Items where Subject is "QU Biochemistry > Cell biology and genetics"

Up a level
Export as [feed] Atom [feed] RSS 1.0 [feed] RSS 2.0
Group by: Creators | Item Type
Jump to: A | B | D | E | F | G | H | I | J | K | M | N | O | P | R | S | T | V | Y | Z
Number of items at this level: 166.

A

Abbasi, S. and Zamanzad, B. (2015) Genotypic and phenotypic characteristics of vancomycin-resistant enterococcus isolated from clinical specimens of patients in shahrekord. Journal of Mazandaran University of Medical Sciences, 24 (122). pp. 98-106.

Abbasi, S. and Zamanzad, B. and Golipour, A. and Damavandi, M.S. (2015) Prevalence of constitutive and inducible resistance to clindamycin in staphylococci isolates from Hajar and Kashani hospitals in Shahrekord, 2014. Journal of Shahrekord Uuniversity of Medical Sciences, 17.

Abdian, N. and Allahbakhshian-Farsani, M. and Ghasemi-Dehkordi, P. and Mirzaeian, A. and Saffari-Chaleshtori, J. and Sadeghiani, M. and Hashemzadeh-Chaleshtori, M. and Yazdanpanahi, N. (2015) Effects of lentiviral vectors on DNA damage of human dermal fibroblasts (HDFs). Journal of Pure and Applied Microbiology, 9 (1). pp. 307-317.

Abolhassani, M. and Hashemzade Chaleshtori, M. and Iziy, E. and Motovalibashi, M. and Khazraei, H. and Ramazi, Sh. (2015) Association of interleukin-18 gene polymorphism-137 G/C with allergic rhinitis. Journal of Gorgan University of Medical Sciences, 17 (2).

Aghaei, M. and Ghanadian, M. and Faez, F. and Esfandiary, E. (2015) Cytotoxic activities of <em>Euphorbia kopetdaghi</em> against OVCAR-3 and EJ-138 cell lines. Journal of HerbMed Pharmacology, 4.

Ahani, A. and Khoramkhorshid, H. and Behnam, B. and Akbari, M.T. (2012) Report of a novel mutation in Rb1 gene from an Iranian retinoblastoma patient and its effect on splicing pattern of mRNA. Journal of Shahrekord Uuniversity of Medical Sciences, 14.

Ahmadi, A. and Hasanzadeh, J. and Ghaem, H. and Khosravi, Sh. and Reisi, R. (2009) The survey of family history of diabetes in patients with type 2 diabetes in Chaharmahal va Bakhteyari province, Iran, 2008. Journal of Shahrekord Uuniversity of Medical Sciences, 11.

Ahmadinejad, F. and Honardoost, M.A. and Amiri, M. and Jami, M.S. (2015) Genetics and epidemiology of Middle East Respiratory Syndrome-Coronavirus (MERS-CoV). International Journal of Epidemiologic Research, 2 (4). pp. 204-208.

Ahmadinejad, F. and Mowla, S.J. and Honardoost, M.A. and Gholami Arjenaki, M. and Moazeni-Bistgani, M. and Kheiri, S. and Teimori, H. (2017) Lower expression of miR-218 in human breast cancer is associated with lymph node metastases, higher grades, and poorer prognosis. Tumour biology : the journal of the International Society for Oncodevelopmental Biology and Medicine, 39 (8). p. 1010428317698362. ISSN 1423-0380

Akbari, A. and Agah, S. and Heidari, M. and Mobini, G.R. and Faghihloo, E. and Sarveazad, A. and Mirzaei, A. (2017) Homeodomain protein transforming growth factor beta-induced factor 2 like, X-linked function in colon adenocarcinoma cells. Asian Pacific Journal of Cancer Prevention, 18 (8). pp. 2101-2108.

Alijany-Renany, H. and Tamaddoni, A. and Haghighy-zadeh, M. and Pourhosein, S. (2012) The effect of using partnership care model on the quality of life in the school-age children with β-thalassemia. Journal of Shahrekord Uuniversity of Medical Sciences, 14.

Alipour, P. and Tabatabaiefar, M.A. and Reiisi, S. and Fattahi, N. and Pourahmadian, A. and Hashemzadeh-Chaleshtori, M. (2015) Genetic linkage analysis of the DFNB63 locus in families with autosomal recessive nonsyndromic hearing loss from Hamadan and Kohgiluyeh and Boyer-Ahmad Provinces, Iran. Journal of Isfahan Medical School, 33 (346). pp. 1308-1317.

Allahbakhshian-Farsani, M. and Abdian, N. and Ghasemi-Dehkordi, P. and Sadeghiani, M. and Saffari-Chaleshtori, J. and Hashemzadeh-Chaleshtori, M. and Khosravi-Farsani, S. (2014) Cytogentic analysis of human dermal fibroblasts (HDFs) in early and late passages using both karyotyping and comet assay techniques. CYTOTECHNOLOGY, 66 (5). pp. 815-822.

Allahbakhshian-Farsani, M. and Ghasemi-Dehkordi, P. and Abdian, N. and Khosravi-Farsani, S. and Mirzaeian, A. and Nasri, M. and Karimi-Taghanaki, A. and Mardani, G. and Amiri, S. and Hashemzadeh-Chaleshtori, M. (2014) The assessment of lentiviral vectors application for gene transformation in human dermal fibroblasts (HDFs). Journal of Shahrekord Uuniversity of Medical Sciences, 15.

Amini-Farsani, Z. and Ahadi, A.M. and Teimori, H. and Haeri-Ruhani, A. and Heidari, S. (2013) Investigation of mutation in cystatin‌ B gene in patients affected by idiopathic generalized epilepsy in Chaharmahal and Bakhtiari province. journal of shahrekord university of medical sciences, 15 (1).

Andonian, L. and Khorramizadeh, M.R. and Farhud, D.D. and Chaleshtori, M.H. and Naieni, K.H. and Razi, A. and Sanadizadeh, J. and Pourmand, G. and Nouraie, M. and Rezaie, S. and Saadat, F. and Yepiskoposyan, L. and Norouzi, M. and Soleimanpour, H. and Berahme, A. and Aalizadeh, N. (2005) Molecular detection of prostate specific antigen in patients with prostate cancer or benign prostate hyperplasia the first investigation from Iran. Iranian Journal of Public Health, 34 (3). pp. 20-26.

Arefkhah, N. and Shirzad, H. and Mosaviasl, F. and taghipor, S. and daneshpor, Sh. and yousofidarani, H. (2013) Title: Effects of hydatid cyst antigen on Hella cells in vitro. Journal of Shahrekord Uuniversity of Medical Sciences, 15.

Ayat, H. and Musavian, S.A. and Ahadi, A.M. and behvandi, E. and pirali, Kh. and Mahzounieh, M.R. (2014) Construction of single domain camel antibody library against breast cancer cellular antigens. Journal of Shahrekord Uuniversity of Medical Sciences, 16.

Azadegan Dehkordi, F. and Rashki, A. and Bagheri, N. and Hashemzadeh Chaleshtori, M. and Memarzadeh, E. and Salehi, A. and Ghatreh, H. and Zandi, F. and Yazdanpanahi, N. and Tabatabaiefar, M.A. and Hashemzadeh Chaleshtori, M. (2013) Study of VSX1 Mutations in Patients with Keratoconus in Southwest Iran Using PCR-Single-Strand Conformation Polymorphism/Heteroduplex Analysis and Sequencing Method. ACTA CYTOLOGICA, 57 (6). pp. 646-651.

Azizi, F. and Fallahi, S. and Asadi-Samani, M. and Goudarzian, M. (2014) Comparing thrB gene sequencing and multiplex PCR method in grouping of the different strains of escherichia coli. Journal of Mazandaran University of Medical Sciences, 24 (115). pp. 101-112.

akrami, H. and mahmoodi, F. (2015) Ibuprofen inhibits metastasis and invasion of Gastric cancer stem cells. Journal of Shahrekord Uuniversity of Medical Sciences, 17.

anbara, H. and Shahrooz, R. and razi, M. and Malekinejad, H. (2015) Evaluating the protective effect of co-administrating of vitamin C and royal jelly on Phenylhydrazine-induced hemolytic anemia’s derangements on sperm quality and serum parameters in mice Running Title: Role of vitamin C in anemia. Journal of Shahrekord Uuniversity of Medical Sciences, 17.

B

Bagheri, N. and Taghikhani, A. and Rahimian, Gh. and Salimzadeh, L. and Azadegan Dehkordi, F. and Zandi, F. and Hashemzadeh Chaleshtori, M. and Rafieian-Kopaei, M. and Shirzad, H. (2013) Association between virulence factors of helicobacter pylori and gastric mucosal interleukin-18 mRNA expression in dyspeptic patients. MICROBIAL PATHOGENESIS, 65. pp. 7-13.

Baharara, J. and Haddad, F. and Shariatzadeh, M.A. and Razavi, T. (2008) Genotoxic effect of hydrogen peroxide on bone marrow erythrocytes of female Balb/C mouse. Journal of Shahrekord Uuniversity of Medical Sciences, 10.

Baharara, J. and Zafar-Balanezhad, S. and Nejad-Shahrokhabadi, K. and Hesami, Z. (2012) The effects of different doses of atorvastatin on angiogenesis of chorioallantoic membrane of chick embryo. Journal of Shahrekord Uuniversity of Medical Sciences, 14.

Bakhshalizadeh, Sh. and Esmaeili, F. and Houshmand, F. and Shirzad, H. and Saedi, M. (2011) Effects of selegiline, a monoamine oxidase B inhibitor, on differentiation of P19 embryonal carcinoma stem cells, into neuron-like cells. IN VITRO CELLULAR & DEVELOPMENTAL BIOLOGY-ANIMAL, 47 (8). pp. 550-557.

Bakhshalizadeh, Sh. and Esmaeili, F. and Shirzad, H. and Houshmand, F. and Ebrahimi-Hafshejani, M. and Ghasemi, S. (2014) Neuronal differentiation of GFP expressing P19 embryonal carcinoma cells by deprenyl, an antiparkinson drug. Journal of Shahrekord Uuniversity of Medical Sciences, 16.

Banitalebi, E. and Gharakhanlou, R. and Ghatreh-Samani, K. and Mohammad-Amoli, M. and Teimori, H. (2012) The effect of resistance training on plasma and skeletal muscles sphingosine-1-phosphate levels of male Wistar rat. Journal of Shahrekord Uuniversity of Medical Sciences, 14.

Banitalebi, E. and Gharakhanlou, R. and Ghatrehsamani, K. and Parnow, A.H. and Teimori, H. and Mohammad Amoli, M. (2013) The study of effect of resistance training on plasma S1P level and gene expression of S1P1,2,3 receptors in male Wistar rat. MINERVA ENDOCRINOLOGICA, 38 (4). pp. 395-400.

Banitalebi, G. and Montazerzohor, M. and Farokhi, E. and Abolhasani, M. and Reissi, S. and Heydari, S. and Ataii, Z. and Azadegan-Dehkordi, F. and Hoseinipoor, A. and Hashemzadeh-Chaleshtory, M. (2012) Study of three common mitochondrial mutations in Arab patients with nonsyndromic hearing loss in Khuzestan province, I.R.Iran. Journal of Shahrekord Uuniversity of Medical Sciences, 14.

Banoei, M.M. and Hashemzade Chaleshtori, M. and Sanati, M.H. and Sharait Panahi, M.S. and Majidizadeh, T. and Rostami, M. and Manshadi, M.D. and Golalipour, M. (2007) Diversity and relationship between Iranian ethnic groups: Human dopamine transporter gene (DAT1) VNTR genotyping. American Journal of Human Biology, 19 (6). pp. 821-826.

Banoei, M.M. and Hashemzade Chaleshtori, M. and Sanati, M.H. and Shariati, P. and Houshmand, M. and Majidizadeh, T. and Jahangir Soltani, N. and Golalipour, M. (2008) Variation of DAT1 VNTR alleles and genotypes among old ethnic groups in Mesopotamia to the Oxus region. Human Biology, 80 (1). pp. 73-81.

Barati, A.H. and Fazeli, F. and Lotfipour, M. (2015) Effect of Aloe vera on some indicators of cell damage after a period of aerobic exercise in male athletes. Journal of Herbmed Pharmacology, 4.

Boroujeni, H.R. and Pourgheysari, B. and Hasheminia, A. and Boroujeni, P.R. and Drees, F. (2014) Effect of platelet glycoprotein IIb/IIIa PLA2 polymorphism on severity of pulmonary thromboembolism. Tanaffos, 13 (3). pp. 14-22.

D

Darani, Yousoff H. and Shirzad, H. and Mansoori, F. (2009) The effects of two parasite antigens (Toxoplasma gondii and Toxocara canis) on WEHI-164 fibrosarcoma growth in mouse model. SWISS MEDICAL WEEKLY, 139 (9-10). 29S.

Dehghani, L. and Tahani, S. and Hashemibeni, B. and Zamani, S. and esfandiari, E. (2013) Comparative Analysis of Collagen Type I and II Synthesis in Chondrocytes Derived Adipose Derived Stem Cells Versus Natural Articular Chondrocytes. Cell Journal (Yakhteh), 15.

Dehkordi, F. and Rashki, A. and Bagheri, N. and Chaleshtori, M. and Memarzadeh, E. and Salehi, A. and Ghatreh, H. and Hydari, S. and Yazdanpanahi, N. and Ghalehnoo, Z. and Merzaeyan, A. and Ghalehstori, M. (2013) Studying VSX1 gene mutations in patients with Keratoconus of Chaharmahal and Bakhtiari province, Iran. Journal of Kerman University of Medical Sciences, 20 (6). pp. 546-554.

Doosti, A. and Davoudi, N. and Mahboudi, F. (2007) Construction of a novel recombinant vector carrying. Journal of Shahrekord Uuniversity of Medical Sciences, 9.

E

Ebrahimi Hafshejani, M. and Esmaeili, F. and Houshmand, F. (2013) Differentiation of embryonal carcinoma stem cells into insulin-producing cells by using pancreas extract in vitro. Iranian Journal of Endocrinology and Metabolism, 15 (4). pp. 395-401.

Ebrahiminia, M. and Esmaeili, F. and Kharazian, N. and Houshmand, F. and Ebrahimi, M. (2014) Effect of flavonoids of extract of cichorium intybus L. leaf on induction of P19 stem-cells differentiation to insulin-producing cells. Journal of Mazandaran University of Medical Sciences, 23 (110). pp. 92-100.

Esmaeili, F. and Bamdad, T. and Ghasemi, S. (2010) Stable suppression of gene expression by short interfering RNAs targeted to promoter in a mouse embryonal carcinoma stem cell line. In Vitro Cellular and Developmental Biology - Animal, 46 (10). pp. 834-840.

F

Fallahi, E. and Parchami Barjuii, S. and Reiisi, S. and Salehi, A. and Amiri, B. and Heybati, F. and Teimori, H. (2015) Mutation screening of 3’UTR and exons 1-2 of vsx1 gene by PCR-SSCP/HA and sequencing in patients with Vernal Keratoconjuctivis (VKC) in Shahrekord. Journal of Zanjan University of Medical Sciences and Health Services, 23 (100).

Farhud, D. D. and Lotfi, A. S. and Hashemzadeh Chaleshtori, M. and Akhondi, M. and Sadighi, H. (2009) Progress of Education, Research and Services in Medical Genetics, in Some Institutions of Iran. IRANIAN JOURNAL OF PUBLIC HEALTH, 38 (1). pp. 115-118.

Fatahi, F. and Khazraei, H. and Ghatreh, K. and Amiri, M. and Hashemzadeh Chaleshtori, M. (2012) Analysis Of IL-17A And IL17F Genetic Polymorphisms As Risk Factors For Allergic Rhinitis In Iranian Females. JOURNAL OF MEDICAL GENETICS, 49 (1). S89.

Fatehi, D. (2009) Chromosomal aberrations induced by a low dose of neutron irradiation and hyperthermia. International Journal of Low Radiation, 6 (4). pp. 283-293.

Fatehi, D. (2010) Chromosomal damage to human lymphocytes induced by hyperthermia pre and post extremely low dose neutron or gamma radiation. Australasian Medical Journal, 1 (4). pp. 236-247.

Fathi, M. and Gharakanlou, R. and Rezaei, R. (2015) The effect of endurance training on left ventricle serum response factor gene expression in Wistar male rats. Journal of Shahrekord Uuniversity of Medical Sciences, 17.

Fattahi, N. and Tabatabaiefar, M.A. and Reeisi, S. and Alipour, P. and Pourahmadian, A. and Hashemzadeh Chaleshtory, M. (2015) Genetic linkage analysis of DFNB59 loci involved in autosomal recessive non-syndromic hearing loss (ARNSHL) in western provinces of Iran. journal of shahrekord university of medical sciences, 17 (4).

G

Ghasemi-Dehkordi, P. and Allahbakhshian-Farsani, M. and Abdian, N. and Jafari-Ghahfarokhi, H. and Saffari-Chaleshtori, J. and Sadeghiani, M. and Mirzaeian, A. and Hashemzadeh-Chaleshtori, M. (2015) A study of cytogenetic stability of induced pluripotent stem cells using karyotyping and comet assay techniques. Journal of Kerman University of Medical Sciences, 22 (4). pp. 370-384.

Ghasemi-Dehkordi, P. and Allahbakhshian-Farsani, M. and Abdian, N. and Mirzaeian, A. and Hashemzadeh-Chaleshtori, M. and Jafari-Ghahfarokhi, H. (2015) Effects of Feeder Layers, Culture Media, Conditional Media, Growth Factors, and Passages Number on Stem Cell Optimization. Proceedings of the National Academy of Sciences India Section B - Biological Sciences, 85 (3). pp. 711-717.

Ghasempour, E. and Emadi‑Baygi, M. and Nikpour, P. and Baradaran, A. (2016) Evaluation of expression ratio of HOXB13:IL17BR in patients with breast cancer by qRT-PCR method using SYBR Green dye. journal of shahrekord university of medical sciences, 18 (4).

Ghatreh Samani, K. and Noori, M. and Rohbani Nobar, M. and Hashemzadeh Chaleshtory, M. and Farrokhi, E. and Darabi Amin, M. (2012) The -514C/T Polymorphism of Hepatic Lipase Gene among Iranian Patients with Coronary Heart Disease. Iranian journal of public health, 41 (1). pp. 59-65. ISSN 2251-6085

Ghatreh Samani, K. and Noori, M. and Rohbani Nobar, M. and Hashemzadeh Chaleshtory, M. and Farrokhi, E. and Darabi Amin, M. (2012) The -514C/T polymorphism of hepatic lipase gene among iranian patients with coronary heart Disease. Iranian Journal of Public Health, 41 (1). pp. 59-65.

Gholipoor, A. and Peshva, A. and Tamizi, H. and Salehi, M. and Solemani, N. (2005) Determination of Brucella melitensis biotypes in human and sheep. Journal of Shahrekord Uuniversity of Medical Sciences, 6.

Gholipour, A. and Soleimani, N. and Shokri, D. and Mobasherizadeh, S. and Kardi, M. and Baradaran, A. (2014) Phenotypic and Molecular Characterization of Extended-Spectrum beta-Lactamase Produced by Escherichia coli, and Klebsiella pneumoniae Isolates in an Educational Hospital. JUNDISHAPUR JOURNAL OF MICROBIOLOGY, 7 (10).

Ghorbani, M. and Hashemibani, B. and Bahramian, H. and Karimi, Z. and Zamani, S. and Mirhosseini, S.A. and Zarkesh Isfahani, S.H. (2012) Recognition of Cytokeratin 18 Marker by Flow Cytometry of Nucleus Pulposus Cells in Human Intervertebral Disc and Comparison of Proliferation and Morphology of these Cells in Chitosan-Gelatin and Alginate Scaffolds. Journal of Isfahan Medical School, 30 (188).

Golshan Iranpour, F. and Rezazadeh Valojerdi, M. (2013) The epididymal sperm viability, motility and DNA integrity in dead mice maintained at 4-6 degrees C. IRANIAN JOURNAL OF REPRODUCTIVE MEDICINE, 11 (3). pp. 195-200.

Golshan-Iranpour, F. and Emami, E. (2011) The effects of lead on motility, viability and DNA denaturation of cauda epididymal spermatozoa of mouse. Journal of Shahrekord Uuniversity of Medical Sciences, 13.

H

Habibian, S. and Shadnoush, F. and Arabi, M. and Safar, B. (2013) Evaluation of the cytotoxicity and protein expression alteration induced by nanoparticles of silver in the rat sperm and testis. Journal of Shahrekord Uuniversity of Medical Sciences, 15.

Haghjooy Javanmard, Sh. and Ziaei, A. and Ziaei, S. and Ziaei, E. and Mirmohammad-Sadeghi, M. (2013) The Effect of Preoperative Melatonin on Nuclear Erythroid 2-Related Factor 2 Activation in Patients Undergoing Coronary Artery Bypass Grafting Surgery. OXIDATIVE MEDICINE AND CELLULAR LONGEVITY.

Hamidi, M. and Karimipoor, M. and Hashemzadeh Chaleshtori, M. and Akbari, M.T. (2009) A novel 355-357delGAG mutation and frequency of connexin-26 (GJB2) mutations in Iranian patients. JOURNAL OF GENETICS, 88 (3). pp. 359-362.

Hasheminia, S.J. and Tolouei, S. and Zarkesh-Esfahani, S.H. and Shaygannejad, V. and Shirzad, H.A. and Torabi, R. and Chaloshtory, M.H.Z. (2015) Cytokine gene expression in newly diagnosed multiple sclerosis patients. Iranian Journal of Allergy, Asthma and Immunology, 14 (2). pp. 208-216.

Hasheminia, S.J. and Zarkesh-Esfahani, S.H. and Tolouei, S. and Shaygannejad, V. and Shirzad, H. and Chaleshtory, M.H. (2014) Toll like receptor 2 and 4 expression in peripheral blood mononuclear cells of multiple sclerosis patients. Iranian Journal of Immunology, 11 (2). pp. 74-83.

Hashemzadeh Chaleshtori, M. and Farhud, D.D. and Crosby, A.H. and Farrokhi, E. and Jafari Pour, H. and Ghatreh Samani, K. and Safa Chaleshtori, K. and Kasiri, M. and Shahrani, M. and Mobini, G.R. and Banitalebi, M. and Mansouri, M. and Modarresinia, D. and Jafari, M. (2008) Molecular pathology of 6 novel GJB2 allelic variants detected in familial and sporadic Iranian non syndromic hearing loss cases. IRANIAN JOURNAL OF PUBLIC HEALTH, 37 (3). pp. 9-18.

Hashemzadeh Chaleshtori, M. and Farhud, D.D. and Patton, M.A. (2007) Familial and sporadic GJB2-related deafness in iran: Review of gene mutations. IRANIAN JOURNAL OF PUBLIC HEALTH, 36 (1). pp. 1-14.

Hashemzadeh Chaleshtori, M. and Farrokhi, E. and Shahrani, M. and Kheiri, S. and Dolati, M. and Hoghooghi Rad, L. and Pour-Jafari, H. and Ghatreh Samani, K. and Safa Chaleshtori, K. and Crosby, A.H. (2007) High carrier frequency of the GJB2 mutation (35delG) in the north of Iran. INTERNATIONAL JOURNAL OF PEDIATRIC OTORHINOLARYNGOLOGY, 71 (6). pp. 863-867.

Hashemzadeh Chaleshtori, M. and Hoghooghi Rad, L. and Dolati, M. and Sasanfar, R. and Hoseinipour, A. and Montazer Zohour, M. and Pourjafari, H. and Tolooi, A. and Ghadami, M. and Farhud, D.D. and Patton, M.A. (2005) Frequencies of mutations in the connexin 26 gene (GJB2) in two populations of Iran (Tehran and Tabriz). Iranian Journal of Public Health, 34 (1). pp. 1-7.

Hashemzadeh Chaleshtori, M. and Montazer Zohour, M. and Hoghooghi Rad, L. and Pour-Jafari, H. and Farhud, D.D. and Dolati, M. and Safa Chaleshtori, K. and Sasanfar, R. and Hosseinipour, A. and Andonian, L. and Tolouei, A. and Ghadami, M. and Patton, M.A. (2006) Autosomal recessive and sporadic non syndromic hearing loss and the incidence of Cx26 mutations in a province of Iran. Iranian Journal of Public Health, 35 (1). pp. 88-91.

Hashemzadeh Chaleshtori, M. and Simpson, M.A. and Farrokhi, E. and Dolati, M. and Hoghooghi Rad, L. and Amani Geshnigani, S. and Crosby, A.H. (2007) Novel mutations in the pejvakin gene are associated with autosomal recessive non-syndromic hearing loss in Iranian families. CLINICAL GENETICS, 72 (3). pp. 261-263.

Hashmzade Chaleshtori, M. and Akbari, M.T. and Khazraei, H. and Abolhasani, M. and Reisi, S. and Ataei, Z. and Saedi-Marghmaleki, M. and Shirmardi, S.A. and Farrokhi,, E. and Montazer-Zohouri, M. and Azadegan-Dehkordi, F. (2011) Screening of three common mtDNA mutations among subjects with autosomal recessive non-syndromic hearing loss in Sistan va Baluchestan province, Iran. Zahedan Journal of Research in Medical Sciences, 13 (5).

Hatamnia, Z. and Esmaeili, F. and Houshmand, F. and Dehdehi, L. (2014) Effect of pancreatic extract on insulin secreting cell differentiation from mouse bone marrow mesenchymal stem cells. Journal of Shahrekord Uuniversity of Medical Sciences, 16.

Hematian, H. and Khaksar, Z. and Jelodar, Gh. (2010) Evaluation of maternal diabetes effects on Lumbosacral portion of spinal cord in neonate rats by morphometry. Journal of Shahrekord Uuniversity of Medical Sciences, 12.

Heydari, S. and Khaledifar, A. and Pourahmad, R. and Hashemzadeh-Chaleshtori, M. and Heydari, S. and Bagheri, N. and Reisi, S. and Abolhasani, M. (2013) Investigation of mutations in exons 19-23 MYH7 gene in hypertrophic cardiomyopathy patients using PCR-SSCP/HA technique in Chaharmahal va Bakhtiari province. Journal of Shahrekord Uuniversity of Medical Sciences, 15.

Honari, H. and Mehrazin, H. and Saadati, M. and Minaei, M.E. (2013) Production of polycolonal antibody against domain 2-4 of protective antigen of Bacillus anthracis in laboratory animals. Journal of Shahrekord Uuniversity of Medical Sciences, 15.

Hosseini, A. and Estiri, H. and Akhavan Niaki, H. and Alizadeh, A. and Abdolhossein Zadeh, B. and Ghaderian, S.M.H. and Farjadfar, A. and Fallah, A.A. (2017) Multiple Sclerosis Gene Therapy Using Recombinant Viral Vectors: Overexpression of IL-4, IL-10 and Leukemia Inhibitory Factor in Wharton's Jelly Stem Cells in The EAE Mice Model. CELL JOURNAL, 19 (3). pp. 361-374.

Hosseinipour, A. and Chaleshtori, M.H. and Sasanfar, R. and Farhud, D.D. and Tolooi, A. and Doulati, M. and Rad, L.H. and Montazer Zohour, M. and Ghadami, M. (2005) Report of a new mutation and frequency of connexin 26 gene (GJB2) mutations in patients from three provinces of Iran. Iranian Journal of Public Health, 34 (1). pp. 47-50.

I

Ilkhanizade, Sh. and Ayat, H. and Ahadi, A.M. and Pirali, Kh. (2011) Sequencing and comparative-bioinformatic analysis of chlorotoxin-like peptide from Iranian scorpion Mesobuthus eupeus. Journal of Shahrekord Uuniversity of Medical Sciences, 13.

Iranpoor, H.r. and Vatankhah, V. and Lotfizadeh, M. (2015) Optimization and Construction of Human Insulin-like Growth Factor 1 Gene related to human health. International Journal of Epidemiologic Research, 2 (3). pp. 140-145.

J

Jafari, H. and Hojati, Z. (2015) Construction of eukaryotic integrative vectors by insertion of the integration region attB in pSVM. Journal of Shahrekord Uuniversity of Medical Sciences, 16.

Jafari Ghahfarokhi, H. and Ashoori, S. and Akbari, M.T. and Lotfizadeh, M. and Karimi, A. and Teimori, H. (2014) ZAP70 Expression Within del6q21, del11q13 and del17p13 Cytogenetic Subgroups of Iranian Patients with Chronic Lymphocytic Leukemia. IRANIAN RED CRESCENT MEDICAL JOURNAL, 16 (11).

Jafarzadeh, L. and Danesh, A. and Sadeghi, M. and Heybati, F. and Hashemzadeh, M. (2013) Analysis of relationship between tumor necrosis factor alpha gene (G308A polymorphism) with preterm labor. International Journal of Preventive Medicine, 4 (8). pp. 896-901.

K

Kamali, E. and Tavassoli, M. and Hemmati, S. (2015) Association between the polymorphism of CA dinucleotide repeat in intron 1 of NFκB1 gene and risk of breast cancer. Journal of Shahrekord Uuniversity of Medical Sciences, 17.

Karimi, A. and Nafisi, M.R. and Tamizi, H. (2004) Investigation of host cell protein synthesis shut-off inhibition by a Herpes simplex virus type-1 gene, ICP34.5, in a neuronal cell line, SK-N-SH. Journal of Shahrekord Uuniversity of Medical Sciences, 6.

Karimi, n. and Saffar, b. and Ghaedi, k. and Mobini-Dehkordi, m. (2013) Optimization of expression, purification and handling anti bacteria feature protein of bovine neutrophil B-defensing BNBD2. Journal of Shahrekord Uuniversity of Medical Sciences, 15.

Kazemi Arababadi, M. and Mosavi, R. and Ravari, A. and Teimori, H. and Hassanshahi, Gh. (2012) Association of interleukin-4 polymorphisms with multiple sclerosis in southeastern Iranian patients. ANNALS OF SAUDI MEDICINE, 32 (2). pp. 127-130.

Khademi, S. and Ahadi, A.M. and Mehvari, J. and Ayat, H. and Farokhi, E. and Moradi, M.T. and Hashemzadeh-Chaleshtori, M. (2011) Detection of A1430G mutation in SCN1A gene in a patient affected by GEFS-Like epilepsy in Chaharmahal va Bakhtiari Province. Journal of Shahrekord Uuniversity of Medical Sciences, 13.

Khorvash, F. and Khorvash, A. and Meidani, M. and Abasi, S. and Yaran, M. and Zolfaghari, M.R. and Rezaei, S.A. and Ataei, B. (2015) Detection of Legionella pneumophila in the bronchoalveolar lavage samples by real time PCR in patients with ventilator-associated pneumonia in ICU. Journal of Shahrekord Uuniversity of Medical Sciences, 17.

Khorvash, F. and Nikooei, M. and Meidani, M. and Shokri, D. and Zolfaghari, M.R. (2016) Reduction of vancomycin resistance inVanAand VanBcontainingVancomycin Resistant Enterococci (VRE) isolatesin presence of lactoferrin protein. Journal of Shahrekord Uuniversity of Medical Sciences, 17.

Khoshdel, Abolfazl and Kheiri, Soleman and Habibian, Roya and Nozari, Ahora and Baradaran, Azar (2012) Lack of association between TNF-α gene polymorphisms at position -308 A, -850T and risk of simple febrile convulsion in pediatric patients. Advanced biomedical research, 1. p. 85. ISSN 2277-9175

Khosravi, A. and Hashemi Shahraki, A. (2005) Differentiation of Mycobacterium tuberculosis clinical strains using restrikction fragment length polymorphism technique based on hsp65 gene. Journal of Shahrekord Uuniversity of Medical Sciences, 7.

Kooshavar, D. and Tabatabaiefar, M.A. and Farrokhi, E. and Abolhasani, M. and Noori-Daloii, M.R. and Hashemzadeh Chaleshtori, M. (2013) Digenic inheritance in autosomal recessive non-syndromic hearing loss cases carrying GJB2 heterozygote mutations: Assessment of GJB4, GJA1, and GJC3. INTERNATIONAL JOURNAL OF PEDIATRIC OTORHINOLARYNGOLOGY, 77 (2). pp. 189-193.

M

Mansouri-Bidekani, A. and Esmaeili, F. and Houshmand, F. and Hajisharifi, Z. (2013) Evaluation of pdx-1 gene expression in insulin producing cells, derived from embryonal carcinoma stem cells. Journal of Shahrekord Uuniversity of Medical Sciences, 15.

Mehdinejadiani, K. and Jalili, A. and Kopaei, M.R. and Salimzadeh, L. and Mehdinejadiani, S. and Mousavi, S.M.J. and Shirzad, H. (2015) Effect of glycyrrhetinic acid and glycyrrhizic acid on the expression of CXCR4 in epithelial cells of gastric carcinoma. Journal of Mazandaran University of Medical Sciences, 25 (123). pp. 152-161.

Mehri-Ghahfarrokhi, A. and Hashemzadeh-Chaleshtori, M. and Shojaeian, A. and Mahmoudian-Sani, M.R. (2017) Studying gap junction beta 2-related deafness in Iranian population. Otorinolaringologia, 67 (3). pp. 89-95.

Mohammadali Beigi, F. and Mehrabi, S. and Javaherforooshzadeh, A. (2007) Varicocele in brothers of patients with varicocele. Urology journal, 4 (1). pp. 33-35.

Mohandes-Samani, N. and Ghatre-Samani, K. and Fathpour, H. and Farokhi, E. and Salehian-Dehkordi, M. (2014) Decreases of osteonectin gene expression by gallic acid in vascular smooth muscle cells. Journal of Shahrekord Uuniversity of Medical Sciences, 16.

Mojtabavi Naeini, M. and Mesrian Tanha, H. and Hashemzadeh Chaleshtori, M. and Vallian-Brojeni, S. (2014) Genotyping Data and Novel Haplotype Diversity of STR Markers in the SLC26A4 Gene Region in Five Ethnic Groups of the Iranian Population. GENETIC TESTING AND MOLECULAR BIOMARKERS, 18 (12). pp. 820-825.

Mokhtari-Farsani, A. and Doosti, A. (2015) Investigation of antibiotic resistance and frequency of Clostridium difficile tcdA and tcdB genes in feces of calves in Chaharmahal and Bakhtiari province. Journal of Shahrekord Uuniversity of Medical Sciences, 17.

Montazer Zohour, M. and Tabatabaiefar, M.A. and Azadegan Dehkordi, F. and Farrokhi, E. and Akbari, M.T. and Hashemzade Chaleshtori, M. (2012) Large-Scale Screening of Mitochondrial DNA Mutations Among Iranian Patients with Prelingual Nonsyndromic Hearing Impairment. GENETIC TESTING AND MOLECULAR BIOMARKERS, 16 (4). pp. 271-278.

Montazer- Zohour, M. and Hashemzadeh-Chaleshtori, M. and Akbari, M. T. (2012) Frequency of the common mitochondrial DNA (mtDNA) mutations in non-syndromic hearing impairment in southwest subpopulations of Iran. Journal of Shahrekord Uuniversity of Medical Sciences, 14.

Mortezaee, F.T. and Chaleshtori, M.H. and Kheiri, S. and Farrokhi, E. and Shariati, L. and Tabatabaiefar, M.A. and Miraj, S. (2015) Interleukin-1 β gene polymorphisms in Iranian patients with uterine fibroid, a case-control study. Biosciences Biotechnology Research Asia, 12 (1). pp. 341-345.

Motamedi, S. and Hashemzadeh-Chaleshtori, M. and Mojtabavi-Naeini, M. and Teimori, H. (2015) Genetic variation of D9S1837 Marker located at TMC1 gene in Iranian population. Journal of Shahrekord Uuniversity of Medical Sciences, 16.

Mousavi, M. and Baharara, J. and Asadi-Samani, M. (2014) Anti-angiogenesis effect of <em>crocous sativus </em>L. extract on matrix metalloproteinase gene activities in human breast carcinoma cells. Journal of HerbMed Pharmacology, 3.

Mousavi, S.M. and Kamali, E. and Karimi, P. and Salehi, M. (2014) An overview on the evolution of language and genetics of speech disorders. Journal of Isfahan Medical School, 32 (301). pp. 1509-1529.

N

Naeini, M.M. and Boroujeni, S.V. and Chaleshtori, M.H. (2014) Population data on d7s2425 marker in five ethnic groups of the iranian population: A highly informative marker for molecular diagnosis of ARNSHL. Journal of Kerman University of Medical Sciences, 21 (6). pp. 540-550.

Namjoo, A.R. and Kargar, A. and Heidarian, E. and Ashje, A. and Malki, S. (2012) The toxicity effect of methyl mercury chloride on newborn rat: Enzymatic, histology change and mercury accumulation. Journal of Shahrekord Uuniversity of Medical Sciences, 14.

Nasri, H. and Rafieian-Kopaei, M. (2013) Significant association of serum H. pylori IgG antibody titer with kidney function in renal transplanted patients. Journal of renal injury prevention, 2 (1). pp. 23-5. ISSN 2345-2781

Navid, S. and Rastegar, T. and Baazm, M. and Alizadeh, R. and Talebi, A. and Gholami, K. and Khosravi-Farsani, S. and Koruji, M. and Abbasi, M. (2017) In vitro effects of melatonin on colonization of neonate mouse spermatogonial stem cells. Systems Biology in Reproductive Medicine. pp. 1-12.

Nikbakht Dastjerdi, M. and Zamani, S. and Mardani, M. and Hashemi Beni, B. (2016) All-trans retinoic acid and genistein induce cell apoptosis in OVCAR-3 cells by increasing the P14 tumor suppressor gene. Research in Pharmaceutical Sciences, 11 (6).

Nikooei, M. and Meidani, M. and Khorvash, F. and Karimi, M. and Parsaei, P. (2014) Evaluation of the frequency of phenotype and genotype of Van A and Van B genes in vancomycine resistant enterococcus isolated from clinical sample of Alzahra Hospitals in Isfahan. Journal of Shahrekord Uuniversity of Medical Sciences, 16.

Nozar, A. and Foroghmand, A.m. and Ahadi, A.M. and Khoshdel, A. and Salehian, Sh. and Bagheri, H. and Hashem Zadeh-Chaleshtori, M. (2010) Assosiation study between IL1RA gene polymorphism with febrile convulsion in Shahrekord children. Journal of Shahrekord Uuniversity of Medical Sciences, 12.

nekouei, A. and kordi, M.R. and Choobineh, S. and Soleimani, M. and Shafiee, A. and Hadidi, V. (2016) The Effect Of Eight Week Continuous Training On Expression Of Mir29mRNA, In Healthy Male Rat’s Cardiac Muscle. Journal of Shahrekord Uuniversity of Medical Sciences, 17.

O

Olad, Gh. and Tavalaee, M. and mohamad hasan, z. and Ebrahimi, f. and Salimian, J. and Nazarean, sh. and Rahimi, a. (2011) Shigella dysentery stxA mutant (R170L-A231D-G234E) gene design and optimization of recombinant protein expression and purification. Journal of Shahrekord Uuniversity of Medical Sciences, 13.

P

Parchami Barjui, S. and Reiisi, S. and bayati, A. (2017) Human glutathione s-transferase enzyme gene variations and risk of multiple sclerosis in Iranian population cohort. Multiple Sclerosis and Related Disorders, 17. pp. 41-46.

Parchami-Barjui, S. and Reiisi, S. and Rezaiean, F. and Heybati, F. and Hashemzadeh-Chaleshtori, M. (2014) Screening LRTOMT gene (DFNB63 locus) in patients with recessive nonsyndromic hearing loss in hormozgan province, Iran. Journal of Isfahan Medical School, 32 (298). pp. 1330-1337.

Pour-Jafari, H. and Chaleshtori, M.H. and Farhud, D.D. (2005) Dermatoglyphics in patients with oligo/azospermia. Iranian Journal of Public Health, 34 (3). pp. 56-61.

Pourgheysari, B. and Beshkar, P. and Azadegan, F. (2012) Factor XIIIA-V34L and factor XIIIB-H95R gene polymorphisms in Shahrekord, 2010, I.R.Iran. Journal of Shahrekord Uuniversity of Medical Sciences, 14.

Pourgheysari, B. and Bruton, R. and Parry, H. and Billingham, L. and Fegan, Ch. and Murray, J. and Moss, P. (2010) The number of cytomegalovirus-specific CD4(+) T cells is markedly expanded in patients with B-cell chronic lymphocytic leukemia and determines the total CD4(+) T-cell repertoire. BLOOD, 116 (16). pp. 2968-2974.

Pourgheysari, B. and Rouhi Boroujeni, H. and Hasheminia, A.M. and Drees, F. (2013) PLA2 polymorphism of platelet glycoprotein IIb/IIIa but not Factor V Leiden and prothrombin G20210A polymorphisms is associated with venous thromboembolism and more recurrent events in central Iran. BLOOD COAGULATION & FIBRINOLYSIS, 24 (5). pp. 471-476.

R

Rabiee-Faradonbeh, M. and Darban-Sarokhalil, D. and Feizabadi, M.M. and Alvandi, A.H. and Momtaz, H. and Soleimani, N. and Gholipour, A. (2014) Cloning of the Recombinant Cytochrome P450 Cyp141 Protein of Mycobacterium tuberculosis as a Diagnostic Target and Vaccine Candidate. IRANIAN RED CRESCENT MEDICAL JOURNAL, 16 (11).

Rafieian-Kopaei, M. and Baradaran, A. and Nasri, H. (2013) Significance of extracapillary proliferation in IgA-nephropathy patients with regard to clinical and histopathological variables. HIPPOKRATIA, 17 (3). pp. 258-261.

Rahimian, Gh. and Bagheri, N. and Shirzad, H. (2015) Correlation between expression levels of mRNA IL-6 and H. pylori-infected patients with cagA. Journal of Shahrekord Uuniversity of Medical Sciences, 17.

Rahimifard, M. and Sadeghi, F. and Asadi-Samani, M. and Nejati-Koshki, K. (2017) Effect of quercetin on secretion and gene expression of leptin in breast cancer. JOURNAL OF TRADITIONAL CHINESE MEDICINE, 37 (3). pp. 321-325.

Rahmani, F. and esfandiari, E. (2000) Cephalometric parameters in Schizophrenic patients. Journal of Shahrekord Uuniversity of Medical Sciences, 2.

Ramazi, Sh. and Motovalibashi, M. and Hashemzade-Chaleshtori, M. and Khazraei, H. (2014) Introduction of Interleukin-18 genotype as a risk factor for allergic rhinitis in Chaharmahal va Bakhtiari province. Journal of Shahrekord Uuniversity of Medical Sciences, 16.

Reiisi, S. and Sanati, M.H. and Tabatabaiefar, M.A. and Pourjafari, H.R. and Minuchehr, Z. and Shavarzi, A. and Ataie, M. and Kasiri, M. and Hashemzadeh-Chaleshtori, M. (2014) Study of the association of DFNB3 locus with autosomal recessive non-syndromic hearing loss in iranian deaf population using genetic linkage analysis. Journal of Isfahan Medical School, 32 (285). pp. 669-677.

Rezaee, M. and Honari, H. and Zand, A.m. (2012) Molecular cloning and expression of Bacillus anthracis Lethal Factor domain 1 gene in Escherichia coli. Journal of Shahrekord Uuniversity of Medical Sciences, 14.

Rezaeian, F. and Tabatabaiefar, M.A. and Heybati, F. and Reiisi, S. and Parchami, Sh. and Abolhasani, M. and Amiri, B. and Salehi, A.R. and Hashemzadeh-Chaleshtori, M. (2014) Genetic linkage analysis of DFNB93 locus in a group of families with autosomal recessive non-syndromic hearing loss in Chahar Mahal & Bakhtiari and Kohkiluyeh & Boyer Ahmad provinces of Iran. Journal of Shahrekord Uuniversity of Medical Sciences, 16.

S

Sadeghi, A. and Sanati, M.H. and Alasti, F. and Chaleshtori, M.H. and Mahmoudian, S. and Ataei, M. (2009) Contribution of GJB2 mutations and Four common DFNB loci in autosomal recessive non-syndromic hearing impairment in Markazi and Qom provinces of Iran. Iranian Journal of Biotechnology, 7 (2). 108-111+120.

Sadrizade, N. and Parchami-Barjui, S. and Reiisi, S. and Hashemzadeh-Chaleshtori, M. and Hajhashemi, M. (2015) Screening BRCA1 and BRCA2 Mutation Frequencies In Breast Cancer Patients Of West Iran Reveals a Novel Polymorphism In BRCA1 Gene «L’indagine sulla frequenza di mutazione dei BRCA1 e BRCA2 in pazienti con tumore mammario dell’Iran occidentale evidenzia un nuovo polimorfismo del gene BRCA1». European Journal of Oncology, 20 (2). pp. 94-99.

Saee-Rad, S. and Hashemi, H. and Miraftab, M. and Noori-Daloii, M.R. and Hashemzadeh Chaleshtori, M. and Raoofian, R. and Jafari, F. and Greene, W. and Fakhraie, Gh. and Rezvan, F. and Heidari, M. (2011) Mutation analysis of VSX1 and SOD1 in Iranian patients with keratoconus. MOLECULAR VISION, 17 (336-37). pp. 3128-3136.

Saeidi, E. and Hashemzadeh Chaleshtori, M. and Doosti, A. and Parchami Bajue, Sh. investigation of mutation in Exon 27 and exon 29 of MYBPC3 gene by using PCR-SSCP/HA in cardiomyopathic hypertrophy patients in chahahrmahal va bakhtiari province. journal of shahrekord university of medical sciences.

Salehi Chaleshtori, A.R. and Tabatabaiefar, M.A. and Salehi, H.R. and Chaleshtori, M.H. (2014) Analysis of CABP2 c.637+1G>T mutation in iranian patients with non-syndromic sporadic hearing loss. Genetics in the Third Millennium, 12 (2). pp. 3504-3511.

Salek Abdollahi, F. and Baharara, J. and NejadShahrokhabadi, Kh. and Namvar, F. and Amini, E. (2015) Effect of Phoenix dactylifera pollen grain on maturation of preantral follicles in NMRI mice. Journal of Herbmed Pharmacology, 4.

Schrauwen, I. and Helfmann, S. and Inagaki, A. and Predoehl, F. and Tabatabaiefar, M.A. and Picher, M.M. and Sommen, M. and Seco, C.Z. and Oostrik, J. and Kremer, H. and Dheedene, A. and Claes, Ch. and Fransen, E. and Hashemzadeh Chaleshtori, M. and Coucke, P. and Lee, A. and Moser, T. and Van Camp, G. (2012) A Mutation in CABP2, Expressed in Cochlear Hair Cells, Causes Autosomal-Recessive Hearing Impairment. AMERICAN JOURNAL OF HUMAN GENETICS, 91 (4). pp. 636-645.

Seyedalipour, B. and Barimani, N. and Hoseini, S.M. (2015) Embryonic malformations following exposure to copper oxide nanoparticles in Mus musculus. Journal of Shahrekord Uuniversity of Medical Sciences, 17.

Shahbazi-Gahrouei, D. and Williams, M. and Allen, B. (2001) In vitro study of relationship between signal intensity and gadolinium-DTPA concentration at high magnetic field strength. Australasian Radiology, 45 (3). pp. 298-304.

Shahpari, A. and Dehghan, M. and Pourahmad, R. and Hashemzadeh-Chaleshtori, M. and Amiri, M. and Kazemi, S. (2015) Association of ApaI and Taq1 polymorphic site of vitamin D receptor gene with bone mineral density in women aged 45 years and older. Journal of Shahrekord Uuniversity of Medical Sciences, 17.

Shahriari, H. and Farid-Hosseini, R. and Jabbari Azad, F. and Rafatpanah, H. and Jafari, M. and Khashyarmanesh, Z. and Rezaee, A.R. and Asadi-Samani, M. (2015) Evaluation of Indoleamine 2, 3-Dioxygenase Gene Expression and Activation in Chronic Spontaneous Urticaria. INTERNATIONAL JOURNAL OF ADVANCED BIOTECHNOLOGY AND RESEARCH, 8 (2). pp. 1102-1107.

Sharafi, S.M. and Rostami-Nejad, M. and Moazeni, M. and Yousefi, M. and Saneie, B. and Hosseini-Safa, A. and Yousofi-Darani, H. (2014) Echinococcus granulosus genotypes in Iran. Gastroenterology and Hepatology from Bed to Bench, 7 (2). pp. 82-88.

Shayesteh Moghadam, M. and Nasr-Esfahani, M.H. and Razavi, Sh. and Nazem, H. and Deemeh, M.R. and Tavalaee, M. (2008) The efficiency of Zeta method in separation of sperm. Journal of Shahrekord Uuniversity of Medical Sciences, 10.

Shirzad, H. and Bagheri, N. and Azadegan-Dehkordi, F. and Zamanzad, B. and Izadpanah, E. and Abdi, M. and Ramazani, G. and Sanei, M.H. and Ayoubian, H. and Ahmadi, A. and Jamalzehi, S. and Aslani, P. and Zandi, F. (2015) New insight to IL-23/IL-17 axis in iranian infected adult patients with gastritis : Effects of genes polymorphisms on expression of cytokines. Acta Gastro-Enterologica Belgica, 78 (2). pp. 212-218.

Shirzad, H. and Zamanzad, B. and Shahabi, Gh.A. (2009) Expression of NC-2 Receptor on MCL Cells and Its Natural Cytotoxicity Against Cancer Cells. KUWAIT MEDICAL JOURNAL, 41 (2). pp. 112-116.

Shirzade, H. and Meshkat, R. and Ganjalikhani-Hakemi, M. and Mosayebian, A. and Ghasemi, R. and Deress, F. and Parchami barjui, S. and Sadri, M. and Salehi, R. (2015) Association analysis of -416 G>C polymorphism of T-cell immunoglobulin and mucin domain-1 gene with asthma in Iran. International Journal of Immunogenetics, 42 (4). pp. 265-269.

Soleimani, A. and Mobedi, Z. and Hashemzadeh-Chaleshtori, M. and Alerasoul, M. and Sadeghi, B. and Kazemi-Vardanjani, A. and Sharifi-Faradonbeh, A. (2014) The effect of HLADRB1 subtypes, on clinical diseases activity index in rheumatoid arthritis patients referred to rheumatology clinic of Shahrekord University of Medical Sciences. Journal of Shahrekord Uuniversity of Medical Sciences, 16.

T

Tabatabaiefar, M.A. and Alasti, F. and Montazer Zohour, M. and Shariati, L. and Farrokhi, E. and Farhud, D.D. and Camp, G.V. and Noori-Daloii, M.R. and Hashemzadeh Chaleshtori, M. (2011) Genetic Linkage Analysis of 15 DFNB Loci in a Group of Iranian Families with Autosomal Recessive Hearing Loss. IRANIAN JOURNAL OF PUBLIC HEALTH, 40 (2). pp. 34-48.

Tabatabaiefar, M.A. and Alasti, F. and Shariati, L. and Farrokhi, E. and Fransen, E. and Nooridaloii, M.R. and Chaleshtori, M.H. and Van Camp, G. (2011) DFNB93, a novel locus for autosomal recessive moderate-to-severe hearing impairment. CLINICAL GENETICS, 79 (6). pp. 594-598.

Taghipour-Sheshdeh, A. and Tabatabaiefar, M.A. and Nemati-Zargaran, F. and Moradi, F. and Zarepour, N. and Hashemzadeh Chaleshtori, M. (2016) Genetic linkage analysis of the DFNB48 and DFNB98 loci in families with Autosomal Recessive Non-Syndromic Hearing Loss (ARNSHL) from Khouzestan province. journal of shahrekord university of medical sciences, 18 (6).

Taghizade Mortezaee, F. and Tabatabaiefar, M.A. and Hashemzadeh Chaleshtori, M. and Miraj, S. (2014) Lack of Association between ESR1 and CYP1A1 Gene Polymorphisms and Susceptibility to Uterine Leiomyoma in Female Patients of Iranian Descent. CELL JOURNAL, 16 (2). pp. 225-230.

Taghizadeh, S.H. and Kazeminezhad, S.R. and Sefidgar, S.A.A. and Yazdanpanahi, N. and Tabatabaeifar, M.A. and Yousefi, A. and Lesani, S.M. and Abolhasani, M. and Hashemzadeh Chaleshtori, M. (2013) Investigation of LRTOMT gene (locus DFNB63) mutations in Iranian patients with autosomal recessive non-syndromic hearing loss. International journal of molecular and cellular medicine, 2 (1). pp. 41-5. ISSN 2251-9637

TahrzadehGharofi, M. and Farkhoi, E. and Shirmardi, S.A. and Safari Chaleshtori, J. and Asadi, S. and Ghatreh Samani, K. and Abolhasani, M. and HajiHoseyni, R. and HashemzadehChaleshtori, M. (2010) DFNB59 gene mutations screening in non syndromic deaf subjects in Chaharmahal va Bakhtiari province. Journal of Shahrekord Uuniversity of Medical Sciences, 11.

Tavalaee, M. and Parivar, K. and Javadian Elyadari, S. and Nasr Isfahani, M.H. Centrosome and its role in gametogenesis and embryonic development. journal of shahrekord university of medical sciences.

Teimori, H. and Akbari, M.T. and Hamid, M. and Forouzandeh, M. and Bibordi, E. (2011) Analysis of CD38 and ZAP70 mRNA expression among cytogenetic subgroups of Iranian chronic-lymphocytic-leukemia patients. GENETICS AND MOLECULAR RESEARCH, 10 (4). pp. 2415-2423.

Torshizi, R. and Zamanzad, B. and Mokhtareyan, K. and Karimi, A. (2011) Determination of CTX-M genes in enterobacteriaceae producing extended-spectrum beta-lactamase using PCR method. Journal of Shahrekord Uuniversity of Medical Sciences, 13.

Tousizadeh, B. and Moghim, Sh. and Salehi Chaleshtori, A.R. and Ghanbarian, M. and Mirian, M. and Salehi, M. and Tousizadeh, S. and Zaboli, F. (2017) Application of Epstein-Barr Virus for Optimization of Immortalized B-lymphocyte Production as a Positive Control in Genetic Studies. Advanced biomedical research, 6. p. 80. ISSN 2277-9175

V

Vand Rajabpour, F. and Raoofian, R. and Youssefian, L. and Vahidnezhad, H. and Mirshams Shahshahani, M. and Fathi, H. and Noormohammadpour, P. and Kamyab Hesari, K. and Hashemzadeh-Chaleshtori, M. and Tabrizizadeh, M. (2014) BMI1 and TWIST1 Downregulated mRNA Expression in Basal Cell Carcinoma. ASIAN PACIFIC JOURNAL OF CANCER PREVENTION, 15 (8). pp. 3797-3800.

Vanwesemael, M. and Schrauwen, I. and Ceuppens, R. and Alasti, F. and Jorssen, E. and Farrokhi, E. and Chaleshtori, M.H. and Van Camp, G. (2011) A 1bp deletion in the dual reading frame deafness gene LRTOMT causes a frameshift from the first into the second reading frame. American Journal of Medical Genetics, Part A, 155 (8). pp. 2021-2023.

Vanwesemael, Maarten and Schrauwen, Isabelle and Ceuppens, Ruben and Alasti, Fatemeh and Jorssen, Ellen and Farrokhi, Effat and Chaleshtori, Morteza Hashemzadeh and Van Camp, Guy (2011) A 1 bp Deletion in the Dual Reading Frame Deafness Gene LRTOMT Causes a Frameshift From the First Into the Second Reading Frame. AMERICAN JOURNAL OF MEDICAL GENETICS PART A, 155A (8). pp. 2021-2023.

Y

Yazdanpanahi, N. and Hashemzadeh Chaleshtori, M. and Tabatabaiefar, M.A. and Noormohammadi, Z. and Farrokhi, E. and Najmabadi, H. and Shahbazi, Sh. and Hosseinipour, A. (2012) Two novel SLC26A4 mutations in Iranian families with autosomal recessive hearing loss. INTERNATIONAL JOURNAL OF PEDIATRIC OTORHINOLARYNGOLOGY, 76 (6). pp. 845-850.

Yazdanpanahi, N. and Tabatabaiefar, M.A. and Farrokhi, E. and Abdian, N. and Bagheri, N. and Shahbazi, Sh. and Noormohammadi, Z. and Hashennzadeh Chaleshtori, M. (2013) Compound Heterozygosity for Two Novel SLC26A4 Mutations in a Large Iranian Pedigree with Pendred Syndrome. CLINICAL AND EXPERIMENTAL OTORHINOLARYNGOLOGY, 6 (4). pp. 201-208.

Yousofi, H. and Hashemzadeh-Chaleshtori, M. and Aliyari, Z. and Farrokhi, E. and Zebardast, N. (2007) Molecular characterization of the strains cause sheep-Hydatid cyst, in Chaharmahal va Bakhtiary province using restriction fragment length polymorphism. Journal of Shahrekord Uuniversity of Medical Sciences, 9.

Z

Zamani, S. and Aflaki, M. and Imani Fooladi, A.A. and Darban-Sarokhalil, D. and Bameri, Z. and Khazaee, S. and Nasiri, M.J. and Feizabadi, M.M. (2013) MIRU-VNTR analysis of the Mycobacterium tuberculosis isolates from three provinces of Iran. SCANDINAVIAN JOURNAL OF INFECTIOUS DISEASES, 45 (2). pp. 124-130.

Zandi, F. and Shirzad, H. and Bagheri, N. and Ahmadi, A. and Azadegan, F. and Gharib, A. and Hosseini, J. and Salimzadeh, L. and Ayoubian, H. and Menbari, N. and Zamanzad, B. (2013) Evaluation of IL-17A and IL-17F genes polymorphism in Iranian dyspeptic patients. Life Science Journal, 10 (SPL.IS). pp. 544-551.

Zandi, F. and Shirzad, H. and Bagheri, N. and Rahimian, G. and Salimzadeh, L. and Azadegan, F. and Yousefzadeh Eshkevari, K. and Fatahi, F. and Ahmadi, A. and Gharib, A. and Gholami, S. and Zamanzad, B. (2014) Evaluation of H.pylori infection and IL23R gene polymorphism in dyspeptic subjects. Life Science Journal, 11 (SPEC.I). pp. 40-46.

Zarghampoor, F. and Pourahmad, R. and Dehghan, M. and Hashemzadeh-Chaleshtori, M. (2015) Association of Taq1 restriction site of Calcitonine gene and Alu1 (rs1801197) polymorphism of Calcitonin receptor gene with bone mineral density in 200 women over 45 years in Shahrekord city. Journal of Shahrekord Uuniversity of Medical Sciences, 17.

Zohour, M.M. and Akbari, M.T. and Chaleshtori, M.H. (2012) Frequency of the mitochondrial A1555G mutation in Iranian patients with non-syndromic hearing impairment. Indian Journal of Science and Technology, 5 (10). pp. 3378-3383.

This list was generated on Mon Sep 25 01:00:57 2017 IRST.