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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CD25 targeted therapy of chemotherapy resistant leukemic stem cells using DR5 specific TRAIL peptide.
TL;DR: CD25 and DR5 specific targeting by IL2-TRAIL peptide may be an effective strategy for targeting drug resistant leukemic cells and LSCs.
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Enhancing the anti-cancer therapeutic efficacy by optimizing molecular weight of metal-free fully alternating semi-aromatic polyester as nano-drug carriers
Piyush Kumar Gupta,Santosh Gupta,Sreenath Pappuru,Siva Chander Chabattula,Debashis Chakraborty,Rama Shanker Verma +5 more
TL;DR: It is proved that poly(tBGE-alt-PA) copolymer of Mn = 9.2 kDa can be used further in the broader applications of drug delivery.
Journal Article
Absence of derepression of amino acids transport in Candida.
TL;DR: It appears that derepression of amino acids transport, a well known phenomenon in S. cerevisiae, may not exist in Candida species.
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Identification of novel target genes involved in Indian Fanconi anemia patients using microarray.
TL;DR: A gene expression profile of Fanconi anemia patients from the Indian population and a pool of genes that might aid in the acquisition and progression of the FA phenotype are reported for the first time.
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Targeting c-kit receptor in neuroblastomas and colorectal cancers using stem cell factor (SCF)-based recombinant bacterial toxins
Swati Choudhary,Alessa Pardo,Reinhard Rosinke,Janendra K. Batra,Stefan Barth,Stefan Barth,Rama Shanker Verma +6 more
TL;DR: This study demonstrates the role of stem cell factor (SCF)-based toxin conjugates for targeting WT-KIT-overexpressing malignancies such as NBs and CRCs and proves that these novel targeting agents have promising potential as KIT receptor tyrosine kinase targeting system.