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Shilpee Dutt

Researcher at Homi Bhabha National Institute

Publications -  54
Citations -  2506

Shilpee Dutt is an academic researcher from Homi Bhabha National Institute. The author has contributed to research in topics: Medicine & Cancer research. The author has an hindex of 19, co-authored 46 publications receiving 2204 citations. Previous affiliations of Shilpee Dutt include University of Manchester & University of Zurich.

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Microscopic activity in ulcerative colitis: what does it mean?

TL;DR: The presence of a chronic inflammatory cell infiltrate or crypt architectural irregularities bore no relation to the frequency of colitis relapse and relapse rates were higher in the presence of crypt abscesses, mucin depletion, and breaches in the surface epithelium.
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Haploinsufficiency for ribosomal protein genes causes selective activation of p53 in human erythroid progenitor cells

TL;DR: The findings indicate that the erythroid lineage has a low threshold for the induction of p53, providing a basis for the failure of erythropoiesis in the 5q-syndrome, DBA, and perhaps other bone marrow failure syndromes.
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The AID antibody diversification enzyme is regulated by protein kinase A phosphorylation

TL;DR: AID from non-lymphoid cells can be functionally phosphorylated by recombinant PKA to allow interaction with RPA and promote deamination of transcribed dsDNA substrates, and PKA has a critical role in post-translational regulation of AID activity in B cells.
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Comparison of delayed release 5 aminosalicylic acid (mesalazine) and sulphasalazine in the treatment of mild to moderate ulcerative colitis relapse.

TL;DR: In this paper, the authors compared sulphasalazine, low dose mesalazine and high dose mesaline in the treatment of mild to moderate relapse of ulcerative colitis.
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Comparison of delayed-release 5-aminosalicylic acid (mesalazine) and sulfasalazine as maintenance treatment for patients with ulcerative colitis

TL;DR: Delayed-release mesalazine is an effective treatment for maintaining ulcerative colitis remission and is associated with fewer side effects than equivalent doses of enteric-coated sulfasalazine.