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Sahar Bayat
Sahar Bayat
PhD Student, Isfahan university of medical science
No verified email
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Year
Downregulation of HDAC2 and HDAC3 via oleuropein as a potent prevention and therapeutic agent in MCF‐7 breast cancer cells
S Bayat, S Mansoori Derakhshan, N Mansoori Derakhshan, ...
Journal of cellular biochemistry 120 (6), 9172-9180, 2019
442019
HDACis (class I), cancer stem cell, and phytochemicals: Cancer therapy and prevention implications
S Bayat, MS Khaniani, J Choupani, MR Alivand, SM Derakhshan
Biomedicine & Pharmacotherapy 97, 1445-1453, 2018
442018
Narrower insight to SIRT1 role in cancer: A potential therapeutic target to control epithelial–mesenchymal transition in cancer cells
J Choupani, S Mansoori Derakhshan, S Bayat, MR Alivand, ...
Journal of cellular physiology 233 (6), 4443-4457, 2018
432018
The hopeful anticancer role of oleuropein in breast cancer through histone deacetylase modulation
N Mansouri, MR Alivand, S Bayat, MS Khaniani, SM Derakhshan
Journal of Cellular Biochemistry 120 (10), 17042-17049, 2019
192019
Association study of FOXP3 gene and the risk of 0020 pre-eclampsia
M Gholami, R Mirfakhraie, R Pirjani, R Taheripanah, S Bayat, ...
Clinical and Experimental Hypertension 40 (7), 613-616, 2018
152018
Investigation of CEBPA and CEBPA-AS genes expression in acute myeloid leukemia
M Gholami, S Bayat, S Manoochehrabadi, H Pashaiefar, MD Omrani, ...
Reports of Biochemistry & Molecular Biology 7 (2), 136, 2019
132019
RAR‐related orphan receptor A: One gene with multiple functions related to migraine
S Farahani, L Solgi, S Bayat, A Abedin Do, S Zare‐Karizi, ...
CNS Neuroscience & Therapeutics 26 (12), 1315-1321, 2020
112020
Whole exome sequencing identified a novel homozygous ARV1 mutation in an Iranian family with developmental and epileptic encephalopathy-38
E Esmaeilzadeh, S Bayat, R Mirfakhraie, M Gholami
Meta Gene 30, 100953, 2021
42021
A homozygous missense mutation of WFS1 gene causes Wolfram's syndrome without hearing loss in an Iranian family (a report of clinical heterogeneity)
S Torkamandi, S Rezaei, R Mirfakhraie, S Bayat, S Piltan, M Gholami
Journal of Clinical Laboratory Analysis 34 (8), e23358, 2020
42020
Targeted sequencing of CDH23 and GJB2 genes in an Iranian pedigree with Usher syndrome and non-syndromic hearing loss
S Torkamandi, S Bayat, R Mirfakhraie, S Rezaei, M Askari, S Piltan, ...
Gene Reports 23, 101149, 2021
22021
Mutational Analysis of FLT3 Internal Tandem Duplication and D835 in De novo Adult Acute Myeloid Leukemia
FB and Reza Mirfakhraie Milad Gholami, Hossein Pashaiefar, Mohammad Reza ...
Journal of Advances in Medicine and Medical Research, 2017
12017
Mutational screening of RTK-BRAF genes in de novo adult acute myeloid leukemia
M Gholami, S Bayat, H Pashaiefar, S Pouriamanesh, S Manoochehrabadi, ...
Gene Reports 21, 100904, 2020
2020
HDACis (Class I), Cancer Stem Cell, and Phytochemicals: Cancer Therapy and Prevention Implications
SMD Sahar Bayat , Mohammad Reza Alivand
Third International Private Medical Congress of Iran, 2019
2019
Simultaneous Down Regulation Of HDAC2 And HDAC3 Through Oleuropein As A Potent Prevention And Therapeutic Agent In Breast Cancer Cells
MRA Sahar Bayat, Sima Mansoori Derakhshan
11th international congress of laboratory and clinic, 2019
2019
Mutational Analysis of FLT3 Internal Tandem Duplication and D835 in De novo Adult Acute Myeloid Leukemia
MDO Sahar Bayat,Milad Gholami,Reza Mirfakhraie ,Farkhondeh Behjati
2nd International Personalized Medical Congress, 2018
2018
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Articles 1–15