نتایج جستجو برای: dna methyltransferase

تعداد نتایج: 521977  

Journal: :The Analyst 2014
Lan Ma Min Su Tao Li Zhenxin Wang

A microarray-based resonance light scattering assay, with the combination of methylation-sensitive endonuclease and gold nanoparticle (GNP) probes, has been proposed to sensitively distinguish the DNA methylation level as low as 0.01% (10 pM methylated DNA in 100 nM total DNA) and detect human DNA methyltransferase 1 (Dnmt1) down to 0.1 U mL(-1).

Journal: :iranian red crescent medical journal 0
ebrahim faghihloo department of virology, school of public health, tehran university of medical sciences, tehran, ir iran majid sadeghizadeh department of genetics, faculty of biological sciences, tarbiat modares university, tehran, ir iran shohreh shahmahmoodi department of virology, school of public health, tehran university of medical sciences, tehran, ir iran talat mokhtari-azad department of virology, school of public health, tehran university of medical sciences, tehran, ir iran; department of virology, school of public health, tehran university of medical sciences, tehran, ir iran. tel/fax: +98-2188962343

results hpv-16 e6 and e7 proteins reduced e-cadherin expression 3.7 and 2.2 times when compared with control cells (p = 0.0221 and p = 0.0461, respectively). this reduction was greater in hpv-16 e6-expressing cells than in hpv-16 e7-expressing cells. although hpv-16 e6 and e7 increased dna methyltransferase 1 expression 2.6 and 3.4 times, respectively (p = 0.0133 and p = 0.0113) when compared w...

2015
Liming Li Cui Xu Jia Long Danbei Shen Wuqing Zhou Qiyan Zhou Jia Yang Mingjun Jiang

In SiHa and CaSki cells, E6 and E7-targeting shRNA specifically and effectively knocked down human papillomavirus (HPV) 16 E6 and E7 at the transcriptional level, reduced the E6 and E7 mRNA levels by more than 80% compared with control cells that expressed a scrambled-sequence shRNA. E6 and E7 repression resulted in down-regulation of DNA methyltransferase mRNA and protein expression, decreased...

Journal: :Nucleic acids research 1997
C Finta A Kiss

The interaction between the GGCC-specific Bsp RI DNA methyltransferase (M. Bsp RI) and substrate DNA was studied with footprinting techniques using a DNA fragment that was unmodified on both strands. Footprinting with DNase I revealed an approximately 14 bp protected region. Footprinting with dimethylsulfate detected major groove interactions with the guanine bases of the recognition sequence. ...

Journal: :Science 2006
Mary Grace Goll Finn Kirpekar Keith A Maggert Jeffrey A Yoder Chih-Lin Hsieh Xiaoyu Zhang Kent G Golic Steven E Jacobsen Timothy H Bestor

The sequence and the structure of DNA methyltransferase-2 (Dnmt2) bear close affinities to authentic DNA cytosine methyltransferases. A combined genetic and biochemical approach revealed that human DNMT2 did not methylate DNA but instead methylated a small RNA; mass spectrometry showed that this RNA is aspartic acid transfer RNA (tRNA(Asp)) and that DNMT2 specifically methylated cytosine 38 in ...

Journal: :Trends in genetics : TIG 2001
L Duret

Determination of trace amounts of 5-methylcytosine in DNA by reverse-phase highperformance liquid chromatography. Anal. Biochem. 164, 164–169 6 Bird, A.P. (1995) Gene number, noise reduction and biological complexity. Trends Genet. 11, 94–100 7 Bird, A.P. and Wolffe, A.P. (1999) Methylationinduced repression – belts, braces, and chromatin. Cell 99, 451–454 8 Hung, M.S. et al. (1999) Drosophila ...

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