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Veronica van Heyningen
Veronica van Heyningen
Honorary Professor University of Edinburgh; Honorary Professor University College London
Geverifieerd e-mailadres voor igmm.ed.ac.uk - Homepage
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Mouse small eye results from mutations in a paired-like homeobox-containing gene
VH RE Hill, J Favor, BL Hogan, CC Ton, GF Saunders, IM Hanson, J Prosser, T ...
Nature 354, 4, 1991
1514*1991
Pax6 controls progenitor cell identity and neuronal fate in response to graded Shh signaling
J Ericson, P Rashbass, A Schedl, S Brenner-Morton, A Kawakami, ...
Cell 90 (1), 169-180, 1997
11591997
Long-range control of gene expression: emerging mechanisms and disruption in disease
DA Kleinjan, V Van Heyningen
The American Journal of Human Genetics 76 (1), 8-32, 2005
10272005
Positional cloning and characterization of a paired box-and homeobox-containing gene from the aniridia region
CCT Ton, H Hirvonen, H Miwa, MM Weil, P Monaghan, T Jordan, ...
Cell 67 (6), 1059-1074, 1991
9971991
The candidate Wilms' tumour gene is involved in genitourinary development
K Pritchard-Jones, S Fleming, D Davidson, W Bickmore, D Porteous, ...
Nature 346 (6280), 194-197, 1990
9871990
The human PAX6 gene is mutated in two patients with aniridia
T Jordan, I Hanson, D Zaletayev, S Hodgson, J Prosser, A Seawright, ...
Nature genetics 1 (5), 328-332, 1992
6131992
Mutations in SOX2 cause anophthalmia
J Fantes, NK Ragge, SA Lynch, NI McGill, JRO Collin, ...
Nature genetics 33 (4), 462-463, 2003
5932003
Subnuclear localization of WT1 in splicing or transcription factor domains is regulated by alternative splicing
SH Larsson, JP Charlieu, K Miyagawa, D Engelkamp, M Rassoulzadegan, ...
Cell 81 (3), 391-401, 1995
5831995
Mutations at the PAX6 locus are found in heterogeneous anterior segment malformations including Peters' anomaly
IM Hanson, JM Fletcher, T Jordan, A Brown, D Taylor, RJ Adams, ...
Nature genetics 6 (2), 168-173, 1994
5521994
Influence of PAX6 gene dosage on development: overexpression causes severe eye abnormalities
A Schedl, A Ross, M Lee, D Engelkamp, P Rashbass, V van Heyningen, ...
Cell 86 (1), 71-82, 1996
4871996
Position effect in human genetic disease
DJ Kleinjan, V Van Heyningen
Human molecular genetics 7 (10), 1611-1618, 1998
4411998
Graded sonic hedgehog signaling and the specification of cell fate in the ventral neural tube
J Ericson, J Briscoe, P Rashbass, V Van Heyningen, TM Jessell
Cold Spring Harbor symposia on quantitative biology 62, 451-466, 1997
4091997
The level of the transcription factor Pax6 is essential for controlling the balance between neural stem cell self-renewal and neurogenesis
SN Sansom, DS Griffiths, A Faedo, DJ Kleinjan, Y Ruan, J Smith, ...
PLoS genetics 5 (6), e1000511, 2009
3982009
The β2-microglobulin gene is on chromosome 15 and not in the HL-A region
PN Goodfellow, EA Jones, V Van Heyningen, E Solomon, M Bobrow, ...
Nature 254 (5497), 267-269, 1975
3551975
Role of Pax6 in development of the cerebellar system
D Engelkamp, P Rashbass, A Seawright, V van Heyningen
Development 126 (16), 3585-3596, 1999
3211999
Heterozygous mutations of OTX2 cause severe ocular malformations
NK Ragge, AG Brown, CM Poloschek, B Lorenz, RA Henderson, ...
The American Journal of Human Genetics 76 (6), 1008-1022, 2005
3172005
PAX6 mutations reviewed
J Prosser, V van Heyningen
Human mutation 11 (2), 93-108, 1998
3061998
Pax6 is required to regulate the cell cycle and the rate of progression from symmetrical to asymmetrical division in mammalian cortical progenitors
G Estivill-Torrus, H Pearson, V van Heyningen, DJ Price, P Rashbass
Oxford University Press for The Company of Biologists Limited 129 (2), 455-466, 2002
3002002
Domain disruption and mutation of the bZIP transcription factor, MAF,associated with cataract, ocular anterior segment dysgenesis and coloboma
RV Jamieson, R Perveen, B Kerr, M Carette, J Yardley, E Heon, MG Wirth, ...
Human molecular genetics 11 (1), 33-42, 2002
2942002
National study of microphthalmia, anophthalmia, and coloboma (MAC) in Scotland: investigation of genetic aetiology
D Morrison, D FitzPatrick, I Hanson, K Williamson, V Van Heyningen, ...
Journal of medical genetics 39 (1), 16-22, 2002
2912002
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Artikelen 1–20