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Reza Ebrahimzadeh-Vesal
Reza Ebrahimzadeh-Vesal
Department of Basic Medical Sciences, Neyshabur University of Medical Sciences, Neyshabur, IRAN
在 nums.ac.ir 的电子邮件经过验证
标题
引用次数
引用次数
年份
Lactobacillus acidophilus and Lactobacillus crispatus culture supernatants downregulate expression of cancer-testis genes in the MDA-MB-231 cell line
R Azam, S Ghafouri-Fard, M Tabrizi, MH Modarressi, ...
Asian Pacific Journal of Cancer Prevention 15 (10), 4255-4259, 2014
832014
Expression analysis of aurora-C and Survivin, two testis-specific genes, in patients with colorectal cancer
S Hosseini, S Hashemzadeh, MA Estiar, R Ebrahimzadeh, MB Fakhree, ...
Clin Lab 61 (5-6), 475-80, 2015
412015
Next Generation Sequencing approach to molecular diagnosis of Duchenne muscular dystrophy; identification of a novel mutation
R Ebrahimzadeh-Vesal, A Teymoori, M Azimi-Nezhad, FS Hosseini
Gene 644, 1-3, 2018
152018
Molecular characterization of KRAS, BRAF, and EGFR genes in cases with prostatic adenocarcinoma; reporting bioinformatics description and recurrent mutations
A Salmaninejad, S Ghadami, MZ Dizaji, Z Golchehre, MA Estiar, ...
Clin Lab 61 (7), 749-59, 2015
152015
Association of CYP11B2 gene polymorphism with preeclampsia in north east of Iran (Khorasan province)
M Azimi-Nezhad, A Teymoori, R Ebrahimzadeh-Vesal
Gene 733, 144358, 2020
142020
Identification of Spata-19 new variant with expression beyond meiotic phase of mouse testis development
S Nourashrafeddin, R Ebrahimzadeh-Vesal, MH Modarressi, A Zekri, ...
Reports of biochemistry & molecular biology 2 (2), 89, 2014
122014
Identification of a novel nonsense mutation in kyphoscoliosis peptidase gene in an Iranian patient with myofibrillar myopathy
R Ebrahimzadeh-Vesal, A Teymoori, AM Dourandish, M Azimi-Nezhad
Genes & diseases 5 (4), 331-334, 2018
112018
Genetic screening of Iranian patients with 46, XY disorders of sex development
A Shojaei, R Ebrahimzadeh-Vesal, A Ahani, M Razzaghy-Azar, F Ghazi, ...
Reports of biochemistry & molecular biology 6 (1), 59, 2017
102017
Expression analysis of PAWP during mouse embryonic stem cell-based spermatogenesis in vitro
S Nourashrafeddin, M Aarabi, M Miryounesi, R Ebrahimzadeh-Vesal, ...
In Vitro Cellular & Developmental Biology-Animal 50, 475-481, 2014
92014
Analysis of SPATA19 gene expression during male germ cells development, lessons from in vivo and in vitro study
S Nourashrafeddin, R Ebrahimzadeh‐Vesal, M Miryounesi, M Aarabi, ...
Cell biology international reports 21 (1), 1-7, 2014
82014
Gene dosage analysis of proximal spinal muscular atrophy carriers using real-time PCR
MR Abbaszadegan, F Keify, F Ashrafzadeh, M Farshchian, ...
Archives of Iranian medicine 14 (3), 188-191, 2011
82011
Association of MTHFR C677T polymorphism with preeclampsia in North East of Iran (Khorasan Province)
M Azimi-Nezhad, A Teymoori, A Salmaninejad, R Ebrahimzadeh-Vesal
Fetal and Pediatric Pathology 39 (5), 373-380, 2020
72020
AKT family and miRNAs expression in IL-2 induced CD4+ T cells
N Ranji, M Sadeghizadeh, M Karimipoor, MA Shokrgozar, ...
Iranian Journal of Basic Medical Sciences 17 (11), 886, 2014
62014
High Frequency of Mutations in the PIK3CA Gene Helical and Kinase Coding Regions in a Group of Iranian Patients with High-Grade Glioblastomas: Five Novel …
P Derakhshandeh-Peykar, J Alivi, A Hosseinnejad, B Rautenstrauss, ...
Journal of Neurogenetics 25 (4), 189-194, 2011
62011
Recurrent pregnancy loss in a subject with heterozygote factor V Leiden mutation; a case report
R Ebrahimzadeh-Vesal, R Azam, A Ghazarian, M Hajesmaeili, N Ranji, ...
Reports of Biochemistry & Molecular Biology 2 (2), 98, 2014
52014
The relationship between MTHFR polymorphisms and abortion in Iranian women
F Keyfi, R Ebrahimzadeh-Vesal, N Zhiyan, M Nayebi, M Nasseri, ...
Gene Reports 13, 130-133, 2018
42018
Identification of a new splice-acceptor mutation in HFM1 and functional analysis through molecular docking in nonobstructive azoospermia
N Saebnia, R Ebrahimzadeh-Vesal, A Haddad-Mashhadrizeh, ...
Journal of assisted reproduction and genetics 39 (5), 1195-1203, 2022
32022
Identification of novel missense HEXB gene mutation in Iranian-child with juvenile Sandhoff disease
R Ebrahimzadeh-Vesal, S Hosseini, M Moghaddassian, ...
Meta Gene 12, 83-87, 2017
32017
MicroRNA profiling during germline differentiation of mouse embryonic stem cells
R Ebrahimzadeh-Vesal, MA Shokrgozar, K Nayernia, L Teimoori-Toolabi, ...
Cellular and Molecular Biology 61 (3), 84-91, 2015
32015
Mutation analysis of androgen receptor gene: Multiple uses for a single test
A Shojaei, F Behjati, R Ebrahimzadeh-Vesal, M Razzaghy-Azar, ...
Gene 552 (2), 234-238, 2014
32014
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