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Maternal vitamin B12 deficiency in rats alters DNA methylation in metabolically important genes in their offspring.
Tanwar VS, Ghosh S, Sati S, Ghose S, Kaur L, Kumar KA, Shamsudheen KV, Patowary A, Singh M, Jyothi V, Kommineni P, Sivasubbu S, Scaria V, Raghunath M, Mishra R, Chandak GR, Sengupta S. Tanwar VS, et al. Among authors: shamsudheen kv. Mol Cell Biochem. 2020 May;468(1-2):83-96. doi: 10.1007/s11010-020-03713-x. Epub 2020 Mar 18. Mol Cell Biochem. 2020. PMID: 32189172
LncRNA VEAL2 regulates PRKCB2 to modulate endothelial permeability in diabetic retinopathy.
Sehgal P, Mathew S, Sivadas A, Ray A, Tanwar J, Vishwakarma S, Ranjan G, Shamsudheen KV, Bhoyar RC, Pateria A, Leonard E, Lalwani M, Vats A, Pappuru RR, Tyagi M, Jakati S, Sengupta S, B K B, Chakrabarti S, Kaur I, Motiani RK, Scaria V, Sivasubbu S. Sehgal P, et al. Among authors: shamsudheen kv. EMBO J. 2021 Aug 2;40(15):e107134. doi: 10.15252/embj.2020107134. Epub 2021 Jun 28. EMBO J. 2021. PMID: 34180064 Free PMC article.
Investigating Coronary Artery Disease methylome through targeted bisulfite sequencing.
Ghose S, Ghosh S, Tanwar VS, Tolani P, Kutum R, Sharma A, Bhardwaj N, Shamsudheen KV, Verma A, Jayarajan R, Dash D, Sivasubbu S, Scaria V, Seth S, Sengupta S. Ghose S, et al. Among authors: shamsudheen kv. Gene. 2019 Dec 30;721:144107. doi: 10.1016/j.gene.2019.144107. Epub 2019 Sep 6. Gene. 2019. PMID: 31499127
Autosomal recessive epidermolysis bullosa simplex: report of three cases from India.
Yenamandra VK, Shamsudheen KV, Madhumita RC, Rijith J, Ankit V, Scaria V, Sridhar S, Kabra M, Sharma VK, Sethuraman G. Yenamandra VK, et al. Among authors: shamsudheen kv. Clin Exp Dermatol. 2017 Oct;42(7):800-803. doi: 10.1111/ced.13182. Clin Exp Dermatol. 2017. PMID: 28925504 No abstract available.
14 results