Search Results - "Mansour Heidari"

Retraction Notice to “Possible involvement of CREB/BDNF signaling pathway in neuroprotective effects of topiramate against methylphenidate induced apoptosis, oxidative stress and inflammation in hippocampus of rats: Molecular, biochemical and histological evidences” [Brain. Res. Bull. 132 (2017) 82–98] by Motaghinejad, Majid, Motevalian, Manijeh, Babalouei, Fatemeh, Abdollahi, Mohammad, Heidari, Mansour, Madjd, Zahra

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Identification of Two Novel Mutations in ABCA4 Gene in a Patient With Stargardt Disease by Mohebbi, Masoumeh, Heidari, Matin, Heidari, Mansour

“…Herein we investigated mutations in the ABCA4 gene in an Iranian patient with Stargardt disease using whole exome sequencing (WES). We evaluated genetic…”
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The relationship between common mutations in CFTR, AR genes, Y chromosome microdeletions and karyotyping abnormalities with very severe oligozoospermia in Iranian men by Jafari, Leyla, Safinejad, Kyumars, Nasiri, Mahboobeh, Heidari, Mansour, Houshmand, Massoud

“…Background Male infertility due to very severe oligozoospermia has been associated with some genetic risk factors. Objective To investigate the distribution of…”
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The Role of MicroRNA Signature as Diagnostic Biomarkers in Different Clinical Stages of Colorectal Cancer by Eslamizadeh, Sara, Heidari, Mansour, Agah, Shahram, Faghihloo, Ebrahim, Ghazi, Hossein, Mirzaei, Alireza, Akbari, Abolfazl

“…Colorectal cancer (CRC) is one of the most common cancers and a major cause of cancer-related death worldwide. The early diagnosis of colorectal tumors is one…”
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Human Homeobox TGIFLX Regulates CDX1, CDX2, and OCT1 Genes Expression in Colorectal Cancer Cell Lines by Soroosh Shahryarhesami, Mansour Heidari, Masoud Heidari, Nahid Sadighi

“…Background: Homeodomain transcriptional regulatory proteins, which are encoded by Homeobox (HOX) genes, play critical roles in both normal development and…”
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Identification of Two Novel Mutations in PKHD1 Gene from Two Families with Polycystic Kidney Disease by Whole Exome Sequencing by Heidari, Masoud, Gharshasbi, Hamid, Isazadeh, Alireza, Soleyman-Nejad, Morteza, Taskhiri, Mohammad Hossein, Shapouri, Javad, Bolhassani, Manzar, Sadighi, Nahid, Heidari, Mansour

“…Background: Polycystic kidney disease (PKD) is an autosomal recessive disorder resulting from mutations in the PKHD1 gene on chromosome 6 (6p12), a large gene…”
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Inhibition of Colorectal Cancer Cell Line CaCo-2 by Essential Oil of Eucalyptus camaldulensis Through Induction of Apoptosis by Taheri, Elham, Ghorbani, Saba, Safi, Maryam, Seyyed Sani, Nasrin, Firouzi Amoodizaj, Fatemeh, Heidari, Masoud, Chavoshi, Reza, Hajazimian, Saba, Isazadeh, Alireza, Heidari, Mansour

“…Treatment of colorectal cancer is one of the important challenges due to the increase of resistance to chemotherapeutic drugs. Isolated natural compounds from…”
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Mutations in CNNM4 Cause Jalili Syndrome, Consisting of Autosomal-Recessive Cone-Rod Dystrophy and Amelogenesis Imperfecta by Parry, David A., Mighell, Alan J., El-Sayed, Walid, Shore, Roger C., Jalili, Ismail K., Dollfus, Hélène, Bloch-Zupan, Agnes, Carlos, Roman, Carr, Ian M., Downey, Louise M., Blain, Katharine M., Mansfield, David C., Shahrabi, Mehdi, Heidari, Mansour, Aref, Parissa, Abbasi, Mohsen, Michaelides, Michel, Moore, Anthony T., Kirkham, Jennifer, Inglehearn, Chris F.

“…The combination of recessively inherited cone-rod dystrophy (CRD) and amelogenesis imperfecta (AI) was first reported by Jalili and Smith in 1988 in a family…”
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Thalidomide attenuates the hyporesponsiveness of isolated atria to chronotropic stimulation in BDL rats: The involvement of TNF-α, IL-6 inhibition, and SOCS1 activation by Hosseini-Chegeni, Ali, Jazaeri, Farahnaz, Yousefi-Ahmadipour, Aliakbar, Heidari, Mansour, Abdollahie, Alireza, Dehpour, Ahmad Reza

“…Cirrhotic cardiomyopathy is a complication of uncured cirrhosis which is associated with hyporesponsiveness of the heart to sympathetic stimulation. The…”
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Identification of Two Novel Mutations in the ATM Gene from Patients with Ataxia-Telangiectasia by Whole Exome Sequencing by Heidari, Masoud, Soleyman-Nejad, Morteza, Taskhiri, Mohammad H, Shahpouri, Javad, Isazadeh, Alireza, Ahangari, Roghayyeh, Mohamadi, Ali R, Ebrahimi, Masoumeh, Karimi, Hadi, Bolhassani, Manzar, Karimi, Zahra, Heidari, Mansour

“…Background: Ataxia telangiectasia (AT) is one of the most common autosomal recessive hereditary ataxia presenting in childhood. The responsible gene for AT…”
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Identification of a novel homozygous mutation in the DDR2 gene from a patient with spondylo-meta-epiphyseal dysplasia by whole exome sequencing by Heidari, Masoud, Soleyman-Nejad, Morteza, Isazadeh, Alireza, Taskiri, Mohammad Hossein, Bolhassani, Manzar, Sadighi, Nahid, Shiri, Zahra, Karimi, Zahra, Heidari, Mansour

“…The spondylo-meta-epiphyseal dysplasia (SMED) short limbs-hand type is a rare autosomal recessive disease, which is characterized by premature calcification…”
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Change in the Expression of BAK، FAS، BAX، TNF-A، BCL-2 and Survivin Apoptosis Genes of the Human Breast Adenocarcinoma Cells (MCF-7) by Staphylococcal Enterotoxin B by Afzali, Sara, Doosti, Abbas, Heidari, Mansour, Babaei, Nahid, Keshavarz, Parvaneh

“…Introduction: Breast cancer is one of the most prevalent malignancies among women. Patients whose suffering from this condition, as a result of the use of…”
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First Report of Hartmannella keratitis in a Cosmetic Soft Contact Lens Wearer in Iran by Abedkhojasteh, Hoda, Niyyati, Maryam, Rahimi, Firoozeh, Heidari, Mansour, Farnia, Shohreh, Rezaeian, Mostafa

“…Poor hygiene will provide good condition for corneal infections by opportunistic free-living amoebae (FLA) in soft contact lens wearers. In the present study…”
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The effect of antimicrobial photodynamic therapy on the expression of novel methicillin resistance markers determined using cDNA-AFLP approach in Staphylococcus aureus by Hoorijani, Mohammad Neshvan, Rostami, Hosein, Pourhajibagher, Maryam, Chiniforush, Nasim, Heidari, Mansour, Pourakbari, Babak, Kazemian, Hossein, Davari, Kambiz, Amini, Vahid, Raoofian, Reza, Bahador, Abbas

“…Highlights • cDNA-AFLP is suitable approach for identification of new target genes implicated in antimicrobial resistance. • Serine hydrolase family protein…”
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Down-regulation of miR-135b in colon adenocarcinoma induced by a TGF-β receptor I kinase inhibitor (SD-208) by Abolfazl Akbari, Mohammad Hossein Ghahremani, Gholam Reza Mobini, Mahdi Abastabar, Javad Akhtari, Manzar Bolhassani, Mansour Heidari

“…Objective(s):Transforming growth factor-β(TGF-β) is involved in colorectal cancer (CRC). The SD-208 acts as an anti-cancer agent in different malignancies via…”
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Association of a novel homozygous mutation in the HMGCS2 gene with an HMGCSD in an Iranian patient by Heidari, Masoud, Soleyman‐Nejad, Morteza, Isazadeh, Alireza, Shapouri, Javad, Taskhiri, Mohammad Hossein, Ahangari, Roghayyeh, Mohamadi, Ali Reza, Ebrahimi, Masoumeh, Karimi, Hadi, Bolhassani, Manzar, Karimi, Zahra, Heidari, Mansour

“…Background 3‐Hydroxy‐3‐methylglutaryl‐CoA (HMG‐CoA) synthase 2 gene (HMGCS2) encodes a mitochondrial enzyme catalyzing the first reaction of ketogenesis…”
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Mutation analysis of connexin 50 gene among Iranian families with autosomal dominant cataracts by Mohebi, Masoumeh, Chenari, Saeed, Akbari, Abolfazl, Ghassemi, Fariba, Zarei-Ghanavati, Mehran, Fakhraie, Ghasem, Babaie, Nahid, Heidari, Mansour

“…Childhood cataract is a genetically heterogeneous eye disorder that results in visual impairment. The aim of this study was to identify the genetic mutations…”
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A Heterozygous STXBP1 Gene de novo Mutation in an Iranian Child With Epileptic Encephalopathy: Case Report by Heidari, Masoud, Soleyman-Neja, Morteza d, Taskhiri, Mohammad Hossein, Isazadeh, Alireza, Bolhassani, Manzar, Shahpouri, Javad, Heidari, Mansour, Sadighi, Nahid

“…The Syntaxin Binding Protein 1 (STXBP1) plays an important role in regulating neurotransmitter release and synaptic vesicle fusion through binding to…”
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Evaluation of SD-208, a TGF-β-RI Kinase Inhibitor, as an Anticancer Agent in Retinoblastoma by Fadakar, Puran, Akbari, Abolfazl, Ghassemi, Fariba, Mobini, Gholam Reza, Mohebi, Masoumeh, Bolhassani, Manzar, Abed Khojasteh, Hoda, Heidari, Mansour

“…Retinoblastoma is the most common intraocular tumor in children resulting from genetic alterations and transformation of mature retinal cells. The objective of…”
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Transforming Growth Factor Beta-Induced Factor 2-Linked X (TGIF2LX) Regulates Two Morphogenesis Genes, Nir1 and Nir2 in Human Colorectal by Mobini, Gholam Reza, Ghahremani, Mohammad Hossein, Amanpour, Saeid, Dehpour, Ahmad Reza, Akbari, Abolfazl, Hoseiniharouni, Seyed Mojtaba, Muhammadnejad, Samad, Sheikhzade, Maryam, Abedkhojasteh, Hoda, Mohebi, Masoumeh, Bolhassani, Manzar, Heidari, Mansour

“…A member of homeodomain protein namely TGIF2LX has been implicated as a tumor suppressor gene in human malignancy as well as in spermatogenesis. However, to…”
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