نتایج جستجو برای: dna release

تعداد نتایج: 711962  

Journal: :Physical chemistry chemical physics : PCCP 2013
Hidehiko Asanuma Zhifeng Jiang Katsuyoshi Ikeda Kohei Uosaki Hua-Zhong Yu

Plasmonic heating to trigger release of oligonucleotides from nanoconjugates is potentially useful for therapeutic purposes and designed assembly of DNA nanostructures. In the past, great controllability has been achieved by introducing distinctive absorption nanoparticle centers, where the anchoring bond (e.g., sulfur-gold bond) has been selectively broken. Instead of releasing the surface-bou...

2012
Olga Zafra María Lamprecht-Grandío Carolina González de Figueras José Eduardo González-Pastor

Extracellular DNA (eDNA) release is a widespread capacity described in many microorganisms. We identified and characterized lysis-independent eDNA production in an undomesticated strain of Bacillus subtilis. DNA fragments are released during a short time in late-exponential phase. The released eDNA corresponds to whole genome DNA, and does not harbour mutations suggesting that is not the result...

2011
Yongguang Tao Shuang Liu Victorino Briones Theresa M. Geiman Kathrin Muegge

Inactivation of tumor suppressor genes plays an important role in tumorigenesis, and epigenetic modifications such as DNA methylation are frequently associated with transcriptional repression. Here, we show that gene silencing at selected genes with signs of DNA hypermethylation in breast cancer cells involves Pol II stalling. We studied several repressed genes with DNA hypermethylation within ...

Journal: :iranian journal of chemistry and chemical engineering (ijcce) 2015
m. christe sonia mary s. sasikumar

in the present study, floating drug delivery beads (fdds) were prepared with sodium alginate/ starch blend as a matrix, sodium hydrogen carbonate as a pore forming agent, methyl cellulose as a binder and barium chloride solution as a hardening agent. in order to prepare the beads with different porosity and morphology the ratio between pore forming agent to polymer blend and ratio of the consti...

Journal: :Zeitschrift fur Naturforschung. C, Journal of biosciences 1995
M Reitz G Löber P Kleemann W Dick

After incubation with DNA human lymphocytes release neutral and acid DNase activities into the culture medium; the release depends on DNA concentration and time of cultivation. The electrophoretic mobility of the released neutral DNase activity is in accordance with DNase I and the electrophoretic mobility of the released acid DNase activity with DNase II. The released DNase activities do not o...

Journal: :Medicine in drug discovery 2022

• When PLA/PEG/Chitosan/FA/DNA nanoparticles interact with MCF-7 cells, their loading percentage and biocompatibility improve. Physicochemical properties of for properly targeted transfer to cells. An increase in Chitosan-FA on gene efficiency was seen positively by nanoparticles. The ability Chitosan-Folic acid PLA-PEG polymers delivery into cells evaluated. copolymer is one the most appealing...

Journal: :Proceedings of the National Academy of Sciences of the United States of America 2014
Mohammad R Ebrahimkhani Ali Daneshmand Aprotim Mazumder Mariacarmela Allocca Jennifer A Calvo Nona Abolhassani Iny Jhun Sureshkumar Muthupalani Cenk Ayata Leona D Samson

Inflammation is accompanied by the release of highly reactive oxygen and nitrogen species (RONS) that damage DNA, among other cellular molecules. Base excision repair (BER) is initiated by DNA glycosylases and is crucial in repairing RONS-induced DNA damage; the alkyladenine DNA glycosylase (Aag/Mpg) excises several DNA base lesions induced by the inflammation-associated RONS release that accom...

Journal: :Journal of virology 1974
B Labedan J Legault-Demare

Each T5 stock contains a population of particular phages that, just after adsorption onto the host bacteria. release their entire chromosome outside the bacterial membrane in a place where it is sensitive to bacterial enzymes. This release takes place before the sensitization step to deprivation of calcium and before the transfer of the first-step DNA fragment. Secondarily, this released DNA is...

Journal: :The Journal of biological chemistry 1985
C Andrews J P Richardson

Dissociation of RNA and DNA from Escherichia coli RNA polymerase in transcription complexes prepared with enzyme molecules located within and near a rho-dependent transcription termination region on bacteriophage T7 D111 DNA has been studied using a membrane filter-binding assay. Rho protein with ATP present mediated rapid (half-time approximately 27 s) simultaneous dissociation of about 50% of...

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