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Densities, length proportions, and other distributional features of repetitive sequences in the human genome estimated from 430 megabases of genomic sequence.
Z Gu et al.
Gene 259 (1-2), 81-8 (23 Dec 2000)
Posted by gwynne_yvr to Alu line L1 repeats human on Thu Jan 25 2007 at 00:36 UTC | info | related
 
Biased distribution of inverted and direct Alus in the human genome: implications for insertion, exclusion, and genome stability.
J E Stenger et al.
Genome research 11 (1), 12-27 (Jan 2001)
 
Similar integration but different stability of Alus and LINEs in the human genome.
A Pavlícek et al.
Gene 276 (1-2), 39-45 (03 Oct 2001)
Posted by gwynne_yvr to human L1 line Alu integration on Thu Jan 25 2007 at 00:29 UTC | info | related
 
Nonrandom distribution of alu elements in genes of various functional categories: insight from analysis of human chromosomes 21 and 22.
Deepak Grover et al.
Molecular biology and evolution 20 (9), 1420-4 (Sep 2003)
Posted by gwynne_yvr to genomics human Alu on Thu Jan 25 2007 at 00:18 UTC | info | related
 
Why are young and old repetitive elements distributed differently in the human genome?
Elise Belle, Matthew Webster, and Adam Eyre-Walker
Journal of molecular evolution 60 (3), 290-6 (Mar 2005)
Posted by gwynne_yvr to human evolution Alu on Wed Jan 24 2007 at 22:33 UTC | info | related
 
The length of CpG islands is associated with the distribution of Alu and L1 retroelements.
Moo-Il Kang et al.
Genomics 87 (5), 580-90 (May 2006)
Posted by gwynne_yvr to Alu retroelement cpg TE L1 on Wed Jan 24 2007 at 22:26 UTC | info | related
 
Alu elements contain many binding sites for transcription factors and may play a role in regulation of development processes
www.biomedcentral.com

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