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Vojdani, S., Milanizadeh, S., Molaei, F., (...), Talee, M.R., Abbaszadegan, M.R. Mutation Screening of KCNQ1 and KCNE1 Genes in Iranian Patients With Jervell and Lange-Nielsen Syndrome. Fetal and Pediatric Pathology 2019

 

 

Khorasani, Z.M., Bagheri, R.K., Yaghoubi, M.A., (...), Abbaszadegan, M.R., Sahebkar, A. The association between serum irisin levels and cardiovascular disease in diabetic patients. Diabetes and Metabolic Syndrome: Clinical Research and Reviews Volume 13, Issue 1, January - February 2019, 786-790

 

 

Golyan, F.F., Moghaddassian, M., Forghanifard, M.M., Mahmoudian, R.A., Abbaszadegan, M.R. Whole Exome Sequencing Reveals a Novel Damaging Mutation in Human Fibroblast Activation Protein in a Family with Esophageal Squamous Cell Carcinoma. Journal of Gastrointestinal Cancer2019

 

 

Forghanifard, M.M., Naeimi Khorasanizadeh, P., Abbaszadegan, M.R., Javdani Mallak, A., Moghbeli, M. Role of DIDO1 in Progression of Esophageal Squamous Cell Carcinoma. Journal of Gastrointestinal Cancer2019

 

 

 Forghanifard, M.M., Abbaszadegan, M.R., Moghbeli, M. Role of SIZN1 in esophageal squamous cell carcinoma. Middle East Journal of Cancer, Volume 10, Issue 1, 1 January 2019, 37-42

 

 

 Moghbeli, M., Makhdoumi, Y., Soltani Delgosha, M., Abdollahi, A., Abbaszadegan, M.R. ErbB1 and ErbB3 co-over expression as a prognostic factor in gastric cancer. Biological research.Volume 52, Issue 1, 8 January 2019, 2

 

 

Ghaemi, N., Ghahraman, M., Noroozi Asl, S., (...), Moghbeli, M., Abbaszadegan, M.R. Novel DNA variation of GPR54 gene in familial central precocious puberty. Italian Journal of Pediatrics. Volume 45, Issue 1, 11 January 2019, Article number 10

 

 

 Keyfi, F., Abbaszadegan, M.R., Sankian, M., Alijanpour, M., Varasteh, A. Mutation analysis of genes related to methylmalonic acidemia: identification of eight novel mutations. Molecular Biology ReportsVolume 46, Issue 1, 1 February 2019,271-285

 

   Bagheri, V., Abbaszadegan, M.R., Memar, B., Mahmoudian, R.A., Gholamin, M. Induction of T cell-mediated immune response by dendritic cells pulsed with mRNA of sphere-forming cells isolated from patients with gastric cancer. Life SciencesVolume 219, 15 February 2019,136-143  
   Shariat Razavi, S.M., Forghanifard, M.M., Kordi-Tamandani, D.M., Abbaszadegan, M.R.MAML1 regulates EMT markers expression through NOTCH-independent pathway in breast cancer cell line MCF7. Biochemical and Biophysical Research Communications.2019.510(3), pp. 376-382  
   Tafazoli, A., Behjati, F., Farhud, D.D., Abbaszadegan, M.R. Combination of genetics and nanotechnology for down syndrome modification: A potential hypothesis and review of the literature. Iranian Journal of Public Health.Volume 48, Issue 3, 12 March 2019, 371-378  

 

Moghbeli, M., Mosannen Mozaffari, H., Memar, B., Gholamin, M., Abbaszadegan, M.R. Role of MAML1 in targeted therapy against the esophageal cancer stem cells. Journal of Translational Medicine. Volume 17, Issue 1, 16 April 2019, Article number 126

 

 

Ardalan Khales, S., Abbaszadegan, M.R., Majd, A., Forghanifard, M. M. Linkage between EMT and stemness state through molecular association between TWIST1 and NY-ESO1 in esophageal squamous cell carcinoma. BiochimieVolume 163, August 2019, 84-93

 

 

 Ebrahimi V, Aliaghaei A, Piryaei A, Haghir H, Abdollahifar MA, Sadeghi Y: Nigral injection of 6-hydroxydopamine induces changes in spatial arrangement of striatal neuron and glial cells. Front Biosci (Schol Ed). 2019 Jan 1;11:1 

 
  Khoshdel-Sarkarizi H, Hami J, Mohammadipour A, Sadr-Nabavi A, Mahmoudi M, Kheradmand H, Peyvandi M, Nourmohammadi E, Haghir H: Developmental regulation and lateralization of GABA receptors in the rat hippocampus. Int J Dev Neurosci. 2019 Jan 7;76:52-60  
  Alimardani M, Hosseini SM, Khaniani MS, Haghi MR, Eslahi A, Farjami M, Chezgi J, Derakhshan SM, Mojarrad M. Targeted Mutation Analysis of the SLC26A4, MYO6, PJVK and CDH23 Genes in Iranian Patients with AR Nonsyndromic Hearing Loss. Fetal Pediatr Pathol. 2019 Apr;38(2):93-102  
  Darabi H, Salmaninejad A, Jaripour ME, Azarpazhooh MR, Mojarrad MSadr-Nabavi A. Association of the genetic polymorphisms in immunoinflammatory microRNAs with risk of ischemic stroke and subtypes in an Iranian population. J Cell Physiol. 2019 Apr;234(4):3874-3886.  
  Bozorg Qomi S, Asghari A, Salmaninejad A, Mojarrad M. Spinal Muscular Atrophy and Common Therapeutic Advances. Fetal Pediatr Pathol. 2019 Jun;38(3):226-238. doi: 10.1080/15513815.2018.1520374. Epub 2019 May 7.  
  Maryam Zare, Jina Khayatzadeh, Hamidreza Sadegh Nia, Majid Mojarad, Fatemeh Baghbani, Javad Sargolzaei, HAMID SADEGHIAN, MOHSEN SISAKHTI, MOHAMMAD SOUKHTANLOO. EFFECTS OF BEE VENOM ON ACTIVITY AND EXPRESSION OF 15-LIPOXYGENASE-1 IN HUMAN HT29 COLON CANCER. ACTA POLONIAE PHARMACEUTICA,2019  
  Hashemian, S., Vakili, R., Sadr-Nabavi, A., Esfehani, R.J., Jaripour, M.E. Molecular evaluation of children with clinical russell-silver phenotypes: The first report from Iran .Iranian Journal of PediatricsOpen AccessVolume 29, Issue 2, April 2019, Article number e81388  
  Kerachian, M.A,Kerachian, M. Long interspersed nucleotide element-1 (LINE-1) methylation in colorectal cancer Clinica Chimica ActaVolume 488, January 2019, Pages 209-21  
  Mollazadeh, S.Fazly Bazzaz, B.Neshati, V.De Vries, A.ANaderi-Meshkin, H.Mojarad, M. Mirahmadi, M.Neshati, Z.Kerachian, MOverexpression of MicroRNA-148b-3p stimulates osteogenesis of human bonemarrow-derived mesenchymal stem cells: The role of MicroRNA-148b-3p in osteogenesis  BMC Medical Genetics,Volume 20, Issue 1, 1 July 2019, Article number 117  
  Hamzehzadeh, L. ,Khadangi, F. ,Ghayoor Karimiani, E. ,Pasdar, A. Kerachian, M.A.a,  Common KRAS and NRAS gene mutations in sporadic colorectal cancer in Northeastern Iranian patients. Current Problems in CancerVolume 42, Issue 6, November 2018, Pages 572-581