Search Results - "Sima Mansoori"
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Molecular Mechanisms of Apoptosis and Roles in Cancer Development and Treatment
Published in Asian Pacific journal of cancer prevention : APJCP (03-04-2015)Get full text
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Narrower insight to SIRT1 role in cancer: A potential therapeutic target to control epithelial–mesenchymal transition in cancer cells
Published in Journal of cellular physiology (01-06-2018)“…The epithelial–mesenchymal transition (EMT) is a highly networked cellular process which involves cell transition from the immotile epithelial to the motile…”
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Downregulation of HDAC2 and HDAC3 via oleuropein as a potent prevention and therapeutic agent in MCF‐7 breast cancer cells
Published in Journal of cellular biochemistry (01-06-2019)“…Breast cancer is the most common malignancy in the world with the highest rate of morbidity and mortality. Due to the several side effects of chemotherapy and…”
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A new insight on serum microRNA expression as novel biomarkers in breast cancer patients
Published in Journal of cellular physiology (01-11-2019)“…Breast cancer (BC) is one of the widespread lethal diseases affecting a large number of women worldwide. As such, employing and identifying significant markers…”
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The hopeful anticancer role of oleuropein in breast cancer through histone deacetylase modulation
Published in Journal of cellular biochemistry (01-10-2019)“…Breast cancer (BC) is one of the most common cancers among women worldwide. Genetic, epigenetic, and environmental factors play a crucial role in BC…”
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A novel missense variant in ESRRB gene causing autosomal recessive non-syndromic hearing loss: in silico analysis of a case
Published in BMC medical genomics (01-02-2022)“…Hereditary hearing loss (HHL) is a common heterogeneous disorder affecting all ages, ethnicities, and genders. The most common form of HHL is autosomal…”
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An update of common autosomal recessive non-syndromic hearing loss genes in Iranian population
Published in International journal of pediatric otorhinolaryngology (01-06-2017)“…Abstract Autosomal-recessive genes are responsible for about 80% of the hereditary non-syndromic hearing loss (NSHL) cases. In Iran, due to consanguineous…”
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A Novel Pathogenic Mutation in WNK1 Gene Causing HSAN Type II in Three Siblings
Published in Journal of molecular neuroscience (23-10-2024)“…Hereditary sensory and autonomic neuropathy (HSAN) is a rare genetic disorder that primarily affects the peripheral nervous system, leading to a progressive…”
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The impact of microRNAs on the resistance of breast cancer subtypes to chemotherapy
Published in Pathology, research and practice (01-09-2023)“…Breast cancer (BC) formation is primarily influenced by genetics, epigenetics and environmental factors. Aberrant Genetics and epigenetics leads to a condition…”
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miR‐449a: A Promising Biomarker and Therapeutic Target in Cancer and Other Diseases
Published in Cell biochemistry and biophysics (01-09-2024)“…In the regulation of gene expression, epigenetic factors like non-coding RNAs (ncRNAs) play an equal role in genetics. The role of microRNAs (miRNAs), which…”
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Potential brain biomarkers in patients with Autism spectrum syndrome
Published in Research in autism spectrum disorders (01-10-2024)“…Autism spectrum disorder (ASD) is referred as a cluster of neurodevelopmental disorders with relatively high incidence. ASD is believed to be a multifactorial…”
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HDACis (class I), cancer stem cell, and phytochemicals: Cancer therapy and prevention implications
Published in Biomedicine & pharmacotherapy (01-01-2018)“…Epigenetics is independent of the sequence events that physically affect the condensing of chromatin and genes expression. The unique epigenetic memories of…”
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Restoration of correct splicing in IVSI-110 mutation of β-globin gene with antisense oligonucleotides: implications and applications in functional assay development
Published in Iranian journal of basic medical sciences (01-06-2017)“…The use of antisense oligonucleotides (AOs) to restore normal splicing by blocking the recognition of aberrant splice sites by the spliceosome represents an…”
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Differential Expression Pattern of Epithelial Mesenchymal Transition Gens: AXL, GAS6, Claudin-1, and Cofilin-1, in Different Stages of Epithelial Ovarian Cancer
Published in Iranian journal of public health (01-09-2019)“…Epithelial ovarian cancer (EOC), is the fatal form of gynecological cancer. Almost 70% of ovarian cancer patients are detected at an advanced stage (III-IV)…”
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Evaluation of Association Between HLA Class II DR4-DQ8 Haplotype and Type I Diabetes Mellitus in Children of East Azerbaijan State of Iran
Published in Advanced pharmaceutical bulletin (01-03-2015)“…Purpose: Association between HLA-DR4–DQ8 haplotype and type 1 Diabetes Mellitus (DM-1A) was investigated in children of East Azerbaijan state of Iran because…”
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The HLA-G 14-bp Insertion/ Deletion Polymorphism in Recurrent Spontaneous Abortion among Iranian Women
Published in Iranian journal of allergy, asthma, and immunology (01-10-2014)“…HLA-G is a non-classical HLA class Ib molecule with limited protein variability generated by alternative splicing. HLA-G displays immunotolerant properties and…”
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The worldwide frequency of MYO15A gene mutations in patients with non-syndromic hearing loss: A meta-analysis
Published in Iranian journal of basic medical sciences (01-07-2020)“…MYO15A is the third most crucial gene in hereditary sensorineural hearing loss after GJB2 and SLC26A4 . In the present study, we reviewed the prevalence of…”
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Molecular Mechanisms of Apoptosis and Roles in Cancer Development and Treatment
Published in Asian Pacific journal of cancer prevention : APJCP (2015)“…Programmed cell death (PCD) or apoptosis is a mechanism which is crucial for all multicellular organisms to control cell proliferation and maintain tissue…”
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Cloning of Soluble Human Stem Cell Factor in pET-26b(+) Vector
Published in Advanced pharmaceutical bulletin (2014)“…Purpose: Stem cell factor (SCF) plays an important role in the survival, proliferation and differentiation of hematopoietic stem cells and progenitor cells…”
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NUCB2/Nesfatin-1: A Potent Meal Regulatory Hormone and its Role in Diabetes
Published in The Egyptian journal of medical human genetics (01-04-2017)“…Nesfatin-1, a newly discovered calcium and DNA binding peptide, originate from nucleobindin 2 (NUCB2) precursors and expressed by central and peripheral…”
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