Showing results (11-20 of 61) with videos related to

Sort By:
Pageof 7
Journal of Cell Science|June 3, 2004
Impairment of SHOX nuclear localization as a cause for Léri-Weill syndromeNitin Sabherwal, Katja U Schneider, Rüdiger J Blaschke, et al.
Human Mutation|August 30, 2007
The novel human SHOX allelic variant databaseBeate Niesler, Ralph Röth, Steffi Wilke, et al.
European Journal of Human Genetics : EJHG|December 10, 2009
Enhancer elements upstream of the SHOX gene are active in the developing limbClaudia Durand, Fiona Bangs, Jason Signolet, et al.
Journal of Cell Science|December 14, 2011
SrGAP3 interacts with lamellipodin at the cell membrane and regulates Rac-dependent cellular protrusionsVolker Endris, Lydia Haussmann, Elena Buss, et al.
Plos One|March 31, 2011
Alternative splicing and nonsense-mediated RNA decay contribute to the regulation of SHOX expressionClaudia Durand, Ralph Roeth, Harsh Dweep, et al.
Human Molecular Genetics|September 21, 2007
BNP is a transcriptional target of the short stature homeobox gene SHOXAntonio Marchini, Beate Häcker, Tiina Marttila, et al.
Human Molecular Genetics|January 29, 2011
FGFR3 is a target of the homeobox transcription factor SHOX in limb developmentEva Decker, Claudia Durand, Sebastian Bender, et al.
Pageof 7