Search Results - "Damavandi, Elia"
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CircZNF609 and circNFIX as possible regulators of glioblastoma pathogenesis via miR-145-5p/EGFR axis
Published in Scientific reports (12-06-2024)“…Glioblastoma is a rare and deadly malignancy with a low survival rate. Emerging evidence has shown that aberrantly expressed circular RNAs (circRNAs) play a…”
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Investigation of promoter methylation of FSCN1 gene and FSCN1 protein expression in differentiated thyroid carcinomas
Published in Molecular biology reports (01-03-2020)“…FSCN1 gene encodes an actin-bundling protein, FSCN1, which is involved in formation of actin-based structures that contribute to cell migration. High levels of…”
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Comparison of Plasma Levels of MicroRNA-155-5p, MicroRNA-210-3p, and MicroRNA-16-5p in Rheumatoid Arthritis Patients with Healthy Controls in a Case-control Study
Published in Iranian journal of allergy, asthma, and immunology (01-08-2023)“…Rheumatoid arthritis is a chronic autoimmune disease that causes inflammation and destruction of the joints. The objective of the current study was to evaluate…”
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Plasma Levels of MicroRNA-146a-5p, MicroRNA-24-3p, and MicroRNA-125a-5p as Potential Diagnostic Biomarkers for Rheumatoid Arthris
Published in Iranian journal of allergy, asthma, and immunology (06-06-2021)“…Rheumatoid arthritis (RA) is an autoimmune disease that is characterized by inflammation of the articular tissue. This study aims to evaluate the expression of…”
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RET Proto-Oncogene Mutational Analysis in 45 Iranian Patients Affected with Medullary Thyroid Carcinoma: Report of a New Variant
Published in Journal of thyroid research (2021)“…Background. The aim of this study was to identify germline mutation of the RET (rearranged during transfection) gene in patients with medullary thyroid…”
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Involvement of Bax Redistribution in the Induction of Germ Cell Apoptosis in Neonatal Mouse Testes
Published in ACTA HISTOCHEMICA ET CYTOCHEMICA (01-01-2002)“…Germ cell death is very common in mammalian testis, during both early testicular development and in the adult period, however the molecular mechanisms…”
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Plasma Levels of MicroRNA-146a-5p, MicroRNA-24-3p, and MicroRNA-125a-5p as Potential Diagnostic Biomarkers for Rheumatoid Arthris Diagnostic Biomarkers for Rheumatoid Arthritis
Published in Iranian journal of allergy, asthma, and immunology (01-01-2021)“…Rheumatoid arthritis (RA) is an autoimmune disease that is characterized by inflammation of the articular tissue. This study aims to evaluate the expression of…”
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Evaluation of the Prevalence of Exons 1 And 10 Polymorphisms of LHCGR Gene and Its Relationship with IVF Success
Published in Journal of reproduction & infertility (01-10-2019)“…Luteinizing hormone receptor gene shows four nonsynonymous polymorphisms within the exons. Three of these polymorphisms, . rs4539842 (an insertion of 6bp…”
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Molecular histochemical analysis of estrogen receptor alpha and beta expressions in the mouse ovary: in situ hybridization and Southwestern histochemistry
Published in Medical electron microscopy (01-06-2003)“…It is well known that estrogen plays important roles in the female reproductive organs, including the ovary, through estrogen receptors (ERalpha and ERbeta)…”
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Molecular histochemical analysis of estrogen receptor [alpha] and [beta] expressions in the mouse ovary: in situ hybridization and Southwestern histochemistry
Published in Medical molecular morphology (01-06-2003)“…It is well known that estrogen plays important roles in the female reproductive organs, including the ovary, through estrogen receptors (ER[alpha] and…”
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Isolated congenital anosmia with morphologically normal olfactory bulb in two Iranian families: A new clinical entity?
Published in American journal of medical genetics. Part A (15-06-2004)“…Congenital total loss of the sense of smell occurs as a part of a syndrome or isolated anosmia. Kallmann syndrome is the most well known congenital anosmia…”
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Bardet-Biedl syndrome type 3 in an Iranian family: Clinical study and confirmation of disease localization
Published in American journal of medical genetics (23-10-2000)“…Bardet‐Biedl syndrome (BBS) is a group of autosomal recessive MCA/MR syndromes characterized by pigmentary retinopathy, postaxial polydactyly, hypogenitalism,…”
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Confirmation of genetic homogeneity of syndactyly type 1 in an Iranian family
Published in American journal of medical genetics (22-11-2001)“…Syndactyly type 1 (SD1) is the most common type of syndactyly, inherited in an autosomal dominant fashion and characterized by complete or partial webbings…”
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