نتایج جستجو برای: multiplex ligation dependentprobe amplification

تعداد نتایج: 97340  

Journal: :Annals of Hematology 2021

Abstract Chromosomal abnormalities play an important role in classification and prognostication of myelodysplastic syndrome (MDS) patients. However, more than 50% low-risk MDS patients harbor a normal karyotype. Recently, multiplex ligation-dependent probe amplification (MLPA) has emerged as effective robust method for the detection cytogenetic aberrations To characterize subset with karyotype ...

2013
Ali Ahani Mohammad Taghi Akbari Kioomars Saliminejad Babak Behnam Mohammad Mehdi Akhondi Parvaneh Vosoogh Farriba Ghassemi Masood Naseripour Gholamreza Bahoush Hamid Reza Khorram Khorshid

PURPOSE To screen deletions/duplications of the RB1 gene in a large cohort of Iranian patients using the multiplex ligation-dependent probe amplification (MLPA) technique. METHODS A total of 121 patients with retinoblastoma, involving 55 unilateral and 66 bilateral or familial retinoblastomas, were included in this study. Among these patients, 121 blood and 43 tissue samples were available. D...

Journal: :Clinica chimica acta; international journal of clinical chemistry 2006
Lourdes R Desviat Belén Pérez Magdalena Ugarte

BACKGROUND Multiplex ligation probe amplification (MLPA) is a sensitive and efficient technique for molecular diagnosis of diseases involving deletions or duplications of large genomic regions. In phenylketonuria (PKU), most of the mutant alleles correspond to missense mutations and large deletions have been scarcely identified. In this study, we report for the first time the use of MLPA analys...

2012
Carles Garcia-Linares Jaume Mercadé Bernat Gel Josep Biayna Ernest Terribas Conxi Lázaro Eduard Serra

The study of somatic genetic alterations in tumors contributes to the understanding and management of cancer. Genetic alterations, such us copy number or copy neutral changes, generate allelic imbalances (AIs) that can be determined using polymorphic markers. Here we report the development of a simple set of calculations for analyzing microsatellite multiplex PCR data from control-tumor pairs t...

2007
U. Felbor D. J. Verlaan R. Vijzelaar G. A. Rouleau A. M. Siegel

Cerebral cavernous malformations (CCM) are vascular lesions that predispose to headaches, seizures, and hemorrhagic stroke. Hereditary CCMs are usually associated with the occurrence of multiple CCMs and occur with a frequency of 1:2,000 to 1:10,000. In this study, eight isolated cases with multiple CCMs but no CCM1-3 point mutation were analyzed using the multiplex ligation-dependent probe amp...

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...

Journal: :Genetic testing 2004
Marianne Schwartz Morten Dunø

Mutation detection in the DMD gene defective in Duchenne (DMD) and Becker muscular dystrophies (BMD) is complicated by the presence of 79 exons. The majority of recognized mutations are, however, copy number changes of individual exons, which traditionally have been identified by three common multiplex polymerase chain reaction (PCR) assays and/or Southern blotting. Here we report the use of th...

Journal: :Neuroscience letters 2006
Nathan Pankratz Michael W Pauciulo Veronika E Elsaesser Diane K Marek Cheryl A Halter Joanne Wojcieszek Alice Rudolph Clifford W Shults Tatiana Foroud William C Nichols

Mutations in DJ-1 (PARK7) are one cause of early-onset autosomal-recessive parkinsonism. We screened for DJ-1 mutations in 93 affected individuals from the 64 multiplex Parkinson disease (PD) families in our sample that had the highest family-specific multipoint LOD scores at the DJ-1 locus. In addition to sequencing all coding exons for alterations, we used multiplex ligation-dependent probe a...

2014
Shujuan Jiang Jiubin Zhang Dan Huang Yuanyuan Zhang Xiaoliang Liu Yinzhao Wang Rong He Yanyan Zhao

Nail patella syndrome (NPS) is an autosomal dominant disorder characterized by nail malformations, patellar apoplasia, or patellar hypoplasia. Mutations within the LMX1B gene are found in 85% of families with NPS; thus, this gene has been characterized as the causative gene of NPS. In this study, we identified a heterozygous microdeletion of the entire LMX1B gene using multiplex ligation-depend...

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