Show items per page
Elements: 5
Page 1 on 1
 TitleAuthors / EditorsDate
add to browser selection
A switch between topological domains underlies HoxD genes collinearity in mouse limbs Andrey, Guillaume; Montavon, Thomas; Mascrez, Bénédicte; Gonzalez, Federico; ... Duboule, Denis 2013
add to browser selection
A systematic enhancer screen using lentivector transgenesis identifies conserved and non-conserved functional elements at the Olig1 and Olig2 locus Friedli, Marc; Barde, Isabelle; Arcangeli, Mélanie; Verp, Sonia; ... Antonarakis, Stylianos 2010
add to browser selection
A t(2;8) balanced translocation with breakpoints near the human HOXD complex causes mesomelic dysplasia and vertebral defects Spitz, François; Montavon, Thomas; Monso-Hinard, Christine; Morris, Michael Andréw; ... Duboule, Denis 2002
add to browser selection
Characterization of mouse Dactylaplasia mutations: a model for human ectrodactyly SHFM3 Friedli, Marc; Nikolaev, Sergey Igorievich; Lyle, Robert; Arcangeli, Mélanie; ... Antonarakis, Stylianos 2008
add to browser selection
Uncoupling Time and Space in the Collinear Regulation of Hox Genes Tschopp, Patrick; Tarchini, Basile; Spitz, François; Zakany, Jozsef; Duboule, Denis 2009