Salehi M - Search Results

1

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

Koohiyan M, Noori-Daloii MR, Hashemzadeh-Chaleshtori M, Salehi M, Abtahi H, Tabatabaiefar MA. Koohiyan M, et al. Among authors: salehi m. Audiol Neurootol. 2019;24(5):258-263. doi: 10.1159/000502251. Epub 2019 Oct 29. Audiol Neurootol. 2019. PMID: 31661684

2

A new compound heterozygous mutation in GJB2 causes nonsyndromic hearing loss in a consanguineous Iranian family.

Keivani A, Haghighat-Nia A, Fazel-Najafabadi E, Hosseinzadeh M, Salehi M. Keivani A, et al. Among authors: salehi m. Int J Pediatr Otorhinolaryngol. 2015 Apr;79(4):553-6. doi: 10.1016/j.ijporl.2015.01.027. Epub 2015 Jan 30. Int J Pediatr Otorhinolaryngol. 2015. PMID: 25708704

3

A Lentiviral Vector Expressing Desired Gene Only in Transduced Cells: An Approach for Suicide Gene Therapy.

Mohammadi Z, Shariati L, Khanahmad H, Kolahdouz M, Kianpoor F, Ghanbari JA, Hejazi Z, Salehi M, Nikpour P, Tabatabaiefar MA. Mohammadi Z, et al. Among authors: salehi m. Mol Biotechnol. 2015 Sep;57(9):793-800. doi: 10.1007/s12033-015-9872-3. Mol Biotechnol. 2015. PMID: 26014225

4

Mutation spectrum of autosomal recessive non-syndromic hearing loss in central Iran.

Haghighat-Nia A, Keivani A, Nadeali Z, Fazel-Najafabadi E, Hosseinzadeh M, Salehi M. Haghighat-Nia A, et al. Among authors: salehi m. Int J Pediatr Otorhinolaryngol. 2015 Nov;79(11):1892-5. doi: 10.1016/j.ijporl.2015.08.039. Epub 2015 Sep 2. Int J Pediatr Otorhinolaryngol. 2015. PMID: 26409293

5

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

Shariati L, Modaress M, Khanahmad H, Hejazi Z, Tabatabaiefar MA, Salehi M, Modarressi MH. Shariati L, et al. Among authors: salehi m. Biotechnol Lett. 2016 Aug;38(8):1243-50. doi: 10.1007/s10529-016-2101-8. Epub 2016 Apr 13. Biotechnol Lett. 2016. PMID: 27075690

6

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

Shariati L, Khanahmad H, Salehi M, Hejazi Z, Rahimmanesh I, Tabatabaiefar MA, Modarressi MH. Shariati L, et al. Among authors: salehi m. J Gene Med. 2016 Oct;18(10):294-301. doi: 10.1002/jgm.2928. J Gene Med. 2016. PMID: 27668420

7

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: salehi m. 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

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: salehi m. 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

Screening of 10 DFNB Loci Causing Autosomal Recessive Non-Syndromic Hearing Loss in Two Iranian Populations Negative for GJB2 Mutations.

Koohiyan M, Reiisi S, Azadegan-Dehkordi F, Salehi M, Abtahi H, Hashemzadeh-Chaleshtori M, Noori-Daloii MR, Tabatabaiefar MA. Koohiyan M, et al. Among authors: salehi m. Iran J Public Health. 2019 Sep;48(9):1704-1713. Iran J Public Health. 2019. PMID: 31700827 Free PMC article.

10

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

Koohiyan M, Hashemzadeh-Chaleshtori M, Salehi M, Abtahi H, Noori-Daloii MR, Tabatabaiefar MA. Koohiyan M, et al. Among authors: salehi m. Audiol Neurootol. 2020;25(5):258-262. doi: 10.1159/000506500. Epub 2020 Jun 2. Audiol Neurootol. 2020. PMID: 32485727

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