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Andrew D. Ellington

Researcher at University of Texas at Austin

Publications -  599
Citations -  48723

Andrew D. Ellington is an academic researcher from University of Texas at Austin. The author has contributed to research in topics: Aptamer & RNA. The author has an hindex of 96, co-authored 569 publications receiving 43262 citations. Previous affiliations of Andrew D. Ellington include Harvard University & UPRRP College of Natural Sciences.

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In vitro selection of RNA molecules that bind specific ligands.

TL;DR: Subpopulations of RNA molecules that bind specifically to a variety of organic dyes have been isolated from a population of random sequence RNA molecules.
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The zebrafish reference genome sequence and its relationship to the human genome.

Kerstin Howe, +174 more
- 25 Apr 2013 - 
TL;DR: A high-quality sequence assembly of the zebrafish genome is generated, made up of an overlapping set of completely sequenced large-insert clones that were ordered and oriented using a high-resolution high-density meiotic map, providing a clearer understanding of key genomic features such as a unique repeat content, a scarcity of pseudogenes, an enrichment of zebra fish-specific genes on chromosome 4 and chromosomal regions that influence sex determination.
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Aptamers as therapeutics.

TL;DR: A series of aptamers currently in development may change how nucleic acid therapeutics are perceived and will increasingly find use in concert with other therapeutic molecules and modalities.
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The DNA sequence of human chromosome 22

Ian Dunham, +223 more
- 02 Dec 1999 - 
TL;DR: The sequence of the euchromatic part of human chromosome 22 is reported, which consists of 12 contiguous segments spanning 33.4 megabases, contains at least 545 genes and 134 pseudogenes, and provides the first view of the complex chromosomal landscapes that will be found in the rest of the genome.
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Selection in vitro of single-stranded DNA molecules that fold into specific ligand-binding structures

TL;DR: A set of ligand-binding DNA sequences are isolated from a large pool of random sequence DNAs by selection and amplification in vitro, revealing that ligand binding is DNA-specific; RNAs of identical sequence could not interact with the same ligands.