Functional genome-wide siRNA screen identifies KIAA0586 as mutated in Joubert syndrome

Roosing, S, Hofree, M, Kim, S et al. (42 more authors) (2015) Functional genome-wide siRNA screen identifies KIAA0586 as mutated in Joubert syndrome. eLife, 4. e06602. ISSN 2050-084X

Abstract

Metadata

Authors/Creators:
  • Roosing, S
  • Hofree, M
  • Kim, S
  • Scott, E
  • Copeland, B
  • Romani, M
  • Silhavy, JL
  • Rosti, RO
  • Schroth, J
  • Mazza, T
  • Miccinilli, E
  • Zaki, MS
  • Swoboda, KJ
  • Milisa-Drautz, J
  • Dobyns, WB
  • Mikati, M
  • İncecik, F
  • Azam, M
  • Borgatti, R
  • Romaniello, R
  • Boustany, RM
  • Clericuzio, CL
  • D Arrigo, S
  • Strømme, P
  • Boltshauser, E
  • Stanzial, F
  • Mirabelli-Badenier, M
  • Moroni, I
  • Bertini, E
  • Emma, F
  • Steinlin, M
  • Hildebrandt, F
  • Johnson, CA
  • Freilinger, M
  • Vaux, KK
  • Gabriel, SB
  • Aza-Blac, P
  • Heynen, SG
  • Ideker, T
  • Dynlacht, BD
  • Lee, JE
  • Valente, EM
  • Valente, EM
  • Kim, J
  • Gleeson, JG
Copyright, Publisher and Additional Information: © 2015, Roosing et alThis article is distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use and redistribution provided that the original author and source are credited. - See more at: http://elifesciences.org/content/4/e06602#.dpuf
Keywords: Joubert syndrome; KIAA0586; Talpid3; ciliopathy; developmental biology; high-content screen; human; human biology; medicine; siRNA; stem cells
Dates:
  • Published: 30 May 2015
  • Accepted: 28 May 2015
Institution: The University of Leeds
Academic Units: The University of Leeds > Faculty of Medicine and Health (Leeds) > School of Medicine (Leeds) > Inst of Biomed & Clin Sciences (LIBACS) (Leeds)
Depositing User: Symplectic Publications
Date Deposited: 22 Jul 2015 13:44
Last Modified: 25 Jan 2018 18:59
Published Version: http://dx.doi.org/10.7554/eLife.06602
Status: Published
Identification Number: https://doi.org/10.7554/eLife.06602
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