Her primary scientific interests are in Cell biology, Genetics, Spinal muscular atrophy, Molecular biology and SMA*. Her Cell biology research integrates issues from Transcription factor, Eye development and Fibroblast growth factor. Her research in Spinal muscular atrophy tackles topics such as Exon which are related to areas like Pancreas.
Her Molecular biology research is multidisciplinary, relying on both Translation, Messenger RNA and RNA-binding protein. The SMA* study combines topics in areas such as Motor neuron and Atrophy. The concepts of her Motor neuron study are interwoven with issues in Phenotype, Neuromuscular junction, RHOA and Anatomy.
Rashmi Kothary focuses on Cell biology, Spinal muscular atrophy, SMA*, Dystonin and Molecular biology. Rashmi Kothary combines subjects such as Chromatin, Genetics and Cytoskeleton with her study of Cell biology. The various areas that she examines in her Spinal muscular atrophy study include Motor neuron and Neuroscience.
Her research in SMA* intersects with topics in Endocrinology, Skeletal muscle, Pathogenesis, Degeneration and Atrophy. Her work carried out in the field of Dystonin brings together such families of science as Neurodegeneration, Sensory neuron, Hereditary sensory and autonomic neuropathy, Dystonia and Gene isoform. As a member of one scientific family, Rashmi Kothary mostly works in the field of Molecular biology, focusing on Transgene and, on occasion, Regulation of gene expression.
Her primary areas of study are Spinal muscular atrophy, SMA*, Pathology, Cell biology and SMN1. Her Spinal muscular atrophy study integrates concerns from other disciplines, such as Endocrinology, Motor neuron, Muscle atrophy and Fatty acid metabolism. Her research integrates issues of Dyslipidemia, Pathogenesis, Immune system, Skeletal muscle and Cell type in her study of SMA*.
Her Pathology research includes themes of Nerve fiber layer, Retinal ganglion cell and Denervation. Her Cell biology research is multidisciplinary, incorporating elements of Chromatin, Wild type, Dystonin, Cytoskeleton and Epigenetics. Her SMN1 study combines topics in areas such as Molecular biology, Gene knockdown and SOD1.
The scientist’s investigation covers issues in SMA*, Spinal muscular atrophy, Anatomy, SMN1 and Pathology. Rashmi Kothary has included themes like Endocrinology, Internal medicine, Pathogenesis, Neuroinflammation and Motor neuron in her SMA* study. Her studies deal with areas such as Muscle atrophy and Atrophy as well as Motor neuron.
Rashmi Kothary works mostly in the field of Spinal muscular atrophy, limiting it down to topics relating to Immune system and, in certain cases, Lymphatic system, as a part of the same area of interest. In her research on the topic of Anatomy, Visual phototransduction, Cell biology, Retina and Retinal degeneration is strongly related with Transplantation. Her SMN1 research includes elements of Amyotrophic lateral sclerosis and RNA-Binding Protein FUS, RNA-binding protein.
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Inducible expression of an hsp68-lacZ hybrid gene in transgenic mice
R. Kothary;S. Clapoff;S. Darling;M.D. Perry.
Correction: Corrigendum: Establishment of a cone photoreceptor transplantation platform based on a novel cone-GFP reporter mouse line
Sheila Smiley;Philip E. Nickerson;Lacrimioara Comanita;Narsis Daftarian.
Scientific Reports (2016)
A SEQUENCE MOTIF FOUND IN A DROSOPHILA HETEROCHROMATIN PROTEIN IS CONSERVED IN ANIMALS AND PLANTS
P B Singh;J R Miller;J Pearce;R Kothary.
Nucleic Acids Research (1991)
The mouse dystonia musculorum gene is a neural isoform of bullous pemphigoid antigen 1.
Arthur Brown;Gilbert Bernier;Martine Mathieu;Janet Rossant;Janet Rossant.
Nature Genetics (1995)
The Splotch mutation interferes with muscle development in the limbs
T. Franz;R. Kothary;M. A. H. Surani;Z. Halata.
Anatomy and Embryology (1993)
A transgene containing lacZ inserted into the dystonia locus is expressed in neural tube
R. Kothary;S. Clapoff;A. Brown;R. Campbell.
Chx10 repression of Mitf is required for the maintenance of mammalian neuroretinal identity
D. Jonathan Horsford;Minh-Thanh T. Nguyen;Grant C. Sellar;Rashmi Kothary.
Genome imprinting and development in the mouse
M A Surani;R Kothary;N D Allen;P B Singh.
MEF2 is upregulated during cardiac hypertrophy and is required for normal post-natal growth of the myocardium.
Steven M. Kolodziejczyk;Ling Wang;Kim Balazsi;Yves DeRepentigny.
Current Biology (1999)
Rho-kinase inactivation prolongs survival of an intermediate SMA mouse model
Mélissa Bowerman;Ariane Beauvais;Ariane Beauvais;Carrie L. Anderson;Carrie L. Anderson;Rashmi Kothary.
Human Molecular Genetics (2010)
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