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Rashmi Kothary
Rashmi Kothary
Ottawa Hospital Research Institute
Verified email at ohri.ca - Homepage
Title
Cited by
Cited by
Year
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
3951989
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
3671991
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
3121995
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
2581988
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
2352005
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
2341993
Genome imprinting and development in the mouse
MA Surani, R Kothary, ND Allen, PB Singh, R Fundele, ...
Development 108 (Supplement), 89-98, 1990
2231990
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
2161999
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
2062010
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
1922012
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
1842007
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
1762002
The myogenic kinome: protein kinases critical to mammalian skeletal myogenesis
JDR Knight, R Kothary
Skeletal muscle 1, 1-18, 2011
1692011
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
1662009
Polytene chromosomes in mouse trophoblast giant cells
S Varmuza, V Prideaux, R Kothary, J Rossant
Development 102 (1), 127-134, 1988
1661988
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
1522012
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
1522003
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
1491996
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
1452012
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
1412013
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