نتایج جستجو برای: multiplex ligation dependentprobe amplification

تعداد نتایج: 97340  

Journal: :BioTechniques 2007
Piotr Kozlowski Mei Lin Lynsey Meikle David J Kwiatkowski

Transgenic mouse alleles continue to be used heavily in biomedical research (1). Transgenes insert into the genome at random sites, typically in a tandem array of 1 to 20 copies. Both Southern blot analysis and real-time PCR can be used for determining the zygosity of transgenes, but each have practical and technical limitations (2–4). Here we describe a robust, easily implemented method for de...

Journal: :The Malaysian journal of pathology 2014
N H Hamidah A R Munirah A Hafiza A R Farisah A Shuhaila M N Norzilawati M Y Jamil O Ainoon

Prenatal diagnosis is essential in the new era of diagnosis and management of genetic diseases in obstetrics. Multiple ligation-dependent probe amplification (MLPA) is a recent technique for prenatal diagnosis for the relative quantification of 40 different nucleic acid sequences in one single reaction. We had utilized the MLPA technique in detecting aneuploidies in amniotic fluid samples from ...

2013
Cathy B. Moelans Frederik Holst Olaf Hellwinkel Ronald Simon Paul J. van Diest

Prevalence of ESR1 amplification in breast cancer is highly disputed and discrepancies have been related to different technical protocols and different scoring approaches. In addition, pre-mRNA artifacts have been proposed to influence outcome of ESR1 FISH analysis. We analyzed ESR1 gene copy number status combining an improved RNase FISH protocol with multiplex ligation-dependent probe amplifi...

Journal: :Molecular Cytogenetics 2021

Abstract Background Molecular genetic testing for the 11p15-associated imprinting disorder Beckwith-Wiedemann syndrome (BWS) is challenging because of molecular heterogeneity and complexity affected imprinted regions. An integrated approach to analyze epigenetic-genetic alterations required accurate diagnosis BWS. Case presentation : We reported a Chinese case with BWS detected by SNP array ana...

Journal: :Genetic testing 2003
Anna Erlandson Lena Samuelsson Bengt Hagberg Mårten Kyllerman Mihailo Vujic Jan Wahlström

Mutations in the methyl-CpG-binding protein-2 (MECP2) gene on Xq28 have been found to be a cause of Rett syndrome (RS). In a previous mutation screening, we found MECP2 mutations in 81% of Swedish classical Rett women. In this study, we have analyzed 22 patients for MECP2 deletions using multiplex-ligation-dependent probe amplification (MLPA). Clinically, 11 of the patients who were classical R...

Journal: :Electrophoresis 2005
Tommy Gerdes Maria Kirchhoff Thue Bryndorf

For use in routine prenatal diagnostics, we developed software and methods for automatic aneuploidy detection based on a commercial multiplex ligation-dependent probe amplification (MLPA) kit. Software and methods ensure a reliable, objective, and fast workflow, and may be applied to other types of MLPA kits. Following CE of MLPA amplification products, the software automatically identified the...

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