نتایج جستجو برای: dhplc

تعداد نتایج: 390  

Journal: :Journal of clinical microbiology 2005
Oliver Goldenberg Stefanie Herrmann Thomas Adam Gina Marjoram George Hong Ulf B Göbel Barbara Graf

A novel denaturing high-performance liquid chromatography (DHPLC)-based technique allows rapid high-resolution analysis of PCR products. We used this technique for unequivocal molecular identification of seven Candida species. We show the application of this PCR/DHPLC approach for direct detection and identification of yeast species from blood cultures and for detection of Candida colonization ...

Journal: :Prenatal diagnosis 2001
P Bénit J P Bonnefont A Kara Mostefa C Francannet A Munnich P F Ray

Tuberous sclerosis (TSC) is a frequent autosomal-dominant condition (affecting 1 in 6000 individuals) caused by various mutations in either the hamartin (TSC1) or the tuberin gene (TSC2). This allelic and non-allelic heterogeneity makes genetic counseling and prenatal diagnosis difficult, especially as a significant proportion of TSC cases are due to de novo mutations. For this reason the ident...

Journal: :Journal of clinical microbiology 2003
William Hurtle Luther Lindler Wei Fan David Shoemaker Erik Henchal David Norwood

Denaturing high-performance liquid chromatography (DHPLC) has been used extensively to detect genetic variation. We used this method to detect and identify Yersinia pestis KIM5 ciprofloxacin-resistant isolates by analyzing the quinolone resistance-determining region (QRDR) of the gyrase A gene. Sequencing of the Y. pestis KIM5 strain gyrA QRDR from 55 ciprofloxacin-resistant isolates revealed f...

Journal: :international journal of reproductive biomedicine 0
mir davood omrani agneta nordenskhold

background: for screening sequence variations in genes, rapid turnover time is of fundamental importance. while, many of the current methods are unfortunately time consuming and technically difficult to implement. denaturing high-performance liquid chromatography (dhplc) method had been shown to be a high-throughput, time saving, and economical tool for mutation screening. objective: in the pre...

2006
Monia Magliozzi Maria Piane Isabella Torrente Lorenzo Sinibaldi Giovanni Rizzo Camilla Savio Patrizia Lulli Alessandro De Luca Bruno Dallapiccola Luciana Chessa

The gene for ataxia-telangiectasia (A-T:MIM: #208900), ATM, spans about 150 kb of genomic DNA and is composed of 62 coding exons. ATM mutations are found along the entire coding sequence of the gene, without evidence of mutational hot spots. Using DNA as the starting material, we used denaturing high performance liquid chromatography (DHPLC) technique to search for ATM gene mutations. Initially...

Journal: :Nucleic acids research 2002
Dajun Deng Guoren Deng Michael F Smith Jing Zhou Huijun Xin Steven M Powell Youyong Lu

We report here a novel method to simultaneously detect CpG methylation and single nucleotide polymorphisms (SNPs) using denaturing high performance liquid chromatography (DHPLC). PCR products of bisulfite-modified CpG islands were separated using DHPLC. BstUI digestion and DNA sequencing were used in confirmation studies. Consistent with the BstUI digestion assay, the 294 bp PCR product of the ...

Journal: :Methods in molecular biology 2005
Donna Lee Fackenthal Pei Xian Chen Ted Howe Soma Das

Denaturing high-performance liquid chromatography (DHPLC) is an accurate and efficient screening technique used for detecting DNA sequence changes by heteroduplex analysis. It can also be used for genotyping of single nucleotide polymorphisms (SNPs). The high sensitivity of DHPLC has made this technique one of the most reliable approaches to mutation analysis and, therefore, used in various are...

Journal: :Journal of Biomedicine and Biotechnology 2008
Renata Guedes Koyama Rosa M. R. P. S. Castro Marco Túlio De Mello Sergio Tufik Mario Pedrazzoli

Insertion-deletion polymorphism (InDeL) is the second most frequent type of genetic variation in the human genome. For the detection of large InDeLs, researchers usually resort to either PCR gel analysis or RFLP, but these are time consuming and dependent on human interpretation. Therefore, a more efficient method for genotyping this kind of genetic variation is needed. In this report, we descr...

Journal: :Human mutation 2005
Yi-Ning Su Chia-Cheng Hung Hung Li Chien-Nan Lee Wen-Fang Cheng Po-Nien Tsao Ming-Cheng Chang Chia-Li Yu Wu-Shiun Hsieh Win-Li Lin Su-Ming Hsu

Autosomal recessive spinal muscular atrophy (SMA) is a common, fatal neuromuscular disease caused by homozygous absence of the SMN1 gene in approximately 94% of patients. However, a highly homologous SMN2 gene exists in the same chromosome interval, centromeric to SMN1, and hampers detection of SMN1. We present a new, rapid, simple, and highly reliable method for detecting the SMN1 deletion/con...

Journal: :Journal of clinical microbiology 2003
Jianduan Li Daniela S Gerhard Zhengyan Zhang Phyllis C Huettner Jason Wright Loan Nguyen Danielle Lu Janet S Rader

Human papillomaviruses (HPVs) are important in the development of human cancers, including cervical and oral tumors. However, most existing methods for HPV typing cannot routinely distinguish among the more than 100 distinct types of HPV or the natural HPV intratypic variants that have also been documented. To address this problem, we developed a novel method, general primer-denaturing high-per...

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