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Resource

A platform for curated products from novel open reading frames prompts reinterpretation of disease variants

  • Matthew D.C. Neville
  • Robin Kohze
  • Chaitanya Erady
  • Narendra Meena
  • Matthew Hayden
  • David N. Cooper
  • Matthew Mort
  • Sudhakaran Prabakaran
  • First Published January 19, 2021
Research

Loss of exon identity is a common mechanism of human inherited disease

  • Timothy Sterne-Weiler
  • Jonathan Howard
  • Matthew Mort
  • David N. Cooper
  • Jeremy R. Sanford
  • First Published July 12, 2011
Letter

Splicing factor SFRS1 recognizes a functionally diverse landscape of RNA transcripts

  • Jeremy R. Sanford
  • Xin Wang
  • Matthew Mort
  • Natalia VanDuyn
  • David N. Cooper
  • Sean D. Mooney
  • Howard J. Edenberg
  • Yunlong Liu
  • First Published December 30, 2008
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