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Mahmoud Shekari Khaniani
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Year
Molecular mechanisms of apoptosis and roles in cancer development and treatment
S Goldar, MS Khaniani, SM Derakhshan, B Baradaran
Asian Pacific journal of cancer prevention 16 (6), 2129-2144, 2015
6612015
Small CGG repeat expansion alleles of FMR1 gene are associated with parkinsonism
DZ Loesch, MS Khaniani, HR Slater, JP Rubio, QM Bui, K Kotschet, ...
Clinical genetics 76 (5), 471-476, 2009
772009
An improved diagnostic PCR assay for identification of cryptic heterozygosity for CGG triplet repeat alleles in the fragile X gene (FMR1)
MS Khaniani, P Kalitsis, T Burgess, HR Slater
Molecular Cytogenetics 1, 1-6, 2008
662008
Inhibition of MEK/ERK1/2 signaling affects the fatty acid composition of HepG2 human hepatic cell line
B Yousefi, M Darabi, B Baradaran, MS Khaniani, M Rahbani, M Darabi, ...
BioImpacts: BI 2 (3), 145, 2012
492012
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
Simultaneous downregulation of miR‐21 and miR‐155 through oleuropein for breast cancer prevention and therapy
M Abtin, MR Alivand, MS Khaniani, M Bastami, M Zaeifizadeh, ...
Journal of cellular biochemistry 119 (9), 7151-7165, 2018
432018
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
422018
RIT2 Polymorphisms: Is There a Differential Association?
B Emamalizadeh, J Jamshidi, A Movafagh, M Ohadi, MS Khaniani, ...
Molecular neurobiology 54, 2234-2240, 2017
352017
The HLA-G 14-bp insertion/deletion polymorphism in recurrent spontaneous abortion among Iranian women
F Afkhami, MS Khaniani, L Farzadi, Z Paknejad, SM Derakhshan
Iranian Journal of Allergy, Asthma and Immunology, 364-369, 2014
352014
HLA‐G regulatory variants and haplotypes with susceptibility to recurrent pregnancy loss
N Yazdani, M Shekari Khaniani, M Bastami, T Ghasemnejad, F Afkhami, ...
International Journal of Immunogenetics 45 (4), 181-189, 2018
322018
An update of common autosomal recessive non-syndromic hearing loss genes in Iranian population
T Ghasemnejad, MS Khaniani, F Zarei, M Farbodnia, SM Derakhshan
International journal of pediatric otorhinolaryngology 97, 113-126, 2017
322017
A new insight on serum microRNA expression as novel biomarkers in breast cancer patients
Z Bahmanpour, R Sheervalilou, J Choupani, M Shekari Khaniani, ...
Journal of Cellular Physiology 234 (11), 19199-19211, 2019
312019
NUCB2/Nesfatin-1: a potent meal regulatory hormone and its role in diabetes
S Khalili, MS Khaniani, F Afkhami, SM Derakhshan
Egyptian Journal of Medical Human Genetics 18 (2), 105-109, 2017
292017
Linking the FMR1 alleles with small CGG expansions with neurodevelopmental disorders: preliminary data suggest an involvement of epigenetic mechanisms
DZ Loesch, DE Godler, M Khaniani, E Gould, G Freya, C Dissanayake, ...
American journal of medical genetics. Part A, 2306, 2009
292009
PPARγ agonist-induced alterations in Δ6-desaturase and stearoyl-CoA desaturase 1: Role of MEK/ERK1/2 pathway
N Saliani, M Darabi, B Yousefi, B Baradaran, MS Khaniani, M Darabi, ...
World journal of hepatology 5 (4), 220, 2013
282013
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
The analysis of association between SNCA, HUSEYO and CSMD1 gene variants and Parkinson’s disease in Iranian population
N Shahmohammadibeni, S Rahimi-Aliabadi, J Jamshidi, ...
Neurological Sciences 37, 731-736, 2016
152016
Prenatal diagnosis of spinal muscular atrophy: clinical experience and molecular genetics of SMN gene analysis in 36 cases
MS Khaniani, SM Derakhshan, S Abasalizadeh
Journal of prenatal medicine 7 (3), 32, 2013
152013
Molecular study of deletional and nondeletional mutations on the α-globin locus in the Azeri population of Northwestern Iran
SM Derakhshan, MS Khaniani, F Afkhami, AH PourFeizi
Hemoglobin 40 (5), 319-322, 2016
132016
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Articles 1–20