Inducible expression of an hsp68-lacZ hybrid gene in transgenic mice R Kothary, S Clapoff, S Darling, MD Perry, LA Moran, J Rossant Development 105 (4), 707-714, 1989 | 401 | 1989 |
A sequence motif found in a Drosophila heterochromatin protein is conserved in animals and plants PB Singh, JR Miller, J Pearce, R Kothary, RD Burton, R Paro, TC James, ... Nucleic acids research 19 (4), 789-794, 1991 | 367 | 1991 |
The mouse dystonia musculorum gene is a neural isoform of bullous pemphigoid antigen 1 A Brown, G Bernier, M Mathieu, J Rossant, R Kothary Nature genetics 10 (3), 301-306, 1995 | 315 | 1995 |
A transgene containing lacZ inserted into the dystonia locus is expressed in neural tube R Kothary, S Clapoff, A Brown, R Campbell, A Peterson, J Rossant Nature 335 (6189), 435-437, 1988 | 256 | 1988 |
Chx10 repression of Mitf is required for the maintenance of mammalian neuroretinal identity DJ Horsford, MTT Nguyen, GC Sellar, R Kothary, H Arnheiter, ... Oxford University Press for The Company of Biologists Limited 132 (1), 177-187, 2005 | 238 | 2005 |
The Splotch mutation interferes with muscle development in the limbs T Franz, R Kothary, MAH Surani, Z Halata, M Grim Anatomy and embryology 187, 153-160, 1993 | 231 | 1993 |
Genome imprinting and development in the mouse MA Surani, R Kothary, ND Allen, PB Singh, R Fundele, ... Development 108 (Supplement), 89-98, 1990 | 223 | 1990 |
MEF2 is upregulated during cardiac hypertrophy and is required for normal post-natal growth of the myocardium SM Kolodziejczyk, L Wang, K Balazsi, Y DeRepentigny, R Kothary, ... Current Biology 9 (20), 1203-1206, 1999 | 220 | 1999 |
Rho-kinase inactivation prolongs survival of an intermediate SMA mouse model M Bowerman, A Beauvais, CL Anderson, R Kothary Human molecular genetics 19 (8), 1468-1478, 2010 | 208 | 2010 |
Glucose metabolism and pancreatic defects in spinal muscular atrophy M Bowerman, KJ Swoboda, JP Michalski, GS Wang, C Reeks, A Beauvais, ... Annals of neurology 72 (2), 256-268, 2012 | 199 | 2012 |
The myogenic kinome: protein kinases critical to mammalian skeletal myogenesis JDR Knight, R Kothary Skeletal muscle 1, 1-18, 2011 | 185 | 2011 |
Smn depletion alters profilin II expression and leads to upregulation of the RhoA/ROCK pathway and defects in neuronal integrity M Bowerman, D Shafey, R Kothary Journal of molecular neuroscience 32, 120-131, 2007 | 184 | 2007 |
SRp30c-dependent stimulation of survival motor neuron (SMN) exon 7 inclusion is facilitated by a direct interaction with hTra2β1 PJ Young, CJ DiDonato, D Hu, R Kothary, EJ Androphy, CL Lorson Human molecular genetics 11 (5), 577-587, 2002 | 180 | 2002 |
SMN, profilin IIa and plastin 3: a link between the deregulation of actin dynamics and SMA pathogenesis M Bowerman, CL Anderson, A Beauvais, PP Boyl, W Witke, R Kothary Molecular and Cellular Neuroscience 42 (1), 66-74, 2009 | 166 | 2009 |
Polytene chromosomes in mouse trophoblast giant cells S Varmuza, V Prideaux, R Kothary, J Rossant Development 102 (1), 127-134, 1988 | 166 | 1988 |
A critical smn threshold in mice dictates onset of an intermediate spinal muscular atrophy phenotype associated with a distinct neuromuscular junction pathology M Bowerman, LM Murray, A Beauvais, B Pinheiro, R Kothary Neuromuscular Disorders 22 (3), 263-276, 2012 | 156 | 2012 |
Lung tumors in mice expressing an antisense RARβ2 transgene J Bérard, F Laboune, M Mukuna, S Massé, R Kothary, WEC Bradley The FASEB journal 10 (9), 1091-1097, 1996 | 155 | 1996 |
Transgenic expression of the activating natural killer receptor Ly49H confers resistance to cytomegalovirus in genetically susceptible mice SH Lee, A Zafer, Y de Repentigny, R Kothary, ML Tremblay, P Gros, ... The Journal of experimental medicine 197 (4), 515-526, 2003 | 152 | 2003 |
Fasudil improves survival and promotes skeletal muscle development in a mouse model of spinal muscular atrophy M Bowerman, LM Murray, JG Boyer, CL Anderson, R Kothary BMC medicine 10, 1-14, 2012 | 149 | 2012 |
A novel function for the survival motoneuron protein as a translational regulator G Sanchez, AY Dury, LM Murray, O Biondi, H Tadesse, R El Fatimy, ... Human molecular genetics 22 (4), 668-684, 2013 | 145 | 2013 |