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Results: 8

Cited In for PubMed (Select 20502635)

1.

Emerging epigenetic mechanisms of long non-coding RNAs.

Schaukowitch K, Kim TK.

Neuroscience. 2014 Apr 4;264:25-38. doi: 10.1016/j.neuroscience.2013.12.009. Epub 2013 Dec 14. Review.

2.

Great ape genomics.

Wall JD.

ILAR J. 2013;54(2):82-90. doi: 10.1093/ilar/ilt048. Review.

3.

A model-based analysis of GC-biased gene conversion in the human and chimpanzee genomes.

Capra JA, Hubisz MJ, Kostka D, Pollard KS, Siepel A.

PLoS Genet. 2013;9(8):e1003684. doi: 10.1371/journal.pgen.1003684. Epub 2013 Aug 15.

4.

Bidirectional promoters as important drivers for the emergence of species-specific transcripts.

Gotea V, Petrykowska HM, Elnitski L.

PLoS One. 2013;8(2):e57323. doi: 10.1371/journal.pone.0057323. Epub 2013 Feb 27.

5.

Human-specific CpG "beacons" identify loci associated with human-specific traits and disease.

Bell CG, Wilson GA, Butcher LM, Roos C, Walter L, Beck S.

Epigenetics. 2012 Oct;7(10):1188-99. doi: 10.4161/epi.22127. Epub 2012 Sep 11.

6.

The role of GC-biased gene conversion in shaping the fastest evolving regions of the human genome.

Kostka D, Hubisz MJ, Siepel A, Pollard KS.

Mol Biol Evol. 2012 Mar;29(3):1047-57. doi: 10.1093/molbev/msr279. Epub 2011 Nov 10.

7.

Ongoing GC-biased evolution is widespread in the human genome and enriched near recombination hot spots.

Katzman S, Capra JA, Haussler D, Pollard KS.

Genome Biol Evol. 2011;3:614-26. doi: 10.1093/gbe/evr058. Epub 2011 Jun 21.

8.

Substitution patterns are GC-biased in divergent sequences across the metazoans.

Capra JA, Pollard KS.

Genome Biol Evol. 2011;3:516-27. doi: 10.1093/gbe/evr051. Epub 2011 Jun 13.

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