7;54(2):124-30. Epub 2014 Oct 7.

* Department of Biochemistry, Falavarjan Branch, Islamic Azad University , Isfahan , Iran.

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http://dx.doi.org/10.3109/14992027.2014.944276DOI Listing
February 2015

Significant expressivity of Wolfram syndrome: phenotypic assessment of two known and one novel mutation in the WFS1 gene in three Iranian families.

Mol Biol Rep 2014 Nov 31;41(11):7499-505. Epub 2014 Aug 31.

Department of Medical Genetics, School of Medicine, Tehran University of Medical Sciences, Poursina Ave, 16 Azar St. Keshavarz BLVD, 1417613151, Tehran, Iran.

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http://link.springer.com/content/pdf/10.1007/s11033-014-3642
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http://link.springer.com/10.1007/s11033-014-3642-3
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http://dx.doi.org/10.1007/s11033-014-3642-3DOI Listing
November 2014

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

Cell J 2014 25;16(2):225-30. Epub 2014 May 25.

Deparmment of Obstetrics and Gynecology, Hajar Hospital, Shahrekord University of Medical Sciences, Shahrekord, Iran.

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http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4072073PMC
July 2014

The role of epigenetics in the induction of fetal hemoglobin: a combination therapy approach.

Int J Hematol Oncol Stem Cell Res 2014 ;8(1):9-14

Health research center, Research Center of Thalassemia & Hemoglobinopathy, Ahvaz Jundishapur University of Medical Sciences, Ahvaz, Iran.

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http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3913159PMC
February 2014

Compound Heterozygosity for Two Novel SLC26A4 Mutations in a Large Iranian Pedigree with Pendred Syndrome.

Clin Exp Otorhinolaryngol 2013 Dec 29;6(4):201-8. Epub 2013 Nov 29.

Cellular and Molecular Research Center, School of Medicine, Shahrekord University of Medical Sciences, Shahrekord, Iran.

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http://dx.doi.org/10.3342/ceo.2013.6.4.201DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3863667PMC
December 2013

Genotyping of carbapenem resistant Acinetobacter baumannii isolated from tracheal tube discharge of hospitalized patients in intensive care units, Ahvaz, Iran.

Iran J Microbiol 2013 Dec;5(4):315-22

Department of Microbiology, School of Medicine, Infectious & Tropical Diseases Research Center, Ahvaz Jundishapur University of Medical Sciences, Ahvaz, Iran.

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http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4385154PMC
December 2013

Is the IL-10 -819 polymorphism associated with visceral leishmaniasis?

Inflammation 2013 Dec;36(6):1513-8

Department of Immunology, Faculty of Medicine, Hamadan University of Medical Sciences, Hamadan, Iran.

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http://dx.doi.org/10.1007/s10753-013-9693-0DOI Listing
December 2013

Molecular characterization of WFS1 in an Iranian family with Wolfram syndrome reveals a novel frameshift mutation associated with early symptoms.

Gene 2013 Oct 8;528(2):309-13. Epub 2013 Jul 8.

Department of Medical Genetics, School of Medicine, Tehran University of Medical Sciences, Tehran, Iran.

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http://dx.doi.org/10.1016/j.gene.2013.06.040DOI Listing
October 2013

A transversion mutation in non-coding exon 3 of the TMC1 gene in two ethnically related Iranian deaf families from different geographical regions; evidence for founder effect.

Int J Pediatr Otorhinolaryngol 2013 May 21;77(5):821-6. Epub 2013 Mar 21.

Department of Molecular Medicine, Biotechnology Research Center, Pasteur Institute of Iran, Pasteur St., Tehran, Iran.

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http://dx.doi.org/10.1016/j.ijporl.2013.02.021DOI Listing
May 2013

Association of P1635 and P1655 polymorphisms in dysbindin (DTNBP1) gene with schizophrenia.

Acta Neuropsychiatr 2012 Jun;24(3):155-9

Department of Medical Genetics, School of Medicine, Tehran University of Medical Sciences, Tehran, Iran.

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http://dx.doi.org/10.1111/j.1601-5215.2011.00598.xDOI Listing
June 2012

Two novel SLC26A4 mutations in Iranian families with autosomal recessive hearing loss.

Int J Pediatr Otorhinolaryngol 2012 Jun 23;76(6):845-50. Epub 2012 Mar 23.

Department of Biology, Science and Research Branch, Islamic Azad University, Tehran, Iran.

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http://dx.doi.org/10.1016/j.ijporl.2012.02.056DOI Listing
June 2012

Two novel SLC26A4 mutations in Iranian families with autosomal recessive hearing loss.

Int J Pediatr Otorhinolaryngol 2012 Jun 23;76(6):845-50. Epub 2012 Mar 23.

Department of Biology, Science and Research Branch, Islamic Azad University, Tehran, Iran.

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http://dx.doi.org/10.1016/j.ijporl.2012.02.056DOI Listing
June 2012

Large-scale screening of mitochondrial DNA mutations among Iranian patients with prelingual nonsyndromic hearing impairment.

Genet Test Mol Biomarkers 2012 Apr 11;16(4):271-8. Epub 2011 Nov 11.

Department of Medical Genetics, Faculty of Medical Sciences, Tarbiat Modares University, Tehran, Iran.

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http://dx.doi.org/10.1089/gtmb.2011.0176DOI Listing
April 2012

Estrogen receptor alpha gene polymorphisms are associated with type 2 diabetes and fasting glucose in male subjects.

Mol Cell Biochem 2012 Jan 12;359(1-2):225-33. Epub 2011 Aug 12.

The Department of Biochemistry, Faculty of Medicine, Tehran University of Medical Sciences, Tehran, IR, Iran.

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http://link.springer.com/10.1007/s11010-011-1017-9
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http://dx.doi.org/10.1007/s11010-011-1017-9DOI Listing
January 2012

Novel human pathological mutations. Gene symbol: SLC26A4. Disease: Pendred syndrome.

Hum Genet 2010 Apr;127(4):468-9

Department of Medical Genetics, The University and University Hospital of Antwerp, Antwerp, Belgium.

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April 2010

Comparison of real-time PCR with disk diffusion, agar screen and E-test methods for detection of methicillin-resistant Staphylococcus aureus.

Curr Microbiol 2010 Dec 20;61(6):520-4. Epub 2010 Apr 20.

Department of Microbiology and Immunology, Cellular and Molecular Research Center, Shahrekord University of Medical Sciences, Shahrekord, Iran.

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http://dx.doi.org/10.1007/s00284-010-9647-9DOI Listing
December 2010