نتایج جستجو برای: histone

تعداد نتایج: 43029  

Journal: :jundishapur journal of natural pharmaceutical products 0
maryam moradi binabaj biochemistry and metabolic disorders research center, golestan university of medical sciences, gorgan, ir iran seyed ahmad hosseini nutrition and metabolic disease research center, ahvaz jundishapur university of medical sciences, ahvaz, ir iran alireza khoshbin khoshnazar biochemistry and metabolic disorders research center, golestan university of medical sciences, gorgan, ir iran jahanbakhsh asadi biochemistry and metabolic disorders research center, golestan university of medical sciences, gorgan, ir iran; biochemistry and metabolic disorders research center, golestan university of medical sciences, gorgan, ir iran. tel: +98-1732440225, fax: +98-1732421651

conclusions the increasing cell toxicity, apoptosis-inducing effects and decreasing telomerase activity may play an important role in the valproic acid and radiation mechanism. the current survey suggested that it is likely beneficial to combine valproic acid and gamma radiation to treat breast cancer. results combination of valproic acid and gamma radiation increased significantly cell toxicit...

Interaction between DNA and histone H, was investigated in the presence and absence of sodium-n-dodecyl sulphate (SDS) and dodecyl trimethylammonium bromide (DTAB) at temperatures of 27 and 37?C, in 2.5 mM phosphate buffer, pH 6.4 by UV spectrophotometry, equilibriumdialysis and titration. The presence of 1.33 mM SDS caused histone H to fold and to further contact DNA. Binding data were use...

Journal: :journal of sciences islamic republic of iran 0

interaction between dna and histone h, was investigated in the presence and absence of sodium-n-dodecyl sulphate (sds) and dodecyl trimethylammonium bromide (dtab) at temperatures of 27 and 37?c, in 2.5 mm phosphate buffer, ph 6.4 by uv spectrophotometry, equilibriumdialysis and titration. the presence of 1.33 mm sds caused histone h to fold and to further contact dna. binding data were used in...

Journal: :international journal of hematology-oncology and stem cell research 0
ali dehghani fard sarem cell research center-scrc, sarem women's hospital, tehran, iran. seyed ahmad hosseini department of nutrition, allied health sciences school, ahvaz jundishapur university of medical sciences, ahvaz, iran. mohammad shahjahani department of hematology and blood banking, faculty of medical sciences, tarbiat modares university, tehran, iran. fatemeh salari thalassemia and hemoglobinopathy research center, jundishapur university of medical sciences, ahvaz, iran. kaveh jaseb thalassemia and hemoglobinopathy research center, jundishapur university of medical sciences, ahvaz, iran.

objective: the use of fetal hemoglobin (hbf) inducer drugs is considered as a novel approach in treatment of β-hemoglobinopathies, especially β- thalassemia and sickle cell disease. hbf inducers including hydroxyurea, histone deacetylase (hdac) inhibitor agents such as sodium butyrate, azacitidine, decitabine and new immunomodulator drugs like pomalidomide, lenalidomide and thalidomide can redu...

Journal: :iranian red crescent medical journal 0
ladan akbarzadeh department of pharmacology, shahid beheshti university, tehran, ir iran; department of pharmacology, shahid beheshti university, tehran, ir iran. tel: +98-9121034458, fax: +98-2122439969 taraneh moini zanjani department of pharmacology, shahid beheshti university, tehran, ir iran masoumeh sabetkasaei department of pharmacology, shahid beheshti university, tehran, ir iran

conclusions vpa and cbz treatments caused a decrease in β-catenin and vegf levels in sw480 colon cancer cell lines. these results suggest that cbz can be considered a potential antitumor drug with potencies different from vpa. methods in the present experimental study, implemented during 2014 - 2015 in iran, after incubation of cells into 96-well plates with 5,500 cells/well, the tested drugs w...

Effect of trichostatin A on histone deacetylase 1 (HDAC 1) and CIP/KIP (p21CIP1/WAF1, p27KIP1, and p57KIP2) gene expression, cell growth inhibition and apoptosis induction in lung cancer COR-L105 cell line. Abstract Background: Lung cancer is one the leading cause of cancer-related death worldwide, with more than 1.2 million deaths each year. In addition to genetic mutations, epigenetic modif...

Journal: :medical journal of islamic republic of iran 0
azra rabbani from the institute of biochemistry and biophysics, university of tehran, tehran mahvash jafari the department of biochemistry, faculty of medicine, baghiatollah university of medical sciences, tehran, i.r. iran.

in this study calf thymus chromatin was fractionated into active (s1 and s2) and inactive (p 2) chromatin. then the interaction of an anthracyc1ine antibiotic, adriamycin, with these fractions was investigated employing absorption and difference uv nis spectroscopy and sds and agarose gel electrophoreses. the results suggest that the binding of adriamycin to the s 1 fraction is slight but s2 an...

E Kordestani Shrgh MA Sadighi Gilani, N Sodeifi R Favaedi,

Background During mammalian spermatogenesis unique and dynamic epigenetic events occur leading to chromatin condensation. Through these events, histone demethylases such as JMJD1A play important roles in compaction of sperm chromatin, due to regulation of histone methylation dynamics and alteration of chromatin structure. As �histone methylation� is one of the best-characterized modifications i...

Journal: :medical journal of islamic republic of iran 0
azra rabbani from the institute of biochemistry and biophysics, tehran university of medical sciences, tehran, islamic republic of iran. marzieh hagsharifia tagavi bahram goliaei

isotherms of the binding of the anthracyciine antibiotic, adriamycin (adriblastin), to dna histone complexes was studied by means of spectroscopic analysis. the results indicated that: (a) binding of adriamycin to histones reduced the interaction of histones with dna, (b) binding of the drug to dna did not change the binding affinity of histone to dna and, (c) in the explored binding range of r

Journal: :iranian journal of pharmaceutical research 0
afshin zarghi department of medicinal chemistry, faculty of pharmacy, shahid beheshti university of medical sciences atefeh haji agha bozorgi department of medicinal chemistry, faculty of pharmacy, shahid beheshti university of medical sciences

histone deacetylase inhibitors have gained a great deal of attention recently for the treatment of cancers and inflammatory diseases. so design of new inhibitors is of great importance in pharmaceutical industries and labs. creating pharmacophor models in order to design new molecules or search a library for finding lead compounds is of great interest. this approach reduces the overall cost ass...

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