نتایج جستجو برای: array cgh

تعداد نتایج: 134291  

2007
A.-C. Thuresson M.-L. Bondeson C. Edeby P. Ellis C. Langford J.P. Dumanski G. Annerén

Chromosomal imbalances are the major cause of mental retardation (MR). Many of these imbalances are caused by submicroscopic deletions or duplications not detected by conventional cytogenetic methods. Microarray-based comparative genomic hybridization (array-CGH) is considered to be superior for the investigation of chromosomal aberrations in children with MR, and has been demonstrated to impro...

Journal: :American journal of medical genetics. Part A 2007
Gokce A Toruner Deanna L Streck Marvin N Schwalb James J Dermody

Developmental delay (DD) and mental retardation (MR) are important child heath issues with a one percent prevalence. Karyotyping with or without subtelomeric FISH (fluorescent in situ hybridization), unless the phenotype of the patient suggests a specific aberration for a specific FISH assay, is the most common procedure in cytogenetic evaluation of MR/DD. In addition, there are several platfor...

2009
Michael Seifert Ali Banaei Jens Keilwagen Michael Florian Mette Andreas Houben François Roudier Vincent Colot Ivo Grosse Marc Strickert

Abstract: Arabidopsis thaliana is an important model organism in plant biology with a broad geographic distribution including ecotypes from Africa, America, Asia, and Europe. The natural variation of different ecotypes is expected to be reflected to a substantial degree in their genome sequences. Array comparative genomic hybridization (Array-CGH) can be used to quantify the natural variation o...

2017
Mi-Na Lee Jiwon Lee Hee Joon Yu Jeehun Lee Sun-Hee Kim

Pallister-Killian syndrome (PKS) is a rare multisystem disorder characterized by isochromosome 12p and tissue-limited mosaic tetrasomy 12p. In this study, we diagnosed three pediatric patients who were suspicious of having PKS using array-based comparative genomic hybridization (array CGH) and FISH analyses performed on peripheral lymphocytes. Patients 1 and 2 presented with craniofacial dysmor...

2008
Nha Nguyen Heng Huang Soontorn Oraintara

Array based comparative genomic hybridization (array-CGH) has merged as a highly efficient technique for the detection of chromosomal imbalances. Characteristics of these DNA copy number aberrations provide the insights into cancer, and they are useful for the diagnostic and therapy strategies. In this paper, we propose a statistical bivariate model for array CGH data in the stationary wavelet ...

2015
U. Fischer N. Ludwig A. Keller C. Backes E. Meese

There is growing evidence that gene amplifications were present in neural stem and progenitor cells during differentiation. We used array-CGH to discover copy number changes including gene amplifications and deletions during differentiation of mouse neural stem cells using TGF-ß and FCS for differentiation induction. Array data were deposited in GEO (Gene Expression Omnibus, NCBI) under accessi...

Journal: :International journal of oncology 2014
Hong Zhu Maria Pik Wong Vicky Tin

Genomic abnormalities are the hallmark of cancers and may harbor potential candidate genes important for cancer development and progression. We performed array comparative genomic hybridization (array CGH) on 36 cases of primary lung adenocarcinoma (AD) using an array containing 2621 BAC or PAC clones spanning the genome at an average interval of 1 Mb. Array CGH identified the commonest aberrat...

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