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Items: 1 to 20 of 39

1.

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

Shariati L, Validi M, Hasheminia AM, Ghasemikhah R, Kianpour F, Karimi A, Nafisi MR, Tabatabaiefar MA.

Jundishapur J Microbiol. 2016 Jan 2;9(1):e28291. doi: 10.5812/jjm.28291. eCollection 2016 Jan.

2.

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.

Biotechnol Lett. 2016 Aug;38(8):1243-50. doi: 10.1007/s10529-016-2101-8. Epub 2016 Apr 13.

PMID:
27075690
3.

Using intron splicing trick for preferential gene expression in transduced cells: an approach for suicide gene therapy.

Pourzadegan F, Shariati L, Taghizadeh R, Khanahmad H, Mohammadi Z, Tabatabaiefar MA.

Cancer Gene Ther. 2016 Jan;23(1):7-12. doi: 10.1038/cgt.2015.57. Epub 2015 Dec 18.

PMID:
26679755
4.

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

Khosravi A, Javan B, Tabatabaiefar MA, Ebadi H, Fathi D, Shahbazi M.

J Neuroimmunol. 2015 Nov 15;288:114-9. doi: 10.1016/j.jneuroim.2015.09.009. Epub 2015 Sep 25.

PMID:
26531703
5.

Correlation Between Mucosal IL-6 mRNA Expression Level and Virulence Factors of Helicobacter pylori in Iranian Adult Patients With Chronic Gastritis.

Azadegan-Dehkordi F, Bagheri N, Shirzad M, Sanei MH, Hashemzadeh-Chaleshtori M, Rafieian-Kopaei M, Tabatabaiefar MA, Shirzad H.

Jundishapur J Microbiol. 2015 Aug 29;8(8):e21701. doi: 10.5812/jjm.21701. eCollection 2015 Aug.

6.

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

Jalilian N, Tabatabaiefar MA, Farhadi M, Bahrami T, Noori-Daloii MR.

Int J Pediatr Otorhinolaryngol. 2015 Oct;79(10):1736-40. doi: 10.1016/j.ijporl.2015.07.039. Epub 2015 Aug 3.

PMID:
26279250
7.

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

Jalilian N, Tabatabaiefar MA, Farhadi M, Bahrami T, Emamdjomeh H, Noori-Daloii MR.

Gene. 2015 Dec 15;574(2):302-7. doi: 10.1016/j.gene.2015.08.023. Epub 2015 Aug 11.

PMID:
26275939
8.

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

Farrokhi E, Samani KG, Chaleshtori MH, Tabatabaiefar MA.

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

9.

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.

Mol Biotechnol. 2015 Sep;57(9):793-800. doi: 10.1007/s12033-015-9872-3.

PMID:
26014225
10.
11.

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

Farajzadeh Sheikh A, Rostami S, Jolodar A, Tabatabaiefar MA, Khorvash F, Saki A, Shoja S, Sheikhi R.

Jundishapur J Microbiol. 2014 Nov;7(11):e12289. doi: 10.5812/jjm.12289. Epub 2014 Nov 1.

12.

Post Neurosurgical Meningitis due to Colistin Heteroresistant Acinetobacter baumannii.

Moosavian M, Shoja S, Nashibi R, Ebrahimi N, Tabatabaiefar MA, Rostami S, Peymani A.

Jundishapur J Microbiol. 2014 Oct;7(10):e12287. doi: 10.5812/jjm.12287. Epub 2014 Oct 1.

13.

The Study of SLC26A4 Gene Causing Autosomal Recessive Hearing Loss by Linkage Analysis in a Cohort of Iranian Populations.

Reiisi S, Sanati MH, Tabatabaiefar MA, Ahmadian S, Reiisi S, Parchami S, Porjafari H, Shahi H, Shavarzi A, Hashemzade Chaleshtori M.

Int J Mol Cell Med. 2014 Summer;3(3):176-82.

14.

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

Yazdanpanahi N, Tabatabaiefar MA, Bagheri N, Azadegan Dehkordi F, Farrokhi E, Hashemzadeh Chaleshtori M.

Int J Audiol. 2015 Feb;54(2):124-30. doi: 10.3109/14992027.2014.944276. Epub 2014 Oct 7.

PMID:
25290043
15.

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

Sobhani M, Tabatabaiefar MA, Rajab A, Kajbafzadeh AM, Noori-Daloii MR.

Mol Biol Rep. 2014 Nov;41(11):7499-505. doi: 10.1007/s11033-014-3642-3. Epub 2014 Aug 31.

PMID:
25173644
16.

Characterization of wild-type and mutated RET proto- oncogene associated with familial medullary thyroid cancer.

Masbi MH, Mohammadiasl J, Galehdari H, Ahmadzadeh A, Tabatabaiefar MA, Golchin N, Haghpanah V, Rahim F.

Asian Pac J Cancer Prev. 2014;15(5):2027-33.

17.

Identification of Xq22.1-23 as a region linked with hereditary recurrent spontaneous abortion in a family.

Shekouhi S, Baghbani F, Hasanzadeh Nazar-Abadi M, Hamzehloie T, Abbaszadegan MR, Saghafi N, Raoofian R, Zavar Reza J, Ahmadzadeh S, Tabatabaiefar MA, Mojarrad M.

Iran J Reprod Med. 2013 Aug;11(8):659-64.

18.

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

Taghizade Mortezaee F, Tabatabaiefar MA, Hashemzadeh Chaleshtori M, Miraj S.

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

19.

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

Ahmadvand M, Noruzinia M, Fard AD, Zohour MM, Tabatabaiefar MA, Soleimani M, Kaviani S, Abroun S, Beiranvand S, Saki N.

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

20.

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

Yazdanpanahi N, Tabatabaiefar MA, Farrokhi E, Abdian N, Bagheri N, Shahbazi S, Noormohammadi Z, Chaleshtori MH.

Clin Exp Otorhinolaryngol. 2013 Dec;6(4):201-8. doi: 10.3342/ceo.2013.6.4.201. Epub 2013 Nov 29.

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