The product of the mouse Xist gene is a 15 kb inactive X-specific transcript containing no conserved ORF and located in the nucleus N Brockdorff, A Ashworth, GF Kay, VM McCabe, DP Norris, PJ Cooper, ... Cell 71 (3), 515-526, 1992 | 1241 | 1992 |
Conservation of position and exclusive expression of mouse Xist from the inactive X chromosome N Brockdorff, A Ashworth, GF Kay, P Cooper, S Smith, VM McCabe, ... Nature 351 (6324), 329-331, 1991 | 759 | 1991 |
Nodal signalling in the epiblast patterns the early mouse embryo J Brennan, CC Lu, DP Norris, TA Rodriguez, RSP Beddington, ... Nature 411 (6840), 965-969, 2001 | 639 | 2001 |
Pitx2 determines left–right asymmetry of internal organs in vertebrates AK Ryan, B Blumberg, C Rodriguez-Esteban, S Yonei-Tamura, K Tamura, ... Nature 394 (6693), 545-551, 1998 | 611 | 1998 |
A comparison of the properties of Sox-3 with Sry and two related genes, Sox-1 and Sox-2 J Collignon, S Sockanathan, A Hacker, M Cohen-Tannoudji, D Norris, ... Development 122 (2), 509-520, 1996 | 575 | 1996 |
Cell fate decisions within the mouse organizer are governed by graded Nodal signals SD Vincent, NR Dunn, S Hayashi, DP Norris, EJ Robertson Genes & development 17 (13), 1646-1662, 2003 | 410 | 2003 |
Nodal activity in the node governs left-right asymmetry J Brennan, DP Norris, EJ Robertson Genes & development 16 (18), 2339-2344, 2002 | 343 | 2002 |
Evidence that random and imprinted Xist expression is controlled by preemptive methylation DP Norris, D Patel, GF Kay, GD Penny, N Brockdorff, SA Sheardown, ... Cell 77 (1), 41-51, 1994 | 319 | 1994 |
The Foxh1-dependent autoregulatory enhancer controls the level of Nodal signals in the mouse embryo DP Norris, J Brennan, EK Bikoff, EJ Robertson Oxford University Press for The Company of Biologists Limited 129 (14), 3455 …, 2002 | 277 | 2002 |
Cited2 controls left-right patterning and heart development through a Nodal-Pitx2c pathway SD Bamforth, J Bragança, CR Farthing, JE Schneider, C Broadbent, ... Nature genetics 36 (11), 1189-1196, 2004 | 229 | 2004 |
Pkd1l1 establishes left-right asymmetry and physically interacts with Pkd2 S Field, KL Riley, DT Grimes, H Hilton, M Simon, N Powles-Glover, ... Development 138 (6), 1131-1142, 2011 | 209 | 2011 |
Asymmetric and node-specific nodal expression patterns are controlled by two distinct cis-acting regulatory elements DP Norris, EJ Robertson Genes & development 13 (12), 1575-1588, 1999 | 207 | 1999 |
A Mutation in the Mitochondrial Fission Gene Dnm1l Leads to Cardiomyopathy H Ashrafian, L Docherty, V Leo, C Towlson, M Neilan, V Steeples, ... Plos genetics 6 (6), e1001000, 2010 | 179 | 2010 |
Methylation status of CpG-rich islands on active and inactive mouse X chromosomes DP Norris, N Brockdorff, S Rastan Mammalian Genome 1, 78-83, 1991 | 142 | 1991 |
Towards high resolution maps of the mouse and human genomes—a facility for ordering markers to 0.1 cM resolution M Breen, L Deakln, B Macdonald, S Miller, R Sibson, E Tarttelln, P Avner, ... Human Molecular Genetics 3 (4), 621-627, 1994 | 131 | 1994 |
The novel mouse mutant, chuzhoi, has disruption of Ptk7 protein and exhibits defects in neural tube, heart and lung development and abnormal planar cell polarity … A Paudyal, C Damrau, VL Patterson, A Ermakov, C Formstone, Z Lalanne, ... BMC developmental biology 10, 1-22, 2010 | 118 | 2010 |
Arkadia enhances Nodal/TGF-β signaling by coupling phospho-Smad2/3 activity and turnover KJ Mavrakis, RL Andrew, KL Lee, C Petropoulou, JE Dixon, ... PLoS Biology 5 (3), e67, 2007 | 117 | 2007 |
Mouse models of ciliopathies: the state of the art DP Norris, DT Grimes Disease models & mechanisms 5 (3), 299-312, 2012 | 113 | 2012 |
Foxj1 regulates floor plate cilia architecture and modifies the response of cells to sonic hedgehog signalling C Cruz, V Ribes, E Kutejova, J Cayuso, V Lawson, D Norris, J Stevens, ... Development 137 (24), 4271-4282, 2010 | 112 | 2010 |
Zic2 -associated holoprosencephaly is caused by a transient defect in the organizer region during gastrulation N Warr, N Powles-Glover, A Chappell, J Robson, D Norris, RM Arkell Human molecular genetics 17 (19), 2986-2996, 2008 | 111 | 2008 |