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Whole-exome analyses of congenital muscular dystrophy and congenital myopathy patients from India reveal a wide spectrum of known and novel mutations.
Sanga S, Ghosh A, Kumar K, Polavarapu K, Preethish-Kumar V, Vengalil S, Nashi S, Bardhan M, Arunachal G, Raju S, Gayathri N, Biswas NK, Chakrabarti S, Nalini A, Roy S, Acharya M. Sanga S, et al. Among authors: chakrabarti s. Eur J Neurol. 2021 Mar;28(3):992-1003. doi: 10.1111/ene.14616. Epub 2020 Nov 26. Eur J Neurol. 2021. PMID: 33124102
KLK5 induces shedding of DPP4 from circulatory Th17 cells in type 2 diabetes.
Nargis T, Kumar K, Ghosh AR, Sharma A, Rudra D, Sen D, Chakrabarti S, Mukhopadhyay S, Ganguly D, Chakrabarti P. Nargis T, et al. Among authors: chakrabarti p, chakrabarti s. Mol Metab. 2017 Nov;6(11):1529-1539. doi: 10.1016/j.molmet.2017.09.004. Epub 2017 Sep 27. Mol Metab. 2017. PMID: 29107298 Free PMC article.
Analysis of Pan-omics Data in Human Interactome Network (APODHIN).
Biswas N, Kumar K, Bose S, Bera R, Chakrabarti S. Biswas N, et al. Among authors: chakrabarti s. Front Genet. 2020 Dec 8;11:589231. doi: 10.3389/fgene.2020.589231. eCollection 2020. Front Genet. 2020. PMID: 33363571 Free PMC article.
Variability in the Responses of Hepatitis B Virus D-Subgenotypes to Antiviral Therapy: Designing Pan-D-Subgenotypic Reverse Transcriptase Inhibitors.
Khatun M, Kumar K, Baidya A, Mondal RK, Baszczyňski O, Kalčic F, Banerjee S, Dhali GK, Das K, Chowdhury A, Janeba Z, Chakrabarti S, Datta S. Khatun M, et al. Among authors: chakrabarti s. J Virol. 2022 Jan 26;96(2):e0180021. doi: 10.1128/JVI.01800-21. Epub 2021 Nov 3. J Virol. 2022. PMID: 34730399 Free PMC article.
2,296 results