Oligonucleotide microarray analysis of genomic imbalance in children with mental retardation
Article Abstract:
Whole-genome sampling analysis with Affymetrix GeneChip Human Mapping 100K arrays is used to study 100 children with idiopathic mental retardation and normal results of standard chromosomal analysis. It is found that this technology can detect at least twice as many potentially pathogenic de novo copy-number variants, as conventional cytogenetic analysis can in people with mental retardation.
Publication Name: American Journal of Human Genetics
Subject: Biological sciences
ISSN: 0002-9297
Year: 2006
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Rebuilding microbial genomes
Article Abstract:
A model system in which a donor genome from H. influenza was fragmented and the pieces then modified and reassembled in an Escherichia coli host cell was examined to understand the process of genetic engineering in rebuilding microbial genomes. It was found that rebuilding and booting a genome is a feasible and efficient approach to creating a synthetic microbial cell.
Publication Name: BioEssays
Subject: Biological sciences
ISSN: 0265-9247
Year: 2007
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The molecular signature and cis-regulatory architecture of a C. elegans gustatory neuron
Article Abstract:
A serial analysis of gene expression (SAGE) libraries were generated from two distinct populations of single, isolated sensory neuron classes, the gustatory neuron class ASE from Caenorhabditis elegans. It was shown that the ASE motif is a binding site for the C2H2 zinc finger TF CHE-1 which is essential for the correct differentiation of the ASE gustatory neuron.
Publication Name: Genes & Development
Subject: Biological sciences
ISSN: 0890-9369
Year: 2007
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- Abstracts: Phylogenetic analysis of snow sheep (Ovis nivicola) and closely related taxa. SNP identification and analysis in part of intron 2 of goat MSTN gene and variation within and among species
- Abstracts: Forensic application of microbiological culture analysis to identify mail intentionally contaminated with bacillus anthracis spores
- Abstracts: Evidence that mutations in the X-linked DDP gene cause incompletely penetrant and variable skewed X inactivation