نتایج جستجو برای: g genotyping

تعداد نتایج: 462990  

2015
Samaneh HAJIHOSEINI Majid MOTOVALI-BASHI Mohammad Amin HONARDOOST Nader ALERASOOL

BACKGROUND β-thalassemia, a monogenic autosomal recessive disorder, is prevalent in Middle East, particularly in Iran. In Iran, near to 20 mutations in the β-globin gene are introduced as common mutations with varying incidence frequencies in each city. Therefore, detection and screening for couples at high risk can help to solve the problems of this disease. In this study, optimized genotyping...

Journal: :Clinical chemistry 2009
Jin Li Lilin Wang Pasi A Jänne G Mike Makrigiorgos

BACKGROUND DNA genotyping with mutation-specific TaqMan(R) probes (Applied Biosystems) is broadly used in detection of single-nucleotide polymorphisms but is less so for somatic mutations because of its limited selectivity for low-level mutations. We recently described coamplification at lower denaturation temperature-PCR (COLD-PCR), a method that amplifies minority alleles selectively from mix...

2017
Bugi Ratno Budiarto

Background: A reliable method to detect gene polymorphisms must be established to eliminate genotyping errors due to false PCR amplification. In the previous study, we have developed AS-PCR (Allele Specific-Polymerase Chain Reaction) to detect HER2 Ile655Val gene polymorphism with good specificity and sensitivity, yet it produces some errors. This study is aimed to eliminate the source of genot...

Journal: :Blood 2002
Dorothea Zucker-Franklin

3. Xu Y, Carr LG, Bosron WF, Li T-K, Edenberg HJ. Genotyping of human alcohol dehydrogenases at the ADH2 and ADH3 loci following DNA sequence amplification. Genomics. 1988;2:209-214. 4. Aoshima T, Umetsu K, Yuasa I, Watanabe G, Suzuki T. Simultaneous genotyping of alcohol dehydrogenase 2 (ADH2) and aldehyde dehydrogenase 2 (ALDH2) loci by amplified product length polymorphism (APLP) analysis. E...

2014
Anna Szpakowicz Witold Pepinski Ewa Waszkiewicz Dominika Maciorkowska Małgorzata Skawronska Anna Niemcunowicz-Janica Robert Milewski Sławomir Dobrzycki Włodzimierz Jerzy Musial Karol Adam Kaminsk

The authors and the editors retract this publication. The authors have identified a mistake in the genotyping analyses underlying this study. Although the result that a 9p21.3 polymorphism affects the prognosis after STEMI in high-risk patients stands, the re-evaluation of the data shows that the allele A is the correct risk allele for death for the rs4977574 polymorphism, and not allele G as r...

2015
Linda Chapdeleine Mekue Mouafo Hélène Péré Angélique Ndjoyi-Mbiguino Donato Koyalta Jean De Dieu Longo François-Xavier Mbopi-Kéou Coumba Toure Kane Laurent Bélec

Resistance genotypes in pol gene of HIV-1 were obtained by the ViroSeq(®) HIV-1 Genotyping System v2.0 (Celera Diagnostics, Alameda, CA, USA) in 138 of 145 (95%) antiretroviral treatment-experienced adults in virological failure living in Central Africa (Cameroon, Central African Republic, Chad, Gabon). HIV-1 group M exhibited broad genetic diversity. Performance of the 7 ViroSeq(®) sequencing ...

2005
Tatsuo Kanno Werner Aufsatz Estelle Jaligot M. Florian Mette Marjori Matzke Antonius J.M. Matzke

Supplementary Methods Primers used for genotyping: The α’ promoter silencing system and the drd1 mutant alleles have been described previously (Kanno et al., 2004). The work reported here was carried out using plants carrying the drd1-6 allele. The drd1-6 mutation produces a G to A substitution (TGGTCA to TGATCA), producing a new NdeII restriction enzyme site (/GATC) that can be used for genoty...

Journal: :Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics 2000
X Jiang G Hou J Yu B Huang D Xu

OBJECTIVE To analyze the sequence difference between human A, B, and O alleles and establish the method of ABO genotyping by PCR direct sequencing. METHODS PCR-direct sequencing technique was used to analyze two regions of cDNA from A transferase gene, 233-433 and 660-788. RESULTS Two nucleotide substitutions at 258th and 297th were found in 233-433 region, and a nucleotide substitution at ...

پایان نامه :وزارت علوم، تحقیقات و فناوری - دانشگاه تربیت مدرس - دانشکده علوم زیستی 1390

در جوامع پزشکی مهار موثر لخته شدن پلاکت به نقطه عطفی در درمان بیماران مبتلا به بیماری های قلبی مبدل گشته است. تجویز همزمان پلاویکس و آسپیرین کاهش چشمگیری را در بروز مجدد وقایع قلبی-عروقی در بیماران مبتلا به بیماری قلبی از خود نشان داده است. با این وجود مطالعات بیانگر این حقیقت است که پاسخ درمانی به پلاویکس در میان بیماران متفاوت می باشد و مهار کنندگی کم یا ناقص در بیماران، رابطه مستقیمی با افزا...

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