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Rakesh K. Jain

Researcher at Harvard University

Publications -  1528
Citations -  198912

Rakesh K. Jain is an academic researcher from Harvard University. The author has contributed to research in topics: Angiogenesis & Cancer. The author has an hindex of 200, co-authored 1467 publications receiving 177727 citations. Previous affiliations of Rakesh K. Jain include Government Medical College, Thiruvananthapuram & University of Oslo.

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Hepatic granulomas due to visceral larva migrans in adults: appearance on US and MRI.

TL;DR: Three adult patients with hepatic lesions which on histopathology demonstrated characteristic granulomas of visceral larva migrans are described.
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Dynamics of cancer cell interactions with microvasculature and interstitium

TL;DR: Interactions of cancer cells with the microvasculature and the interstitium of non-malignant tissue were studied in a rabbit ear chamber preparation using intravital fluorescent microscopy and implantation of VX2 carcinoma cells in the interstitial space led to increases in theinterstitial diffusion coefficients and the microvascular permeability.
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Genetics of Thrips palmi (Thysanoptera: Thripidae)

TL;DR: Genetics of T. palmi genes will assist elucidation of thrips identification, means of adaptation in diverse ecological niches, mechanisms of insecticide resistance, and transmission of plant viruses, as well as assist in integrated thrips management.
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Synthesis of α-d-galactopyranosyl-linked oligosaccharides containing the α-Gal → β-Gal → GlcNAc sequence employing methyl-2,3,4,6-tetra-O-(4-methoxybenzyl)-1-thio- β-d-galactopyranoside as an efficient glycosyl donor☆

TL;DR: In this paper, the synthesis of two trisaccharides and a tetrasaccharide using a key α- galactosyl donor, methyl 2,3,4,6-tetra-O-(4-methoxybenzyl)-1-thio-β- d - galactopyranoside (1).
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Cellular Membrane Permeability of Anthracyclines Does Not Correlate with Their Delivery in a Tissue-isolated Tumor

TL;DR: The observed similarities in clearance of the anthracyclines was largely explained by differences in their protein binding and tissue diffusion gradients.