A
Anju Chadha
Researcher at Indian Institute of Technology Madras
Publications - 140
Citations - 3089
Anju Chadha is an academic researcher from Indian Institute of Technology Madras. The author has contributed to research in topics: Candida parapsilosis & Enantiomeric excess. The author has an hindex of 30, co-authored 135 publications receiving 2800 citations. Previous affiliations of Anju Chadha include Indian Institute of Science & National Institutes of Health.
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Biocatalytic deracemization of alkyl-2-hydroxy-4-arylbut-3-ynoates using whole cells of Candida parapsilosis ATCC 7330
Thangavel Saravanan,Anju Chadha +1 more
TL;DR: Racemic alkyl-2-hydroxy-4-arylbut-3-ynoates were deracemized to the (S)-alkyl- 2-Hydroxy- 4- Darylbut- 3-ynOates in excellent enantiomeric excesses and good isolated yields with the biocatalyst Candida parapsilosis ATCC 7330.
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Docosahexaenoic acid production by a novel high yielding strain of Thraustochytrium sp. of Indian origin: Isolation and bioprocess optimization studies
TL;DR: In this article, a high yielding strain from the mangroves of South India for the production of DHA resulted in a strain which showed promising yields of biomass and DHA.
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Cyclotides from the Indian Medicinal Plant Viola odorata (Banafsha): Identification and Characterization.
TL;DR: This study was undertaken to detect and identify known and new cyclotides in Viola odorata, a commercially important medicinal plant, from three geographical locations in India.
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Phospholipid stabilized gold nanorods: towards improved colloidal stability and biocompatibility.
TL;DR: A facile method for the efficient removal of CTAB molecules with 1,2-dimyristoyl-sn-glycero-3-phosphocholine (DMPC) phospholipid molecules, which are naturally present in cell membranes are reported and provide insights into the important factors to be considered while designing biocompatible GNRs suitable for applications in nanomedicine.
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Structures of covalent nucleoside adducts formed from adenine, guanine, and cytosine bases of DNA and the optically active bay-region 3,4-diol 1,2-epoxides of benz[a]anthracene
Albert M. Cheh,Anju Chadha,Jane M. Sayer,Herman J. C. Yeh,Haruhiko Yagi,Lewis K. Pannell,Donald M. Jerina +6 more
TL;DR: In this paper, the structure of the principal covalent adducts formed from DNA upon reaction in vitro with the four optically active 3,4-diol 1,2-epoxides of benz[a]anthracene have been elucidated at the nucleoside level.