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NeuroArray: A Customized aCGH for the Analysis of Copy Number Variations in Neurological Disorders

Title: NeuroArray: A Customized aCGH for the Analysis of Copy Number Variations in Neurological Disorders
Authors: La Cognata, Valentina; Morello, Giovanna; Gentile, Giulia; Cavalcanti, Francesca; Cittadella, Rita; Conforti, Francesca Luisa; De Marco, Elvira Valeria; Magariello, Angela; Muglia, Maria; Patitucci, Alessandra; Spadafora, Patrizia; D'Agata, Velia; Ruggieri, Martino; Cavallaro, Sebastiano
Source: Current genomics 19 (2018): 431–443. doi:10.2174/1389202919666180404105451 ; info:cnr-pdr/source/autori:La Cognata, Valentina; Morello, Giovanna; Gentile, Giulia; Cavalcanti, Francesca; Cittadella, Rita; Conforti, Francesca Luisa; De Marco, Elvira Valeria; Magariello, Angela; Muglia, Maria; Patitucci, Alessandra; Spadafora, Patrizia; D'Agata, Velia; Ruggieri, Martino; Cavallaro, Sebastiano/titolo:NeuroArray: A Customized aCGH for the Analysis of Copy Number Variations in Neurological Disorders/doi:10.21741389202919666180404105451/rivista:Current genomics/anno:2018/pagina_da:431/pagina_a:443/intervallo_pagine:431–443/volume:19
Publisher Information: Bentham Science Publishers, Hilversum , Paesi Bassi
Publication Year: 2018
Collection: PUMAlab (ISTI CNR - Consiglio Nazionale delle Ricerche / National Research Council)
Subject Terms: Methods; aCGH; CNVs; Neurological diseases; Genes; Custom array
Description: Background: Neurological disorders are a highly heterogeneous group of pathological conditions that affect both the peripheral and the central nervous system. These pathologies are characterized by a complex and multifactorial etiology involving numerous environmental agents and genetic susceptibility factors. For this reason, the investigation of their pathogenetic basis by means of traditional methodological approaches is rather arduous. High-throughput genotyping technologies, including the microarray-based comparative genomic hybridization (aCGH), are currently replacing classical detection methods, providing powerful molecular tools to identify genomic unbalanced structural rearrangements and explore their role in the pathogenesis of many complex human diseases.
Document Type: article in journal/newspaper
Language: English
Relation: info:cnr-pdr/author/idpersonaleesterno:21822/LA COGNATA/VALENTINA; info:cnr-pdr/author/idpersonaleesterno:28467/MORELLO/GIOVANNA; info:cnr-pdr/author/matricola:4172/DE MARCO/ELVIRA VALERIA; info:cnr-pdr/author/matricola:5327/CAVALLARO/SEBASTIANO; info:cnr-pdr/author/matricola:5735/D'AGATA/VELIA MARIA; info:cnr-pdr/author/matricola:5808/CAVALCANTI/FRANCESCA; info:cnr-pdr/author/matricola:5809/CONFORTI/FRANCESCA LUISA; info:cnr-pdr/author/matricola:5813/SPADAFORA/PATRIZIA; info:cnr-pdr/author/matricola:8035/RUGGIERI/MARTINO; info:cnr-pdr/author/matricola:8233/PATITUCCI/ALESSANDRA; info:cnr-pdr/author/matricola:9874/MAGARIELLO/ANGELA; info:cnr-pdr/author/matricola:17223/GUARNACCIA/MARIA; info:cnr-pdr/author/matricola:17224/GENTILE/GIULIA; info:cnr-pdr/author/matricola:29550/CITTADELLA/RITA; info:cnr-pdr/author/matricola:39037/MUGLIA/MARIA; http://www.cnr.it/prodotto/i/389655; https://publications.cnr.it/doc/389655; https://dx.doi.org/10.2174/1389202919666180404105451; info:doi:10.2174/1389202919666180404105451; https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6128384/
DOI: 10.2174/1389202919666180404105451
Availability: http://www.cnr.it/prodotto/i/389655; https://publications.cnr.it/doc/389655; https://doi.org/10.2174/1389202919666180404105451; https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6128384/
Rights: info:eu-repo/semantics/openAccess
Accession Number: edsbas.2572D82E
Database: BASE