Repository of Research and Investigative Information

Repository of Research and Investigative Information

دانشگاه علوم پزشکی و خدمات بهداشتی درمانی زنجان

Items where Division is "Education Vice-Chancellor Department > Faculty of Medicine > Department of Basic Science > Department of Molecular Medicine and Genetics" and Year is 2019

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Number of items: 20.


(2019) Metabolomics in early detection and prognosis of acute coronary syndrome. Clinica Chimica Acta. pp. 43-53. ISSN 0009-8981, 1873-3492

(2019) Ataxia-telangiectasia: A review of clinical features and molecular pathology. Pediatric Allergy and Immunology. pp. 277-288. ISSN 0905-6157

(2019) Mutation Analysis of GJB2 and GJB6 Genes and Screening of Nine Common DFNB Loci in Iranian Pedigrees with Autosomal Recessive Nonsyndromic Hearing Loss. Indian Journal of Otology. pp. 97-102. ISSN 0971-7749, 2249-9520


(2019) Prenatal stress increased gamma 2 GABAA receptor subunit gene expression in hippocampus and potentiated pentylenetetrazol-induced seizure in rats. Iranian Journal of Basic Medical Sciences. pp. 724-729. ISSN 2008-3866, 2008-3874


(2019) Insights into the roles of miRNAs; miR-193 as one of small molecular silencer in osteosarcoma therapy. Biomedicine & Pharmacotherapy. pp. 873-881. ISSN 0753-3322


(2019) The impact of genetic variation on metabolism of heavy metals: Genetic predisposition? Biomedicine & Pharmacotherapy. ISSN 0753-3322


(2019) GATA4 screening in Iranian patients of various ethnicities affected with congenital heart disease: Co-occurrence of a novel de novo translocation (5;7) and a likely pathogenic heterozygous GATA4 mutation in a family with autosomal dominant congenital heart disease. J Clin Lab Anal. e22923. ISSN 0887-8013

(2019) Genetic Analysis of Congenital Heart Disease in Iranian Pediatric Patients. International Cardiovascular Research Journal. pp. 56-61. ISSN 2251-9130


(2019) A novel homozygous LRRK1 stop gain mutation in a patient suspected with osteosclerotic metaphyseal dysplasia. Ann Hum Genet. pp. 102-106. ISSN 0003-4800

(2019) Cardioprotective microRNAs: Lessons from stem cell-derived exosomal microRNAs to treat cardiovascular disease. Atherosclerosis. pp. 1-9. ISSN 0021-9150


(2019) Whole exome sequencing identifies a homozygous pycr1 missense variant in a patient with autosomal recessive cutis laxa type 2b: A case report. Journal of Comprehensive Pediatrics. ISSN 2251-8150

(2019) A rare De novo robertsonian translocation t(21q; 21q) in an Iranian child with down syndrome: A case report. Acta medica iranica. ISSN 0044-6025


(2019) Metabolomics in early detection and prognosis of acute coronary syndrome. Clin Chim Acta. pp. 43-53. ISSN 0009-8981


(2019) Preparation and investigation of indirubin-loaded SLN nanoparticles and their anti-cancer effects on human glioblastoma U87MG cells. Cell Biol Int. pp. 2-11. ISSN 1065-6995


(2019) In vitro osteogenic differentiation potential of the human induced pluripotent stem cells augments when grown on Graphene oxide-modified nanofibers. Gene. pp. 72-79. ISSN 0378-1119

(2019) Evaluation of Relationship between Awareness of Islamic Citizenship Rights and Organizational Similar-to-me of Education Managers of Zanjan University of Medical Sciences. Journal of Medical Education Development. pp. 34-42. ISSN 2251-9521

(2019) Decision tree-based classifiers for lung cancer diagnosis and subtyping using TCGA miRNA expression data. Oncol Lett. pp. 2125-2131. ISSN 1792-1074


(2019) تهیه فیلم های زیست تخریب پذیر فعال آلژینات سدیم غنی شده با رزوراترول و اسانس آویشن شیرازی و بررسی خصوصیات آنتی اکسیدانی آنها در شرایط آزمایشگاهی. completed.


(2019) بررسی اتصال فاکتور رونویسی OCT4به الیگودئوکسی نوکلئوتیدهای تله طراحی شده بر اساس ناحیه‌ی تنظیمی E-box در رده سلولی HT29 حاوی سلول های بنیادی سرطانی غنی سازی شده با روش EMSA. completed.

(2019) بررسی اثر مهار فاکتور رونویسی Tcf3 با استفاده از استراتژی تله الیگود‌ئوکسی نوکلئوتیدی بر ژن‌های اصلی تنظیم‌کننده خاصیت بنیادینگی در سلول‌های بنیادی جنینی موشی. completed.

This list was generated on Tue Jan 26 18:34:14 2021 +0330.