Regulation from a distance: long-range control of gene expression in development and disease

Por van Heyningen, Veronica, Bickmore, Wendy
Publicado em 2013

Frequent Chromosome Aberrations Revealed by Molecular Cytogenetic Studies in Patients with Aniridia

Por Crolla, John A., van Heyningen, Veronica
Publicado em 2002

Long-Range Control of Gene Expression: Emerging Mechanisms and Disruption in Disease

Por Kleinjan, Dirk A., van Heyningen, Veronica
Publicado em 2005

Aniridia

Por Hingorani, Melanie, Hanson, Isabel, van Heyningen, Veronica
Publicado em 2012

Hsp90 Selectively Modulates Phenotype in Vertebrate Development

Por Yeyati, Patricia L, Bancewicz, Ruth M, Maule, John, van Heyningen, Veronica
Publicado em 2007

Clinical utility gene card for: WAGR syndrome

Por Clericuzio, Carol, Hingorani, Melanie, Crolla, John A, van Heyningen, Veronica, Verloes, Alain
Publicado em 2011

DNaseI Hypersensitivity and Ultraconservation Reveal Novel, Interdependent Long-Range Enhancers at the Complex Pax6 Cis-Regulatory Region

Por McBride, David J., Buckle, Adam, van Heyningen, Veronica, Kleinjan, Dirk A.
Publicado em 2011

Clinical utility gene card for: Aniridia

Por Richardson, Rose, Hingorani, Melanie, Van Heyningen, Veronica, Gregory-Evans, Cheryl, Moosajee, Mariya
Publicado no Eur J Hum Genet (2016)

Raised risk of Wilms tumour in patients with aniridia and submicroscopic WT1 deletion

Por van Heyningen, Veronica, Hoovers, Jan M N, de Kraker, Jan, Crolla, John A
Publicado em 2007

The Developmental Regulator Pax6 Is Essential for Maintenance of Islet Cell Function in the Adult Mouse Pancreas

Por Hart, Alan W., Mella, Sebastien, Mendrychowski, Jacek, van Heyningen, Veronica, Kleinjan, Dirk A.
Publicado em 2013

Complete sequencing of the Fugu WAGR region from WT1 to PAX6: Dramatic compaction and conservation of synteny with human chromosome 11p13

Por Miles, Colin, Elgar, Greg, Coles, Edward, Kleinjan, Dirk-Jan, van Heyningen, Veronica, Hastie, Nicholas
Publicado em 1998

Discovery and assessment of conserved Pax6 target genes and enhancers

Por Coutinho, Pedro, Pavlou, Sofia, Bhatia, Shipra, Chalmers, Kevin J., Kleinjan, Dirk A., van Heyningen, Veronica
Publicado em 2011

Pleiotropic Effects of Sox2 during the Development of the Zebrafish Epithalamus

Por Pavlou, Sofia, Astell, Katy, Kasioulis, Ioannis, Gakovic, Milica, Baldock, Richard, van Heyningen, Veronica, Coutinho, Pedro
Publicado em 2014

Functional conservation of Pax6 regulatory elements in humans and mice demonstrated with a novel transgenic reporter mouse

Por Tyas, David A, Simpson, T Ian, Carr, Catherine B, Kleinjan, Dirk A, van Heyningen, Veronica, Mason, John O, Price, David J
Publicado em 2006

The Level of the Transcription Factor Pax6 Is Essential for Controlling the Balance between Neural Stem Cell Self-Renewal and Neurogenesis

Por Sansom, Stephen N., Griffiths, Dean S., Faedo, Andrea, Kleinjan, Dirk-Jan, Ruan, Youlin, Smith, James, van Heyningen, Veronica, Rubenstein, John L., Livesey, Frederick J.
Publicado em 2009

Long-range downstream enhancers are essential for Pax6 expression

Por Kleinjan, Dirk A., Seawright, Anne, Mella, Sebastien, Carr, Catherine B., Tyas, David A., Simpson, T. Ian, Mason, John O., Price, David J., van Heyningen, Veronica
Publicado em 2006

Disruption of Autoregulatory Feedback by a Mutation in a Remote, Ultraconserved PAX6 Enhancer Causes Aniridia

Por Bhatia, Shipra, Bengani, Hemant, Fish, Margaret, Brown, Alison, Divizia, Maria Teresa, de Marco, Riccardo, Damante, Guiseppe, Grainger, Robert, van Heyningen, Veronica, Kleinjan, Dirk A.
Publicado em 2013

PAX6, brain structure and function in human adults: advanced MRI in aniridia

Por Yogarajah, Mahinda, Matarin, Mar, Vollmar, Christian, Thompson, Pamela J., Duncan, John S., Symms, Mark, Moore, Anthony T., Liu, Joan, Thom, Maria, van Heyningen, Veronica, Sisodiya, Sanjay M.
Publicado no Ann Clin Transl Neurol (2016)

GDF6, a Novel Locus for a Spectrum of Ocular Developmental Anomalies

Por Asai-Coakwell, Mika , French, Curtis R. , Berry, Karyn M. , Ye, Ming , Koss, Ron , Somerville, Martin , Mueller, Rosemary , van Heyningen, Veronica , Waskiewicz, Andrew J. , Lehmann, Ordan J. 
Publicado em 2007

A rare de novo nonsense mutation in OTX2 causes early onset retinal dystrophy and pituitary dysfunction

Por Henderson, Robert H., Williamson, Kathleen A., Kennedy, Joanna S., Webster, Andrew R., Holder, Graham E., Robson, Anthony G., FitzPatrick, David R., van Heyningen, Veronica, Moore, Anthony T.
Publicado em 2009