Items where Author is "Abbaszadegan, M. R."

Up a level
Export as [feed] Atom [feed] RSS 1.0 [feed] RSS 2.0
Group by: Item Type | No Grouping
Jump to: Article
Number of items: 63.

Article

Rafieenia, F. and Abbaszadegan, M. R. and Poursheikhani, A. and Razavi, S. M. S. and Jebelli, A. and Molaei, F. and Aghaee-Bakhtiari, S. H. (2020) In silico evidence of high frequency of miRNA-related SNPs in Esophageal Squamous Cell Carcinoma. Journal of Cellular Physiology, 235 (2). pp. 966-978.

Rafigh, M. and Salmaninejad, A. and Sorouri Khorashad, B. and Arabi, A. and Milanizadeh, S. and Hiradfar, M. and Abbaszadegan, M. R. (2020) Novel Deleterious Mutation in Steroid-5α-Reductase-2 in 46, XY Disorders of Sex Development: Case Report Study. Fetal and Pediatric Pathology.

Tafazoli, A. and Behjati, F. and Farhud, D. D. and Abbaszadegan, M. R. (2019) Combination of genetics and nanotechnology for down syndrome modification: A potential hypothesis and review of the literature. Iranian Journal of Public Health, 48 (3). pp. 371-378.

Tavakolian, S. and Bagherabad, M. B. and Kordi-Tamandani, D. M. and Abbaszadegan, M. R. and Kerachian, M. A. (2019) Epigenetic inactivation of protocadherin 10 by methylation in colorectal cancer. Acta Medica Iranica, 57 (8). pp. 472-477.

Moghbeli, M. and Makhdoumi, Y. and Soltani Delgosha, M. and Aarabi, A. and Dadkhah, E. and Memar, B. and Abdollahi, A. and Abbaszadegan, M. R. (2019) ErbB1 and ErbB3 co-over expression as a prognostic factor in gastric cancer. Biological research, 52 (1). p. 2.

Abbaszadegan, M. R. and Keyvani, V. and Moghbeli, M. (2019) Genetic and molecular bases of esophageal Cancer among Iranians: An update. Diagnostic Pathology, 14 (1).

Shariat Razavi, S. M. and Forghanifard, M. M. and Kordi-Tamandani, D. M. and Abbaszadegan, M. R. (2019) MAML1 regulates EMT markers expression through NOTCH-independent pathway in breast cancer cell line MCF7. Biochemical and Biophysical Research Communications, 510 (3). pp. 376-382.

Mahmoudian, R. A. and Bahadori, B. and Rad, A. and Abbaszadegan, M. R. and Forghanifard, M. M. (2019) MEIS1 knockdown may promote differentiation of esophageal squamous carcinoma cell line KYSE-30. Molecular Genetics and Genomic Medicine, 7 (7).

Vojdani, S. and Amirsalari, S. and Milanizadeh, S. and Molaei, F. and Ajalloueyane, M. and Khosravi, A. and Hamzehzadeh, L. and Ghasemi, M. M. and Talee, M. R. and Abbaszadegan, M. R. (2019) Mutation Screening of KCNQ1 and KCNE1 Genes in Iranian Patients With Jervell and Lange-Nielsen Syndrome. Fetal and Pediatric Pathology, 38 (4). pp. 273-281.

Ghaemi, N. and Ghahraman, M. and Noroozi Asl, S. and Vakili, R. and Fardi Golyan, F. and Moghbeli, M. and Abbaszadegan, M. R. (2019) Novel DNA variation of GPR54 gene in familial central precocious puberty. Italian Journal of Pediatrics, 45 (1).

Keyvani, V. and Farshchian, M. and Esmaeili, S. A. and Yari, H. and Moghbeli, M. and Nezhad, S. R. K. and Abbaszadegan, M. R. (2019) Ovarian cancer stem cells and targeted therapy. Journal of Ovarian Research, 12 (1).

Moghbeli, M. and Mosannen Mozaffari, H. and Memar, B. and Forghanifard, M. M. and Gholamin, M. and Abbaszadegan, M. R. (2019) Role of MAML1 in targeted therapy against the esophageal cancer stem cells. Journal of Translational Medicine, 17 (1).

Shirkani, A. and Mansouri, A. and Hosseini, R. F. and Azad, F. J. and Mahmoudian, R. A. and Montazer, M. and Samimi, A. and Momtazi-Borojeni, A. A. and Abbaszadegan, M. R. and Gholamin, M. (2019) The role of interleukin-4 and 13 gene polymorphisms in allergic rhinitis: A case control study. Reports of Biochemistry and Molecular Biology, 8 (2). pp. 111-118.

Motamedi Rad, N. and Rezaeishahmirzadi, M. and Shakeri, S. and Abbaszadegan, M. R. and Shekari, M. (2018) Association of IL-1B+3954 and IL-1RN polymorphisms in chronic gastritis and peptic ulcer. Iranian Journal of Public Health, 47 (9). pp. 1363-1369.

Khorashad, B. S. and Roshan, G. M. and Reid, A. G. and Aghili, Z. and Moghadam, M. D. and Khazai, B. and Hiradfar, M. and Afkhamizadeh, M. and Ghaemi, N. and Talaei, A. and Abbaszadegan, M. R. and Aarabi, A. and Dastmalchi, S. and Van de Grift, T. C. (2018) Childhood Sex-Typed Behavior and Gender Change in Individuals with 46,XY and 46,XX Disorders of Sex Development: An Iranian Multicenter Study. Archives of Sexual Behavior, 47 (8). pp. 2287-2298.

Abbaszadegan, M. R. and Taghehchian, N. and Li, L. and Aarabi, A. and Moghbeli, M. (2018) Contribution of KCTD12 to esophageal squamous cell carcinoma. BMC Cancer, 18 (1).

Khaleghizadeh, M. and Forghanifard, M. M. and Rad, A. and Farshchian, M. and Hejazi, Z. and Gholamin, M. and Memar, B. and Abbaszadegan, M. R. (2018) Ectopic expression of human DPPA2 gene in ESCC cell line using retroviral system. Avicenna Journal of Medical Biotechnology, 10 (2). pp. 75-82.

Khalilipour, N. and Baranova, A. and Jebelli, A. and Heravi-Moussavi, A. and Bruskin, S. and Abbaszadegan, M. R. (2018) Familial Esophageal Squamous Cell Carcinoma with damaging rare/germline mutations in KCNJ12/KCNJ18 and GPRIN2 genes. Cancer Genetics, 221. pp. 46-52.

Abbaszadegan, M. R. and Moghbeli, M. (2018) Genetic and molecular origins of colorectal Cancer among the Iranians: An update. Diagnostic Pathology, 13 (1).

Bagheri, V. and Memar, B. and Behzadi, R. and Aliakbarian, M. and Jangjoo, A. and Bahar, M. M. and Talebi, S. and Gholamin, M. and Abbaszadegan, M. R. (2018) Isolation and identification of chemotherapy-enriched sphere-forming cells from a patient with gastric cancer. Journal of Cellular Physiology, 233 (10). pp. 7036-7046.

Molaei, F. and Forghanifard, M. M. and Fahim, Y. and Abbaszadegan, M. R. (2018) Molecular signaling in tumorigenesis of gastric cancer. Iranian Biomedical Journal, 22 (4). pp. 217-230.

Moghbeli, M. and Naghibzadeh, B. and Ghahraman, M. and Fatemi, S. and Taghavi, M. and Vakili, R. and Abbaszadegan, M. R. (2018) Mutations in HNF1A Gene are not a Common Cause of Familial Young-Onset Diabetes in Iran. Indian Journal of Clinical Biochemistry, 33 (1). pp. 91-95.

Tafazoli, A. and Eshraghi, P. and Pantaleoni, F. and Vakili, R. and Moghaddassian, M. and Ghahraman, M. and Muto, V. and Paolacci, S. and Golyan, F. F. and Abbaszadegan, M. R. (2018) Novel mutations and their genotype-phenotype correlations in patients with Noonan syndrome, using next-generation sequencing. Advances in Medical Sciences, 63 (1). pp. 87-93.

Madani, G. K. and Rad, A. and Molavi, M. and Khales, S. A. and Abbaszadegan, M. R. and Forghanifard, M. M. (2018) Predicting the correlation of EZH2 and cancer stem cell markers in esophageal squamous cell carcinoma. Journal of Gastrointestinal Cancer, 49 (4). pp. 437-441.

Bagerabad, M. B. and Tavakolian, S. and Abbaszadegan, M. R. and Kerachian, M. A. (2018) Promoter hypermethylation of the eyes absent 4 gene is a tumor-specific epigenetic biomarker in Iranian colorectal cancer patients. Acta Medica Iranica, 56 (1). pp. 21-27.

Abbaszadegan, M. R. and Riahi, A. and Forghanifard, M. M. and Moghbeli, M. (2018) WNT and NOTCH signaling pathways as activators for epidermal growth factor receptor in esophageal squamous cell carcinoma. Cellular and Molecular Biology Letters, 23 (1).

Mahmoudian, R. A. and Abbaszadegan, M. R. and Gholamin, M. (2017) Applying Subtractive Hybridization Technique to Enrich and Amplify Tumor-Specific Transcripts of Esophageal Squamous Cell Carcinoma. Pathology and Oncology Research, 23 (2). pp. 271-279.

Izadpanah, M. H. and Abbaszadegan, M. R. and Fahim, Y. and Forghanifard, M. M. (2017) Ectopic expression of TWIST1 upregulates the stemness marker OCT4 in the esophageal squamous cell carcinoma cell line KYSE30. Cellular and Molecular Biology Letters, 22 (1).

Fairoozy, R. H. and Futema, M. and Vakili, R. and Abbaszadegan, M. R. and Hosseini, S. and Aminzadeh, M. and Zaeri, H. and Mobini, M. and Humphries, S. E. and Sahebkar, A. (2017) The Genetic Spectrum of Familial Hypercholesterolemia (FH) in the Iranian Population. Scientific Reports, 7 (1).

Forouzanfar, N. and Baranova, A. and Milanizadeh, S. and Heravi-Moussavi, A. and Jebelli, A. and Abbaszadegan, M. R. (2017) Novel candidate genes may be possible predisposing factors revealed by whole exome sequencing in familial esophageal squamous cell carcinoma. Tumor Biology, 39 (5).

Moaven, O. and Raziee, H. and Bowne, W. and Abbaszadegan, M. R. and Fuchs, B. C. (2016) Disease Biomarkers in Gastrointestinal Malignancies. Disease Markers, 2016.

Keyfi, F. and Abbaszadegan, M. R. and Rolfs, A. and Orolicki, S. and Moghaddassian, M. and Varasteh, A. (2016) Identification of a novel deletion in the MMAA gene in two Iranian siblings with vitamin B12-responsive methylmalonic acidemia. Cellular and Molecular Biology Letters, 21 (1).

Aghdam, M. N. and Abbaszadegan, M. R. and Tafazoli, A. and Aslzare, M. and Mosavi, Z. (2016) Presence of the RET Cys634Tyr mutation and Gly691Ser functional polymorphism in Iranian families with multiple endocrine neoplasia type 2A. Hormones, 15 (1). pp. 65-72.

Barooei, R. and Mahmoudian, R. A. and Abbaszadegan, M. R. and Mansouri, A. and Gholamin, M. (2015) Evaluation of thymic stromal lymphopoietin (TSLP) and its correlation with lymphatic metastasis in human gastric cancer. Medical Oncology, 32 (8).

Mansouri, A. and Foroughm, A. M. and Abbaszadegan, M. R. and Memar, B. and Mahmoudian, R. A. and Gholamin, M. (2015) Expression analysis of CD44 isoforms S and V3, in patients with esophageal squamous cell carcinoma. Iranian Journal of Basic Medical Sciences, 18 (4). pp. 380-384.

Gholamin, M. and Bazi, A. and Abbaszadegan, M. R. (2015) Idiopathic lymphocytopenia. Current Opinion in Hematology, 22 (1). pp. 46-52.

Forghanifard, M. M. and Taleb, S. and Abbaszadegan, M. R. (2015) Notch Signaling Target Genes are Directly Correlated to Esophageal Squamous Cell Carcinoma Tumorigenesis. Pathology and Oncology Research, 21 (2). pp. 463-467.

Moghbeli, M. and Forghanifard, M. M. and Sadrizadeh, A. and Mozaffari, H. M. and Golmakani, E. and Abbaszadegan, M. R. (2015) Role of Msi1 and MAML1 in Regulation of Notch Signaling Pathway in Patients with Esophageal Squamous Cell Carcinoma. Journal of Gastrointestinal Cancer, 46 (4). pp. 365-369.

Haghnejad, L. and Emamalizadeh, B. and Jamshidi, J. and Bidoki, A. Z. and Ghaedi, H. and Ahmadi, E. and Abdollahi, S. and Shahmohammadibeni, N. and Taghavi, S. and Fazeli, A. and Motallebi, M. and Zarneh, A. E. S. and Mohammadihosseinabad, S. and Abbaszadegan, M. R. and Torkamandi, S. and Gavenaroudi, M. A. and Pedram, N. and Shahidi, G. A. and Tafakhori, A. and Darvish, H. and Movafagh, A. (2015) Variation in the miRNA-433 binding site of FGF20 is a risk factor for Parkinson's disease in Iranian population. Journal of the Neurological Sciences, 355 (1-2). pp. 72-74.

Homayouni-Tabrizi, M. and Asoodeh, A. and Abbaszadegan, M. R. and Shahrokhabadi, K. and Nakhaie Moghaddam, M. (2015) An identified antioxidant peptide obtained from ostrich (Struthio camelus) egg white protein hydrolysate shows wound healing properties. Pharmaceutical Biology, 53 (8). pp. 1155-1162.

Zand Karimi, M. R. and Faridhosseini, R. and Abbaszadegan, M. R. and Jabbari Azad, F. and Shirkani, A. and Riyahi, A. and Montazar, M. and Gholamin, M. (2014) Association of ADAM33 gene polymorphisms with allergic asthma. Iranian Journal of Basic Medical Sciences, 17 (9). pp. 716-721.

Taleb, S. and Abbaszadegan, M. R. and Moghbeli, M. and Roudbari, N. H. and Forghanifard, M. M. (2014) HES1 as an Independent Prognostic Marker in Esophageal Squamous Cell Carcinoma. Journal of Gastrointestinal Cancer, 45 (4). pp. 466-471.

Torkamandi, S. and Moghbeli, M. and Farshchian, M. and Rad, A. and Tafazoli, A. and Abbaszadegan, M. R. (2014) Role of Brg1 in progression of esophageal squamous cell carcinoma. Iranian Journal of Basic Medical Sciences, 17 (11). pp. 912-916.

Moghbeli, M. and Abbaszadegan, M. R. and Farshchian, M. and Montazer, M. and Raeisossadati, R. and Abdollahi, A. and Forghanifard, M. M. (2013) Association of PYGO2 and EGFR in esophageal squamous cell carcinoma. Medical Oncology, 30 (2).

Shekouhi, S. and Baghbani, F. and Nazar-Abadi, M. H. and Hamzehloie, T. and Abbaszadegan, M. R. and Saghafi, N. and Raoofian, R. and Reza, J. Z. and Ahmadzadeh, S. and Tabatabaiefar, M. A. and Mojarrad, M. (2013) Identification of Xq22.1-23 as a region linked with hereditary recurrent spontaneous abortion in a family. International Journal of Reproductive BioMedicine, 11 (8). pp. 659-664.

Dadkhah, E. and Ziaee, M. and Davari, M. H. and Kazemi, T. and Abbaszadegan, M. R. (2012) Informative STR markers for marfan syndrome in Birjand, Iran. Iranian Journal of Basic Medical Sciences, 15 (5). pp. 1020-1025.

Moghbeli, M. and Maleknejad, M. and Arabi, A. and Abbaszadegan, M. R. (2012) Mutational analysis of uroporphyrinogen III cosynthase gene in Iranian families with congenital erythropoietic porphyria. Molecular Biology Reports, 39 (6). pp. 6731-6735.

Keify, F. and Zhiyan, N. and Mirzaei, F. and Tootian, S. and Ghazaey, S. and Abbaszadegan, M. R. (2012) Two novel familial balanced translocations t(8;11)(p23;q21) and t(6;16)(q26;p12) implicated in recurrent spontaneous abortion. Archives of Iranian Medicine, 15 (4). pp. 249-252.

Bonakdaran, S. and Abbaszadegan, M. R. and Dadkhah, E. and Khajeh-Dalouie, M. (2012) Vitamin D receptor gene polymorphisms in type 1 diabetes mellitus: A new pattern from Khorasan province, Islamic Republic of Iran. Eastern Mediterranean Health Journal, 18 (6). pp. 614-619.

Rafatpanah, H. and Rezaee, A. and Etemadi, M. M. and Hosseini, R. F. and Khorram, B. and Afsahr, L. and Taylor, G. and Mokhber, N. and Mahmoudi, M. and Abbaszadegan, M. R. and Foroghipor, M. and Hashemi, P. and Amiri, A. and Tehrani, M. and Azarpazhooh, A. and Azarpazhooh, M. R. (2012) The impact of interferon-alpha treatment on clinical and immunovirological aspects of HTLV-1-associated myelopathy in northeast of Iran. Journal of Neuroimmunology, 250 (1-2). pp. 87-93.

Forghanifard, M. M. and Gholamin, M. and Farshchian, M. and Moaven, O. and Memar, B. and Forghani, M. N. and Dadkhah, E. and Naseh, H. and Moghbeli, M. and Raeisossadati, R. and Abbaszadegan, M. R. (2011) Cancer-testis gene expression profiling in esophageal squamous cell carcinoma: Identification of specific tumor marker and potential targets for immunotherapy. Cancer Biology and Therapy, 12 (3). pp. 191-197.

Moghbeli, M. and Moaven, O. and Dadkhah, E. and Farzadnia, M. and Roshan, N. M. and Asadzadeh-Aghdaee, H. and Bahar, M. M. and Raeisossadati, R. and Forghanifard, M. M. and Bakhtiari, S. R. E. A. and Baradaran, A. and Abbaszadegan, M. R. (2011) High frequency of microsatellite instability in sporadic colorectal cancer patients in Iran. Genetics and Molecular Research, 10 (4). pp. 3520-3529.

Taghavi, N. and Biramijamal, F. and Sotoudeh, M. and Moaven, O. and Khademi, H. and Abbaszadegan, M. R. and Malekzadeh, R. (2010) Association of p53/p21 expression with cigarette smoking and prognosis in esophageal squamous cell carcinoma patients. World Journal of Gastroenterology, 16 (39). pp. 4958-4967.

Taghavi, N. and Biramijamal, F. and Sotoudeh, M. and Moaven, O. and Khademi, H. and Abbaszadegan, M. R. and Malekzadeh, R. (2010) Association of p53/p21 expression with cigarette smoking and prognosis in esophageal squamous cell carcinoma patients. World Journal of Gastroenterology, 16 (39). pp. 4958-4967.

Gholamin, M. and Moaven, O. and Farshchian, M. and Mahmoudi, M. and Sankian, M. and Memar, B. and Forghani, M. N. and Malekzadeh, R. and Rajabi-Mashhadi, M. T. and Abbaszadegan, M. R. (2010) Induction of cytotoxic T lymphocytes primed with Tumor RNA-loaded Dendritic Cells in esophageal squamous cell carcinoma: Preliminary step for DC vaccine design. BMC Cancer, 10.

Gholamin, M. and Moaven, O. and Farshchian, M. and Mahmoudi, M. and Sankian, M. and Memar, B. and Forghani, M. N. and Malekzadeh, R. and Rajabi-Mashhadi, M. T. and Abbaszadegan, M. R. (2010) Induction of cytotoxic T lymphocytes primed with Tumor RNA-loaded Dendritic Cells in esophageal squamous cell carcinoma: Preliminary step for DC vaccine design. BMC Cancer, 10.

Taghavi, N. and Biramijamal, F. and Sotoudeh, M. and Khademi, H. and Malekzadeh, R. and Moaven, O. and Memar, B. and A'Rabi, A. and Abbaszadegan, M. R. (2010) P16INK4ahypermethylation and p53, p16 and MDM2 protein expression in Esophageal Squamous Cell Carcinoma. BMC Cancer, 10.

Taghavi, N. and Biramijamal, F. and Sotoudeh, M. and Khademi, H. and Malekzadeh, R. and Moaven, O. and Memar, B. and A'Rabi, A. and Abbaszadegan, M. R. (2010) P16INK4ahypermethylation and p53, p16 and MDM2 protein expression in Esophageal Squamous Cell Carcinoma. BMC Cancer, 10.

Taghavi, N. and Biramijamal, F. and Abbaszadegan, M. R. and Khademi, H. and Sotoudeh, M. and Khoshbakht, S. (2010) P21 (Waf1/Cip1) gene polymorphisms and possible interaction with cigarette smoking in esophageal squamous cell carcinoma in northeastern Iran: A preliminary study. Archives of Iranian Medicine, 13 (3). pp. 235-242.

Abbaszadegan, M. R. and Moaven, O. and Sima, H. R. and Ghafarzadegan, K. and A'Rabi, A. and Forghani, M. N. and Raziee, H. R. and Mashhadinejad, A. and Jafarzadeh, M. and Esmaili-Shandiz, E. and Dadkhah, E. (2008) p16 promoter hypermethylation: A useful serum marker for early detection of gastric cancer. World Journal of Gastroenterology, 14 (13). pp. 2055-2060.

Vakili, R. and Baradaran-Heravi, A. and Barid-Fatehi, B. and Gholamin, M. and Ghaemi, N. and Abbaszadegan, M. R. (2005) Molecular analysis of the CYP21 gene and prenatal diagnosis in families with 21-hydroxylase deficiency in Northeastern Iran. Hormone Research, 63 (3). pp. 119-124.

Vakili, R. and Baradaran-Heravi, A. and Barid-Fatehi, B. and Gholamin, M. and Ghaemi, N. and Abbaszadegan, M. R. (2005) Molecular analysis of the CYP21 gene and prenatal diagnosis in families with 21-hydroxylase deficiency in Northeastern Iran. Hormone Research, 63 (3). pp. 119-124.

Abbaszadegan, M. R. and Gholamin, M. and Tabatabaee, A. and Farid, R. and Houshmand, M. and Abbaszadegan, M. (2003) Prevalence of human T-lymphotropic virus type 1 among blood donors from Mashhad, Iran. Journal of Clinical Microbiology, 41 (6). pp. 2593-2595.

This list was generated on Fri Apr 23 04:01:49 2021 EDT.