Journal article
Microarray mRNA expression profiling to study cystic fibrosis
Methods in molecular biology (Clifton, N.J.), Vol.742, pp.193-212
2011
DOI: 10.1007/978-1-61779-120-8_12
PMID: 21547734
Abstract
To understand the links between CFTR mutations and the development of cystic fibrosis (CF) phenotypes, it is imperative to study the transcriptome in affected cell types. Microarray expression profiling provides a platform to study global gene expression in detail. This approach may provide the necessary information to segregate phenotypic characteristics of CF, differentiate between genetic or environmental factors, and assess the advent and progression of disease phenotypes. Moreover, if a "CF signature" of genes with altered expression is defined, this can be used to monitor effectiveness of treatment. We provide here detailed protocols and tips for collecting and preserving tissues and cells, and preparing total RNA. We also outline novel strategies for experimental design and data analysis, and describe some powerful gene and pathway discovery tools.
Details
- Title: Subtitle
- Microarray mRNA expression profiling to study cystic fibrosis
- Creators
- Shyam Ramachandran - Interdisciplinary Program in Genetics, Department of Pediatrics, University of Iowa, Iowa City, IA, USA. shyam-ramachandran@uiowa.eduLuka A ClarkeTodd E ScheetzMargarida D AmaralPaul B McCray Jr
- Resource Type
- Journal article
- Publication Details
- Methods in molecular biology (Clifton, N.J.), Vol.742, pp.193-212
- DOI
- 10.1007/978-1-61779-120-8_12
- PMID
- 21547734
- NLM abbreviation
- Methods Mol Biol
- eISSN
- 1940-6029
- Publisher
- United States
- Language
- English
- Date published
- 2011
- Academic Unit
- Roy J. Carver Department of Biomedical Engineering; Electrical and Computer Engineering; Microbiology and Immunology; Pulmonary Medicine; Stead Family Department of Pediatrics; Internal Medicine; Ophthalmology and Visual Sciences
- Record Identifier
- 9983980060802771
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