Vijaya Ramesh mainly focuses on Genetics, Tumor suppressor gene, Molecular biology, Carcinogenesis and Gene. Her research integrates issues of Merlin, Mutation, Ectoderm, Mesoderm and Gene targeting in her study of Tumor suppressor gene. The various areas that she examines in her Merlin study include Moesin, COS cells and Filopodia.
Her Carcinogenesis research includes themes of Cancer research and Neurofibromatosis. Her work is dedicated to discovering how Cancer research, TSC2 are connected with Cell cycle and other disciplines. Vijaya Ramesh has researched Exon in several fields, including Locus and Loss of heterozygosity.
Her main research concerns Genetics, Merlin, Molecular biology, Cell biology and Gene. Her Merlin research also works with subjects such as
Her Cell biology research incorporates themes from Moesin, Actin-binding protein, Actin cytoskeleton, Immunoprecipitation and Radixin. Her studies examine the connections between Moesin and genetics, as well as such issues in Actin, with regards to PDZ domain. Her Neurofibromatosis study combines topics from a wide range of disciplines, such as Carcinogenesis, Cancer research and Meningioma.
Cancer research, Schwannomatosis, mTORC1, Neurofibromatosis and Kinome are her primary areas of study. The concepts of her Cancer research study are interwoven with issues in Tuberous sclerosis, Genetic enhancement, Tumor suppressor gene and TSC2, PI3K/AKT/mTOR pathway. Her TSC2 study is concerned with the larger field of Genetics.
Particularly relevant to TSC1 is her body of work in Genetics. Her Neurofibromatosis type 2 study, which is part of a larger body of work in Neurofibromatosis, is frequently linked to Foundation, bridging the gap between disciplines. Her Neurofibromatosis type 2 research includes elements of Merlin and Clinical trial, Bioinformatics.
Her primary scientific interests are in TSC1, mTORC1, Cancer research, Kinome and TSC2. Her studies in TSC1 integrate themes in fields like Transcriptome, Ubiquitin ligase and RHEB. Her mTORC1 study contributes to a more complete understanding of Cell biology.
Her Cancer research research is multidisciplinary, relying on both mTORC2, Immediate early protein, Molecular biology, Signal transduction and Meningioma. Her research in Kinome intersects with topics in Proto-oncogene tyrosine-protein kinase Src, Receptor tyrosine kinase, Erythropoietin-producing hepatocellular receptor, Tumor suppressor gene and Tumor progression. Her study on TSC2 is covered under Genetics.
This overview was generated by a machine learning system which analysed the scientist’s body of work. If you have any feedback, you can contact us here.
Reversal of learning deficits in a Tsc2+/− mouse model of tuberous sclerosis
Dan Ehninger;Sangyeul Han;Carrie Shilyansky;Yu Zhou.
Nature Medicine (2008)
The FERM domain: A unique module involved in the linkage of cytoplasmic proteins to the membrane
Athar H. Chishti;Anthony C. Kim;Shirin M. Marfatia;Mohini Lutchman.
Trends in Biochemical Sciences (1998)
Analysis of the neurofibromatosis 2 gene reveals molecular variants of meningioma.
R. Wellenreuther;J. A. Kraus;D. Lenartz;A. G. Menon.
American Journal of Pathology (1995)
NHE-RF, a Regulatory Cofactor for Na+-H+Exchange, Is a Common Interactor for Merlin and ERM (MERM) Proteins
Anita Murthy;Charo Gonzalez-Agosti;Etchell Cordero;Denise Pinney.
Journal of Biological Chemistry (1998)
NF2/Merlin Is a Novel Negative Regulator of mTOR Complex 1, and Activation of mTORC1 Is Associated with Meningioma and Schwannoma Growth
Marianne James;S Han;Carolyn Polizzano;Scott Randall Plotkin.
Molecular and Cellular Biology (2009)
Mutations in transcript isoforms of the neurofibromatosis 2 gene in multiple human tumour types.
Bianchi Ab;Hara T;Ramesh;Gao J.
Nature Genetics (1994)
Association of Mammalian Trp4 and Phospholipase C Isozymes with a PDZ Domain-containing Protein, NHERF
Yufang Tang;Jisen Tang;Zhangguo Chen;Claudia Trost.
Journal of Biological Chemistry (2000)
Exon scanning for mutation of the NF2 gene in schwannomas
Lee B. Jacoby;Mia MacCollin;David N. Louls;Trina Mohney.
Human Molecular Genetics (1994)
The Nf2 tumor suppressor gene product is essential for extraembryonic development immediately prior to gastrulation.
A I McClatchey;I Saotome;V Ramesh;J F Gusella.
Genes & Development (1997)
Mutant torsinA, responsible for early-onset torsion dystonia, forms membrane inclusions in cultured neural cells
Jeffrey Hewett;Charo Gonzalez-Agosti;Damien Slater;Philipp Ziefer.
Human Molecular Genetics (2000)
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