Tabatabaiefar MA - Search Results

1

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

Shadmehri AA, Fattahi N, Pourreza MR, Koohiyan M, Zarifi S, Darbouy M, Sharifi R, Tavakkoly Bazzaz J, Tabatabaiefar MA. Shadmehri AA, et al. Among authors: tabatabaiefar ma. J Cell Biochem. 2019 Mar;120(3):3367-3372. doi: 10.1002/jcb.27607. Epub 2018 Sep 11. J Cell Biochem. 2019. PMID: 30203563

2

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

Soltani M, Tabatabaiefar MA, Mohsenifar Z, Pourreza MR, Moridnia A, Shariati L, Razavi SM. Soltani M, et al. Among authors: tabatabaiefar ma. J Oral Pathol Med. 2018 Jan;47(1):86-90. doi: 10.1111/jop.12610. Epub 2017 Nov 7. J Oral Pathol Med. 2018. PMID: 28650588

3

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

Tabatabaiefar MA, Alipour P, Pourahmadiyan A, Fattahi N, Shariati L, Golchin N, Mohammadi-Asl J. Tabatabaiefar MA, et al. J Neurol Sci. 2017 Aug 15;379:212-216. doi: 10.1016/j.jns.2017.06.012. Epub 2017 Jun 12. J Neurol Sci. 2017. PMID: 28716242

4

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

Modares Sadeghi M, Shariati L, Hejazi Z, Shahbazi M, Tabatabaiefar MA, Khanahmad H. Modares Sadeghi M, et al. Among authors: tabatabaiefar ma. J Cell Biochem. 2018 Mar;119(3):2512-2519. doi: 10.1002/jcb.26412. Epub 2017 Nov 30. J Cell Biochem. 2018. PMID: 28941328

5

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

Tabatabaiefar MA, Pourreza MR, Tahmasebi P, Saki N, Hashemzadeh Chaleshtori M, Salehi R, Mohammadi-Asl J. Tabatabaiefar MA, et al. Otolaryngol Head Neck Surg. 2018 Jun;158(6):1084-1092. doi: 10.1177/0194599818759007. Epub 2018 Feb 27. Otolaryngol Head Neck Surg. 2018. PMID: 29484972

6

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

Koohiyan M, Hashemzadeh-Chaleshtori M, Salehi M, Abtahi H, Reiisi S, Pourreza MR, Noori-Daloii MR, Tabatabaiefar MA. Koohiyan M, et al. Among authors: tabatabaiefar ma. Int J Pediatr Otorhinolaryngol. 2018 Apr;107:121-126. doi: 10.1016/j.ijporl.2018.01.012. Epub 2018 Jan 31. Int J Pediatr Otorhinolaryngol. 2018. PMID: 29501291

7

Applying Two Different Bioinformatic Approaches to Discover Novel Genes Associated with Hereditary Hearing Loss via Whole-Exome Sequencing: ENDEAVOUR and HomozygosityMapper.

Pourreza MR, Mohammadi H, Sadeghian L, Asgharzadeh S, Sehhati M, Tabatabaiefar MA. Pourreza MR, et al. Among authors: tabatabaiefar ma. Adv Biomed Res. 2018 Oct 31;7:141. doi: 10.4103/abr.abr_80_18. eCollection 2018. Adv Biomed Res. 2018. PMID: 30505812 Free PMC article.

8

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

Shariati L, Modarressi MH, Tabatabaiefar MA, Kouhpayeh S, Hejazi Z, Shahbazi M, Sabzehei F, Salehi M, Khanahmad H. Shariati L, et al. Among authors: tabatabaiefar ma. J Cell Biochem. 2019 May;120(5):8438-8446. doi: 10.1002/jcb.28130. Epub 2018 Dec 16. J Cell Biochem. 2019. PMID: 30556211

9

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

Sadeghian L, Tabatabaiefar MA, Fattahi N, Pourreza MR, Tahmasebi P, Alavi Z, Hashemzadeh Chaleshtori M. Sadeghian L, et al. Among authors: tabatabaiefar ma. Int J Pediatr Otorhinolaryngol. 2019 Sep;124:99-105. doi: 10.1016/j.ijporl.2019.05.023. Epub 2019 May 21. Int J Pediatr Otorhinolaryngol. 2019. PMID: 31176026

10

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

Pourahmadiyan A, Alipour P, Fattahi N, Kasiri M, Rezaeian F, Taghipour-Sheshdeh A, Mohammadi-Asl J, Tabatabaiefar MA, Hashemzadeh Chaleshtori M. Pourahmadiyan A, et al. Among authors: tabatabaiefar ma. Int J Audiol. 2019 Oct;58(10):628-634. doi: 10.1080/14992027.2019.1619945. Epub 2019 Jun 12. Int J Audiol. 2019. PMID: 31187663

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