Items where Author is "Karimian, M."

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Number of items: 19.

Article

Noureddini, M. and Mobasseri, N. and Karimian, M. and Behjati, M. and Nikzad, H. (2018) Arg399Gln substitution in XRCC1 as a prognostic and predictive biomarker for prostate cancer: Evidence from 8662 subjects and a structural analysis. Journal of Gene Medicine, 20 (10-11).

Talebi, E. and Karimian, M. and Nikzad, H. (2018) Association of sperm mitochondrial DNA deletions with male infertility in an Iranian population. Mitochondrial DNA Part A: DNA Mapping, Sequencing, and Analysis, 29 (4). pp. 615-623.

Talebi, E. and Karimian, M. and Nikzad, H. (2018) Association of sperm mitochondrial DNA deletions with male infertility in an Iranian population. Mitochondrial DNA Part A: DNA Mapping, Sequencing, and Analysis, 29 (4). pp. 615-623.

Rafatmanesh, A. and Nikzad, H. and Ebrahimi, A. and Karimian, M. and Zamani, T. (2018) Association of the c.-9C>T and c.368A>G transitions in H2BFWT gene with male infertility in an Iranian population. Andrologia, 50 (1).

Hashemi, M. and Karimian, M. and Nilforoush, P. and Taheri, M. and Behjati, M. (2018) Evaluation of the predictive value of Gensini score on determination of severity of coronary artery disease in cases with left bundle branch block. Comparative Clinical Pathology. pp. 1-5.

Zamani-Badi, T. and Nikzad, H. and Karimian, M. (2018) IL-1RA VNTR and IL-1α 4845G>T polymorphisms and risk of idiopathic male infertility in Iranian men: A case�control study and an in silico analysis. Andrologia, 50 (9).

Zamani-Badi, T. and Nikzad, H. and Karimian, M. (2018) IL-1RA VNTR and IL-1α 4845G>T polymorphisms and risk of idiopathic male infertility in Iranian men: A case�control study and an in silico analysis. Andrologia, 50 (9).

Zamani-Badi, T. and Karimian, M. and Azami Tameh, A. and Nikzad, H. (2018) Il-1� C376a transversion variant and risk of idiopathic male infertility in Iranian men: A genetic association study. International Journal of Fertility and Sterility, 12 (3). pp. 229-234.

Nejati, M. and Atlasi, M.A. and Karimian, M. and Nikzad, H. and Azami Tameh, A. (2018) Lipoprotein lipase gene polymorphisms as risk factors for stroke: A computational and meta-analysis. Iranian Journal of Basic Medical Sciences, 21 (7). pp. 701-708.

Tameh, A.A. and Karimian, M. and Zare-Dehghanani, Z. and Aftabi, Y. and Beyer, C. (2018) Role of Steroid Therapy after Ischemic Stroke by N-Methyl-D-Aspartate Receptor Gene Regulation. Journal of Stroke and Cerebrovascular Diseases, 27 (11). pp. 3066-3075.

Karimian, M. and Aftabi, Y. and Mazoochi, T. and Babaei, F. and Khamechian, T. and Boojari, H. and Nikzad, H. (2018) Survivin polymorphisms and susceptibility to prostate cancer: A genetic association study and an in Silico analysis. EXCLI Journal, 17. pp. 479-491.

Sharif, A. and Kheirkhah, D. and Sharif, M.R. and Karimian, M. and Karimian, Z. (2017) ABCB1-C3435T polymorphism and breast cancer risk: A case-control study and a meta-analysis. Journal of B.U.ON., 22 (2). pp. 355-364.

Mazaheri, M. and Karimian, M. and Behjati, M. and Raygan, F. and Hosseinzadeh Colagar, A. (2017) Association analysis of rs1049255 and rs4673 transitions in p22phox gene with coronary artery disease: A case-control study and a computational analysis. Irish Journal of Medical Science. pp. 1-8.

Talebi, E. and Karimian, M. and Nikzad, H. (2017) Association of sperm mitochondrial DNA deletions with male infertility in an Iranian population. Mitochondrial DNA Part A: DNA Mapping, Sequencing, and Analysis. pp. 1-9.

Rafatmanesh, A. and Nikzad, H. and Ebrahimi, A. and Karimian, M. and Zamani, T. (2017) Association of the c.-9C>T and c.368A>G transitions in H2BFWT gene with male infertility in an Iranian population. Andrologia.

Raygan, F. and Karimian, M. and Rezaeian, A. and Bahmani, B. and Behjati, M. (2016) Angiotensinogen-M235T as a risk factor for myocardial infarction in Asian populations: A genetic association study and a bioinformatics approach. Croatian Medical Journal, 57 (4). pp. 351-362.

Soleimani, Z. and Kheirkhah, D. and Sharif, M.R. and Sharif, A. and Karimian, M. and Aftabi, Y. (2016) Association of CCND1 Gene c.870G>A Polymorphism with Breast Cancer Risk: A Case-ControlStudy and a Meta-Analysis. Pathology and Oncology Research. pp. 1-11.

Jamali, S. and Karimian, M. and Nikzad, H. and Aftabi, Y. (2016) The c.-190 C>A transversion in promoter region of protamine1 gene as a genetic risk factor for idiopathic oligozoospermia. Molecular Biology Reports, 43 (8). pp. 795-802.

Nikzad, H. and Karimian, M. and Sareban, K. and Khoshsokhan, M. and Hosseinzadeh Colagar, A. (2015) MTHFR-Ala222Val and male infertility: A study in Iranian men, an updated meta-analysis and an in silico-analysis. Reproductive BioMedicine Online, 31 (5). pp. 668-680.

This list was generated on Wed Apr 24 18:44:38 2019 EDT.