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Page 1
EFHC1 mutation in Indian juvenile myoclonic epilepsy patient.
Thounaojam R, Langbang L, Itisham K, Sobhani R, Srivastava S, Ramanujam B, Verma R, Tripathi M, Aguan K. Thounaojam R, et al. Among authors: aguan k. Epilepsia Open. 2017 Feb 1;2(1):84-89. doi: 10.1002/epi4.12037. eCollection 2017 Mar. Epilepsia Open. 2017. PMID: 29750216 Free PMC article.
Mutations in EFHC1 cause juvenile myoclonic epilepsy.
Suzuki T, Delgado-Escueta AV, Aguan K, Alonso ME, Shi J, Hara Y, Nishida M, Numata T, Medina MT, Takeuchi T, Morita R, Bai D, Ganesh S, Sugimoto Y, Inazawa J, Bailey JN, Ochoa A, Jara-Prado A, Rasmussen A, Ramos-Peek J, Cordova S, Rubio-Donnadieu F, Inoue Y, Osawa M, Kaneko S, Oguni H, Mori Y, Yamakawa K. Suzuki T, et al. Among authors: aguan k. Nat Genet. 2004 Aug;36(8):842-9. doi: 10.1038/ng1393. Epub 2004 Jul 18. Nat Genet. 2004. PMID: 15258581
Complexation of turmeric and curcumin mediated silver nanoparticles with human serum albumin: Further investigation into the protein-corona formation, anti-bacterial effects and cell cytotoxicity studies.
Baruah K, Konthoujam I, Lyndem S, Aguan K, Singha Roy A. Baruah K, et al. Among authors: aguan k. Spectrochim Acta A Mol Biomol Spectrosc. 2023 Jun 5;294:122540. doi: 10.1016/j.saa.2023.122540. Epub 2023 Feb 21. Spectrochim Acta A Mol Biomol Spectrosc. 2023. PMID: 36848856
45 results