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William R. Jeck

Researcher at Duke University

Publications -  46
Citations -  12496

William R. Jeck is an academic researcher from Duke University. The author has contributed to research in topics: Medicine & Gene. The author has an hindex of 18, co-authored 35 publications receiving 10233 citations. Previous affiliations of William R. Jeck include Harvard University & University of North Carolina at Chapel Hill.

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Circular RNAs are abundant, conserved, and associated with ALU repeats

TL;DR: High-throughput sequencing of libraries prepared from ribosome-depleted RNA with or without digestion with the RNA exonuclease showed that ecircRNAs are abundant, stable, conserved and nonrandom products of RNA splicing that could be involved in control of gene expression.
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Genomic Classification of Cutaneous Melanoma

Rehan Akbani, +351 more
- 18 Jun 2015 - 
TL;DR: This clinicopathological and multi-dimensional analysis suggests that the prognosis of melanoma patients with regional metastases is influenced by tumor stroma immunobiology, offering insights to further personalize therapeutic decision-making.
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Evolution of genes and genomes on the Drosophila phylogeny.

Andrew G. Clark, +429 more
- 08 Nov 2007 - 
TL;DR: These genome sequences augment the formidable genetic tools that have made Drosophila melanogaster a pre-eminent model for animal genetics, and will further catalyse fundamental research on mechanisms of development, cell biology, genetics, disease, neurobiology, behaviour, physiology and evolution.
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Detecting and characterizing circular RNAs

TL;DR: Evidence is emerging that some circRNAs might regulate microRNA (miRNA) function, and roles in transcriptional control have also been suggested.
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Expression of Linear and Novel Circular Forms of an INK4/ARF-Associated Non-Coding RNA Correlates with Atherosclerosis Risk

TL;DR: The results identify novel circular RNA products emanating from the ANRIL locus and suggest causal variants at 9p21.3 regulate INK4/ARF expression and ASVD risk by modulating ANRil expression and/or structure.