Items where Author is "Hashemzadeh-Chaleshtori, Morteza."

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Khaledifar, Arsalan. and Hashemzadeh-Chaleshtori, Morteza. and Solati Dehkordi, Seyed kamal. and Poustchi, Hossein. and Bollati, Valentina. and Ahmadi, Ali. and Kheiri, Soleiman. and Ghatreh Samani, Keihan. and Banitalebi, Mehdi. and Sedehi, Morteza. and Malekzadeh, Reza. (2018) The protocol of a population-based prospective cohort study in southwest of Iran to analyze common non-communicable diseases: Shahrekord cohort study. BMC Public Health., 18 (1).

Mahmoudian Sani, Mohammad Reza. and Mehri-Ghahfarrokhi, Ameneh. and Hashemzadeh-Chaleshtori, Morteza. and Saidijam, Masoud. and Jami, Mohammad-Saeid. (2017) Comparison of Three Types of Mesenchymal Stem Cells (Bone Marrow, Adipose Tissue, and Umbilical Cord-Derived) as Potential Sources for Inner Ear Regeneration. The International Tinnitus Journal, 21 (2).

Zeinalian, Mehrdad. and Hadian, Mahdi. and Hashemzadeh-Chaleshtori, Morteza. and Salehi, Rasoul. and Emami, Mohammad Hassan. (2017) Familial colorectal cancertype X in central Iran: A new clinicopathologic description. International Journal of Hematology-Oncology and Stem Cell Research, 11 (3). pp. 241-246.

Khosrofar, Mahtab. and Pourreza, Mohammad Reza. and Asgharzadeh, Samira. and Tahmasebi, Parisa. and Ali Asgari, Elahe. and Ghasemikhah, Reza. and Saki, Nader. and Mohammadi-Asl, Javad. and Hashemzadeh-Chaleshtori, Morteza. and Tabatabaiefar, Mohammad Amin. (2017) Genetic Linkage Analysis of the DFNB21 Locus in Autosomal Recessive Hearing Loss in Large Families from Khuzestan Province. Arak Medical University Journal, 20 (3).

Sadeghian, Ladan. and Tabatabaiefar, Mohammad Amin. and Zarepour, Narges. and Hashemzadeh-Chaleshtori, Morteza. (2017) Genetic linkage analysis of DFNB24 locus in a group of families with autosomal recessive non-syndromic hearing loss in Khouzestan province of Iran. Journal of Shahrekord Uuniversity of Medical Sciences, 19.

Zarepour, Narges. and Tabatabaiefar, Mohammad Amin. and taghipour, Afsaneh. and Nemati, Fatemeh. and Sadeghian, Ladan. and Hashemzadeh-Chaleshtori, Morteza. (2017) Genetic linkage analysis of DFNB39 locus in families with autosomal recessive non-syndromic hearing loss (ARNSHL) from Khuzestan province. journal of shahrekord university of medical sciences, 19 (3).

Nemati-Zargaran, Fatemeh. and Tabatabaiefar, Mohammad Amin. and Taghipour-Sheshdeh, Afsaneh. and Moradi, Fahimeh. and Zarepour, Narges. and Hashemzadeh-Chaleshtori, Morteza. (2017) Genetic linkage analysis of the DFNB35 and DFNB42 loci in families with autosomal recessive non-syndromic hearing loss from Khuzestan province. journal of shahrekord university of medical sciences, 19 (1).

Mahmoudian Sani, Mohammad Reza. and Hashemzadeh-Chaleshtori, Morteza. and Asadi-Samani, Majid. and Yang, Qian. (2017) Ginkgo Biloba in the treatment of tinnitus: An updated literature review. International Tinnitus Journal, 21 (1). pp. 58-62.

Karami-Eshkaftaki, Raziyeh. and Ahmadinejad, Fereshteh. and Aghaei, Shahrzad. and Moghim, Hassan. and Hashemzadeh-Chaleshtori, Morteza. and Jami, Mohammad-Saeid. (2017) Hearing loss: A review on molecular genetics and epidemiologic aspects. International Journal of Epidemiologic Research, 4 (2). pp. 166-172.

Saffari-Chaleshtori, Javad. and Tabatabaiefar, Mohammad Amin. and Ghasemi-Dehkordi, Payam. and Farokhi, Effat. and Moradi, Mohammad-Taghi. and Hashemzadeh-Chaleshtori, Morteza. (2017) THE LACK OF CORRELATION BETWEEN TP53 MUTATIONS AND GASTRIC CANCER: A REPORT FROM A PROVINCE OF IRAN. GENETIKA-BELGRADE, 49 (1). pp. 235-246.

Mahmoudian Sani, Mohammad Reza. and Mehri-Ghahfarrokhi, Ameneh. and Ahmadinejad, Fereshteh. and Hashemzadeh-Chaleshtori, Morteza. and Saidijam, Massoud. and Jami, Mohammad-Saeid. (2017) MicroRNAs: effective elements in ear-related diseases and hearing loss. European Archives of Oto-Rhino-Laryngology, 274 (6). pp. 2373-2380.

Mahmoudian Sani, Mohammad Reza. and Mehri-Ghahfarrokhi, Ameneh. and Ahmadinejad, Fereshteh. and Hashemzadeh-Chaleshtori, Morteza. and Saidijam, Massoud. and Jami, Mohammad Saeid. (2017) MicroRNAs: effective elements in ear-related diseases and hearing loss. European Archives of Oto-Rhino-Laryngology. pp. 1-8.

Ahmadinejad, Fereshteh. and Geir Møller, Simon. and Hashemzadeh-Chaleshtori, Morteza. and Bidkhori, Gholamreza. and Jami, Mohammad-Saeid. (2017) Molecular Mechanisms behind Free Radical Scavengers Function against Oxidative Stress. Antioxidants, 6 (3).

Asgharzadeh, Samira. and Reiisi, Somayeh. and Tabatabaiefar, Mohammad Amin. and Hashemzadeh-Chaleshtori, Morteza. (2017) Screening of Myo7A mutations in Iranian patients with autosomal recessive hearing loss from west of Iran. Iranian Journal of Public Health, 46 (1). pp. 76-82.

Mahmoudian Sani, Mohammad Reza. and Mehri-Ghahfarrokhi, Ameneh. and Ahmadi, Hamed. and Shojaeian, Ali. and Hashemzadeh-Chaleshtori, Morteza. and Mahdavinezhad, Ali. and Saidijam, Massoud. (2017) Study of common mitochondrial mutations in patients with nonsyndromic hearing loss. Otorinolaringologia, 67 (2). pp. 61-67.

Mehri-Ghahfarrokhi, Ameneh. and Hashemzadeh-Chaleshtori, Morteza. and Shojaeian, Ali. and Mahmoudian Sani, Mohammad Reza. (2017) Studying gap junction beta 2-related deafness in Iranian population. Otorinolaringologia, 67 (3). pp. 89-95.

Sadeghiani, Marzieh. and Bagheri, Nader. and Shahi, Heshmat. and Reiisi, Somayeh. and Rahimian, Ghorbanali. and Rashidi, Reza. and Mahsa, Majid. and Shafigh Ardestani, Mohammad Hadi. and Salimi, Elahe. and Rafieian-Kopaei, Mahmoud. and Hashemzadeh-Chaleshtori, Morteza. and shirzad, Hedayatollah. (2017) cag Pathogenicity island-dependent upregulation of matrix metalloproteinase-7 in infected patients with Helicobacter pylori. Journal of Immunoassay and Immunochemistry. pp. 1-13.

Mahmoudian Sani, Mohammad Reza. and Hashemzadeh-Chaleshtori, Morteza. and Asadi-Samani, Majid. and Luther, Tahra. (2017) A review of medicinal plants for the treatment of earache and tinnitus in Iran. International Tinnitus Journal, 21 (1). pp. 44-49.

Bagheri, Nader. and Azadegan-Dehkordi, Fatemeh. and Rahimian, Ghorbanali. and Hashemzadeh-Chaleshtori, Morteza. and Rafieian-Kopaei, Mahmoud. and Kheiri, Soleiman. and Gholipour, Abolfazl. and shirzad, Hedayatollah. (2016) Altered Th17 Cytokine Expression in Helicobacter pylori Patients with TLR4 (D299G) Polymorphism. Immunological Investigations, 45 (2). pp. 161-171.

Fatahi, Fardin. and Chaleshtori, A. R. S. and Ghatreh Samani, Keihan. and Mousavi, S. M. and Zandi, F. and Heydari, Seyed taghi. and Hashemzadeh-Chaleshtori, Morteza. and Valiollahpour Amiri, Majid. and Khazraee, Hamid. (2016) Assessment of the Effects of IL9, IL9R, IL17A, and IL17F Gene Polymorphisms on Women with Allergic Rhinitis in Shahrekord, Iran. ANNALS OF MEDICAL AND HEALTH SCIENCES RESEARCH, 6 (4). pp. 216-223.

Sadeghiani, Marzieh. and Shahi, Heshmat. and Bagheri, Nader. and Reiisi, Somayeh. and Rahimian, Ghorbanali. and Rashidii, Reza. and Shafighe ardestani, Mohammadhadi. and Hashemzadeh-Chaleshtori, Morteza. and Rafieian-Kopaei, Mahmoud. and Ramezani, Ghasem. and Fatollahi, Fereshteh. and Shahverdi, Elahe. and shirzad, Hedayatollah. (2016) Comparing the expression levels of mRNA for MMP-7 in gastric mucosa of patients with H. pylori infection and uninfected patients. Journal of Mazandaran University of Medical Sciences, 26 (138). pp. 108-117.

Momeni, Ali. and Hashemzadeh-Chaleshtori, Morteza. and Saadatmand, Saeed. and Kheiri, Soleiman. (2016) Correlation of endothelial nitric oxide synthase gene polymorphism (GG, TT and GT genotype) with proteinuria and retinopathy in type 2 diabetic patients. Journal of Clinical and Diagnostic Research, 10 (2). OC32-OC35.

Bakhshian dehkordi, Ehsan. and Hashemzadeh-Chaleshtori, Morteza. and saadat Haerian, Batool. and Mohamadinejad, Parisa. (2016) Correlation study of rs833061, rs2010963 polymorphisms in VEGF-A gene in Iranian colorectal cancer patients. journal of shahrekord university of medical sciences, 18 (5).

Mardani, Gashtasb. and Mahvi, Amir Hossein. and Hashemzadeh-Chaleshtori, Morteza. and Nasseri, Simin. and Dehghani, Mohammad hadi. and Ghasemi-Dehkordi, Payam. (2016) Degradation of phenanthrene and pyrene using genetically engineered dioxygenase producing Pseudomonas putida in soil. Genetika, 48 (3). pp. 837-858.

Farahani, Najmeh. and Nikpour, Parvaneh. and Emami, Mohammad Hassan. and Hashemzadeh-Chaleshtori, Morteza. and Zeinalian, Mehrdad. and Shariatpanahi, Seyed Shervin. and Salehi, Rasoul. (2016) Evaluation of MT1XT20 single quasi-monomorphic mononucleotide marker for characterizing microsatellite instability in persian lynch syndrome patients. Asian Pacific Journal of Cancer Prevention, 17 (9). pp. 4259-4265.

Ghasemi-Dehkordi, Payam. and Jaafari, Azar. and Parchami Barjui, Shahrbanoo. and Reiisi, Sepideh. and Hashemzadeh-Chaleshtori, Morteza. and Miraj, Somayeh. (2016) Evaluation of Serum Level Parameters and C677T Polymorphism of MTHFR Gene in Preeclampsia Patients. GENETIC EPIDEMIOLOGY, 40 (7). pp. 637-638.

Pourahmadiyan, Azam. and Tabatabaiefar, Mohammad Amin. and Reiisi, Somayeh. and Alipour, Paria. and Fattahi, Najmeh. and Hashemzadeh-Chaleshtori, Morteza. (2016) Genetic linkage analysis of DFNB40 and DFNB48 loci in families with autosomal recessive non-syndromic hearing loss (ARNSHL) from western provinces of Iran. Journal of Isfahan Medical School, 34 (374).

Pourahmadiyan, Azam. and Tabatabaiefar, Mohammad Amin. and Reiisi, Somayeh. and Alipour, Paria. and Fattahi, Najmeh. and Hashemzadeh-Chaleshtori, Morteza. (2016) Genetic linkage analysis of DFNB7/11 locus in patients with autosomal recessive non syndromic hearing loss from Hamedan province. journal of shahrekord university of medical sciences, 18 (3).

Taghipour-Sheshdeh, Afsaneh. and Tabatabaiefar, Mohammad Amin. and Nemati-Zargaran, Fatemeh. and Moradi, Fahimeh. and Zarepour, Narges. and Hashemzadeh-Chaleshtori, Morteza. (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).

Ashrafi Dehkordi, Korosh. and Hashemzadeh-Chaleshtori, Morteza. and Sharifi, Mohamadreza. and Jalili, Ali. and Fathi, Fardin and Roshani, Daem. and Nikkhoo, Bahram. and Hakhamaneshi, Mohammad Saeed. and Mahmoodian Sani, Mohammad Reza. and Ganji-Arjenaki, Mahboube (2016) Inhibition of MicroRNA miR-222 with LNA Inhibitor Can Reduce Cell Proliferation in B Chronic Lymphoblastic Leukemia. Indian Journal of Hematology and Blood Transfusion. pp. 1-6.

Farahani, Najmeh. and Nikpour, Parvaneh. and Emami, Mohammad Hassan. and Hashemzadeh-Chaleshtori, Morteza. and Zeinalian, Mehrdad. and Salehi, Rasoul. (2016) MT1XT20 single quasi-monomorphic mononucleotide marker for detection of microsatellite instability in iranian patients with hereditary nonpolyposis colorectal cancer (HNPCC). Journal of Isfahan Medical School, 33 (362). pp. 2120-2130.

Mahmoudian Sani, Mohammad Reza. and Hashemzadeh-Chaleshtori, Morteza. and Mehri-Ghahfarrokhi, Ameneh. and Ghasemi-Dehkordi, Payam. and Saidijam, Massoud. and Jami, Mohammad-Saeid. (2016) MicroRNA-183 family in inner ear: Hair cell development and deafness. Journal of audiology and otology, 20 (3). pp. 131-138.

Asgharzadeh, Samira. and Hashemzadeh-Chaleshtori, Morteza. and Tabatabaiefar, Mohammad Amin. and Reisi, Somayeh and Modarressi, Mohammad Hossein. (2016) Mutation in second exon of myo15a gene cause of nonsyndromic hearing loss and its association in the Arab population in Iran. Genetika, 48 (2). pp. 587-596.

Moradipour, Negar. and Ghasemi-Dehkordi, Payam. and Heibati, Fatemeh. and Parchami Barjui, Shahrbanoo. and Abolhasani, Marziyeh. and Rashki, Ahmad. and Hashemzadeh-Chaleshtori, Morteza. (2016) Mutation screening of exons 7 and 13 of the TMC1 gene in autosomal recessive non-syndromic hearing loss (ARNSHL) in Iran. Iranian Red Crescent Medical Journal, 18 (2).

Ziaei, Ehsan. and Hashemzadeh-Chaleshtori, Morteza. and Ziaei, Amin. and Banitalebi-dehkordi, golandam. and Pooryamofrad, Amirarsham. and Kashani, Shima. and Batenipoor, Maede. and Miraj, Sepideh (2016) Polymorphisms of p53 promoter and susceptibility to uterine leiomyoma. Clinical and Experimental Obstetrics and Gynecology, 43 (5). pp. 713-717.

Reiisi, Somayeh. and Tabatabaiefar, Mohammad Amin. and Sanati, Mohammad Hossein. and Hashemzadeh-Chaleshtori, Morteza. (2016) Screening of DFNB3 in Iranian families with autosomal recessive non-syndromic hearing loss reveals a novel pathogenic mutation in the MyTh4 domain of the MYO15A gene in a linked family. Iranian Journal of Basic Medical Sciences, 19 (7). pp. 772-778.

Banitalebi Dehkordi, Mehdi. and Madjd, Zahra. and Hashemzadeh-Chaleshtori, Morteza. and Meshkani, Reza. and Nikfarjam, Laleh. and Kajbafzadeh, Abdol-Mohammad. (2016) A Simple, Rapid, and Efficient Method for Isolating Mesenchymal Stem Cells From the Entire Umbilical Cord. Cell transplantation, 25 (7). pp. 1287-1297.

Karami-Eshkaftaki, Razieh. and Farrokhi, Effat. and Zia, Nosha. and Hashemzadeh-Chaleshtori, Morteza. (2016) Study of rs6050307 polymorphism of VSX1 gene in patient with keratoconus in Chaharmahal and Bakhtiari. Journal of Shahrekord Uuniversity of Medical Sciences, 18.

Sheikhshahrokh, Amir Hossein. and Hashemzadeh-Chaleshtori, Morteza. and Doosti, Abbas. and Parchami Barjui, Shahrbanoo. (2016) Study the presence of mutations in exons 30 and 33 MYBPC3 gene in patients with hypertrophic cardiomyopathy by PCR-SSCP/HA method in Chaharmahal and Bakhtiari. journal of shahrekord university of medical sciences, 18 (2).

Banitalebi Dehkordi, Mehdi. and Madjd, Zahra. and Hashemzadeh-Chaleshtori, Morteza. and Meshkani, Reza. and Nikfarjam, Laleh. and Kajbafzadeh, Abdol-Mohammad. (2016) A simple, rapid, and efficient method for isolating mesenchymal stem cells from the entire umbilical cord. Cell Transplantation, 25 (7). pp. 1287-1297.

Azadegan-Dehkordi, Fatemeh. and Bagheri, Nader. and Shirzad, Mahsa. and Sanei, Mohammad Hossein. and Hashemzadeh-Chaleshtori, Morteza. and Rafieian-Kopaei, Mahmoud. and Tabatabaiefar, Mohammad Amin. and shirzad, Hedayatollah. (2015) Correlation Between Mucosal IL-6 mRNA Expression Level and Virulence Factors of Helicobacter pylori in Iranian Adult Patients With Chronic Gastritis. Jundishapur journal of microbiology, 8 (8). e21701. ISSN 2008-3645

Zeinalian, Mehrdad. and Emami, Mohammad Hassan. and Salehi, Rasoul. and Naimi, Azar. and Kazemi, Mohammad. and Hashemzadeh-Chaleshtori, Morteza. (2015) Molecular analysis of Iranian colorectal cancer patients at risk for Lynch syndrome: a new molecular, clinicopathological feature. Journal of gastrointestinal cancer, 46 (2). pp. 118-25. ISSN 1941-6636

Zeinalian, Mehrdad. and Hashemzadeh-Chaleshtori, Morteza. and Salehi, Rasoul. and Kazemi, Mohammad. and Emami, Mohammad Hassan. (2015) Tumor microsatellite instability and clinicopathologic features in Iranian colorectal cancer patients at risk for Lynch syndrome. Journal of research in medical sciences : the official journal of Isfahan University of Medical Sciences, 20 (2). pp. 154-60. ISSN 1735-1995

Shahpari, Akram. and Dehghan, Morteza. and Pourahmad, Razieh. and Hashemzadeh-Chaleshtori, Morteza. and Amiri, Masoud. and Kazemi, Sedigheh. (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.

Zarghampoor, Farzaneh. and Pourahmad, Razieh. and Dehghan, Morteza. and Hashemzadeh-Chaleshtori, Morteza. (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.

Ghasemi-Dehkordi, Payam. and Allahbakhshian-Farsani, Mehdi. and Abdian, Narges. and Mirzaeian, Amin. and Saffari-Chaleshtori, Javad. and Heybati, Fatemeh. and Mardani, Gashtasb. and Karimi-Taghanaki, Alireza. and Doosti, Abbas. and Jami, Mohammad-Saeid. and Abolhasani, Marziyeh. and Hashemzadeh-Chaleshtori, Morteza. (2015) Comparison between the cultures of human induced pluripotent stem cells (hiPSCs) on feeder- and serum-free system (Matrigel matrix), MEF and HDF feeder cell lines. JOURNAL OF CELL COMMUNICATION AND SIGNALING, 9 (3). pp. 233-246.

Azadegan-Dehkordi, Fatemeh. and Bagheri, Nader. and Shirzad, Mahsa. and Sanei, Mohammad Hossein. and Hashemzadeh-Chaleshtori, Morteza. and Rafieian-Kopaei, Mahmoud. and Tabatabaiefar, Mohammad Amin. and shirzad, Hedayatollah. (2015) Correlation Between Mucosal IL-6 mRNA Expression Level and Virulence Factors of Helicobacter pylori in Iranian Adult Patients With Chronic Gastritis. JUNDISHAPUR JOURNAL OF MICROBIOLOGY, 8 (8).

Hasheminia, Seyed Javad. and Tolouei, Sepideh. and Zarkesh Esfahani, Hamid. and Shaygannejad, Vahid. and shirzad, Hedayatollah. and Torabi, Reza. and Hashemzadeh-Chaleshtori, Morteza. (2015) Cytokine gene expression in newly diagnosed multiple sclerosis patients. Iranian Journal of Allergy, Asthma and Immunology, 14 (2). pp. 208-216.

Hojati, Zohreh. and Zamanzad, Behnam. and Hashemzadeh-Chaleshtori, Morteza. and Molaie, Razieh. and Gholipour, Abolfazl. (2015) Detection of FimH Gene in Uropathogenic Escherichia coli Strains Isolated From Patients With Urinary Tract Infection. JUNDISHAPUR JOURNAL OF MICROBIOLOGY, 8 (2).

Jami, Mohammad-Saeid. and Salehi-Najafabadi, Zahra. and Ahmadinejad, Fereshteh. and Hoedt, Esthelle. and Hashemzadeh-Chaleshtori, Morteza. and Ghatreh samani, Mahdi. and Neubert, Thomas.A. and Larsen, Jan Petter. and Moller, Simon Geir. (2015) Edaravone leads to proteome changes indicative of neuronal cell protection in response to oxidative stress. NEUROCHEMISTRY INTERNATIONAL, 90. pp. 134-141.

Farrokhi, Effat. and Ghatreh Samani, Keihan. and Hashemzadeh-Chaleshtori, Morteza. and Tabatabaiefar, Mohammad Amin. (2015) Effect of Oxidized Low Density Lipoprotein on the Expression of Runx2 and SPARC Genes in Vascular Smooth Muscle Cells. Iranian biomedical journal, 19 (3). pp. 160-4. ISSN 2008-823X

Ghasemi-Dehkordi, Payam. and Allahbakhshian-Farsani, Mehdi. and Abdian, Narges. and Mirzaeian, Amin. and Hashemzadeh-Chaleshtori, Morteza. and Jafari-Ghahfarokhi, Hamideh. (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.

Mahvi, Amirhossein. and Mardani, Gashtasb. and Ghasemi-Dehkordi, Payam. and Saffari-Chaleshtori, Javad. and Hashemzadeh-Chaleshtori, Morteza. and Allahbakhshian-Farsani, Mehdi. and Abdian, Narges. (2015) Effects of Phenanthrene and Pyrene on Cytogenetic Stability of Human Dermal Fibroblasts Using Alkaline Comet Assay Technique. Proceedings of the National Academy of Sciences India Section B - Biological Sciences, 85 (4). pp. 1055-1063.

Abdian, Narges. and Allahbakhshian-Farsani, Mehdi. and Ghasemi-Dehkordi, Payam. and Mirzaeian, Amin. and Saffari-Chaleshtori, Javad. and Sadeghiani, Marzieh. and Hashemzadeh-Chaleshtori, Morteza. and Yazdanpanahi, Nasrin. (2015) Effects of lentiviral vectors on DNA damage of human dermal fibroblasts (HDFs). Journal of Pure and Applied Microbiology, 9 (1). pp. 307-317.

Zeinalian, Mehrdad. and Hashemzadeh-Chaleshtori, Morteza. and Akbarpour, Mohammad Javad. and Emami, Mohammad Hassan. (2015) Epidemioclinical Feature of Early-Onset Colorectal Cancer at-Risk for Lynch Syndrome in Central Iran. Asian Pacific journal of cancer prevention : APJCP, 16 (11). pp. 4647-52. ISSN 2476-762X

Salimzadeh, Loghman. and Bagheri, Nader. and Zamanzad, Behnam. and Azadegan-Dehkordi, Fatemeh. and Rahimian, Ghorbanali. and Hashemzadeh-Chaleshtori, Morteza. and Rafieian-Kopaei, Mahmoud. and Sanei, Mohammad Hossein. and shirzad, Hedayatollah. (2015) Frequency of virulence factors in Helicobacter pylori-infected patients with gastritis. MICROBIAL PATHOGENESIS, 80. pp. 67-72.

Fattahi, Najmeh. and Tabatabaiefar, Mohammad Amin. and Reeisi, Somayeh. and Alipour, Paria. and Pourahmadian, Azam. and Hashemzadeh-Chaleshtori, Morteza. (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).

Alipour, Paria. and Tabatabaiefar, Mohammad Amin. and Reiisi, Somayeh. and Fattahi, Najmeh. and Pourahmadian, Azam. and Hashemzadeh-Chaleshtori, Morteza. (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.

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

Fouladi, Bahman. and Yadegari, Mohammad Hossein. and Rajabibazl, Masoumeh. and Fazaeli, Asghar. and Hashemzadeh-Chaleshtori, Morteza. (2015) Identification of candida species in patients with vulvovaginitis presenting different clinical symptoms. Journal of Zanjan University of Medical Sciences and Health Services, 23 (98). pp. 57-68.

Zeinalian, Mehrdad. and Emami, Mohammad Hassan. and Naimi, Azar. and Salehi, Rasoul. and Hashemzadeh-Chaleshtori, Morteza. (2015) Immunohistochemical analysis of mismatch repair proteins in Iranian Colorectal Cancer patients at risk for Lynch syndrome. IRANIAN JOURNAL OF CANCER PREVENTION, 8 (1). pp. 11-17.

Taghizade Mortezaee, Fatemeh. and Hashemzadeh-Chaleshtori, Morteza. and Kheiri, Soleiman. and Farrokhi, Effat. and Shariati, Laleh. and Tabatabaiefar, Mohammad Amin. and Miraj, Sepide. (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.

Sadrizade, N. and Parchami Barjui, Shahrbanoo. and Reiisi, Somayeh. and Hashemzadeh-Chaleshtori, Morteza. 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.

Jafari-Ghahfarokhi, Hamideh. and Moradi-Chaleshtori, Maryam. and Liehr, Thomas. and Hashemzadeh-Chaleshtori, Morteza. and Teimori, Hossein. and Ghasemi-Dehkordi, Payam. (2015) Small supernumerary marker chromosomes and their correlation with specific syndromes. Advanced biomedical research, 4. p. 140. ISSN 2277-9175

Arbabi, Mohsen. and Hashemzadeh-Chaleshtori, Morteza. and Mardani, Gashtasb. and Sadeghi, Mehraban. and Najafi-Chaleshtori, Akram. and Shakeri, Kobra. (2015) Survey of the residual polycyclic aromatic hydrocarbons in petroleum contaminated soils in Shahrekord in 2013. Journal of Shahrekord Uuniversity of Medical Sciences, 17.

Karimi, Ali. and Abolhasani, Marziyeh. and Hashemzadeh-Chaleshtori, Morteza. and Pourgheysari, Batoul. (2015) A preliminary study of inherited thrombophilic risk factors in different clinical manifestations of venous thromboembolism in central Iran. INDIAN JOURNAL OF MEDICAL RESEARCH, 142. pp. 46-52.

Yazdanpanahi, Nasrin. and Tabatabaiefar, Mohammad Amin. and Bagheri, Nader. and Azadegan-Dehkordi, Fatemeh. and Farrokhi, Effat. and Hashemzadeh-Chaleshtori, Morteza. (2015) The role and spectrum of SLC26A4 mutations in Iranian patients with autosomal recessive hereditary deafness. INTERNATIONAL JOURNAL OF AUDIOLOGY, 54 (2). pp. 124-130.

Ghasemi-Dehkordi, Payam. and Allahbakhshian-Farsani, Mehdi. and Abdian, Narges. and Jafari-Ghahfarokhi, Hamideh. and Saffari-Chaleshtori, Javad. and Sadeghiani, Marzieh. and Mirzaeian, Amin. and Hashemzadeh-Chaleshtori, Morteza. (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.

Salehi Chaleshtori, Ahmad Reza. and Tabatabaiefar, Mohammad Amin. and Salehi, Hamid Reza. and Hashemzadeh-Chaleshtori, Morteza. (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.

Bagheri, Nader. and Azadegan-Dehkordi, Fatemeh. and Sanei, Hossein. and Taghikhani, Afshin. and Rahimian, Ghorbanali. and Salimzadeh, Loghman. and Hashemzadeh-Chaleshtori, Morteza. and Rafieian-Kopaei, Mahmoud. and Shirzad, Mahsa. and shirzad, Hedayatollah. (2014) Associations of a TLR4 single-nucleotide polymorphism with H. pylori associated gastric diseases in iranian patients. CLINICS AND RESEARCH IN HEPATOLOGY AND GASTROENTEROLOGY, 38 (3). pp. 366-371.

Vand Rajabpour, Fatemeh. and Raoofian, Reza. and Youssefian, Leila. and Vahidnezhad, Hassan. and Mirshams Shahshahani, Mostafa. and Fathi, Hamidreza. and Noormohammadpour, Pedram. and Kamyab Hesari, Kambiz. and Hashemzadeh-Chaleshtori, Morteza. and Tabrizi, Mina. (2014) BMI1 and TWIST1 Downregulated mRNA Expression in Basal Cell Carcinoma. ASIAN PACIFIC JOURNAL OF CANCER PREVENTION, 15 (8). pp. 3797-3800.

Allahbakhshian-Farsani, Mehdi. and Abdian, Narges. and Ghasemi-Dehkordi, Payam. and Sadeghiani, Marzieh. and Saffari-Chaleshtori, Javad. and Hashemzadeh-Chaleshtori, Morteza. and Khosravi-Farsani, Somayeh. (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.

Abolhasani, Marziyeh. and Hashemzadeh-Chaleshtori, Morteza. and Doosti, Abbas. and Amini Sarteshnizi, Neamatollah. and Gholami-Arjenaki, Mostafa. and Teimori, Hossein. (2014) Evaluation of the effect of Chrysin and Caffeic acid phenethyl ester on eIF4E expression in AGS cell line. Journal of HerbMed Pharmacology, 3.

Bagheri, Nader. and Rahimian, Ghorbanali. and Salimzadeh, Loghman. and Taghikhani, Afshin. and Mahsa, Majid. and Hashemzadeh-Chaleshtori, Morteza. and Azadegan-Dehkordi, Fatemeh. and Solimani, Neda. and shirzad, Hedayatollah. (2014) Expression of IL-18 cytokine mRNA in gastric mucosa tissue of patients with H. pylori infection in Chahar Mahal and Bakhtiari. ISMJ, 17 (4).

Pourgheysari, Batoul. and Deris, Fatemeh. and Hashemzadeh-Chaleshtori, Morteza. (2014) Factor XIIIA-V34L and factor XIIIB-H95R in venous thromboembolism in central Iran: protective and neutral. BLOOD COAGULATION & FIBRINOLYSIS, 25 (5). pp. 439-443.

Rezaeian, Fatemeh. and Tabatabaiefar, Mohammad Amin. and Heybati, Fatemeh. and Reiisi, Somayeh. and Parchami Barjui, Shahrbanoo. and Abolhasani, Marziyeh. and Amiri, Beheshteh. and Salehi Chaleshtori, Ahmad Reza. and Hashemzadeh-Chaleshtori, Morteza. (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.

Mojtabavi Naeini, Marjan. and Mesrian Tanha, Hamzeh. and Hashemzadeh-Chaleshtori, Morteza. and Vallian-Brojeni, Sadegh. (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.

Mojtabavi Naeini, Marjan. and Vallian-Brojeni, Sadegh. and Hashemzadeh-Chaleshtori, Morteza. (2014) Investigation of D7S496 marker characteristics in five Iranian ethnic groups for linkage analysis of autosomal recessive non syndromic hearing loss. journal of shahrekord university of medical sciences, 15 (6).

Taghizade Mortezaee, Fatemeh. and Tabatabaiefar, Mohammad Amin. and Hashemzadeh-Chaleshtori, Morteza. and Miraj, Sepide. (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.

Mojtabavi Naeini, Mojgan. and Vallian Boroujeni, Sadeq. and Hashemzadeh-Chaleshtori, Morteza. (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.

Parchami Barjui, Shahrbanoo. and Reiisi, Somayeh. and Rezaiean, Fatemeh. and Heybati, Fatemeh. and Hashemzadeh-Chaleshtori, Morteza. (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.

Reiisi, Somayeh. and Sanati, Mohammad Hossein. and Tabatabaiefar, Mohammad Amin. and Ahmadian, Shahla. and Reiisi, Salimeh. and Parchami Barjui, Shahrbanoo. and Porjafari, Hamid. and Shahi, Heshmat. and Shavarzi, Afsaneh. and Hashemzadeh-Chaleshtori, Morteza. (2014) The Study of SLC26A4 Gene Causing Autosomal Recessive Hearing Loss by Linkage Analysis in a Cohort of Iranian Populations. International journal of molecular and cellular medicine, 3 (3). pp. 176-82. ISSN 2251-9637

Reiisi, Somayeh. and Sanati, Mohammad Hossein. and Tabatabaiefar, Mohammad Amin. and PourJafari, Hamid Reza. and Minuchehr, Zarrin. and Shavarzi, Afsaneh. and Ataiee, Mitra. and kasiri, mahboobeh. and Hashemzadeh-Chaleshtori, Morteza. (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.

Hasheminia, Seyed Javad. and Zarkesh Esfahani, Hamid. and Tolouei, Sepideh. and Shaygannejad, Vahid. and shirzad, Hedayatollah. and Hashemzadeh-Chaleshtori, Morteza. (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.

Rahimian, Ghorbanali. and Sanei, Mohammad Hossein. and shirzad, Hedayatollah. and Azadegan-Dehkordi, Fatemeh. and Taghikhani, Afshin. and Salimzadeh, Loghman. and Hashemzadeh-Chaleshtori, Morteza. and Rafieian-Kopaei, Mahmoud. and Bagheri, Nader. (2014) Virulence factors of Helicobacter pylori vacA increase markedly gastric mucosal TGF-beta 1 mRNA expression in gastritis patients. MICROBIAL PATHOGENESIS, 67-68. pp. 1-7.

Rahimian, Ghorbanali. and Sanei, Mohammad Hossein. and shirzad, Hedayatollah. and Azadegan-Dehkordi, Fatemeh. and Taghikhani, Afshin. and Salimzadeh, Loghman. and Hashemzadeh-Chaleshtori, Morteza. and Rafieian-Kopaei, Mahmoud. and Bagheri, Nader. (2014) Virulence factors of Helicobacter pylori vacA increase markedly gastric mucosal TGF-β1 mRNA expression in gastritis patients. Microbial pathogenesis, 67.

Allahbakhshian-Farsani, Mehdi. and Ghasemi-Dehkordi, Payam. and Abdian, Narges. and Khosravi-Farsani, Somayeh. and Mirzaeian, Amin. and Nasri, Masoud. and Karimi-Taghanaki, Alireza. and Mardani, Gashtasb. and Amiri, Seyedeh beheshteh. and Hashemzadeh-Chaleshtori, Morteza. (2014) The assessment of lentiviral vectors application for gene transformation in human dermal fibroblasts (HDFs). Journal of Shahrekord Uuniversity of Medical Sciences, 15.

Soleimani, Akbar. and Mobedi, Zahra. and Hashemzadeh-Chaleshtori, Morteza. and Alerasoul, Maryam. and Sadeghi, Bahman. and Kazemi-Vardanjani, Abdolrahim. and Sharifi Faradonbeh, Abolghasem. (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.

Jafarzadeh, Lobat. and danesh, Azar. and Sadeghi, Marzieh. and Heybati, Fateme and Hashemzadeh-Chaleshtori, Morteza. (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.

Bagheri, Nader. and Taghikhani, Afshin. and Rahimian, Ghorbanali. and Salimzadeh, Loghman. and Azadegan-Dehkordi, Fatemeh. and Zandi, Farid. and Hashemzadeh-Chaleshtori, Morteza. and Rafieian-Kopaei, Mahmoud. and shirzad, Hedayatollah. (2013) Association between virulence factors of helicobacter pylori and gastric mucosal interleukin-18 mRNA expression in dyspeptic patients. MICROBIAL PATHOGENESIS, 65. pp. 7-13.

Yazdanpanahi, Nasrin. and Tabatabaiefar, Mohammad Amin. and Farrokhi, Effat. and Abdian, Narges. and Bagheri, Nader. and Shahbazi, Shirin. and Noormohammadi, Zahra. and Hashemzadeh-Chaleshtori, Morteza. (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.

norbahksh, Seyed Mohammad Kazem. and Kasiri, Karamali. and Jalili, Ali. and Hashemzadeh-Chaleshtori, Morteza. (2013) Determining the frequency of glucose-6-phosphate dehydrogenase deficiency in newborn infants in Shahrekord. Journal of Shahrekord Uuniversity of Medical Sciences, 15.

Kooshavar, Daniz. and Tabatabaiefar, Mohammad Amin. and Farrokhi, Effat. and Abolhasani, Marziyeh. and Noori-Daloii, Mohammad Reza. and Hashemzadeh-Chaleshtori, Morteza. (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.

Bagheri, Nader. and Salimzadeh, Loghman. and Azadegan-Dehkordi, Fatemeh. and Hashemzadeh-Chaleshtori, Morteza. and Heidari, soraya. and Rahimian, Razieh. and Rahimian, Ghorbanali. and Taghikhani, Afshin. and Rafieian-Kopaei, Mahmoud. and shirzad, Hedayatollah. (2013) Expression levels of mRNA cytokines of IL-17 and IL-23 in epithelialfiber of stomach inpatients with Helicobacter pylori using Real-Time PCR in Chahar Mahal and Bakhtiari province. Journal of Shahrekord Uuniversity of Medical Sciences, 15.

Teimori, Hossein. and Ashoori, Saeede. and Akbari, Mohamad Taghi. and Mojtabavi Naeini, Marjan. and Hashemzadeh-Chaleshtori, Morteza. (2013) FISH Analysis for del6q21 and del17p13 in B-cell Chronic Lymphocytic Leukemia in Iranians. IRANIAN RED CRESCENT MEDICAL JOURNAL, 15 (2). pp. 107-112.

Taghizadeh, Seyyed Hossein. and Kazeminezhad, Seyyed Reza and Sefidgar, Seyyed Ali and Yazdanpanahi, Nasrin. and Tabatabaeifar, Mohammad Amin. and Yousefi, Ahmad. and Lesani, Seyyed Mohammad. and Abolhasani, Marziyeh. and Hashemzadeh-Chaleshtori, Morteza. (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

Heydari, Soraya. and Khaledifar, Arsalan. and Pourahmad-Jaktaji, Razieh. and Hashemzadeh-Chaleshtori, Morteza. and Heydari, Somayeh. and Bagheri, Nader. and Reisi, Somayeh and Abolhasani, Marziyeh. (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.

Moazeni-Bistgani, Mohammad. and Taghipoor, Simin. and Abolhasani, Marziyeh. and Hashemzadeh-Chaleshtori, Morteza. and Zarean, Elham. and Yousofi Darani, Hossein. (2013) Molecular characterization of the human and sheep hydatid cyst strains in Chaharmahal va Bakhtiari province of Iran using restriction fragment length plolymorphism (PCR RFLP). Cell biology, 2 (2).

Azadegan-Dehkordi, Fatemeh. and Rashki, Ahmad. and Bagheri, Nader. and Hashemzadeh-Chaleshtori, Morteza. and Memarzadeh, Ezzatollah. and Salehi, Ali. and Ghatreh, Homan. and Zandi, Farid. and Yazdanpanahi, Nasrin. and Tabatabaiefar, Mohammad Amin. and Hashemzadeh-Chaleshtori, Morteza. (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.

Zeinalian, Mehrdad. and Fadaei Nobari, Reza. and Moafi, Alireza. and Salehi, Mansour. and Hashemzadeh-Chaleshtori, Morteza. (2013) Two decades of pre-marital screening for beta-thalassemia in central Iran. Journal of Community Genetics, 4 (4). pp. 517-522.

Taghizade Mortezaee, Fatemeh. and Farrokhi, Effat. and Shahinfard, Najmeh. and Ashoori, Saeede. and Gatreh Samani, Keihan. and Hashemzadeh-Chaleshtori, Morteza. and Miraj, Sepide. (2012) Association of (Ile462Val in genetic polymorphisms CYP1A1) and uterine leiomyoma risk in women in Charmahal va Bakhtiari, I.R. Iran. Journal of Shahrekord Uuniversity of Medical Sciences, 14.

Montazer- Zohour, Mostafa. and Hashemzadeh-Chaleshtori, Morteza. and Akbari, mohammad taghi. (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.

Montazer Zohouri, Mostafa. and Akbari, mohammad taghi. and Hashemzadeh-Chaleshtori, Morteza. (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.

Montazer Zohouri, Mostafa. and Tabatabaiefar, Mohammad Amin. and Azadegan-Dehkordi, Fatemeh. and Farrokhi, Effat. and Akbari, mohammad taghi. and Hashemzadeh-Chaleshtori, Morteza. (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.

Khosravi, Sharifeh. and Hossein Hejazi, Saied. and Hashemzadeh-Chaleshtori, Morteza. and Eslami, Gilda. and Yousofi Darani, Hossein. (2012) Molecular diagnosis of Old World leishmaniasis: Real-time PCR based on tryparedoxin peroxidase gene for the detection and identification of Leishmania spp. JOURNAL OF VECTOR BORNE DISEASES, 49 (1). pp. 15-18.

Banitalebi, Golandam. and Montazerzohor, Mostafa. and Farrokhi, Effat. and Abolhasani, Marzieh. and Reissi, Somayeh. and Heydari, Soraya. and Ataii, Zohreh. and Azadegan-Dehkordi, Fatemeh. and Hoseinipoor, Azam. and Hashemzadeh-Chaleshtori, Morteza. (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.

Ghatreh-Samani, Keihan. and Farrokhi, Effat. and Hashemzadeh-Chaleshtori, Morteza. and Sadeghi, Masoud. (2012) Study the relationship between Q192R paraoxonase gene polymorphism and high density lipoprotein composition after Lovastatin Trapy. Journal of Shahrekord Uuniversity of Medical Sciences, 14.

Yazdanpanahi, Nasrin. and Hashemzadeh-Chaleshtori, Morteza. and Tabatabaiefar, Mohammad Amin. and Noormohammadi, Zahra. and Farrokhi, Effat. and Najmabadi, Hossein. and Shahbazi, Shirin. and Hosseinipour, Azam. (2012) Two novel SLC26A4 mutations in Iranian families with autosomal recessive hearing loss. INTERNATIONAL JOURNAL OF PEDIATRIC OTORHINOLARYNGOLOGY, 76 (6). pp. 845-850.

Vanwesemael, Maarten. and Schrauwen, Isabelle. and Ceuppens, Ruben. and Alasti, Fatemeh. and Jorssen, Ellen. and Farrokhi, Effat. and Hashemzadeh-Chaleshtori, Morteza. 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.

Vanwesemael, Maarten. and Schrauwen, Isabelle and Ceuppens, Ruben. and Alasti, Fatemeh. and Jorssen, Ellen. and Farrokhi, Effat. and Hashemzadeh-Chaleshtori, Morteza. and Van Camp, Guy. (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.

Tabatabaiefar, Mohammad Amin. and Alasti, Fatemeh. and Shariati, Laleh. and Farrokhi, Effat. and Fransen, Erik. and Nooridaloii, MohammadReza. and Hashemzadeh-Chaleshtori, Morteza. and Camp, Guy.Van. (2011) DFNB93, a novel locus for autosomal recessive moderate-to-severe hearing impairment. CLINICAL GENETICS, 79 (6). pp. 594-598.

Manouchehri Naeini, Koorosh. and Asadi-Samani, Majid. and Hashemzadeh-Chaleshtori, Morteza. (2011) Detection and molecular characterization of Cryptosporidium Species in recreational waters of Chaharmahal va Bakhtiyari Province of Iran using nested PCR-RFLP. Iranian Journal of Parasitology, 6 (1). pp. 20-27.

Khademi, Solmaz. and Ahadi, AliMohammad. and Mehvari, Jafar. and Ayat, Hoda. and Farokhi, Effat. and Moradi, Mohammad-Taghi. and Hashemzadeh-Chaleshtori, Morteza. (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.

Tabatabaiefar, Mohammad Amin. and Montazer Zohouri, Mostafa. and Alasti, Fatemeh. and Shariati, Laleh. and Farrokhi, Effat. and Farhud, D.D. and Camp, Guy.Van. and Noori-Daloii, M.R. and Hashemzadeh-Chaleshtori, Morteza. (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).

Tabatabaiefar, Mohammad Amin. and Alasti, Fatemeh. and Montazer Zohouri, Mostafa. and Shariati, Laleh. and Farrokhi, Effat. and Farhud, D.D. and Camp, Guy.Van. and Noori-Daloii, Mohammad Reza. and Hashemzadeh-Chaleshtori, Morteza. (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.

Farrokhi, Effat. and Shayesteh, Fatemeh. and Asadi Mobarakeh, S. and Roghani Dehkordi, F. and Ghatreh Samani, Keihan. and Hashemzadeh-Chaleshtori, Morteza. (2011) Molecular characterization of Iranian patients with possible familial hypercholesterolemia. Indian Journal of Clinical Biochemistry, 26 (3).

Saee-Rad, Samira. and Hashemi, Hassan. and Miraftab, Mohammad and Noori-Daloii, Mohammad Reza. and Hashemzadeh-Chaleshtori, Morteza. and Raoofian, Reza. and Jafari, Fatemeh. and Greene, Wayne. and Fakhraie, Ghasem. and Rezvan, Farhad. and Heidari, Mansour. (2011) Mutation analysis of VSX1 and SOD1 in Iranian patients with keratoconus. MOLECULAR VISION, 17 (336-37). pp. 3128-3136.

Hashemzadeh-Chaleshtori, Morteza. and Akbari, mohammad taghi. and Khazraei, Hamid. and Abolhasani, Marzieh. and Reisi, Somayeh and Ataei, Zohreh. and Saedi-Marghmaleki, Mojtaba. and Shirmardi, Seyed Abolfath. and Farrokhi, Effat. and Montazer Zohouri, Mostafa and Azadegan-Dehkordi, Fatemeh. (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).

Nozari, Ahora and Foroghmand, Alimohammad. and Ahadi, AliMohammad. and Khoshdel, Abolfazl. and Salehian, Shahla. and Bagheri, Homayoun. and Hashemzadeh-Chaleshtori, Morteza. and Farrokhi, Effat. (2010) Assosiation study between IL1RA gene polymorphism with febrile convulsion in Shahrekord children. Journal of Shahrekord Uuniversity of Medical Sciences, 12.

Azadegan-Dehkordi, Fatemeh. and Farrokhi, Effat. and Montazer Zohouri, Mostafa. and Mobini, Gholam Reza. and Taherzadeh Ghahfarrokhi, Maryam. and Raiesi, Marzieh. and Raiesi, Somayeh. and Banitalebi, Mehdi. and Hashemzadeh-Chaleshtori, Morteza. and Soleimani, Mahshid. and kasiri, mahboobeh. and Shirmardi, Seyed Abolfath. and Taji, Fatemeh. and Asgari, Azam. and Banitalebi, Golandam. and safari, javad. (2010) DFNB59 Gene Mutation Screening Using PCR-SSCP/HA Technique in Non-syndromic Genetic Hearing Loss in Bushehr Province. ISMJ, 13 (3).

Hashemzadeh-Chaleshtori, Morteza. and Banitalebi, Golandam. and Reisi, Somayeh and Azadegan-Dehkordi, Fatemeh. and Abolhasani, Marzieh. and Ghasemi, Soraya. and Shirmardi, Seyed Abolfath. and Farrokhi, Effat. and Taherzadeh Ghahfarrokhi, Maryam. (2010) DFNB59 Gene Mutations and its Association with Deafness in Schoolchildren in Kohgilooyeh & Boyerahmad Province. Armaghane danesh, 14 (4).

Taherzadeh Ghahfarrokhi, Maryam. and Farrokhi, Effat. and Shirmardi, Seyed Abolfath. and Safari Chaleshtori, Javad. and Asadi, Somayeh. and Ghatreh Samani, Keihan. and Abolhasani, Marziyeh. and Haji Hoseini, Reza. and Hashemzadeh-Chaleshtori, Morteza. and Parvin, Neda. and Raeisi, Marziye. and Mobini, Gholam Reza. and Banitalebi, Golandam. and Azadegan-Dehkordi, Fatemeh. and Reiisi, Somayeh. (2010) DFNB59 gene mutations screening in non syndromic deaf subjects in Chaharmahal va Bakhtiari province. Journal of Shahrekord Uuniversity of Medical Sciences, 11.

Tabatabaiefar, Mohammad Amin. and Montazer Zohouri, Mostafa. and Shariati, Laleh. and Safari Chaleshtori, Javad. and Ashrafi, Koorosh. and Gholami, A. and Farokhi, Effat. and Hashemzadeh-Chaleshtori, Morteza. and Noori-Daloii, Mohammad Reza. (2010) Mutation analysis of GJB2 and GJB6 genes and the genetic linkage analysis of five common DFNB loci in the Iranian families with autosomal recessive non-syndrom. JOURNAL OF SCIENCES ISLAMIC REPUBLIC OF IRAN, 21 (2).

Tabatabaiefar, Mohammad Amin. and Shariati, Laleh. and Montazer Zohouri, Mostafa. and Ashrafi, Koorosh. and Saffari-Chaleshtori, Javad. and Ghasemikhah, Reza. and Farrokhi, Effat. and Noori-Daloii, Mohammad Reza. and Hashemzadeh-Chaleshtori, Morteza. (2010) Mutation screening of GJB2 and GJB6 and genetic linkage study of three prevalent DFNB loci in Iranian families with autosomal recessive non-syndromic hearing loss. journal of shahrekord university of medical sciences, 12 (2).

Asadi, Somayeh. and Gatreh Samani, Keihan. and Banitalebi, Mehdi. and Mobini, Gholam Reza. and Saffari Chaleshtori, Javad. and Taherzadeh Ghahfarrokhi, Maryam. and Shayesteh, Fatemeh. and Nazem, Habibollah. and HajiHosayni BaghdadAbadi, Reza. and Hashemzadeh-Chaleshtori, Morteza. (2010) Study of LDL receptor gene mutations in patients with familial hypercholesterolemia in Chaharmahal va Bakhtiari province. Journal of Shahrekord Uuniversity of Medical Sciences, 11.

Sadeghi, Abdolrahim. and Sanati, Mohammad Hossein. and Alasti, Fatemeh. and Hashemzadeh-Chaleshtori, Morteza. and Mahmoudian, Saeid. and Ataei, Mitra. (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.

Safari Chaleshtori, Javad. and Moradi, Mohammad-Taghi. and Farokhi, Effat. and Tabatabaee Far, Mohammad Amin. and Taherzadeh Ghahfarrokhi, Maryam. and Shayesteh, Fatemeh. and Mobini, Gholam Reza. and Banitalbi, Mehdi. and Mardani, Gashtasb. and Hashemzadeh-Chaleshtori, Morteza. (2009) Detection of mutations in exons 5-8 of the P53 gene in gastric cancer samples using PCR-SSCP in Chaharmahal va Bakhtiari province 2006-2007. Journal of Shahrekord Uuniversity of Medical Sciences, 11.

Farrokhi, Effat. and Shirmardi, Abolfath. and Khoshdel, Abolfazl. and Amani, Soroush. and Soleimani, Mahshid. and kasiri, mahboobeh. and Rahbarian, Jahanbakhsh. and Parvin, Neda. and Shahinfard, Najmeh. and Hashemzadeh-Chaleshtori, Morteza. (2009) Genetic study of 45 big hearing loss pedigrees and GJB2 gene mutations frequency in Chaharmahal va Bakhtiari province, Iran, 2008. journal of shahrekord university of medical sciences, 10 (4).

Ghatreh Samani, Keihan. and Noori, Mohammad. and Rohbani Nobar, Mohammad. and Hashemzadeh-Chaleshtori, Morteza. and Farrokhi, Effat. and Darabi Amin, Masoud. (2009) I405V and -629C/A polymorphisms of the cholesteryl ester transfer protein gene in patients with coronary artery disease. Iranian Biomedical Journal, 13 (2). pp. 103-108.

Farhud, Daryoush. and Lotfi, A. S. and Hashemzadeh-Chaleshtori, Morteza. and Akhondi, Mohammad Mehdi. 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.

Shayesteh, Fatemeh. and Ghatreh Samani, Keihan. and Shirani, Manoochehr. and Parvin, Neda. and Saffari Chaleshtori, Javad. and Taherzadeh Ghahfarrokhi, Maryam. and Mobini, Gholam Reza. and Modaresi, Mehrdad. and Hashemzadeh-Chaleshtori, Morteza. and Banitalebi, Mehdi. (2009) Study of three common ApoB gene mutations in possible familial hypercholesterolemia patients in Cheharmahal va Bakhtiari province, Iran, 2003. journal of shahrekord university of medical sciences, 10 (4).

Saffari-Chaleshtori, Javad. and Moradi, Mohammad-Taghi. and Farrokhi, Effat. and Tabatabaiefar, Mohammad Amin. and Taherzadeh Ghahfarrokhi, Maryam. and Shayesteh, Fatemeh. and Mobini, Gholam Reza. and Banitalebi, Mehdi. and Khademi, Solmaz. and Hashemzadeh-Chaleshtori, Morteza. and Nazem, Habibollah. and Rahimian, Ghorbanali. and Shahinfard, Najmeh. and Parvin, Neda. and Shahrani, Mehrdad. and Mardani, Gashtasb. (2009) Study of two common P53 gene mutations in gastric cancer using PCR-RFLP in Chaharmahal va Bakhtiari province, Iran, 2003. journal of shahrekord university of medical sciences, 10 (4).

Parvin, Neda. and Shahinfard, Najmeh. and Farrokhi, Effat. and kasiri, mahboobeh. and Khoshdel, Abolfazl. and Amani, Soroush. and Hoseynzadeh, Shahryar. and Shirmardi, Abolfazl. and Noeparast, Zahra. and Hashemzadeh-Chaleshtori, Morteza. (2009) The frequenc of hearing loss etiology among deaf students in Chaharmahal va Bakhtiari province Iran 2008-2009. Journal of Shahrekord Uuniversity of Medical Sciences, 11.

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

Hamid, Mohammad. and Karimipoor, MORTEZA. and Hashemzadeh-Chaleshtori, Morteza. and Akbari, mohammad taghi. (2009) A novel 355–357delGAG mutation and frequency of connexin-26 (GJB2) mutations in Iranian patients. Journal of genetics, 88 (3).

Hashemzadeh-Chaleshtori, Morteza. and Farhud, Daryoush. and Crosby, Andrew.H. and Farrokhi, Effat. and Jafari Pour, H. and Ghatreh Samani, Keihan. and Safa Chaleshtori, K. and Kasiri, Mansureh. and Shahrani, Mehrdad. and Mobini, GholamReza. 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.

Banoei, Mohammad Mehdi. and Hashemzadeh-Chaleshtori, Morteza. and Sanati, Mohammad Hossein. and Shariati, PARVIN. and Houshmand, MASSOUD. and Majidizadeh, TAYEBEH. and Jahangir Soltani, NILOOFAR. and Golalipour, MASSOUD. (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.

Banoei, Mohammad Mehdi. and Hashemzadeh-Chaleshtori, Morteza. and Sanati, Mohammad Hossein. and Shafa Sharait Panahi, Mehdi. and Majidizadeh, TAYEBEH. and Rostami, Maryam. and DEHGHAN Manshadi, Massoumeh. and Golalipour, Masoud. (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.

Shahrani, Mehrdad. and Rafieian-Kopaei, Mahmoud. and shirzad, Hedayatollah. and Hashemzadeh-Chaleshtori, Morteza. and Yousefi, Hossein. and khadivi, Reza. and Amini, Seyed Asadollah. and Dehghan, Morteza. and Kheiri, Soleiman. and Moradi, Mohammad-Taghi. and Rahimian, Ghorbanali. and Gheitasi, Izadpanah. (2007) Effect of Allium sativum L. extract on acid and pepsin secretion in basal condition and stimulated with vag stimulate in rat. Journal of Medicinal Plants, 6 (24). pp. 28-37.

Moradi, Mohammad-Taghi. and Kheiri, Soleiman. and Dehghan, Morteza. and Amini, Seyed Asadollah. and khadivi, Reza. and Yousefi, Hossein. and Hashemzadeh-Chaleshtori, Morteza. and shirzad, Hedayatollah. and Rafieian-Kopaei, Mahmoud. and Shahrani, Mehrdad. (2007) Effect of Allium sativum L. extract on acid and pepsin secretion in basal condition and stimulated with vag stimulate in rat. Journal of Medicinal Plants, 4 (24).

Hashemzadeh-Chaleshtori, Morteza. and Farrokhi, Effat. and Shahrani, Mehrdad. and Kheiri, Soleiman. and Dolati, Masoumeh. and Hoghooghi Rad, Laleh. and Pour-Jafari, Hamid. and Ghatreh Samani, Keihan. and Safa Chaleshtori, Katayoon. and Crosby, Andrew 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.

Yousofi Darani, Hossein. and Hashemzadeh-Chaleshtori, Morteza. and Aliyari, Zahra. and Farrokhi, Effat. and Zebardast, Nozhat. (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.

Shahrani, Mehrdad. and Rafieian-Kopaei, Mahmoud. and Pilehvarian, Ali Asghar. and shirzad, Hedayatollah. and Hashemzadeh-Chaleshtori, Morteza. and Yousefi, Hossein. and Moradi, Mohammad-Taghi. and Ebrahimzadeh, Azam. and HasanPour-Dehkordi, Ali. and Sadeghi, Mehraban. and Imani, Reza. and Ganji, Forouzan. and Moghadasi, Jafar. (2007) The effect of Amirkabiria odoratissima M extract on gastric acid and pepsin secretion level in rat. Journal of Shahrekord Uuniversity of Medical Sciences, 8.

Hashemzadeh-Chaleshtori, Morteza. and Montazer Zohouri, Mostafa. and Hoghooghi Rad, L. and Pour-Jafari, Hamid. and Farhud, Daryoush. and Dolati, M. and Safa Chaleshtori, K. and Sasanfar, Roksana. and Hosseinipour, A. and Andonian, Laris. 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.

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

Hashemzadeh-Chaleshtori, Morteza. and Hoghooghi Rad, Laleh. and Dolati, Masoumeh. and Sasanfar, Roksana. and Hoseinipour, Abedin. and Montazer Zohouri, Mostafa. and PourJafari, Hamid Reza. and Tolooi, A. and Ghadami, Mohammad Rasoul. and Farhud, D.D. and Patton, Michael. (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.

Andonian, Laris. and Khorramizadeh, M.R. and Farhud, Daryoush. and Hashemzadeh-Chaleshtori, Morteza. and Holakouie Naieni, K. 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.

Sadeghi, Abdolrahim. and Sanati, Mohammad Hossein. and Alasti, Fatemeh. and Ataei, Mitra. and Hashemzadeh-Chaleshtori, Morteza. (2005) Mutation analysis of connexin 26 gene and del (GJB6-D13S1830) in patients with hereditary deafness from two provinces in Iran. IRANIAN JOURNAL OF BIOTECHNOLOGY, 3 (4).

Hosseinipour, A. and Hashemzadeh-Chaleshtori, Morteza. and Sasanfar, Roksana. and Farhud, Daryoush. and Tolooi, A. and Doulati, M. and Rad, L.H. and Montazer Zohouri, Mostafa. 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.

Sasanfar, Roksana. and Tolouei, A. and Hoseinipour, Abedin. and Farhud, Daryoush. and Dolati, Masoumeh. and Hoghooghi Rad, Laleh. and Montazer Zohouri, Mostafa. and Ghadami, M. and Pour-Jafari, Hamid. and Hashemzadeh-Chaleshtori, Morteza. (2004) Frequency of a very rare 35delG mutation in two ethnic groups of Iranian populations. Iranian Journal of Public Health, 33 (4). pp. 26-30.

Pour-Jafari, Hamid. and Hashemzadeh-Chaleshtori, Morteza. (2004) Pedigree patterns of families having at least one member with sensorineural deafness in Hamadan. journal of shahrekord university of medical sciences, 5 (4).

Pour-Jafari, Hamid. and Farhud, D.D. and Yazdani, A. and Hashemzadeh-Chaleshtori, Morteza. (2003) Dermatoglyphics in patients with eczema, psoriasis and alopecia areata. Skin research and technology, 9 (3).

Hashemzadeh-Chaleshtori, Morteza. and Farhud, D.D. and Taylor, R. and Hadavi, V. and Patton, Michael. and Afzal, A.R. and Gharavi, Mohammad javad. (2002) Deafness–associated connexin 26 gene (GJB2) mutations in Iranian population. Iranian Journal of Public Health, 31 (3-4).

Saeidi, Elnaz. and Hashemzadeh-Chaleshtori, Morteza. and Doosti, Abbas. and Parchami Barjui, Shahrbanoo. 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.

This list was generated on Mon Jun 17 01:11:25 2019 IRDT.