Publications by authors named "Annick Francis"

15Publications

Stalk cell phenotype depends on integration of Notch and Smad1/5 signaling cascades.

Dev Cell 2012 Mar 23;22(3):501-14. Epub 2012 Feb 23.

VIB11 Center for the Biology of Disease, Laboratory of Developmental Signaling, VIB and Center for Human Genetics, KU Leuven, 3000 Leuven, Belgium.

View Article

Download full-text PDF

Source
http://dx.doi.org/10.1016/j.devcel.2012.01.007DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4544746PMC
March 2012

Neural crest-specific removal of Zfhx1b in mouse leads to a wide range of neurocristopathies reminiscent of Mowat-Wilson syndrome.

Hum Mol Genet 2007 Jun 3;16(12):1423-36. Epub 2007 May 3.

Laboratory of Molecular Biology (Celgen), KULeuven, Herestraat 49,B-3000 Leuven, Belgium.

View Article

Download full-text PDF

Source
http://academic.oup.com/hmg/article/16/12/1423/2355959/Neura
Publisher Site
http://dx.doi.org/10.1093/hmg/ddm093DOI Listing
June 2007

Smad5 determines murine amnion fate through the control of bone morphogenetic protein expression and signalling levels.

Development 2006 Sep 3;133(17):3399-409. Epub 2006 Aug 3.

Department of Developmental Biology (VIB7 for Biotechnology (VIB) and Laboratory of Molecular Biology (Celgen), University of Leuven, B-3000 Leuven, Belgium.

View Article

Download full-text PDF

Source
http://dev.biologists.org/cgi/doi/10.1242/dev.02497
Publisher Site
http://dx.doi.org/10.1242/dev.02497DOI Listing
September 2006

Generation of a floxed allele of Smad5 for cre-mediated conditional knockout in the mouse.

Genesis 2003 Sep;37(1):5-11

Department of Developmental Biology (VIB 7), Flanders Interuniversity Institute for Biotechnology (VIB), and Laboratory of Molecular Biology (CELGEN), University of Leuven, Leuven, Belgium.

View Article

Download full-text PDF

Source
http://dx.doi.org/10.1002/gene.10219DOI Listing
September 2003

Mice lacking ZFHX1B, the gene that codes for Smad-interacting protein-1, reveal a role for multiple neural crest cell defects in the etiology of Hirschsprung disease-mental retardation syndrome.

Am J Hum Genet 2003 Feb 9;72(2):465-70. Epub 2003 Jan 9.

Department of Developmental Biology, Flanders Interuniversity Institute for Biotechnology, and Laboratory of Molecular Biology (Celgen), University of Leuven, Leuven, Belgium.

View Article

Download full-text PDF

Source
http://dx.doi.org/10.1086/346092DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC379238PMC
February 2003