| A narrative review of tumor-associated macrophages in lung cancer: regulation of macrophage polarization and therapeutic implications SS Sedighzadeh, AP Khoshbin, S Razi, M Keshavarz-Fathi, N Rezaei Translational lung cancer research 10 (4), 1889, 2021 | 94 | 2021 |
| Biallelic loss of LDB3 leads to a lethal pediatric dilated cardiomyopathy TT Koopmann, Y Jamshidi, M Naghibi-Sistani, HM van der Klift, H Birjandi, ... European Journal of Human Genetics 31 (1), 97-104, 2023 | 8 | 2023 |
| The endocannabinoid, anandamide, acts as a novel inhibitor of LPS‐induced inflammasome activation in human gastric cancer AGS cell line: Involvement of CB1 and TRPV1 receptors SS Sedeighzadeh, H Galehdari, MR Tabandeh, M Shamsara, ... Mediators of Inflammation 2021 (1), 6698049, 2021 | 8 | 2021 |
| The clinical and genetic spectrum of autosomal-recessive TOR1A-related disorders A Saffari, T Lau, H Tajsharghi, EG Karimiani, A Kariminejad, S Efthymiou, ... Brain 146 (8), 3273-3288, 2023 | 5 | 2023 |
| Identification of three novel mutations in the FANCA, FANCC, and ITGA2B genes by whole exome sequencing S Negahdari, M Zamani, T Seifi, S Sedighzadeh, N Mazaheri, J Zeighami, ... International journal of preventive medicine 11 (1), 117, 2020 | 4 | 2020 |
| Fusion Protein Strategy to Increase Expression and Solubility of Hypervariable Region of VP2 Protein of Infectious Bursal Disease Virus in Escherichia coli SS Sedighzadeh, M Shamsara, A Shahpiri The Protein Journal 31, 580-584, 2012 | 4 | 2012 |
| Childhood‐Onset Choreo‐Dystonia Due to a Recurrent Novel Homozygous Nonsense HPCA Variant: Case Series and Literature Review F Magrinelli, KP Bhatia, M Beiraghi Toosi, F Arab, EG Karimiani, ... Movement Disorders Clinical Practice 10 (1), 101-108, 2023 | 3 | 2023 |
| Whole-exome sequencing application for genetic diagnosis of kidney diseases: A study from southwest of Iran M Zamani, T Seifi, S Sedighzadeh, S Negahdari, J Zeighami, A Sedaghat, ... Kidney360 2 (5), 873-877, 2021 | 2 | 2021 |
| Whole exome sequencing reveals several novel variants in congenital disorders of glycosylation and glycogen storage diseases in seven patients from Iran A Papi, M Zamani, G Shariati, A Sedaghat, T Seifi, S Negahdari, ... Molecular Genetics & Genomic Medicine 11 (2), e2099, 2023 | 1 | 2023 |
| Whole-exome sequencing deciphers the genetic profile of visual impairments in patients from Southwest Iran M Zamani, S Sedighzadeh, T Seifi, S Negahdari, J Zeighami, A Sedaghat, ... Molecular Genetics and Genomics 297 (5), 1289-1300, 2022 | 1 | 2022 |
| Whole exome sequencing identified a novel frameshift variant in the BHLHA9 in an Iranian family with mesoaxial synostotic syndactyly SS Sedighzadeh, A Sedaghat, M Zamani, T Seifi, G Shariati, J Zeighami, ... Congenital Anomalies 61 (6), 220-225, 2021 | 1 | 2021 |
| The LPS-Treated Human Gastric Cancer Cells (AGS) Show a Significant Higher Tendency to Proliferation, Inflammation and Cannabinoid Receptor 1 Expression SS Sedighzadeh, H Galehdari, MR Tabandeh, A Roohbakhsh, ... Jentashapir Journal of Cellular and Molecular Biology 11 (4), 2020 | 1 | 2020 |
| Biallelic loss of LDB3 leads to a lethal pediatric dilated cardiomyopathy Y Jamshidi, T Koopmann, M Naghibi-Sistani, HM van der Klift, H Birjandi, ... | | 2022 |
| identification of three novel mutations in the fanca, fancc, and itga2b genes by whole exome sequencing journal of preventive medicine, 2020 | | 2020 |
| Cloning and Codon-optimized Expression of Structural Protein Hypervariable Region of VP2 from Infectious Bursal Disease Virus SS Sedighzadeh, M Shamsara, KS HAJI, OA NASROLLAHI INTERNATIONAL JOURNAL OF MOLECULAR AND CLINICAL MICROBIOLOGY 2 (1), 119-123, 2012 | | 2012 |
| IMMUNOLOGY AND IMMUNOTHERAPY: P-87: EXTRACTION AND DETECTION OF HYPERVARIABLE REGION OF VP2 PROTEIN FROM INFECTIOUS BURSAL DISEASE VIRUS IN ESCHERICHIA COLI S Sedighzadeh, M Shamsara, A Shahpiri, KS HAJI CELL JOURNAL (YAKHTEH) 12 (11), 78-79, 2011 | | 2011 |
| Cloning and Codon-optimized Expression of Structural Protein Hypervariable Region of VP2 from Infectious Bursal Disease Virus S sadat Sedighzadeh, M Shamsara, SH Khodadad, AN Omran | | |
Mehdi ShamsaraNational Institute for Genetic Engineering and Biotechnology在 nigeb.ac.ir 的电子邮件经过验证
