Publications by authors named "Akrami Seyed Mohammad"

34Publications

Plasma 5-miRNA as Biomarkers for Identifying Prostate Cancer Patients.

Iran J Public Health 2019 Sep;48(9):1743-1745

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

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September 2019

Mitochondrial Variants in Pompe Disease: A Comparison between Classic and Non-Classic Forms.

Cell J 2018 Oct 15;20(3):333-339. Epub 2018 May 15.

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

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October 2018

Inflammation, a significant player of Ataxia-Telangiectasia pathogenesis?

Inflamm Res 2018 Jul 26;67(7):559-570. Epub 2018 Mar 26.

Research Center for Immunodeficiencies, Children's Medical Center Hospital, Tehran University of Medical Science, 62 Qarib St., Keshavarz Blvd., Tehran, 14194, Iran.

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July 2018

Ataxia telangiectasia syndrome: moonlighting ATM.

Expert Rev Clin Immunol 2017 12 20;13(12):1155-1172. Epub 2017 Oct 20.

b Research Center for Immunodeficiencies, Children's Medical Center , Tehran University of Medical Science , Tehran , Iran.

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December 2017

Mitochondrial Copy Number and D-Loop Variants in Pompe Patients.

Cell J 2016 24;18(3):405-15. Epub 2016 Aug 24.

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

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September 2016

Effect of Copper Sulfate on Expression of Endogenous L1 Retrotransposons in HepG2 Cells (Hepatocellular Carcinoma).

Biol Trace Elem Res 2015 Jun 8;165(2):131-4. Epub 2015 Feb 8.

Tasnim Biotechnology Research Center (TBRC), Faculty of Medicine, AJA University of Medical Sciences, Etemadzadeh Ave., West Fatemi, Tehran, Iran.

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June 2015

Note: High-speed Z tip scanner with screw cantilever holding mechanism for atomic-resolution atomic force microscopy in liquid.

Rev Sci Instrum 2014 Dec;85(12):126106

Division of Electrical Engineering and Computer Science, Kanazawa University, Kakuma-machi, Kanazawa 920-1192, Japan.

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December 2014

Novel trends in genetics: transposable elements and their application in medicine.

Arch Iran Med 2014 Oct;17(10):702-12

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

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October 2014

The effect of homozygous deletion of the BBOX1 and Fibin genes on carnitine level and acyl carnitine profile.

BMC Med Genet 2014 Jul 1;15:75. Epub 2014 Jul 1.

Center for Integrative Genomics, University of Lausanne, 1015 Lausanne, Switzerland.

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July 2014

Exposure of hepatocellular carcinoma cells to low-level As₂O₃‎ causes an extra toxicity pathway via L1 retrotransposition ‎induction.

Toxicol Lett 2014 Aug 21;229(1):111-7. Epub 2014 Jun 21.

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

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August 2014

Evaluating the extent of LINE-1 mobility following exposure to heavy metals in HepG2 cells.

Biol Trace Elem Res 2014 Jul 5;160(1):143-51. Epub 2014 Jun 5.

Department of Molecular Medicine, Faculty of Advanced Technologies in Medicine (FATiM), Iran University of Medical Sciences, Tehran, Iran.

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July 2014

Retrotransposons and pediatric genetic disorders: Importance and implications.

J Pediatr Genet 2014 Mar;3(1):9-16

Department of Medical Genetics, School of Medicine, Tehran University of Medical Sciences, Tehran, Iran; Nanotechnology Research Center, Faculty of Pharmacy, Tehran University of Medical Sciences, Tehran, Iran.

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March 2014

Mercury specifically induces LINE-1 activity in a human neuroblastoma cell line.

Mutat Res Genet Toxicol Environ Mutagen 2014 Jan 13;759:9-20. Epub 2013 Nov 13.

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

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January 2014

Normal and tumour cervical cells respond differently to vaginal lactobacilli, independent of pH and lactate.

J Med Microbiol 2013 Jul 25;62(Pt 7):1065-1072. Epub 2013 Apr 25.

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

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July 2013

Genetics of consanguineous marriage: Impact and importance of counseling.

J Pediatr Genet 2012 Dec;1(4):217-20

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

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December 2012

2q34-qter duplication and 4q34.2-qter deletion in a patient with developmental delay.

Eur J Med Genet 2012 Mar 4;55(3):203-10. Epub 2012 Feb 4.

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

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March 2012

Is there a significant trend in prevalence of consanguineous marriage in Tehran? A review of three generations.

J Genet Couns 2009 Feb 9;18(1):82-6. Epub 2008 Oct 9.

Department of Medical Genetics, Tehran University of Medical Sciences, Poursina St., Tehran, 14176, Iran.

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February 2009

Genetic counseling in southern Iran: consanguinity and reason for referral.

J Genet Couns 2008 Oct 13;17(5):472-9. Epub 2008 Jun 13.

Human Genetic Rresearch Group, Iranian Academic Center for Education, Culture & Research, Fars Province Branch, Shiraz, Iran.

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October 2008

The common -866G/A polymorphism of the UCP2 gene in healthy Iranians compared with world populations.

Hum Biol 2007 Feb;79(1):103-10

Endocrinology and Metabolism Research Center, Medical Sciences/University of Tehran, Shariati Hospital, North Kargar St., Tehran 14114, Iran.

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February 2007

Genetics of hereditary nonpolyposis colorectal cancer.

Arch Iran Med 2006 Oct;9(4):381-9

Department of Medical Genetics, Endocrinology and Metabolism Research Center (EMRC), Tehran University of Medical Sciences, Tehran, Iran.

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October 2006

Is consanguineous marriage religiously encouraged? Islamic and Iranian considerations.

J Biosoc Sci 2007 Mar 23;39(2):313-6. Epub 2006 Oct 23.

Medical Genetics Department, Tehran University of Medical Sciences (TUMS), Tehran, Iran.

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March 2007

Diabetes mellitus following pituitary adenomectomy in euglycemic patients with acromegaly.

J Coll Physicians Surg Pak 2005 Jul;15(7):430-2

Endocrinology and Metabolism Research Centre (EMRC), Tehran University of Medical Sciences (TUMS), Iran.

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July 2005

Screening for exonic copy number mutations at MSH2 and MLH1 by MAPH.

Fam Cancer 2005 ;4(2):145-9

Institute of Genetics, University of Nottingham, Queen's Medical Centre, Nottingham NG7 2UH, UK.

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September 2005