Salehi M - Search Results

1

Detection of rifampin resistance patterns in Mycobacterium tuberculosis strains isolated in Iran by polymerase chain reaction-single-strand conformation polymorphism and direct sequencing methods.

Isfahani BN, Tavakoli A, Salehi M, Tazhibi M. Isfahani BN, et al. Among authors: salehi m. Mem Inst Oswaldo Cruz. 2006 Sep;101(6):597-602. doi: 10.1590/s0074-02762006000600004. Mem Inst Oswaldo Cruz. 2006. PMID: 17072470 Free article.

2

Comparison of distribution of virulence determinants in clinical and environmental isolates of Vibrio cholera.

Bakhshi B, Pourshafie MR, Navabakbar F, Tavakoli A, Shahcheraghi F, Salehi M, Faradjzadegan Z, Zahraei SM. Bakhshi B, et al. Among authors: salehi m. Iran Biomed J. 2008 Jul;12(3):159-65. Iran Biomed J. 2008. PMID: 18762819

3

Simultaneous Detection of Integrase and Antibiotic Resistance Genes within SXT Constin in Vibrio cholerae O1 El Tor Strains Isolated from Iran Using Multiplex-PCR.

Marashi SM, Nasr Esfahani B, Tavakoli A, Moghim S, Pourshafie MR, Salehi M. Marashi SM, et al. Among authors: salehi m. Iran J Basic Med Sci. 2012 May;15(3):885-9. Iran J Basic Med Sci. 2012. PMID: 23493053 Free PMC article.

4

Investigation of sensitivity, specificity and accuracy of Tetra primer ARMS PCR method in comparison with conventional ARMS PCR, based on sequencing technique outcomes in IVS-II-I genotyping of beta thalassemia patients.

Honardoost MA, Tabatabaeian H, Akbari M, Salehi M. Honardoost MA, et al. Among authors: salehi m. Gene. 2014 Oct 1;549(1):1-6. doi: 10.1016/j.gene.2014.05.071. Epub 2014 Jun 2. Gene. 2014. PMID: 24946023

5

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

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: 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

7

A Comparison Between Full-COLD PCR/HRM and PCR Sequencing for Detection of Mutations in Exon 9 of PIK3CA in Breast Cancer Patients.

Ghalamkari S, Khosravian F, Mianesaz H, Kazemi M, Behjati M, Hakimian SM, Salehi M. Ghalamkari S, et al. Among authors: salehi m. Appl Biochem Biotechnol. 2019 Mar;187(3):975-983. doi: 10.1007/s12010-018-2859-3. Epub 2018 Aug 15. Appl Biochem Biotechnol. 2019. PMID: 30109561

8

Two novel mutations in hMLH1 gene in Iranian hereditary non-polyposis colorectal cancer patients.

Shahmoradi S, Bidmeshkipour A, Salamian A, Emami MH, Kazemi Z, Salehi M. Shahmoradi S, et al. Among authors: salehi m. Fam Cancer. 2012 Mar;11(1):13-7. doi: 10.1007/s10689-011-9478-2. Fam Cancer. 2012. PMID: 21901500

9

Association between mismatch repair gene MSH3 codons 1036 and 222 polymorphisms and sporadic prostate cancer in the Iranian population.

Jafary F, Salehi M, Sedghi M, Nouri N, Jafary F, Sadeghi F, Motamedi S, Talebi M. Jafary F, et al. Among authors: salehi m. Asian Pac J Cancer Prev. 2012;13(12):6055-7. doi: 10.7314/apjcp.2012.13.12.6055. Asian Pac J Cancer Prev. 2012. PMID: 23464402 Free article.

10

Detection of intragenic SMN1 mutations in spinal muscular atrophy patients with a single copy of SMN1.

Ganji H, Nouri N, Salehi M, Aryani O, Houshmand M, Basiri K, Fazel-Najafabadi E, Sedghi M. Ganji H, et al. Among authors: salehi m. J Child Neurol. 2015 Apr;30(5):558-62. doi: 10.1177/0883073814521297. Epub 2014 Feb 20. J Child Neurol. 2015. PMID: 24563475

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