نتایج جستجو برای: multiplex ligation

تعداد نتایج: 42263  

2017
Robbert D.A. Weren Arjen R. Mensenkamp Michiel Simons Astrid Eijkelenboom Aisha S. Sie Hicham Ouchene Monique van Asseldonk Encarna B. Gomez‐Garcia Marinus J. Blok Joanne A. de Hullu Marcel R. Nelen Alexander Hoischen Johan Bulten Bastiaan B.J. Tops Nicoline Hoogerbrugge Marjolijn J.L. Ligtenberg

With the recent introduction of Poly(ADP-ribose) polymerase inhibitors, a promising novel therapy has become available for ovarian carcinoma (OC) patients with inactivating BRCA1 or BRCA2 mutations in their tumor. To select patients who may benefit from these treatments, assessment of the mutation status of BRCA1 and BRCA2 in the tumor is required. For reliable evaluation of germline and somati...

Journal: :Nucleic Acids Research 2005
Anders O. H. Nygren Najim Ameziane Helena M. B. Duarte Raymon N. C. P. Vijzelaar Quinten Waisfisz Corine J. Hess Jan P. Schouten Abdellatif Errami

Copy number changes and CpG methylation of various genes are hallmarks of tumor development but are not yet widely used in diagnostic settings. The recently developed multiplex ligation-dependent probe amplification (MLPA) method has increased the possibilities for multiplex detection of gene copy number aberrations in a routine laboratory. Here we describe a novel robust method: the methylatio...

Journal: :Nucleic acids research 1994
P D Grossman W Bloch E Brinson C C Chang F A Eggerding S Fung D M Iovannisci S Woo E S Winn-Deen

We describe a non-isotopic, semi-automated method for large-scale multiplex analysis of nucleic acid sequences, using the cystic fibrosis transmembrane regulator (CFTR) gene as an example. Products of a multiplex oligonucleotide ligation assay (OLA) are resolved electrophoretically from one another and from unligated probes under denaturing conditions with fluorescence detection. One ligation p...

Journal: :Haematologica 2009
Marion Phylipsen Antonio Amato Maria Pia Cappabianca Jan Traeger-Synodinos Emmanuel Kanavakis Nazli Basak Renzo Galanello Teresa Tuveri Giovanni Ivaldi Cornelis L Harteveld Piero C Giordano

When the molecular background of couples requesting prevention is unclear, family analysis and tools to define rare mutations are essential. We report two novel deletion defects observed in an Italian and in a Turkish couple. The first proband presented with microcytic hypochromic parameters without iron deficiency, a normal HbA(2) and an elevated HbF (10.6%). His father presented with a simila...

2014
Steffi Werler Joachim Wistuba

Other novel techniques are also available that can provide fast and reliable diagnosis of KS, for example, array based multiplex ligation-dependent probe amplification (MLPA)4 for the rapid screening of chromosomal aneuploidies or the equally elegant assessment of the copy number of the androgen receptor by quantitative polymerase chain reaction (qPCR).5 These techniques should also be consider...

2015
Emmanuelle Souzeau Melanie Hayes Jonathan B. Ruddle James E. Elder Sandra E. Staffieri Lisa S. Kearns David A. Mackey Tiger Zhou Bronwyn Ridge Kathryn P. Burdon Andrew Dubowsky Jamie E. Craig

PURPOSE To evaluate the prevalence and the diagnostic utility of testing for CYP1B1 copy number variation (CNV) in primary congenital glaucoma (PCG) cases unexplained by CYP1B1 point mutations in The Australian and New Zealand Registry of Advanced Glaucoma. METHODS In total, 50 PCG cases either heterozygous for disease-causing variants or with no CYP1B1 sequence variants were included in the ...

Journal: :Journal of separation science 2011
Virginia García-Cañas Monica Mondello Alejandro Cifuentes

New DNA amplification methods are continuously developed for sensitive detection and quantification of specific DNA target sequences for, e.g. clinical, environmental or food applications. These new applications often require the use of long DNA oligonucleotides as probes for target sequences hybridization. Depending on the molecular technique, the length of DNA probes ranges from 40 to 450 nuc...

2012
Gabriella Ujhelyi Jeroen P van Dijk Theo W Prins Marleen M Voorhuijzen AM Angeline Van Hoef Henriek G Beenen Dany Morisset Kristina Gruden Esther J Kok

BACKGROUND With the increasing number of GMOs on the global market the maintenance of European GMO regulations is becoming more complex. For the analysis of a single food or feed sample it is necessary to assess the sample for the presence of many GMO-targets simultaneously at a sensitive level. Several methods have been published regarding DNA-based multidetection. Multiplex ligation detection...

2015
Eileen M Boyle Paula Z Proszek Martin F Kaiser Dil Begum Nasrin Dahir Suvi Savola Christopher P Wardell Xavier Leleu Fiona M Ross Laura Chiecchio Gordon Cook Mark T Drayson Richard G Owen John M Ashcroft Graham H Jackson James Anthony Child Faith E Davies Brian A Walker Gareth J Morgan

Risk stratification in myeloma requires an accurate assessment of the presence of a range of molecular abnormalities including the differing IGH translocations and the recurrent copy number abnormalities that can impact clinical behavior. Currently, interphase fluorescence in situ hybridization is used to detect these abnormalities. High failure rates, slow turnaround, cost, and labor intensive...

2012
David J. Bunyan Jonathan L.A. Callaway Nadja Laddach

BACKGROUND In recent studies, partial deletions of the azoospermia factor c region (AZFc) on the Y-chromosome have been detected in males with infertility problems. However, there has been a lot of debate about their significance. In order to study such deletions, a simple but accurate method for their detection was applied in this study. METHODS We present data obtained from the Multiplex Li...

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