نتایج جستجو برای: Non-viral gene delivery

تعداد نتایج: 2602772  

Journal: :journal of paramedical sciences 0
afshin khavari department of hepatitis and aids, pasteur institute of iran, tehran, iran zahra orafa department of hepatitis and aids, pasteur institute of iran, tehran, iran mehrdad hashemi department of genetics, islamic azad university, tehran medical sciences branch,tehran,iran noorieh habibzadeh department of hepatitis and aids, pasteur institute of iran, tehran, iran azam bolhassani department of hepatitis and aids, pasteur institute of iran, tehran, iran

delivery of exogenous materials such as nucleic acids, peptides, proteins, and drugs into cells is an important strategy in modern cellular and molecular biology. recently, the development of gene carriers for efficient gene transfer into cells has attracted a great attention. furthermore, lack of effective drug delivery is one of the major problems of cancer chemotherapy. many physical methods...

Journal: :iranian journal of basic medical sciences 0
faezeh moghadam ariaee pharmaceutical research center, school of pharmacy, mashhad university of medical sciences, mashhad, iran maryam hashemi nanotechnology research center, school of pharmacy, mashhad university of medical sciences, mashhad, iran sara amel farzad pharmaceutical research center, school of pharmacy, mashhad university of medical sciences, mashhad, iran khalil abnous pharmaceutical research center, school of pharmacy, mashhad university of medical sciences, mashhad, iran mohammad ramezani nanotechnology research center, school of pharmacy, mashhad university of medical sciences, mashhad, iran

objective(s): first, 10-bromodecanoic acid was covalently attached to all available surface primary amines of ppi g2 and g3 to increase their lipophilicity. in the subsequent step, ppis were conjugated to the alkylcarboxylate groups of alkylcarboxylate-ppi derivatives to increase the number of surface primary amines. physicochemical properties of modified ppis were determined. transfection expe...

Journal: :nanomedicine journal 0
hamideh parhiz pharmaceutical research center, school of pharmacy, mashhad university of medical sciences, mashhad, iran department of pharmaceutical biotechnology, school of pharmacy, mashhad university of medical sciences, mashhad, iranسازمان اصلی تایید شده: دانشگاه علوم پزشکی مشهد (mashhad university of medical sciences) maryam hashemi nanotechnology research center, school of pharmacy, mashhad university of medical sciences, mashhad, iranسازمان اصلی تایید شده: دانشگاه علوم پزشکی مشهد (mashhad university of medical sciences) mohammad ramezani pharmaceutical research center, school of pharmacy, mashhad university of medical sciences, mashhad, iran department of pharmaceutical biotechnology, school of pharmacy, mashhad university of medical sciences, mashhad, iranسازمان اصلی تایید شده: دانشگاه علوم پزشکی مشهد (mashhad university of medical sciences)

gene therapy as a modern therapeutic approach has not yet advanced to a globally-approved therapeutic approach. lack of adequate reliable gene delivery system seems to be one of the major reasons from the pharmaceutical biotechnology point of view. main obstacles delaying successful application of human gene therapy are presented in this review. the unique advantages of non-biological gene carr...

Journal: :iranian journal of pharmaceutical research 0
e süleymano?lu

thermodynamic features related to preparation and use of self-assemblies formed between multilamellar and unilamellar zwitterionic liposomes and polynucleotides with various conformation and sizes are presented. the divalent metal cation or surfactant-induced adsorption, aggregation and adhesion between single- and double-stranded polyribonucleotides and phosphatidylcholine vesicles was followe...

Journal: Nanomedicine Journal 2019
Anum Habib, Faisal Qaisar Maira Riaz, Zia Ur Rehman

Cystic fibrosis (CF) is an autosomal recessive disorder caused by mutations in CFTR genes that affect chloride ion channel. The CF is a good nominee for gene therapy as the asymptomatic carriers are phenotypically normal, and the desired cells are accessible for vector delivery. Gene therapy shows promising effects involving the correction of gene or replacement of the mutant gene with the func...

Journal: :modares journal of medical sciences: pathobiology 2008
azam bolhasani mohammad taghikhani nahid ghasemi hooriyeh soleimanjahi sima rafati

objective: dna vaccines have been widely used to develop immunity against various pathogens including parasites and viruses. the potential of dna vaccine to induce an effective immune response is related to the expression levels of the encoded protein in eukaryotic cells. therefore, optimization of plasmid dna delivery system is a major concern in protein expression in order to make an efficien...

Human gene therapy has attracted increasing attention as a highly encouraging therapeutic approach to treat wide variety of diseases, other than genetically inherited and monogenic disorders. This approach entails the introduction and expression of a variety of nucleic acids into human target cells for therapeutic purposes. In this article, we review the history, highlights, recently progresses...

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