R
Rama Shanker Verma
Researcher at Indian Institute of Technology Madras
Publications - 167
Citations - 3945
Rama Shanker Verma is an academic researcher from Indian Institute of Technology Madras. The author has contributed to research in topics: Stem cell & Mesenchymal stem cell. The author has an hindex of 30, co-authored 159 publications receiving 3160 citations. Previous affiliations of Rama Shanker Verma include University of Pennsylvania & Thapar University.
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Organotypic cancer tissue models for drug screening: 3D constructs, bioprinting and microfluidic chips.
TL;DR: This review projects the progress toward biomimetic tissue model development, highlighting the emergence of bioprinting and microfluidic technology in in vitro cancer drug screening and pertaining challenges.
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Effect of perturbation of specific folate receptors during in vitro erythropoiesis.
TL;DR: Data support the conclusion that folate receptors on marrow cells provide an important function in the cellular uptake of folates during in vitro erythropoiesis and play a pivotal role in the differentiation and proliferation of erythroid progenitor cells.
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Evaluation of platelet lysate as a substitute for FBS in explant and enzymatic isolation methods of human umbilical cord MSCs
Sangeetha Kandoi,Praveen Kumar L,Bamadeb Patra,Prasanna Vidyasekar,Divya Sivanesan,S. Vijayalakshmi,Kalyanaraman Rajagopal,Rama Shanker Verma +7 more
TL;DR: Platelet lysate from expired platelets is a viable alternative to FBS for generating clinically relevant numbers of MSC from explant cultures over enzymatic method and shows typical immunophenotype, plasticity, immunomodulatory property and chromosomal stability.
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Role of protein tyrosine phosphorylation in H2O2-induced activation of endothelial cell phospholipase D.
TL;DR: Results suggest that tyrosine kinase activation may be involved in H2O2-induced PLD activation in vascular endothelial cells.
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Cardiomyocyte culture - an update on the in vitro cardiovascular model and future challenges.
TL;DR: This review discusses the use of freshly isolated murine cardiomyocytes andCardiomyocyte alternatives for use in cardiac disease models and other related studies.