نتایج جستجو برای: heteroduplex

تعداد نتایج: 1227  

ژورنال: :مجله دانشگاه علوم پزشکی شهرکرد 0
مریم طاهرزاده قهفرخی mryam tahrzadehgharofi عفت فرخی efat farkhoi سید ابوالفتح شیرمردی seyed abolfateh shirmardi جواد صفاری چالشتری javad safari chaleshtori سمیه اسدی somayeh asadi کیهان قطره سامانی keyhan ghatreh samani مرضیه ابوالحسنی

زمینه و هدف: وقوع ناشنوایی پیش زبانی حدود 1 در 1000 تولد است که بیش از 60% موارد آن ارثی هستند. ناشنوایی اختلالی هتروژن محسوب می شود و ممکن است به علل محیطی، ژنتیکی یا هر دو رخ دهد. اخیراً جهش های ژن dfnb59 که رمز کننده پروتئین پژواکین است به عنوان عامل ناشنوایی نوع عصبی معرفی شده اند. این مطالعه با هدف بررسی نوع و فراوانی جهش های ژن dfnb59 در 100 ناشنوای غیرسندرومی، در استان چهارمحال و بختیاری ...

Journal: :Clinical chemistry 2005
Jeffrey W Stephens M Mert Sozen Ros A Whittall Muriel J Caslake Dorothy Bedford Jayshree Acharya Steven J Hurel Steve E Humphries

BACKGROUND Apolipoprotein E (apoE) is found in association with triglyceride-rich lipoproteins and is the ligand for the removal of these particles from the plasma. Genetic variations in exon 4 lead to three common gene variants: E2, E3, and E4. METHODS We performed apoE genotyping in 765 individuals with type 2 diabetes. RESULTS We identified three new variant heteroduplex patterns. Sequen...

Journal: :Journal of virology 1985
B A Wiggins S Hilliker

The genomes of temperate Salmonella typhimurium phages P22 and L share approximately 69% homology, as measured by DNA heteroduplex analysis. Alignment of the P22/L heteroduplex molecules with a P22 physical map places most of this homology between the capsid genes and genes in the vicinity of the prophage attachment sites. The degree of genetic relatedness between these phages and the lambdoid ...

Journal: :Nucleic acids research 1996
R Landgraf K S Ramamurthi D S Sigman

We have used R-loop formation and direct hybridization techniques to analyze the kinetics by which RNA is displaced from a heteroduplex by DNA of identical sequence. Using random walk simulations we were able to calculate the step times for a single displacement reaction. For RNA with a GC content of 57-60% the data indicate an RNA exchange probability of 50.06%, which is indicative of a modest...

Journal: :Blood 1994
M Bottaro E Berti A Biondi N Migone L Crosti

The possibility to detect markers of T-cell clonality at the T-cell receptor (TCR) beta and gamma loci in skin biopsy samples has proven to be helpful for the often difficult clinical and immunohistochemical diagnosis of cutaneous T-cell lymphoma (CTCL). However, particularly at the early stage of the neoplastic infiltration, an emerging clonal pattern at Southern may be obscured by the germlin...

Journal: :The Analyst 2013
Feng Chen Yongxi Zhao

Herein, using DNA adenine methylation (Dam) methyltransferase (MTase) as a model analyte, a novel fluorescence sensing strategy was developed for facile, rapid and highly sensitive detection of the activity and inhibition of the target based on methylation-blocked enzymatic recycling amplification. In this sensing system, nicking endonuclease Nt.AlwI with the methylation-sensitive property was ...

Journal: :The Journal of biological chemistry 1999
I Biswas C Ban K G Fleming J Qin J W Lary D A Yphantis W Yang P Hsieh

The MutS DNA mismatch protein recognizes heteroduplex DNAs containing mispaired or unpaired bases. We have examined the oligomerization of a MutS protein from Thermus aquaticus that binds to heteroduplex DNAs at elevated temperatures. Analytical gel filtration, cross-linking of MutS protein with disuccinimidyl suberate, light scattering, and matrix-assisted laser desorption/ionization time-of-f...

Journal: :Analytical biochemistry 2009
Bisheng Zhou Changjiang Huang Junhua Yang Jianxin Lu Qiaoxiang Dong Lu-Zhe Sun

Preparation of heteroduplexes in large quantities with high purity is essential for the measurement of DNA mismatch repair (MMR) activity. Here we report a rapid, less labor-intensive method for the preparation of a heteroduplex plasmid that expresses the enhanced green fluorescent protein (EGFP) if the mismatch is repaired correctly. The method involves the use of a wild-type and a mutated EGF...

Journal: :Cell 2001
Thorsten Allers Michael Lichten

Unitary models of meiotic recombination postulate that a central intermediate containing Holliday junctions is resolved to generate either noncrossover or crossover recombinants, both of which contain heteroduplex DNA. Contrary to this expectation, we find that during meiosis in Saccharomyces cerevisiae, noncrossover heteroduplex products are formed at the same time as Holliday junction interme...

Journal: :Cell 2004
Olga M Mazina Alexander V Mazin Takuro Nakagawa Richard D Kolodner Stephen C Kowalczykowski

Crossover and noncrossover recombinants can form by two different pathways during meiotic recombination in Saccharomyces cerevisiae. The MER3 gene is known to affect selectively crossover, but not noncrossover, recombination. The Mer3 protein is a DNA helicase that unwinds duplex DNA in the 3' to 5' direction. To define the underlying molecular steps of meiotic recombination, we investigated th...

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