نتایج جستجو برای: dhplc

تعداد نتایج: 390  

Journal: :Anesthesia and analgesia 2005
Huei-Ming Yeh Mei-Chuan Tsai Yi-Ning Su Rong-Ching Shen Jeuy-Jen Hwang Wei-Zen Sun Ling-Ping Lai

We performed the present study to identify the mutation in patients in Taiwan with malignant hyperthermia (MH). We also test the hypothesis that a denaturing high-performance liquid chromatography (DHPLC) protocol can be used for mutation detection in these patients. We identified five Taiwanese patients with typical clinical presentations of MH after general anesthesia. We also enrolled 50 hea...

Journal: :Mitochondrion 2005
David Meierhofer Johannes A Mayr Sabine Ebner Wolfgang Sperl Barbara Kofler

Alterations of the mitochondrial DNA (mtDNA) are implicated in various pathological conditions. In this study, we used denaturing high performance liquid chromatography (DHPLC) as a method to rapidly screen the entire mtDNA for mutations. Overlapping DNA fragments, amplified by one single cycling protocol from frozen pre-formulated PCR mixes, were subjected to DHPLC analysis. Single DHPLC injec...

Journal: :iranian biomedical journal 0
حمیدرضا خرم خورشید hamid reza khorram khorshid raymond dalgleish

background: several methods have been developed for detection of sequence variation in genes and each has its advantages and disadvantages. a disadvantage of them is that the simpler, cost-effective methods are commonly perceived as being less sensitive in their detection of sequence variation, whereas those with proven sensitivity have a requirement for complex or expensive laboratory equipmen...

Journal: :Clinical chemistry 2001
E Schaeffeler T Lang U M Zanger M Eichelbaum M Schwab

BACKGROUND The thiopurine S:-methyltransferase (TPMT) genetic polymorphism has a significant clinical impact on the toxicity of thiopurine drugs, which are used in the treatment of leukemia and as immunosuppressants. To date, 10 mutant alleles are known that are associated with intermediate or low TPMT activity. To facilitate rapid screening of clinically relevant TPMT mutations, we developed a...

Journal: :Molecular Vision 2008
Ana Bustamante-Aragones Elena Vallespin Marta Rodriguez de Alba Maria Jose Trujillo-Tiebas Cristina Gonzalez-Gonzalez Dan Diego-Alvarez Rosa Riveiro-Alvarez Isabel Lorda-Sanchez Carmen Ayuso Carmen Ramos

PURPOSE Leber congenital amaurosis (LCA) is one of the most severe inherited retinal dystrophies with the earliest age of onset. Mutations in the Crumbs homologue 1 (CRB1; OMIM 600105) gene explain 10%-24% of cases with LCA depending on the population. The aim of the present work was to study a fetal mutation associated to LCA in maternal plasma by a new methodology in the noninvasive prenatal ...

Journal: :Nucleic acids research 1998
W Liu D I Smith K J Rechtzigel S N Thibodeau C D James

Denaturing high performance liquid chromatography (DHPLC) has been described recently as a method for screening DNA samples for single nucleotide polymorphisms and inherited mutations. Thirty-eight DNAs, 22 of which were heterozygous for previously characterized rearranged transforming gene (RET) or cystic fibrosis transmembrane conductance regulator gene (CFTR) mutations or polymorphisms, were...

Journal: :Journal of clinical microbiology 2002
Liran I Shlush Doron M Behar Adrian Zelazny Nathy Keller James R Lupski Arthur L Beaudet Dani Bercovich

A serogroup C meningococcal outbreak that occurred in an Israeli Arab village led to a massive vaccination campaign. During the subsequent 18 months, new cases of type B Neisseria meningitidis infection were revealed. To investigate the influence of vaccination on bacteriological epidemiology, bacteria were isolated from individuals at the outbreak location, patients with several additional oth...

Journal: :Human mutation 2001
W Xiao P J Oefner

Denaturing high-performance liquid chromatography (DHPLC) compares two or more chromosomes as a mixture of denatured and reannealed PCR amplicons, revealing the presence of a mutation by the differential retention of homo- and heteroduplex DNA on reversed-phase chromatography supports under partial denaturation. Temperature determines sensitivity, and its optimum can be predicted by computation...

Journal: :Neuroepidemiology 2011
K C Bueno S P Gouvea A B Genari C A Funayama D L Zanette W A Silva A B Oliveira R H Scola L C Werneck W Marques

BACKGROUND Spinal muscular atrophy is a common autosomal recessive neuromuscular disorder caused by mutations in the SMN1 gene. Identification of spinal muscular atrophy carriers has important implications for individuals with a family history of the disorder and for genetic counseling. The aim of this study was to determine the frequency of carriers in a sample of the nonconsanguineous Brazili...

2013
Hassan Dastsooz Nazanin Vahedi Majid Fardaei

OBJECTIVE(S) Denaturing high performance liquid chromatography (DHPLC) is a high throughput approach for screening DNA sequence variations. To assess oven calibration, cartridge performance, buffer composition and stability, the WAVE Low and High Range Mutation Standards are employed to ensure reproducibility and accuracy of the chromatographic analysis. The purpose of this study was to provide...

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